WO2015062596A1 - Hair treatment agent containing l-carnitine or an l-carnitine derivative and an oligopeptide containing the sequence glu-glu-glu - Google Patents
Hair treatment agent containing l-carnitine or an l-carnitine derivative and an oligopeptide containing the sequence glu-glu-glu Download PDFInfo
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- WO2015062596A1 WO2015062596A1 PCT/DE2014/200477 DE2014200477W WO2015062596A1 WO 2015062596 A1 WO2015062596 A1 WO 2015062596A1 DE 2014200477 W DE2014200477 W DE 2014200477W WO 2015062596 A1 WO2015062596 A1 WO 2015062596A1
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- 0 CCCC(*(NC(CCC(O)=O)C(NC(C(C)CC)C(NC(CCCNC(N)=[N+])C(NC(C(C)C)C(NC(CC(C)C)C(O)=O)=O)=O)=O)=O)=O)NC(C(CCC(O)=O)NC(C(CC(C)=CC=C)N)=O)=O Chemical compound CCCC(*(NC(CCC(O)=O)C(NC(C(C)CC)C(NC(CCCNC(N)=[N+])C(NC(C(C)C)C(NC(CC(C)C)C(O)=O)=O)=O)=O)=O)=O)NC(C(CCC(O)=O)NC(C(CC(C)=CC=C)N)=O)=O 0.000 description 1
- CCLKILWPWYDIQD-UHFFFAOYSA-N COC(CCC(C(NC(CCC(O)=O)C(NC(CCC(O)=O)C(O)=O)=O)=O)N)O Chemical compound COC(CCC(C(NC(CCC(O)=O)C(NC(CCC(O)=O)C(O)=O)=O)=O)N)O CCLKILWPWYDIQD-UHFFFAOYSA-N 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q7/00—Preparations for affecting hair growth
Definitions
- the invention relates to the use of hair treatment compositions with certain ingredients to promote or enhance the hair growth and / or reduce hair loss and / or activation of the hair root cells and / or activation of hair follicles and / or thickening of the hair.
- hair loss is thus meant the permanent hair loss, in which the failed hair again very late, usually getting thinner or not at all, regrow.
- Hair loss is a widespread cosmetic problem for both men and women and can be psychologically stressful. In men, it is mainly characterized by a receding hairline on the forehead and decreasing hair density in the vertex area. In women, there is usually a general reduction in hair density over the entire head.
- Hair loss occurs when, due to various causes, the so-called hair cycle is disturbed.
- the hair cycle the hair usually regenerates itself.
- a growth phase in which about 80-90% of the hair is and takes between 2 and 6 years, follows the so-called regression phase (catagen, about 3-6 weeks), in the metabolic processes in the hair root be reduced.
- about 2% of the hair is usually in this resting phase.
- this phase forms the transition between the anagen phase and the telogen phase.
- the Telogen phase which is constantly about 10-20% of the hair, is the resting phase (duration about 3 months), after which the hair fails and a new growth phase begins in this follicle. With increased hair loss, it can be e.g. An increase in telogen, and a shortening of the anagen phase, so that the proportion of failing hair increases without being replaced by new, beginning the growth phase.
- HGF and KGF are important growth factors that are released by the dermal papilla to control the proliferation of hair keratinocytes. In a potentially growth-promoting and hair-strengthening substance, these parameters should be influenced in any case.
- the treatment of thin hair is a consumer need.
- conventional structurally improving and smoothing molecules can complain the hair and lead to a "over-care"
- Improving the hair structure from the root, the production site for hair-building keratins, is an efficient and sustainable method of treating thin hair.
- the object of the present invention was to provide agents that promote or enhance hair growth and reduce hair loss and activate the hair root cells and / or hair follicles. Thickening the hair was another object of the present invention.
- agents which contain at least one compound selected from L-carnitine and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine citrate, lauroyl-L-carnitine and L.
- amino group is free or protonated and the carboxy groups may be free or deprotonated.
- the present invention therefore relates to the use of a hair treatment composition containing
- amino group may be free or protonated and the carboxy groups may be free or deprotonated
- Hair treatment compositions in the context of the present invention are, for example, hair shampoos, hair conditioners, conditioning shampoos, hairsprays, hair conditioners, hair conditioners, hair wraps, hair tonics, perming solutions, hair dye shampoos, hair dyes, hair fixatives, hair dressings, hairstyling preparations, hair lotions, mousses, hair gels , Hair waxes or their combinations.
- means according to the invention are preferably agents which the man applies anyway.
- Preferred agents according to the invention are therefore shampoos, conditioners or hair tonics.
- the hair treatment agents used according to the invention are capable of positively influencing hair growth by repressing or reducing specific inhibiting hair-specific genes.
- the repression or reduction of the inhibiting genes causes the hair root can be reactivated.
- the hair structure is already influenced on the hair roots, so that the hair can grow strong and healthy and thicker.
- the hair is positively influenced in its growth and metabolism by the application of said agents.
- the hair treatment compositions used according to the invention contain as essential ingredient at least one compound selected from L-carnitine and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine citrate, lauroyl L-carnitine and L-carnitine tartrate ,
- the agents used according to the invention may contain L-carnitine and / or an L-carnitine derivative or else a plurality of different L-carnitine derivatives.
- L-carnitine or L-carnitine derivatives are contained in the compositions according to the invention preferably in amounts of 0.001 to 10 wt .-%, based on the total preparation. Levels of 0.1 to 10 wt .-% are particularly preferred, amounts of 0.1 to 5 wt .-% are particularly preferred, and amounts of 1 to 3 wt .-% are very particularly preferred.
- Particularly preferred hair treatment agents used according to the invention are characterized in that they are 0.0005 to 7.5 wt .-%, preferably 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4 wt % and in particular 0.1 to 3 wt .-% of at least one compound selected from L-carnitine, and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine citrate, lauroyl Carnitine and in particular L-carnitine tartrate included.
- Hair treatment agents preferably used according to the invention contain from 0.0001 to 10% by weight of at least one compound selected from L-carnitine, and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine citrate, lauroyl- Carnitine and in particular L-carnitine tartrate.
- the hair treatment agent - based on its weight - 0.0005 to 7.5 wt .-%, preferably 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4% by weight and in particular 0.1 to 3% by weight of at least one compound selected from L-carnitine, and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine Citrate, lauroyl-L-carnitine and especially L-carnitine tartrate.
- the hair treatment compositions used according to the invention contain as further essential ingredient at least one oligopeptide containing at least one amino acid sequence Glu-Glu-Glu
- amino group may be free or protonated and the carboxy groups may be free or deprotonated.
- the hair treatment composition contains, based on its weight, 0.0001 to 10% by weight of at least one oligopeptide containing at least one amino acid sequence Glu-Glu-Glu
- amino group may be free or protonated and the carboxy groups may be free or deprotonated
- the parenthetized hydrogen atom of the amino group, as well as the parenthetical group of the acid function means that the groups concerned may be present as such (then an oligopeptide having the relevant number of amino acids as shown (in the above) Formula 3) or that the amino acid sequence is present in an oligopeptide, which also comprises other amino acids - depending on where the other amino acid (s) is / are bound, the parenthetical components of the above formula by the / the other Replaced amino acid residue (s).
- compositions according to the invention contain - based on their weight - 0.0001 to 10 wt .-% of at least one oligopeptide having at least one amino acid residue Glu-Glu-Glu, ie at least three consecutive glutamic acids.
- Oligopeptides in the sense of the present application are acid amide-like linked condensation products of amino acids which comprise at least 3 and at most 25 amino acids by peptide bonds
- the oligopeptide comprises 5 to 15 amino acids, preferably 6 to 13 amino acids, particularly preferably 7 to 12 amino acids and in particular 8, 9 or 10 amino acids.
- the molecular weight of the oligopeptide contained in the agents used according to the invention may vary.
- Preferred hair treatment agents used according to the invention are characterized in that the oligopeptide has a molecular weight of from 650 to 3000 Da, preferably from 750 to 2500 Da, particularly preferably from 850 to 2000 Da and in particular from 1000 to 1600 Da.
- the oligopeptide comprises 5 to 15 amino acids, preferably 6 to 13 amino acids, more preferably 7 to 12 amino acids and especially 8, 9 or 10 amino acids and a molecular weight of 650 to 3000 Da, preferably 750 to 2500 Since, more preferably from 850 to 2000 Da and in particular from 1000 to 1600 Da has.
- oligopeptides which do not consist solely of the three glutamic acids but have further amino acids bound to this sequence.
- These other amino acids are preferably selected from certain amino acids, while certain other representatives are less preferred in the present invention.
- oligopeptides used in the agents used according to the invention contain no methionine.
- oligopeptides used in the agents used according to the invention do not contain cysteine and / or cystine.
- oligopeptides used in the agents used according to the invention contain no aspartic acid and / or asparagine.
- oligopeptides used in the agents used according to the invention do not contain serine and / or threonine.
- oligopeptides used in the agents used according to the invention contain tyrosine.
- oligopeptides used in the agents according to the invention contain leucine.
- the oligopeptides used in the agents used according to the invention contain isoleucine. It is further preferred if the oligopeptides used in the agents used according to the invention contain arginine.
- oligopeptides used in the agents according to the invention contain valine.
- oligopeptides or amino acid sequences contained in the preferred oligopeptides are described below:
- a particularly preferred oligopeptide additionally contains tyrosine, which is preferably linked via its acid function to the Glu-Glu-Glu sequence.
- Hair treatment compositions which are preferred according to the invention are therefore characterized in that the oligopeptide contained in them has at least one amino acid sequence Tyr-Glu-Glu-Glu, where the amino group may be free or protonated and the carboxy groups may be free or deprotonated.
- Another particularly preferred oligopeptide additionally contains isoleucine, which is preferably linked to the Glu-Glu-Glu sequence via its amino function.
- Hair treatment agents which are preferred according to the invention are therefore characterized in that the oligopeptide contained in them has at least one amino acid sequence Glu-Glu-Glu-Ile, wherein the amino group can be free or protonated and the carboxy groups can be free or deprotonated.
- Oligopeptides which have both the abovementioned amino acids (tyrosine and isoleucine) are preferred according to the invention. Particular preference is given to uses according to the invention in which the oligopeptide contained in the hair treatment agent has at least one amino acid sequence Tyr-Glu-Glu-Glu-Ile, where the amino group may be free or protonated and the carboxy groups may be free or deprotonated.
- oligopeptides additionally contain arginine, which is preferably bound to isoleucine
- the oligopeptide contained in the hair treatment agent has at least one amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg, wherein the amino groups may be free or protonated and the carboxy groups may be free or deprotonated.
- Still further preferred oligopeptides additionally contain valine, which is preferably bound to the arginine.
- the oligopeptide contained in the hair treatment agent has at least one amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val, wherein the amino groups are free or protonated and the carboxy groups are free or deprotonated can.
- Still further preferred oligopeptides additionally contain leucine, which is preferably bound to the valine.
- the oligopeptide contained in the hair treatment agent has at least one amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu, wherein the amino groups are free or protonated and the carboxy groups may be present freely or deprotonated.
- oligopeptides additionally contain leucine, which is preferably bound to the tyrosine.
- the oligopeptide contained in the hair treatment agent has at least one amino acid sequence Leu-Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu, wherein the amino groups are free or protonated and the carboxy groups may be free or deprotonated.
- agents used according to the invention comprise at least two oligopeptides which satisfy the abovementioned criteria but which differ from one another.
- Such mutually different oligopeptides A and B correspond to each other in that they carry three consecutive Glu amino acids in their amino acid sequence, but have differences in the upstream or downstream amino acids. Preference is given to mutually different peptides with partial agreement, which may well be greater than in the above-mentioned three amino acids.
- the hair treatment composition contains at least two mutually different oligopetides A and B, both of which contain the amino acid sequence Glu-Glu-Glu-Ile.
- hair treatment compositions containing at least two mutually different oligopetides A and B, both containing the amino acid sequence Tyr-Glu-Glu-Glu.
- Hair treatment agent contains at least two mutually different oligopeptides A and B, both of which contain the amino acid sequence Glu-Glu-Glu-Ile-Arg.
- Hair treatment agent contains at least two mutually different oligopeptides A and B, both of which contain the amino acid sequence Tyr-Glu-Glu-Glu-Ile.
- Oligopeptid has at least one amino acid sequence Tyr-Glu-Glu-Glu-Ile, wherein the
- Amino group is free or protonated and the carboxy groups may be free or deprotonated.
- hair treatment agent at least two mutually different oligopeptides A and B. Both contain the amino acid sequence Glu-Glu-Glu-Ile-Arg.
- the hair treatment agent contains at least two mutually different oligopeptides A and B, both containing the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg.
- the hair treatment compositions contain at least two distinct oligopetides A and B both containing the amino acid sequence Glu-Glu-Glu-Ile-Arg-Val are further preferred embodiments of the present invention. Also preferred embodiments are uses in which the hair treatment agents contain at least two mutually different oligopetides A and B, both containing the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val.
- hair treatment agents contain at least two mutually different oligopetides A and B, both containing the amino acid sequence Glu-Glu-Glu-Ile-Arg-Val-Leu.
- hair treatment agents contain at least two mutually different oligopetides A and B, both containing the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu.
- the oligopeptide has at least one amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu, where the amino groups may be free or protonated and the carboxy groups may be free or deprotonated,
- the hair treatment compositions contain at least two mutually different oligopetides A and B, the oligopeptide A having the amino acid sequence Leu-Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu, where the amino- Groups may be free or protonated and the carboxy groups may be free or deprotonated
- the oligopeptide B has the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu, wherein the amino groups may be free or protonated and the carboxy groups may be free or deprotonated.
- the hair treatment compositions contain, based on the weight of the composition, from 0.00001 to 1% by weight of oligopeptide A and from 0.00001 to 1% by weight of oligopeptide B.
- the hair treatment compositions contain, based on the weight of the composition, from 0.00005 to 0.1% by weight of oligopeptide A and from 0.00005 to 0.1% by weight of oligopeptide B.
- the hair treatment agents - based on the weight of the composition - 0.0001 to 0.01 wt .-% oligopeptide A and 0.0001 to 0.001 wt .-% oligopeptide B.
- oligopeptides used in the context of the present invention which satisfy the abovementioned conditions, can advantageously be obtained from keratinic materials. It is preferred according to the invention that these oligopeptides are used in high proportions, based on the total keratinic peptide content of the agents. It is very particularly preferred that the highest possible proportion of all the keratinic peptides contained in the agent used according to the invention satisfies the conditions mentioned above.
- Preferred hair treatment agents used according to the invention are characterized in that at least 0.1% by weight, preferably at least 0.5% by weight, more preferably at least 1% by weight, more preferably at least 2.5% by weight, still further preferably at least 5% by weight and in particular at least 10% by weight of all the keratinic peptides contained in the middle have the amino acid sequence Glu-Glu-Glu.
- Further preferred hair treatment agents used according to the invention are characterized in that at least 0.1 wt .-%, preferably at least 0.5 wt .-%, more preferably at least 1 wt .-%, more preferably at least 2.5 wt .-%, still more preferably at least 5% by weight, and in particular at least 10% by weight, of all the keratinic peptides contained in the middle have the amino acid sequence Glu-Glu-Glu-Ile.
- Further preferred hair treatment agents used according to the invention are characterized in that at least 0.1% by weight, preferably at least 0.5% by weight, more preferably at least 1% by weight, more preferably at least 2.5% by weight, even more preferably at least 5% by weight, and in particular at least 10% by weight, of all the keratinic peptides contained in the middle have the amino acid sequence Tyr-Glu-Glu-Glu.
- Particularly preferred hair treatment agents used according to the invention are characterized in that at least 0.1 wt .-%, preferably at least 0.5 wt .-%, more preferably at least 1 wt .-%, more preferably at least 2.5 wt .-%, still more preferably at least 5% by weight and in particular at least 10% by weight of all the keratinic peptides contained in the middle have the amino acid sequence Tyr-Glu-Glu-Glu-Ile.
- Very particularly preferred hair treatment agents used according to the invention are characterized in that at least 0.1% by weight, preferably at least 0.5% by weight, particularly preferably at least 1% by weight, more preferably at least 2.5% by weight, even more preferably at least 5% by weight, and in particular at least 10% by weight, of all the keratinic peptides contained in the composition have the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg.
- Still further preferred hair treatment agents used according to the invention are characterized characterized in that at least 0.1% by weight, preferably at least 0.5% by weight, more preferably at least 1% by weight, more preferably at least 2.5% by weight, even more preferably at least 5% by weight. % and in particular at least 10 wt .-% of all keratinic peptides contained in the middle have the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val.
- Particularly preferred hair treatment agents used according to the invention are characterized in that at least 0.1% by weight, preferably at least 0.5% by weight, more preferably at least 1% by weight, more preferably at least 2.5% by weight, still more preferably at least 5% by weight, and in particular at least 10% by weight, of all the keratinic peptides contained in the middle have the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu.
- the above conditions relate to the total content of the agents used according to the invention to peptides derived from keratinic materials.
- oligopeptides of keratinic origin of course, other peptides and / or protenihydrolysates can be used, for example from other native sources.
- wheat protein hydrolysates is preferred, see below. It has been found that the combination of two active substances in the hair treatment compositions used according to the invention can be successfully supplemented by a third active substance, whereby the promotion or enhancement of hair growth, the reduction of hair loss, the activation of the hair root cells, the activation of hair follicles and the thickening of the hair can be further enhanced.
- the hair treatment composition contains at least one extract of Pisum sativium.
- Preferred agents used according to the invention are characterized in that they contain - based on their weight - 0.0005 to 7.5 wt .-%, preferably 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4 wt .-% and in particular 0, 1 to 3 wt .-% of at least one extract of Pisum sativium included.
- the hair treatment agent - based on its weight - 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4 wt .-% and in particular 0, 1 contains up to 3 wt .-% of at least one extract of Pisum sativium.
- the positive properties of the agents used according to the invention can be increased still further, in particular with regard to the positive effects on the hair roots and the inner structural strengthening of the keratin fibers, if the agents used according to the invention contain purine or purine derivatives.
- Preferred uses according to the invention are characterized in that the Hair treatment agent - based on its weight - 0.0005 to 7.5 wt .-%, preferably 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4 wt .-% and in particular 0.1 to 3 wt .-% purine and / or purine derivative (s) of the formula (I)
- radicals R 1 , R 2 and R 3 are independently selected from -H, - OH, -NH 2, -SH and the radicals R 4 , R 5 and R 6 are independently selected from -H, -CH 3 and -CH 2 -CH 3 , with the following compounds being preferred:
- Preferred agents used according to the invention contain purine and / or purine derivatives in narrower ranges.
- Cosmetic compositions preferably used according to the invention are characterized in that they contain, based on their weight, from 0.001 to 2.5% by weight, preferably from 0.0025 to 1% by weight, particularly preferably from 0.005 to 0.5% by weight. and in particular from 0.01 to 0.1% by weight of purine (s) and / or purine derivative (s).
- Caffeine has proved particularly useful in hair cosmetic formulations, for example in shampoos and conditioners, preferably in amounts of from 0.005 to 0.25% by weight, more preferably from 0.01 to 0.1% by weight and in particular from 0.01 to 0.05 wt .-% (in each case based on the agent) can be used.
- Hair-treatment compositions preferably used according to the invention contain - in each case based on their weight
- oligopeptide (s) having the amino acid sequence preferably 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4 wt .-% and in particular 0.1 to 3 wt .-% of at least one compound selected from L-carnitine, and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine citrate, lauroyl-L-carnitine and in particular L-carnitine tartrate; - 0.0002 to 5 wt .-%, preferably 0.0005 to 2.5 wt .-%, more preferably 0.00075 to 1 wt .-%, particularly preferably 0.001 to 0.5 wt .-%, more preferably 0.002 to 0.25 wt .-% and in particular 0.005 to 0.1 wt .-% oligopeptide (s) having the amino acid sequence
- 0.001 to 2.5 wt .-% preferably 0.0025 to 1 wt .-%, particularly preferably 0.005 to 0.5 wt .-% and in particular 0.01 to 0.1 wt .-% caffeine.
- Hair treatment agents used particularly preferably according to the invention contain - in each case based on their weight
- oligopeptide (s) having the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val wherein the amino groups are free or protonated and the Carboxy groups may be free or deprotonated,
- 0.001 to 2.5 wt .-% preferably 0.0025 to 1 wt .-%, particularly preferably 0.005 to 0.5 wt .-% and in particular 0.01 to 0, 1 wt .-% caffeine.
- the agents used in the invention may contain other active ingredients and adjuvants. These are described below.
- the agents used according to the invention preferably additionally comprise at least one emulsifier or a surfactant, surface-active substances being referred to as surfactants or as emulsifiers, depending on the field of use, and selected from anionic, cationic, zwitterionic, ampholytic and nonionic surfactants and emulsifiers.
- Preferred uses according to the invention are characterized in that the hair treatment agent - based on its weight - 0.5 to 70 wt .-%, preferably 1 to 60 wt .-%, more preferably 2.5 to 35 wt .-% and in particular 5 to 25% by weight of anionic and / or nonionic and / or cationic and / or amphoteric surfactant (s).
- Suitable anionic surfactants and emulsifiers for the compositions used according to the invention are all anionic surfactants suitable for use on the human body. These are characterized by a water-solubilizing, anionic group such as.
- Example a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group having about 8 to 30 carbon atoms.
- glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups may be present in the molecule.
- suitable anionic surfactants and emulsifiers are, in each case in the form of the sodium, potassium and ammonium as well as mono-, di- and trialkanolammonium salts having 2 to 4 C atoms in the alkanol group,
- Alpha-sulfofatty acid methyl esters of fatty acids having 8 to 30 carbon atoms are alpha-sulfofatty acids having 8 to 30 carbon atoms.
- R 1 CO is a linear or branched acyl radical having 6 to 22 carbon atoms and 0, 1, 2 or 3 double bonds and X is hydrogen, an alkali and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium, for example acylglutamates, which are derived from fatty acids having 6 to 22, preferably 12 to 18 carbon atoms, such as, for example, C 12/14 or C 12/18 coconut fatty acid, lauric acid, myristic acid, palmitic acid and / or stearic acid, in particular sodium N-cocoyl and sodium N-stearoyl-L-glutamate,
- Sulfosuccinic acid mono- and dialkyl esters having 8 to 24 C atoms in the alkyl group and sulfosuccinic monoalkylpolyoxyethyl esters having 8 to 24 C atoms in the alkyl group and 1 to 6 oxyethyl groups,
- R- alkyl sulfates and alkyl polyglycol ether sulfates of the formula R- (O-CH 2 -CH 2 ) x-OSO 3 H, in which R is a preferably linear alkyl group having 8 to 30 carbon atoms and x 0 or 1-12, esters of tartaric acid and Citric acid with alcohols which are adducts of about 2-15 molecules of ethylene oxide and / or propylene oxide onto C8-22 fatty alcohols, alkyl and / or alkenyl ether phosphates,
- Monoglyceride sulfates and monoglyceride ether sulfates Monoglyceride sulfates and monoglyceride ether sulfates.
- Preferred anionic surfactants and emulsifiers are acylglutamates, acyl isethionates, acyl sarcosinates and acyl taurates, each with a linear or branched acyl radical having 6 to 22 carbon atoms and 0, 1, 2 or 3 double bonds, which are particularly preferred Embodiments of an octanoyl, decanoyl, lauroyl, myristoyl, palmitoyl and stearoyl radical is selected, esters of tartaric acid, citric acid or succinic acid or the salts of these acids with alkylated glucose, in particular the products with the INCI name Disodium Coco Glucoside Citrate, Sodium Coco-Glucoside Tartrate and Disodium Coco-Glucoside Sulfosuccinates, alkyl polyglycol ether sulfates and ether carboxylic acids containing 8 to 18 carbon atoms in the alkyl group and up to 12 ethoxy groups in
- Zwitterionic surfactants and emulsifiers are those surface-active compounds which carry in the molecule at least one quaternary ammonium group and at least one -COO (_) or -SO 3 H group.
- Particularly suitable zwitterionic surfactants and emulsifiers are the so-called betaines, such as N-alkyl-N, N-dimethylammonium glycinates, for example cocoalkyldimethylammonium glycinate, N-acylaminopropyl- ⁇ , ⁇ -dimethylammonium glycinates, for example cocoacylaminopropyldimethylammonium glycinate, and 2-alkyl 3-carboxymethyl-3-hydroxyethylimidazolines having in each case 8 to 18 carbon atoms in the alkyl or acyl group, and also the cocoacylaminoethylhydroxyethylcarboxymethylglycinate.
- Ampholytic surfactants and emulsifiers are understood as meaning those surface-active compounds which, apart from a Ca-C2-alkyl or -acyl group, contain at least one free amino group and at least one -COOH or -SOsH group and are capable of forming internal salts.
- ampholytic surfactants are N-alkylglycines, N-alkylaminopropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids each having about 8 to 24 C atoms in the alkyl group.
- Particularly preferred ampholytic surfactants are N-cocoalkylaminopropionate, cocoacylaminoethylaminopropionate and C12-C18 acylsarcosine.
- Nonionic surfactants and emulsifiers contain as hydrophilic group z.
- a polyol group a polyalkylene glycol ether group or a combination of polyol and polyglycol ether group.
- Preferred nonionic surface-active substances are the alkylpolyglycosides, optionally mixed with fatty alcohols, alkoxylated polydialkylsiloxanes, alkylene oxide addition products of saturated linear fatty alcohols and fatty acids with in each case 2 to 30 moles of ethylene oxide per mole of fatty alcohol or fatty acid.
- cationic surfactants of the quaternary ammonium compound type are ammonium halides, in particular chlorides and bromides, such as alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkylmethylammonium chlorides.
- the long alkyl chains of these surfactants preferably have 10 to 18 carbon atoms, such as.
- cetyltrimethylammonium chloride stearyltrimethylammonium chloride, distearyldimethylammonium chloride, lauryldimethylammonium chloride, lauryldimethylbenzylammonium chloride and tricetylmethylammonium chloride.
- Further preferred cationic surfactants are the imidazolium compounds known under the INCI names Quaternium-27 and Quaternium-83.
- Very particularly preferred agents used according to the invention additionally comprise fatty alcohol (s) and / or fatty alcohol alkoxylate (s), preferably C 12-22 fatty alcohol (s) and / or C 12-22 fatty alcohol ethoxylate (s) with 10 to 30 EO units, especially preferably C16-18 fatty alcohol (s) and / or Ci6-ie fatty alcohol ethoxylate (s) having 12 to 20 EO units, preferably in amounts of 5 to 20 wt .-%, preferably from 7.5 to 17.5 wt .-% and in particular from 10 to 15 wt .-%, each based on the weight of the composition.
- hair treatment agents used according to the invention are preferred, which - based on their weight - 0.1 to 20 wt .-%, preferably 0.25 to 17.5 wt .-% and in particular 5 to 15 wt .-% anionic (s) surfactant (E), particularly preferably Fettal kholethersulfate the formula
- n represents values of from 5 to 21, preferably from 7 to 19, particularly preferably from 9 to 17 and in particular from 1 to 13 and k for values of 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10, preferably 1, 2 or 3 and especially 2
- M is a cation from the group Na + , K + NH 4 + , Vz Mg 2+ , 1 / Zn 2+ , preferably Na + , stand.
- Preferred hair-treatment agents used according to the invention are further characterized in that they additionally contain amphoteric surfactant (s), preferably from the groups of
- N-alkylglycines N-alkylpropionic acids, N-alkylaminobutyric acids, N-alkylimidodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids having in each case about 8 to 24 C atoms in the alkyl group, Alkylaminoacetic acids having in each case about 8 to 24 carbon atoms in the alkyl group, N-cocoalkylaminopropionate, cocoacylaminoethylaminopropionate, C 12 -C 18 -acylsarcosine, N-alkyl-N, N-dimethylammonium glycinates, for example cocoalkyldimethylammonium glycinate, N-acylaminopropyl -N, N-dimethylammonium gly
- Cationic or amphoteric polymers are to be understood as meaning polymers which have a group in the main and / or side chain which may be “temporary” or “permanent” cationic.
- "permanently cationic” refers to those polymers which have a cationic group, irrespective of the pH of the agent. These are usually polymers containing a quaternary nitrogen atom, for example in the form of an ammonium group.
- Preferred cationic groups are quaternary ammonium groups.
- those polymers in which the quaternary ammonium group is bonded via a C 1-4 hydrocarbon group to a polymer main chain constructed from acrylic acid, methacrylic acid or derivatives thereof have proven to be particularly suitable.
- the agents used in the invention may also contain amphoteric polymers. These additionally have at least one negatively charged group in the molecule and are also referred to as zwitterionic polymers.
- the polymer or polymers are used within narrower ranges.
- agents used according to the invention are preferred which, based on their weight, contain 0.05 to 7.5% by weight, preferably 0.1 to 5% by weight, particularly preferably 0.2 to 3.5% by weight. and in particular from 0.25 to 2.5% by weight of amphoteric polymer (s).
- amphoteric polymers are or are not included in the compositions
- further preferred agents used according to the invention are characterized in that they contain, based on their weight, from 0.05 to 7.5% by weight, preferably from 0.1 to 5% by weight .-%, particularly preferably 0.2 to 3.5 wt .-% and in particular 0.25 to 2.5 wt .-% cationic (s) polymer (s) included.
- Cationic polymers which can preferably be used according to the invention are described below: Homopolymers of the general formula (G1-I),
- R 1 is a methyl group
- R 2 , R 3 and R 4 are methyl groups
- m has the value 2.
- Suitable physiologically tolerated counterions X " are, for example, halide ions, sulfate ions, phosphate ions, methosulfate ions and organic ions such as lactate, citrate, tartrate and acetate ions.Holyidene ions, in particular chloride, are particularly suitable.
- a particularly suitable homopolymer is the, if desired crosslinked, poly (methacryloyloxyethyltrimethylammonium chloride) with the INCI name Polyquaternium-37.
- such products are, for example, under the names Rheocare ® CTH (Cosmetic Rheologies) and Synthalen® ® CR (Ethnichem) commercially available.
- the crosslinking can, if desired, with the help of olefinically polyunsaturated compounds, for example divinylbenzene , Tetraallyloxyethane, methylenebisacrylamide, diallyl ether, polyallylpolyglyceryl ethers, or allyl ethers of sugars or sugar derivatives such as erythritol, pentaerythritol, arabitol, mannitol, sorbitol, sucrose or glucose methylenebisacrylamide is a preferred crosslinking site ns.
- olefinically polyunsaturated compounds for example divinylbenzene , Tetraallyloxyethane, methylenebisacrylamide, diallyl ether, polyallylpolyglyceryl ethers, or allyl ethers of sugars or sugar derivatives such as erythritol, pentaerythritol, arabitol, mannitol, sorbitol
- the homopolymer is preferably used in the form of a nonaqueous polymer dispersion which should not have a polymer content of less than 30% by weight.
- Such polymer dispersions are (under the names Salcare ® SC 95 about 50% polymer content, additional components: mineral oil (INCI name: Mineral Oil) and tridecyl polyoxypropylene polyoxyethylene ether (INCI name: PPG-1 trideceth-6) ) and Salcare ® SC 96 (about 50% polymer content, additional components: mixture of diesters of propylene glycol (with a mixture of caprylic and capric acid INCI name: propylene glycol Dicaprylate / Dicaprate) and tridecyl-polyoxypropylene-polyoxyethylene ether (INCI name: PPG-1 -Trideceth-6)) are commercially available.
- Copolymers with monomer units of the formula (G1 -I) contain as nonionic monomer units preferably acrylamide, methacrylamide, acrylic acid C-alkyl esters and methacrylic acid C 1-4 -alkyl esters. Among these nonionic monomers, the acrylamide is particularly preferred. These copolymers can also be crosslinked, as described above in the case of the homopolymers.
- a copolymer preferred according to the invention is the crosslinked acrylamide-methacryloyloxyethyltrimethylammonium chloride copolymer.
- Such copolymers in which the monomers are present in a weight ratio of about 20:80 are commercially available as approximately 50% non-aqueous polymer dispersion 92 under the name Salcare ® SC.
- polymers known under the names Polyquaternium-24 commercial product eg Quatrisoft® LM 200
- Polyquaternium-24 commercial product eg Quatrisoft® LM 200
- copolymers of vinylpyrrolidone such as the commercial products Copolymer 845 (manufacturer: ISP), Gaffix® VC 713 (manufacturer: ISP), Gafquat®ASCP 101 1, Gafquat®HS 1 10, Luviquat® 8155 and Luviquat® MS 370 are available.
- Cationic protein hydrolysates may also be used as cationic polymers, preferred agents being one or more cationic protein hydrolyzates from the group Cocodimonium Hydroxypropyl Hydrolyzed Collagen, Cocodimonium Hydroxypropyl Hydrolyzed Casein, Cocodimonium Hydroxypropyl Hydrolyzed Collagen, Cocodimonium Hydroxypropyl Hydrolyzed Hair Keratin, Cocodimonium Hydroxypropyl Hydrolyzed Keratin, Cocodimonium Hydroxypropyl Hydrolyzed Rice Protein, Cocodimonium Hydroxypropyl Hydrolyzed Soy Protein, Cocodimonium Hydroxypropyl Hydrolyzed Wheat Protein, Hydroxypropyl Arginine Lauryl / Myristyl Ether HCl, Hydroxypropyltrimonium Gelatin, Hydroxypropyltrimonium Hydrolyzed Casein, Hydroxypropyltrimonium Hydrolyzed Collagen, Hydroxypropyltrimonium Hydrolyzed Con
- the hair treatment composition - based on its weight - 0.05 to 7.5 wt .-%, preferably 0.1 to 5 wt .-%, particularly preferably 0.2 to 3.5 wt.
- cationic polymer (s) with preferred cationic polymer (s) being / are selected from poly (methacryloyloxyethyltrimethylammonium chloride) (INCI: Polyquaternium) 37) and / or quaternized cellulose derivatives (INCI: Polyquaternium 10) and / or cationic alkylpolyglycosides and / or cationised honey and / or cationic guar derivatives and / or polymeric dimethyldiallylammonium salts and their copolymers with esters and amides of acrylic acid and methacrylic acid and / or copolymers of vinylpyrrolidone with quaternized derivatives of Diaikyiaminoalkyiacryiats and -methacrylate and / or vinylpyrrolidone-Vinylimidazoliummethochlorid copolymers and / or quaternized polyvinyl alcohol
- the agents used in the invention may contain amphoteric polymers.
- amphoteric polymers preferably usable amphoteric polymers are composed essentially together
- R 1 -CH CR 2 -CO-Z- (C n H 2n ) -N ( + ) R 3 R 4 R 5 A ⁇ " ) ⁇ Z" ')
- R and R 2 are independently of each other hydrogen or a methyl group and R 3 , R 4 and R ⁇ independently represent alkyl groups having 1 to 4 carbon atoms, Z is an NH group or an oxygen atom, n is an integer of 2 to 5 and
- a ⁇ -> is the anion of an organic or inorganic acid
- R 6 and fiJ are independently hydrogen or
- Suitable starting monomers are, for. Dimethylaminoethylacrylamide, dimethylaminoethylmethacrylamide, dimethylaminopropylacrylamide, dimethylaminopropylmethacrylamide and diethylaminoethylacrylamide when Z is an NH group or dimethylaminoethyl acrylate, dimethylaminoethyl methacrylate and diethylaminoethyl acrylate when Z is an oxygen atom.
- the monomers containing a tertiary amino group are then quaternized in a known manner, methyl chloride, dimethyl sulfate or diethyl sulfate being particularly suitable as alkylating reagents.
- the quaternization reaction can be carried out in aqueous solution or in the solvent.
- those monomers of formula (ZI) which are derivatives of acrylamide or methacrylamide. Preference is furthermore given to those monomers which contain halide, methoxysulfate or ethoxysulfate ions as counterions. Also preferred are those monomers of formula (ZI) wherein R 1, R 4 and R 5 are methyl groups.
- the acrylamidopropyltrimethylammonium chloride is a very particularly preferred monomer of the formula (ZI).
- Suitable monomeric carboxylic acids of the formula (Z-I) are acrylic acid, methacrylic acid, crotonic acid and 2-methylcrotonic acid. Preference is given to using acrylic or methacrylic acid, in particular acrylic acid.
- the zwitterionic polymers which can be used according to the invention are prepared from monomers of the formulas (Z-1) and (Z-II) by polymerization processes known per se.
- the polymerization can be carried out either in aqueous or aqueous-alcoholic solution.
- the alcohols used are alcohols having 1 to 4 carbon atoms, preferably isopropanol, which simultaneously serve as polymerization regulators.
- other components than regulators may also be added to the monomer solution, eg.
- formic acid or mercaptans such as thioethanol and thioglycolic acid.
- the initiation of the polymerization takes place with the aid of free-radical-forming substances.
- redox systems and / or thermally decomposing radical formers of the azo compound type such.
- azoisobutyronitrile azo-bis (cyanopentanoic acid) or azo-bis (amidinopropane) dihydrochloride can be used.
- redox systems are z. B. combinations of hydrogen peroxide, potassium or ammonium peroxodisulfate and tertiary butyl hydroperoxide with sodium sulfite, sodium dithionite or hydroxylamine hydrochloride as a reduction component.
- the polymerization can be carried out isothermally or under adiabatic conditions, depending on the concentration ratios by the heat of polymerization released, the temperature range for the course of the reaction between 20 and 200 ° C may vary, and the reaction may be carried out under the autogenous pressure. Preferably, the reaction temperature is between 20 and 100 ° C.
- the pH during the copolymerization may vary within a wide range.
- polymerization is carried out at low pH values; however, pH values above the neutral point are also possible.
- an aqueous base for. As sodium hydroxide, potassium hydroxide or ammonia, to a pH between 5 and 10, preferably 6 to 8 set. Further details of the polymerization process can be found in the examples.
- amphoteric polymer (s) comprises monomers A) and B), wherein A) and B) are selected from
- R 1 -CH CR 2 -CO-Z- (C n H 2n ) -N ( + ) R 3 R 4 R 5 A ⁇ ( Z_l )
- R and R 2 independently represent hydrogen or a
- Methyl group and R 3 , R 4 and R 5 are independently alkyl groups having 1 to 4 carbon atoms, Z is an NH group or an oxygen atom, n is an integer from 2 to 5 and A (-) the anion of an organic or inorganic Acid is
- R 6 and R 7 are independently hydrogen or methyl groups.
- amphoteric polymers used in the compositions according to the invention contain monomers from the group of acrylamides and / or methacrylamides with alkylammonium groups.
- Acrylic acid and / or methacrylic acid and / or crotonic acid and / or 2-methyl-crotonic acid have proven useful as monomers with anionic groups which are additionally present in the polymers.
- agents used according to the invention are preferred in which the amphoteric polymer (s) are copolymers of at least one of the monomers trimethylammoniumethylacrylamide and / or trimethylammoniumethylmethacrylamide and / or trimethylammoniumpropylacrylamide and / or trimethylammonium propylmethacrylamide and / or trimethylammoniumethylacrylamide and / or trimethylammoniumethylacrylate and / or trimethylammoniumethylmethacrylate and / or trimethylammoniumethylacrylate and / or ethyldimethylammoniumethylacrylamide and / or ethyldimethylammoniumethylmethacrylamide and / or ethyldimethylammoniumpropylacrylamide and / or ethyldimethylammoniumpropylmethacrylamide and / or ethyldimethylammoniumpropylmethacrylamide and / or ethyldimethylammoniumpropy
- amphoteric polymers according to the invention are:
- the agents used according to the invention may furthermore contain all active ingredients, additives and auxiliaries known for such preparations.
- the agents contain at least one surfactant, with both anionic and zwitterionic, ampholytic, nonionic and cationic surfactants being suitable in principle.
- anionic and zwitterionic, ampholytic, nonionic and cationic surfactants being suitable in principle.
- compositions used according to the invention may also contain plant extracts (L).
- extracts are produced by extraction of the whole plant. However, in individual cases it may also be preferred to prepare the extracts exclusively from flowers and / or leaves of the plant.
- Especially suitable for the use according to the invention are the extracts of green tea, almond, aloe vera, coconut, mango, apricot, lime, wheat, kiwi and melon.
- alcohols and mixtures thereof can be used as extraction agent for the preparation of said plant extracts water.
- the alcohols are lower alcohols such as ethanol and isopropanol, but especially polyhydric alcohols such as ethylene glycol and propylene glycol, both as sole extractant and in admixture with water, are preferred.
- Plant extracts based on water / propylene glycol in a ratio of 1:10 to 10: 1 have proven to be particularly suitable.
- the plant extracts can be used according to the invention both in pure and in diluted form. If they are used in diluted form, they usually contain about 2 to 80 wt .-% of active substance and as a solvent used in their extraction agent or extractant mixture. Furthermore, it may be preferable to use mixtures of several, in particular two, different plant extracts in the compositions used according to the invention.
- the agents used according to the invention contain penetration aids and / or swelling agents (M).
- M penetration aids and / or swelling agents
- M include, for example, urea and urea derivatives, guanidine and its derivatives, arginine and derivatives thereof, water glass, imidazole and its derivatives, histidine and its derivatives, benzyl alcohol, glycerol, glycol and glycol ethers, propylene glycol and propylene glycol ethers, for example propylene glycol monoethyl ether, carbonates, hydroxides.
- gencarbonates diols and triols, and in particular 1, 2-diols and 1, 3-diols such as 1, 2-propanediol, 1, 2-pentanediol, 1, 2-hexanediol, 1, 2-dodecanediol, 1, 3-propanediol , 1, 6-hexanediol, 1, 5-pentanediol, 1, 4-butanediol.
- 1, 2-diols and 1, 3-diols such as 1, 2-propanediol, 1, 2-pentanediol, 1, 2-hexanediol, 1, 2-dodecanediol, 1, 3-propanediol , 1, 6-hexanediol, 1, 5-pentanediol, 1, 4-butanediol.
- hair treatment agents preferably used according to the invention are therefore transparent or translucent, transparent or translucent in the context of the present invention means a composition having an NTU value of less than 100.
- the NTU (Nephelometry Turbidity Unit) value is a fluid turbidity measurement unit used in water treatment and is the unit of turbidity of a fluid measured with a calibrated nephelometer.
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Abstract
Description
HAARBEHANDLUNGSMITTEL ENTHALTEND L-CARNITIN HAIR TREATMENT CONTAINING L-CARNITINE
ODER EIN L-CARNITINDERIVAT UND EIN OLIGOPEPTID OR AN L-CARNITINE DERIVATIVE AND AN OLIGOPEPTIDE
ENTHALTEND DIE SEQUENZ GLU-GLU-GLU CONTAINING THE SEQUENCE GLU-GLU-GLU
Die Erfindung betrifft die Verwendung von Haarbehandlungsmitteln mit bestimmten Inhaltsstoffen zur Förderung oder Verstärkung des Haarwuchses und/oder Verminderung von Haarausfall und/oder Aktivierung der Haarwurzelzellen und/oder Aktivierung von Haarfollikeln und/oder Verdickung des Haares. The invention relates to the use of hair treatment compositions with certain ingredients to promote or enhance the hair growth and / or reduce hair loss and / or activation of the hair root cells and / or activation of hair follicles and / or thickening of the hair.
Dem Menschen fallen durchschnittlich zwischen 70 und 100 Kopfhaare pro Tag aus, aber da die Haarwurzeln normalerweise in der Kopfhaut verbleiben und wieder nachwachsen, werden die ausgefallenen Haare ständig ersetzt und der Haarausfall ist nicht sichtbar. Mit Haarausfall ist somit der permanente Haarausfall gemeint, bei dem die ausgefallenen Haare erst sehr spät wieder, meist immer dünner werdend oder gar nicht mehr, nachwachsen. On average, between 70 and 100 hairs per day are lost by humans, but as the hair roots usually remain in the scalp and regrow, hair loss is constantly replaced and hair loss is not visible. With hair loss is thus meant the permanent hair loss, in which the failed hair again very late, usually getting thinner or not at all, regrow.
Haarausfall ist ein weit verbreitetes kosmetisches Problem sowohl für Männer als auch Frauen und kann psychisch stark belastend sein. Bei Männern ist er vor allem durch zurückgehendem Haaransatz an der Stirn und sich verringernder Haardichte im Vertexbereich charakterisiert. Bei Frauen kommt es meist zu einer generellen Verminderung der Haardichte über den gesamten Kopf. Hair loss is a widespread cosmetic problem for both men and women and can be psychologically stressful. In men, it is mainly characterized by a receding hairline on the forehead and decreasing hair density in the vertex area. In women, there is usually a general reduction in hair density over the entire head.
Zu Haarausfall kommt es, wenn, durch verschiedene Ursachen bedingt, der so genannte Haarzyklus gestört ist. Im Haarzyklus regeneriert sich das Haar im Normalfall selber. Nach einer Wachstumsphase (Anagen), in der sich etwa 80 - 90% der Haare befinden und die zwischen 2 und 6 Jahre dauert, folgt die so genannte Regressionsphase (Katagen, ca. 3-6 Wochen), in der metabolische Prozesse in der Haarwurzel verringert werden. Etwa 2% der Haare befinden sich normalerweise in dieser Ruhephase. Im Laufe des Haarzyklus bildet diese Phase den Übergang zwischen der Anagenphase und der Telogen-Phase. Hair loss occurs when, due to various causes, the so-called hair cycle is disturbed. In the hair cycle, the hair usually regenerates itself. After a growth phase (anagen), in which about 80-90% of the hair is and takes between 2 and 6 years, follows the so-called regression phase (catagen, about 3-6 weeks), in the metabolic processes in the hair root be reduced. About 2% of the hair is usually in this resting phase. During the hair cycle, this phase forms the transition between the anagen phase and the telogen phase.
Die Telogenphase, inder sich ständig ca 10-20% der Haare befinden, ist die Ruhephase (Dauer ca. 3 Monate), nach der das Haar ausfällt und eine neue Wachstumsphase in diesem Follikel beginnt. Bei vermehrtem Haarausfall kann es z.B. zu einer Verlängerung der Telogen, und zu einer Verkürzung der Anagenphase kommen, so dass der Anteil ausfallender Haare steigt ohne durch neue, die Wachstumsphase beginnende ersetzt zu werden. The Telogen phase, which is constantly about 10-20% of the hair, is the resting phase (duration about 3 months), after which the hair fails and a new growth phase begins in this follicle. With increased hair loss, it can be e.g. An increase in telogen, and a shortening of the anagen phase, so that the proportion of failing hair increases without being replaced by new, beginning the growth phase.
Zurzeit existieren auf dem Markt kaum kosmetische Präparate, die das Haarwachstum und die Haarstruktur signifikant verbessern bzw. Haarausfall verhindern. At present, there are hardly any cosmetic preparations on the market which significantly improve hair growth and structure or prevent hair loss.
HGF und KGF sind wichtige Wachstumsfaktoren, die von der dermalen Papille ausgeschüttet werden, um die Proliferation der Haar-Keratinozyten zu steuern. Bei einer potentiell wachstumsfördernden und das Haar stärkenden Substanz sollten diese Parameter in jedem Fall beeinflusst werden. Die Behandlung von dünnem Haar ist ein Verbraucherbedürfnis. Dabei können jedoch herkömmliche strukturverbessernde und glättende Moleküle das Haar beschweren und zu einer„Überpflege" führen HGF and KGF are important growth factors that are released by the dermal papilla to control the proliferation of hair keratinocytes. In a potentially growth-promoting and hair-strengthening substance, these parameters should be influenced in any case. The treatment of thin hair is a consumer need. However, conventional structurally improving and smoothing molecules can complain the hair and lead to a "over-care"
Die Haarstruktur von der Wurzel her, der Produktionsstätte für die das Haar aufbauenden Keratine, zu verbessern ist eine effiziente und nachhaltige Methode zur Behandlung von dünnem Haar. Improving the hair structure from the root, the production site for hair-building keratins, is an efficient and sustainable method of treating thin hair.
Durch geeignete Wirkstoffformulierungen die Jugendlichkeit der Haare zu erhalten oder sie verjüngen zu können, ist eine Herausforderung für die kosmetische Forschung. Maintaining or rejuvenating the youthfulness of hair through suitable formulations of active ingredients is a challenge for cosmetic research.
Die Aufgabe der vorliegenden Erfindung bestand darin, Mittel bereitzustellen, die den Haarwuchs fördern oder verstärken sowie Haarausfall vermindern und die Haarwurzelzellen und/oder Haarfollikeln aktivieren. Eine Verdickung des Haares herbeizuführen, war eine weitere Aufgabe der vorliegenden Erfindung. The object of the present invention was to provide agents that promote or enhance hair growth and reduce hair loss and activate the hair root cells and / or hair follicles. Thickening the hair was another object of the present invention.
Diese Aufgabe wird erfindungsgemäß gelöst durch den Einsatz von Mitteln, welche mindestens eine Verbindung ausgewählt aus L-Carnitin und/oder den Carnitinderivaten Acetyl-L-Carnitin, L-Carnitin-Fumarat, L-Carnitin-Citrat, Lauroyl- L-Carnitin und L-Carnitin- Tartrat und mindestens ein Oligopetid, das mindestens eine Aminosäuresequenz Glu-Glu-Glu This object is achieved according to the invention by the use of agents which contain at least one compound selected from L-carnitine and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine citrate, lauroyl-L-carnitine and L. Carnitine tartrate and at least one oligopetide having at least one amino acid sequence Glu-Glu-Glu
aufweist, wobei die Amino-Gruppe frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können, enthalten. where the amino group is free or protonated and the carboxy groups may be free or deprotonated.
Die vorliegende Erfindung betrifft daher die Verwendung eines Haarbehandlungsmittels enthaltend The present invention therefore relates to the use of a hair treatment composition containing
a) mindestens eine Verbindung ausgewählt aus L-Carnitin und/oder den Carnitinderivaten Acetyl-L-Carnitin, L-Carnitin-Fumarat, L-Carnitin-Citrat, Lauroyl- L- Carnitin und L-Carnitin-Tartrat; a) at least one compound selected from L-carnitine and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine citrate, lauroyl-L-carnitine and L-carnitine tartrate;
b) mindestens ein Oligopetid, das mindestens eine Aminosäuresequenz Glu-Glu-Glu b) at least one oligopetide having at least one amino acid sequence Glu-Glu-Glu
aufweist, wobei die Amino-Gruppe frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können wherein the amino group may be free or protonated and the carboxy groups may be free or deprotonated
zur to
Förderung oder Verstärkung des Haarwuchses und/oder Promotion or enhancement of hair growth and / or
Verminderung von Haarausfall und/oder Reduction of hair loss and / or
Aktivierung der Haarwurzelzellen und/oder Activation of hair root cells and / or
Aktivierung von Haarfollikeln und/oder Activation of hair follicles and / or
Verdickung des Haares. Thickening of the hair.
Haarbehandlungsmittel im Sinne der vorliegenden Erfindung sind beispielsweise Haarshampoos, Haarkonditionierer, konditionierenden Shampoos, Haarsprays, Haarspülungen, Haarkuren, Haarpackungen, Haar-Tonics, Dauerwell-Fixierlösungen, Haarfärbeshampoos, Haarfärbemittel, Haarfestiger, Haarlegemittel, Haarstyling- Zubereitungen, Fönwell-Lotionen, Schaumfestiger, Haargele, Haarwachse oder deren Kombinationen. Im Hinblick auf die Tatsache, daß Männer oft die Anwendung mehrerer unterschiedlicher Mittel und/oder mehrere Anwendungsschritte scheuen, sind erfindungsgemäße Mittel bevorzugt solche Mittel, die der Mann ohnehin anwendet. Bevorzugte erfindungsgemäße Mittel sind daher Shampoos, Konditioniermittel oder Haar- Tonics. Hair treatment compositions in the context of the present invention are, for example, hair shampoos, hair conditioners, conditioning shampoos, hairsprays, hair conditioners, hair conditioners, hair wraps, hair tonics, perming solutions, hair dye shampoos, hair dyes, hair fixatives, hair dressings, hairstyling preparations, hair lotions, mousses, hair gels , Hair waxes or their combinations. In view of the fact that men often shy away from the use of several different agents and / or several application steps, means according to the invention are preferably agents which the man applies anyway. Preferred agents according to the invention are therefore shampoos, conditioners or hair tonics.
Die erfindungsgemäß verwendeten Haarbehandlungsmittel sind in der Lage, den Haarwuchs positiv zu beeinflussen, indem spezielle inhibierende haarspezifische Gene reprimiert bzw. reduziert werden. Die Repression bzw. Reduktion der inhibierenden Gene, führt dazu, dass die Haarwurzel wieder reaktiviert werden kann. Zudem wird die Haarstruktur bereits an den Haarwurzeln beeinflusst, so dass das Haar kräftig und gesund sowie dicker nachwachsen kann. The hair treatment agents used according to the invention are capable of positively influencing hair growth by repressing or reducing specific inhibiting hair-specific genes. The repression or reduction of the inhibiting genes, causes the hair root can be reactivated. In addition, the hair structure is already influenced on the hair roots, so that the hair can grow strong and healthy and thicker.
Weiterhin wurde gefunden, dass durch die Applikation der genannten Mittel das Haar in seinem Wachstum und seinem Stoffwechsel positiv beeinflusst werden. Furthermore, it has been found that the hair is positively influenced in its growth and metabolism by the application of said agents.
Die Penetration von Wirkstoffen zum Follikel ist üblicherweise erschwert, da das entsprechende Target, die dermale Papille sowie die ORS-Keratinozyten, ca. 2 mm tief in der Kopfhaut eingebettet ist. Die Verwendung von Liposomen erhöht die Penetration eines Wirkstoffes, so daß Haarbehandlungsmittel, die die o.g. Wirkstoffe liposomal verkapselt enthalten, sehr gut wirken. Überraschenderweise wurde festgestellt, daß diese Zusammensetzungen selbst dann eine ausreichende Penetration zum Wirkungsort zeigen, wenn die Verwendung von Liposomen aus formulierungstechnischen Gründen nicht möglich ist. The penetration of active substances into the follicle is usually more difficult since the corresponding target, the dermal papilla and the ORS keratinocytes, are embedded approximately 2 mm deep in the scalp. The use of liposomes increases the penetration of one Active ingredient, so that hair treatment agents that contain the above-mentioned drugs liposomal encapsulated, work very well. Surprisingly, it has been found that these compositions show sufficient penetration to the site of action even if the use of liposomes is not possible for formulation-technical reasons.
Die erfindungsgemäß verwendeten Haarbehandlungsmittel enthalten als wesentlichen Inhaltstoff mindestens eine Verbindung ausgewählt aus L-Carnitin und/oder den Carnitinderivaten Acetyl-L-Carnitin, L-Carnitin-Fumarat, L-Carnitin-Citrat, Lauroyl- L-Carnitin und L-Carnitin-Tartrat. The hair treatment compositions used according to the invention contain as essential ingredient at least one compound selected from L-carnitine and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine citrate, lauroyl L-carnitine and L-carnitine tartrate ,
Die erfindungsgemäß verwendeten Mittel können L-Carnitin und/oder ein L-Carnitinderivat oder auch mehrere voneinander verschiedene L-Carnitinderivate enthalten. The agents used according to the invention may contain L-carnitine and / or an L-carnitine derivative or else a plurality of different L-carnitine derivatives.
L-Carnitin bzw. L-Carnitinderivate sind in den erfindungsgemäß verwendeten Mitteln bevorzugt in Mengen von 0,001 bis 10 Gew.-%, bezogen auf die gesamte Zubereitung, enthalten. Mengen von 0,1 bis 10 Gew.-% sind besonders bevorzugt, Mengen von 0,1 bis 5 Gew.-% sind in besonderem Maße bevorzugt, und Mengen von 1 bis 3 Gew.-% sind ganz besonders bevorzugt. L-carnitine or L-carnitine derivatives are contained in the compositions according to the invention preferably in amounts of 0.001 to 10 wt .-%, based on the total preparation. Levels of 0.1 to 10 wt .-% are particularly preferred, amounts of 0.1 to 5 wt .-% are particularly preferred, and amounts of 1 to 3 wt .-% are very particularly preferred.
Besonders bevorzugte erfindungsgemäß verwendete Haarbehandlungsmittel sind dadurch gekennzeichnet, daß sie 0,0005 bis 7,5 Gew.-%, vorzugsweise 0,001 bis 6 Gew.-%, weiter bevorzugt 0,005 bis 5 Gew.-%, weiter bevorzugt 0,01 bis 4 Gew.-% und insbesondere 0,1 bis 3 Gew.-% mindestens einer Verbindung ausgewählt aus L-Carnitin, und/oder den Carnitinderivaten Acetyl-L-Carnitin, L-Carnitin-Fumarat, L-Carnitin-Citrat, Lauroyl- L-Carnitin und insbesondere L-Carnitin-Tartrat enthalten. Particularly preferred hair treatment agents used according to the invention are characterized in that they are 0.0005 to 7.5 wt .-%, preferably 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4 wt % and in particular 0.1 to 3 wt .-% of at least one compound selected from L-carnitine, and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine citrate, lauroyl Carnitine and in particular L-carnitine tartrate included.
Erfindungsgemäß bevorzugt verwendete Haarbehandlungsmittel enthalten 0,0001 bis 10 Gew.-% mindestens einer Verbindung ausgewählt aus L-Carnitin, und/oder den Carnitinderivaten Acetyl-L-Carnitin, L-Carnitin-Fumarat, L-Carnitin-Citrat, Lauroyl- L-Carnitin und insbesondere L-Carnitin-Tartrat. Hair treatment agents preferably used according to the invention contain from 0.0001 to 10% by weight of at least one compound selected from L-carnitine, and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine citrate, lauroyl- Carnitine and in particular L-carnitine tartrate.
Bevorzugte erfindungsgemäße Verwendungen sind zusammenfassend dadurch gekennzeichnet, daß das Haarbehandlungsmittel - bezogen auf sein Gewicht - 0,0005 bis 7,5 Gew.-%, vorzugsweise 0,001 bis 6 Gew.-%, weiter bevorzugt 0,005 bis 5 Gew.-%, weiter bevorzugt 0,01 bis 4 Gew.-% und insbesondere 0,1 bis 3 Gew.-% mindestens einer Verbindung ausgewählt aus L-Carnitin, und/oder den Carnitinderivaten Acetyl-L-Carnitin, L- Carnitin-Fumarat, L-Carnitin-Citrat, Lauroyl- L-Carnitin und insbesondere L-Carnitin-Tartrat enthält. Preferred uses of the invention are summarized in that the hair treatment agent - based on its weight - 0.0005 to 7.5 wt .-%, preferably 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4% by weight and in particular 0.1 to 3% by weight of at least one compound selected from L-carnitine, and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine Citrate, lauroyl-L-carnitine and especially L-carnitine tartrate.
Die erfindungsgemäß verwendeten Haarbehandlungsmittel enthalten als weiteren wesentlichen Inhaltstoff mindestens ein Oligopetids, das mindestens eine Aminosäuresequenz Glu-Glu-Glu The hair treatment compositions used according to the invention contain as further essential ingredient at least one oligopeptide containing at least one amino acid sequence Glu-Glu-Glu
aufweist, wobei die Amino-Gruppe frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können. wherein the amino group may be free or protonated and the carboxy groups may be free or deprotonated.
Bevorzugte erfindungsgemäße Verwendungen sind dadurch gekennzeichnet, daß das Haarbehandlungsmittel - bezogen auf sein Gewicht - 0,0001 bis 10 Gew.-% mindestens eines Oligopetids enthält, das mindestens eine Aminosäuresequenz Glu-Glu-Glu Preferred uses according to the invention are characterized in that the hair treatment composition contains, based on its weight, 0.0001 to 10% by weight of at least one oligopeptide containing at least one amino acid sequence Glu-Glu-Glu
aufweist, wobei die Amino-Gruppe frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können wherein the amino group may be free or protonated and the carboxy groups may be free or deprotonated
In dieser wie in allen nachstehenden Formeln bedeutet das eingeklammerte Wasserstoffatom der Aminogruppe ebenso wie die eingeklammerte Hydroxygruppe der Säurefunktion, daß die betreffenden Gruppen als solche vorhanden sein können (dann handelt es sich um ein Oligopeptid mit der betreffenden Anzahl an Aminosäuren wie dargestellt (in der vorstehenden Formel 3) oder aber, daß die Aminosäuresequenz in einem Oligopeptid vorliegt, das noch weitere Anminosäuren umfaßt - je nachdem, wo die weitere(n) Aminosäure(n) gebunden ist/sind, sind die eingeklammerten Bestandteile der o.g. Formel durch den/die weiteren Aminosäurerest(e) ersetzt. In this formula as well as in the formulas below, the parenthetized hydrogen atom of the amino group, as well as the parenthetical group of the acid function, means that the groups concerned may be present as such (then an oligopeptide having the relevant number of amino acids as shown (in the above) Formula 3) or that the amino acid sequence is present in an oligopeptide, which also comprises other amino acids - depending on where the other amino acid (s) is / are bound, the parenthetical components of the above formula by the / the other Replaced amino acid residue (s).
Diese bevorzugten erfindungsgemäß verwendeten Haarbehandlungsmittel enthalten - bezogen auf ihr Gewicht - 0,0001 bis 10 Gew.-% mindestens eines Oligopeptids, das mindestens eine Aminosäuresequent Glu-Glu-Glu, d.h. mindestens drei aufeinander folgende Glutaminsäuren aufweist. Oligopeptide im Sinne der vorliegenden Anmeldung sind durch Peptid-Bindungen Säureamid- artig verknüpfte Kondensationsprodukte von Aminosäuren, die mindestens 3 und maximal 25 Aminosäuren umfassen These preferred hair treatment compositions according to the invention contain - based on their weight - 0.0001 to 10 wt .-% of at least one oligopeptide having at least one amino acid residue Glu-Glu-Glu, ie at least three consecutive glutamic acids. Oligopeptides in the sense of the present application are acid amide-like linked condensation products of amino acids which comprise at least 3 and at most 25 amino acids by peptide bonds
In bevorzugten erfindungsgemäß verwendeten Haarbehandlungsmitteln umfaßt das Oligopeptid 5 bis 15 Aminosäuren, vorzugsweise 6 bis 13 Aminosäuren, besonders bevorzugt 7 bis 12 Aminosäuren und insbesondere 8, 9 oder 10 Aminosäuren. In preferred hair treatment compositions used according to the invention, the oligopeptide comprises 5 to 15 amino acids, preferably 6 to 13 amino acids, particularly preferably 7 to 12 amino acids and in particular 8, 9 or 10 amino acids.
Je nachdem, ob weitere Aminosäuren an die Sequenz Glu-Glu-Glu gebunden sind und je nach Art dieser Aminosäuren kann die Molmasse des in den erfindungsgemäß verwendeten Mitteln enthaltenen Oligopeptids variieren. Bevorzugte erfindungsgemäß verwendete Haarbehandlungsmittel sind dadurch gekennzeichnet, daß das Oligopeptid eine Molmasse von 650 bis 3000 Da, vorzugsweise von 750 bis 2500 Da, besonders bevorzugt von 850 bis 2000 Da und insbesondere von 1000 bis 1600 Da aufweist. Depending on whether further amino acids are bound to the sequence Glu-Glu-Glu and depending on the nature of these amino acids, the molecular weight of the oligopeptide contained in the agents used according to the invention may vary. Preferred hair treatment agents used according to the invention are characterized in that the oligopeptide has a molecular weight of from 650 to 3000 Da, preferably from 750 to 2500 Da, particularly preferably from 850 to 2000 Da and in particular from 1000 to 1600 Da.
Zusammenfassend sind bevorzugte Verwendungen dadurch gekennzeichnet, daß das Oligopeptid 5 bis 15 Aminosäuren, vorzugsweise 6 bis 13 Aminosäuren, besonders bevorzugt 7 bis 12 Aminosäuren und insbesondere 8, 9 oder 10 Aminosäuren umfaßt und eine Molmasse von 650 bis 3000 Da, vorzugsweise von 750 bis 2500 Da, besonders bevorzugt von 850 bis 2000 Da und insbesondere von 1000 bis 1600 Da aufweist. In summary, preferred uses are characterized in that the oligopeptide comprises 5 to 15 amino acids, preferably 6 to 13 amino acids, more preferably 7 to 12 amino acids and especially 8, 9 or 10 amino acids and a molecular weight of 650 to 3000 Da, preferably 750 to 2500 Since, more preferably from 850 to 2000 Da and in particular from 1000 to 1600 Da has.
Wie aus der bevorzugten Anzahl von Aminosäuren in den Oligopeptiden und dem bevorzugten Molmassenbereich zu ersehen ist, werden vorzugsweise Oligopeptide eingesetzt, die nicht allein aus den drei Glutaminsäuren bestehen, sondern weitere, an diese Sequenz gebundene Aminosäuren aufweisen. Diese weiteren Aminosäuren sind vorzugsweise aus bestimmten Aminosäuren ausgewählt, während bestimmte andere Vertreter erfindungsgemäß weniger bevorzugt sind. As can be seen from the preferred number of amino acids in the oligopeptides and the preferred molecular weight range, it is preferred to use oligopeptides which do not consist solely of the three glutamic acids but have further amino acids bound to this sequence. These other amino acids are preferably selected from certain amino acids, while certain other representatives are less preferred in the present invention.
So ist es bevorzugt, wenn die in den erfindungsgemäß verwendeten Mitteln eingesetzten Oligopeptide kein Methionin enthalten. Thus it is preferred if the oligopeptides used in the agents used according to the invention contain no methionine.
Weiter bevorzugt ist es, wenn die in den erfindungsgemäß verwendeten Mitteln eingesetzten Oligopeptide kein Cystein und/oder Cystin enthalten. It is further preferred if the oligopeptides used in the agents used according to the invention do not contain cysteine and / or cystine.
Weiter bevorzugt ist es, wenn die in den erfindungsgemäß verwendeten Mitteln eingesetzten Oligopeptide keine Asparaginsäure und/oder Asparagin enthalten. It is further preferred if the oligopeptides used in the agents used according to the invention contain no aspartic acid and / or asparagine.
Weiter bevorzugt ist es, wenn die in den erfindungsgemäß verwendeten Mitteln eingesetzten Oligopeptide kein Serin und/oder Threonin enthalten. It is further preferred if the oligopeptides used in the agents used according to the invention do not contain serine and / or threonine.
Demgegenüber ist es bevorzugt, wenn die in den erfindungsgemäß verwendeten Mitteln eingesetzten Oligopeptide Tyrosin enthalten. In contrast, it is preferred if the oligopeptides used in the agents used according to the invention contain tyrosine.
Weiter bevorzugt ist es, wenn die in den erfindungsgemäß verwendeten Mitteln eingesetzten Oligopeptide Leucin enthalten. It is further preferred if the oligopeptides used in the agents according to the invention contain leucine.
Weiter bevorzugt ist es, wenn die in den erfindungsgemäß verwendeten Mitteln eingesetzten Oligopeptide Isoleucin enthalten. Weiter bevorzugt ist es, wenn die in den erfindungsgemäß verwendeten Mitteln eingesetzten Oligopeptide Arginin enthalten. It is further preferred if the oligopeptides used in the agents used according to the invention contain isoleucine. It is further preferred if the oligopeptides used in the agents used according to the invention contain arginine.
Weiter bevorzugt ist es, wenn die in den erfindungsgemäß verwendeten Mitteln eingesetzten Oligopeptide Valin enthalten. It is further preferred if the oligopeptides used in the agents according to the invention contain valine.
Besonders bevorzugte Oligopeptide bzw. in den bevorzugten Oligopeptiden enthaltene Aminosäuresequenzen werden nachstehend beschrieben: Particularly preferred oligopeptides or amino acid sequences contained in the preferred oligopeptides are described below:
Ein besonders bevorzugtes Oligopeptid enthält zusätzlich Tyrosin, das vorzugsweise über seine Säurefunktion an die Glu-Glu-Glu-Sequenz gebunden ist. Erfindungsgemäß bevorzugte Haarbehandlungsmittel sind daher dadurch gekennzeichnet, daß das in ihnen enthaltene Oligopeptid mindestens eine Aminosäuresequenz Tyr-Glu-Glu-Glu aufweist, wobei die Amino- Gruppe frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können. Ein weiteres besonders bevorzugtes Oligopeptid enthält zusätzlich Isoleucin, das vorzugsweise über seine Aminofunktion an die Glu-Glu-Glu-Sequenz gebunden ist. Erfindungsgemäß bevorzugte Haarbehandlungsmittel sind daher dadurch gekennzeichnet, daß das in ihnen enthaltene das Oligopeptid mindestens eine Aminosäuresequenz Glu-Glu- Glu-Ile aufweist, wobei die Amino-Gruppe frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können. A particularly preferred oligopeptide additionally contains tyrosine, which is preferably linked via its acid function to the Glu-Glu-Glu sequence. Hair treatment compositions which are preferred according to the invention are therefore characterized in that the oligopeptide contained in them has at least one amino acid sequence Tyr-Glu-Glu-Glu, where the amino group may be free or protonated and the carboxy groups may be free or deprotonated. Another particularly preferred oligopeptide additionally contains isoleucine, which is preferably linked to the Glu-Glu-Glu sequence via its amino function. Hair treatment agents which are preferred according to the invention are therefore characterized in that the oligopeptide contained in them has at least one amino acid sequence Glu-Glu-Glu-Ile, wherein the amino group can be free or protonated and the carboxy groups can be free or deprotonated.
Oligopeptide, die beide vorgenannten Aminosäuren (Tyrosin und Isoleucin) aufweisen, sind erfindungsgemäß bevorzugt. Besonders bevorzugt sind dabei erfindungsgemäße Verwendungen, bei denen das im Haarbehandlungsmittel enthaltene Oligopeptid mindestens eine Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile aufweist, wobei die Amino-Gruppe frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können. Oligopeptides which have both the abovementioned amino acids (tyrosine and isoleucine) are preferred according to the invention. Particular preference is given to uses according to the invention in which the oligopeptide contained in the hair treatment agent has at least one amino acid sequence Tyr-Glu-Glu-Glu-Ile, where the amino group may be free or protonated and the carboxy groups may be free or deprotonated.
Weiter bevorzugte Oligopeptide enthalten zusätzlich Arginin, das vorzugsweise an Isoleucin gebunden vorliegt Further preferred oligopeptides additionally contain arginine, which is preferably bound to isoleucine
Besonders bevorzugt sind dabei erfindungsgemäße Verwendungen, bei denen das im Haarbehandlungsmittel enthaltene Oligopeptid mindestens eine Aminosäuresequenz Tyr-Glu- Glu-Glu-Ile-Arg aufweist, wobei die Amino-Gruppen frei oder protoniert und die Carboxy- Gruppen frei oder deprotoniert vorliegen können. Particular preference is given to uses according to the invention in which the oligopeptide contained in the hair treatment agent has at least one amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg, wherein the amino groups may be free or protonated and the carboxy groups may be free or deprotonated.
Noch weiter bevorzugte Oligopeptide enthalten zusätzlich Valin, das vorzugsweise an das Arginin gebunden vorliegt. Erfindungsgemäß weiter bevorzugte Verwendungen sind daher dadurch gekennzeichnet, daß das im Haarbehandlungsmittel enthaltene Oligopeptid mindestens eine Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile-Arg-Val aufweist, wobei die Amino- Gruppen frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können. Still further preferred oligopeptides additionally contain valine, which is preferably bound to the arginine. Further preferred uses according to the invention are therefore characterized in that the oligopeptide contained in the hair treatment agent has at least one amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val, wherein the amino groups are free or protonated and the carboxy groups are free or deprotonated can.
Noch weiter bevorzugte Oligopeptide enthalten zusätzlich Leucin, das vorzugsweise an das Valin gebunden vorliegt. Erfindungsgemäß weiter bevorzugte Verwendungen sind daher dadurch gekennzeichnet, daß das im Haarbehandlungsmittel enthaltene Oligopeptid mindestens eine Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu aufweist, wobei die Amino-Gruppen frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können. Still further preferred oligopeptides additionally contain leucine, which is preferably bound to the valine. Further preferred uses according to the invention are therefore characterized in that the oligopeptide contained in the hair treatment agent has at least one amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu, wherein the amino groups are free or protonated and the carboxy groups may be present freely or deprotonated.
Insbesondere bevorzugte Oligopeptide enthalten zusätzlich Leucin, das vorzugsweise an das Tyrosin gebunden vorliegt. Erfindungsgemäß weiter bevorzugte Verwendungen sind daher dadurch gekennzeichnet, daß das im Haarbehandlungsmittel enthaltene Oligopeptid mindestens eine Aminosäuresequenz Leu-Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu aufweist, wobei die Amino-Gruppen frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können. Particularly preferred oligopeptides additionally contain leucine, which is preferably bound to the tyrosine. Further preferred uses according to the invention are therefore characterized in that the oligopeptide contained in the hair treatment agent has at least one amino acid sequence Leu-Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu, wherein the amino groups are free or protonated and the carboxy groups may be free or deprotonated.
Ganz besonders bevorzugt enthalten erfindungsgemäß verwendete Mittel mindestens zwei Oligopeptide, die den vorstehend genannten Kriterien genügen, sich aber voneinander unterscheiden. So ist beispielsweise die Verwendung von Haarbehandlungsmitteln bevorzugt, die mindestens zwei voneinander verschiedene Oligopetide A und B enthalten, die beide die Aminosäuresequenz Glu-Glu-Glu enthalten. With very particular preference, agents used according to the invention comprise at least two oligopeptides which satisfy the abovementioned criteria but which differ from one another. For example, it is preferable to use hair treatment agents containing at least two mutually different oligopetides A and B both containing the amino acid sequence Glu-Glu-Glu.
Solche voneinander unterschiedlichen Oligopeptide A und B entsprechen einander darin, daß sie drei aufeinander folgende Glu-Aminosäuren in ihrer Aminosäuresequenz tragen, besitzen aber in den davor oder dahinter gebundenen Aminosäuren Unterschiede. Bevorzugt sind voneinander verschiedene Peptide mit partieller Übereinstimmung, die durchaus größer sein kann als in den vorstehend genannten drei Aminosäuren. Such mutually different oligopeptides A and B correspond to each other in that they carry three consecutive Glu amino acids in their amino acid sequence, but have differences in the upstream or downstream amino acids. Preference is given to mutually different peptides with partial agreement, which may well be greater than in the above-mentioned three amino acids.
So sind weiter bevorzugte Verwendungen dadurch gekennzeichnet, daß im Haarbehandlungsmittel mindestens zwei voneinander verschiedene Oligopetide A und B enthalten sind, die beide die Aminosäuresequenz Glu-Glu-Glu-Ile enthalten. Thus, further preferred uses are characterized in that the hair treatment composition contains at least two mutually different oligopetides A and B, both of which contain the amino acid sequence Glu-Glu-Glu-Ile.
Ebenfalls bevorzugt sind Verwendungen von Haarbehandlungsmitteln, die mindestens zwei voneinander verschiedene Oligopetide A und B enthalten, die beide die Aminosäuresequenz Tyr-Glu-Glu-Glu enthalten. Also preferred are uses of hair treatment compositions containing at least two mutually different oligopetides A and B, both containing the amino acid sequence Tyr-Glu-Glu-Glu.
Noch weiter bevorzugte Verwendungen sind dadurch gekennzeichnet, daß das Still further preferred uses are characterized in that
Haarbehandlungsmittel mindestens zwei voneinander verschiedene Oligopetide A und B enthält, die beide die Aminosäuresequenz Glu-Glu-Glu-Ile-Arg enthalten. Hair treatment agent contains at least two mutually different oligopeptides A and B, both of which contain the amino acid sequence Glu-Glu-Glu-Ile-Arg.
Ebenfalls noch weiter bevorzugte Verwendungen sind dadurch gekennzeichnet, daß das Also still further preferred uses are characterized in that the
Haarbehandlungsmittel mindestens zwei voneinander verschiedene Oligopetide A und B enthält, die beide die Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile enthalten. Hair treatment agent contains at least two mutually different oligopeptides A and B, both of which contain the amino acid sequence Tyr-Glu-Glu-Glu-Ile.
Erfindungsgemäße bevorzugte Verwendungen sind daher dadurch gekennzeichnet, daß das Preferred uses according to the invention are therefore characterized in that
Oligopeptid mindestens eine Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile aufweist, wobei dieOligopeptid has at least one amino acid sequence Tyr-Glu-Glu-Glu-Ile, wherein the
Amino-Gruppe frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können. Amino group is free or protonated and the carboxy groups may be free or deprotonated.
Ganz besonders bevorzugte Verwendungen sind dadurch gekennzeichnet, daß das Haarbehandlungsmittel mindestens zwei voneinander verschiedene Oligopetide A und B enthält, die beide die Aminosäuresequenz Glu-Glu-Glu-Ile-Arg enthalten. Very particularly preferred uses are characterized in that the hair treatment agent at least two mutually different oligopeptides A and B. Both contain the amino acid sequence Glu-Glu-Glu-Ile-Arg.
Ebenfalls ganz besonders bevorzugte Verwendungen sind dadurch gekennzeichnet, daß das Haarbehandlungsmittel mindestens zwei voneinander verschiedene Oligopetide A und B enthält, die beide die Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile-Arg enthalten. Also very particularly preferred uses are characterized in that the hair treatment agent contains at least two mutually different oligopeptides A and B, both containing the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg.
Vorzugsweise besteht eine noch größere strukturelle Übereinstimmung in den Oligopeptiden. So sind Verwendungen, bei denen die Haarbehandlungsmittel mindestens zwei voneinander verschiedene Oligopetide A und B enthalten, die beide die Aminosäuresequenz Glu-Glu-Glu- Ile-Arg-Val enthalten, weitere bevorzugte Ausführungsformen der vorliegenden Erfindung. Ebenfalls bevorzugte Ausführungsformen sind Verwendungen, bei denen die Haarbehandlungsmittel mindestens zwei voneinander verschiedene Oligopetide A und B enthalten, die beide die Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile-Arg-Val enthalten. Preferably, there is an even greater structural match in the oligopeptides. Thus, uses in which the hair treatment compositions contain at least two distinct oligopetides A and B both containing the amino acid sequence Glu-Glu-Glu-Ile-Arg-Val are further preferred embodiments of the present invention. Also preferred embodiments are uses in which the hair treatment agents contain at least two mutually different oligopetides A and B, both containing the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val.
Noch weiter bevorzugte erfindungsgemäße Verwendungen sind dadurch gekennzeichnet, daß die Haarbehandlungsmittel mindestens zwei voneinander verschiedene Oligopetide A und B enthalten, die beide die Aminosäuresequenz Glu-Glu-Glu-Ile-Arg-Val-Leu enthalten. Still further preferred uses of the invention are characterized in that the hair treatment agents contain at least two mutually different oligopetides A and B, both containing the amino acid sequence Glu-Glu-Glu-Ile-Arg-Val-Leu.
Ebenfalls noch weiter bevorzugte erfindungsgemäße Verwendungen sind dadurch gekennzeichnet, daß die Haarbehandlungsmittel mindestens zwei voneinander verschiedene Oligopetide A und B enthalten, die beide die Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile-Arg-Val- Leu enthalten. Still further preferred uses of the invention are characterized in that the hair treatment agents contain at least two mutually different oligopetides A and B, both containing the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu.
Erfindungsgemäße bevorzugte Verwendungen sind daher dadurch gekennzeichnet, daß das Oligopeptid mindestens eine Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu aufweist, wobei die Amino-Gruppen frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können, Preferred uses according to the invention are therefore characterized in that the oligopeptide has at least one amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu, where the amino groups may be free or protonated and the carboxy groups may be free or deprotonated,
Insbesondere bevorzugte erfindungsgemäße Verwendungen sind dadurch gekennzeichnet, daß die Haarbehandlungsmittel mindestens zwei voneinander verschiedene Oligopetide A und B enthalten, wobei das Oligopeptid A die Aminosäuresequenz Leu-Tyr-Glu-Glu-Glu-Ile-Arg- Val-Leu aufweist, wobei die Amino-Gruppen frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können Particularly preferred uses according to the invention are characterized in that the hair treatment compositions contain at least two mutually different oligopetides A and B, the oligopeptide A having the amino acid sequence Leu-Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu, where the amino- Groups may be free or protonated and the carboxy groups may be free or deprotonated
und das Oligopeptid B die Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu aufweist, wobei die Amino-Gruppen frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können. and the oligopeptide B has the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu, wherein the amino groups may be free or protonated and the carboxy groups may be free or deprotonated.
In ganz besonders bevorzugten Verwendungen dieser letztgenannten Ausführungsform enthalten die Haarbehandlungsmittel - bezogen auf das Gewicht des Mittels - 0,00001 bis 1 Gew.-% Oligopeptid A und 0,00001 bis 1 Gew.-% Oligopeptid B. In most preferred uses of this latter embodiment, the hair treatment compositions contain, based on the weight of the composition, from 0.00001 to 1% by weight of oligopeptide A and from 0.00001 to 1% by weight of oligopeptide B.
In weiter bevorzugten Verwendungen dieser letztgenannten Ausführungsform enthalten die Haarbehandlungsmittel - bezogen auf das Gewicht des Mittels -0,00005 bis 0, 1 Gew.-% Oligopeptid A und 0,00005 bis 0,1 Gew.-% Oligopeptid B. In further preferred uses of this latter embodiment, the hair treatment compositions contain, based on the weight of the composition, from 0.00005 to 0.1% by weight of oligopeptide A and from 0.00005 to 0.1% by weight of oligopeptide B.
In noch weiter bevorzugten Verwendungen dieser letztgenannten Ausführungsform enthalten die Haarbehandlungsmittel - bezogen auf das Gewicht des Mittels -0,0001 bis 0,01 Gew.-% Oligopeptid A und 0,0001 bis 0,001 Gew.-% Oligopeptid B. In still further preferred uses of this latter embodiment the hair treatment agents - based on the weight of the composition - 0.0001 to 0.01 wt .-% oligopeptide A and 0.0001 to 0.001 wt .-% oligopeptide B.
Die im Rahmen der vorliegenden Erfindung eingesetzten Oligopeptide, die den vorstehend genannten Bedingungen genügen, können vorteilhafterweise aus keratinischen Materialien gewonnen werden. Es ist erfindungsgemäß bevorzugt, daß diese Oligopeptide in hohen Anteilen, bezogen auf den gesamten keratinischen Peptidgehalt der Mittel, eingesetzt werden. Ganz besonders bevorzugt ist es, daß ein möglichst hoher Anteil aller im erfindungsgemäß verwendeten Mittel enthaltenen keratinischen Peptide den vorstehend genannten Bedingungen genügt. The oligopeptides used in the context of the present invention, which satisfy the abovementioned conditions, can advantageously be obtained from keratinic materials. It is preferred according to the invention that these oligopeptides are used in high proportions, based on the total keratinic peptide content of the agents. It is very particularly preferred that the highest possible proportion of all the keratinic peptides contained in the agent used according to the invention satisfies the conditions mentioned above.
Bevorzugte erfindungsgemäß verwendete Haarbehandlungsmittel sind dadurch gekennzeichnet, daß mindestens 0, 1 Gew.-%, vorzugsweise mindestens 0,5 Gew.-%, besonders bevorzugt mindestens 1 Gew.-%, weiter bevorzugt mindestens 2,5 Gew.-%, noch weiter bevorzugt mindestens 5 Gew.-% und insbesondere mindestens 10 Gew.-% aller im Mittel enthaltenen keratinischen Peptide die Aminosäuresequenz Glu-Glu-Glu aufweisen. Weiter bevorzugte erfindungsgemäß verwendete Haarbehandlungsmittel sind dadurch gekennzeichnet, daß mindestens 0,1 Gew.-%, vorzugsweise mindestens 0,5 Gew.-%, besonders bevorzugt mindestens 1 Gew.-%, weiter bevorzugt mindestens 2,5 Gew.-%, noch weiter bevorzugt mindestens 5 Gew.-% und insbesondere mindestens 10 Gew.-% aller im Mittel enthaltenen keratinischen Peptide die Aminosäuresequenz Glu-Glu-Glu-Ile aufweisen. Noch weiter bevorzugte erfindungsgemäß verwendete Haarbehandlungsmittel sind dadurch gekennzeichnet, daß mindestens 0, 1 Gew.-%, vorzugsweise mindestens 0,5 Gew.-%, besonders bevorzugt mindestens 1 Gew.-%, weiter bevorzugt mindestens 2,5 Gew.-%, noch weiter bevorzugt mindestens 5 Gew.-% und insbesondere mindestens 10 Gew.-% aller im Mittel enthaltenen keratinischen Peptide die Aminosäuresequenz Tyr-Glu-Glu-Glu aufweisen. Besonders bevorzugte erfindungsgemäß verwendete Haarbehandlungsmittel sind dadurch gekennzeichnet, daß mindestens 0,1 Gew.-%, vorzugsweise mindestens 0,5 Gew.-%, besonders bevorzugt mindestens 1 Gew.-%, weiter bevorzugt mindestens 2,5 Gew.-%, noch weiter bevorzugt mindestens 5 Gew.-% und insbesondere mindestens 10 Gew.-% aller im Mittel enthaltenen keratinischen Peptide die Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile aufweisen. Preferred hair treatment agents used according to the invention are characterized in that at least 0.1% by weight, preferably at least 0.5% by weight, more preferably at least 1% by weight, more preferably at least 2.5% by weight, still further preferably at least 5% by weight and in particular at least 10% by weight of all the keratinic peptides contained in the middle have the amino acid sequence Glu-Glu-Glu. Further preferred hair treatment agents used according to the invention are characterized in that at least 0.1 wt .-%, preferably at least 0.5 wt .-%, more preferably at least 1 wt .-%, more preferably at least 2.5 wt .-%, still more preferably at least 5% by weight, and in particular at least 10% by weight, of all the keratinic peptides contained in the middle have the amino acid sequence Glu-Glu-Glu-Ile. Further preferred hair treatment agents used according to the invention are characterized in that at least 0.1% by weight, preferably at least 0.5% by weight, more preferably at least 1% by weight, more preferably at least 2.5% by weight, even more preferably at least 5% by weight, and in particular at least 10% by weight, of all the keratinic peptides contained in the middle have the amino acid sequence Tyr-Glu-Glu-Glu. Particularly preferred hair treatment agents used according to the invention are characterized in that at least 0.1 wt .-%, preferably at least 0.5 wt .-%, more preferably at least 1 wt .-%, more preferably at least 2.5 wt .-%, still more preferably at least 5% by weight and in particular at least 10% by weight of all the keratinic peptides contained in the middle have the amino acid sequence Tyr-Glu-Glu-Glu-Ile.
Ganz besonders bevorzugte erfindungsgemäß verwendete Haarbehandlungsmittel sind dadurch gekennzeichnet, daß mindestens 0,1 Gew.-%, vorzugsweise mindestens 0,5 Gew.- %, besonders bevorzugt mindestens 1 Gew.-%, weiter bevorzugt mindestens 2,5 Gew.-%, noch weiter bevorzugt mindestens 5 Gew.-% und insbesondere mindestens 10 Gew.-% aller im Mittel enthaltenen keratinischen Peptide die Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile-Arg aufweisen. Very particularly preferred hair treatment agents used according to the invention are characterized in that at least 0.1% by weight, preferably at least 0.5% by weight, particularly preferably at least 1% by weight, more preferably at least 2.5% by weight, even more preferably at least 5% by weight, and in particular at least 10% by weight, of all the keratinic peptides contained in the composition have the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg.
Noch weiter bevorzugte erfindungsgemäß verwendete Haarbehandlungsmittel sind dadurch gekennzeichnet, daß mindestens 0, 1 Gew.-%, vorzugsweise mindestens 0,5 Gew.-%, besonders bevorzugt mindestens 1 Gew.-%, weiter bevorzugt mindestens 2,5 Gew.-%, noch weiter bevorzugt mindestens 5 Gew.-% und insbesondere mindestens 10 Gew.-% aller im Mittel enthaltenen keratinischen Peptide die Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile-Arg-Val aufweisen. Still further preferred hair treatment agents used according to the invention are characterized characterized in that at least 0.1% by weight, preferably at least 0.5% by weight, more preferably at least 1% by weight, more preferably at least 2.5% by weight, even more preferably at least 5% by weight. % and in particular at least 10 wt .-% of all keratinic peptides contained in the middle have the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val.
Insbesondere bevorzugte erfindungsgemäß verwendete Haarbehandlungsmittel sind dadurch gekennzeichnet, daß mindestens 0, 1 Gew.-%, vorzugsweise mindestens 0,5 Gew.-%, besonders bevorzugt mindestens 1 Gew.-%, weiter bevorzugt mindestens 2,5 Gew.-%, noch weiter bevorzugt mindestens 5 Gew.-% und insbesondere mindestens 10 Gew.-% aller im Mittel enthaltenen keratinischen Peptide die Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile-Arg-Val- Leu aufweisen. Particularly preferred hair treatment agents used according to the invention are characterized in that at least 0.1% by weight, preferably at least 0.5% by weight, more preferably at least 1% by weight, more preferably at least 2.5% by weight, still more preferably at least 5% by weight, and in particular at least 10% by weight, of all the keratinic peptides contained in the middle have the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val-Leu.
Die vorstehend genannten Bedingungen betreffen den Gesamtgehalt der erfindungsgemäß verwendeten Mittel an Peptiden, welche aus keratinischen Materialien stammen. Zusätzlich zu den Oligopeptiden keratinischer Herkunft können selbstverständlich weitere Peptide und/oder Protenihydrolysate eingesetzt werden, beispielsweise aus anderen nativen Quellen. Bevorzugt ist beispielsweise der zusätzliche Einsatz von Weizenproteinydrolysaten, siehe weiter unten. Es hat sich gezeigt, daß die Kombination aus zwei Aktivstoffen in den erfindungsgemäß verwendeten Haarbehandlungsmitteln durch einen dritten Aktivstoff erfolgreich ergänzt werden kann, wodurch die Förderung oder Verstärkung des Haarwuchses, die Verminderung von Haarausfall, die Aktivierung der Haarwurzelzellen, die Aktivierung von Haarfollikeln und die Verdickung des Haares noch weiter verstärkt werden können. The above conditions relate to the total content of the agents used according to the invention to peptides derived from keratinic materials. In addition to the oligopeptides of keratinic origin, of course, other peptides and / or protenihydrolysates can be used, for example from other native sources. For example, the additional use of wheat protein hydrolysates is preferred, see below. It has been found that the combination of two active substances in the hair treatment compositions used according to the invention can be successfully supplemented by a third active substance, whereby the promotion or enhancement of hair growth, the reduction of hair loss, the activation of the hair root cells, the activation of hair follicles and the thickening of the hair can be further enhanced.
Hier haben sich bestimmte Extrakte als dritter Aktivstoff in besonderer weise bewährt. Here certain extracts have proven to be the third active ingredient in a special way.
In erfindungsgemäß bevorzugten Verwendungen enthält das Haarbehandlungsmittel mindestens einen Extrakt von Pisum sativium. In preferred uses according to the invention, the hair treatment composition contains at least one extract of Pisum sativium.
Bevorzugte erfindungsgemäß verwendete Mittel sind dabei dadurch gekennzeichnet, daß sie - bezogen auf ihr Gewicht - 0,0005 bis 7,5 Gew.-%, vorzugsweise 0,001 bis 6 Gew.-%, weiter bevorzugt 0,005 bis 5 Gew.-%, weiter bevorzugt 0,01 bis 4 Gew.-% und insbesondere 0, 1 bis 3 Gew.-% mindestens eines Extraktes von Pisum sativium enthalten. Preferred agents used according to the invention are characterized in that they contain - based on their weight - 0.0005 to 7.5 wt .-%, preferably 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4 wt .-% and in particular 0, 1 to 3 wt .-% of at least one extract of Pisum sativium included.
Bevorzugte erfindungsgemäße Verwendungen sind dadurch gekennzeichnet, daß das Haarbehandlungsmittel - bezogen auf sein Gewicht - 0,001 bis 6 Gew.-%, weiter bevorzugt 0,005 bis 5 Gew.-%, weiter bevorzugt 0,01 bis 4 Gew.-% und insbesondere 0, 1 bis 3 Gew.-% mindestens eines Extraktes von Pisum sativium enthält. Preferred uses according to the invention are characterized in that the hair treatment agent - based on its weight - 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4 wt .-% and in particular 0, 1 contains up to 3 wt .-% of at least one extract of Pisum sativium.
Es hat sich gezeigt, daß die positiven Eigenschaften der erfindungsgemäß verwendeten Mittel insbesondere im Hinblick auf die positiven Effekte auf die Haarwurzeln und die innerstrukturelle Stärkung der Keratinfasern noch weiter gesteigert werden können, wenn die erfindungsgemäß verwendeten Mittel Purin bzw. Purinderivate enthalten. It has been found that the positive properties of the agents used according to the invention can be increased still further, in particular with regard to the positive effects on the hair roots and the inner structural strengthening of the keratin fibers, if the agents used according to the invention contain purine or purine derivatives.
Bevorzugte erfindungsgemäße Verwendungen sind dadurch gekennzeichnet, daß das Haarbehandlungsmittel - bezogen auf sein Gewicht - 0,0005 bis 7,5 Gew.-%, vorzugsweise 0,001 bis 6 Gew.-%, weiter bevorzugt 0,005 bis 5 Gew.-%, weiter bevorzugt 0,01 bis 4 Gew.- % und insbesondere 0,1 bis 3 Gew.-% Purin und/oder Purinderivat(e) der Formel (I) enthält Preferred uses according to the invention are characterized in that the Hair treatment agent - based on its weight - 0.0005 to 7.5 wt .-%, preferably 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4 wt .-% and in particular 0.1 to 3 wt .-% purine and / or purine derivative (s) of the formula (I)
in der die Reste R1, R2 und R3 unabhängig voneinander ausgewählt sind aus -H, - OH, -NH2, -SH und die Reste R4, R5 und R6 unabhängig voneinander ausgewählt sind aus -H, -CH3 und -CH2-CH3, wobei folgende Verbindungen bevorzugt sind: in which the radicals R 1 , R 2 and R 3 are independently selected from -H, - OH, -NH 2, -SH and the radicals R 4 , R 5 and R 6 are independently selected from -H, -CH 3 and -CH 2 -CH 3 , with the following compounds being preferred:
Purin (R1 = R2 = R3 = R4 = R5 = R6 = H), Adenin (R1 = NH2, R2 = R3 = R4 = R5 = R6 = H), Guanin (R1 = OH, R2 = NH2, R3 = R4 = R5 = R6 = H), Harnsäure (R1 = R2 = R3 = OH, R4 = R5 = R6 = H), Hypoxanthin (R1 = OH, R2 = R3 = R4 = R5 = R6 = H), 6-Purinthiol (R1 = SH, R2 = R3 = R = R5 = R6 = H) 6-Thioguanin (R1 = SH, R2 = NH2, R3 = R4 = R5 = R6 = H), Xanthin (R1 = R2 = OH, R3 = R4 = R5 = R6 = H), Coffein (R1 = R2 = OH, R3 = H, R4 = R5 = R6 = CH3), Theobromin (R1 = R2 = OH, R3 = R4 = H, R5 = R6 = H), Theophyllin (R1 = R2 = OH, R3 = H, R4 = CH3, R5 = CH3, R6 = H). Purine (R 1 = R 2 = R 3 = R 4 = R 5 = R 6 = H), adenine (R 1 = NH 2 , R 2 = R 3 = R 4 = R 5 = R 6 = H), guanine (R 1 = OH, R 2 = NH 2 , R 3 = R 4 = R 5 = R 6 = H), uric acid (R 1 = R 2 = R 3 = OH, R 4 = R 5 = R 6 = H ), Hypoxanthine (R 1 = OH, R 2 = R 3 = R 4 = R 5 = R 6 = H), 6-purinethiol (R 1 = SH, R 2 = R 3 = R = R 5 = R 6 = H) 6-thioguanine (R 1 = SH, R 2 = NH 2 , R 3 = R 4 = R 5 = R 6 = H), xanthine (R 1 = R 2 = OH, R 3 = R 4 = R 5 = R 6 = H), caffeine (R 1 = R 2 = OH, R 3 = H, R 4 = R 5 = R 6 = CH 3 ), theobromine (R 1 = R 2 = OH, R 3 = R 4 = H, R 5 = R 6 = H), theophylline (R 1 = R 2 = OH, R 3 = H, R 4 = CH 3 , R 5 = CH 3 , R 6 = H).
Bevorzugte erfindungsgemäß verwendete Mittel enthalten Purin und/oder Purinderivate in engeren Mengenbereichen. Hier sind erfindungsgemäß bevorzugt verwendete kosmetische Mittel dadurch gekennzeichnet, daß sie - bezogen auf ihr Gewicht - 0,001 bis 2,5 Gew.-%, vorzugsweise 0,0025 bis 1 Gew.-%, besonders bevorzugt 0,005 bis 0,5 Gew.-% und insbesondere 0,01 bis 0,1 Gew.-% Purin(e) und/oder Purinderivat(e) enthalten. Preferred agents used according to the invention contain purine and / or purine derivatives in narrower ranges. Cosmetic compositions preferably used according to the invention are characterized in that they contain, based on their weight, from 0.001 to 2.5% by weight, preferably from 0.0025 to 1% by weight, particularly preferably from 0.005 to 0.5% by weight. and in particular from 0.01 to 0.1% by weight of purine (s) and / or purine derivative (s).
Je nach gewünschtem Anwendungszweck der kosmetischen Mittel kann dabei die Art und Menge des Purinderivates variieren. In haarkosmetischen Formulierungen hat sich insbesondere Coffein bewährt, das beispielsweise in Shampoos und Conditionern vorzugsweise in Mengen von 0,005 bis 0,25 Gew.-%, weiter bevorzugt von 0,01 bis 0,1 Gew.- % und insbesondere von 0,01 bis 0,05 Gew.-% (jeweils bezogen auf das Mittel) eingesetzt werden kann. Depending on the desired application of the cosmetic agent may vary the nature and amount of purine derivative. Caffeine has proved particularly useful in hair cosmetic formulations, for example in shampoos and conditioners, preferably in amounts of from 0.005 to 0.25% by weight, more preferably from 0.01 to 0.1% by weight and in particular from 0.01 to 0.05 wt .-% (in each case based on the agent) can be used.
Erfindungsgemäß bevorzugt verwendete Haarbehandlungsmittel enthalten - jeweils bezogen auf ihr Gewicht Hair-treatment compositions preferably used according to the invention contain - in each case based on their weight
0,0005 bis 7,5 Gew.-%, vorzugsweise 0,001 bis 6 Gew.-%, weiter bevorzugt 0,005 bis 5 Gew.-%, weiter bevorzugt 0,01 bis 4 Gew.-% und insbesondere 0,1 bis 3 Gew.-% mindestens einer Verbindung ausgewählt aus L-Carnitin, und/oder den Carnitinderivaten Acetyl-L-Carnitin, L-Carnitin-Fumarat, L-Carnitin-Citrat, Lauroyl- L- Carnitin und insbesondere L-Carnitin-Tartrat; - 0,0002 bis 5 Gew.-%, vorzugsweise 0,0005 bis 2,5 Gew.-%, weiter bevorzugt 0,00075 bis 1 Gew.-%, besonders bevorzugt 0,001 bis 0,5 Gew.-%, weiter bevorzugt 0,002 bis 0,25 Gew.-% und insbesondere 0,005 bis 0,1 Gew.-% Oligopeptid(e) mit der Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile-Arg-Val wobei die Amino-Gruppen frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können, 0.0005 to 7.5 wt .-%, preferably 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4 wt .-% and in particular 0.1 to 3 wt .-% of at least one compound selected from L-carnitine, and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine citrate, lauroyl-L-carnitine and in particular L-carnitine tartrate; - 0.0002 to 5 wt .-%, preferably 0.0005 to 2.5 wt .-%, more preferably 0.00075 to 1 wt .-%, particularly preferably 0.001 to 0.5 wt .-%, more preferably 0.002 to 0.25 wt .-% and in particular 0.005 to 0.1 wt .-% oligopeptide (s) having the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val wherein the amino groups are free or protonated and the Carboxy groups may be free or deprotonated,
0,001 bis 2,5 Gew.-%, vorzugsweise 0,0025 bis 1 Gew.-%, besonders bevorzugt 0,005 bis 0,5 Gew.-% und insbesondere 0,01 bis 0,1 Gew.-% Coffein. 0.001 to 2.5 wt .-%, preferably 0.0025 to 1 wt .-%, particularly preferably 0.005 to 0.5 wt .-% and in particular 0.01 to 0.1 wt .-% caffeine.
Erfindungsgemäß besonders bevorzugt verwendete Haarbehandlungsmittel enthalten - jeweils bezogen auf ihr Gewicht Hair treatment agents used particularly preferably according to the invention contain - in each case based on their weight
0,0005 bis 7,5 Gew.-%, vorzugsweise 0,001 bis 6 Gew.-%, weiter bevorzugt 0,005 bis 5 Gew.-%, weiter bevorzugt 0,01 bis 4 Gew.-% und insbesondere 0,1 bis 3 Gew.-% mindestens einer Verbindung ausgewählt aus L-Carnitin, und/oder den Carnitinderivaten Acetyl-L-Carnitin, L-Carnitin-Fumarat, L-Carnitin-Citrat, Lauroyl- L- Carnitin und insbesondere L-Carnitin-Tartrat; 0.0005 to 7.5 wt .-%, preferably 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4 wt .-% and in particular 0.1 to 3 wt .-% of at least one compound selected from L-carnitine, and / or the carnitine derivatives acetyl-L-carnitine, L-carnitine fumarate, L-carnitine citrate, lauroyl-L-carnitine and in particular L-carnitine tartrate;
- 0,0002 bis 5 Gew.-%, vorzugsweise 0,0005 bis 2,5 Gew.-%, weiter bevorzugt 0,00075 bis 1 Gew.-%, besonders bevorzugt 0,001 bis 0,5 Gew.-%, weiter bevorzugt 0,002 bis 0,25 Gew.-% und insbesondere 0,005 bis 0, 1 Gew.-% Oligopeptid(e) mit der Aminosäuresequenz Tyr-Glu-Glu-Glu-Ile-Arg-Val wobei die Amino-Gruppen frei oder protoniert und die Carboxy-Gruppen frei oder deprotoniert vorliegen können, - 0.0002 to 5 wt .-%, preferably 0.0005 to 2.5 wt .-%, more preferably 0.00075 to 1 wt .-%, particularly preferably 0.001 to 0.5 wt .-%, more preferably 0.002 to 0.25 wt .-% and in particular 0.005 to 0, 1 wt .-% oligopeptide (s) having the amino acid sequence Tyr-Glu-Glu-Glu-Ile-Arg-Val wherein the amino groups are free or protonated and the Carboxy groups may be free or deprotonated,
0,0005 bis 7,5 Gew.-%, vorzugsweise 0,001 bis 6 Gew.-%, weiter bevorzugt 0,005 bis 5 Gew.-%, weiter bevorzugt 0,01 bis 4 Gew.-% und insbesondere 0,1 bis 3 Gew.-% mindestens eines Extraktes von Pisum sativium, 0.0005 to 7.5 wt .-%, preferably 0.001 to 6 wt .-%, more preferably 0.005 to 5 wt .-%, more preferably 0.01 to 4 wt .-% and in particular 0.1 to 3 wt .-% of at least one extract of Pisum sativium,
0,001 bis 2,5 Gew.-%, vorzugsweise 0,0025 bis 1 Gew.-%, besonders bevorzugt 0,005 bis 0,5 Gew.-% und insbesondere 0,01 bis 0, 1 Gew.-% Coffein. 0.001 to 2.5 wt .-%, preferably 0.0025 to 1 wt .-%, particularly preferably 0.005 to 0.5 wt .-% and in particular 0.01 to 0, 1 wt .-% caffeine.
Die erfindungsgemäß verwendeten Mittel können weitere Wirk- und Hilfsstoffe beinhalten. Diese werden nachfolgend beschrieben. The agents used in the invention may contain other active ingredients and adjuvants. These are described below.
Vorzugsweise enthalten die erfindungsgemäß verwendeten Mittel zusätzlich mindestens einen Emulgator bzw. ein Tensid, wobei oberflächenaktive Substanzen je nach Anwendungsgebiet als Tenside oder als Emulgatoren bezeichnet werden und aus anionischen, kationischen, zwitterionischen, ampholytischen und nichtionischen Tensiden und Emulgatoren ausgewählt sind. The agents used according to the invention preferably additionally comprise at least one emulsifier or a surfactant, surface-active substances being referred to as surfactants or as emulsifiers, depending on the field of use, and selected from anionic, cationic, zwitterionic, ampholytic and nonionic surfactants and emulsifiers.
Bevorzugte erfindungsgemäße Verwendungen sind dadurch gekennzeichnet, daß das Haarbehandlungsmittel - bezogen auf sein Gewicht - 0,5 bis 70 Gew.-%, vorzugsweise 1 bis 60 Gew.-%, weiter bevorzugt 2,5 bis 35 Gew.-% und insbesondere 5 bis 25 Gew.-% anionische(s) und/oder nichtionische(s) und/oder kationische(s) und/oder amphotere(s) Tensid(e), enthält. Als anionische Tenside und Emulgatoren eignen sich für die erfindungsgemäß verwendeten Zusammensetzungen alle für die Verwendung am menschlichen Körper geeigneten anionischen oberflächenaktiven Stoffe. Diese sind gekennzeichnet durch eine wasserlöslich machende, anionische Gruppe wie z. B. eine Carboxylat-, Sulfat-, Sulfonat- oder Phosphat- Gruppe und eine lipophile Alkylgruppe mit etwa 8 bis 30 C-Atomen. Zusätzlich können im Molekül Glycol- oder Polyglycolether-Gruppen, Ester-, Ether- und Amidgruppen sowie Hydroxylgruppen enthalten sein. Beispiele für geeignete anionische Tenside und Emulgatoren sind, jeweils in Form der Natrium-, Kalium- und Ammonium- sowie der Mono-, Di- und Trialka- nolammoniumsalze mit 2 bis 4 C-Atomen in der Alkanolgruppe, Preferred uses according to the invention are characterized in that the hair treatment agent - based on its weight - 0.5 to 70 wt .-%, preferably 1 to 60 wt .-%, more preferably 2.5 to 35 wt .-% and in particular 5 to 25% by weight of anionic and / or nonionic and / or cationic and / or amphoteric surfactant (s). Suitable anionic surfactants and emulsifiers for the compositions used according to the invention are all anionic surfactants suitable for use on the human body. These are characterized by a water-solubilizing, anionic group such as. Example, a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group having about 8 to 30 carbon atoms. In addition, glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups may be present in the molecule. Examples of suitable anionic surfactants and emulsifiers are, in each case in the form of the sodium, potassium and ammonium as well as mono-, di- and trialkanolammonium salts having 2 to 4 C atoms in the alkanol group,
lineare und verzweigte Fettsäuren mit 8 bis 30 C-Atomen (Seifen), linear and branched fatty acids with 8 to 30 carbon atoms (soaps),
Ethercarbonsäuren der Formel R-0-(CH2-CH20)x-CH2-COOH, in der R eine lineare Alkylgruppe mit 8 bis 30 C-Atomen und x = 0 oder 1 bis 16 ist, Ethercarbonsäuren the formula R-0- (CH 2 -CH 2 0) x-CH 2 -COOH, in which R is a linear alkyl group having 8 to 30 carbon atoms and x = 0 or 1 to 16,
Acylsarcoside mit 8 bis 24 C-Atomen in der Acylgruppe, Acylsarcosides having 8 to 24 carbon atoms in the acyl group,
Acyltauride mit 8 bis 24 C-Atomen in der Acylgruppe, Acyltaurides having 8 to 24 carbon atoms in the acyl group,
Acylisethionate mit 8 bis 24 C-Atomen in der Acylgruppe, Acyl isethionates having 8 to 24 carbon atoms in the acyl group,
lineare Alkansulfonate mit 8 bis 24 C-Atomen, linear alkanesulfonates having 8 to 24 C atoms,
lineare Alpha-Olefinsulfonate mit 8 bis 24 C-Atomen, linear alpha-olefin sulfonates having 8 to 24 C atoms,
Alpha-Sulfofettsäuremethylester von Fettsäuren mit 8 bis 30 C-Atomen, Alpha-sulfofatty acid methyl esters of fatty acids having 8 to 30 carbon atoms,
Acylglutamate der Formel (T-l), Acylglutamates of the formula (T-1),
XOOC-CH2CH2CH-COOX (T-l) XOOC-CH2CH2CH-COOX (T-1)
I I
HN-COR1 HN-COR 1
in der R1CO für einen linearen oder verzweigten Acylrest mit 6 bis 22 Kohlenstoffatomen und 0, 1 , 2 oder 3 Doppelbindungen und X für Wasserstoff, ein Alkali- und/oder Erdalkalimetall, Ammonium, Alkylammonium, Alkanolammonium oder Glucammonium steht, beispielsweise Acylglutamate, die sich von Fettsäuren mit 6 bis 22, vorzugsweise 12 bis 18 Kohlenstoffatomen ableiten, wie beispielsweise C12/14- bzw. C 12/18- Kokosfettsäure, Laurin- säure, Myristinsäure, Palmitinsäure und/oder Stearinsäure, insbesondere Natrium-N- cocoyl- und Natrium-N-stearoyl-L-glutamat, in which R 1 CO is a linear or branched acyl radical having 6 to 22 carbon atoms and 0, 1, 2 or 3 double bonds and X is hydrogen, an alkali and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium, for example acylglutamates, which are derived from fatty acids having 6 to 22, preferably 12 to 18 carbon atoms, such as, for example, C 12/14 or C 12/18 coconut fatty acid, lauric acid, myristic acid, palmitic acid and / or stearic acid, in particular sodium N-cocoyl and sodium N-stearoyl-L-glutamate,
Ester einer hydroxysubstituierten Di- oder Tricarbonsäure der allgemeinen Formel ("T-l I) , Esters of a hydroxy-substituted di- or tricarboxylic acid of the general formula ( " T1 " ),
XX
II
HO— C— COOR1 (T-Il) HOCCOOR 1 (T-II)
I I
Y— CH— COOR2 in der X=H oder eine -ChbCOOR-Gruppe ist, Y=H oder -OH ist unter der Bedingung, dass Y=H ist, wenn X—CH2COOR ist, R, R1 und R2 unabhängig voneinander ein Wasserstoffatom, ein Alkali- oder Erdalkalimetallkation, eine Ammoniumgruppe, das Kation einer ammonium-organischen Base oder einen Rest Z bedeuten, der von einer poly- hydroxylierten organischen Verbindung stammt, die aus der Gruppe der veretherten (C6-Ci8)-Alkylpolysaccharide mit 1 bis 6 monomeren Saccharideinheiten und/oder der veretherten aliphatischen (C6-Ci6)-Hydroxyalkylpolyole mit 2 bis 16 Hydroxylresten ausgewählt sind, unter der Maßgabe, dass wenigstens eine der Gruppen R, R1 oder R2 ein Rest Z ist, Y-CH-COOR 2 wherein X = H or a -ChbCOOR group, Y = H or -OH is under the condition that Y = H when X is -CH 2 COOR, R, R 1 and R 2 are independently a hydrogen atom, an alkali or alkaline earth metal cation, an ammonium group, the cation of an ammonium organic base or a radical Z derived from a polyhydroxylated organic compound selected from the group of etherified (C6-Ci 8 ) -alkyl polysaccharides having 1 to 6 monomeric saccharide units and / or the etherified aliphatic (C 6 -C 16) -hydroxyalkylpolyols having 2 to 16 hydroxyl radicals are selected, provided that at least one of the groups R, R 1 or R 2 is a radical Z,
Ester der Sulfobernsteinsäure oder der Sulfosuccinate der allgemeinen Formel (TT- III), Esters of sulfosuccinic acid or sulfosuccinates of the general formula (TT-III),
H2C— COOR1 (T-Ill) in der M'n+ n) für n = 1 ein Wasserstoffatom, ein Alkalimetallkation, eine Ammoniumgruppe oder das Kation einer ammonium-organischen Base und für n = 2 ein Erdalkalimetallkation darstellt und R1 und R2 unabhängig voneinander ein Wasserstoffatom, ein Alkali- oder Erdalkalimetallkation, eine Ammoniumgruppe, das Kation einer ammonium-organischen Base oder einen Rest Z bedeuten, der von einer polyhydroxylierten organischen Verbindung stammt, die aus der Gruppe der veretherten (C6-Ci8)-Alkylpolysaccharide mit 1 bis 6 monomeren Saccharideinheiten und/oder der veretherten aliphatischen (C6-Ci6)-Hydro- xyalkylpolyole mit 2 bis 16 Hydroxylresten ausgewählt ist, unter der Maßgabe, dass wenigstens eine der Gruppen R1 oder R2 ein Rest Z ist, H 2 C COOR 1 (T-III) in M ' n + n) for n = 1 represents a hydrogen atom, an alkali metal cation, an ammonium group or the cation of an ammonium organic base and for n = 2 an alkaline earth metal cation and R 1 and R 2 independently represent a hydrogen atom, an alkali metal or Alkaline earth metal cation, an ammonium group, the cation of an ammonium organic base or a radical Z derived from a polyhydroxylated organic compound selected from the group of etherified (C6-Ci8) alkyl polysaccharides having 1 to 6 monomeric saccharide units and / or the etherified aliphatic (C 6 -C 16) -hydroxyalkyl polyols having 2 to 16 hydroxyl radicals, with the proviso that at least one of the groups R 1 or R 2 is a radical Z,
Sulfobernsteinsäuremono- und -dialkylester mit 8 bis 24 C-Atomen in der Alkylgruppe und Sulfobernsteinsäuremonoalkylpolyoxyethylester mit 8 bis 24 C-Atomen in der Alkylgruppe und 1 bis 6 Oxyethylgruppen, Sulfosuccinic acid mono- and dialkyl esters having 8 to 24 C atoms in the alkyl group and sulfosuccinic monoalkylpolyoxyethyl esters having 8 to 24 C atoms in the alkyl group and 1 to 6 oxyethyl groups,
- Alkylsulfate und Alkylpolyglycolethersulfate der Formel R-(0-CH2-CH2)x-OS03H, in der R eine bevorzugt lineare Alkylgruppe mit 8 bis 30 C-Atomen und x = 0 oder 1 - 12 ist, Ester der Weinsäure und Zitronensäure mit Alkoholen, die Anlagerungsprodukte von etwa 2-15 Molekülen Ethylenoxid und/oder Propylenoxid an C8-22-Fettalkohole darstellen, Alkyl- und/oder Alkenyletherphosphate, - alkyl sulfates and alkyl polyglycol ether sulfates of the formula R- (O-CH 2 -CH 2 ) x-OSO 3 H, in which R is a preferably linear alkyl group having 8 to 30 carbon atoms and x = 0 or 1-12, esters of tartaric acid and Citric acid with alcohols which are adducts of about 2-15 molecules of ethylene oxide and / or propylene oxide onto C8-22 fatty alcohols, alkyl and / or alkenyl ether phosphates,
sulfatierte Fettsäurealkylenglycolester, sulfated fatty acid alkylene glycol esters,
Monoglyceridsulfate und Monoglyceridethersulfate. Monoglyceride sulfates and monoglyceride ether sulfates.
Bevorzugte anionische Tenside und Emulgatoren sind Acylglutamate, Acylisethionate, Acylsarcosinate und Acyltaurate, jeweils mit einem linearen oder verzweigten Acylrest mit 6 bis 22 Kohlenstoffatomen und 0, 1 , 2 oder 3 Doppelbindungen, der in besonders bevorzugten Ausführungsformen aus einem Octanoyl-, Decanoyl-, Lauroyl-, Myristoyl-, Palmitoyl- und Stearoylrest ausgewählt ist, Ester der Weinsäure, Zitronensäure oder Bernsteinsäure bzw. der Salze dieser Säuren mit alkylierter Glucose, insbesondere die Produkte mit der INCI- Bezeichnung Disodium Coco-Glucoside Citrate, Sodium Coco-Glucoside Tartrate und Disodium Coco-Glucoside Sulfosuccinate, Alkylpolyglycolethersulfate und Ethercarbonsäuren mit 8 bis 18 C-Atomen in der Alkylgruppe und bis zu 12 Ethoxygruppen im Molekül, Sulfo- bernsteinsäuremono- und -dialkylester mit 8 bis 18 C-Atomen in der Alkylgruppe und Sulfo- bernsteinsäuremonoalkylpolyoxyethylester mit 8 bis 18 C-Atomen in der Alkylgruppe und 1 bis 6 Ethoxygruppen. Preferred anionic surfactants and emulsifiers are acylglutamates, acyl isethionates, acyl sarcosinates and acyl taurates, each with a linear or branched acyl radical having 6 to 22 carbon atoms and 0, 1, 2 or 3 double bonds, which are particularly preferred Embodiments of an octanoyl, decanoyl, lauroyl, myristoyl, palmitoyl and stearoyl radical is selected, esters of tartaric acid, citric acid or succinic acid or the salts of these acids with alkylated glucose, in particular the products with the INCI name Disodium Coco Glucoside Citrate, Sodium Coco-Glucoside Tartrate and Disodium Coco-Glucoside Sulfosuccinates, alkyl polyglycol ether sulfates and ether carboxylic acids containing 8 to 18 carbon atoms in the alkyl group and up to 12 ethoxy groups in the molecule, sulfonated succinic acid mono- and dialkyl esters of 8 to 18 carbon atoms in the alkyl group and sulfosuccinic monoalkylpolyoxyethyl esters having 8 to 18 C atoms in the alkyl group and 1 to 6 ethoxy groups.
Als zwitterionische Tenside und Emulgatoren werden solche oberflächenaktiven Verbindungen bezeichnet, die im Molekül mindestens eine quartäre Ammoniumgruppe und mindestens eine -COO(_) - oder -S03H -Gruppe tragen. Besonders geeignete zwitterionische Tenside und Emulgatoren sind die sogenannten Betaine wie die N-Alkyl-N,N-dimethylammoni- umglycinate, beispielsweise das Kokosalkyldimethylammoniumglycinat, N-Acyl-aminopropyl- Ν,Ν-dimethylammoniumglycinate, beispielsweise das Kokosacylaminopropyldimethyl- ammoniumglycinat, und 2-Alkyl-3-carboxymethyl-3-hydroxyethylimidazoline mit jeweils 8 bis 18 C-Atomen in der Alkyl- oder Acylgruppe sowie das Kokosacylaminoethylhydroxyethylcarb- oxymethylglycinat. Ein bevorzugtes zwitterionisches Tensid ist das unter der INCI- Bezeichnung Cocamidopropyl Betaine bekannte Fettsäureamidderivat. Zwitterionic surfactants and emulsifiers are those surface-active compounds which carry in the molecule at least one quaternary ammonium group and at least one -COO (_) or -SO 3 H group. Particularly suitable zwitterionic surfactants and emulsifiers are the so-called betaines, such as N-alkyl-N, N-dimethylammonium glycinates, for example cocoalkyldimethylammonium glycinate, N-acylaminopropyl-Ν, Ν-dimethylammonium glycinates, for example cocoacylaminopropyldimethylammonium glycinate, and 2-alkyl 3-carboxymethyl-3-hydroxyethylimidazolines having in each case 8 to 18 carbon atoms in the alkyl or acyl group, and also the cocoacylaminoethylhydroxyethylcarboxymethylglycinate. A preferred zwitterionic surfactant is the fatty acid amide derivative known by the INCI name Cocamidopropyl Betaine.
Unter ampholytischen Tensiden und Emulgatoren werden solche oberflächenaktiven Verbindungen verstanden, die außer einer Ca - C2 - Alkyl- oder -Acylgruppe mindestens eine freie Aminogruppe und mindestens eine -COOH- oder -SOsH-Gruppe enthalten und zur Ausbildung innerer Salze befähigt sind. Beispiele für geeignete ampholytische Tenside sind N-Alkyl- glycine, N-Alkylaminopropionsäuren, N-Alkylaminobuttersäuren, N-Alkyliminodipropionsäuren, N-Hydroxyethyl-N-alkylamidopropylglycine, N-Alkyltaurine, N-Alkylsarcosine, 2-Alkylamino- propionsäuren und Alkylaminoessigsäuren mit jeweils etwa 8 bis 24 C-Atomen in der Alkylgruppe. Besonders bevorzugte ampholytische Tenside sind das N-Kokosalkylaminopropionat, das Kokosacylaminoethylaminopropionat und das C12 - C18 - Acylsarcosin. Ampholytic surfactants and emulsifiers are understood as meaning those surface-active compounds which, apart from a Ca-C2-alkyl or -acyl group, contain at least one free amino group and at least one -COOH or -SOsH group and are capable of forming internal salts. Examples of suitable ampholytic surfactants are N-alkylglycines, N-alkylaminopropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids each having about 8 to 24 C atoms in the alkyl group. Particularly preferred ampholytic surfactants are N-cocoalkylaminopropionate, cocoacylaminoethylaminopropionate and C12-C18 acylsarcosine.
Nichtionische Tenside und Emulgatoren enthalten als hydrophile Gruppe z. B. eine Polyol- gruppe, eine Polyalkylenglycolethergruppe oder eine Kombination aus Polyol- und Polyglycol- ethergruppe. Nonionic surfactants and emulsifiers contain as hydrophilic group z. For example, a polyol group, a polyalkylene glycol ether group or a combination of polyol and polyglycol ether group.
Als bevorzugte nichtionische oberflächenaktive Substanzen haben sich die Alkylpolyglycoside, gegebenenfalls im Gemisch mit Fettalkoholen, alkoxylierte Polydialkylsiloxane, Alkylenoxid- Anlagerungsprodukte an gesättigte lineare Fettalkohole und Fettsäuren mit jeweils 2 bis 30 Mol Ethylenoxid pro Mol Fettalkohol bzw. Fettsäure erwiesen. Preferred nonionic surface-active substances are the alkylpolyglycosides, optionally mixed with fatty alcohols, alkoxylated polydialkylsiloxanes, alkylene oxide addition products of saturated linear fatty alcohols and fatty acids with in each case 2 to 30 moles of ethylene oxide per mole of fatty alcohol or fatty acid.
Erfindungsgemäß einsetzbar sind weiterhin kationische Tenside vom Typ der quartären Ammoniumverbindungen, der Esterquats und der Amidoamine. Bevorzugte quaternäre Ammoniumverbindungen sind Ammoniumhalogenide, insbesondere Chloride und Bromide, wie Alkyltrimethylammoniumchloride, Dialkyldimethylammoniumchloride und Trialkylmethyl- ammoniumchloride. Die langen Alkylketten dieser Tenside weisen bevorzugt 10 bis 18 Kohlenstoffatome auf, wie z. B. in Cetyltrimethylammoniumchlorid, Stearyltrimethylammonium- chlorid, Distearyldimethylammoniumchlorid, Lauryldimethylammoniumchlorid, Lauryldi- methylbenzylammoniumchlorid und Tricetylmethylammoniumchlorid. Weitere bevorzugte kationische Tenside sind die unter den INCI-Bezeichnungen Quaternium-27 und Quaternium- 83 bekannten Imidazolium-Verbindungen. Also usable according to the invention are cationic surfactants of the quaternary ammonium compound type, the esterquats and the amidoamines. Preferred quaternary Ammonium compounds are ammonium halides, in particular chlorides and bromides, such as alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkylmethylammonium chlorides. The long alkyl chains of these surfactants preferably have 10 to 18 carbon atoms, such as. In cetyltrimethylammonium chloride, stearyltrimethylammonium chloride, distearyldimethylammonium chloride, lauryldimethylammonium chloride, lauryldimethylbenzylammonium chloride and tricetylmethylammonium chloride. Further preferred cationic surfactants are the imidazolium compounds known under the INCI names Quaternium-27 and Quaternium-83.
Ganz besonders bevorzugte erfindungsgemäß verwendete Mittel, enthalten zusätzlich Fettalkohol(e) und/oder Fettalkoholalkoxylat(e), vorzugsweise Ci2-22-Fettalkohol(e) und/oder Ci2-22-Fettalkoholethoxylat(e) mit 10 bis 30 EO-Einheiten, besonders bevorzugt C16-18- Fettalkohol(e) und/oder Ci6-ie-Fettalkoholethoxylat(e) mit 12 bis 20 EO-Einheiten, vorzugsweise in Mengen von 5 bis 20 Gew.-%, bevorzugt von 7,5 bis 17,5 Gew.-% und insbesondere von 10 bis 15 Gew.-%, jeweils bezogen auf das Gewicht des Mittels. Very particularly preferred agents used according to the invention additionally comprise fatty alcohol (s) and / or fatty alcohol alkoxylate (s), preferably C 12-22 fatty alcohol (s) and / or C 12-22 fatty alcohol ethoxylate (s) with 10 to 30 EO units, especially preferably C16-18 fatty alcohol (s) and / or Ci6-ie fatty alcohol ethoxylate (s) having 12 to 20 EO units, preferably in amounts of 5 to 20 wt .-%, preferably from 7.5 to 17.5 wt .-% and in particular from 10 to 15 wt .-%, each based on the weight of the composition.
Zusammenfassend sind erfindungsgemäß verwendete Haarbehandlungsmittel bevorzugt, die - bezogen auf ihr Gewicht - 0,1 bis 20 Gew.-%, vorzugsweise 0,25 bis 17,5 Gew.-% und insbesondere 5 bis 15 Gew.-% anionische(s) Tensid(e), besonders bevorzugt Fettal koholethersulfate der Formel In summary, hair treatment agents used according to the invention are preferred, which - based on their weight - 0.1 to 20 wt .-%, preferably 0.25 to 17.5 wt .-% and in particular 5 to 15 wt .-% anionic (s) surfactant (E), particularly preferably Fettal kholethersulfate the formula
H3C-(CH2)n-(OCH2CH2)k-OS03- M+ H 3 C- (CH 2) n (OCH 2 CH 2) k-OS03- M +
enthalten, in der n für Werte von 5 bis 21 , vorzugsweise von 7 bis 19, besonders bevorzugt von 9 bis 17 und insbesondere von 1 1 bis 13 und k für Werte von 1 , 2, 3, 4, 5, 6, 7, 8, 9 oder 10, vorzugsweise für 1 , 2 oder 3 und insbesondere für 2 stehen, und M für ein Kation aus der Gruppe Na+, K+ NH4 +, Vz Mg2+, 1/ Zn2+, vorzugsweise für Na+, stehen. in which n represents values of from 5 to 21, preferably from 7 to 19, particularly preferably from 9 to 17 and in particular from 1 to 13 and k for values of 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10, preferably 1, 2 or 3 and especially 2, and M is a cation from the group Na + , K + NH 4 + , Vz Mg 2+ , 1 / Zn 2+ , preferably Na + , stand.
Bevorzugte erfindungsgemäß verwendete Haarbehandlungsmittel sind weiter dadurch gekennzeichnet, daß sie zusätzlich amphotere(s) Tensid(e), vorzugsweise aus den Gruppen der Preferred hair-treatment agents used according to the invention are further characterized in that they additionally contain amphoteric surfactant (s), preferably from the groups of
N-Alkylglycine, N-Alkylpropionsäuren, N-Alkylaminobuttersäuren, N-Alkylimino- dipropionsäuren, N-Hydroxyethyl-N-alkylamidopropylglycine, N-Alkyltaurine, N-Alkylsarcosine, 2-Alkylaminopropionsäuren mit jeweils etwa 8 bis 24 C-Atomen in der Alkylgruppe, Alkylaminoessigsäuren mit jeweils etwa 8 bis 24 C-Atomen in der Alkylgruppe, N-Kokosalkyl- aminopropionat, Kokosacylaminoethylaminopropionat, C12 - C18 - Acylsarcosin, N-Alkyl-N,N- dimethylammonium-glycinate, beispielsweise Kokosalkyl-dimethylammoniumglycinat, N-Acyl- aminopropyl-N,N-dimethylammoniumglycinate, beispielsweise Kokosacylaminopropyl- dimethylammoniumglycinat, 2-Alkyl-3-carboxymethyl-3-hydroxyethyl-imidazoline mit jeweils 8 bis 18 C-Atomen in der Alkyl- oder Acylgruppe, Kokosacylaminoethylhydroxyethylcarboxy- methylglycinat, der unter der INCI-Bezeichnung Cocamidopropyl Betain bekannten Verbindungen, der unter der INCI-Bezeichnung Disodium Cocoamphodiacetate bekannten Verbindungen, enthalten, wobei bevorzugte erfindungsgemäß verwendete Mittel das bzw. die amphotere(n) Tensid(e) in Mengen von 1 bis 15 Gew.-%, vorzugsweise von 2,5 bis 12 Gew.- % und insbesondere von 5 bis 10 Gew.-%, jeweils bezogen auf das gesamte Mittel, enthalten. Als weiteren optionalen Bestandteil können die erfindungsgemäß verwendeten Mittel 0,01 bis 10 Gew.-% mindestens eines Polymers aus der Gruppe der kationischen und/oder amphoteren Polymere enthalten. N-alkylglycines, N-alkylpropionic acids, N-alkylaminobutyric acids, N-alkylimidodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids having in each case about 8 to 24 C atoms in the alkyl group, Alkylaminoacetic acids having in each case about 8 to 24 carbon atoms in the alkyl group, N-cocoalkylaminopropionate, cocoacylaminoethylaminopropionate, C 12 -C 18 -acylsarcosine, N-alkyl-N, N-dimethylammonium glycinates, for example cocoalkyldimethylammonium glycinate, N-acylaminopropyl -N, N-dimethylammonium glycinates, for example Kokosacylaminopropyl- dimethylammoniumglycinat, 2-alkyl-3-carboxymethyl-3-hydroxyethyl imidazoline having in each case 8 to 18 carbon atoms in the alkyl or acyl group, cocoacylaminoethylhydroxyethylcarboxymethylglycinat, the INCI name Cocamidopropyl betaine known compounds known under the INCI name Disodium Cocoamphodiacetate Compounds containing, preferred means according to the invention the amphoteric surfactant (s) in amounts of 1 to 15 wt .-%, preferably from 2.5 to 12% by weight and in particular from 5 to 10 wt .-%, each based on the total agent included. As a further optional component, the agents used according to the invention may contain from 0.01 to 10% by weight of at least one polymer from the group of cationic and / or amphoteric polymers.
Unter kationischen bzw. amphoteren Polymeren sind Polymere zu verstehen, welche in der Haupt- und/oder Seitenkette eine Gruppe aufweisen, welche "temporär" oder "permanent" kationisch sein kann. Als "permanent kationisch" werden erfindungsgemäß solche Polymere bezeichnet, die unabhängig vom pH-Wert des Mittels eine kationische Gruppe aufweisen. Dies sind in der Regel Polymere, die ein quartäres Stickstoffatom, beispielsweise in Form einer Ammoniumgruppe, enthalten. Bevorzugte kationische Gruppen sind quartäre Ammoniumgruppen. Insbesondere solche Polymere, bei denen die quartäre Ammoniumgruppe über eine C1-4-Kohlenwasserstoffgruppe an eine aus Acrylsäure, Methacrylsäure oder deren Derivaten aufgebaute Polymerhauptkette gebunden sind, haben sich als besonders geeignet erwiesen. Cationic or amphoteric polymers are to be understood as meaning polymers which have a group in the main and / or side chain which may be "temporary" or "permanent" cationic. According to the invention, "permanently cationic" refers to those polymers which have a cationic group, irrespective of the pH of the agent. These are usually polymers containing a quaternary nitrogen atom, for example in the form of an ammonium group. Preferred cationic groups are quaternary ammonium groups. In particular, those polymers in which the quaternary ammonium group is bonded via a C 1-4 hydrocarbon group to a polymer main chain constructed from acrylic acid, methacrylic acid or derivatives thereof have proven to be particularly suitable.
Zusätzlich zu kationischen Polymerisaten oder an ihrer Stelle können die erfindungsgemäß verwendeten Mittel auch amphotere Polymere enthalten. Diese weisen zusätzlich mindestens eine negativ geladene Gruppe im Molekül auf und werden auch als zwitterionische Polymere bezeichnet. In addition to cationic polymers or in their place, the agents used in the invention may also contain amphoteric polymers. These additionally have at least one negatively charged group in the molecule and are also referred to as zwitterionic polymers.
Vorzugsweise wird das Polymer bzw. werden die Polymere innerhalb engerer Mengenbereiche eingesetzt. So sind erfindungsgemäß verwendete Mittel bevorzugt, die - bezogen auf ihr Gewicht - 0,05 bis 7,5 Gew.-%, vorzugsweise 0,1 bis 5 Gew.-%, besonders bevorzugt 0,2 bis 3,5 Gew.-% und insbesondere 0,25 bis 2,5 Gew.-% amphotere(s) Polymer(e), enthalten. Preferably, the polymer or polymers are used within narrower ranges. Thus, agents used according to the invention are preferred which, based on their weight, contain 0.05 to 7.5% by weight, preferably 0.1 to 5% by weight, particularly preferably 0.2 to 3.5% by weight. and in particular from 0.25 to 2.5% by weight of amphoteric polymer (s).
Unabhängig davon, ob in den Mitteln amphotere Polymere enthalten sind oder nicht, sind weiter bevorzugte erfindungsgemäß verwendete Mittel dadurch gekennzeichnet, daß sie - bezogen auf ihr Gewicht - 0,05 bis 7,5 Gew.-%, vorzugsweise 0,1 bis 5 Gew.-%, besonders bevorzugt 0,2 bis 3,5 Gew.-% und insbesondere 0,25 bis 2,5 Gew.-% kationische(s) Polymer(e), enthalten. Regardless of whether amphoteric polymers are or are not included in the compositions, further preferred agents used according to the invention are characterized in that they contain, based on their weight, from 0.05 to 7.5% by weight, preferably from 0.1 to 5% by weight .-%, particularly preferably 0.2 to 3.5 wt .-% and in particular 0.25 to 2.5 wt .-% cationic (s) polymer (s) included.
Erfindungsgemäß bevorzugt einsetzbare kationische Polymere werden nachstehend beschrieben: Homopolymere der allgemeinen Formel (G1-I), Cationic polymers which can preferably be used according to the invention are described below: Homopolymers of the general formula (G1-I),
R1 R 1
-[CH2-C-]n (G1-I) - [CH 2 -C-] n (G1-I)
CO-0-(CH2)m-N+R2R3R4 in der R1= -H oder -CH3 ist, R2, R3 und R4 unabhängig voneinander ausgewählt sind aus C1- 4-Alkyl-, -Alkenyl- oder -Hydroxyalkylgruppen, m = 1 , 2, 3 oder 4, n eine natürliche Zahl und X" ein physiologisch verträgliches organisches oder anorganisches Anion ist, sowie Copolymere, bestehend im wesentlichen aus den in Formel (G1-I) aufgeführten Monomereinheiten sowie nichtionogenen Monomereinheiten, sind besonders bevorzugte kationische Polymere. Im Rahmen dieser Polymere sind diejenigen erfindungsgemäß bevorzugt, für die mindestens eine der folgenden Bedingungen gilt: CO-O- (CH 2 ) m -N + R 2 R 3 R 4 in which R 1 is -H or -CH 3 , R 2 , R 3 and R 4 are independently selected from C 1-4 -alkyl, Alkenyl or hydroxyalkyl groups, m = 1, 2, 3 or 4, n is a natural number and X "is a physiologically acceptable organic or inorganic anion, as well as copolymers consisting essentially of the monomer units listed in formula (G1-I) and nonionic monomer units, are particularly preferred cationic polymers. Within the scope of these polymers, preference is given to those according to the invention for which at least one of the following conditions applies:
R1 steht für eine Methylgruppe R 1 is a methyl group
R2, R3 und R4 stehen für Methylgruppen R 2 , R 3 and R 4 are methyl groups
m hat den Wert 2. m has the value 2.
Als physiologisch verträgliches Gegenionen X" kommen beispielsweise Halogenidionen, Sulfationen, Phosphationen, Methosulfationen sowie organische Ionen wie Lactat-, Citrat-, Tartrat- und Acetationen in Betracht. Bevorzugt sind Halogenidionen, insbesondere Chlorid. Ein besonders geeignetes Homopolymer ist das, gewünschtenfalls vernetzte, Poly(methacryloyloxyethyltrimethylammoniumchlorid) mit der INCI-Bezeichnung Polyquaternium-37. Solche Produkte sind beispielsweise unter den Bezeichnungen Rheocare® CTH (Cosmetic Rheologies) und Synthalen® CR (Ethnichem) im Handel erhältlich. Die Vernetzung kann gewünschtenfalls mit Hilfe mehrfach olefinisch ungesättigter Verbindungen, beispielsweise Divinylbenzol, Tetraallyloxyethan, Methylenbisacrylamid, Diallylether, Polyallylpolyglycerylether, oder Allylethern von Zuckern oder Zuckerderivaten wie Erythritol, Pentaerythritol, Arabitol, Mannitol, Sorbitol, Sucrose oder Glucose erfolgen. Methylenbisacrylamid ist ein bevorzugtes Vernetzungsagens. Suitable physiologically tolerated counterions X " are, for example, halide ions, sulfate ions, phosphate ions, methosulfate ions and organic ions such as lactate, citrate, tartrate and acetate ions.Holyidene ions, in particular chloride, are particularly suitable A particularly suitable homopolymer is the, if desired crosslinked, poly (methacryloyloxyethyltrimethylammonium chloride) with the INCI name Polyquaternium-37. such products are, for example, under the names Rheocare ® CTH (Cosmetic Rheologies) and Synthalen® ® CR (Ethnichem) commercially available. the crosslinking can, if desired, with the help of olefinically polyunsaturated compounds, for example divinylbenzene , Tetraallyloxyethane, methylenebisacrylamide, diallyl ether, polyallylpolyglyceryl ethers, or allyl ethers of sugars or sugar derivatives such as erythritol, pentaerythritol, arabitol, mannitol, sorbitol, sucrose or glucose methylenebisacrylamide is a preferred crosslinking site ns.
Das Homopolymer wird bevorzugt in Form einer nichtwäßrigen Polymerdispersion, die einen Polymeranteil nicht unter 30 Gew.-% aufweisen sollte, eingesetzt. Solche Polymerdispersionen sind unter den Bezeichnungen Salcare® SC 95 (ca. 50 % Polymeranteil, weitere Komponenten: Mineralöl (INCI-Bezeichnung: Mineral Oil) und Tridecyl-polyoxypropylen- polyoxyethylen-ether (INCI-Bezeichnung: PPG-1-Trideceth-6)) und Salcare® SC 96 (ca. 50 % Polymeranteil, weitere Komponenten: Mischung von Diestern des Propylenglykols mit einer Mischung aus Capryl- und Caprinsäure (INCI-Bezeichnung: Propylene Glycol Dicaprylate/Dicaprate) und Tridecyl-polyoxypropylen-polyoxyethylen-ether (INCI-Bezeichnung: PPG-1 -Trideceth-6)) im Handel erhältlich. The homopolymer is preferably used in the form of a nonaqueous polymer dispersion which should not have a polymer content of less than 30% by weight. Such polymer dispersions are (under the names Salcare ® SC 95 about 50% polymer content, additional components: mineral oil (INCI name: Mineral Oil) and tridecyl polyoxypropylene polyoxyethylene ether (INCI name: PPG-1 trideceth-6) ) and Salcare ® SC 96 (about 50% polymer content, additional components: mixture of diesters of propylene glycol (with a mixture of caprylic and capric acid INCI name: propylene glycol Dicaprylate / Dicaprate) and tridecyl-polyoxypropylene-polyoxyethylene ether (INCI name: PPG-1 -Trideceth-6)) are commercially available.
Copolymere mit Monomereinheiten gemäß Formel (G1 -I) enthalten als nichtionogene Monomereinheiten bevorzugt Acrylamid, Methacrylamid, Acrylsäure-C- -alkylester und Methacrylsäure-Ci-4-alkylester. Unter diesen nichtionogenen Monomeren ist das Acrylamid besonders bevorzugt. Auch diese Copolymere können, wie im Falle der Homopolymere oben beschrieben, vernetzt sein. Ein erfindungsgemäß bevorzugtes Copolymer ist das vernetzte Acrylamid-Methacryloyloxyethyltrimethylammoniumchlorid-Copolymer. Solche Copolymere, bei denen die Monomere in einem Gewichtsverhältnis von etwa 20:80 vorliegen, sind im Handel als ca. 50 %ige nichtwäßrige Polymerdispersion unter der Bezeichnung Salcare® SC 92 erhältlich. Copolymers with monomer units of the formula (G1 -I) contain as nonionic monomer units preferably acrylamide, methacrylamide, acrylic acid C-alkyl esters and methacrylic acid C 1-4 -alkyl esters. Among these nonionic monomers, the acrylamide is particularly preferred. These copolymers can also be crosslinked, as described above in the case of the homopolymers. A copolymer preferred according to the invention is the crosslinked acrylamide-methacryloyloxyethyltrimethylammonium chloride copolymer. Such copolymers in which the monomers are present in a weight ratio of about 20:80, are commercially available as approximately 50% non-aqueous polymer dispersion 92 under the name Salcare ® SC.
Gleichfalls als kationische Polymere eingesetzt werden können die unter den Bezeichnungen Polyquaternium-24 (Handelsprodukt z. B. Quatrisoft® LM 200), bekannten Polymere. Ebenfalls erfindungsgemäß verwendbar sind die Copolymere des Vinylpyrrolidons, wie sie als Handelsprodukte Copolymer 845 (Hersteller: ISP), Gaffix® VC 713 (Hersteller: ISP), Gafquat®ASCP 101 1 , Gafquat®HS 1 10, Luviquat®8155 und Luviquat® MS 370 erhältlich sind. Als kationische Polymere können auch kationische Proteinhydrolysate eingesetzt werden, wobei bevorzugte Mittel ein oder mehrere kationische Proteinhydrolysate aus der Gruppe Cocodimonium Hydroxypropyl Hydrolyzed Collagen, Cocodimonium Hydroxypropyl Hydrolyzed Casein, Cocodimonium Hydroxypropyl Hydrolyzed Collagen, Cocodimonium Hydroxypropyl Hydrolyzed Hair Keratin, Cocodimonium Hydroxypropyl Hydrolyzed Keratin, Cocodimonium Hydroxypropyl Hydrolyzed Rice Protein, Cocodimonium Hydroxypropyl Hydrolyzed Soy Protein, Cocodimonium Hydroxypropyl Hydrolyzed Wheat Protein, Hydroxypropyl Arginine Lauryl/Myristyl Ether HCl, Hydroxypropyltrimonium Gelatin, Hydroxypropyltrimonium Hydrolyzed Casein, Hydroxypropyltrimonium Hydrolyzed Collagen, Hydroxypropyltrimonium Hydrolyzed Conchiolin Protein, Hydroxypropyltrimonium Hydrolyzed Keratin, Hydroxypropyltrimonium Hydrolyzed Rice Bran Protein, Hydroxypropyltrimonium Hydrolyzed Soy Protein, Hydroxypropyl Hydrolyzed Vegetable Protein, Hydroxypropyltrimonium Hydrolyzed Wheat Protein, Hydroxypropyltrimonium Hydrolyzed Wheat Pro- tein/Siloxysilicate, Laurdimonium Hydroxypropyl Hydrolyzed Soy Protein, Laurdimonium Hydroxypropyl Hydrolyzed Wheat Protein, Laurdimonium Hydroxypropyl Hydrolyzed Wheat Protein/Siloxysilicate, Lauryldimonium Hydroxypropyl Hydrolyzed Casein, Lauryldimonium Hydroxypropyl Hydrolyzed Collagen, Lauryldimonium Hydroxypropyl Hydrolyzed Keratin, Lauryldimonium Hydroxypropyl Hydrolyzed Soy Protein, Steardimonium Hydroxypropyl Hydrolyzed Casein, Steardimonium Hydroxypropyl Hydrolyzed Collagen, Steardimonium Hydroxypropyl Hydrolyzed Keratin, Steardimonium Hydroxypropyl Hydrolyzed Rice Protein, Steardimonium Hydroxypropyl Hydrolyzed Soy Protein, Steardimonium Hydroxypropyl Hydrolyzed Vegetable Protein, Steardimonium Hydroxypropyl Hydrolyzed Wheat Protein, Steartrimonium Hydroxyethyl Hydrolyzed Collagen, Quaternium-76 Hydrolyzed Collagen, Quaternium-79 Hydrolyzed Collagen, Quaternium-79 Hydrolyzed Keratin, Quaternium-79 Hydrolyzed Milk Protein, Quaternium-79 Hydrolyzed Soy Protein, Quaternium-79 Hydrolyzed Wheat Protein enthalten. It is likewise possible to use the polymers known under the names Polyquaternium-24 (commercial product eg Quatrisoft® LM 200) as cationic polymers. Also suitable for use in accordance with the invention are the copolymers of vinylpyrrolidone, such as the commercial products Copolymer 845 (manufacturer: ISP), Gaffix® VC 713 (manufacturer: ISP), Gafquat®ASCP 101 1, Gafquat®HS 1 10, Luviquat® 8155 and Luviquat® MS 370 are available. Cationic protein hydrolysates may also be used as cationic polymers, preferred agents being one or more cationic protein hydrolyzates from the group Cocodimonium Hydroxypropyl Hydrolyzed Collagen, Cocodimonium Hydroxypropyl Hydrolyzed Casein, Cocodimonium Hydroxypropyl Hydrolyzed Collagen, Cocodimonium Hydroxypropyl Hydrolyzed Hair Keratin, Cocodimonium Hydroxypropyl Hydrolyzed Keratin, Cocodimonium Hydroxypropyl Hydrolyzed Rice Protein, Cocodimonium Hydroxypropyl Hydrolyzed Soy Protein, Cocodimonium Hydroxypropyl Hydrolyzed Wheat Protein, Hydroxypropyl Arginine Lauryl / Myristyl Ether HCl, Hydroxypropyltrimonium Gelatin, Hydroxypropyltrimonium Hydrolyzed Casein, Hydroxypropyltrimonium Hydrolyzed Collagen, Hydroxypropyltrimonium Hydrolyzed Conchiolin Protein, Hydroxypropyltrimonium Hydrolyzed Keratin, Hydroxypropyltrimonium Hydrolyzed Rice Bran Protein, Hydroxypropyltrimonium Hydrolyzed Soy Protein, Hydroxypropyl Hydrolyzed Vegetable Protein, Hydroxypropyltrimon Hydroxylzed Wheat Protein, Hydroxypropyltrimonium Hydrolyzed Wheat Protein / Siloxysilicate, Lauridimonium Hydroxypropyl Hydrolyzed Soy Protein, Lauridimonium Hydroxypropyl Hydrolyzed Wheat Protein, Laurodimonium Hydroxypropyl Hydrolyzed Wheat Protein / Siloxysilicate, Lauryldimonium Hydroxypropyl Hydrolyzed Casein, Lauryldimonium Hydroxypropyl Hydrolyzed Collagen, Lauryldimonium Hydroxypropyl Hydrolyzed Keratin, Lauryldimonium Hydroxypropyl Hydrolyzed Soy Protein, Steardimonium Hydroxypropyl Hydrolyzed Casein, Steardimonium Hydroxypropyl Hydrolyzed Collagen, Steardimonium Hydroxypropyl Hydrolyzed Keratin, Steardimonium Hydroxypropyl Hydrolyzed Rice Protein, Steardimonium Hydroxypropyl Hydrolyzed Soy Protein, Steardimonium Hydroxypropyl Hydrolyzed Vegetable Protein, Steardimonium Hydroxypropyl Hydrolyzed Wheat Protein, Steartrimonium Hydroxyethyl Hydrolyzed Collagen, Quaternium-76 Hydrolyzed Collagen, Quaternium-79 Hydrolyzed Collagen, Quaternium-79 Hydrolyzed Keratin, Quaternium-79 Hydrolyzed Milk Protein, Quaternium-79 Hydrolyzed Soy Protein, Quaternium-79 Hydrolyzed Wheat Protein included.
Zusammenfassend sind erfindungsgemäße Verwendungen bevorzugt, bei denen das Haarbehandlungsmittel - bezogen auf sein Gewicht - 0,05 bis 7,5 Gew.-%, vorzugsweise 0,1 bis 5 Gew.-%, besonders bevorzugt 0,2 bis 3,5 Gew.-% und insbesondere 0,25 bis 2,5 Gew.-% kationische(s) Polymer(e), enthält, wobei bevorzugte kationische(s) Polymer(e) ausgewählt ist/sind aus Poly(methacryloyloxyethyltrimethylammoniumchlorid) (INCI: Polyquaternium-37) und/oder quaternisierten Cellulose-Derivaten (INCI: Polyquaternium 10) und/oder kationischen Alkylpolyglycosiden und/oder kationisertem Honig und/oder kationischen Guar-Derivaten und/oder polymeren Dimethyldiallylammoniumsalzen und deren Copolymeren mit Estern und Amiden von Acrylsäure und Methacrylsäure und/oder Copolymeren des Vinylpyrrolidons mit quaternierten Derivaten des Diaikyiaminoalkyiacryiats und -methacrylats und/oder Vinylpyrrolidon-Vinylimidazoliummethochlorid-Copolymeren und/oder quaterniertem Polyvinylalkohol und/oder Polyquaternium 2 und/oder Polyquaternium-7 und/oder Polyquaternium 17 und/oder Polyquaternium 18 und/oder Polyquaternium 24 und/oder Polyquaternium 27. In summary, uses according to the invention are preferred in which the hair treatment composition - based on its weight - 0.05 to 7.5 wt .-%, preferably 0.1 to 5 wt .-%, particularly preferably 0.2 to 3.5 wt. % and in particular 0.25 to 2.5% by weight of cationic polymer (s), with preferred cationic polymer (s) being / are selected from poly (methacryloyloxyethyltrimethylammonium chloride) (INCI: Polyquaternium) 37) and / or quaternized cellulose derivatives (INCI: Polyquaternium 10) and / or cationic alkylpolyglycosides and / or cationised honey and / or cationic guar derivatives and / or polymeric dimethyldiallylammonium salts and their copolymers with esters and amides of acrylic acid and methacrylic acid and / or copolymers of vinylpyrrolidone with quaternized derivatives of Diaikyiaminoalkyiacryiats and -methacrylate and / or vinylpyrrolidone-Vinylimidazoliummethochlorid copolymers and / or quaternized polyvinyl alcohol and / or Polyquaternium 2 and / or Polyquaternium-7 and / or Polyquaternium 17 and / or Polyquaternium 18 and / or Polyquaternium 24 and / or Polyquaternium 27.
Zusätzlich zu den kationischen Polymeren oder an ihrer Stelle können die erfindungsgemäß verwendeten Mittel amphotere Polymere enthalten. Im Rahmen der vorliegenden Erfindung bevorzugt einsetzbare amphotere Polymerisate setzen sich im wesentlichen zusammen aus In addition to or in place of the cationic polymers, the agents used in the invention may contain amphoteric polymers. In the context of the present invention preferably usable amphoteric polymers are composed essentially together
A) Monomeren mit quartären Ammoniumgruppen der allgemeinen Formel (Z-l), A) monomers having quaternary ammonium groups of the general formula (Z-1),
R1-CH=CR2-CO-Z-(CnH2n)-N(+)R3R4R5 A<") <Z"') R 1 -CH = CR 2 -CO-Z- (C n H 2n ) -N ( + ) R 3 R 4 R 5 A <" ) <Z"')
In der R und R2 unabhängig voneinander stehen für Wasserstoff oder eine Methylgruppe und R3, R4 und R^ unabhängig voneinander für Alkylgruppen mit 1 bis 4 Kohlenstoff- Atomen, Z eine NH-Gruppe oder ein Sauerstoffatom, n eine ganze Zahl von 2 bis 5 undIn the R and R 2 are independently of each other hydrogen or a methyl group and R 3 , R 4 and R ^ independently represent alkyl groups having 1 to 4 carbon atoms, Z is an NH group or an oxygen atom, n is an integer of 2 to 5 and
A<-> das Anion einer organischen oder anorganischen Säure ist und A <-> is the anion of an organic or inorganic acid and
B) monomeren Carbonsäuren der allgemeinen Formel (Z-l I) , B) monomeric carboxylic acids of the general formula (Z-1 I),
R6-CH=CR7-COOH (Z-Il) R 6 -CH = CR 7 -COOH (Z-II)
in denen R6 und fiJ unabhängig voneinander Wasserstoff oder in which R 6 and fiJ are independently hydrogen or
Methylgruppen sind. Geeignete Ausgangsmonomere sind z. B. Dimethylaminoethylacrylamid, Dimethylaminoethylmethacrylamid, Dimethylaminopropylacrylamid, Dimethylaminopropylmethacrylamid und Diethylaminoethylacrylamid, wenn Z eine NH-Gruppe bedeutet oder Dimethylaminoethylacrylat, Dimethylaminoethylmethacrylat und Diethylaminoethylacrylat, wenn Z ein Sauerstoffatom ist. Are methyl groups. Suitable starting monomers are, for. Dimethylaminoethylacrylamide, dimethylaminoethylmethacrylamide, dimethylaminopropylacrylamide, dimethylaminopropylmethacrylamide and diethylaminoethylacrylamide when Z is an NH group or dimethylaminoethyl acrylate, dimethylaminoethyl methacrylate and diethylaminoethyl acrylate when Z is an oxygen atom.
Die eine tertiäre Aminogruppe enthaltenden Monomeren werden dann in bekannter Weise quarterniert, wobei als Alkylierungsreagenzien Methylchlorid, Dimethylsulfat oder Diethylsulfat besonders geeignet sind. Die Quaternisierungsreaktion kann in wäßriger Lösung oder im Lösungsmittel erfolgen. The monomers containing a tertiary amino group are then quaternized in a known manner, methyl chloride, dimethyl sulfate or diethyl sulfate being particularly suitable as alkylating reagents. The quaternization reaction can be carried out in aqueous solution or in the solvent.
Vorteilhafterweise werden solche Monomere der Formel (Z-l) , die Derivate des Acrylamids oder Methacrylamids darstellen. Weiterhin bevorzugt sind solche Monomeren, die als Gegenionen Halogenid-, Methoxysulfat- oder Ethoxysulfat-Ionen enthalten. Ebenfalls bevorzugt sind solche Monomeren der Formel (Z-l), bei denen R^, R4 und R5 Methylgruppen sind. Das Acrylamidopropyl-trimethylammoniumchlorid ist ein ganz besonders bevorzugtes Monomer der Formel (Z-l). Advantageously, those monomers of formula (ZI) which are derivatives of acrylamide or methacrylamide. Preference is furthermore given to those monomers which contain halide, methoxysulfate or ethoxysulfate ions as counterions. Also preferred are those monomers of formula (ZI) wherein R 1, R 4 and R 5 are methyl groups. The acrylamidopropyltrimethylammonium chloride is a very particularly preferred monomer of the formula (ZI).
Als monomere Carbonsäuren der Formel (Z-l I) eignen sich Acrylsäure, Methacrylsäure, Crotonsäure und 2-Methyl-crotonsäure. Bevorzugt werden Acryl- oder Methacrylsäure, insbesondere Acrylsäure, eingesetzt. Suitable monomeric carboxylic acids of the formula (Z-I) are acrylic acid, methacrylic acid, crotonic acid and 2-methylcrotonic acid. Preference is given to using acrylic or methacrylic acid, in particular acrylic acid.
Die erfindungsgemäß einsetzbaren zwitterionischen Polymerisate werden aus Monomeren der Formeln (Z-l) und (Z-Il) nach an sich bekannten Polymerisationsverfahren hergestellt. Die Polymerisation kann entweder in wäßriger oder wäßrig-alkoholischer Lösung erfolgen. Als Alkohole werden Alkohole mit 1 bis 4 Kohlenstoffatomen, vorzugsweise Isopropanol, verwendet, die gleichzeitig als Polymerisationsregler dienen. Der Monomerlösung können aber auch andere Komponenten als Regler zugesetzt werden, z. B. Ameisensäure oder Mercaptane, wie Thioethanol und Thioglykolsäure. Die Initiierung der Polymerisation erfolgt mit Hilfe von radikalbildenden Substanzen. Hierzu können Redoxsysteme und/oder thermisch zerfallende Radikalbildner vom Typ der Azoverbindungen, wie z. B. Azoisobuttersäurenitril, Azo-bis- (cyanopentansäure) oder Azo-bis-(amidinopropan)dihydrochlorid verwendet werden. Als Redoxsysteme eignen sich z. B. Kombinationen aus Wasserstoffperoxid, Kalium- oder Ammoniumperoxodisulfat sowie tertiäres Butylhydroperoxid mit Natriumsulfit, Natriumdithionit oder Hydroxylaminhydrochlorid als Reduktionskomponente. The zwitterionic polymers which can be used according to the invention are prepared from monomers of the formulas (Z-1) and (Z-II) by polymerization processes known per se. The polymerization can be carried out either in aqueous or aqueous-alcoholic solution. The alcohols used are alcohols having 1 to 4 carbon atoms, preferably isopropanol, which simultaneously serve as polymerization regulators. However, other components than regulators may also be added to the monomer solution, eg. For example, formic acid or mercaptans, such as thioethanol and thioglycolic acid. The initiation of the polymerization takes place with the aid of free-radical-forming substances. For this purpose, redox systems and / or thermally decomposing radical formers of the azo compound type, such. As azoisobutyronitrile, azo-bis (cyanopentanoic acid) or azo-bis (amidinopropane) dihydrochloride can be used. As redox systems are z. B. combinations of hydrogen peroxide, potassium or ammonium peroxodisulfate and tertiary butyl hydroperoxide with sodium sulfite, sodium dithionite or hydroxylamine hydrochloride as a reduction component.
Die Polymerisation kann isotherm oder unter adiabatischen Bedingungen durchgeführt werden, wobei in Abhängigkeit von den Konzentrationsverhältnissen durch die freiwerdende Polymerisationswärme der Temperaturbereich für den Ablauf der Reaktion zwischen 20 und 200 °C schwanken kann, und die Reaktion gegebenenfalls unter dem sich einstellenden Überdruck durchgeführt werden muß. Bevorzugterweise liegt die Reaktionstemperatur zwischen 20 und 100 °C. Der pH-Wert während der Copolymerisation kann in einem weiten Bereich schwanken. Vorteilhafterweise wird bei niedrigen pH-Werten polymerisiert; möglich sind jedoch auch pH- Werte oberhalb des Neutralpunktes. Nach der Polymerisation wird mit einer wäßrigen Base, z. B. Natronlauge, Kalilauge oder Ammoniak, auf einen pH-Wert zwischen 5 und 10, vorzugsweise 6 bis 8, eingestellt. Nähere Angaben zum Polymerisationsverfahren können den Beispielen entnommen werden. The polymerization can be carried out isothermally or under adiabatic conditions, depending on the concentration ratios by the heat of polymerization released, the temperature range for the course of the reaction between 20 and 200 ° C may vary, and the reaction may be carried out under the autogenous pressure. Preferably, the reaction temperature is between 20 and 100 ° C. The pH during the copolymerization may vary within a wide range. Advantageously, polymerization is carried out at low pH values; however, pH values above the neutral point are also possible. After the polymerization is treated with an aqueous base, for. As sodium hydroxide, potassium hydroxide or ammonia, to a pH between 5 and 10, preferably 6 to 8 set. Further details of the polymerization process can be found in the examples.
Als besonders wirksam haben sich solche Polymerisate erwiesen, bei denen die Monomeren der Formel (Z-l) gegenüber den Monomeren der Formel (Z-Il) im Überschuß vorlagen. Es ist daher erfindungsgemäß bevorzugt, solche Polymerisate zu verwenden, die aus Monomeren der Formel (Z-l) und die Monomeren der Formel (Z-Il) in einem Molverhältnis von 60:40 bis 95:5, insbesondere von 75:25 bis 95:5, bestehen. Be particularly effective, such polymers have proven in which the monomers of the formula (Z-l) were present in excess over the monomers of formula (Z-II). It is therefore preferred in accordance with the invention to use those polymers which consist of monomers of the formula (Z1) and the monomers of the formula (Z-II) in a molar ratio of 60:40 to 95: 5, in particular 75:25 to 95: 5 , consist.
Bevorzugte erfindungsgemäß zu verwendende Mittel sind dadurch gekennzeichnet, daß das/die amphotere(n) Polymer(e) Monomere A) und B) umfassen, wobei A) und B) ausgewählt sind aus Preferred agents to be used according to the invention are characterized in that the amphoteric polymer (s) comprises monomers A) and B), wherein A) and B) are selected from
A) Monomeren mit quartären Ammoniumgruppen der allgemeinen Formel (Z-l), A) monomers having quaternary ammonium groups of the general formula (Z-1),
R1-CH=CR2-CO-Z-(CnH2n)-N(+)R3R4R5 A^ (Z_l) R 1 -CH = CR 2 -CO-Z- (C n H 2n ) -N ( + ) R 3 R 4 R 5 A ^ ( Z_l )
in der R und R2 unabhängig voneinander stehen für Wasserstoff oder einein which R and R 2 independently represent hydrogen or a
Methylgruppe und R3, R4 und R5 unabhängig voneinander für Alkylgruppen mit 1 bis 4 Kohlenstoff-Atomen, Z eine NH-Gruppe oder ein Sauerstoffatom, n eine ganze Zahl von 2 bis 5 und A(-) das Anion einer organischen oder anorganischen Säure ist Methyl group and R 3 , R 4 and R 5 are independently alkyl groups having 1 to 4 carbon atoms, Z is an NH group or an oxygen atom, n is an integer from 2 to 5 and A (-) the anion of an organic or inorganic Acid is
und and
B) monomeren Carbonsäuren der allgemeinen Formel (Z-Il), B) monomeric carboxylic acids of the general formula (Z-II),
R6-CH=CR7-COOH (Z-Il) R 6 -CH = CR 7 -COOH (Z-II)
in der R6 und R7 unabhängig voneinander Wasserstoff oder Methylgruppen sind. in which R 6 and R 7 are independently hydrogen or methyl groups.
Mit besonderem Vorzug enthalten die in den erfindungsgemäß verwendeten Mitteln eingesetzten amphoteren Polymere Monomere aus der Gruppe der Acrylamide und/oder Methacrylamide mit Alkylammoniumgruppen. Als zusätzlich in den Polymeren enthaltene Monomere mit anionischen Gruppen haben sich Acrylsäure und/oder Methacrylsäure und/oder Crotonsäure und/oder 2-Methyl-crotonsäure bewährt. With particular preference, the amphoteric polymers used in the compositions according to the invention contain monomers from the group of acrylamides and / or methacrylamides with alkylammonium groups. Acrylic acid and / or methacrylic acid and / or crotonic acid and / or 2-methyl-crotonic acid have proven useful as monomers with anionic groups which are additionally present in the polymers.
Zusammenfassend sind erfindungsgemäß verwendete Mittel bevorzugt, bei denen das/die amphotere(n) Polymer(e) Co-Polymerisate mindestens eines der Monomere Trimethylammoniumethylacrylamid und/oder Trimethylammoniumethylmethacrylamid und/oder Trimethylammoniumpropylacrylamid und/oder Trimethylammonium- propylmethacrylamid und/oder Trimethylammoniumethylacrylamid und/oder Trimethylammoniumethylacrylat und/oder Trimethylammoniumethylmethacrylat und/oder Trimethylammoniumethylacrylat und/oder Ethyldimethylammoniumethylacrylamid und/oder Ethyldimethylammoniumethylmethacrylamid und/oder Ethyldimethylammonium- propylacrylamid und/oder Ethyldimethylammoniumpropylmethacrylamid und/oder Ethyldimethylammoniumethylacrylamid und/oder Ethyldimethylammoniumethylacrylat und/oder Ethyldimethylammoniumethylmethacrylat und/oder Ethyldimethyl- ammoniumethylacrylat mit mindestens einem der Monomere Acrylsäure und/oder Methacrylsäure und/oder Crotonsäure und/oder 2-Methyl-crotonsäure sind. In summary, agents used according to the invention are preferred in which the amphoteric polymer (s) are copolymers of at least one of the monomers trimethylammoniumethylacrylamide and / or trimethylammoniumethylmethacrylamide and / or trimethylammoniumpropylacrylamide and / or trimethylammonium propylmethacrylamide and / or trimethylammoniumethylacrylamide and / or trimethylammoniumethylacrylate and / or trimethylammoniumethylmethacrylate and / or trimethylammoniumethylacrylate and / or ethyldimethylammoniumethylacrylamide and / or ethyldimethylammoniumethylmethacrylamide and / or ethyldimethylammoniumpropylacrylamide and / or ethyldimethylammoniumpropylmethacrylamide and / or ethyldimethylammoniumethylacrylamide and / or ethyldimethylammoniumethylacrylate and / or ethyldimethylammoniumethylmethacrylate and / or Ethyldimethyl- ammonium ethyl acrylate with at least one of the monomers acrylic acid and / or methacrylic acid and / or crotonic acid and / or 2-methyl crotonic acid.
Erfindungsgemäß besonders bevorzugte amphotere Polymere sind: Particularly preferred amphoteric polymers according to the invention are:
Copolymere von Tr me thylammoniumethylacrylamid mit Acrylsäure Copolymers of trimethylammonium ethylacrylamide with acrylic acid
Copolymere von Tr me thylammoniumethylacrylamid mit Methacrylsäure Copolymers of methyl thylammonium ethylacrylamide with methacrylic acid
Copolymere von Tr me thylammoniumethylacrylamid mit Crotonsäure Copolymers of trimethylammonium ethylacrylamide with crotonic acid
Copolymere von Tr me thylammoniumethylacrylamid mit 2-Methyl-crotonsäure Copolymers of trimethylammonium ethylacrylamide with 2-methyl-crotonic acid
Copolymere von Tr me thylammoniumethylmethacrylamid mit Acrylsäure Copolymers of trimethylammonium ethylmethacrylamide with acrylic acid
Copolymere von Tr me thylammoniumethylmethacrylamid mit Methacrylsäure Copolymers of trimethylammonium ethylmethacrylamide with methacrylic acid
Copolymere von Tr me thylammoniumethylmethacrylamid mit Crotonsäure Copolymers of trimethylammonium ethylmethacrylamide with crotonic acid
Copolymere von Tr me thylammoniumethylmethacrylamid mit 2-Methyl-crotonsäure Copolymers of trimethylammonium ethylmethacrylamide with 2-methyl-crotonic acid
Copolymere von Tr me thylammoniumpropylacrylamid mit Acrylsäure Copolymers of trimethylammonium propylacrylamide with acrylic acid
Copolymere von Tr me thylammoniumpropylacrylamid mit Methacrylsäure Copolymers of methyl thylammoniumpropylacrylamide with methacrylic acid
Copolymere von Tr me thylammoniumpropylacrylamid mit Crotonsäure Copolymers of trimethylammonium propylacrylamide with crotonic acid
Copolymere von Tr me thylammoniumpropylacrylamid mit 2-Methyl-crotonsäure Copolymers of trimethylammonium propylacrylamide with 2-methylcrotonic acid
Copolymere von Tr me thylammoniumpropylmethacrylamid mit Acrylsäure Copolymers of trimethylammonium propylmethacrylamide with acrylic acid
Copolymere von Tr me thylammoniumpropylmethacrylamid mit Methacrylsäure Copolymers of methyl ammonium propyl methacrylamide with methacrylic acid
Copolymere von Tr me thylammoniumpropylmethacrylamid mit Crotonsäure Copolymers of trimethylammopropylpropylmethacrylamide with crotonic acid
Copolymere von Tr me thylammoniumpropylmethacrylamid mit 2-Methyl-crotonsäure Copolymers of trimethylammopropylpropylmethacrylamide with 2-methyl-crotonic acid
Copolymere von Tr me thylammoniumethylacrylamid mit Acrylsäure Copolymers of trimethylammonium ethylacrylamide with acrylic acid
Copolymere von Tr me thylammoniumethylacrylamid mit Methacrylsäure Copolymers of methyl thylammonium ethylacrylamide with methacrylic acid
Copolymere von Tr me thylammoniumethylacrylamid mit Crotonsäure Copolymers of trimethylammonium ethylacrylamide with crotonic acid
Copolymere von Tr me thylammoniumethylacrylamid mit 2-Methyl-crotonsäure Copolymers of trimethylammonium ethylacrylamide with 2-methyl-crotonic acid
Copolymere von Tr me thylammoniumethylacrylat mit Acrylsäure Copolymers of methyl methacrylate with acrylic acid
Copolymere von Tr me thylammoniumethylacrylat mit Methacrylsäure Copolymers of methyl methacrylate with methacrylic acid
Copolymere von Tr me thylammoniumethylacrylat mit Crotonsäure Copolymers of trimethyl ammonium ethyl acrylate with crotonic acid
Copolymere von Tr me thylammoniumethylacrylat mit 2-Methyl-crotonsäure Copolymers of tr methyl ammonium ethyl acrylate with 2-methyl crotonic acid
Copolymere von Tr me thylammoniumethylmethacrylat mit Acrylsäure Copolymers of trimethylammonium ethyl methacrylate with acrylic acid
Copolymere von Tr me thylammoniumethylmethacrylat mit Methacrylsäure Copolymers of methyl methacrylate with methacrylic acid
Copolymere von Tr me thylammoniumethylmethacrylat mit Crotonsäure Copolymere von Trimethylammoniumethylmethacrylat mit 2-Methyl-crotonsäure Copolymere von Trimethylammoniumethylacrylat mit Acrylsäure Copolymers of methyl methacrylate with crotonic acid Copolymers of trimethylammoniumethyl methacrylate with 2-methyl-crotonic acid copolymers of trimethylammonium ethyl acrylate with acrylic acid
Copolymere von Trimethylammoniumethylacrylat mit Methacrylsäure Copolymers of trimethylammonium ethyl acrylate with methacrylic acid
Copolymere von Trimethylammoniumethylacrylat mit Crotonsäure Copolymers of trimethylammonium ethyl acrylate with crotonic acid
Copolymere von Trimethylammoniumethylacrylat mit 2-Methyl-crotonsäure Copolymers of trimethylammonium ethyl acrylate with 2-methyl-crotonic acid
Copolymere von Ethyldimethylammoniumethylacrylamid mit Acrylsäure Copolymers of ethyldimethylammoniumethylacrylamide with acrylic acid
Copolymere von Ethyldimethylammoniumethylacrylamid mit Methacrylsäure Copolymers of ethyldimethylammoniumethylacrylamide with methacrylic acid
Copolymere von Ethyldimethylammoniumethylacrylamid mit Crotonsäure Copolymers of ethyldimethylammoniumethylacrylamide with crotonic acid
Copolymere von Ethyldimethylammoniumethylacrylamid mit 2-Methyl-crotonsäure Copolymere von Ethyldimethylammoniumethylmethacrylamid mit Acrylsäure Copolymers of ethyldimethylammoniumethylacrylamide with 2-methyl-crotonic acid Copolymers of ethyldimethylammoniumethylmethacrylamide with acrylic acid
Copolymere von Ethyldimethylammoniumethylmethacrylamid mit Methacrylsäure Copolymere von Ethyldimethylammoniumethylmethacrylamid mit Crotonsäure Copolymere von Ethyldimethylammoniumethylmethacrylamid mit 2-Methyl-crotonsäure Copolymere von Ethyldimethylammoniumpropylacrylamid mit Acrylsäure Copolymers of ethyldimethylammoniumethylmethacrylamide with methacrylic acid Copolymers of ethyldimethylammoniumethylmethacrylamide with crotonic acid Copolymers of ethyldimethylammoniumethylmethacrylamide with 2-methylcrotonic acid Copolymers of ethyldimethylammoniumpropylacrylamide with acrylic acid
Copolymere von Ethyldimethylammoniumpropylacrylamid mit Methacrylsäure Copolymers of ethyldimethylammoniumpropylacrylamide with methacrylic acid
Copolymere von Ethyldimethylammoniumpropylacrylamid mit Crotonsäure Copolymers of ethyldimethylammoniumpropylacrylamide with crotonic acid
Copolymere von Ethyldimethylammoniumpropylacrylamid mit 2-Methyl-crotonsäure Copolymere von Ethyldimethylammoniumpropylmethacrylamid mit Acrylsäure Copolymere von Ethyldimethylammoniumpropylmethacrylamid mit Methacrylsäure Copolymere von Ethyldimethylammoniumpropylmethacrylamid mit Crotonsäure Copolymere von Ethyldimethylammoniumpropylmethacrylamid mit 2-Methyl- crotonsäure Copolymers of ethyldimethylammoniumpropylacrylamide with 2-methyl-crotonic acid Copolymers of ethyldimethylammoniumpropylmethacrylamide with acrylic acid Copolymers of ethyldimethylammoniumpropylmethacrylamide with methacrylic acid Copolymers of ethyldimethylammoniumpropylmethacrylamide with crotonic acid Copolymers of ethyldimethylammoniumpropylmethacrylamide with 2-methylcrotonic acid
Copolymere von Ethyldimethylammoniumethylacrylamid mit Acrylsäure Copolymers of ethyldimethylammoniumethylacrylamide with acrylic acid
Copolymere von Ethyldimethylammoniumethylacrylamid mit Methacrylsäure Copolymers of ethyldimethylammoniumethylacrylamide with methacrylic acid
Copolymere von Ethyldimethylammoniumethylacrylamid mit Crotonsäure Copolymers of ethyldimethylammoniumethylacrylamide with crotonic acid
Copolymere von Ethyldimethylammoniumethylacrylamid mit 2-Methyl-crotonsäure Copolymere von Ethyldimethylammoniumethylacrylat mit Acrylsäure Copolymers of ethyldimethylammoniumethylacrylamide with 2-methyl-crotonic acid Copolymers of ethyldimethylammonium ethylacrylate with acrylic acid
Copolymere von Ethyldimethylammoniumethylacrylat mit Methacrylsäure Copolymers of ethyldimethylammonium ethyl acrylate with methacrylic acid
Copolymere von Ethyldimethylammoniumethylacrylat mit Crotonsäure Copolymers of ethyldimethylammonium ethyl acrylate with crotonic acid
Copolymere von Ethyldimethylammoniumethylacrylat mit 2-Methyl-crotonsäure Copolymere von Ethyldimethylammoniumethylmethacrylat mit Acrylsäure Copolymers of ethyldimethylammonium ethylacrylate with 2-methyl-crotonic acid Copolymers of ethyldimethylammoniumethylmethacrylate with acrylic acid
Copolymere von Ethyldimethylammoniumethylmethacrylat mit Methacrylsäure Copolymers of ethyldimethylammonium ethyl methacrylate with methacrylic acid
Copolymere von Ethyldimethylammoniumethylmethacrylat mit Crotonsäure Copolymers of ethyldimethylammonium ethyl methacrylate with crotonic acid
Copolymere von Ethyldimethylammoniumethylmethacrylat mit 2-Methyl-crotonsäure Copolymere von Ethyldimethylammoniumethylacrylat mit Acrylsäure Copolymers of ethyldimethylammoniumethyl methacrylate with 2-methylcrotonic acid Copolymers of ethyldimethylammonium ethylacrylate with acrylic acid
Copolymere von Ethyldimethylammoniumethylacrylat mit Methacrylsäure Copolymers of ethyldimethylammonium ethyl acrylate with methacrylic acid
Copolymere von Ethyldimethylammoniumethylacrylat mit Crotonsäure Copolymere von Ethyldimethylammoniumethylacrylat mit 2-Methyl-crotonsäure Die erfindungsgemäß verwendeten Mittel können weiterhin alle für solche Zubereitungen bekannten Wirk-, Zusatz- und Hilfsstoffe enthalten. In vielen Fällen enthalten die Mittel mindestens ein Tensid, wobei prinzipiell sowohl anionische als auch zwitterionische, am- pholytische, nichtionische und kationische Tenside geeignet sind. In vielen Fällen hat es sich aber als vorteilhaft erwiesen, die Tenside aus anionischen, zwitterionischen oder nichtionischen Tensiden auszuwählen. Diese Tenside wurden weiter oben ausführlich beschrieben. Copolymers of ethyldimethylammonium ethyl acrylate with crotonic acid Copolymers of ethyldimethylammonium ethyl acrylate with 2-methyl-crotonic acid The agents used according to the invention may furthermore contain all active ingredients, additives and auxiliaries known for such preparations. In many cases, the agents contain at least one surfactant, with both anionic and zwitterionic, ampholytic, nonionic and cationic surfactants being suitable in principle. In many cases, however, it has proved to be advantageous to select the surfactants from anionic, zwitterionic or nonionic surfactants. These surfactants have been described in detail above.
Schließlich können die erfindungsgemäß verwendeten Mittel auch Pflanzenextrakte (L) enthalten. Finally, the compositions used according to the invention may also contain plant extracts (L).
Üblicherweise werden diese Extrakte durch Extraktion der gesamten Pflanze hergestellt. Es kann aber in einzelnen Fällen auch bevorzugt sein, die Extrakte ausschließlich aus Blüten und/oder Blättern der Pflanze herzustellen. Usually these extracts are produced by extraction of the whole plant. However, in individual cases it may also be preferred to prepare the extracts exclusively from flowers and / or leaves of the plant.
Erfindungsgemäß sind vor allem die Extrakte aus Grünem Tee, Eichenrinde, Brennessel, Hamamelis, Hopfen, Henna, Kamille, Klettenwurzel, Schachtelhalm, Weißdorn, Lindenblüten, Mandel, Aloe Vera, Fichtennadel, Roßkastanie, Sandelholz, Wacholder, Kokosnuß, Mango, Aprikose, Limone, Weizen, Kiwi, Melone, Orange, Grapefruit, Salbei, Rosmarin, Birke, Malve, Wiesenschaumkraut, Quendel, Schafgarbe, Thymian, Melisse, Hauhechel, Huflattich, Eibisch, Meristem, Ginseng und Ingwerwurzel bevorzugt. The extracts of green tea, oak bark, stinging nettle, witch hazel, hops, henna, chamomile, burdock root, horsetail, hawthorn, linden, almond, aloe vera, spruce needle, horse chestnut, sandalwood, juniper, coconut, mango, apricot, lime , Wheat, kiwi, melon, orange, grapefruit, sage, rosemary, birch, mallow, meadowfoam, quenelle, yarrow, thyme, lemon balm, toadstool, coltsfoot, marshmallow, meristem, ginseng and ginger root.
Besonders bevorzugt sind die Extrakte aus Grünem Tee, Eichenrinde, Brennessel, Hamamelis, Hopfen, Kamille, Klettenwurzel, Schachtelhalm, Lindenblüten, Mandel, Aloe Vera, Kokosnuß, Mango, Aprikose, Limone, Weizen, Kiwi, Melone, Orange, Grapefruit, Salbei, Rosmarin, Birke, Wiesenschaumkraut, Quendel, Schafgarbe, Hauhechel, Meristem, Ginseng und Ingwerwurzel. Particularly preferred are the extracts of green tea, oak bark, stinging nettle, witch hazel, hops, chamomile, burdock root, horsetail, lime blossom, almond, aloe vera, coconut, mango, apricot, lime, wheat, kiwi, melon, orange, grapefruit, sage, Rosemary, birch, meadowfoam, quenelle, yarrow, toadstool, meristem, ginseng and ginger root.
Ganz besonders für die erfindungsgemäße Verwendung geeignet sind die Extrakte aus Grünem Tee, Mandel, Aloe Vera, Kokosnuß, Mango, Aprikose, Limone, Weizen, Kiwi und Melone. Especially suitable for the use according to the invention are the extracts of green tea, almond, aloe vera, coconut, mango, apricot, lime, wheat, kiwi and melon.
Als Extraktionsmittel zur Herstellung der genannten Pflanzenextrakte können Wasser, Alkohole sowie deren Mischungen verwendet werden. Unter den Alkoholen sind dabei niedere Alkohole wie Ethanol und Isopropanol, insbesondere aber mehrwertige Alkohole wie Ethylenglykol und Propylenglykol, sowohl als alleiniges Extraktionsmittel als auch in Mischung mit Wasser, bevorzugt. Pflanzenextrakte auf Basis von Wasser/Propylenglykol im Verhältnis 1 :10 bis 10:1 haben sich als besonders geeignet erwiesen. As extraction agent for the preparation of said plant extracts water, alcohols and mixtures thereof can be used. Among the alcohols are lower alcohols such as ethanol and isopropanol, but especially polyhydric alcohols such as ethylene glycol and propylene glycol, both as sole extractant and in admixture with water, are preferred. Plant extracts based on water / propylene glycol in a ratio of 1:10 to 10: 1 have proven to be particularly suitable.
Die Pflanzenextrakte können erfindungsgemäß sowohl in reiner als auch in verdünnter Form eingesetzt werden. Sofern sie in verdünnter Form eingesetzt werden, enthalten sie üblicherweise ca. 2 - 80 Gew.-% Aktivsubstanz und als Lösungsmittel das bei ihrer Gewinnung eingesetzte Extraktionsmittel oder Extraktionsmittelgemisch. Weiterhin kann es bevorzugt sein, in den erfindungsgemäß verwendeten Mitteln Mischungen aus mehreren, insbesondere aus zwei, verschiedenen Pflanzenextrakten einzusetzen. The plant extracts can be used according to the invention both in pure and in diluted form. If they are used in diluted form, they usually contain about 2 to 80 wt .-% of active substance and as a solvent used in their extraction agent or extractant mixture. Furthermore, it may be preferable to use mixtures of several, in particular two, different plant extracts in the compositions used according to the invention.
Zusätzlich kann es sich als vorteilhaft erweisen, wenn in den erfindungsgemäß verwendeten Mitteln Penetrationshilfsstoffe und/ oder Quellmittel (M) enthalten sind. Hierzu sind beispielsweise zu zählen Harnstoff und Harnstoffderivate, Guanidin und dessen Derivate, Arginin und dessen Derivate, Wasserglas, Imidazol und dessen Derivate, Histidin und dessen Derivate, Benzylalkohol, Glycerin, Glykol und Glykolether, Propylenglykol und Propylenglykolether, beispielsweise Propylenglykolmonoethylether, Carbonate, Hydro- gencarbonate, Diole und Triole, und insbesondere 1 ,2-Diole und 1 ,3-Diole wie beispielsweise 1 ,2-Propandiol, 1 ,2-Pentandiol, 1 ,2-Hexandiol, 1 ,2-Dodecandiol, 1 ,3-Propandiol, 1 ,6- Hexandiol, 1 ,5-Pentandiol, 1 ,4-Butandiol. In addition, it may prove advantageous if the agents used according to the invention contain penetration aids and / or swelling agents (M). These include, for example, urea and urea derivatives, guanidine and its derivatives, arginine and derivatives thereof, water glass, imidazole and its derivatives, histidine and its derivatives, benzyl alcohol, glycerol, glycol and glycol ethers, propylene glycol and propylene glycol ethers, for example propylene glycol monoethyl ether, carbonates, hydroxides. gencarbonates, diols and triols, and in particular 1, 2-diols and 1, 3-diols such as 1, 2-propanediol, 1, 2-pentanediol, 1, 2-hexanediol, 1, 2-dodecanediol, 1, 3-propanediol , 1, 6-hexanediol, 1, 5-pentanediol, 1, 4-butanediol.
Aus ästhetischen Gründen werden „klare" Produkte von Verbrauchern oft bevorzugt. Erfindungsgemäß bevorzugt verwendete Haarbehandlungsmittel sind daher dadurch gekennzeichnet, daß sie transparent bzw. transluzent sind. Unter transparent oder transluzent wird im Rahmen der vorliegenden Erfindung eine Zusammensetzung verstanden, die einen NTU-Wert von unter 100 aufweist. Der NTU-Wert (Nephelometrie Turbidity Unit, Nephelometrischer Trübungswert; NTU) ist eine in der Wasseraufbereitung verwendete Einheit für Trübungsmessungen in Flüssigkeiten. Sie ist die Einheit einer mit einem kalibrierten Nephelometer gemessenen Trübung einer Flüssigkeit. For aesthetic reasons, "clear" products are often preferred by consumers, hair treatment agents preferably used according to the invention are therefore transparent or translucent, transparent or translucent in the context of the present invention means a composition having an NTU value of less than 100. The NTU (Nephelometry Turbidity Unit) value is a fluid turbidity measurement unit used in water treatment and is the unit of turbidity of a fluid measured with a calibrated nephelometer.
Claims
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE112014004999.9T DE112014004999A5 (en) | 2013-10-31 | 2014-09-16 | Hair treatment composition containing L-carnitine or an L-carnitine derivative and an oligopeptide containing the sequence Glu-Glu-Glu |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102013222212.2 | 2013-10-31 | ||
| DE201310222212 DE102013222212A1 (en) | 2013-10-31 | 2013-10-31 | Use of special hair treatment products III |
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| WO2015062596A1 true WO2015062596A1 (en) | 2015-05-07 |
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| PCT/DE2014/200477 Ceased WO2015062596A1 (en) | 2013-10-31 | 2014-09-16 | Hair treatment agent containing l-carnitine or an l-carnitine derivative and an oligopeptide containing the sequence glu-glu-glu |
Country Status (2)
| Country | Link |
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| DE (2) | DE102013222212A1 (en) |
| WO (1) | WO2015062596A1 (en) |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030086893A1 (en) * | 2000-06-05 | 2003-05-08 | Yohei Hirai | Oligopeptides for promoting hair growth |
| EP1709956A1 (en) * | 2001-03-19 | 2006-10-11 | Henkel Kommanditgesellschaft auf Aktien | Hair treatment composition comprising betains |
| WO2007003307A1 (en) * | 2005-07-05 | 2007-01-11 | Henkel Kommanditgesellschaft Auf Aktien | Agent containing l-carnitine or l-carnitine derivatives and at least one other specific substance |
| WO2011042323A2 (en) * | 2009-10-05 | 2011-04-14 | Henkel Ag & Co. Kgaa | Hair treatment agents comprising surfactant(s) and proteolipid(s) |
| US20120101038A1 (en) * | 2005-08-23 | 2012-04-26 | The General Hospital Corporation | Use of glp-1, glp-1 derivatives or glp-1 fragments for skin regeneration, stimulation of hair growth, or treatment of diabetes |
| DE102012215046A1 (en) * | 2012-08-24 | 2013-05-02 | Henkel Ag & Co. Kgaa | Use of (6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaene for producing cosmetic composition e.g. for stimulating hair keratins synthesis and cell viability |
| EP2724711A2 (en) * | 2012-10-25 | 2014-04-30 | Henkel AG & Co. KGaA | Hair care product with selected amino acids and/or selected oligopeptides and a selected cationic keratin hydrolysate |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4413686C2 (en) | 1994-04-20 | 1996-10-24 | Henkel Kgaa | Cationic sugar surfactants, process for their preparation and their use |
-
2013
- 2013-10-31 DE DE201310222212 patent/DE102013222212A1/en not_active Withdrawn
-
2014
- 2014-09-16 WO PCT/DE2014/200477 patent/WO2015062596A1/en not_active Ceased
- 2014-09-16 DE DE112014004999.9T patent/DE112014004999A5/en not_active Withdrawn
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|---|---|---|---|---|
| US20030086893A1 (en) * | 2000-06-05 | 2003-05-08 | Yohei Hirai | Oligopeptides for promoting hair growth |
| EP1709956A1 (en) * | 2001-03-19 | 2006-10-11 | Henkel Kommanditgesellschaft auf Aktien | Hair treatment composition comprising betains |
| WO2007003307A1 (en) * | 2005-07-05 | 2007-01-11 | Henkel Kommanditgesellschaft Auf Aktien | Agent containing l-carnitine or l-carnitine derivatives and at least one other specific substance |
| US20120101038A1 (en) * | 2005-08-23 | 2012-04-26 | The General Hospital Corporation | Use of glp-1, glp-1 derivatives or glp-1 fragments for skin regeneration, stimulation of hair growth, or treatment of diabetes |
| WO2011042323A2 (en) * | 2009-10-05 | 2011-04-14 | Henkel Ag & Co. Kgaa | Hair treatment agents comprising surfactant(s) and proteolipid(s) |
| DE102012215046A1 (en) * | 2012-08-24 | 2013-05-02 | Henkel Ag & Co. Kgaa | Use of (6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaene for producing cosmetic composition e.g. for stimulating hair keratins synthesis and cell viability |
| EP2724711A2 (en) * | 2012-10-25 | 2014-04-30 | Henkel AG & Co. KGaA | Hair care product with selected amino acids and/or selected oligopeptides and a selected cationic keratin hydrolysate |
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| R. L. ECKERT: "Sequence of the human 40-kDa keratin reveals an unusual structure with very high sequence identity to the corresponding bovine keratin.", PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES, vol. 85, no. 4, 1 February 1988 (1988-02-01), pages 1114 - 1118, XP055163143, ISSN: 0027-8424, DOI: 10.1073/pnas.85.4.1114 * |
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| DE112014004999A5 (en) | 2016-08-11 |
| DE102013222212A1 (en) | 2015-04-30 |
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