WO2002038121A1 - Composition cosmetique pour le traitement, le soin ou la protection de la peau - Google Patents
Composition cosmetique pour le traitement, le soin ou la protection de la peau Download PDFInfo
- Publication number
- WO2002038121A1 WO2002038121A1 PCT/EP2001/012672 EP0112672W WO0238121A1 WO 2002038121 A1 WO2002038121 A1 WO 2002038121A1 EP 0112672 W EP0112672 W EP 0112672W WO 0238121 A1 WO0238121 A1 WO 0238121A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- extract
- acid
- composition according
- composition
- antarctica
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/02—Algae
- A61K36/05—Chlorophycota or chlorophyta (green algae), e.g. Chlorella
-
- 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
- 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
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9706—Algae
- A61K8/9722—Chlorophycota or Chlorophyta [green algae], e.g. Chlorella
Definitions
- UV-A light characteristic wavelength range from 315 to 400 nm
- typical sunscreens often pass very easily, since these sunscreens often only contain the UV-B- that is the main cause of sunburn. Filter out light effectively. This explains in particular the need for novel substances that absorb in the area of UV-A light.
- green algae there are substances with suitable absorption spectra. It is known (Post and Larkum (1993), Aquat. Bot., 45, pp. 231-243) that the methanolic extract from Prasiola crispa ssp. antarctica shows an absorption band at 325 nm. It is probably a mycosporin-like amino acid (MAA).
- MAA mycosporin-like amino acid
- Another object of the present invention is the use of this UV-absorbing substance or a derivative thereof in cosmetic preparations.
- polyglycerol esters e.g. Polyglycerol polyricinoleate, polyglycerol poly-12-hydroxystearate or polyglycerol dimerate. Mixtures of compounds from several of these classes of substances are also suitable;
- UV light protection filters can be added to the composition according to the invention.
- the further UV light protection filters that can be added to the cosmetic composition are preferably soluble compounds or insoluble pigments or mixtures thereof.
- UV light protection filters are understood to mean organic substances which are able to absorb ultraviolet rays and release the absorbed energy in the form of longer-wave radiation, for example heat.
- the organic substances can be oil-soluble or water-soluble.
- benzoylmethane such as 1- (4'-tert-butylphenyl) -3- (4'-methoxyphenyl) propane-1,3-dione, 4-tert-butyl
- benzoylmethane such as 1- (4'-tert-butylphenyl) -3- (4'-methoxyphenyl) propane-1,3-dione, 4-tert-butyl
- typical UV-A filters -4'-methoxydibenzoylmethane or 1-phenyl-3- (4 ' ⁇ isopropylphenyl) propane-1,3-dione.
- the UV-A and UV-B filters can of course also be used in mixtures.
- the cosmetic composition can also contain, among other things, caring components such as oils, waxes, fats, lipid-replenishing substances, thickeners, emulsifiers and fragrances.
- caring components such as oils, waxes, fats, lipid-replenishing substances, thickeners, emulsifiers and fragrances.
- a high proportion of nourishing substances is particularly advantageous for topical prophylactic or cosmetic treatment of the skin. It is particularly advantageous if, in addition to the animal and vegetable fats and oils, which in many cases also have a care effect, the composition also contains further care components.
- the group of nourishing active ingredients that can be used includes, for example: fatty alcohols with 8 - 22 carbon atoms, in particular fatty alcohols from natural fatty acids; animal and vegetable protein hydrolyzates, in particular elastin, collagen, keratin, milk protein, soy protein, silk protein, oat protein, pea protein, almond protein and wheat protein hydrolyzates; Vitamins and vitamin precursors, especially those of vitamin groups A and B; Mono-, di- and oligosaccharides; Plant extracts; Honey extracts; ceramides; phospholipids; Petroleum jelly, paraffin and silicone oils; Fatty acid and fatty alcohol esters, especially the monoesters of fatty acids with alcohols with 3 to 24 carbon atoms.
- the vitamins, provitamins or vitamin precursors to be used preferably in the composition according to the invention include, among others:
- the 2-furanone derivative which is extremely preferred according to the invention is pantolactone (dihydro-3-hydroxy-4,4-dimethyl-2 (3H) - furanone), where in formula (I) R 1 is a hydroxyl group, R 2 is a hydrogen atom, R 3 and R 4 represent a methyl group and R 5 and R 6 represent a hydrogen atom.
- the stereoisomer (R) -pantolactone is formed when pantothenic acid is broken down.
- Vitamin B 6 which does not mean a uniform substance, but rather the derivatives of 5-hydroxymethyl-2-methylpyridin-3-ol known under the trivial names pyridoxine, pyridoxamine and pyridoxal. Vitamin B 6 is contained in the agents according to the invention preferably in amounts of 0.0001 to 1.0% by weight, in particular in amounts of 0.001 to 0.01% by weight.
- topical preparations for example aqueous and aqueous / alcoholic solutions, aqueous gels, sprays, foams, foam aerosols, ointments, emulsions of the O / W or W / O type or microemulsions, can be prepared in a simple manner from the extracts mentioned ,
- the composition contains at least one mycosporin-like amino acid (MAA).
- MAA mycosporin-like amino acid
- Prasiola crispa ssp. antarctica contains traces of mycosporin-glycine and a large amount of a structurally not yet elucidated UV-absorbing substance, which shows an absorption maximum at 324 nm and which is determined by HPLC analysis (5 vol.% aqueous methanol, 0.1 vol. % Acetic acid; flow rate: 0.7 ml min "1 ; Phenomenex Sphereclone RP-8 column, 5 ⁇ m, 250 x 4 mm ID) is available with a retention time of 3.4 min.
- HPLC analysis 5 vol.% aqueous methanol, 0.1 vol. % Acetic acid; flow rate: 0.7 ml min "1 ; Phenomenex Sphereclone RP-8 column, 5 ⁇ m, 250 x 4 mm ID
- the structurally as yet unidentified UV-absorbing substance is also a mycosporin-like amino acid.
- composition according to the invention preferably contains 0.01 to 10% by weight of the extract, based on the dry mass of the extract. Contents of 0.05 to 1% by weight, in particular 0.1 to 0.5% by weight, based on the dry mass of the extract, are particularly preferred.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Birds (AREA)
- Botany (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Dermatology (AREA)
- Chemical & Material Sciences (AREA)
- Alternative & Traditional Medicine (AREA)
- Medical Informatics (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Cosmetics (AREA)
Abstract
L'invention concerne une composition cosmétique pour le traitement, le soin ou la protection de la peau, comprenant un support et caractérisée en ce qu'elle contient un extrait de l'algue verte <i>Prasiola crispa ssp. antarctica</i>.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2002224822A AU2002224822A1 (en) | 2000-11-09 | 2001-11-02 | Cosmetic skin treatment, care or protection composition |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10055558A DE10055558A1 (de) | 2000-11-09 | 2000-11-09 | Kosmetische Zusammensetzung zur Behandlung, zur Pflege oder zum Schutz der Haut |
| DE10055558.6 | 2000-11-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2002038121A1 true WO2002038121A1 (fr) | 2002-05-16 |
Family
ID=7662703
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2001/012672 Ceased WO2002038121A1 (fr) | 2000-11-09 | 2001-11-02 | Composition cosmetique pour le traitement, le soin ou la protection de la peau |
Country Status (3)
| Country | Link |
|---|---|
| AU (1) | AU2002224822A1 (fr) |
| DE (1) | DE10055558A1 (fr) |
| WO (1) | WO2002038121A1 (fr) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004105722A1 (fr) * | 2003-05-30 | 2004-12-09 | Gianfranco De Paoli Ambrosi | Formulation servant a realiser une exfoliation chimique |
| CN104352554A (zh) * | 2014-10-21 | 2015-02-18 | 河南牧翔动物药业有限公司 | 一种复方头孢喹肟抗菌药物 |
| CN104352566A (zh) * | 2014-10-21 | 2015-02-18 | 河南牧翔动物药业有限公司 | 一种水包油型复方金霉素纳米乳 |
| CN104474164A (zh) * | 2014-11-21 | 2015-04-01 | 范影 | 一种治疗阴虚阳亢型神经衰弱的小验方 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10259966A1 (de) * | 2002-12-15 | 2004-07-08 | Henkel Kgaa | Kosmetische oder pharmazeutische Zubereitung zur Verbesserung der Sauerstoffaufnahme bei Menschen oder Tieren |
| CH701253A1 (de) | 2009-06-12 | 2010-12-15 | Mibelle Ag | Verwendung eines Extraktes aus Schneealgen in kosmetischen oder dermatologischen Formulierungen. |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2674126A1 (fr) * | 1991-03-19 | 1992-09-25 | Secma | Utilisation d'algues rouges calcaires pour la preparation de compositions cosmetiques. |
| WO2000024369A1 (fr) * | 1998-10-23 | 2000-05-04 | Nouvab Inc | Composition de protection contre le rayonnement solaire |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19643365C2 (de) * | 1996-10-09 | 1998-08-20 | Holger Wohner | Protein- und vitaminhaltige Kosmetikzusammensetzung |
-
2000
- 2000-11-09 DE DE10055558A patent/DE10055558A1/de not_active Ceased
-
2001
- 2001-11-02 WO PCT/EP2001/012672 patent/WO2002038121A1/fr not_active Ceased
- 2001-11-02 AU AU2002224822A patent/AU2002224822A1/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2674126A1 (fr) * | 1991-03-19 | 1992-09-25 | Secma | Utilisation d'algues rouges calcaires pour la preparation de compositions cosmetiques. |
| WO2000024369A1 (fr) * | 1998-10-23 | 2000-05-04 | Nouvab Inc | Composition de protection contre le rayonnement solaire |
Non-Patent Citations (1)
| Title |
|---|
| COCKELL C., KNOWLAND J.: "Ultraviolet radiation screening compounds", BIOLOGICAL REVIEWS OF THE CAMBRIDGE PHILOSOPHICAL SOCIETY, 1999, United Kingdom, pages 311 - 345, XP002196313, Retrieved from the Internet <URL:http://www.botany.hawaii.edu/Bot482/Biol%20Rev%20UV%20abs%20compounds.pdf> [retrieved on 20020415] * |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004105722A1 (fr) * | 2003-05-30 | 2004-12-09 | Gianfranco De Paoli Ambrosi | Formulation servant a realiser une exfoliation chimique |
| HRP20050972B1 (hr) * | 2003-05-30 | 2013-09-30 | Gianfranco De Paoli Ambrosi | Formulacija za kemijsko lupljenje (piling) |
| CN104352554A (zh) * | 2014-10-21 | 2015-02-18 | 河南牧翔动物药业有限公司 | 一种复方头孢喹肟抗菌药物 |
| CN104352566A (zh) * | 2014-10-21 | 2015-02-18 | 河南牧翔动物药业有限公司 | 一种水包油型复方金霉素纳米乳 |
| CN104474164A (zh) * | 2014-11-21 | 2015-04-01 | 范影 | 一种治疗阴虚阳亢型神经衰弱的小验方 |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2002224822A1 (en) | 2002-05-21 |
| DE10055558A1 (de) | 2002-06-06 |
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