WO2012084876A2 - Copolymères cationiques de styrène/acrylate dans des agents de traitement capillaire - Google Patents

Copolymères cationiques de styrène/acrylate dans des agents de traitement capillaire Download PDF

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WO2012084876A2
WO2012084876A2 PCT/EP2011/073310 EP2011073310W WO2012084876A2 WO 2012084876 A2 WO2012084876 A2 WO 2012084876A2 EP 2011073310 W EP2011073310 W EP 2011073310W WO 2012084876 A2 WO2012084876 A2 WO 2012084876A2
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hair
cleansing
weight
cationic
total weight
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PCT/EP2011/073310
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German (de)
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WO2012084876A3 (fr
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Erik Schulze Zur Wiesche
Volker Scheunemann
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Henkel Ag & Co. Kgaa
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Priority to EP11802075.9A priority Critical patent/EP2654901A2/fr
Publication of WO2012084876A2 publication Critical patent/WO2012084876A2/fr
Publication of WO2012084876A3 publication Critical patent/WO2012084876A3/fr

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    • 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
    • A61Q5/12—Preparations containing hair conditioners
    • 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
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35—Ketones, e.g. benzophenone
    • A61K8/355—Quinones
    • 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
    • A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated 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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
    • 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
    • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
    • A61K8/4953—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom containing pyrimidine ring derivatives, e.g. minoxidil
    • 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
    • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
    • 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
    • A61K8/673—Vitamin B group
    • 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
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9706—Algae
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9783—Angiosperms [Magnoliophyta]
    • A61K8/9789—Magnoliopsida [dicotyledons]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9783—Angiosperms [Magnoliophyta]
    • A61K8/9794—Liliopsida [monocotyledons]
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q7/00—Preparations for affecting hair growth

Definitions

  • the invention is in the field of cosmetics and relates to hair cleansing and / or hair conditioning compositions containing a cationic styrene / acrylate copolymer and at least one active substance influencing the metabolic activity at the hair root.
  • the invention further relates to the use of the hair cleansing and / or hair conditioning agents for increasing the hair volume and / or the cell activity of the scalp and / or the hair root.
  • human hair In addition to their actual physiological role, such as thermal insulation and light protection, human hair has a psychosocial function that should not be underestimated. Among other things, they serve as a means of interpersonal communication and are a sign of their own individuality. Changes, including age-related, in hair growth, hair density, hair color and / or hair structure can lead to a massive impairment of the self-esteem of the person concerned.
  • Combination preparations often have the disadvantage that they contain a large number of very different cosmetic active ingredients, which interact with each other in an undesirable interaction and can deactivate.
  • the hair-treatment compositions should contain suitable active ingredients and / or combinations of active substances which can alleviate, eliminate, prevent and / or delay undesired (age-related) changes in the hair without impairing the stability of the means.
  • the hair treatment agents should positively affect keratin synthesis, hair growth, hair structure and / or hair repigmentation.
  • Another object of the invention was to find caring active ingredients or combinations of active ingredients for hair cleansing and / or hair conditioners that do not over-condition and / or complain the hair, but give the hair a natural shine, suppleness and increased volume.
  • the invention relates to hair cleansing and / or hair conditioning agents which are in a cosmetic carrier
  • At least one active substance influencing the metabolic activity at the hair root selected from
  • the hair cleansing and / or hair conditioning compositions according to the invention contain the components a) and b) in a cosmetic carrier, which may preferably be aqueous or aqueous-alcoholic.
  • a cosmetic carrier which may preferably be aqueous or aqueous-alcoholic.
  • the cosmetic carrier preferably contains at least 40% by weight of water.
  • the cosmetic carrier may contain 0.01 to 60% by weight, preferably 0.05 to 45% by weight and in particular 0.1 to 40% by weight of at least one alcohol which may be selected from ethanol, ethyl diglycol, 1-Propanol, 2-propanol, isopropanol, 1, 2-propylene glycol, glycerol, 1-butanol, 2-butanol, 1, 2-butanediol, 1, 3-butanediol, 1-pentanol, 2-pentanol, 1, 2 Pentanediol, 1, 5-pentanediol, 1, hexanol, 2-hexanol, 1, 2-hexanediol, 1, 6-hexanediol, sorbitol, benzyl alcohol, phenoxyethanol or mixtures of these alcohols.
  • at least one alcohol which may be selected from ethanol, ethyl diglycol, 1-Propanol, 2-propanol, isopropano
  • ethanol ethyl diglycol
  • 1-propanol 2-propanol
  • isopropanol 1, 2-propylene glycol
  • glycerol benzyl alcohol and / or phenoxyethanol and mixtures of these alcohols.
  • the hair cleansing and / or hair conditioning compositions according to the invention can be formulated as a shampoo, rinse, hair conditioner, hair tonic, hair tonic, hair spray, hair tip fluid, foam aerosol, hair wax, hair gel, hair dye, bleaching agent and / or hair shaping agent, and in principle contain all ingredients customary for these preparation forms.
  • compositions according to the invention are formulated as hair tonic and / or hair tonic and contain, based on their total weight, preferably 0 to 70% by weight of at least one alcohol.
  • hair lotions and / or hair tonics containing 10 to 65 wt .-%, especially 20 to 60 wt .-% and in particular 25 to 50 wt .-% of at least one alcohol.
  • Suitable alcohols which can be used in hair lotions and / or tonics according to the invention are the abovementioned alcohols.
  • C 1 -C 4 -alcohols such as ethanol, ethyldiglycol, 1-propanol, 2-propanol, isopropanol, 1, 2-propylene glycol, glycerol, 1-butanol, 2-butanol, 1, 2 Butanediol and / or 1, 3-butanediol and More preferred are ethanol, 1 - propanol, 2-propanol and / or isopropanol, and particularly preferred is ethanol.
  • Shampoo, conditioner, hair conditioner, hair dye, bleaching and / or hair shaping compositions and contain - based on their total weight - preferably 0.1 to 50 wt .-% of at least one surfactant which may be selected from anionic, nonionic, cationic and / or amphoteric / zwitterionic surfactants.
  • compositions according to the invention are formulated as a shampoo, rinse and / or hair conditioner.
  • Anionic surfactants and / or amphoteric / zwitterionic surfactants are preferably used in hair shampoos.
  • hair treatment compositions according to the invention which are formulated as hair shampoo,
  • Suitable anionic surfactants are the inventive agents - based on their total weight - preferably in amounts of from 0.5 to 25 wt .-%, more preferably from 1 to 20% by weight, particularly preferably from 2 to 17.5 wt .-% and especially from 3 to 15% by weight.
  • Suitable anionic surfactants include, for example:
  • Sulfosuccinic acid mono- and / or dialkyl esters having 8 to 24 C atoms in the alkyl group and sulfosuccinic acid monoalkylpolyoxyethyl esters having 8 to 24 C atoms in the alkyl group and 1 to 6 oxyethyl groups,
  • Alpha-olefin sulfonates having 8 to 24 C atoms
  • R-0 (CH 2 -CH 2 0) x -OS0 3 " X + , in which R is a preferably linear or branched, saturated or unsaturated alkyl group having 8 to 30 carbon atoms, x 0 or 1 to 12 and X is an alkali or ammonium ion,
  • R 1 is preferably an aliphatic hydrocarbon radical having 8 to 30 carbon atoms
  • R 2 is hydrogen, a radical (CH 2 CH 2 0) n R or X, n is from 1 to 10 and X is hydrogen, an alkali or alkaline earth metal or NR 3 R 4 R 5 R 6 , with R 3 to R 6 independently of one another represents a C 1 to C 4 hydrocarbon radical.
  • Preferred anionic surfactants are ether carboxylic acids of the abovementioned formula, acylsarcosides having 8 to 24 carbon atoms in the acyl group, sulfosuccinic mono- and / or dialkyl esters having 8 to 24 carbon atoms in the alkyl group and sulfosuccinic acid mono-alkylpolyoxyethyl esters having 8 to 24C -Atomen in the alkyl group and 1 to 6 oxyethyl groups, alpha-olefin sulfonates having 8 to 24 carbon atoms and / or alkyl sulfate and / or Alkylpolyglykolethersulfatsalze the aforementioned formula.
  • Particularly preferred anionic surfactants are straight-chain or branched alkyl ether sulfates which contain an alkyl radical having 8 to 18 and in particular 10 to 16 carbon atoms and 1 to 8 and in particular 2 to 4 ethylene oxide units.
  • anionic surfactants are straight-chain or branched alkyl sulfonates which contain an alkyl radical having 8 to 20 and in particular 10 to 18 carbon atoms. Particular preference is given to the sodium, magnesium and / or triethanolamine salts of linear or branched lauryl, tridecyl and / or myristyl sulfates which have a degree of ethoxylation of from 1 to 8.
  • Suitable amphoteric / zwitterionic surfactants may preferably be added to the compositions according to the invention, based on their total weight, in amounts of from 0.1 to 20% by weight, more preferably from 0.25 to 15% by weight, particularly preferably from 0.5 to 12 , 5 wt .-% and in particular from 1 to 10 wt .-% are added.
  • Suitable amphoteric / zwitterionic surfactants may be selected from compounds of the following formulas (i) to (v) in which the radical R is in each case a straight-chain or branched, saturated or mono- or polyunsaturated alkyl or alkene radical having 8 to 24 Carbon atoms, (I) l + 3
  • amphoteric / zwitterionic surfactants are alkylamidoalkylbetaines and / or alkylampho (di) acetates of the abovementioned formulas (i) to (v).
  • amphoteric / zwitterionic surfactants include the surfactants cocamidopropyl betaine and disodium cocoamphodiacetate known under the INCI name.
  • Cationic surfactants are preferably used in hair conditioning agents according to the invention (such as, for example, hair rinses and / or hair treatments).
  • Suitable cationic surfactants are, for example, quaternary ammonium compounds, esterquats and / or amidoamines.
  • Preferred quaternary ammonium compounds are ammonium halides, especially chlorides and bromides, such as alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkylmethylammonium chlorides, e.g.
  • alkyltrimethylammonium chlorides dialkyldimethylammonium chlorides and trialkylmethylammonium chlorides, e.g.
  • cetyltrimethylammonium chloride, stearyltrimethylammonium chloride, distearyldimethylammonium chloride, lauryldimethylammonium chloride, lauryldimethylbenzylammonium chloride and tricetylmethylammonium chloride as well as the imidazolium compounds known under the INCI names Quaternium-27, Quaternium-83 and Quaternium-87.
  • the alkyl chains of the above-mentioned surfactants preferably have 10 to 18 carbon atoms.
  • Esterquats are known substances which contain both at least one ester function and at least one quaternary ammonium group as a structural element.
  • Preferred esterquats are quaternized ester salts of fatty acids with triethanolamine, quaternized ester salts of fatty acids with diethanolalkylamines and quaternized ester salts of fatty acids with 1,2-dihydroxypropyldialkylamines.
  • Such products are marketed under the trade names Stepantex® ®, Dehyquart® ®, ® and Armocare® Quartamin ®.
  • alkylamidoamines are usually prepared by amidation of natural or synthetic fatty acids and fatty acid cuts with dialkylaminoamines.
  • a particularly suitable compound from this group of substances under the name Tegoamid ® S 18 stearamidopropyl commercially represent.
  • the cationic surfactants may be used in the hair conditioning compositions according to the invention preferably in an amount of 0.05 to 20 wt .-%, based on the total agent. Quantities of 0.1 to 15 wt .-% and in particular from 0.2 to 10 wt .-% are particularly preferred.
  • Suitable nonionic surfactants and / or emulsifiers are in the inventive compositions - based on their total weight - preferably in amounts of 0.01 to 20 wt .-%, preferably 0.05 to 15 wt .-% and in particular 0.1 to 10 wt .-% used.
  • nonionic surfactants / emulsifiers examples include
  • Amine oxides Addition products of 2 to 50 moles of ethylene oxide and / or 0 to 5 moles of propylene oxide to linear and branched fatty alcohols having 8 to 30 carbon atoms, to fatty acids having 8 to 30 carbon atoms and alkylphenols having 8 to 15 carbon atoms in the alkyl group .
  • alkyl oligoglucosides in particular alkyl oligoglucosides based on hydrogenated C 2 / i 4 coconut oil having a DP of 1 -3, as for example under INCI name "coco-glucosides" are commercially available.
  • nonionic surfactants are the C 8 -C 30 fatty acid mono- and diesters of addition products of 1 to 30 moles of ethylene oxide with glycerol. Particularly preferred are the Cio-C 6 -Fetklamono- and diesters of addition products of 1 to 10 moles of ethylene oxide to glycerol. Especially preferred is the PEG-7 glyceryl cocoate known under the INCI name.
  • Preferred surfactant combinations which can be used in hair shampoos according to the invention contain, based on the total weight of the shampoo:
  • Particularly preferred combinations of surfactants that can be used in hair shampoos according to the invention contain, based on the total weight of the shampoo:
  • At least one anionic surfactant selected from ether carboxylic acids, acylsarcosides having 8 to 24 carbon atoms in the acyl group, sulfosuccinic mono- and / or - dialkyl esters having 8 to 24 carbon atoms in the alkyl group and sulfosuccinic acid monoalkylpolyoxyethyl esters having 8 to 24 carbon atoms in the alkyl group and 1 to 6 oxyethyl groups, alpha-olefin sulfonates having 8 to 24 carbon atoms and / or alkyl sulfate and / or or alkyl polyglycol ether sulfate salts of the aforementioned formula and from 0.5 to 12.5% by weight of at least one zwitterionic / amphoteric surfactant selected from alkylamidoalkylbetaines and / or alkylampho (di) acetates of
  • At least one anionic surfactant selected from ether carboxylic acids, acylsarcosides having 8 to 24 carbon atoms in the acyl group, Sulfobernsteinklamono- and / or dialkyl esters having 8 to 24 carbon atoms in the alkyl group and sulfosuccinic monoalkylpolyoxyethylestern with 8 to 24 carbon atoms in the alkyl group and 1 to 6 oxyethyl groups, alpha-olefin sulfonates having 8 to 24 carbon atoms and / or alkyl sulfate and / or Alkylpolyglykolethersulfatsalzen the aforementioned formula and 0.05 to 15 wt .-% of at least one nonionic surfactant selected from C 8 -C 30 - fatty acid mono- and diesters of addition products of 1 to 30 moles of ethylene oxide with glycerol, addition products of
  • At least one anionic surfactant selected from ether carboxylic acids, acylsarcosides having 8 to 24 carbon atoms in the acyl group, Sulfobernsteinklamono- and / or dialkyl esters having 8 to 24 carbon atoms in the alkyl group and sulfosuccinic monoalkylpolyoxyethylestern with 8 to 24 C atoms in the alkyl group and 1 to 6 oxyethyl groups, alpha-olefin sulfonates having 8 to 24 C atoms and / or alkyl sulfate and / or alkylpolyglycol ether sulfate salts of the aforementioned formula, 0.5 to 12.5 wt.
  • anionic surfactant selected from ether carboxylic acids, acylsarcosides having 8 to 24 carbon atoms in the acyl group, Sulfobernsteinklamono- and / or dialkyl esters having 8 to
  • At least one amphoteric / zwitterionic surfactant selected from alkylamidoalkyl betaines and / or alkylampho (di) acetates of the aforementioned formulas (i) to (v) and 0.05 to 15% by weight of at least one nonionic surfactant selected from C 8 -C 30- fatty acid mono- and diesters of addition products of 1 to 30 moles of ethylene oxide with glycerol, addition products of 2 to 50 moles of ethylene oxide and / or 0 to 5 moles of propylene oxide with linear and branched fatty alcohols with 8 up to 30 carbon atoms, addition products of ethylene oxide onto fatty acid alkanolamides and / or alkyl polyglucosides,
  • At least one anionic surfactant selected from ether carboxylic acids, acylsarcosides having 8 to 24 carbon atoms in the acyl group, Sulfobernsteinklamono- and / or dialkyl esters having 8 to 24 carbon atoms in the alkyl group and sulfosuccinic monoalkylpolyoxyethylestern with 8 to 24 C atoms in the alkyl group and 1 to 6 oxyethyl groups, alpha-olefin sulfonates having 8 to 24 C atoms and / or alkyl sulfate and / or alkylpolyglycol ether sulfate salts of the aforementioned formula, 0.5 to 12.5% by weight of at least one amphoteric / zwitterionic surfactant selected from alkylamidoalkylbetaines and / or alkylampho (di) acetates of the abovementi
  • Especially preferred surfactant combinations that can be used in hair shampoos according to the invention contain, based on the total weight of the shampoo:
  • At least one anionic surfactant selected from straight-chain or branched alkyl ether sulfates having an alkyl radical having 8 to 18 and in particular having 10 to 16 carbon atoms and a degree of ethoxylation of 1 to 8, in particular 2 to 4, and / or straight-chain or branched alkyl sulfonates which contain an alkyl radical having 8 to 20 and in particular 10 to 18 carbon atoms and 1 to 10% by weight of at least one of the surfactants cocamidopropyl betaine and disodium cocoamphodiacetate known under the INCI name,
  • At least one anionic surfactant selected from straight-chain or branched alkyl ether sulfates having an alkyl radical having 8 to 18 and in particular having 10 to 16 carbon atoms and a degree of ethoxylation of 1 to 8, in particular 2 to 4, and / or straight-chain or branched alkyl sulfonates which contain an alkyl radical having 8 to 20 and in particular 10 to 18 carbon atoms and 0.1 to 10% by weight of at least one alkylpolyglycoside,
  • At least one anionic surfactant selected from straight-chain or branched alkyl ether sulfates having an alkyl radical having 8 to 18 and in particular having 10 to 16 carbon atoms and a degree of ethoxylation of 1 to 8, in particular 2 to 4, and / or straight-chain or branched alkyl sulfonates which contain an alkyl radical having 8 to 20 and in particular 10 to 18 carbon atoms, 1 to 10 wt.% of at least one of the surfactants cocamidopropyl betaine and disodium cocoamphodiacetates known under the INCI name and 0.1 to 10 %
  • an anionic surfactant selected from straight-chain or branched alkyl ether sulfates having an alkyl radical having 8 to 18 and in particular having 10 to 16 carbon atoms and a degree of ethoxylation of 1 to 8, in particular 2 to 4, and / or straight-chain or branched alkyl sulfonates which contain an alkyl radical having 8
  • At least one anionic surfactant selected from straight-chain or branched alkyl ether sulfates having an alkyl radical having 8 to 18 and in particular having 10 to 16 carbon atoms and a degree of ethoxylation of 1 to 8, in particular 2 to 4, and / or straight-chain or branched alkyl sulfonates which contain an alkyl radical having 8 to 20 and in particular 10 to 18 carbon atoms and 1 to 10 wt.% of at least one of the surfactants cocamidopropyl betaine and disodium cocoamphodiacetates known under the INCI name and 0.2 to 10 % By weight of quaternary ammonium compounds, esterquats and / or amidoamines.
  • the hair-cleansing and / or hair-conditioning compositions according to the invention contain the cationic copolymer X, preferably in an amount of from 0.001 to 10% by weight, preferably from 0.005 to 7.5% by weight, and in particular from 0.01 to - based on their total weight 5% by weight.
  • Suitable cationic copolymers X are preferably obtainable by copolymerization of butyl acrylate, ethyltrimonium chloride methacrylate and styrene and preferably have a weight average molecular weight of 10 to 250 kDa, more preferably 25 to 200 kDa, particularly preferably 50 to 150 kDa and especially of 80 to 120 kDa.
  • Such polymers are commercially available under the INCI name "butyl acrylate / ethyltrimonium chloride methacrylate / styrene copolymer”.
  • cationic copolymers X whose cationic groups are protected. Such protection can be achieved, for example, by nonionic side chains.
  • Polysaf ® 5600 A suitable commercial product that can be used as the cationic copolymer X in the inventive hair cleaning and / or hair conditioners, "Polysaf ® 5600” is. "Polysaf ® 5600” is offered by Dow Reichhold Specialty Latex, and is an approximately 40% aqueous suspension of the polymer known by the INCI name "butyl acrylate / ethyltrimonium chloride methacrylate / styrene copolymer".
  • the hair cleansing and / or hair conditioning compositions according to the invention contain the active substance (s) b) positively influencing the metabolic activity on the hair root.
  • B) - preferably in an amount of 0.001 to 10% by weight, preferably 0.005 to 5%, based on their total weight Wt .-% and in particular from 0.01 to 2 wt .-%.
  • Suitable biochinones are understood as meaning one or more ubiquinone (s) and / or plastoquinone (s).
  • n stands for the integers 6, 7, 8, 9 or 10.
  • compositions according to the invention are - also known under the name coenzyme Q10 - ubiquinone of the aforementioned formula in which n is the number 10.
  • n stands for the integers 6, 7, 8, 9 or 10
  • They can be isolated from chloroplasts and play a role as redox substrates in photosynthesis in cyclic and noncyclic electron transport, reversibly converting into the corresponding hydroquinones (plastoquinol).
  • Particularly preferred active compounds b) which can be used in the hair cleansing and / or hair conditioning compositions according to the invention are selected from taurine, caffeine, pantolactone, carnitine, coenzyme Q 10 and / or theophylline and from physiologically tolerated salts and / or derivatives of these compounds.
  • an inventive hair cleansing and / or hair conditioning composition is formulated as a hair shampoo and contains - based on its total weight - preferred 3 to 15 wt .-% of at least one anionic surfactant selected from straight-chain or branched alkyl ether sulfates having an alkyl radical having 8 to 18 and in particular having 10 to 16 carbon atoms and a degree of ethoxylation of 1 to 8, in particular 2 to 4, and / or straight-chain or branched alkyl sulfonates which contain an alkyl radical having 8 to 20 and in particular 10 to 18 carbon atoms,
  • 0.001 to 10 wt .-% of at least one metabolic activity at the hair root positively affecting drug selected from biotin, a biochinone, taurine, pantolactone, creatine, theophylline, caffeine, carnitine, rice extract, soybean extract, corn extract, wheat extract, rapeseed extract, algae extract Echinaceaex Track and / or physiologically acceptable salts and / or derivatives of these agents.
  • the hair shampoo contains - based on its total weight - 0.005 to 5 wt .-% taurine, caffeine, pantolactone, carnitine, coenzyme Q 10 and / or theophylline.
  • an inventive hair cleansing and / or hair conditioning composition is formulated as a hair shampoo and contains - based on its total weight - preferred
  • At least one anionic surfactant selected from straight-chain or branched alkyl ether sulfates having an alkyl radical having 8 to 18 and in particular having 10 to 16 carbon atoms and a degree of ethoxylation of 1 to 8, in particular 2 to 4, and / or straight-chain or branched alkyl sulfonates which contain an alkyl radical having 8 to 20 and in particular 10 to 18 carbon atoms,
  • the hair shampoo contains - based on its total weight - 0.005 to 5 wt .-% taurine, caffeine, pantolactone, carnitine, coenzyme Q 10 and / or theophylline.
  • a hair conditioning composition according to the invention is formulated as a hair conditioner or rinse and contains-based on its total weight-preferred
  • 0.001 to 10 wt .-% of at least one metabolic activity at the hair root positively affecting drug selected from biotin, a biochinone, taurine, pantolactone, creatine, theophylline, caffeine, carnitine, rice extract, soybean extract, corn extract, wheat extract, rapeseed extract, algae extract Echinaceaex Track and / or physiologically acceptable salts and / or derivatives of these agents.
  • the hair conditioner and / or the hair conditioner contains 0.005 to 5% by weight, based on their total weight, of taurine, caffeine, pantolactone, carnitine, coenzyme Q 10 and / or theophylline.
  • a hair conditioning composition according to the invention is formulated as hair tonic and contains - based on its total weight - preferred
  • 0.001 to 10 wt .-% of at least one metabolic activity at the hair root positively affecting drug selected from biotin, a biochinone, taurine, pantolactone, creatine, theophylline, caffeine, carnitine, rice extract, soybean extract, corn extract, wheat extract, rapeseed extract, algae extract Echinaceaex Track and / or physiologically acceptable salts and / or derivatives of these agents.
  • the cosmetic effect of the hair cleansing and / or hair conditioning compositions according to the invention can be significantly increased if, based on their total weight, they are preferably 0.01 to 10% by weight, more preferably 0.05 to 7.5% by weight. % and in particular 0.1 to 5 wt .-% of at least one - different from X - cationic polymers.
  • Suitable cationic polymers are, for example:
  • quaternized cellulose derivatives such as are available under the names of Celquat ® and Polymer JR ® commercially
  • hydrophobically modified cellulose derivatives for example those sold under the trade name SOFTCAT ® cationic polymers,
  • honey for example the commercial product Honeyquat ® 50,
  • cationic guar derivatives in particular those sold under the tradename Cosmedia Guar ® and Jaguar ® products,
  • Such compounds are available under the Be drawings Gafquat ® 734 and Gafquat ® 755 commercially
  • Vinylpyrrolidone vinylimidazoliummethochloride copolymers such as those offered under the names Luviquat.RTM ® FC 370, FC 550, FC 905 and HM 552,
  • Polyquaternium 2 Polyquaternium 17, Polyquaternium 18, Polyquaternium-24, Polyquaternium 27, Polyquaternium-32, Polyquaternium-37, Polyquaternium 74 and Polyquaternium 89 known polymers.
  • Suitable cationic polymers of the "temporarily cationic" polymers are usually contain an amino group present at certain pH values as a quaternary ammonium group and hence cationic.
  • chitosan and its derivatives are preferred, such as for example, under the trade designations Hydagen ® CMF, Hydagen® ® HCMF, Kytamer ® PC and Chitolam ® NB / 101 are freely available commercially.
  • chitosans are deacetylated, in different degrees of deacetylation and varying degrees of degradation (molecular weights) are commercially available.
  • Particularly preferred cationic polymers which can be used in the hair cleansing and / or hair conditioning compositions according to the invention are quaternized cellulose polymers, cationic guar derivatives and / or cationic polymers based on acrylic acid (derivative), which are selected, in particular, from the polyquaternium polymers known under the INCI names. 6, Polyquaternium-7, Polyquaternium-10, Polyquaternium-37 and / or Polyquaternium-67.
  • the hair cleansing and / or hair conditioning compositions according to the invention may also contain a number of other active ingredients which give them advantageous properties.
  • the preferred optional active substances that can be used in the hair cleansing and / or hair conditioning compositions according to the invention include, for example:
  • Oil, wax and / or fat components which in the respective hair treatment compositions (based on their total weight) preferably in an amount of 0.01 to 20 wt .-%, particularly preferably from 0.05 to 15 wt.% And in particular from 0.1 to 10% by weight can be used,
  • Anti-dandruff active ingredients which in the respective hair treatment compositions (based on their total weight) preferably in an amount of 0.025 to 7.5 wt .-%, particularly preferably from 0.05 to 5 wt .-% and in particular from 0.075 to 3 wt .-% can be used.
  • Suitable oil and / or fat components may preferably be selected from mineral, natural and synthetic oil components and / or fatty substances.
  • natural (vegetable) oils usually triglycerides and mixtures of triglycerides are used.
  • Preferred natural oils are coconut oil, (sweet) almond oil, walnut oil, peach kernel oil, apricot kernel oil, avocado oil, tea tree oil, soybean oil, sesame oil, sunflower oil, tsubaki oil, evening primrose oil, rice bran oil, palm kernel oil, mango seed oil, essence foam herb oil, safflower oil, macadamia nut oil, grapeseed oil, Amaranth seed oil, argan oil, bamboo oil, olive oil, wheat germ oil, pumpkin seed oil, mallow oil, hazelnut oil, safflower oil, canola oil, sasanqua oil, jojoba oil, rambutan oil, cocoa butter and shea butter.
  • mineral oils are used in particular mineral oils, paraffin and Isoparaffinöle and synthetic hydrocarbons.
  • An example of a usable hydrocarbon is for example that available as a commercial product 1, 3-di- (2-ethylhexyl) - cyclohexane (Cetiol ® S).
  • Suitable synthetic oils are silicone compounds. Silicones have excellent conditioning properties on the hair. In particular, they cause better combability of the hair in the wet and dry state and in many cases have a positive effect on the hair and the softness of the hair.
  • Suitable silicones may be selected from:
  • polyalkyl siloxanes polyaryl siloxanes, polyalkylaryl siloxanes which are volatile or nonvolatile, straight chain, branched or cyclic, crosslinked or uncrosslinked;
  • grafted silicone polymers having a non-silicone organic backbone consisting of an organic backbone formed from organic monomers containing no silicone grafted with at least one polysiloxane macromer in the chain and optionally at least one chain end;
  • oil component may further serve a dialkyl ether.
  • Useful dialkyl ethers are, in particular, di-n-alkyl ethers having a total of from 12 to 36 carbon atoms, in particular from 12 to 24 carbon atoms, such as, for example, di-n-octyl ether, di-n-decyl ether, di-n-nonyl ether, di-n undecyl ether, di-n-dodecyl ether, n-hexyl n-octyl ether, n-octyl n-decyl ether, n- Decyl n-undecyl ether, n-undecyl n-dodecyl ether and n-hexyl n-undecyl ether, and also di-tert-butyl ether, di-isopentyl ether, di-3-ethyl decyl ether, tert-butyl n-octyl
  • di-n-octyl ether which is commercially available under the name Cetiol ® OE.
  • Fatty substances are to be understood fatty acids, fatty alcohols and natural and synthetic waxes, which may be present both in solid form and liquid in aqueous dispersion.
  • the fatty acids used can be linear and / or branched, saturated and / or unsaturated fatty acids having 6 to 30 carbon atoms. Preference is given to fatty acids having 10 to 22 carbon atoms. Among these could be mentioned, for example, isostearic as the commercial products Emersol ® 871 and Emersol ® 875, and isopalmitic acids such as the commercial product Edenor ® IP 95, and all other products sold under the trade names Edenor ® (Cognis) fatty acids.
  • fatty acids are caproic, caprylic, 2-ethylhexanoic, capric, lauric, isotridecanoic, myristic, palmitic, palmitoleic, stearic, isostearic, oleic, elaidic, petroselic, linoleic, linolenic as well as their technical mixtures.
  • fatty acid cuttings obtainable from coconut oil or palm oil;
  • stearic acid is usually preferred.
  • fatty alcohols it is possible to use saturated, mono- or polyunsaturated, branched or unbranched fatty alcohols with C 6 -C 30 -, preferably C 10 -C 22 -and very particularly preferably C 12 -C 22 -carbon atoms.
  • the fatty alcohols are derived from preferably natural fatty acids, which can usually be based on recovery from the esters of fatty acids by reduction.
  • those fatty alcohol cuts which are produced by reduction of naturally occurring triglycerides such as beef tallow, palm oil, peanut oil, rapeseed oil, cottonseed oil, soybean oil, sunflower oil and linseed oil or fatty acid esters formed from their transesterification products with corresponding alcohols, and thus represent a mixture of different fatty alcohols.
  • Such substances are, for example, under the names Stenol ® such as Stenol ® 1618 or Lanette ® such as Lanette ® O or Lorol ®, for example, Lorol ® C8, Lorol C14 ®, Lorol C18 ®, ® Lorol C8-18, HD-Ocenol ®, Crodacol ® such as Crodacol CS ®, ® Novol, Eutanol ® G, Guerbitol ® 16, Guerbitol ® 18, Guerbitol ® 20, Isofol ® 12, Isofol ® 16, lsofol ® 24, Isofol ® 36, Isocarb 12, Isocarb 16 or Isocarb 24 commercially available.
  • wool wax alcohols as are commercially available, for example under the names of Corona ®, White Swan ®, Coronet ® or Fluilan ® can be used according to the invention.
  • waxes there may be used solid paraffins or isoparaffins, carnauba waxes, beeswaxes, candelilla waxes, ozokerites, ceresin, spermaceti, sunflower wax, fruit waxes such as apple wax or citrus wax, microwaxes of PE or PP.
  • Such waxes are available, for example, from Kahl & Co., Trittau.
  • fatty substances are, for example
  • Ester oils are to be understood as meaning the esters of C 6 - C 30 fatty acids with C 2 - C 30 fatty alcohols.
  • the monoesters of the fatty acids with alcohols having 2 to 24 carbon atoms are preferred.
  • Examples of fatty acid components used in the esters are caproic, caprylic, 2-ethylhexanoic, capric, lauric, isotridecanoic, myristic, palmitic, palmitoleic, stearic, isostearic, oleic, elaidic, petroselic, linoleic, linolenic Behenic acid and erucic acid and their technical mixtures.
  • fatty alcohol components in the ester oils are isopropyl alcohol, caproic alcohol, capryl alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, linolyl alcohol, linolenyl alcohol, elaeostearyl alcohol, arachyl alcohol, gadoleyl alcohol , Behenyl alcohol, erucyl alcohol and brassidyl alcohol and their technical mixtures.
  • isopropyl myristate IPM Rilanit ®
  • isononanoic acid C16-18 alkyl ester Cetiol ® SN
  • 2-ethylhexyl palmitate Cegesoft ® 24
  • stearic acid-2-ethylhexyl ester Cetiol ® 868
  • cetyl oleate glycerol tricaprylate, caprate Kokosfettalkohol- / caprylate (Cetiol ® LC)
  • n-butyl stearate oleyl erucate
  • isopropyl palmitate IPP Rilanit ®
  • oleyl Oleate Cetiol ®
  • hexyl laurate Cetiol ® A
  • di-n-butyl adipate Cetiol ® B
  • Dicarboxylic acid esters such as di-n-butyl adipate, di- (2-ethylhexyl) adipate, di- (2-ethylhexyl) succinate and di-isotridecyl acelate
  • diol esters such as ethylene glycol dioleate, ethylene glycol diisotridecanoate, propylene glycol di (2- ethylhexanoate), propylene glycol diisostearate,
  • ethoxylated or non ethoxylated mono, - di- and trifatty acid esters of saturated and / or unsaturated linear and / or branched fatty acids with glycerol such as Monomuls 90-018 ®, ® Monomuls 90-L12, Cetiol ® HE or Cutina ® MD.
  • Suitable antidandruff active ingredients may be selected from piroctone olamine, climbazole, zinc pyrithione, ketoconazole, salicylic acid, sulfur, selenium sulfide, tar preparations, undecenoic acid derivatives, burdock root extracts, poplar extracts, nettle extracts, walnut shell extracts, birch extracts, willow bark extracts, rosemary extracts and / or arnica extracts.
  • compositions of the invention include, for example
  • Vitamins Vitamins, vitamin derivatives and / or vitamin precursors
  • Suitable vitamins are preferably the following vitamins, provitamins and vitamin precursors and their derivatives:
  • Vitamin A the group of substances called vitamin A includes retinol (vitamin A) and 3,4-didehydroretinol (vitamin A 2 ).
  • the ß-carotene is the provitamin of retinol.
  • vitamin A component for example, vitamin A acid and its esters, vitamin A aldehyde and vitamin A alcohol and its esters such as the palmitate and the acetate into consideration.
  • Vitamin B belong to the vitamin B group or to the vitamin B complex among others
  • Vitamin B 3 • Vitamin B 3 .
  • the compounds nicotinic acid and nicotinamide (niacinamide) are often performed.
  • Vitamin B 5 pantothenic acid and panthenol.
  • panthenol is preferred.
  • Useful derivatives of panthenol are, in particular, the esters and ethers of panthenol, as well as cationically derivatized panthenols. Individual representatives are, for example, panthenol triacetate, panthenol monoethyl ether and its monoacetate, as well as cationic panthenol derivatives.
  • Vitamin B 6 pyridoxine and pyridoxamine and pyridoxal
  • Vitamin C ascorbic acid: use in the form of palmitic acid ester, glucosides or phosphates may be preferred. The use in combination with tocopherols may also be preferred.
  • Vitamin E tocopherols, especially a-tocopherol.
  • Vitamin F is usually understood as meaning essential fatty acids, in particular linoleic acid, linolenic acid and arachidonic acid.
  • the hair cleansing and / or hair conditioning compositions according to the invention may preferably contain vitamins, provitamins and vitamin precursors from groups A, B and E.
  • nicotinic acid amide or panthenol are particularly preferred.
  • Vitamins, vitamin derivatives and / or vitamin precursors may be present in the hair cleansing and / or hair conditioning agents (based on their total weight) preferably in an amount of 0.001 to 10% by weight, preferably 0.005 to 7.5% by weight and in particular 0.01 be used to 5 wt .-%.
  • Suitable plant extracts are extracts that can be made from any part of a plant.
  • extracts are produced by extraction of the whole plant. However, in individual cases it may also be preferred to prepare the extracts exclusively from flowers and / or leaves of the plant.
  • Particularly preferred for use in the hair treatment compositions according to the invention are the extracts of green tea, stinging nettle, witch hazel, chamomile, aloe vera, ginseng, Echinacea purpurea, Olea europea and / or Boerhavia diffusa roots.
  • alcohols and mixtures thereof can be used as extraction agent for the preparation of said plant extracts water.
  • the alcohols are lower alcohols such as ethanol and isopropanol, but especially polyhydric alcohols such as ethylene glycol and propylene glycol, both as sole extractant and in admixture with water, are preferred.
  • Plant extracts based on water / propylene glycol in a ratio of 1:10 to 10: 1 have proven to be particularly suitable.
  • the plant extracts can be used both in pure and in diluted form. If they are used in diluted form, they usually contain about 2 to 80 wt .-% of active substance and as a solvent used in their extraction agent or extractant mixture.
  • the plant extracts may in the hair cleansing and / or hair conditioning compositions according to the invention (based on their total weight) preferably in an amount of 0.01 to 10 wt .-%, preferably 0.05 to 7.5 wt .-% and in particular 0.1 be used to 5 wt .-%.
  • Suitable humectants or penetrants and / or swelling agents which can be added to the hair cleansing and / or hair conditioning agents according to the invention are, for example, urea and urea derivatives, guanidine and its derivatives, arginine and its derivatives, water glass, imidazole and its derivatives, histidine and its derivatives , Benzyl alcohol, glycerol, glycol and glycol ethers, propylene glycol and propylene glycol ethers, for example propylene glycol monoethyl ether, carbonates, bicarbonates, diols and triols, and in particular 1, 2-diols and 1, 3-diols such as 1, 2-propanediol, 1, 2-pentanediol , 1, 2-hexanediol, 1, 2-dodecanediol, 1, 3-propanediol, 1, 6-hexanediol, 1, 5-pentanedio
  • the humectants may in the compositions of the invention - based on the total weight - preferably in amounts of 0.01 to 10 wt .-%, more preferably in amounts of 0.05 to 5 wt .-% and in particular in amounts of 0.1 to 3 wt .-% are used.
  • Wrk-, auxiliaries and additives that can be used in the hair cleansing and / or hair conditioning according to the invention, for example:
  • Thickening agents such as gelatin or vegetable gums, for example agar-agar, guar gum, alginates, xanthan gum, gum arabic, karaya gum, locust bean gum, linseed gums, dextrans, cellulose derivatives, e.g. As methylcellulose, hydroxyalkylcellulose and carboxymethylcellulose, starch fractions and derivatives such as amylose, amylopectin and dextrins, clays and phyllosilicates such. As bentonite or fully synthetic hydrocolloids such.
  • polyvinyl alcohol the Ca, Mg or Zn - soaps,
  • Structurants such as maleic acid and lactic acid
  • fiber-structure-improving active ingredients in particular mono-, di- and oligosaccharides such as, for example, glucose, galactose, fructose, fructose and lactose,
  • Substances for adjusting the pH for example ⁇ - and ⁇ -hydroxycarboxylic acids such as citric acid, lactic acid, malic acid, glycolic acid,
  • Active ingredients such as bisabolol,
  • Ceramides are understood as meaning N-acylsphingosine (fatty acid amides of sphingosine) or synthetic analogs of such lipids (so-called pseudo-ceramides), Propellants such as propane-butane mixtures, N 2 O, dimethyl ether, C0 2 and air,
  • Bodying agents such as sugar esters, polyol esters or polyol alkyl ethers,
  • Preservatives such as sodium benzoate or salicylic acid
  • Viscosity regulators such as salts (NaCl).
  • the hair cleansing and / or hair conditioning agents according to the invention preferably have pH values in the range from 1 to 7, preferably from 2 to 6.5 and in particular from 3 to 6.
  • the hair cleansing and / or hair conditioning compositions according to the invention have excellent properties when applied to the hair.
  • the hair cleansing and / or hair conditioning agents according to the invention stimulate the metabolic activity at the hair root, whereby the hair is strengthened in its structure. Furthermore, the keratin synthesis is positively influenced, whereby the hair growth can be accelerated.
  • hair after treatment with the hair cleansing and / or hair conditioning compositions according to the invention have a stronger and glossier effect and an increased volume.
  • a second object of the invention is the cosmetic use of a hair cleansing and / or hair conditioning agent according to the invention for increasing the hair volume and / or the cell activity of the scalp and / or the hair root.
  • Salicylic acid 0.2-0.3 0.3

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Abstract

L'invention concerne des agents de lavage et/ou de conditionnement des cheveux, contenant dans un véhicule cosmétique a) au moins un copolymère cationique X renfermant les monomères butylacrylate, chlorure de triméthylammoniuméthylméthacrylate et styrène, et b) au moins un agent actif influençant de façon positive l'activité métabolique sur la racine des cheveux, choisi parmi biotine, bichinone, taurine, pantolactone, créatine, théophylline, caféine, carnitine, un extrait de riz, de soja, de maïs, de blé, de colza, d'algue et/ou d'échinacée, et/ou un sel et/ou dérivé physiologiquement compatible de ces agents actifs. Les agents de lavage et/ou de conditionnement des cheveux confèrent aux cheveux ainsi traités des propriétés avantageuses, notamment plus de volume.
PCT/EP2011/073310 2010-12-20 2011-12-20 Copolymères cationiques de styrène/acrylate dans des agents de traitement capillaire WO2012084876A2 (fr)

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DE102010063584A DE102010063584A1 (de) 2010-12-20 2010-12-20 Kationische Styrol/Acrylat-Copolymere in Haarbehandlungsmitteln
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WO2017202651A1 (fr) * 2016-05-27 2017-11-30 Unilever Plc Compositions antimicrobiennes d'hygiène corporelle
CN110461341A (zh) * 2017-03-31 2019-11-15 莱雅公司 头发处理组合物
US10993896B2 (en) 2015-05-01 2021-05-04 L'oreal Compositions for altering the color of hair
US11083675B2 (en) 2015-11-24 2021-08-10 L'oreal Compositions for altering the color of hair
US11090249B2 (en) 2018-10-31 2021-08-17 L'oreal Hair treatment compositions, methods, and kits for treating hair
US11135150B2 (en) 2016-11-21 2021-10-05 L'oreal Compositions and methods for improving the quality of chemically treated hair
FR3111794A1 (fr) * 2020-06-30 2021-12-31 L'oreal Compositions cosmetiques capables de former une emulsion
US11213470B2 (en) 2015-11-24 2022-01-04 L'oreal Compositions for treating the hair
US11419809B2 (en) 2019-06-27 2022-08-23 L'oreal Hair treatment compositions and methods for treating hair
US11433011B2 (en) 2017-05-24 2022-09-06 L'oreal Methods for treating chemically relaxed hair
US11596588B2 (en) 2017-12-29 2023-03-07 L'oreal Compositions for altering the color of hair
US12048759B2 (en) 2021-11-19 2024-07-30 L'oreal Compositions for treating the hair

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DE102008001770A1 (de) * 2008-05-13 2009-11-19 Beiersdorf Ag Kosmetische Zubereitungen gegen Kopfhautschuppen

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US9913789B2 (en) 2013-07-29 2018-03-13 Evonik Degussa Gmbh Formulations containing sphinganine
WO2015014558A2 (fr) 2013-07-29 2015-02-05 Evonik Industries Ag Formulations contenant de la sphinganine
DE102013214713A1 (de) 2013-07-29 2015-01-29 Evonik Industries Ag Formulierungen enthaltend Sphinganin
WO2016139125A1 (fr) * 2015-03-04 2016-09-09 Henkel Ag & Co. Kgaa Produits cosmétiques contenant une substance bioactive et un dipeptide
US10993896B2 (en) 2015-05-01 2021-05-04 L'oreal Compositions for altering the color of hair
US11083675B2 (en) 2015-11-24 2021-08-10 L'oreal Compositions for altering the color of hair
US11191706B2 (en) 2015-11-24 2021-12-07 L'oreal Compositions for altering the color of hair
US11213470B2 (en) 2015-11-24 2022-01-04 L'oreal Compositions for treating the hair
CN109152708A (zh) * 2016-05-27 2019-01-04 荷兰联合利华有限公司 抗微生物个人清洁组合物
US11364188B2 (en) 2016-05-27 2022-06-21 Conopco, Inc. Antimicrobial personal cleansing compositions
WO2017202651A1 (fr) * 2016-05-27 2017-11-30 Unilever Plc Compositions antimicrobiennes d'hygiène corporelle
US11135150B2 (en) 2016-11-21 2021-10-05 L'oreal Compositions and methods for improving the quality of chemically treated hair
CN110461341A (zh) * 2017-03-31 2019-11-15 莱雅公司 头发处理组合物
EP3615040A4 (fr) * 2017-03-31 2020-12-16 L'Oreal Compositions de traitement capillaire
US11433011B2 (en) 2017-05-24 2022-09-06 L'oreal Methods for treating chemically relaxed hair
US11596588B2 (en) 2017-12-29 2023-03-07 L'oreal Compositions for altering the color of hair
US11090249B2 (en) 2018-10-31 2021-08-17 L'oreal Hair treatment compositions, methods, and kits for treating hair
US11975092B2 (en) 2018-10-31 2024-05-07 L'oreal Hair treatment compositions, methods, and kits for treating hair
US11419809B2 (en) 2019-06-27 2022-08-23 L'oreal Hair treatment compositions and methods for treating hair
WO2022000051A1 (fr) * 2020-06-30 2022-01-06 L'oreal Compositions cosmétiques pouvant former une émulsion
FR3111794A1 (fr) * 2020-06-30 2021-12-31 L'oreal Compositions cosmetiques capables de former une emulsion
US12048759B2 (en) 2021-11-19 2024-07-30 L'oreal Compositions for treating the hair

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