WO2008087765A1 - Composition de traitement capillaire et procédé de traitement capillaire - Google Patents
Composition de traitement capillaire et procédé de traitement capillaire Download PDFInfo
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- WO2008087765A1 WO2008087765A1 PCT/JP2007/067346 JP2007067346W WO2008087765A1 WO 2008087765 A1 WO2008087765 A1 WO 2008087765A1 JP 2007067346 W JP2007067346 W JP 2007067346W WO 2008087765 A1 WO2008087765 A1 WO 2008087765A1
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- Prior art keywords
- hair
- component
- treatment composition
- acid
- hair treatment
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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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
- A61K8/892—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a hydroxy group, e.g. dimethiconol
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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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/345—Alcohols containing more than one hydroxy group
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
Definitions
- the present invention relates to a hair treatment composition and a hair treatment method. More particularly, the present invention relates to hair treatment.
- a unique combination of a natural yarn and a synthetic yarn that eliminates the unique problems of blending alkylpolysiloxanes with terminal hydroxy modification such as dimethiconol, and improves hair strength.
- Hair treatment composition capable of realizing various effects, and this hair treatment composition
- the present invention relates to a hair treatment method used for hair.
- a hair treatment agent containing a silicone derivative has an excellent conditioning effect.
- the silicone derivative accumulates on the hair (build-up), and the conditioning effect gradually decreases.
- Document 1 discloses hair cosmetics that contain a silicone derivative and a sugar component.
- the above-mentioned problems in the formulation of silicone derivatives can be solved.
- Related disclosures are not allowed.
- An object of the present invention is to solve the above-mentioned problems while securing at least the advantages of the blending agent composition containing a silicone derivative.
- the inventor of the present application is particularly preferred in the process of pursuing solutions to the above problems through various trials and errors. It has been found that the above problems can be solved by selectively using a terminal hydroxy-modified alkylpolysiloxane, which is a kind of silicone derivative, and combining with an alicyclic polyol such as inositol. Moreover, it has been found that such a blending can provide a surprising effect of “improving hair strength” in addition to solving the above-mentioned problems. The present invention has been completed based on such novel findings.
- the first invention of the present application is a hair treatment composition containing the following components (A) and (B).
- (B) component terminal polyhydroxy-modified alkylpolysiloxane.
- cycloaliphatic polyol is not particularly limited.
- diol or hexaol of cyclohexane, dieneol or pentaol of cyclopentane, or these A certain range of oligomers as monomer units is included. Particularly preferred is inositol used in the examples described later.
- Inositol is a well-known physiologically active substance, and other alicyclic polyols do not necessarily exhibit the same physiological activity as inositol.
- the unique effects shown below in the first invention are not based on physiological activity, but are thought to be based on the characteristics of the chemical structure of “alicyclic compound having a plurality of hydroxyl groups”. . Therefore, alicyclic polyols other than inositol can be reasonably estimated based on chemical common sense that they exhibit the same effect as inositol.
- the component (A) and the component (B) are combined with the hair treatment composition, an excellent conditioning effect can be ensured based on the component (B) which is a kind of silicone derivative.
- the component (A) increases the hydrophilicity of the component (B), and the accumulation effect on the hair is suppressed because the component (B) is easily washed away during washing, resulting in a decrease in conditioning effect. Is well prevented.
- the hair treatment composition of the first invention improves the hair strength when applied to the hair, both in the (A) component blending system and in the (B) component blending system. 7 067346 was also found to exhibit surprising effects that were not known at all. The reason for this has not been clarified yet, but due to the coating effect of the component (B) on the hair, the component (A) penetrated well into the hair and thus penetrated into the hair. Is estimated to act on the hair structure and improve hair strength.
- the hair treatment composition of the first invention exhibits a good hair strength improving effect even when used for healthy hair, but when this is applied to damaged hair, a particularly remarkable hair strength improving effect is obtained. It was found that it was secured.
- the component in the hair treatment agent and composition according to the first invention, (A) the component is inositol, and (B) the component is dimethiconol, satisfying at least one of the conditions .
- inositol which is a hexol of cyclohexane
- dimethiconol can be exemplified as a terminal hydroxy-modified alkylpolysiloxane.
- the hair treatment composition according to the first invention or the second invention corresponds to one or more of the following (1) and (2).
- the blending amount of the component (A) is in the range of 0.05 mass% to 5.0 mass%.
- the amount of the component (B) is in the range of 0.1% by mass to 10.0% by mass.
- the effect of the first invention is particularly preferably ensured.
- the blending amount of the component (A) is below the above range, the moisture feeling of the hair due to the component (B) can be felt S, the hair is sticky and the smoothness tends to be insufficient, and the hair strength is improved. The effect tends to be insufficient, and the specific effect of the present invention cannot be obtained sufficiently.
- the blending amount of the component exceeds the above range, the blending effect described in the first invention is saturated and uneconomical.
- the blending amount of the component (B) When the blending amount of the component (B) is below the above range, it becomes difficult to ensure the conditioning effect, and the hair moisture tends to be insufficient in smoothness and the hair strength improving effect tends to be insufficient. . If the blending amount of component (B) exceeds the above range, problems such as excessive stickiness may occur, and the blending effect described in the first invention will be saturated, which is uneconomical.
- a fourth invention of the present application is a hair treatment method in which the hair treatment composition according to any of the first to third inventions is applied to damaged hair.
- the hair treatment composition of the present invention is a force that exhibits a good effect of improving hair strength even when used for healthy hair, as defined in the fourth invention, when a hair treatment method is applied in which this is applied to damaged hair Especially, the remarkable effect of improving hair strength is exhibited.
- the hair treatment composition according to the present invention contains at least (A) component: alicyclic polyol, and (B) component: alkylpolysiloxane having a terminal hydroxy modification. More preferably, (C) component: neutral or acidic amino acid, (E) component: pH buffer component consisting of organic acid and organic alcohol, (F) component: oligosaccharide 1 Contains more than ingredients.
- component alicyclic polyol
- component alkylpolysiloxane having a terminal hydroxy modification. More preferably, (C) component: neutral or acidic amino acid, (E) component: pH buffer component consisting of organic acid and organic alcohol, (F) component: oligosaccharide 1 Contains more than ingredients.
- (D) component cellulose derivative can be further exemplified. This component will be described in detail in the section “Other preferred components of the hair treatment composition” described later. Moreover, water is blended as a solvent or dispersion medium for each component of the hair treatment composition, and the concentration (mass percentage) of each component is adjusted.
- the use of the hair treatment agent and composition of the present invention is not particularly limited, it is used, for example, as a shampoo, rinse or styling agent. It can also be used as a post-treatment agent for permanent wave treatment, a hair decoloring treatment, an oxidative hair dyeing treatment or an acid hair dyeing treatment.
- Permanent wave treatment is a second agent that contains at least an oxidizing agent after hair has been reduced with a first agent that contains at least an alkaline agent and a reducing agent, followed by wave shaping on the hair.
- Hair decoloring treatment is a treatment that depilates hair by applying a first agent containing at least an alkaline agent and a second agent containing at least an oxidizing agent such as hydrogen peroxide at the time of use.
- Oxidative hair treatment is a mixture of a first agent containing at least an alkaline agent and an oxidation dye (main intermediate and coupler) and a second agent containing at least an oxidizing agent such as hydrogen peroxide at the time of use. This is a treatment that removes the hair and dyes the hair by coloring the acid.
- Acid hair dyeing refers to a hair dyeing treatment in which an acid dye having a negative charge is applied to hair having a positive charge in advance and ionically bonded.
- the dosage form of the hair treatment composition can be arbitrarily selected from various known dosage forms according to its use and intended purpose.
- liquid form, emulsion, cream form, gel form, paste form, mist form (spray type), aerosol foam and the like can be exemplified.
- the pH of the hair treatment composition is not particularly limited, but generally about pH 3.0 to 8.0 is preferable, and about pH 3.5 to 7.0 is particularly preferable. If the pH is less than 3.0, there is a concern about the poor hair feel due to overconcentration of the hair protein, and if the pH exceeds 8.0, there is a concern about hair damage due to the decomposition of the hair protein.
- the pH buffer component (E) component In order to stably maintain the pH within these ranges in the hair treatment composition, it is preferable to blend the pH buffer component (E) component. This will be described in detail in the section “Main components of the agent composition”.
- the alicyclic polyol as component (A) is a compound having two or more hydroxyl groups in a so-called aliphatic cyclic hydrocarbon.
- the type of the aliphatic cyclic hydrocarbon is not limited, but typical examples include quack-pentane or hexane-hexane having an arbitrary steric structure.
- a compound having 2 to 5 hydroxyl groups can be considered as a polyol of cyclopentane, and a compound having 2 to 6 hydroxyl groups can be considered as a polyol of chicane hexane.
- a particularly preferable component (A) is inositol, which is a hexyl hexane. One of these can be blended alone, or two or more can be blended together. -
- the (B) component terminal hydroxy-modified alkylpolysiloxane refers to various monoalkylpolysiloxanes whose ends are modified with hydroxyl groups, dialkylpolysiloxanes, and the like. Resins that are not hydroxy-terminated at the ends, alkyl polysiloxanes (eg, dimethicone), and polysiloxanes containing aromatic rings or cycloalkane structures (eg, methylphenyl polysiloxane) are excluded.
- dimethiconol dimethylpolysiloxane modified at both ends with hydroxy
- various kinematic viscosities nmi 2 / s
- roxy-modified methylphenol polysiloxane One of these can be blended alone, or two or more can be blended together.
- the hair treatment composition further contains a neutral or acidic amino acid as component (C)
- the hair strength after finishing is further improved.
- neutral or acidic amino acid means a salt of an acidic or neutral amino acid, a modified amino group that is a basic group, or an acidic group as long as it is not basic. It is a concept that includes derivatives such as those containing phonic acid groups.
- the type of neutral or acidic amino acid is not limited, but preferred examples include glycine, araene, taurine, L-theanine, L-phenylalanine, gnoretamic acid, aspartic acid, and proline. One of these can be blended alone, or two or more can be blended together.
- the hair treatment composition preferably stabilizes pH with the component (E), ie, the pH buffer component. Also in this case, the hair strength after finishing is further improved. The reason is that by stabilizing the pH of the hair treatment composition, the structure of the protein constituting the hair can be made more chemically stable, and the physical properties of the protein can be improved accordingly. Because. ⁇ P, the component (E) can be expected to contribute to the improvement of the finished feeling. Since an inorganic pH buffer component is too effective, it is preferable to use an organic acid and an organic alcohol.
- an acid component composed of an organic acid and an alkali component composed of an organic alkali are preferable.
- organic acid carboxylic acid is particularly preferable, and in particular, an acid selected from glycolic acid, lactic acid, malic acid, citrate, tartaric acid and succinic acid is preferable.
- Organic alkalis include volatile alkali components such as morpholine, alkanolamines such as monoethanolamine and triethanolamine, 2-amino-2-methylenole 1-propanol, 2-amino-2-methinole 1, 3 -Basic amino acids such as amino alcoholones such as propanediol, L-arginine, L-lysine, L-histidine and the like. One of these can be blended alone, or two or more can be blended together.
- the hair treatment composition further improves the hair strength after finishing even when it contains an oligosaccharide as the component (F).
- the (F) component oligosaccharide refers to an oligosaccharide in which the same or different monosaccharides as monomers, such as disaccharides, trisaccharides, and tetrasaccharides, are glycoside-bonded in the range of 2 units to 100 units.
- the type of monosaccharide is not limited and may be arbitrary, such as gnolecose, fructose, mannose, and sorbitol. “Oligo cocoon” also includes various oligosaccharide derivatives.
- oligosaccharides include manoleose, cellobiose, lactose, isomanoletose, sucrose, chitobiose, cellotriose, manoleto triose, raffinose, tre / rose, stachoose ⁇ cellotetraose, cellopentose, manoletotetraose And maltopentaose.
- One of these can be blended alone, or two or more can be blended together.
- the hair treatment composition of the present invention preferably contains (D) component: cellulose derivative as a component for improving the strength of the hair.
- Component cellulose derivatives include cationized cellulose, hydroxyethyl cellulose, hydroxypropinoremethenoresenorelose, canoleboxymethinoresenorelose salt, polyquatanumu 4 4 polyquaterum 1 1 0 ( Both are INCI names). One of these can be blended alone, or two or more can be blended together.
- the hair treatment composition of the present invention in addition to the above components, as long as the properties as a hair treatment composition and the effects of the present invention are not impaired, oily components other than the above-described components, hydrocarbons, Surface active agents, cationic compounds, polymer substances, protein hydrolysates, vitamins, ceramides, chelating agents, fragrances, disinfectants, preservatives, UV absorbers, propellants, thickeners, pearlizing agents, etc. It can be blended as necessary or optional. About some of these ingredients Specific examples are listed below.
- silicone derivatives other than the component (B) silicone derivatives other than the component (B), polyhydric alcohol, fats and oils, waxes, higher alcohol, higher fatty acid, final alkyl glyceryl ether, Esters can be blended. In addition to the component (B), one of these can be blended alone, or two or more can be blended together.
- Silicone derivatives include alkylpolysiloxanes that are not terminally hydroxyl-modified.
- polyhydric alcohol examples include glycols and glycerins.
- Glycols include ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, isoprenglycone, 1,3-butylene glycol, etc.
- glycerins include glycerin, diglycerin, polyglycerin, etc. Can be mentioned.
- fats and oils examples include various vegetable oils and animal oils.
- waxes examples include beeswax, candelilla wax, carnauba wax, jojoba oil, and lanolin.
- Higher alcohols include lauryl alcohol, myristyl alcohol, cetyl alcohol monoole (cetanol), stearyl alcohol, cetostearyl alcohol, aralkyl alcohol, behenyl alcohol, 2-hexyldecanol, isostearyl alcohol, 2-octyldodeca Nord, decyltetradecanol, oleyl alcohol, linoleyl alcohol, linolenyl alcohol, lanolin alcohol and the like.
- Higher fatty acids include lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, isostearic acid, hydroxystearic acid, 12-hydroxystearic acid, o Examples include oleic acid, undecylenic acid, linoleic acid, ricinoleic acid, and lanolin fatty acid.
- alkyl glyceryl ether examples include batyl alcohol (monostearyl glycerin ether), chimyl alcohol (monocetyl darseryl ether), ceralkyl alcohol (monooleyl glyceryl ether), and isostearyl glyceryl ether.
- Esters include diisopropyl adipate, diisobutyl adipate, dioctyl adipate, 1-hexyldecyl adipate, disostearyl adipate, isopropyl myristate, cetyl octanoate, cetyl isooctanoate, isononyl isononanoate, isononanoic acid Isosodecyl, Isosodecyl isononanoate, Disopropyl sebacate, Octyldecyl myristate, Isopropyl panolemitate, Ptyl stearate, Stearyl stearate, Hexyl laurate, Myristyl myristate, Decyl oleate, Hexyldecyl dimethyloctylate, Isostearyl myristate, 2-ethylhexyl palmitate,
- hydrocarbons examples include monoolefin oligomer, light isoparaffin, light liquid isoparaffin, liquid isoparaffin, liquid paraffin, liquid squalene, polybutene, paraffin, polyethylene powder, microcrystalline wax, petrolatum and the like. One of these can be blended alone, or two or more can be blended together.
- a cationic, anionic, nonionic or amphoteric surfactant can be combined.
- an amino acid type surfactant as a category focused on the chemical structure can be blended.
- These interfacial surface active active agents are prepared by combining 11 kinds of the substances alone, or more than 22 kinds or more. This is where you can combine and mix together. .
- Aamiminonoic acid type interfacial surface active agents include gayyuonon, katachithioon, non-non-ion, and amphoteric types.
- a amimino acid type interface active agent is used.
- An anionic amiminonoic acid type interfacial surface active agent may be particularly preferred.
- As an anamiononic acid-type interfacial surface active agent having an anionic property it is not limited, but N ⁇ ———Acysilyl type aamiminono acid salt may be preferred. .
- N ⁇ --facilyl glycericin salt N ⁇ --facilyl lanalanin salt, N ⁇ --facilyl lug Gurultataminic acid salt and N ⁇ --facilyl lupus spaparalaginic acid salt are mentioned. .
- Examples include Liumum, —-- Lalauuroloyle Russarul Cocosicin Nanatotrirumum and the like. .
- Tamibu's amiminonoic acid type interfacial surface active agents other than those of non-anionic properties include, for example, Acid syrupyl LL——Arrulgininin ethytyl '' DD LL——Pipyrrololydodoncacarbobonic acid salt, ——— [[Aralkylkilulu ((11 22,, 11 44)) 22——Hydrodoloxyxipropropyryl]] 1 LL 1 1
- Arargigiginin salt hydrochloride salt solution Pipirolog Glutarutamate acid oleileinate acid guglyriceserylyl, etc. Can be mentioned. .
- the catecholthione interfacial surface active agent is a salt chloride.
- Non-Ionion-type interfacial surface active agents include, but are not limited to, Polypolioxyoxyethylene ((hereinafter referred to as “ ⁇ ⁇ ⁇ ”)) ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ Poplari
- alkyl sulfates such as sodium lauryl sulfate
- POE alkyl sulfates such as POE lauryl ether sulfate
- alkyl sulfate esters such as lauryl sulfate triethanol amine, dodecylbenzenesulfonic acid triethanol Mines, sodium tetradecenesulfonate, POE lauryl ether phosphate and its salts 0 0
- amphoteric surfactants examples include 2-undecyl mono-N-carboxymethyl-N-hydroxyethyl imidazoline betaine sodium, cocoa propyl betaine, and lauryl dimethylaminoacetic acid betaine.
- a cationic compound refers to a compound whose aqueous solution is cationic.
- the type of the cationic compound is not limited, but particularly preferable examples include cationic oligomers and cationized sugar derivatives excluding the above-described cationic surfactants, and other examples include cationic polymers. One of these can be blended alone, or two or more can be blended together.
- Examples of the cationic oligomer include cationized hydrolyzed proteins.
- cationized sugar derivative examples include cationized oligosaccharides, cationized honey, and cationized chitosan.
- cationic polymer examples include cationized guar gum, cationized starch, quaternized polyvinylpyrrolidone derivatives, diallyl quaternary ammonium salt polymer derivatives, and the like.
- polymer substance examples include various polymer substances excluding cationic polymers as the following cationic compounds, for example, anionic polymers such as carboxyvinyl polymer, diaryl quaternary ammonium salt Z acrylic acid copolymer, etc.
- cationic polymers such as carboxyvinyl polymer, diaryl quaternary ammonium salt Z acrylic acid copolymer, etc.
- polymers and various water-soluble polymers One of these can be blended alone, or two or more can be blended together.
- the high-molecular substance examples include vegetable polymers such as gum arabic, xanthan gum, carrageenan, pectin, agar and starch, microbial polymers such as dextran and pullulan, Examples include animal polymers such as collagen, casein, and gelatin. Other examples include sodium alginate, carboxyvinyl polymer, polyoxyethylene polymer, sodium polyacryloleate, and polyacrylamide polydimethylmethylene chloride peridinium. .
- protein hydrolysates excluding the above-mentioned cationized hydrolyzed proteins, collagen, keratin, elastin, hive mouth-in, egg, silk, concholine, casein, gelatin and other proteins, rice, wheat, barley, oats
- protein hydrolysates obtained by hydrolyzing proteins obtained from plants such as soybean, endou, almond, brazil nuts, potatoes, and corn with acids, alcohol, enzymes, and the like.
- a hair treatment composition (washing hair treatment) having the composition according to Examples 1 to 4 and Comparative Examples 1 to 10 shown in Table 1 at the end was prepared according to a conventional method. Further, hair treatment compositions having compositions according to Examples 23 to 26 shown in Table 5 at the end were also prepared in the same manner.
- Example 2 3 to Example 26 shown in Table 5 contain only the component (B) as a silicone derivative.
- Each of the hair treatment compositions shown in Tables 1 and 5 has a pH in the range of 3.0 to 8.0.
- phytic acid and sorbi] 1 is a component for comparison with the component (A), and poly (oxyethylene 'oxypropylene) ⁇ Pitylene ⁇ Methylpolysiloxane copolymer, methylphenylpolysiloxane, PEG-12 dimethicone, PEG / PPG-18 / 18 dimethicone, dimethicone and decamethylcyclopentasiloxane are components for comparison with component (B) .
- the amount of each component is expressed as a number, but these values are all in units of “% by mass”.
- an average score is calculated for each of the examples and comparative examples.
- the average score is 3.6 or more, ⁇ (excellent), the average score is 2.6 to 3.
- a case of 5 was marked as ⁇ (good), an average score of 1.6 to 2.5 was evaluated as ⁇ (slightly bad), and an average score of 1.5 or less was rated as X (bad).
- the results are shown in the “Eating feeling after drying” section in the “Evaluation” column of Tables 1 and 5.
- an average score is calculated for each of the examples and comparative examples.
- the average score is 3.6 or more, ⁇ (excellent), the average score is 2.6 to 3. If it is 5, ⁇ (good Favorable), when the average score is L 6 to 2.5, ⁇ (somewhat bad), and when the average score is 1.5 or less, X (bad).
- the results are shown in the section “Softness after time” in the “Evaluation” column of Tables 1 and 5.
- the breaking stress value was determined using a tensile tester (Tensilon UTM-II; manufactured by Toyo Baldwin). It was measured. Then, the increase rate of the measurement value after the treatment with respect to the measurement value before the treatment was calculated as a hair strength increase rate (%). The rate of increase in hair strength was evaluated according to the following criteria, and the results are shown in the section of “Tensile strength of hair” in the “Evaluation” column of Tables 1 and 5.
- ⁇ Hair strength increase rate is 9% or more
- ⁇ Hair strength increase rate is 7% or more and less than 9%
- ⁇ Hair strength increase rate is 5% or more and less than 7%
- X Hair strength increase rate is less than 5% .
- Each of the 10 panelists touched the hair bundle after treatment with the hair treatment composition according to each of the above Examples and Comparative Examples by hand to evaluate the firmness of the finished hair. 4 points when there is sufficient harshness, 3 points when there is harshness, 2 points when there is no harshness, and 1 point when there is no harshness did.
- the average score is calculated for each of the examples and comparative examples. If the average score is 3.6 or more ⁇ (excellent), the average score is 2.6 to 3 ⁇ A case of 5 was marked as ⁇ (good), an average score of 6 to 2.5 was evaluated as ⁇ (somewhat bad), and an average score of 1.5 or less was rated as X (bad). The results are shown in the “Evaluation of hair” section of “Evaluation” in Tables 1 and 5 .
- Example 1 to Example 4 As can be seen from the evaluation results shown in Table 1 and Table 5, Example 1 to Example 4, Example 2 3 to Example 2 6 are very difficult to evaluate in any evaluation item. there were. The slight difference between Example 3 and Example 4 in hair strength and harshness depends on the presence or absence of the C component.
- Example 1 As shown in Table 2, the component (C) in the formulation of “Example 1” according to the first example group described above was mixed in the same amount by changing the type (Example 5 to Example 11). ) In addition, various components (F) were added to the formulation of “Example 1” relating to the first example group (Examples 12 to 15). These hair treatment compositions had the same dosage form as in Example 1 and the same pH.
- each item was As in the case of Example 1 shown in Table 1, all the items were evaluated as “ ⁇ ”.
- the average score of “feeling of hair harshness” in Example 1 was “3.8”, whereas both components (C) and (F) were compared.
- the evaluation average score was “3.9”.
- Example 1 As shown in Table 3, the hair treatment agents according to Examples 16 to 19 in which the amount of component (A) in the formulation of “Example 1” according to the first example group described above was changed, respectively.
- Each composition was prepared according to the same method as in the first example group. These hair treatment compositions had the same dosage form as in Example 1 and the same pH.
- Example 1 6 to Example 19 Using the hair treatment composition according to 9 and performing the same evaluation using the same hair bundle sample as in the case of the first example group, as shown in Table 3. As in the case of Example 1 shown in Table 1, all items were evaluated as “ ⁇ ”. The evaluation average score of “feeling of elasticity of hair” was also not different between Example 16 to Example 19.
- the hair treatment compositions according to Examples 1, 3, 5 and Comparative Examples 1, 4, 9, and 10 were used.
- Examples using the hair treatment compositions according to Examples 1, 3 and 5 were sequentially numbered as Examples 20, 21 and 22 respectively, and were designated as Comparative Examples 1, 4, 9, and 10 respectively.
- the examples using the hair wrinkle treating agent composition were sequentially numbered as Comparative Examples 1 1, 1 2, 1 3 and 14, respectively.
- the same evaluation methods and evaluation criteria were evaluated for the same evaluation items as in the case of the first example group.
- Examples 20 0, 21 and 22 are exactly the same as Examples 1 and 3 in the first example group and Example 5 in the second example group. Evaluation results were obtained.
- Comparative Examples 1 1, 1 2, 1 3 and 14 have relatively higher evaluation ranks than Comparative Examples 1, 4, 9, and 10 of the first example group in many evaluation items. However, in comparison with Examples 2 0, 2 1 and 2 2, there were still significant differences.
- the hair treatment composition according to the present invention has a sufficiently remarkable effect when targeting healthy hair as compared with the prior art, but when treating damaged hair. Means a particularly remarkable effect.
- a hair treatment composition that can ensure an excellent conditioning effect based on the formulation of a silicone derivative, prevent a decrease in the effect due to accumulation on the hair, and improve the strength of the hair.
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Abstract
Cette invention concerne une composition de traitement capillaire comprenant (A) un polyol alicyclique et (B) un alkylpolysiloxane modifié par un groupe hydroxyle aux extrémités, où le polyol alicyclique (A) est particulièrement de préférence de l'inositol et l'alkylpolysiloxane (B) est particulièrement de préférence du diméthiconol ; et un procédé de traitement capillaire par application de la composition de traitement capillaire sur des cheveux endommagés. Selon l'invention, on obtient un excellent effet conditionnant dû au dérivé de silicone et la détérioration de cet effet est inhibée grâce à l'accumulation du dérivé sur les cheveux, tout en améliorant la force des chevaux.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008553953A JP5314431B2 (ja) | 2007-01-15 | 2007-08-30 | 毛髪処理剤組成物及び毛髪処理方法 |
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| Application Number | Priority Date | Filing Date | Title |
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| JP2007-006476 | 2007-01-15 | ||
| JP2007006476 | 2007-01-15 |
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| WO2008087765A1 true WO2008087765A1 (fr) | 2008-07-24 |
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| PCT/JP2007/067346 Ceased WO2008087765A1 (fr) | 2007-01-15 | 2007-08-30 | Composition de traitement capillaire et procédé de traitement capillaire |
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| Country | Link |
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| JP (1) | JP5314431B2 (fr) |
| WO (1) | WO2008087765A1 (fr) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010275286A (ja) * | 2009-05-26 | 2010-12-09 | Sanei Kagaku Kk | 洗い流さない毛髪化粧料 |
| JP2010275285A (ja) * | 2009-05-26 | 2010-12-09 | Sanei Kagaku Kk | 洗い流さない毛髪化粧料 |
| JP2013023471A (ja) * | 2011-07-21 | 2013-02-04 | Kracie Home Products Ltd | ヘアリンス組成物 |
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| JPS63313713A (ja) * | 1987-06-17 | 1988-12-21 | Shiseido Co Ltd | 毛髪化粧料 |
| JPS63313714A (ja) * | 1987-06-17 | 1988-12-21 | Shiseido Co Ltd | 毛髪化粧料 |
| JPH01211518A (ja) * | 1988-02-19 | 1989-08-24 | Shiseido Co Ltd | 毛髪化粧料 |
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| JP2005187359A (ja) * | 2003-12-25 | 2005-07-14 | Lion Corp | ノンエアゾール型泡吐出容器用毛髪洗浄組成物 |
| JP2005350454A (ja) * | 2004-05-12 | 2005-12-22 | Ichimaru Pharcos Co Ltd | 化粧料組成物及びその製造方法 |
| JP2006008611A (ja) * | 2004-06-28 | 2006-01-12 | Lion Corp | 毛髪化粧料 |
| JP2006028113A (ja) * | 2004-07-20 | 2006-02-02 | Kanebo Ltd | 毛髪化粧料 |
| JP2006290787A (ja) * | 2005-04-11 | 2006-10-26 | Nippon Fine Chem Co Ltd | 化粧料用油剤又は皮膚外用剤用油剤、並びに化粧料又は皮膚外用剤 |
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| FR2794998B1 (fr) * | 1999-06-21 | 2001-07-27 | Oreal | Organogels et leurs utilisations notamment cosmetiques |
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| JPS63313713A (ja) * | 1987-06-17 | 1988-12-21 | Shiseido Co Ltd | 毛髪化粧料 |
| JPS63313714A (ja) * | 1987-06-17 | 1988-12-21 | Shiseido Co Ltd | 毛髪化粧料 |
| JPH01211518A (ja) * | 1988-02-19 | 1989-08-24 | Shiseido Co Ltd | 毛髪化粧料 |
| JPH11500458A (ja) * | 1996-11-04 | 1999-01-12 | ザ、プロクター、エンド、ギャンブル、カンパニー | シリコーンエマルジョンを含むヘアムース組成物 |
| JP2003535060A (ja) * | 2000-05-30 | 2003-11-25 | ザ、プロクター、エンド、ギャンブル、カンパニー | 縮れ毛制御剤を含むヘアコンディショニング組成物 |
| JP2004217643A (ja) * | 2002-12-25 | 2004-08-05 | Kao Corp | 毛髪化粧料 |
| JP2005187359A (ja) * | 2003-12-25 | 2005-07-14 | Lion Corp | ノンエアゾール型泡吐出容器用毛髪洗浄組成物 |
| JP2005350454A (ja) * | 2004-05-12 | 2005-12-22 | Ichimaru Pharcos Co Ltd | 化粧料組成物及びその製造方法 |
| JP2006008611A (ja) * | 2004-06-28 | 2006-01-12 | Lion Corp | 毛髪化粧料 |
| JP2006028113A (ja) * | 2004-07-20 | 2006-02-02 | Kanebo Ltd | 毛髪化粧料 |
| JP2006290787A (ja) * | 2005-04-11 | 2006-10-26 | Nippon Fine Chem Co Ltd | 化粧料用油剤又は皮膚外用剤用油剤、並びに化粧料又は皮膚外用剤 |
| JP2006315987A (ja) * | 2005-05-11 | 2006-11-24 | Shiseido Co Ltd | 毛髪化粧料 |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010275286A (ja) * | 2009-05-26 | 2010-12-09 | Sanei Kagaku Kk | 洗い流さない毛髪化粧料 |
| JP2010275285A (ja) * | 2009-05-26 | 2010-12-09 | Sanei Kagaku Kk | 洗い流さない毛髪化粧料 |
| JP2013023471A (ja) * | 2011-07-21 | 2013-02-04 | Kracie Home Products Ltd | ヘアリンス組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPWO2008087765A1 (ja) | 2010-05-06 |
| JP5314431B2 (ja) | 2013-10-16 |
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