EP1001739A1 - Verwendung eines 2-aminoalkan polyol zur behandlung von hautälterung - Google Patents
Verwendung eines 2-aminoalkan polyol zur behandlung von hautälterungInfo
- Publication number
- EP1001739A1 EP1001739A1 EP98941554A EP98941554A EP1001739A1 EP 1001739 A1 EP1001739 A1 EP 1001739A1 EP 98941554 A EP98941554 A EP 98941554A EP 98941554 A EP98941554 A EP 98941554A EP 1001739 A1 EP1001739 A1 EP 1001739A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- use according
- octadecane
- diol
- skin
- amino
- 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.)
- Withdrawn
Links
Classifications
-
- 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
- A61Q19/08—Anti-ageing 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
-
- 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
- A61K8/68—Sphingolipids, e.g. ceramides, cerebrosides, gangliosides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
Definitions
- the present invention relates to the use, as active principle in a cosmetic composition or for the preparation of a pharmaceutical composition, of an effective amount of at least one 2-amino-alkane-1, 3-diol, or of one of its derivatives, intended for treating the signs of skin aging as well as a non-therapeutic method for treating skin aging.
- Skin aging resulting from effects on the skin of intrinsic or extrinsic factors, is manifested by the appearance of fine lines and wrinkles, by the yellowing of the skin which develops a parchment appearance accompanied by the appearance of pigment spots, by the disorganization of the elastin and collagen fibers leading to a loss of elasticity, flexibility and firmness and by the appearance of telangiectasias.
- Some of these signs of aging are more particularly linked to intrinsic or physiological aging, that is to say to “normal” aging linked to age, while others are more specific to extrinsic aging, ie that is to say aging generally caused by the environment; this is more particularly photo-aging due to exposure to the sun, light or any other radiation.
- the invention is concerned with intrinsic or physiological aging as well as extrinsic aging.
- the skin changes resulting from intrinsic or physiological aging are the consequence of genetically programmed senescence in which endogenous factors intervene. This intrinsic aging notably causes a slowing down of the renewal of skin cells. Histologically the skin is generally thinned, both epidermally and dermally. The density of the fibrous macromolecules of the dermis (elastin and collagen) is reduced.
- extrinsic aging leads to clinical alterations such as thick wrinkles and the formation of soft and / or tanned skin, and histopathological changes such as an excessive accumulation of elastic material in the upper dermis and degeneration of the fibers. collagen.
- US Pat. No. 4,603,146 describes the use of retinoic acid and its derivatives in cosmetic compositions, with a view to combating skin aging.
- numerous patents and publications see for example application EP-A-413 528) as well as many commercial cosmetic compositions teach the use of ⁇ -hydroxy acids such as lactic acid, glycolic acid or else citric acid to treat skin aging.
- beta-hydroxy acids and more particularly salicylic acid and its derivatives are known for their flaking properties (see documents WO-A-93/10756 and US-A-4 767 750).
- the subject of the invention is therefore the use of a 2-amino-alkane polyol of formula (I) (below), or of one of its derivatives, in a cosmetic or dermatological composition for topical application, intended to treat certain signs of endogenous and / or exogenous aging.
- This treatment can be carried out as a preventive and / or curative measure.
- the N-acylated derivatives based on sphinganine [(2S, 3R) -2-amino-1, 3-octadecanediol] are ceramides predominantly present in the hair, while analogous derivatives based on phytosphingosine [(2S , 3S, 4R) -2-amino-1, 3,4-octadecane-triol), other ceramides, are part of the lipids mainly present in the stratum corneum of the skin.
- Ceramides are used in cosmetics in natural or synthetic form in compositions intended for example to reinforce the barrier effect of the stratum corneum in order to reduce the loss of water and therefore the drying of the skin (GB 2 178 312, GB 2 213 723 , EP 227 994, EP 282 616, EP 556 957).
- compositions for their properties giving the skin better elasticity EP 500 437) or in compositions for hair use to strengthen the hair and / or repair the damage caused by the continual assaults that this one undergoes.
- the invention relates to the use in a cosmetic composition or for the preparation of a pharmaceutical composition intended for treating the signs of skin aging, of at least one compound of general formula (I):
- R- represents a linear or branched hydrocarbon radical, optionally hydroxylated, saturated or unsaturated, having 4 to 28 carbon atoms
- R2 represents a hydrogen atom or the radical
- R3 represents a linear or branched, saturated or unsaturated hydrocarbon-based radical having from 1 to 11 carbon atoms or a linear or branched, hydroxylated, saturated or unsaturated hydrocarbon-based radical having from 1 to 29 carbon atoms, the hydroxyl being capable of be esterified by an acyl chain having from 2 to 30 carbon atoms, linear or branched, saturated or unsaturated;
- X represents a hydrogen atom or the OH radical; or at least one of its optical isomers or one of the diastereoisomers.
- R-1 preferably contains from 6 to 22 carbon atoms and even more preferably from 10 to 18 carbon atoms.
- R2 represents H or a radical
- O and R3 represents a linear or branched, saturated or unsaturated hydrocarbon radical having from 1 to 9 carbon atoms or a linear or branched, hydroxylated, saturated or unsaturated hydrocarbon radical, having from 1 to 21 carbon atoms.
- Ri represents a saturated and / or linear hydrocarbon radical, more particularly a saturated linear hydrocarbon radical.
- R- represents a saturated hydrocarbon radical having 14 carbon atoms, and even more preferably R ⁇ represents a linear, saturated hydrocarbon radical having 14 carbon atoms.
- the agent promoting the care and / or prevention of aging can be a mixture of compounds of formula (I), for which R, and / or R 2 are chains of different lengths.
- 2-N-acetylamino-octadecane-1, 3-diol or 2-N-octanoylamino-octadecane-1, 3-diol is used.
- a subject of the invention is therefore the use of a 2-amino-alkane-1, 3-diol of formula (I) (below), or of one of its derivatives, in a cosmetic or dermatological composition for topical application, intended to treat wrinkles and / or fine lines and / or yellowing of the skin and / or the parchment appearance of the skin and / or pigmented spots of the skin and / or telangiectasias and or loss elasticity, flexibility and / or firmness of the skin.
- the amount of compounds of formula (I) which can be used according to the invention depends, of course, on the nature of the compound used, on its physicochemical properties and on its mode of application. A person skilled in the art knows how to adjust the amount of compound of formula (I) to be used as required.
- the compounds of formula (I) can be used at concentrations by weight of between 10 ⁇ % and 20%, and preferably between 10 "3 % and 10% in the composition.
- the composition may take the form in particular of an aqueous, alcoholic, hydroalcoholic or oily solution or of dispersion of the lotion or serum type, of an emulsion of liquid or semi-liquid consistency of the milk type, obtained by dispersing a fatty phase in an aqueous phase (O / W) or vice versa (W / O), or a suspension or an emulsion of soft consistency of the cream, foam or aqueous or anhydrous gel type, or still microcapsules or microparticles, or a vesicular dispersion of the ionic and / or nonionic type. It can also take the form of an aerosol composition also comprising a pressurized propellant.
- this composition is prepared according to the usual methods.
- the amounts of the various constituents of the composition according to the invention are those conventionally used in the fields considered.
- the proportion of the fatty phase can range from 5% to 80% by weight, and preferably from 5% to 50% by weight relative to the total weight of the composition.
- the oils, waxes, emulsifiers and co-emulsifiers used in the composition in the form of an emulsion are chosen from those conventionally used in the cosmetic field.
- the emulsifier and the co-emulsifier are present in the composition in a proportion ranging from 0.3% to 30% by weight, and preferably from 0.5 to 20% by weight relative to the total weight of the composition .
- the emulsion may, in addition, contain lipid vesicles.
- the fatty phase can represent more than 90% of the total weight of the composition.
- composition comprising at least one compound of formula (I) as active principle intended to treat and / or prevent aging of the skin is in iiposomal form, as notably described in patent application WO 94 / 22468 filed October 13, 1994 " by Anti Cancer Inc.
- This composition can also contain adjuvants customary in the cosmetic field, such as hydrophilic or iipophilic gelling agents, hydrophilic or Iipophilic additives, preservatives, antioxidants, solvents, perfumes, fillers, filters, odor absorbers and coloring matters.
- adjuvants customary in the cosmetic field, such as hydrophilic or iipophilic gelling agents, hydrophilic or Iipophilic additives, preservatives, antioxidants, solvents, perfumes, fillers, filters, odor absorbers and coloring matters.
- the amounts of these various adjuvants are those conventionally used in the cosmetic field, and for example from 0.01% to 10% of the total weight of the composition.
- These adjuvants depending on their nature, can be introduced into the fatty phase, into the aqueous phase and / or into the lipid spherules.
- emulsifiers which can be used in the invention, there may be mentioned for example glycerol stearate, polysorbate 60 and the mixture of PEG-6 / PEG-32 / Glycol Stearate sold under the name Tefose ⁇ 63 by the company Gattefosse.
- solvents which can be used in the invention mention may be made of lower alcohols, in particular ethanol and isopropanol, propylene glycol.
- hydrophilic gelling agents which can be used in the invention, mention may be made of carboxyvinyl polymers (carbomers), acrylic copolymers such as acrylate / alkylacrylate copolymers, polyacrylamides, polysaccharides such as hydroxypropylcellulose, natural gums and clays, and, as lipophilic gelling agents, mention may be made of modified clays such as bentones, metal salts of fatty acids such as aluminum stearates and hydrophobic silica, ethylcellulose, polyethylene.
- carboxyvinyl polymers carboxyvinyl polymers
- acrylic copolymers such as acrylate / alkylacrylate copolymers
- polyacrylamides polysaccharides
- polysaccharides such as hydroxypropylcellulose
- natural gums and clays and, as lipophilic gelling agents
- modified clays such as bentones, metal salts of fatty acids such as aluminum stearates and hydrophobic silica,
- composition may contain other hydrophilic active agents such as proteins or protein hydrolysates, amino acids, polyols, urea, allantoin, sugars and sugar derivatives, water-soluble vitamins, plant extracts and hydroxy acids.
- hydrophilic active agents such as proteins or protein hydrolysates, amino acids, polyols, urea, allantoin, sugars and sugar derivatives, water-soluble vitamins, plant extracts and hydroxy acids.
- vitamin A As lipophilic active agents, retinol (vitamin A) and its derivatives, tocopherol (vitamin E) and its derivatives, essential fatty acids, ceramides other than the compounds of formula (I), essential oils, salicylic acid and its derivatives.
- - keratolytic agents such as alpha- and beta-hydroxycarboxylic or beta-ketocarboxylic acids, their salts, amides or esters and more particularly hydroxy acids such as glycolic acid, lactic acid, salicylic acid, acid citric and generally fruit acids, and n-octanoyl-5-salicylic acid;
- - anti-free radical agents such as alpha-tocopherol or its esters, superoxide dismutases, certain metal chelating agents or ascorbic acid and its esters;
- - anti-acne drugs such as retinoic acid or benzoyl peroxide.
- antagonists of substance P and / or of CGRP Calcitonin Gene Related Peptide or peptide linked to the calcitonin gene
- substance P and / or CGRP antagonists such as those described in French patent applications FR-2719474 and FR-2729855.
- these pharmaceutical compositions are distinguished in particular from cosmetic compositions by the amount of active agent which they contain.
- the amount of active agent which they contain Those skilled in the art, in this case, know how to determine the quantity of active agent which can be used as a function of the desired result but also of the mode of administration envisaged.
- the compound of formula (I) can be used in the preparation of a pharmaceutical composition at a concentration of between 0.01% and 20% and preferably between 0.1% and 10% by weight relative to the weight of composition.
- the cosmetic or pharmaceutical composition according to the invention can be applied to the skin, generally the skin of the face and / or the neck and / or the hands, and optionally left in contact for several hours and optionally rinsed off.
- These applications can be renewed daily for one or more months depending on the individual.
- the subject of the present invention is also a method of cosmetic treatment of human skin, characterized in that it consists in applying to at least part of the skin of the human body, a cosmetic composition comprising an effective amount of at least one compound of formula (I), to leave it in contact with the skin, and optionally to rinse.
- compositions illustrate the invention without limiting it in any way.
- proportions indicated are percentages by weight unless otherwise indicated.
- Example 1 Measurement of the proliferative effect of 2-amino-octadecane-1, 3-diol and its derivatives on cultured keratinocytes:
- HaCat cells (Boukamp et al., J. Cell Biol. Vol. 106, March 1988, 761-771) are cultured in DMEM medium (Gibco Company) containing amino acids (mixture of nonessential amino acids) at the concentration 0.1 mM, penicillin and streptomycin at respective concentrations of 50 International Units per milliliter and 50 ⁇ g / ml, glutamine at 2 mM concentration, sodium pyruvate at 1 mM concentration and 10% fetal calf serum. These cells were seeded at a density of 10,000 cells per well, in the 24 wells of multi-well type plates (Costar, France).
- DMEM medium Gibco Company
- the cells are brought into contact with the various compounds tested in a KBM medium (Clonetics company) containing 0.15 mM of calcium ion, insulin at 5 ⁇ g / ml, hydrocortisone at 0 , 5 ⁇ g / ml, and delipidated bovine serum albumin at 1 ⁇ g / ml.
- a cell count is carried out 5 days after the addition of the different ceramides using a cell counter of the Coulter Counter type.
- the different compounds are tested at 0.5 nM, 5 nM, 50 nM and 500 nM.
- results expressed as a percentage represent the increase in the number of cells relative to the control, that is to say relative to a culture carried out under the same conditions in the absence of sphinganine.
- A 2-amino-octadecane-1, 3-diol
- B 2-N- (2-hydroxy-hexadecanoyl) -amino-octadecane-1, 3-diol
- C 2-N- acetylamino-octadecane-1, 3-diol
- D 2-N-octanoylamino-octadecane-1, 3-diol.
- HaCat cells are cultured as before. They are then seeded at a density of 20,000 cells per well, in the 24 wells of multi-well plates (Costar, France). 24 hours after inoculation, the cells are brought into contact with the various compounds tested in a KBM medium (Clonetics company) containing insulin at 5 ⁇ g / ml and hydrocortisone at 0.5 ⁇ g / ml. Cell viability is evaluated 48 hours later by measuring the mitochondrial respiration. This is carried out using an XTT kit, sold by the company Boehringer and according to the supplier's instructions.
- results expressed as a percentage represent the increase in the number of cells relative to the control, that is to say relative to a culture carried out under the same conditions in the absence of alkane-diol compounds.
- HaCat cells are cultured as before.
- the cells are brought into contact with the various compounds tested in a KBM medium (Clonetics company) containing insulin at 5 ⁇ g / ml and hydrocortisone at 0.5 ⁇ g / ml and 5- bromo-2 'deoxyuridine (BrdU) at 1 ⁇ .M
- KBM medium Cosmetic and Medical Services company
- RhdU 5- bromo-2 'deoxyuridine
- the cell cycle phase is evaluated 48 hours later by measuring the incorporation of BrdU in genomic deoxyribonucleic acid. This is carried out using a "BrdU fast" kit, sold by the company Boehringer and according to the supplier's instructions.
- results expressed as a percentage represent the increase in the number of cells entered in phase S relative to the control, that is to say relative to a culture carried out under the same conditions in the absence of alkane-diol compounds.
- Example 4 Effect of 2-amino-octadecane-1, 3-diol and its derivatives on cell viability in the presence of a sphingenine-based compound, N-acetyl sphingenine.
- HaCat cells are cultured as in Example 2.
- the cells are brought into contact with the various compounds tested in a KBM medium (Clonetics company) containing insulin at 5 ⁇ g / ml and hydrocortisone at 0.5 ⁇ g / ml.
- the cells are cultured in the presence of 2-amino-octadecane-1, 3-diol to be tested until the evaluation of cell viability.
- N-acetyl sphingenine at a concentration of 10 ⁇ M is added to the culture medium for 2 hours at the start of the experiment.
- Cell viability is evaluated 48 hours later by measuring mitochondrial respiration. This is carried out using an XTT kit, sold by the company Boehringer and according to the supplier's instructions.
- results expressed as a percentage represent the number of cells relative to the control (A), that is to say relative to a culture carried out under the same conditions in the absence of alkane-diol compounds and of N-acetyl sphingenine.
- N-acetyl sphingenine causes a decrease in cell viability.
- Example 5 Examples of compositions to be applied to the skin. These compositions can be prepared by simple mixing. The percentages are given by weight of active material relative to the total weight of the composition.
- Carbopol 940 ® marketed by the company GOODRICH 0.6 0 // o
- Nonionic liposome cream Carbopol 940 ® marketed by the company GOODRICH 0.2% Transcutol ® marketed by the company GATTEFOSSE 3% Triethanolamine 0.2% Polyglyceryl-3-cetyl ether 3.8% ⁇ sitosterol 3.8% Diketyl phosphate 0.4% NaOH 0.007 %
Landscapes
- 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)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Gerontology & Geriatric Medicine (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cosmetics (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9710142 | 1997-08-07 | ||
FR9710142A FR2767056A1 (fr) | 1997-08-07 | 1997-08-07 | Utilisation d'un 2-amino-alcane polyol en tant qu'agent destine a traiter les signes du vieillissement cutane |
PCT/FR1998/001755 WO1999007337A1 (fr) | 1997-08-07 | 1998-08-06 | Utilisation d'un 2-amino-alcane polyol pour le traitement de vieillissement cutane |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1001739A1 true EP1001739A1 (de) | 2000-05-24 |
Family
ID=9510133
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP98941554A Withdrawn EP1001739A1 (de) | 1997-08-07 | 1998-08-06 | Verwendung eines 2-aminoalkan polyol zur behandlung von hautälterung |
Country Status (6)
Country | Link |
---|---|
US (1) | US20020006420A1 (de) |
EP (1) | EP1001739A1 (de) |
JP (1) | JP2001513490A (de) |
CA (1) | CA2299171A1 (de) |
FR (1) | FR2767056A1 (de) |
WO (1) | WO1999007337A1 (de) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2799650B1 (fr) * | 1999-10-14 | 2001-12-07 | Oreal | Procede pour limiter la penetration dans la peau et/ou les fibres keratiniques d'un agent cosmetique et/ou pharmaceutique actif |
FR2811893B1 (fr) * | 2000-07-18 | 2003-04-18 | Oreal | Utilisation d'au moins un extrait d'au moins une iridacee dans une composition destinee a stimuler defenses immunitaires |
US6988268B2 (en) * | 2002-04-30 | 2006-01-17 | Microsoft Corporation | IO completion architecture for user-mode networking |
FR2855047B1 (fr) * | 2003-05-19 | 2007-11-30 | Oreal | Composition comprenant une base sphingoide, un activateur de la voie des 4-et/ou des 6-hydroxylases et un acide gras, utilisation pour renforcer la fonction barriere de la peau |
JP5102198B2 (ja) * | 2006-03-31 | 2012-12-19 | 花王株式会社 | 柔軟洗浄剤組成物 |
KR100823146B1 (ko) | 2006-12-28 | 2008-04-22 | 재단법인 한국원자력의학원 | 신규 파이토스핑고신 유도체 및 이를 이용한 방사선치료증진제 |
DE102011085497A1 (de) * | 2011-10-31 | 2013-05-02 | Evonik Industries Ag | Kosmetische Formulierung |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9124360D0 (en) * | 1991-11-15 | 1992-01-08 | Unilever Plc | Cosmetic compositions |
CA2137001C (en) * | 1992-06-19 | 1999-05-04 | Peter M. Elias | Lipids for epidermal moisturization and repair of barrier function |
GB9308103D0 (en) * | 1993-04-20 | 1993-06-02 | Unilever Plc | Cosmetic composition |
US5368857A (en) * | 1993-11-15 | 1994-11-29 | Elizabeth Arden Company, Division Of Conopco, Inc. | Ceramide cosmetic compositions |
GB9421185D0 (en) * | 1994-10-20 | 1994-12-07 | Unilever Plc | Personal car composition |
FR2728164B1 (fr) * | 1994-12-14 | 1997-03-21 | Oreal | Composition cosmetique ou dermatologique contenant un melange de ceramides, son utilisation pour hydrater la peau |
FR2729079A1 (fr) * | 1995-01-09 | 1996-07-12 | Sederma Sa | Nouvelles compositions cosmetiques contenant des ceramides et autres lipides complexes |
-
1997
- 1997-08-07 FR FR9710142A patent/FR2767056A1/fr active Pending
-
1998
- 1998-08-06 CA CA002299171A patent/CA2299171A1/fr not_active Abandoned
- 1998-08-06 US US09/485,191 patent/US20020006420A1/en not_active Abandoned
- 1998-08-06 JP JP2000506931A patent/JP2001513490A/ja active Pending
- 1998-08-06 WO PCT/FR1998/001755 patent/WO1999007337A1/fr active Search and Examination
- 1998-08-06 EP EP98941554A patent/EP1001739A1/de not_active Withdrawn
Non-Patent Citations (1)
Title |
---|
See references of WO9907337A1 * |
Also Published As
Publication number | Publication date |
---|---|
FR2767056A1 (fr) | 1999-02-12 |
CA2299171A1 (fr) | 1999-02-18 |
WO1999007337A1 (fr) | 1999-02-18 |
US20020006420A1 (en) | 2002-01-17 |
JP2001513490A (ja) | 2001-09-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1064931B1 (de) | Kosmetisches Mittel enthaltend mindestens einen Hydroxystilben und Ascorbinsäure | |
EP1638991B1 (de) | Kosmetische oder dermopharmazeutische zusammensetzung zur verminderung der hautalterungserscheinungen | |
EP0931542B1 (de) | Kosmetische Zusammensetzung, die Phloroglucinol enthält | |
EP1337234B1 (de) | Verwendung von derivaten der 2-oxothiazolidin-4-corbonsäure als prä-abschuppungsmittel | |
CA2255229C (fr) | Utilisation de l'acide cinnamique ou de ses derives dans une composition cosmetique raffermissante | |
FR2777186A1 (fr) | Utilisation d'au moins un hydroxystilbene dans une composition raffermissante | |
EP0790053B1 (de) | Verwendung eines 2-Aminoalkan-1,3-Diol zur Verlangsamung des Haarausfalls und/oder zum Auslösen und Stimulieren des Haarwachstums | |
EP1837013A1 (de) | Zusammensetzung, die Hydroxyapatit und ein Kalziumsalz umfasst, zum Verstärken der Barrierefunktion der Haut und/oder der Halbschleimhäute | |
JP2007515462A (ja) | 生体適合性のガレン基剤の無害製剤方法 | |
EP0756866B1 (de) | Verwendung der Benzosäurederivate zur Stimulierung die Erneuerung der Epidermis und zur Behandlung der Haut | |
EP1278532A1 (de) | Extrakt aus einer pflanze der spezies olea europaea als inhibitor der no-synthase und verwendungen | |
CA2234113C (fr) | Nouveaux derives de l'acide salicylique et leur utilisation dans une composition cosmetique et/ou dermatologique | |
EP1172094B1 (de) | Mittel, insbesondere für Kosmetika, enthaltend DHEA und/oder Vorstufe oder Derivate davon, und mindestens eine Verbindung, die die Glykosaminoglykane-Synthese erhöht | |
EP1337233B1 (de) | Verwendung mindestens eines aminosulfosäure-derivats in einer zusammensetzung zur förderung der abschuppung der haut | |
CA2184402C (fr) | Utilisation de l'acide cysteique ou homocysteique pour favoriser la desquamation de la peau ou stimuler le renouvellement epidermique | |
CA2407334A1 (fr) | Lipochroman-6 comme inhibiteur de no-synthase et utilisations | |
EP1001739A1 (de) | Verwendung eines 2-aminoalkan polyol zur behandlung von hautälterung | |
EP0925779B1 (de) | Zimtsäure oder mindestens ein Zimtsäurederivat enthaltende kosmetische Zusammensetzung und ihre Verwendung | |
EP0858319B1 (de) | Verwendung von carbonsäuren mit einer schwefelhaltigen funktionellen gruppe zur förderung der hautabschälung bzw. stimulierung der epidermisregeneration | |
FR2855049A1 (fr) | Composition comprenant un precurseur de ceramide a base 6-hydroxy-sphingenine et un activeur de la voie des 6-hydroxylases, utilisation pour renforcer la fonction barriere de la peau | |
FR2855048A1 (fr) | Composition comprenant un precurseur de ceramide a base phytosphingosine et un activeur de la voie des 4-hydroxylases, utilisation pour renforcer la fonction barriere de la peau | |
FR2783420A1 (fr) | Utilisation d'au moins un derive de l'acide 10-hydroxy-2-decenoique dans une composition destinee a favoriser la desquamation de la peau, et composition le comprenant | |
FR2828400A1 (fr) | Composition cosmetique ou dermatologique comprenant une association entre de l'igf1 et/ou un compose mimetique de l'igf1, et au moins un retinoide et/ou au moins un derive de retinoide | |
FR2828401A1 (fr) | Composition cosmetique ou dermatologique comprenant une association entre l'igf1 et/ou un compose mimetique de l'igf1, et l'acide ascorbique et/ou au moins l'un de ses derives |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20000307 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): DE ES FR GB IT |
|
17Q | First examination report despatched |
Effective date: 20031107 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 20040518 |