FR2732215A1 - Skin-lightening cosmetic compsns. - Google Patents
Skin-lightening cosmetic compsns. Download PDFInfo
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- FR2732215A1 FR2732215A1 FR9503760A FR9503760A FR2732215A1 FR 2732215 A1 FR2732215 A1 FR 2732215A1 FR 9503760 A FR9503760 A FR 9503760A FR 9503760 A FR9503760 A FR 9503760A FR 2732215 A1 FR2732215 A1 FR 2732215A1
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- proteases
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- cosmetic compositions
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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
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/11—Encapsulated compositions
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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
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/14—Liposomes; Vesicles
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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
- A61K8/31—Hydrocarbons
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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
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/365—Hydroxycarboxylic acids; Ketocarboxylic acids
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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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
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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
- A61K8/60—Sugars; Derivatives thereof
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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
- A61K8/66—Enzymes
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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
- A61K8/67—Vitamins
- A61K8/671—Vitamin A; Derivatives thereof, e.g. ester of vitamin A acid, ester of retinol, retinol, retinal
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/02—Preparations for care of the skin for chemically bleaching or whitening the skin
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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
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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
- A61Q5/02—Preparations for cleaning the hair
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/41—Particular ingredients further characterized by their size
- A61K2800/412—Microsized, i.e. having sizes between 0.1 and 100 microns
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/41—Particular ingredients further characterized by their size
- A61K2800/413—Nanosized, i.e. having sizes below 100 nm
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
Abstract
Description
La pigmentation de la peau est due à la synthèse de mélanine dans les cellules spécialisées, ainsi qu'à la distribution homogène de cette mélanine dans les kératinocytes de l'épiderme. Dans une peau saine, parfaite, cette synthèse est bien règlée, modulée par l'exposition au soleil et par le pucessus de désquamation.The pigmentation of the skin is due to the synthesis of melanin in the specialized cells, as well as to the homogeneous distribution of this melanin in the keratinocytes of the epidermis. In healthy, perfect skin, this synthesis is well regulated, modulated by exposure to the sun and the overdose of despondency.
II arrive, néanmoins, dans de nombreux cas que ce processus complexe est déréglé : un manque de mélanogénèse (soit dû à un problème génétique, soit à la suite d'une blessure de la peau) est aussi possible qu'une surabondance localisée de pigmentation : les tâches de rousseur, les tâches de sénescence, et les tâches diffuses (chloasma, tâches de grossesse) en sont les phénomènes les plus connus. It happens, however, in many cases that this complex process is disordered: a lack of melanogenesis (either due to a genetic problem, or as a result of a skin injury) is also possible that a localized superabundance of pigmentation Freckles, senescence tasks, and diffuse tasks (chloasma, pregnancy tasks) are the most well known phenomena.
Puisque ces symptômes ne constituent pas de véritables pathologies, étant plus un problème d'ésthetique que de santé, et puisque la méhnogénèse à lieu au sein de l'épiderme, c'est plutôt l'industrie cosmétique que celle de la pharmacie qui s'est intéressée à ce problème.Since these symptoms do not constitute true pathologies, being more a problem of aesthetics than of health, and since the mehnogenesis takes place within the epidermis, it is rather the cosmetic industry than that of the pharmacy which is is interested in this problem.
De nombreuses molécules ou substances ont été proposées pour traiter rlTyperpigmenSon de la peau, mais peuvent être retenues pour une application topique cosmétique (problème d'irritation, de législation, de toxicité). Ceux qui restent après cette sélection ne sont en général pas très eI5caces : I'hydroquinone synthétique (limitée à 2% dans les produits cosmétiques), la lutéoline extraite de certaines plantes, la vitamine C s'avèrent les plus utilisées sans que les effets soit très probants. Many molecules or substances have been proposed for treating skin hyperpigmentation, but may be selected for topical cosmetic application (irritation, legislation, toxicity). Those who remain after this selection are generally not very effective: Synthetic hydroquinone (limited to 2% in cosmetics), luteolin extracted from certain plants, vitamin C are the most used without the effects being very convincing.
Une des raisons de cet échec partiel pourrait être recherchée dans la biodisponibilité des molécules (manque de pénétration à travers la couche comée). Les mélanocytes se trouvent dans les couches moyennes de épiderme. One of the reasons for this partial failure could be sought in the bioavailability of molecules (lack of penetration through the comedic layer). Melanocytes are found in the middle layers of the epidermis.
L'objet du présent brevet est la découverte qu'il est possible de pallier à cet inconvénient en combinant la ou les substances intervenant dans rinhibition de la mélanogénèse avec des enzymes protéolytiques, kératolytiques qui pennettent, de façon douce, d'accélérer la desquamation et donc de briser la barrière presque infranchissable des couches supérieures de l'épiderme.The object of this patent is the discovery that it is possible to overcome this disadvantage by combining the substance or substances involved in the inhibition of melanogenesis with proteolytic enzymes, keratolytics which allow, in a gentle way, to accelerate the desquamation and to break the almost impassable barrier of the upper layers of the epidermis.
vautres substances kératolytiques peuvent être utilisées dans ce but, telles que les acides lactiques, glycoliques, salicyliques. Pour être efficaces, ces acides doivent être employés à des doses relativement élevées (S10%) ce qui a plusieurs inconvénients: fort potentiel d'irritation cutanée, pH des préparations très bas, difficultés de tormulation et de parfumage. other keratolytic substances may be used for this purpose, such as lactic, glycolic, salicylic acids. To be effective, these acids must be used at relatively high doses (S10%) which has several disadvantages: high potential for skin irritation, very low preparations pH, difficulty of formulation and perfume.
Les enzymes protéolytiques choisies dans le cadre de notre invention ne possèdent pas ces inconvénients. Le pH des produits peut respecter celui naturel de la peau (5-7), les émulsions ne sont pas perturbées, le parfumage est libre, et les doses actives d'enzyme ne provoquent ni iiatation ni sensibilisation.The proteolytic enzymes chosen in the context of our invention do not have these disadvantages. The pH of the products can respect the natural pH of the skin (5-7), the emulsions are not disturbed, the perfume is free, and the active doses of enzyme do not cause irritation or sensitization.
Alors que tout type de molécule dépigmentante peut être combinée avec les protéases kératolytiques, nous avons observé des effets particulièrement intéressants avec une préparation contenant de l'acide gluconique (en tant que chélsant de cuivre, privant ainsi, enzyme tyrosinase de son métal indispensable pour l'activité d'oxydation de la tyrosine), la glucosaine (inhibiteur puissant de la glycosylation de la tyrosinase, attaquant le processus en amont par rinhibition de l'activation de l'enzyme même), le sel calcique de l'acide pantothène sulfonique (PASS-Ca de la société
SOGO) et les dérivées, précurseurs ou analogues de la vitamine A, en particulier le B carotène. Ces molécules agissent soit seule, soit ensemble pour freiner la mélanogénèse. Leur activité est renforcée in vivo par l'adjonction d'enzymes kératolytiques.While any type of depigmenting molecule can be combined with keratolytic proteases, we have observed particularly interesting effects with a preparation containing gluconic acid (as a copper chelant, thus depriving the enzyme tyrosinase of its essential metal for tyrosine oxidation activity), glucosaine (a potent inhibitor of tyrosinase glycosylation, attacking the upstream process by inhibiting the activation of the enzyme itself), the calcium salt of pantothenesulphonic acid ( PASS-Ca of society
SOGO) and derivatives, precursors or analogues of vitamin A, especially B carotene. These molecules act either alone or together to slow down melanogenesis. Their activity is enhanced in vivo by the addition of keratolytic enzymes.
Les enzymes utilisées préférentiellement sont d'origine végétale (extraits de plantes: bromélaine, papaïne etc...) ou d'origine microbienne obtenues à l'échelle industrielle par fermentation biotechnologique (bacilus subis, aspergillus spp. etc...).The enzymes used preferentially are of plant origin (plant extracts: bromelain, papain, etc.) or of microbial origin obtained on an industrial scale by biotechnological fermentation (bacilus, aspergillus spp., Etc.).
L'activité dépigmentante d'une combinaison de substances inhibitrices de mélanogénèse avec les kératinases a été vérifiée dans un test sur volonlaires sains.The depigmenting activity of a combination of melanogenesis inhibiting substances with keratinases was verified in a healthy volunteers test.
On mesure la couleur de la peau à l'aide d'un Chromamètre (Minolta) pow relever les trois paramètres "clarté", composante "rouge" et composanle "jaune".The color of the skin is measured using a Chromameter (Minolta) to measure the three parameters "clarity", component "red" and component "yellow".
Les produits cosmétiques contenant les substances inhibitrices de mélanogénèse citées ci-dessus et une quantité suffisante de protéase, sont appliqués sur les taches d'hyperpigmentation (chloasma, mélasma) des vobrilaires pendant une période de 8 semaines. Les valeurs chromamétriques sont relevées après 4 et 8 semaines de traitement
A titre d'exemple, les crèmes suivantes ont été testées sur 30 personnes présentant les symptômes d'hyperpigmentation bcale.
Cosmetic products containing the melanogenesis inhibiting substances mentioned above and a sufficient amount of protease are applied to the hyperpigmentation spots (chloasma, melasma) of the vibrilaires for a period of 8 weeks. Chromametric values are found after 4 and 8 weeks of treatment
For example, the following creams have been tested on 30 people with symptoms of ovarian hyperpigmentation.
<tb><Tb>
<SEP> Crème <SEP> A <SEP> Crème <SEP> B <SEP> Crème <SEP> C <SEP>
<tb> Monostéarate <SEP> de <SEP> sorbitan <SEP> 2.00 <SEP> 2.00 <SEP> 2.00
<tb> Po-t > ate60 <SEP> 3.00 <SEP> 3.00 <SEP> 3.00
<tb> Abool <SEP> cétylique <SEP> 1.50 <SEP> 1.50 <SEP> 1.50
<tb> Pabmitate <SEP> d'isopropyle <SEP> 6.00 <SEP> 6.00 <SEP> 6.00
<tb> Huile <SEP> de <SEP> vaseline <SEP> 5.00 <SEP> 5.00 <SEP> 5.00
<tb> Cire <SEP> diabelles <SEP> 4.00 <SEP> 4.00 <SEP> 4.00
<tb> Propylène <SEP> glycol <SEP> 3.00 <SEP> 3.00 <SEP> 3.00
<tb> Acide <SEP> gluconique <SEP> 0.20 <SEP> 0.20
<tb> Glucosarnine <SEP> 0.20 <SEP> 0.20
<tb> Kérallnase200U* <SEP> 3.00
<tb> B <SEP> Carotène <SEP> 0,005 <SEP> 0,005
<tb> Lécitine <SEP> de <SEP> soja <SEP> 0,25 <SEP> 0,25
<tb> Eau <SEP> + <SEP> conservateur <SEP> qsp <SEP> 100 <SEP> qsp <SEP> 100 <SEP> qsp <SEP> 100 <SEP>
<tb>
U = mol. Tyrosine/min/ml
Après 4 semaines de traitement, on constate une différence de pigmentation sur les sites traits aux crèmes A et B par rapport à la crème C (placebo), après 8 semaines les trois sites se différencient nettement ('a clarté chromamétrique augmente de façon significative + 15% sur les sites traités à la crème A, contre +7% sur les sites traités à la crème B et 0.5% sur les sites placebo).<SEP> Cream <SEP> A <SEP> Cream <SEP> B <SEP> Cream <SEP> C <SEP>
<tb> Monostearate <SEP> of <SEP> sorbitan <SEP> 2.00 <SEP> 2.00 <SEP> 2.00
<tb>Po-t> ate60 <SEP> 3.00 <SE> 3.00 <SEP> 3.00
<tb> Abool <SEP> Cetyl <SEP> 1.50 <SEP> 1.50 <SEP> 1.50
<tb> Isopropyl Pabmitate <SEP><SEP> 6.00 <SEP> 6.00 <SEP> 6.00
<tb> Oil <SEP> of <SEP> Vaseline <SEP> 5.00 <SEP> 5.00 <SEP> 5.00
<tb> Wax <SEP> Diabetes <SEP> 4.00 <SEP> 4.00 <SEP> 4.00
<tb> Propylene <SEP> Glycol <SEP> 3.00 <SEP> 3.00 <SEP> 3.00
<tb><SEP> Gluconic acid <SEP> 0.20 <SEP> 0.20
<tb> Glucosamine <SEP> 0.20 <SEP> 0.20
<tb> Kérallnase200U * <SEP> 3.00
<tb> B <SEP> Carotene <SEP> 0.005 <SEP> 0.005
<tb> Lecitin <SEP> of <SEP> soya <SEP> 0.25 <SEP> 0.25
<tb> Water <SEP> + <SEP> preservative <SEP> qsp <SEP> 100 <SEP> qsp <SEP> 100 <SEP> qsp <SEP> 100 <SEP>
<Tb>
U = mol. Tyrosine / min / ml
After 4 weeks of treatment, there is a difference in pigmentation on the sites treated with creams A and B compared to cream C (placebo), after 8 weeks the three sites are clearly differentiated (chromammetric clarity increases significantly + 15% on sites treated with cream A, against + 7% on sites treated with cream B and 0.5% on placebo sites).
Les traitements sont bien tolérés par les volontaires.The treatments are well tolerated by the volunteers.
Pour être efficace, H convient d'utiliser des protéases kératolytiques stables, non irritantes et non sensibilisantes et de les employer à des doses adéquates, c'est-à-dire 0.1 à 20 Unités /g de produit cosmétique fini, prZrentiellement entre 1 et 10 Unités/g. To be effective, stable, non-irritating and non-sensitizing keratolytic proteases should be used and used in adequate doses, ie 0.1 to 20 Units / g of finished cosmetic product, preferably between 1 and 10 Units / g.
Les substances inhibitrices de la mélanogénèse (inhibiteurs de tyrosinase, inhibiteurs de glycosylation etc.) sont employées dans les doses habituelles; par exemple, I'acide gluconique et la glucosamine s'emploient entre 0.01 et 10%, préférentiellement entre 0.1 et 5% dans le produit cosmétique fini, les dérivés précurseurs ou analogues de vitamine A sont utilisés entre 0,00001 et 0,01 %.Substances that inhibit melanogenesis (tyrosinase inhibitors, glycosylation inhibitors, etc.) are used in the usual doses; for example, gluconic acid and glucosamine are used between 0.01 and 10%, preferably between 0.1 and 5% in the finished cosmetic product, precursor derivatives or vitamin A analogues are used between 0.00001 and 0.01% .
La combinaison des kératinases/protéases avec les substances dépigrnentantes simples ou complexes peut être utilisée dans toute forme de produit cosmétique destiné à éclaircir la peau à savoir, les émulsions E/H, hilE, les laits, butions, les gels, les pommades, les shampooings et les produits de traitement du cuir chevelu, les produits de maquillage. Pour l'utilisation dans les produits finis, ces combinaisons peuvent être présentées sous forme de dispersion aqueuse, de pâte, de poudre, de baume, d'huile. Ils peuvent être avantageusement inclus dans des vecteurs cosmétiques tels que les liposomes, les chylomicrons, les micro- ou nanoparScules, les micro- ou nanocasules. Ils peuvent être absorbés sur des supports poreux comme les microéponges, les silicates, bentonites, talcs, polyamides ou polyacrylates.The combination of keratinases / proteases with simple or complex depigmenting substances can be used in any form of cosmetic product intended to lighten the skin, namely W / O emulsions, hilE, milks, preparations, gels, ointments, shampoos and scalp treatment products, makeup products. For use in finished products, these combinations can be presented as an aqueous dispersion, paste, powder, balm, oil. They can advantageously be included in cosmetic vectors such as liposomes, chylomicrons, micro- or nanoparticles, micro- or nanocasules. They can be absorbed on porous substrates such as micro sponges, silicates, bentonites, talcs, polyamides or polyacrylates.
Par ailleurs, les protéases peuvent être de toute origine, préférentiellement d'origine végétale ou biotechnologique, et peuvent être employées sous forme de poudre, de solution, de dispersion; elles peuvent être stabilisées par les moyens connus de l'homme de l'art (encapsulat on,adsorption, modification chimique etc.). Furthermore, the proteases may be of any origin, preferably of plant or biotechnological origin, and may be used in the form of powder, solution or dispersion; they can be stabilized by means known to those skilled in the art (encapsulation, adsorption, chemical modification etc.).
Claims (7)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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FR9503760A FR2732215B1 (en) | 1995-03-28 | 1995-03-28 | NEW DEPIGMENTING COSMETIC COMPOSITIONS |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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FR9503760A FR2732215B1 (en) | 1995-03-28 | 1995-03-28 | NEW DEPIGMENTING COSMETIC COMPOSITIONS |
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FR2732215A1 true FR2732215A1 (en) | 1996-10-04 |
FR2732215B1 FR2732215B1 (en) | 1997-04-30 |
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FR9503760A Expired - Fee Related FR2732215B1 (en) | 1995-03-28 | 1995-03-28 | NEW DEPIGMENTING COSMETIC COMPOSITIONS |
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Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001083031A2 (en) * | 2000-05-01 | 2001-11-08 | Bioderm, Inc. | Topical composition for the treatment of psoriasis and related skin disorders |
EP1384482A1 (en) * | 2001-03-27 | 2004-01-28 | Kanebo, Limited | External skin compositions |
FR2852828A1 (en) * | 2003-03-25 | 2004-10-01 | Oreal | COMPOSITION FOR TREATING KERATINIC MATERIALS COMPRISING A HYDROXYCARBOXYLIC ACID AND A PROTECTIVE AGENT OR CONDITIONER |
WO2010067327A1 (en) | 2008-12-11 | 2010-06-17 | Sederma | Cosmetic composition containing acetylated oligoglucuronans |
WO2010082177A2 (en) | 2009-01-16 | 2010-07-22 | Sederma | New compounds, in particular peptides, compositions comprising them and cosmetic and dermopharmaceutical uses |
WO2010082175A2 (en) | 2009-01-16 | 2010-07-22 | Sederma | New compounds, in particular peptides, compositions comprising them and cosmetic and dermopharmaceutical uses |
WO2010082176A2 (en) | 2009-01-16 | 2010-07-22 | Sederma | Cosmetic composition containing kxk type peptides and uses |
WO2010136965A2 (en) | 2009-05-26 | 2010-12-02 | Sederma | Cosmetic use of tyr-arg dipeptide to combat cutaneous sa |
EP2510982A1 (en) | 2006-05-05 | 2012-10-17 | Sederma | Cosmetic compositions comprising at least one peptide with at least one immobilized aromatic cycle |
US8361516B2 (en) | 2006-08-03 | 2013-01-29 | Sederma | Composition comprising sarsasapogenin |
US8404648B2 (en) | 2006-02-16 | 2013-03-26 | Sederma | Polypeptides KXK and their use |
US8741357B2 (en) | 2005-01-14 | 2014-06-03 | Sederma Sas | Cosmetic or dermopharmaceutical composition comprising an euglena extract |
US8846019B2 (en) | 2005-09-06 | 2014-09-30 | Sederma | Use of protoberberines as an active substance regulating the pilosebaceous unit |
US9050477B2 (en) | 2009-04-17 | 2015-06-09 | Sederma | Cosmetic compositions comprising oridonin and new cosmetic uses |
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JPH01186811A (en) * | 1988-01-20 | 1989-07-26 | Sunstar Inc | Skin beautifying cosmetic |
WO1993013742A1 (en) * | 1992-01-16 | 1993-07-22 | Cosmetics Development Company Limited | Preparation for skin use |
WO1994027569A1 (en) * | 1993-06-01 | 1994-12-08 | Dermatology Home Products, Inc. | Skin treatment method utilizing a composition and a pad |
WO1995007686A1 (en) * | 1993-09-15 | 1995-03-23 | Unilever Plc | Skin care composition comprising thiol proteases from the stratum corneum |
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1995
- 1995-03-28 FR FR9503760A patent/FR2732215B1/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4749719A (en) * | 1983-09-21 | 1988-06-07 | Sogo Pharmaceutical Company Limited | Method of treating skin pigmentation abnormalities with pantetheine-S-sulfonic acid |
JPH01186811A (en) * | 1988-01-20 | 1989-07-26 | Sunstar Inc | Skin beautifying cosmetic |
WO1993013742A1 (en) * | 1992-01-16 | 1993-07-22 | Cosmetics Development Company Limited | Preparation for skin use |
WO1994027569A1 (en) * | 1993-06-01 | 1994-12-08 | Dermatology Home Products, Inc. | Skin treatment method utilizing a composition and a pad |
WO1995007686A1 (en) * | 1993-09-15 | 1995-03-23 | Unilever Plc | Skin care composition comprising thiol proteases from the stratum corneum |
Non-Patent Citations (2)
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CHEMICAL ABSTRACTS, vol. 112, no. 20, 14 May 1990, Columbus, Ohio, US; abstract no. 185579, H. ANDO: "Skin-lightening cosmetics containing unsaturated fatty acids" * |
N. TANAKA: "Effect and Action of Enzymes on Skin", COSMETICS & TOILETRIES, vol. 96, pages 37 - 40 * |
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