EP1496847A1 - Agents coiffants moussants ou expansibles contenant des derives d'amidon pregelatinises a reticulation transversale - Google Patents

Agents coiffants moussants ou expansibles contenant des derives d'amidon pregelatinises a reticulation transversale

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Publication number
EP1496847A1
EP1496847A1 EP03720440A EP03720440A EP1496847A1 EP 1496847 A1 EP1496847 A1 EP 1496847A1 EP 03720440 A EP03720440 A EP 03720440A EP 03720440 A EP03720440 A EP 03720440A EP 1496847 A1 EP1496847 A1 EP 1496847A1
Authority
EP
European Patent Office
Prior art keywords
copolymers
acid
vinylpyrrolidone
use according
vinyl
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
EP03720440A
Other languages
German (de)
English (en)
Inventor
Marion Detert
Kerstin Liebelt
Viola Sass
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 EP1496847A1 publication Critical patent/EP1496847A1/fr
Ceased legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04—Dispersions; Emulsions
    • A61K8/046—Aerosols; Foams
    • 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
    • A61K8/416—Quaternary ammonium compounds
    • 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
    • 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

Definitions

  • the present invention relates to cosmetic hair styling preparations or styling agents with improved properties, in particular foam-like or foamable hairdressing agents with improved behavior when used, in particular when manually distributing the product on 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 a part of the sense of touch that should not be underestimated.
  • 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 in turn is made up of three layers: a central part - the so-called hair mark (medulla), which, however, is reduced in humans and is often completely absent - furthermore the marrow (cortex) and the outer cuticle layer (cuticle), which is 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 foam-like or foamable styling agents or hair setting agents (hair setting agents) based on water or alcohol / 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.
  • Foam stabilizers are aqueous or alcoholic / aqueous preparations which contain blowing agents in addition to setting polymers such as, for example, anionic polymers or preferably combinations of anionic polymers with nonionic or cationic polymers.
  • foam strengthener is the poor quality of the foam, which plays an important role for the consumer.
  • the foam often has a very firm consistency and is difficult to distribute in the hair or breaks very slowly. In other cases, the foam breaks quickly, but feels unkesmetically hard and brittle, similar to partially cured PU construction foam.
  • foamy or foamable aqueous or alcoholic / aqueous hairdressing agents containing blowing agents, one or more pregelatinized, crosslinked starch derivatives and anionic polymers remedy the deficiencies of the prior art.
  • modified starch Structure XL
  • film formers can be used to formulate foam setting agents which achieve very good hair strengthening and additionally act as a "foam booster" for the foam, the quality of the foam being influenced positively Foam becomes creamier, more cosmetic and easier to distribute.
  • the invention also encompasses the use of one or more pregelatinized, crosslinked starch derivatives to improve the distributability of foaming or foamable aqueous or alcoholic / aqueous hairdressing agents containing blowing agent containing anionic polymers.
  • Hydroxypropylated phosphate esters are preferably used as the pregelatinized, cross-linked starch derivatives. Hydroxypropyl distarch phosphate is particularly preferably used as the pregelatinized, cross-linked starch derivative.
  • Hairdressing agents or uses according to the invention are preferably characterized in that as an anionic polymer in the case of water-containing preparations at least one substance selected from the group of vinyl acetate / crotonic acid, vinyl acetate / acrylate and / or vinyl acetate / inylneodecanoate / 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- Vinyl pyrrolidone copolymers, methyl vinyl ether / maleic acid copolymers, which are formed by hydrolysis of vinyl ether / maleic anhydride copolymers and whose ethyl, isopropyl or butyl partial or full ester is used.
  • Hairdressing agents or uses according to the invention are preferably characterized in that the content of pregelatinized, crosslinked starch derivatives is 0.01 to 2% by weight, particularly preferably 0.1 to 0.5% by weight. Hair styling agents or uses according to the invention are particularly preferably characterized in that the weight ratio of solid to pregelatinized, crosslinked starch derivatives is 10 to 1 to 1 to 80, particularly preferably 1 to 4 to 1 to 80.
  • cationic polymers are also present, which are particularly preferably quaternized from the group vinylpyrrolidone / vinylimidazolium methochloride copolymers
  • Vinylpyrrolidone / dialkylaminoalkyl methacrylate copolymers cationic cellulose derivatives, preferably hydroxyethylcellulose / dimethylalkylammonium chloride copolymers, terpolymers of vinylcaprolactam / vinylpyrrolidone with dimethylaminoethyl methacrylate or vinylimmidazolinium methochloride and acrylamidocopolymers.
  • Hairdressing agents or uses according to the invention are preferably characterized in that, in addition to anionic polymers, nonionic polymers are also present, which are particularly preferably selected from the group of vinylpyrrolidone homopolymers or copolymers, preferably polyvinylpyrrolidone, copolymers of N-vinylpyrrolidone and vinyl acetate and / or vinyl propionate , Polyvinylcaprolactam, polyvinylamides and their salts as well as copolymers of vinylpyrrolidone and dimethylaminoethyl methacrylate, terpolymers of vinylcaprolactam, vinylpyrrolidone and dimethylaminoethyl methacrylate and polysiloxanes.
  • US 6248338 describes cosmetic preparations with pregelatinized, crosslinked starch derivatives, but this document could not point the way to the present invention.
  • 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 alcohol-containing hair sprays, liquid setting agents or solutions or as alcohol-free but water-containing foam setting agents, liquid setting agents, syling gels, foam aerosols, emulsions or solutions.
  • agents according to the invention can be present, for example, as preparations which can be removed from aerosol containers, squeeze bottles or by means of a pump, spray or foam device and optionally sprayable, but also in the form of an agent which can be applied from normal bottles and containers.
  • propellant for cosmetic or dermatological preparations which can be sprayed from aerosol containers or can be removed in the form of a foam
  • hair sprays or foaming agents are suitable for the customary, known volatile, liquefied propellants, for example dimethyl ether, hydrocarbons (propane, butane, isobutane), which can be used alone or as a mixture with one another.
  • Compressed air, nitrogen, nitrogen dioxide or carbon dioxide or mixtures of these substances can also be used advantageously.
  • 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.
  • polyurethanes include for example polyurethanes, polyvinyl pyrrolidone, copolymers of N-vinylpyrrolidone and vinyl acetate and / or vinyl propionate in various concentration ratios, polyvinyl caprolactam, polyvinyl amides and salts thereof and copolymers of vinylpyrrolidone and dimethylaminoethyl methacrylate, terpolymers of vinylcaprolactam, vinylpyrrolidone and dimethylaminoethyl methacrylate, polysiloxanes and the like.
  • anionic polymers are, for example, vinyl acetate / crotonic acid, vinyl acetate / acrylate and / or vinyl acetate / inylneodecanoate / 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- Vinyl pyrrolidone copolymers or polystyrene sulfates.
  • 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 which can be contained in preparations according to the invention alone or in a mixture, preferably also with anionic and / or nonionic polymers, are copolymers of N-octylacrylamide, (meth) acrylic acid and tert-butylaminoethyl methacrylate of the “amphomer” type, copolymers Methacryloylethylbetaine and alkyl methacrylates of the "Yukaformer” type, copolymers of monomers containing carboxyl groups or sulfone groups, for example (Meth) acrylic acid and itaconic acid, with basic monomers, in particular those containing amino groups, such as e.g.
  • 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, such as triethanolamine, triisopropanolamine, aminomethyl propanol and / or aminomethyl propanediol, can be used.
  • neutralization can take place partially or completely.
  • 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
  • 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, alcohols , Polyols and their toxicologically compatible ethers and esters, branched and / or unbranched hydrocarbons, further antioxidants, stabilizers, pH regulators, consistency regulators, 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, substances to reduce
  • 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, glycol, ethylene glycol, ethylene glycol monoethyl or monobutyl ether, propylene glycol monomethyl, monoethyl or monobutyl ether, Diethylene glycol monomethyl or monoethyl ether and analog products, furthermore alcohols with a low C number, e.g.
  • 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, aluminum silicates, polysaccharides or their derivatives, for example hyaluronic acid, xanthan gum, hydroxypropylmethyl cellulose, particularly advantageously the group of polyacrylates, preferably a polyacrylate from the group of so-called carbopoles, for example carbopoles of types 980, 981, 1382, 2984, 5984, each individually or in combination.
  • thickeners which one or more 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 the group of polyacrylates, preferably a polyacrylate from the group of so-called carbopoles, for example carbopoles of types 980
  • the proportion of thickeners 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 (eg glycine, histidine, tyrosine, tryptophan) and their derivatives, imidazoles (eg urocanic acid) and their derivatives, peptides such as D, L-carnosine, D-carnosine, L-camosine 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 eg glycine, histidine, tyrosine, tryptophan
  • imidazoles eg urocanic acid
  • peptides such as D, L-carnosine, D-carnosine, L-camosine 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) and sulfoximine compounds (e.g.
  • buthionine sulfoximines in very low tolerable dosages (e.g. pmol to ⁇ mol / kg), further (metal) Chelators (e.g. ⁇ -hydroxy fatty acids, palmitic acid, phytic acid, lactoferrin), ⁇ -hydroxy acids (e.g.
  • citric acid lactic acid, malic acid
  • humic acid bile acid, bile extracts, bilirubin, biliverdin, EDTA, E GTA and its 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. ascorbyl palmitate, Mg ascorbyl phosphate, ascorbyl acetate), tocopherols and derivatives (e.g.
  • vitamin E- acetate vitamin E- acetate
  • vitamin A and derivatives vitamin A palmitate
  • 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 ⁇ / A copolymer, which are sold under the trade name Luviskol VA 64W from the Company BASF or under the name PVP ⁇ / A W735 from the company International Specialty Products (ISP) are available in concentrations of 2 - 8 wt .-% 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 ⁇ / A copolymer, which are sold under the trade
  • 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 polyquaternium-11 (trade name Gafquat 755N, company International Specialty Products (ISP)) or are also preferred -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.
  • 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 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, e.g. based on citric acid / citrate or phosphoric acid phosphate buffer mixtures.
  • buffer mixtures e.g. based on citric acid / citrate or phosphoric acid phosphate buffer mixtures.
  • the pH is below 10, e.g. in the range of 3 to 9.
  • 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. Examples 1-3 Schaumfestiqer

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

Abstract

L'invention concerne des agents coiffants moussants ou expansibles, aqueux ou alcoolisés/aqueux, contenant un principe moussant, un ou plusieurs dérivés d'amidon prégélatinisés à réticulation transversale, et des polymères anioniques.
EP03720440A 2002-04-11 2003-04-09 Agents coiffants moussants ou expansibles contenant des derives d'amidon pregelatinises a reticulation transversale Ceased EP1496847A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE10216498A DE10216498A1 (de) 2002-04-11 2002-04-11 Frisiermittel
DE10216498 2002-04-11
PCT/EP2003/003679 WO2003084494A1 (fr) 2002-04-11 2003-04-09 Agents coiffants moussants ou expansibles contenant des derives d'amidon pregelatinises a reticulation transversale

Publications (1)

Publication Number Publication Date
EP1496847A1 true EP1496847A1 (fr) 2005-01-19

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EP03720440A Ceased EP1496847A1 (fr) 2002-04-11 2003-04-09 Agents coiffants moussants ou expansibles contenant des derives d'amidon pregelatinises a reticulation transversale

Country Status (4)

Country Link
US (1) US20050207992A1 (fr)
EP (1) EP1496847A1 (fr)
DE (1) DE10216498A1 (fr)
WO (1) WO2003084494A1 (fr)

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US20090098077A1 (en) * 2007-10-15 2009-04-16 Kpss-Kao Professional Salon Services Gmbh Two-Phase Composition for Improving Curl Retention
US20130309190A1 (en) * 2012-05-15 2013-11-21 L'oreal S.A. Hair cosmetic and styling compositions based on maleic acid copolymers and polyamines
DE102014225429A1 (de) 2014-12-10 2016-06-16 Henkel Ag & Co. Kgaa Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern
DE102014225438A1 (de) * 2014-12-10 2016-06-16 Henkel Ag & Co. Kgaa Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern
DE102019108227A1 (de) * 2019-03-29 2020-10-01 Henkel Ag & Co. Kgaa Trockenes Texturspray

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WO2003084494A1 (fr) 2003-10-16
DE10216498A1 (de) 2003-10-23

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