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EP1496848A1 - Agents coiffants gelifies contenant des derives d'amidon pregelatinises a reticulation transversale - Google Patents

Agents coiffants gelifies contenant des derives d'amidon pregelatinises a reticulation transversale

Info

Publication number
EP1496848A1
EP1496848A1 EP03745796A EP03745796A EP1496848A1 EP 1496848 A1 EP1496848 A1 EP 1496848A1 EP 03745796 A EP03745796 A EP 03745796A EP 03745796 A EP03745796 A EP 03745796A EP 1496848 A1 EP1496848 A1 EP 1496848A1
Authority
EP
European Patent Office
Prior art keywords
copolymers
hair
derivatives
acid
pregelatinized
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP03745796A
Other languages
German (de)
English (en)
Inventor
Marion Detert
Anke Polzer
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 EP1496848A1 publication Critical patent/EP1496848A1/fr
Ceased 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
    • A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
    • 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • A61K8/732—Starch; Amylose; Amylopectin; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A61K8/8182—Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
    • 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
    • A61K2800/54—Polymers characterized by specific structures/properties
    • A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5422—Polymers characterized by specific structures/properties characterized by the charge nonionic
    • 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
    • A61K2800/54—Polymers characterized by specific structures/properties
    • A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5424—Polymers characterized by specific structures/properties characterized by the charge anionic
    • 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
    • A61K2800/54—Polymers characterized by specific structures/properties
    • A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5426—Polymers characterized by specific structures/properties characterized by the charge cationic

Definitions

  • the present invention relates to cosmetic hair styling preparations or styling agents, in particular gel-shaped hair styling preparations with improved properties, in particular with improved behavior when combing out the product from the hair.
  • the entire human body with the exception of the lips, the palms of the hands and the soles of the feet, is hairy, but for the most part with barely visible wool hairs. Because of the many nerve endings at the hair root, hair is sensitive to external influences such as wind or touch and is therefore one. not to be underestimated part of the sense of touch.
  • the most important function of the human head hair today should be to help shape the human appearance in a characteristic way. Similar to the skin, it fulfills a social function, since its appearance makes a significant contribution to interpersonal relationships and the self-esteem of the individual.
  • the hair consists of the hair shaft protruding freely from the skin - the keratinized (dead) part, which actually represents the visible hair - and the hair root stuck in the skin - the living part, in which the visible hair is constantly being newly formed.
  • the hair shaft for its part, is made up of three layers: a central part - the so-called hair mark (medulla), which, however, is regressed in humans and is often completely absent - as well as the marrow (cortex) and the outer cuticle layer (cuticle) up to ten layers thick that covers the whole hair.
  • One aim of hair care is to protect the scalp and hair from damaging influences and to preserve the natural state of freshly regrown hair for as long as possible and to restore it in the event of loss.
  • Silky shine, low porosity and a pleasant, smooth feeling are characteristics of natural, healthy hair.
  • hair care cosmetics are used nowadays which are either intended to be rinsed out of the hair again after exposure or which are intended to remain on the hair.
  • the latter can be formulated in such a way that they not only serve to care for the individual hair, but also improve the overall appearance of a hairstyle, for example by giving the hair more body, fixing the hairstyle over a longer period of time or improving the manageability.
  • the invention relates to styling agents or hair setting agents (hair setting agents) based on water.
  • Film formers are an essential functional component of such preparations.
  • Various polymers are used as such, for example mixed or copolymers of vinyl acetate and vinylpyrrolidone or also anionic polymers or preferably combinations of anionic polymers with nonionic or cationic polymers.
  • Such preparations are offered in various forms for use, in particular as a hair spray, hairdressing gel, foaming agent or hair lacquer.
  • the styling agents are topical preparations and can also be used to treat and care for the scalp and / or hair or as a sunscreen preparation.
  • Gels are aqueous or alcoholic / aqueous preparations which contain anionic polymers as thickeners in addition to the setting polymers. Often used as thickeners Polyacrylic acids such as (INCI) carbomers used. After styling gels have been applied to the hair, a polymer film forms around the individual hair or parts of the hair. This film tears out of the hair when the product is combed out and leaves small white residues or particles. The appearance of residues is also known as "flaking". This is often observed with styling gels and is completely undesirable.
  • gel-type hairdressing agents containing one or more pregelatinized, crosslinked starch derivatives, anionic polymers, nonionic polymers and water remedy the deficiencies of the prior art.
  • modified starch Structure XL
  • gels can be formulated with which a very good setting of the hair is achieved at the same time by the formation of visible 'residues in the form of white Partkel or scales on the hair of the product during the removal Combing can be significantly reduced.
  • the invention also encompasses the use of one or more pregelatinized, crosslinked starch derivatives to improve the removability of aqueous hairdressing agents containing anionic polymers by combing the product out of the hair.
  • hydroxypropylated phosphate esters very particularly preferably hydroxypropyl distarch phosphates, are used as the pregelatinized, crosslinked starch derivatives.
  • Hairdressing agents or uses according to the invention are preferably characterized in that at least one substance selected from the group consisting of polyacrylic acids with a molar mass of 2,000,000 g / mol to 6,000,000 g / mol, acrylic acid / acrylamide copolymer sodium salts with a molar mass of 2,000,000 g is selected as the anionic polymer / mol to 6000000 g / mol, acrylic acid / methacrylic acid copolymers, acrylate / steareth-2 methacrylate copolymer, stearet-10 allyl ether / acrylate copolymer, acrylate / steareth-20 itaconate copolymer, celluloses, cellulose derivatives, cellulose gums, ethoylated celluloses, starch or Gums, guar gum, guar hydroxypropyltrimonium chloride, xanthan gum, hydroxypropyl guar, karaya gum, bentonite
  • Hair styling agents or uses according to the invention are particularly preferably characterized in that the content of pregelatinized, crosslinked starch derivatives is 0.1 to 4% by weight, particularly preferably 1 to 4% by weight.
  • Hair styling agents or uses according to the invention are very particularly preferably characterized in that their viscosity is 7 to 13 Pa s, preferably 9 to 11 Pa s.
  • hydroxypropylated phosphate esters are used as the pregelatinized, crosslinked starch derivatives.
  • Starch derivatives such as those described in US Pat. No. 6,248,338 are particularly advantageous, and hydroxypropyl distarch phosphate is particularly advantageous.
  • Preparations in the sense of the present invention can advantageously be present as liquid fixers or solutions or syling gels.
  • agents according to the invention can be present, for example, as preparations which can be removed from squeeze bottles or by means of a pump device, but also in the form of an agent which can be applied from normal bottles and containers.
  • Preparations according to the invention advantageously contain, in addition to an effective content of active compound combinations according to the invention, customary active compounds, ingredients, additives and / or auxiliaries.
  • Cosmetic preparations according to the invention for setting and styling the hair usually contain film formers, as are normally used in such preparations, the total amount of the film forming substances, for. B. is between 0.5 and 20 wt .-%, based on the total weight of the preparations.
  • all film formers suitable or customary for cosmetic and / or dermatological applications can be used as cheap film formers.
  • the film-forming agent or films are advantageously selected from the group of polyurethanes, polyureas, silicone resins and / or polyesters which are soluble or dispersible in alcohol or water, and nonionic, anionic, amphoteric and / or cationic polymers.
  • nonionic polymers which can be contained in preparations according to the invention alone or in a mixture, preferably also with anionic and / or amphoteric and / or zwitterionic polymers, are vinylpyrrolidone homopolymers or copolymers.
  • polyvinylpyrrolidone examples include, for example, polyvinylpyrrolidone, copolymers of N-vinylpyrrolidone and vinyl acetate and / or vinyl propionate in various concentration ratios, polyvinylcaprolactam, polyvinylamides and their salts, and copolymers of vinylpyrrolidone and dimethylaminoethyl methacrylate, terpolymers of vinylcaprolactam, vinylpyramino methyl acrylate and vinylpyramino methyl acrylate, and polypyrrino methyl acrylate and the like.
  • anionic polymers are, for example, vinyl acetate / crotonic acid, vinyl acetate / acrylate and / or vinyl acetate / vinyl neodecanoate / crotonic acid copolymers, sodium acrylate / vinyl alcohol copolymers, sodium polystyrene sulfonate, ethyl acrylate / N-tert.-butylacrylamide / acrylic acid copolymers / vinyl pyrrolidone vinyl acetate / itaconic acid
  • Copolymers acrylic acid / acrylamide copolymers and / or their sodium salts, homo- and / or copolymers of acrylic acid and / or methacrylic acid and / or their salts as well as acrylate / hydroxyacrylate, octylacrylamide / acrylate or methacrylic acid esters and / or butyl acrylate / N-vinylpyrrolidone copolymers or polystyrene sulfonates.
  • anionic polymers are methyl vinyl ether / maleic acid copolymers which are formed by hydrolysis of vinyl ether / maleic anhydride copolymers. These polymers can also be partially esterified (ethyl, isopropyl or butyl ester).
  • amphoteric polymers' in formulations of this invention alone or in admixture, preferably with anionic and / or non-ionic polymers may be included, copolymers of N-octyl acrylamide, (meth) acrylic acid and tert.-butylaminoethyl methacrylate of the type "Amphomer” are ,, Copolymers of methacryloylethylbetaine and alkyl methacrylates of the “Yukaformer” type, copolymers of carboxyl groups or sulfone group-containing monomers, for example (meth) acrylic acid and itaconic acid, with basic, in particular amino group-containing monomers such as, for example, mono- or dialkylaminoalkyl (meth) acrylates and / or mono- or dialkylaminoalkyl (meth) acrylamides, copolymers of N-octylacrylamide, methyl methacrylate, hydroxypropyl methacryl
  • Butylaminoethyl methacrylate and acrylic acid although this list is of course not intended to be limiting.
  • alkali or. Alkaline earth bases ammonia and / or various amines, e.g. Triethanolamine, Triisopröpanolamin, Aminomethyl-propanol and / or Aminomethylpropandiol can be used.
  • the neutralization can take place partially or completely, depending on the application.
  • Advantageous cationic polymers are, for example, vinylpyrrolidone / vinylimidazolium methochloride copolymers, quaternized vinylpyrrolidone / dialkylaminoalkyl methacrylate copolymers, cationic cellulose derivatives, such as, for example, hydroxyethyl cellulose / dimethyl alkylammonium chloride copolymers and terpolymers Vinyl caprolactam vinyl pyrrolidone with dimethylaminoethyl methacrylate or
  • film formers on a natural basis, e.g. Chitosan and its derivatives to use, especially in a mixture with synthetic polymers.
  • the preparations according to the invention can contain cosmetic auxiliaries as are usually used in such preparations, e.g. Perfumes, preservatives, substances to reduce or stabilize the foam, dyes, pigments that have a coloring effect, surface-active substances, solubilizers, thickeners, emulsifiers, complexing agents, sequestering agents, pearlescent agents, softening, moisturizing and / or moisturizing substances, refatting agents, alcohol-replenishing agents , Polyols and their toxicologically compatible ethers and esters, branched and / or unbranched hydrocarbons, other antioxidants, stabilizers, pH regulators, consistency agents, bactericides, deodorants, antimicrobial substances, antistatic agents, UV absorbers, polymers, electrolytes, organic solvents, Silicone derivatives, plant extracts, vitamins and / or other active ingredients or other usual components of a cosmetic or dermatological formulation.
  • cosmetic auxiliaries e.g. Perfumes, preservatives
  • the total amount of auxiliaries is, for example, 0.001 to 15% by weight, preferably 0.01 to 10% by weight, in each case based on the total weight of the preparation.
  • the preparations according to the invention optionally advantageously contain 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 one or more can advantageously be selected from the group consisting of silicon dioxide and aluminum silicates , Polysaccharides or their derivatives, for example hyaluronic acid, xanthan gum, hydroxypropylmethyl cellulose, are particularly advantageous the group of polyacrylates, preferably a polyacrylate from the group of so-called carbo
  • 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 thickening agent 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.
  • a thickening agent 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.
  • the proportion of thickeners in the preparations is 0.01 to 20% by weight, preferably 0.01 to 10% by weight, in particular 0.05 to 5% by weight, in each case based on the total weight of the preparation.
  • the water content of the preparations is 50 to 95% by weight, preferably 60 to 95% by weight, in particular 70 to 95% by weight, in each case based on the total weight of the preparation.
  • the proportion of alcohols in the aqueous preparations is, for example, 0 to 30% by weight, preferably 0 to 20, in particular 0 to 15% by weight, in each case based on the total weight of the preparation.
  • the preparations according to the invention can contain water e.g. contained in the amounts introduced by the raw materials used, for example or e.g. also in amounts of up to 30% by weight, based on the total weight of the preparations.
  • antioxidants suitable or customary for cosmetic and / or dermatological applications can be used as antioxidants.
  • the total amount of the antioxidants is, for example, 0.001 to 2% by weight, preferably 0.01 to 1% by weight, in each case based on the total weight of the preparation.
  • antioxidants are advantageously selected from the group consisting of amino acids (for example glycine, histidine, tyrosine, tryptophan) and their derivatives, imidazoles (for example urocanic acid) and their derivatives, peptides such as D, L-camosine, D-camosine, L-carnosine and their derivatives (e.g. anserine), carotenoids, carotenes (e.g. ⁇ -carotene, ß-carotene, lycopene) and their derivatives, chlorogenic acid and their derivatives, lipoic acid and their derivatives (e.g.
  • amino acids for example glycine, histidine, tyrosine, tryptophan
  • imidazoles for example urocanic acid
  • peptides such as D, L-camosine, D-camosine, L-carnosine and their derivatives (e.g. anserine)
  • carotenoids e.g. ⁇
  • thiols e.g. thioredoxin , Glutathione, cysteine, cystine, cystamine and their glycosyl, N-acetyl, methyl, ethyl, propyl, amyl, butyl and lauryl, palmitoyl, oleyl, ⁇ -linoleyl, cholesteryl and Glyceryl esters
  • salts dilauryl thiodipropionate, distearyl thio dipropionate, thiodipropionic acid and their derivatives (esters, ethers, peptides, lipids, nucleotides, nucleosides and salts) as well as sulfoximine compounds (eg buthionine sulfoximines, homocysteine sulfoximine, buthionine sulfones,
  • sulfoximine compounds eg buthionine sulfoximines, homocystein
  • chelators e.g. ⁇ -hydroxy fatty acids, palmitic acid, phytic acid, lactoferrin), ⁇ -hydroxy acids (e.g. citric acid, lactic acid, apple) acid), humic acid, bile acid, bile extracts, bilirubin, biliverdin, EDTA, EGTA and their derivatives, unsaturated fatty acids and their derivatives (e.g. ⁇ -linolenic acid, linoleic acid, oleic acid), folic acid and their derivatives, vitamin C and derivatives (e.g.
  • Preparations according to the invention can also advantageously contain substances which absorb UV radiation in the UV-B range, the total amount of the filter substances being, for example, 0.001% by weight to 30% by weight, preferably 0.05 to 10% by weight, in particular 0.1 to 1.0% by weight, based on the total weight of the preparations, in order to provide cosmetic preparations which protect the hair or the skin from the entire range of ultraviolet radiation. They can also serve as sunscreens for the hair or skin, especially the scalp. If the emulsions according to the invention contain UV-B filter substances, they can advantageously be water-soluble. Examples of advantageous water-soluble UV-B filters are:
  • Triethanolammonium salt as well as the 2-phenylbenzimidazole-5-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.
  • UV-A filters can also be advantageous to add UV-A filters to the preparations according to the invention which have hitherto usually been found in cosmetic preparations.
  • the quantities used for the UV-B combination can be used.
  • nonionic or amphoteric polymers such as e.g. PVP / VA copolymers, e.g. are available from the company BASF under the trade names Luviskol VA 64W or from the company International Specialty Products (ISP) under the name PVP / VA E 335 or nonionic polymers of the type PVP / VA copolymer, which are sold under the trade name Luviskol VA 64W from the Company BASF or under the name PVP / VA W735 from the company International Specialty Products (ISP) are available in concentrations of 2-8% by weight of the total weight of the preparation (based on the active content of the polymer).
  • PVP / VA copolymers e.g. are available from the company BASF under the trade names Luviskol VA 64W or from the company International Specialty Products (ISP) under the name PVP / VA E 335 or nonionic polymers of the type PVP / VA copolymer, which are sold under the trade name Luviskol VA 64W from the Company
  • Amphoteric polymers of the octylacrylamide / acrylate / butylaminoethyl methacrylate copolymer type are e.g. available from National Starch under the trade names Amphomer 28-4910 and LV-71 and will, e.g. in concentrations between 1 - 6 wt .-% of the total weight of the preparation.
  • cationic polymers of the type P ⁇ lyquatemium-11 (trade name Gafquat 755N, company International Specialty Products (ISP)) or -16 (trade name Luviquat FC 550, company BASF), which not only have strengthening but also conditioning properties and thus also act as care substances.
  • cyclic polydimethylsiloxanes in concentrations of e.g. 0.1-1.0% by weight of the total formulation or silicone surfactants (polyether-modified siloxanes) of the Dimethicone Copolyol type, e.g. in conc. 0.01-1.0% by weight of the total weight of the preparation are preferably used.
  • Cyclomethicones are among others under the trade name Abil K4 from the company Goldschmidt or e.g. DC 244, DC 245 or DC 345 offered by Dow Corning.
  • Dimethicone copolyols are e.g. offered under the trade name DC 193 by Dow Corning or Belsil DM 6031 by Wacker.
  • silicone surfactants polyether-modified siloxanes
  • Dimethicone copolyols are e.g. offered under the trade name DC 193 by Dow Corning or Abil B 8851 by Goldschmidt.
  • the application concentrations are e.g. between 0.02 and 1.0% by weight of the total formulation.
  • 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 in particular chelators, form complexes with metal atoms which, if one or more polybasic complexing agents, ie chelators, are metalacycles.
  • Chelates are compounds in which a single ligand occupies more than one coordination site on a central atom. In this case, normally elongated connections 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, aminopolycarboxylic 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 2-dia
  • 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 preparations according to the invention can be prepared in the customary manner by mixing the individual constituents.
  • the active ingredients of the combinations according to the invention or the premixed components of the combinations according to the invention can be added in the mixing process.
  • the pH of the preparations can be adjusted in a known manner by adding acids or bases, preferably by adding buffer mixtures, for example based on citric acid / citrate or phosphoric acid / phosphate buffer mixtures.
  • the pH is preferably below 10, for example in the range from 3 to 9. Unless otherwise stated, all quantities, parts and percentages are based on the weight and the total amount or on the total weight of the preparations or the respective mixture.
  • Luviskol VA 37 E (BASF) is used as the PVP / VA copolymer in the examples.
  • Amphomer 28-4910 National Starch company is used as the octylacrylamide / acrylate / butylaminoethyl methacrylate copolymer in the examples. The amounts in the examples are% by weight.

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Abstract

L'invention concerne des agents coiffants gélifiés contenant un ou plusieurs dérivés d'amidon prégélatinisés à réticulation transversale, des polymères anioniques, des polymères non ioniques et de l'eau.
EP03745796A 2002-04-11 2003-04-09 Agents coiffants gelifies contenant des derives d'amidon pregelatinises a reticulation transversale Ceased EP1496848A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE10216499A DE10216499A1 (de) 2002-04-11 2002-04-11 Frisiermittel
DE10216499 2002-04-11
PCT/EP2003/003678 WO2003084493A1 (fr) 2002-04-11 2003-04-09 Agents coiffants gelifies contenant des derives d'amidon pregelatinises a reticulation transversale

Publications (1)

Publication Number Publication Date
EP1496848A1 true EP1496848A1 (fr) 2005-01-19

Family

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Application Number Title Priority Date Filing Date
EP03745796A Ceased EP1496848A1 (fr) 2002-04-11 2003-04-09 Agents coiffants gelifies contenant des derives d'amidon pregelatinises a reticulation transversale

Country Status (4)

Country Link
US (1) US20050191264A1 (fr)
EP (1) EP1496848A1 (fr)
DE (1) DE10216499A1 (fr)
WO (1) WO2003084493A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102004009158A1 (de) * 2004-02-26 2005-09-15 Beiersdorf Ag Polymerkombination für Stylingmittel
DE102004034265A1 (de) * 2004-07-15 2006-02-16 Wella Ag Haarstylinggel mit Lichtschutzwirkung für Haut und Haare
US20110212145A1 (en) * 2010-03-01 2011-09-01 Honeywell International Inc. Hair fixatives comprising cross linked starches
FR3007286B1 (fr) * 2013-06-20 2015-06-19 Oreal Composition comprenant l'association d'un polymere acrylique, d'un copolymere silicone et d'un amino-acide ou derive d'amino-acide

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL7011183A (fr) * 1969-08-05 1971-02-09
US4508705A (en) * 1980-07-02 1985-04-02 Lever Brothers Company Skin treatment composition
WO1995000104A1 (fr) * 1993-06-23 1995-01-05 Wella Aktiengesellschaft Agent aqueux de fixation capillaire se presentant sous forme de gel tres visqueux pulverisable
FR2713921B1 (fr) * 1993-12-22 1996-01-26 Oreal Procédé de déformation non remanente des fibres kératiniques humaines.
EP0804140A2 (fr) * 1995-01-18 1997-11-05 National Starch and Chemical Investment Holding Corporation Cosmetiques contenant des amidons inhibes thermiquement
FR2734713B1 (fr) * 1995-05-29 1997-07-04 Oreal Utilisation en cosmetique d'une composition solide expansee ayant une matrice constituee d'un reseau alveolaire forme a partir d'un produit naturel ou d'un derive apte a s'expanser
FR2734830B1 (fr) * 1995-05-29 1997-07-11 Oreal Composition solide expansee dont la matrice est constituee d'un reseau alveolaire amidonne et contenant des particules creuses thermoplastiques expansees et ses utilisations en application topique
DE19627498A1 (de) * 1996-07-08 1998-01-15 Nat Starch Chem Invest Stärkehaltige Reinigungs- und Pflegemittel
EP0948960B1 (fr) * 1998-04-09 2008-12-31 National Starch and Chemical Investment Holding Corporation Amidon modifié non ioniquement et son utilisation dans des compositions non en aérosol pour fixer les cheveux à faible teneur en composés organiques volatils
US6344183B2 (en) * 1998-04-09 2002-02-05 National Starch And Chemical Investment Holding Corporation Aerosol hair cosmetic compositions containing non-ionically derivatized starches
US6413505B1 (en) * 1998-04-09 2002-07-02 Nationa L Starch And Chemical Investment Holding Corporation Nonionically derivatized starches and their use in non-aerosol, low VOC hair cosmetic compositions
NO991662L (no) * 1998-04-09 1999-10-11 Nat Starch Chem Invest Ikke-ionisk derivatiserte stivelser og deres anvendelse i polyakrylsyreinneholdende haarkosmetiske sammensetninger med lav VOC
US6562325B2 (en) * 1998-04-09 2003-05-13 National Starch And Chemical Investment Holding Corporation Use of stabilized starches in low VOC, polyacrylic acid-containing hair cosmetic compositions
FR2779648B1 (fr) * 1998-06-15 2001-07-20 Oreal Composition cosmetique ou pharmaceutique se presentant sous forme de solide et pouvant etre deformable
WO2001019404A1 (fr) * 1999-09-15 2001-03-22 Avebe America, Inc. Amidon pregelatinise a epaississement par cisaillement
DE10019314C1 (de) * 2000-04-19 2001-09-20 Wella Ag Gelförmiges Haarbehandlungsmittel
US7083810B2 (en) * 2000-04-19 2006-08-01 Wella Aktiengesellschaft Cosmetic agent in the form of a gel

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO03084493A1 *

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DE10216499A1 (de) 2003-10-23
US20050191264A1 (en) 2005-09-01

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