WO2009092972A2 - Composition cosmétique destinée à bloquer la pigmentation de la peau induite par les rayonnements uv - Google Patents
Composition cosmétique destinée à bloquer la pigmentation de la peau induite par les rayonnements uv Download PDFInfo
- Publication number
- WO2009092972A2 WO2009092972A2 PCT/FR2009/050061 FR2009050061W WO2009092972A2 WO 2009092972 A2 WO2009092972 A2 WO 2009092972A2 FR 2009050061 W FR2009050061 W FR 2009050061W WO 2009092972 A2 WO2009092972 A2 WO 2009092972A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition according
- agent
- derivatives
- cosmetic composition
- blocking
- Prior art date
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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
- 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
- A61K8/96—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
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
-
- 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
-
- 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
Definitions
- the subject of the invention is a topical cosmetic composition intended to block the pigmentation of the skin induced by UV radiation.
- this composition is used in the absence of UVA and UVB filters, on light skin when seeking to minimize the phenomenon of pigmentation.
- the composition is intended more particularly for Asian populations.
- the composition further contains UVA and UVB filters and finds at least two indications.
- the first indication is its use as an anti-bronzer.
- the market concerned is rather the Asian market but also the market of North Africa and the Middle East.
- the second indication corresponds to skin developing hyperpigmentation phenomena in response to the effects of UV rays.
- Melanins are the pigments responsible for the coloring of the skin. They are obtained by mixing a variable amount of two kinds of pigments: phaeo melanins and eumelanines.
- the eumelanines are pigments of black or brown color, totally absorbing the light and thus exerting a real photoprotective power.
- Phaeomelanins are orange-yellow pigments that have a lower protective effect.
- the very light red skins (phototype I) mainly contain phaeomelanines.
- Melanins are made from tyrosine in the presence of tyrosinase in melanocytes, which are located in the basal layer of the epidermis. This is the process of melanogenesis.
- the synthesis of melanins is more particularly carried out in melanosomes, which are transported to the end of the dendrites of melanocytes and then transferred to the keratinocytes.
- the presence of melanins on the surface of the skin makes it possible to absorb some of the visible and UV radiation.
- the Applicant has now developed a novel cosmetic composition which is distinguished from the products of the prior art in that it contains elements which stop melanogenesis not only: by a direct route by inhibiting the synthesis of melanins by inhibition of tyrosinase activity, but also indirectly by inhibiting the production of mediators by keratinocytes, insofar as certain mediators whose production by keratinocytes is stimulated by UV radiation, also take part in the melanogenesis process.
- alpha-MSH alpha-melanocyte stimulating hormone
- MC-I MC-I receptors on the surface of melanocytes
- ET-I endothelin-1
- ETA and ETB melanocyte receptors
- SCF Stem Cell Factor
- ET-1 and SCF act synergistically on the activation of melanogenesis.
- the invention therefore firstly relates to a cosmetic composition which is characterized in that it contains, within a cosmetic vehicle: at least one agent blocking the binding of ⁇ -MSH on MC-receptors. I at the surface of the melanocytes, at least one agent blocking the synthesis of ET-1, at least one agent inhibiting the synthesis of SCF, at least one agent inhibiting the activity of tyrosinase.
- ⁇ -MSH it may be to measure the inhibitory effect of the candidate molecule on the stimulation of melanin synthesis in normal human melanocyte cultures.
- ET-I and SCF it may be to measure the inhibitory effect of the candidate molecule on the secretion of ET-1 and SCF by normal human keratinocytes.
- tyrosinase classical tests are done in tubo, that is to say without cells: tyrosinase is put in the presence of a substrate, which changes color when tyrosinase is activated. In the presence of an active agent inhibiting the activity of tyrosinase, the color change is not done (or less).
- This composition is more particularly used as an anti-pigmenting agent.
- the ⁇ -MSH binding blocking agent on the MC-I receptors is the biomimetic hexapeptide 2 and / or the nonapeptide-1 obtained by chemical synthesis, having an affinity for the the ⁇ -MSH.
- the ⁇ -MSH binding blocking agent, in particular the two abovementioned peptides represent between 0.00001 and 1% by weight of the composition, preferably between 0.0001 and 0.0004% by weight.
- the agent blocking the synthesis of ET-1 is preferably andrographolide, preferably in the form of an extract of leaves of Andrographis paniculata. In practice, it represents between 0.001 and 10%, preferably between 0.01 and 0.1% by weight of the composition.
- the inhibiting agent for the synthesis of SCF and the activity of tyrosinase is the same and is advantageously an aqueous extract of an alga called Palmaria palmata, preferably containing between 5 and 50% by weight of dry matter. .
- the extract is in practice between 0.01 and 25% by weight of the composition, ideally between 1 and 4% by weight.
- the cosmetic composition of the invention additionally contains at least one UVB and UVA and / or UVAAWB filter and optionally at least one mineral screen.
- the invention consists in this case in blocking the penetration of most of the UV rays by means of UVA and UVB filters, or inorganic screens, and then directly inhibiting (inhibition of the stimulation of the activity tyrosinase) and indirectly (inhibition of melanocyte stimulation by mediators secreted by keratinocytes) the production and expression of melanin triggered by the remaining part of the UV having penetrated through the skin.
- the composition of the invention can be used as an anti-bronzer product for skin with little or weakly pigmented, in particular for the Asian market, or as a product intended to fight against photo-induced hyperpigmentation.
- Mineral screens and UVB or UVA / UVB filters are intended to limit the penetration of UVB into the skin. Depending on the nature of the filters, 70 to 98% of the radiation will be stopped.
- the protection of the skin against UVB is characterized by the SPF index. This index corresponds, for a given UVB irradiation, after application of UVB or UVB / UVA filter, to the ratio between the UV dose triggering an erythema on the protected skin and the UV dose triggering erythema on the unprotected skin.
- SPF index corresponds, for a given UVB irradiation, after application of UVB or UVB / UVA filter, to the ratio between the UV dose triggering an erythema on the protected skin and the UV dose triggering erythema on the unprotected skin.
- an SPF of 20 means that it takes 20 times more UV to trigger an erythema, so is to say that 95% of UVB rays are stopped.
- An index of 50 means that
- UVB or UVA organic screening agents chosen from the group comprising:
- Ethyl Dihydroxypropyl PABA (Amerscreen® P sold by Amerchol), Ethylhexyl Dimethyl PABA sold in particular under the name "ESCALOL® 507",
- UVINUL® 400 Benzophenone-1 sold under the trade name "UVINUL® 400”
- Benzophenone-2 sold under the trade name “UVINUL® D50”
- Benzophenone-3 or Oxybenzone sold under the trade name "UVINUL® M40”
- Benzophenone-4 sold under the trade name "UVINUL® MS40", - Benzophenone-5,
- Benzophenone-6 sold under the trade name "HELISORB® 11
- Benzophenone-8 sold under the trade name "SPECTRA-SORB® UV-24”
- Benzophenone-9 sold under the trade name "UNIVUL® DS-49", Benzophenone-12.
- Phenylbenzimidazole Sulfonic Acid sold in particular under the trade name "Eusolex 232"
- UVASORB® HEB - (Bis- Ethylhexyloxyphenol Methoxyphenyl Triazine) Tinosorb S
- imidazoline derivatives Ethylhexyl Dimethoxybenzylidene Dioxoimidazoline Propionate.
- composition of the invention may further comprise nacres, pigments, or even nanopigments (average size of the primary particles: generally between 5 nm and 100 nm, preferably between 10 nm and 50 nm) of coated metal oxides or not, as for example nano-pigments of titanium oxide (amorphous or crystallized in rutile and / or anatase form), iron, zinc, zirconium or cerium and their mixtures which are all UV photoprotective agents well known in itself.
- Conventional coating agents are, moreover, alumina and / or aluminum stearate.
- these filters represent between 2 and 40% by weight of the composition, preferably between 15 and 30% by weight of the composition.
- UVA / UVB filters are advantageously chosen from the group comprising:
- the mineral screens will advantageously be chosen from the group: TiO 2
- the cosmetic composition of the invention is generally applied topically.
- composition may be in any galenical form normally used for topical application to the skin, especially in the form of an oil-in-water or water-in-oil or multiple emulsion, a silicone emulsion, a microemulsion or nanoemulsion.
- This composition may be more or less fluid and have the appearance among others of a white or colored cream, an ointment, a milk, a lotion, a serum or a gel.
- composition of the invention may contain the usual vehicles in the cosmetic and dermatological fields, such as fats, emulsifiers and coemulsifiers, hydrophilic or lipophilic gelling agents, hydrophilic or lipophilic active agents, preservatives, antioxidants, solvents, perfumes, fillers, hydrophilic and lipophilic filters, dyestuffs, neutralizers, pro-penetrating agents, and polymers.
- vehicles in the cosmetic and dermatological fields such as fats, emulsifiers and coemulsifiers, hydrophilic or lipophilic gelling agents, hydrophilic or lipophilic active agents, preservatives, antioxidants, solvents, perfumes, fillers, hydrophilic and lipophilic filters, dyestuffs, neutralizers, pro-penetrating agents, and polymers.
- the invention also relates to cometic skin treatment methods for either depigmenting or stopping tanning, or blocking UV-induced hyperpigmentation by topical application of the previously described composition.
- EXAMPLE 1 Demonstration of the depigmenting activity of a cosmetic formulation on explants of human skin maintained in survival
- Explants of human skin are prepared and maintained in survival in specific medium. The explants are distributed as follows (3 explants per condition):
- UV "T UV” indicator untreated, irradiated Formulation 1 + UV "F UV”: treated, irradiated
- the product (1.5g / cm 2 ) is topically applied to the explants using a small spatula or filter paper discs. Explants are treated every other day.
- the batches "T UV”, “F UV” receive daily, for 8 days, a UVA irradiation of 1.125 J / cm 2 (6-8% UVB) corresponding to the solar irradiation spectrum.
- the irradiations are carried out 30 minutes after the treatment with the product, to avoid a possible filter effect.
- ITA 0 [ArcTan ((L * - 50) / b *)] x 180 / 3,1415
- - L * represents the lightness (from dark to pale)
- - b * represents the range from blue to yellow
- the color of the explants controls do not vary.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Dermatology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Botany (AREA)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Cosmetics (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010543547A JP5536670B2 (ja) | 2008-01-24 | 2009-01-16 | Uv照射によって誘発される皮膚の色素沈着を妨げるための化粧品組成物 |
CN2009801025107A CN101917961B (zh) | 2008-01-24 | 2009-01-16 | 限制由紫外辐射引起的皮肤色素沉积的化妆品组合物 |
HK11102819.2A HK1148494A1 (en) | 2008-01-24 | 2011-03-21 | Cosmetic composition for blocking skin pigmentation induced by uv radiation |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0850454A FR2926720B1 (fr) | 2008-01-24 | 2008-01-24 | Composition cosmetique destinee a bloquer la pigmentation de la peau induite par les rayonnements uv |
FR0850454 | 2008-01-24 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2009092972A2 true WO2009092972A2 (fr) | 2009-07-30 |
WO2009092972A3 WO2009092972A3 (fr) | 2009-10-01 |
Family
ID=39720331
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR2009/050061 WO2009092972A2 (fr) | 2008-01-24 | 2009-01-16 | Composition cosmétique destinée à bloquer la pigmentation de la peau induite par les rayonnements uv |
Country Status (6)
Country | Link |
---|---|
JP (1) | JP5536670B2 (fr) |
KR (1) | KR101574362B1 (fr) |
CN (1) | CN101917961B (fr) |
FR (1) | FR2926720B1 (fr) |
HK (1) | HK1148494A1 (fr) |
WO (1) | WO2009092972A2 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2986154A1 (fr) * | 2012-01-31 | 2013-08-02 | Fabre Pierre Dermo Cosmetique | Nouveau systeme photoprotecteur |
WO2022112476A1 (fr) * | 2020-11-27 | 2022-06-02 | Dsm Ip Assets B.V. | Composition topique |
WO2023062318A1 (fr) * | 2021-10-15 | 2023-04-20 | Naos Institute Of Life Science | Méthodes de mesure de l'effet de protection contre l'hyperpigmentation induite par la lumière visible, sélection de compositions cosmétiques ou pharmaceutique en utilisant ces méthodes et compositions écobiologiques ainsi sélectionnées |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102491963A (zh) * | 2011-11-23 | 2012-06-13 | 常州亚当生物技术有限公司 | 化合物i和ii及其其制备治疗抑制黑色素形成药物中的应用与制备方法 |
KR101694958B1 (ko) * | 2014-04-08 | 2017-01-10 | 바이오스펙트럼 주식회사 | 천심련추출물 또는 안드로그라폴라이드 또는 이의 염을 포함하는 피부상태 개선용 조성물 |
WO2016148324A1 (fr) * | 2015-03-19 | 2016-09-22 | (주)아모레퍼시픽 | Méthode de sélection de matériau fonctionnel de protection contre la lumière du soleil et méthode d'évaluation d'effet de protection contre la lumière du soleil |
FR3034662B1 (fr) * | 2015-04-10 | 2020-08-28 | Isp Investments Inc | Nouvelles utilisations du peptide de sequence his-d-trp-ala-trp-d-phe-lys-nh2 pour diminuer ou retarder l'apparition de la senescence cellulaire et des signes du vieillissement cutane |
CN105168110A (zh) * | 2015-10-14 | 2015-12-23 | 广东三九军大生物科技有限公司 | 一种九肽美白祛斑精华乳 |
FR3042974B1 (fr) * | 2015-11-04 | 2017-12-08 | Isp Investments Inc | Extrait synergique de palmaria palmata et de jasmin, compositions le comprenant et utilisations |
CN109998938B (zh) * | 2015-12-22 | 2020-10-09 | 深圳市维琪医药研发有限公司 | 一种用于美白亮肤淡斑的多肽组合物 |
CN107233223B (zh) * | 2017-06-16 | 2019-01-25 | 湖南御家化妆品制造有限公司 | 控制诱导黑色素靶向组合物及其应用 |
CN107049880A (zh) * | 2017-06-16 | 2017-08-18 | 湖南御家化妆品制造有限公司 | 美白组合物及其应用 |
CN108158866A (zh) * | 2018-02-02 | 2018-06-15 | 广州赛莱拉干细胞科技股份有限公司 | 含有掌状红皮藻提取物的组合物 |
CN109010108A (zh) * | 2018-08-31 | 2018-12-18 | 广州中医药大学(广州中医药研究院) | 亚硫酸氢钠穿心莲内酯抗皮肤光老化的应用及防晒霜 |
Citations (2)
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EP1325738A2 (fr) * | 2001-12-28 | 2003-07-09 | Avon Products, Inc. | Compositions dépigmentantes à usage topique et leurs utilisations |
US20050169860A1 (en) * | 2004-01-30 | 2005-08-04 | Access Business Group International Llc. | Holistic composition and method for reducing skin pigmentation |
Family Cites Families (5)
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JPH0930946A (ja) * | 1995-07-21 | 1997-02-04 | Shiseido Co Ltd | 美白用皮膚外用剤 |
JPH10330219A (ja) * | 1997-05-30 | 1998-12-15 | Noevir Co Ltd | メラニン生成抑制剤及び美白剤 |
JP2001316241A (ja) * | 2000-03-02 | 2001-11-13 | Noevir Co Ltd | 皮膚外用剤 |
JP2006111631A (ja) * | 2005-10-24 | 2006-04-27 | Shiseido Co Ltd | 幹細胞因子の産生・放出の抑制による掻痒、肌荒れ、敏感肌及び美白用薬剤 |
JP2008007442A (ja) * | 2006-06-28 | 2008-01-17 | Univ Kanagawa | 化粧料 |
-
2008
- 2008-01-24 FR FR0850454A patent/FR2926720B1/fr active Active
-
2009
- 2009-01-16 KR KR1020107016011A patent/KR101574362B1/ko active IP Right Grant
- 2009-01-16 CN CN2009801025107A patent/CN101917961B/zh active Active
- 2009-01-16 JP JP2010543547A patent/JP5536670B2/ja active Active
- 2009-01-16 WO PCT/FR2009/050061 patent/WO2009092972A2/fr active Application Filing
-
2011
- 2011-03-21 HK HK11102819.2A patent/HK1148494A1/xx unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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EP1325738A2 (fr) * | 2001-12-28 | 2003-07-09 | Avon Products, Inc. | Compositions dépigmentantes à usage topique et leurs utilisations |
US20050169860A1 (en) * | 2004-01-30 | 2005-08-04 | Access Business Group International Llc. | Holistic composition and method for reducing skin pigmentation |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2986154A1 (fr) * | 2012-01-31 | 2013-08-02 | Fabre Pierre Dermo Cosmetique | Nouveau systeme photoprotecteur |
WO2013113745A3 (fr) * | 2012-01-31 | 2014-02-27 | Pierre Fabre Dermo-Cosmetique | Nouveau système de photoprotection |
AU2013214293B2 (en) * | 2012-01-31 | 2017-07-06 | Pierre Fabre Dermo-Cosmetique | Novel photoprotective system |
US9763867B2 (en) | 2012-01-31 | 2017-09-19 | Pierre Fabre Dermo Cosmetique | Photoprotective system |
RU2635512C2 (ru) * | 2012-01-31 | 2017-11-13 | Пьер Фабр Дермо-Косметик | Новая фотозащитная система |
AU2017239521B2 (en) * | 2012-01-31 | 2019-08-01 | Pierre Fabre Dermo-Cosmetique | Novel photoprotective system |
EP3626226A1 (fr) * | 2012-01-31 | 2020-03-25 | Pierre Fabre Dermo-Cosmétique | Nouveau système photoprotecteur |
WO2022112476A1 (fr) * | 2020-11-27 | 2022-06-02 | Dsm Ip Assets B.V. | Composition topique |
WO2023062318A1 (fr) * | 2021-10-15 | 2023-04-20 | Naos Institute Of Life Science | Méthodes de mesure de l'effet de protection contre l'hyperpigmentation induite par la lumière visible, sélection de compositions cosmétiques ou pharmaceutique en utilisant ces méthodes et compositions écobiologiques ainsi sélectionnées |
Also Published As
Publication number | Publication date |
---|---|
WO2009092972A3 (fr) | 2009-10-01 |
JP5536670B2 (ja) | 2014-07-02 |
FR2926720A1 (fr) | 2009-07-31 |
CN101917961A (zh) | 2010-12-15 |
FR2926720B1 (fr) | 2011-09-09 |
KR101574362B1 (ko) | 2015-12-07 |
HK1148494A1 (en) | 2011-09-09 |
JP2011510053A (ja) | 2011-03-31 |
KR20100105707A (ko) | 2010-09-29 |
CN101917961B (zh) | 2013-06-12 |
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