EP1401428A1 - Utilisation d'acide ascorbique pour produire des preparations topiques a action angiogenique - Google Patents

Utilisation d'acide ascorbique pour produire des preparations topiques a action angiogenique

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Publication number
EP1401428A1
EP1401428A1 EP02754679A EP02754679A EP1401428A1 EP 1401428 A1 EP1401428 A1 EP 1401428A1 EP 02754679 A EP02754679 A EP 02754679A EP 02754679 A EP02754679 A EP 02754679A EP 1401428 A1 EP1401428 A1 EP 1401428A1
Authority
EP
European Patent Office
Prior art keywords
acid
ascorbic acid
water
oil
preservatives
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Withdrawn
Application number
EP02754679A
Other languages
German (de)
English (en)
Inventor
Kirsten Sauermann
Ralph Schimpf
Alexander Filbry
Roger Wepf
Volker Schreiner
Sören JASPERS
Uwe SCHÖNROCK
Joachim Ennen
Gerhard Sauermann
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beiersdorf AG
Original Assignee
Beiersdorf AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Beiersdorf AG filed Critical Beiersdorf AG
Publication of EP1401428A1 publication Critical patent/EP1401428A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • A61K8/676—Ascorbic acid, i.e. vitamin C
    • 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
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • 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
    • A61Q19/001—Preparations for care of the lips
    • 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
    • A61Q19/10—Washing or bathing preparations
    • 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

Definitions

  • the present invention relates to the use of ascorbic acid for the preparation of angiogenetically active topical preparations, in particular cosmetic and dermatological preparations.
  • the blood vessel system serves to supply tissues with nutrients, vitamins, oxygen, to transport hormones from secretion to target organs and to dispose of metabolic end products such as CO 2 to the lung excretory organ or urea for excretion via the kidney.
  • the epidermis is supplied by the microcapillaries of the dermis, which protrude into the epidermis in a regular pattern of papillae (rete cones) in adolescence.
  • This architecture was identified and recognized using classic histology - biposia removal, fixation, staining and countless cuts.
  • the quantitative histometric description is complicated or distorted by process-related shrinkage of the tissue samples.
  • the classic technology age-related degeneration of the microcapillary systems and leveling of the rete cones, i.e. the border zone epidermis / dermis. This entails a reduced supply and disposal of the epidermis (smaller transport area).
  • the extent of the toothing area epidermis / dermis is also reduced, which leads to reduced mechanical strength and elasticity of the skin.
  • the status and changes in the microcapillary system and the reticle pattern can be determined using modern techniques such as confocal microscopy in vivo - ie violated tongue-free, repeatable as often as required and reacting dynamically to current influences - display, track and quantify in test subjects quickly (minutes) both in terms of the density of the rete cones or microcapillaries (number / area unit) and their height, which is an estimate of the size of the exchange area allows.
  • Antioxidants are chemical substances of various structures that inhibit or prevent undesirable changes in the substances to be protected due to the effects of oxygen and other oxidative processes. Antioxidants are used in particular to protect organic products, namely fats and oils, but also active ingredients and additives such as flavorings and the like. Phenols, hydroquinones, pyrocatechols and aromatic amines and their metal complexes substituted by sterically hindering groups are effective as antioxidants.
  • Tocopherol, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), octyl and dodecyl gallate as well as ascorbic, lactic, citric and tartaric acids and their salts are suitable for fats, foodstuffs and in particular also cosmetic and dermatological preparations
  • Excellent antioxidants are selected from the group of ascorbic acid and ascorbyl compounds.
  • L-ascorbic acid ⁇ (R) -5 - [(S) -1, 2-dihydroxyethyl] -3,4-dihydroxy-5-H-furan-2-one, vitamin C ⁇ is characterized by the structural formula
  • Ascorbic acid is an endiol and has a strong reducing effect as a reductone. Ascorbic acid is sensitive to heat and is decomposed by light and atmospheric oxygen, especially in the presence of traces of heavy metals and in an alkaline environment. In a pure, dry state, however, it is relatively resistant to light, air and heat. It was, however, surprising and unforeseeable for the person skilled in the art that the use of ascorbic acid for the preparation of topical preparations with angiogenic activity, in particular cosmetic and dermatological preparations, remedies the disadvantages of the prior art.
  • the cosmetic or dermatological preparations according to the invention can be composed as usual and can be used for the treatment, care and cleaning of the skin and / or hair and as a make-up product in decorative cosmetics. They preferably contain 0.001% by weight to 10% by weight, preferably 0.05% by weight to 5% by weight, in particular 0.1-2.0% by weight, based on the total weight of the preparations, on ascorbic acid.
  • Complexing agents are known auxiliaries in cosmetology and medical galenics.
  • the complexation of interfering metals such as Mn, Fe, Cu and others can, for example, prevent undesirable chemical reactions in cosmetic or dermatological preparations.
  • Complexing agents form complexes with metal atoms which, if one or more polybasic complexing agents, ie chelators, are metallacycles.
  • Chelates are compounds in which a single ligand occupies more than one coordination site on a central atom. In this case, sometimes elongated compounds are closed to form rings by complex formation via a metal atom or ion. The number of ligands bound depends on the coordination number of the central metal. The prerequisite for chelation is that the compound reacting with the metal contains two or more atom groups which act as electron donors.
  • the complexing agent or complexing agents can advantageously be selected from the group of conventional compounds, preferably at least one substance from the group consisting of tartaric acid and its anions, citric acid and its anions, amino polycarboxylic acids and their anions (such as, for example, ethylenediaminetetraacetic acid (EDTA) and their Anions, nitrilotriacetic acid (NTA) and their anions, hydroxyethylenediaminotriesacetic acid (HOEDTA) and their anions, diethylenaminopentaacetic acid (DPTA) and their anions, trans-1,2-diaminocyclohexanetetraacetic acid (CDTA) and their anions).
  • EDTA ethylenediaminetetraacetic acid
  • NTA nitrilotriacetic acid
  • HOEDTA hydroxyethylenediaminotriesacetic acid
  • DPTA diethylenaminopentaacetic acid
  • CDTA trans-1,2-d
  • the complexing agent or complexing agents are advantageous in cosmetic or dermatological preparations, preferably at 0.01% by weight to 10% by weight, preferably at 0.05% by weight to 5% by weight, particularly preferably at 0.1 - 2.0 wt .-%, based on the total weight of the preparations.
  • the cosmetic and dermatological preparations according to the invention are applied to the skin and / or the hair in a sufficient amount in the manner customary for cosmetics.
  • Cosmetic and dermatological preparations according to the invention can be in various forms.
  • they can be a solution, an anhydrous preparation, an emulsion or microemulsion of the water-in-oil (W / O) or oil-in-water (O / W) type, multiple emulsions, for example of the water-in-oil type.
  • Oil-in-water (W / OW) a gel, a solid stick, an ointment or an aerosol.
  • ascorbic acid in encapsulated form for example in collagen matrices and other customary encapsulation materials, for example in the form of cellulose encapsulation, in gelatin, wax matrices or in liposomal encapsulation.
  • wax matrices as described in DE-OS 43 08282 have proven to be favorable. It is also possible and advantageous for the purposes of the present invention to insert active ingredient combinations used according to the invention into aqueous systems or surfactant preparations for cleaning the skin and hair.
  • the cosmetic and dermatological preparations according to the invention can contain cosmetic auxiliaries as are usually used in such preparations, e.g. Preservatives, bactericides, perfumes, substances to prevent foaming, dyes, pigments that have a coloring effect, thickeners, surface-active substances, emulsifiers, softening, moisturizing and / or moisturizing substances, fats, oils, waxes or other usual components of a cosmetic or dermatological formulation such as alcohols, polyols, polymers, foam stabilizers, electrolytes, organic solvents or silicone derivatives.
  • cosmetic auxiliaries e.g. Preservatives, bactericides, perfumes, substances to prevent foaming, dyes, pigments that have a coloring effect, thickeners, surface-active substances, emulsifiers, softening, moisturizing and / or moisturizing substances, fats, oils, waxes or other usual components of a cosmetic or dermatological formulation such as alcohols, polyols, polymers, foam stabilizer
  • active ingredient combinations used according to the invention can also be combined with other antioxidants and / or radical scavengers.
  • antioxidants are advantageously selected from the group consisting of amino acids (eg glycine, histidine, tyrosine, tryptophan) and their derivatives, imidazoles (eg urocanic acid) and their derivatives, peptides such as D, L-carnosine, D-camosine, L- Camosin and its derivatives (e.g. Anserin), carotenoids, carotenes (e.g. ⁇ -carotene, ⁇ -carotene, lycopene) and their derivatives, chlorogenic acid and their derivatives, lipoic acid and their derivatives (e.g.
  • amino acids eg glycine, histidine, tyrosine, tryptophan
  • imidazoles eg urocanic acid
  • peptides such as D, L-carnosine, D-camosine, L- Camosin and its derivatives (e.g. Anserin)
  • carotenoids e.g. ⁇
  • thiols e.g. Thiorexin, glutathione, cysteine, cystine, cystamine and their glycosyl, N-acetyl, methyl, ethyl, propyl, amyl, butyl and lauryl, palmitoyl, oleyl, ⁇ -linoleyl, Cholesteryl and glyceryl esters
  • salts dilaurylthiodipropionate, distearylthiodipropionate, thiodipropionic acid and their derivatives (esters, ethers, peptides, lipids, nucleotides, nucleosides and salts) as well as sulfoximine compounds (e.g.
  • buthioninsulfoximines homocystenesulfoximine, pentane- sulfonimine, buthionine sulfonate Hexa-, heptathioninsulfoximine) in very low tolerable doses (eg pmol to ⁇ mol / kg), also (metal) chelators (eg ⁇ -hydroxy fatty acids, palmitic acid, phytic acid, lactoferrin), ⁇ -hydroxy acids (eg citric acid, lactic acid) , Malic acid), humic acid, bile acid, bile extracts, bilirubin, biliverdin, EDTA, EGTA and their derivatives, unsaturated fatty acids and their derivatives (eg ⁇ -linolenic acid, linoleic acid, oleic acid), folic acid and their derivatives, ubiquinone and ubiquinol and their derivatives , Tocopherols and derivatives (e.g.,
  • vitamin E acetate
  • vitamin A and derivatives Vita min-A-pa imitation
  • the amount of the aforementioned antioxidants (one or more compounds) in the preparations is preferably 0.001 to 30% by weight, particularly preferably 0.05-20% by weight, in particular 1-10% by weight, based on the total weight of the Preparation.
  • vitamin E and / or its derivatives represent the additional antioxidant (s)
  • vitamin A or vitamin A derivatives or carotenes or their derivatives represent the additional antioxidant (s)
  • Emulsions according to the invention are advantageous and contain e.g. the fats, oils, waxes and other fat bodies mentioned, as well as water and an emulsifier, as is usually used for such a type of formulation.
  • the lipid phase can advantageously be selected from the following group of substances: mineral oils, mineral waxes
  • Oils such as triglycerides of capric or caprylic acid as well as natural oils such as e.g. Castor oil;
  • Fats, waxes and other natural and synthetic fat bodies preferably esters of fatty acids with alcohols of low C number, e.g. with isopropanol, propylene glycol or glycerin, or esters of fatty alcohols with low C number alkanoic acids or with fatty acids; benzoates;
  • Silicone oils such as dimethylpolysiloxanes, diethylpolysiloxanes, diphenylpolysiloxanes and mixed forms thereof.
  • the oil phase of the emulsions, oleogels or hydrodispersions or lipodispersions for the purposes of the present invention is advantageously selected from the group of esters from saturated and / or unsaturated, branched and / or unbranched alkane carboxylic acids with a chain length of 3 to 30 carbon atoms and saturated and / or unsaturated, branched and / or unbranched alcohols with a chain length of 3 to 30 C atoms, from the group of esters from aromatic carboxylic acids and saturated and / or unsaturated, branched and / or unbranched alcohols with a chain length of 3 to 30 C- atoms.
  • ester oils can then advantageously be selected from the group of isopropyl myristate, isopropyl palmitate, isopropyl stearate, isopropyl oleate, n-butyl stearate, n-hexyl laurate, n-decyl oleate, isooctyl stearate, isononyl stearate, isononylisononanoate, 2-ethylhexyl ethylhexyl palate, 2-ethylhexyl palylate 2-octyldodecyl palmitate, olefin oleate, olefin erucate, erucyl oleate, erucyl erucate as well as synthetic, semisynthetic and natural mixtures of such esters, for example jojoba oil.
  • the oil phase can advantageously be selected from the group of branched and unbranched hydrocarbons and waxes, the silicone oils, the dialkyl ethers, the group of saturated or unsaturated, branched or unbranched alcohols, and also the fatty acid triglycerides, especially the triglycerol esters of saturated and / or unsaturated, branched and / or unbranched alkane carboxylic acids with a chain length of 8 to 24, in particular 12 - 18 carbon atoms.
  • the fatty acid triglycerides can, for example, advantageously be selected from the group of synthetic, semisynthetic and natural oils, e.g. Olive oil, sunflower oil, soybean oil, peanut oil, rapeseed oil, almond oil, palm oil, coconut oil, palm kernel oil and the like.
  • any mixtures of such oil and wax components can also be used advantageously for the purposes of the present invention. It may also be advantageous to use waxes, for example cetyl palmitate, as the sole lipid component of the oil phase.
  • the oil phase is selected from the group 2-ethylhexyl advantageous, octyldodecanol, isotridecyl isononanoate, isoeicosane, 2-ethylhexyl cocoate, C 12 i 5 alkyl benzoate, caprylic capric acid triglyceride, dicaprylyl ether.
  • hydrocarbons paraffin oil, squalane and squalene can be used advantageously for the purposes of the present invention.
  • the oil phase can advantageously also have a content of cyclic or linear silicone oils or consist entirely of such oils, although it is preferred to use an additional content of other oil phase components in addition to the silicone oil or the silicone oils.
  • Cyclomethicone (octamethylcyclotetrasiloxane) is advantageously used as the silicone oil to be used according to the invention.
  • other silicone oils can also be used advantageously for the purposes of the present invention, for example hexamethylcyclotrisiloxane, polydimethylsiloxane, poly (methylphenylsiloxane).
  • the aqueous phase of the preparations according to the invention optionally advantageously contains alcohols, diols or polyols of low C number, and also their ethers, preferably ethanol, isopropanol, propylene glycol, glycerol, ethylene glycol, ethylene glycol monoethyl or - monobutyl ether, propylene glycol monomethyl, monoethyl or monobutyl ether , Diethylene glycol monomethyl or monoethyl ether and similar products, furthermore alcohols with a low C number, for example ethanol, isopropanol, 1,2-propanediol, glycerol and in particular one or more thickeners which can advantageously be selected from the group consisting of silicon dioxide, Aluminum silicates, polysaccharides or their derivatives, for example hyaluronic acid, xanthan gum, hydroxypropylmethyl cellulose, particularly advantageously from the group of polyacrylates, preferably a polyacrylate from the group
  • Emulsions according to the invention are advantageous and contain e.g. the fats, oils, waxes and other fat bodies mentioned, as well as water and an emulsifier, as is usually used for such a type of formulation.
  • Gels according to the invention usually contain low C number alcohols, e.g. Ethanol, isopropanol, 1,2-propanediol, glycerol and water or an oil mentioned above in the presence of a thickener which is preferably silicon dioxide or an aluminum silicate in the case of oily-alcoholic gels, and is preferably a polyacrylate in the case of aqueous-alcoholic or alcoholic gels.
  • low C number alcohols e.g. Ethanol, isopropanol, 1,2-propanediol, glycerol and water or an oil mentioned above in the presence of a thickener which is preferably silicon dioxide or an aluminum silicate in the case of oily-alcoholic gels, and is preferably a polyacrylate in the case of aqueous-alcoholic or alcoholic gels.
  • Suitable propellants for preparations according to the invention which can be sprayed from aerosol containers are the customary, known volatile, liquefied propellants, for example hydrocarbons (propane, butane, isobutane), which can be used alone or in a mixture with one another. Compressed air can also be used advantageously.
  • hydrocarbons propane, butane, isobutane
  • Preparations according to the invention can also advantageously contain substances which absorb UV radiation in the UVB range, the total amount of filter substances e.g. 0.1% by weight to 30% by weight, preferably 0.5 to 10% by weight, in particular 1.0 to 6.0% by weight, based on the total weight of the preparations, in order to prepare cosmetic preparations To provide that protect the hair or skin from the entire range of ultraviolet radiation. They can also serve as a sunscreen for the hair or skin.
  • UVB filter substances if they contain UVB filter substances, they can be oil-soluble or water-soluble.
  • Oil-soluble UVB filters which are advantageous according to the invention are, for example:
  • 4-aminobenzoic acid derivatives preferably 4- (dimethyfamino) benzoic acid (2-ethylhexyl) ester, 4- (dimethylamino) benzoic acid amyl ester;
  • Esters of cinnamic acid preferably 4-methoxycinnamic acid (2-ethylhexyl) ester, 4-methoxycinnamic acid isopentyl ester;
  • Esters of salicylic acid preferably salicylic acid (2-ethylhexyl) ester, salicylic acid (4-isopropylbenzyl) ester, salicylic acid homomethyl ester,
  • benzophenone preferably 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone;
  • Esters of benzalmalonic acid preferably 4-methoxybenzalmalonic acid di (2-ethylhexyl) ester, 2,4,6-trianilino- (p-carbo-2'-ethyl-r-hexyloxy) -1,3,5-triazine.
  • Salts of 2-phenylbenzimidazole-5-sulfonic acid such as its sodium, potassium or triethanolammonium salt, and also the sulfonic acid itself;
  • Sulfonic acid derivatives of benzophenones preferably 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid and its salts;
  • Sulfonic acid derivatives of 3-benzylidene camphor e.g. 4- (2-oxo-3-bornylidene-methyl) benzenesulfonic acid, 2-methyl-5- (2-oxo-3-bornylidene-methyl) sulfonic acid and their salts and 1,4-di (2-oxo-10-sulfo 3-bornylidene methyl) -benzene and its salts (the corresponding 10-sulfato compounds, e.g. the corresponding sodium, potassium or triethanolammonium salt), also as benzene-1,4-di (2-oxo-3-bornylidene methyl) Designated 10-sulfonic acid
  • UVB filters which can be used in combination with the active compound combinations according to the invention, is of course not intended to be limiting.
  • UVA filters in the preparations according to the invention which have hitherto usually been contained in cosmetic preparations.
  • These substances are preferably derivatives of dibenzoylmethane, in particular 1- (4'-tert-butylphenyl) -3- (4'-methoxyphenyl) propane-1,3-dione and 1-phenyl-3- (4 '-isopropylphenyl) propane-1,3-dione.
  • dibenzoylmethane in particular 1- (4'-tert-butylphenyl) -3- (4'-methoxyphenyl) propane-1,3-dione and 1-phenyl-3- (4 '-isopropylphenyl) propane-1,3-dione.
  • Cosmetic and dermatological preparations according to the invention can also contain inorganic pigments which are usually used in cosmetics to protect the skin from UV rays. These are oxides of titanium, zinc, zirconium, silicon, manganese, cerium and mixtures thereof, as well as modifications in which the oxides are the active agents. It is particularly preferred to use pigments based on titanium dioxide.
  • UVA filter and pigment or preparations containing this combination are also the subject of the invention.
  • the amounts given for the above combinations can be used.
  • the cosmetic and dermatological preparations advantageously contain active substances and auxiliaries, as are usually used for this type of preparations for hair care and hair treatment.
  • Preservatives, surface-active substances, substances for preventing foaming, thickeners, emulsifiers, fats, oils, waxes, organic solvents, bactericides, perfumes, dyes or pigments, the task of which is the hair or the cosmetic or dermatological preparation serve as auxiliary substances to dye themselves, electroyte, substances against greasing the hair.
  • Electrolytes for the purposes of the present invention are water-soluble alkali metal, ammonium, alkaline earth metal (including magnesium) and zinc salts of inorganic anions and any mixtures of such salts, it being necessary to ensure that these salts are pharmaceutically or cosmetically harmless distinguished.
  • the anions according to the invention are preferably selected from the group of chlorides, sulfates and hydrogen sulfates, phosphates, hydrogen phosphates and linear and cyclic oligophosphates as well as carbonates and hydrogen carbonates.
  • Cosmetic preparations which are a skin cleanser preferably contain at least one anionic, non-ionic or amphoteric surface-active substance, or else mixtures of such substances, the active compound combinations according to the invention in the aqueous medium and auxiliaries as are usually used therefor.
  • the surface-active substance or the mixtures of these substances can be present in the shampooing agent in a concentration between 1% by weight and 50% by weight.
  • Aqueous cosmetic cleaning agents according to the invention or water-free or water-free cleaning agent concentrates intended for aqueous cleaning may contain anionic, nonionic and / or amphoteric surfactants, for example conventional soaps, for example sodium fatty acid salts
  • Cosmetic preparations which are cosmetic cleaning preparations for the skin, can be in liquid or solid form.
  • active ingredient combinations used according to the invention they preferably contain at least one anionic, nonionic or amphoteric surface-active substance or mixtures thereof, if desired one or more electrolytes and auxiliaries, as are usually used for this.
  • the surface-active substance can be present in the cleaning preparations in a concentration between 1 and 94% by weight, based on the total weight of the preparations.
  • compositions according to the invention contain water and, if appropriate, the additives customary in cosmetics, for example perfume, thickeners, dyes, deodorants, antimicrobial substances, moisturizing agents, complexing and sequestering agents, pearlescent agents, plant extracts, vitamins, active ingredients and the like.
  • the additives customary in cosmetics for example perfume, thickeners, dyes, deodorants, antimicrobial substances, moisturizing agents, complexing and sequestering agents, pearlescent agents, plant extracts, vitamins, active ingredients and the like.

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Abstract

La présente invention concerne l'utilisation d'acide ascorbique pour produire des préparations topiques à action angiogénique.
EP02754679A 2001-06-15 2002-06-14 Utilisation d'acide ascorbique pour produire des preparations topiques a action angiogenique Withdrawn EP1401428A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE10128911A DE10128911A1 (de) 2001-06-15 2001-06-15 Verwendung von Ascorbinsäure zur Herstellung angiogenetisch wirksamer topischer Zubereitungen
DE10128911 2001-06-15
PCT/EP2002/006598 WO2002102371A1 (fr) 2001-06-15 2002-06-14 Utilisation d'acide ascorbique pour produire des preparations topiques a action angiogenique

Publications (1)

Publication Number Publication Date
EP1401428A1 true EP1401428A1 (fr) 2004-03-31

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EP02754679A Withdrawn EP1401428A1 (fr) 2001-06-15 2002-06-14 Utilisation d'acide ascorbique pour produire des preparations topiques a action angiogenique

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US (1) US20050032888A1 (fr)
EP (1) EP1401428A1 (fr)
DE (1) DE10128911A1 (fr)
WO (1) WO2002102371A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140271507A1 (en) * 2013-03-13 2014-09-18 Stemetrix, Inc. Skin Compositions and Uses

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2556217A1 (fr) * 1983-12-09 1985-06-14 Biosculpture Compositions cosmetiques anti-surcharges graisseuses et application sur le corps humain par ionophorese
CA1291034C (fr) * 1987-10-19 1991-10-22 Mostafa S. Fahim Composition favorisant la regeneration de l'epithelium
JPS6248376A (ja) * 1985-08-23 1987-03-03 Takeda Chem Ind Ltd 細胞の培養法
EP0282746A1 (fr) * 1987-02-19 1988-09-21 Takeda Chemical Industries, Ltd. Procédé de préparation de tissu cultivé de manière artificielle
GR1002610B (el) * 1991-01-02 1997-02-20 Johnson & Johnson Consumer Products Inc. Θεραπευτικες συνθεσεις πληγων που περιεχουν παραγοντα αναπτυξης ινοβλαστων και ασκορβικον οξυ.
DE19509354A1 (de) * 1994-12-08 1996-06-13 Klett Loch Lore M Kombinationspräparat zur Förderung des Haarwachstums und ggf. des Haut- und Nagelwachstums sowie zur Verhinderung bzw. zur Beseitigung von Haarausfall
CA2272306A1 (fr) * 1996-11-22 1998-05-28 The Procter & Gamble Company Compositions cosmetiques
EP1021177A4 (fr) * 1997-02-04 2002-05-15 John V Kosbab Compositions et procedes destines a la prevention et au traitement de maladies degeneratives vasculaires
US6046178A (en) * 1997-04-18 2000-04-04 Deroyal Industries, Inc. Method and compound for treating wounds with starch hydrolysate medication
US6066327A (en) * 1997-12-17 2000-05-23 Color Access, Inc. Antioxidant mixture
US6068848A (en) * 1997-12-17 2000-05-30 Color Access, Inc. Antioxidant mixture comprising tocopherol
AU5334899A (en) * 1998-08-04 2000-02-28 Kosbab, John V. Nutrient and therapeutic compositions for the treatment of cancer
WO2001013865A1 (fr) * 1999-08-20 2001-03-01 Howard Murad Compositions et methodes pharmaceutiques de reduction de l'apparition de la cellulite

Non-Patent Citations (1)

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See references of WO02102371A1 *

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DE10128911A1 (de) 2002-12-19

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