WO2012163406A1 - Composition de traitement des cheveux - Google Patents

Composition de traitement des cheveux Download PDF

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Publication number
WO2012163406A1
WO2012163406A1 PCT/EP2011/058952 EP2011058952W WO2012163406A1 WO 2012163406 A1 WO2012163406 A1 WO 2012163406A1 EP 2011058952 W EP2011058952 W EP 2011058952W WO 2012163406 A1 WO2012163406 A1 WO 2012163406A1
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Prior art keywords
composition according
hair
weight
composition
concentration
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PCT/EP2011/058952
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English (en)
Inventor
Britta Punsch
Christine Cajan
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Kao Germany GmbH
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KPSS Kao Professional Salon Services GmbH
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Priority to PCT/EP2011/058952 priority Critical patent/WO2012163406A1/fr
Publication of WO2012163406A1 publication Critical patent/WO2012163406A1/fr
Anticipated expiration legal-status Critical
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    • 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
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/25—Silicon; Compounds 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
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0241—Containing particulates characterized by their shape and/or structure
    • 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
    • A61K8/044—Suspensions
    • 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
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • 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
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/29—Titanium; Compounds 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
    • A61K8/31—Hydrocarbons
    • 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
    • A61K8/55—Phosphorus compounds
    • A61K8/556—Derivatives containing from 2 to 10 oxyalkylene groups
    • 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
    • A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • 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
    • A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/927—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of insects, e.g. shellac
    • 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
    • A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
    • 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
    • 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
    • A61K2800/41—Particular ingredients further characterized by their size
    • A61K2800/412—Microsized, i.e. having sizes between 0.1 and 100 microns

Definitions

  • Present invention relates to an aqueous composition comprising insoluble particles suspended therein for conditioning, especially styling and matifying of hair.
  • compositions for matifying hair have increasingly been used which are basically emulsions and usually comprising a wax component suspended and or emulsified in an aqueous medium.
  • Such compositions do not provide optimal long lasting conditioning, especially styling and matifying effects and especially, hair styling is laborious because of long drying time of the product on hair, especially when applied onto dry hair, without using hair drier.
  • residues have always been visible on hair and hair has a gray shimmer which disturbs cosmetically appealing appearance of hair.
  • WO 2009/056398 A2 discloses a mat wax composition comprising wax components with a melting temperature above 40 °C and specially treated solid particles with a particle size up to 1 ⁇ .
  • the document does not refer to quick drying properties and does not disclose any composition which may be taken as closely related to the present invention.
  • WO 01 /7431 1 A2 is on leave-in hair conditioning composition comprising non- spherical micro-particles with a size less than 100 ⁇ and a water swellable polymer.
  • Document does not necessarily relate to a wax comprising composition and does not address matifying effect together with quick drying property and visibility of the particles after application and especially drying.
  • an aqueous composition comprising wax, surfactant and particles dispersed therein show excellent
  • conditioning especially styling matifying and effects and composition dries quickly and especially no visible particles have been observed on the hair after application and drying. It has furthermore been found out that the matifying and styling effects and also conditioning effect are long lasting.
  • the first object of the present invention is an aqueous composition for hair comprising at least 20% by weight water, 10 to 60% by weight of at least one wax which is solid at 20 °C, at least one emulsifying surfactant at a concentration in the range of 2 to 25% by weight and dispersed particles with a size below 200 ⁇ measured with sieve analysis at a concentration of 1 to 35% by weight, wherein all values are calculated to total composition.
  • Second object of the present invention is that the aqueous composition comprises inert non-swelling particles.
  • the aqueous composition comprises particles of at least one inert non-swelling inorganic compound.
  • Further object of the present invention is the use of the aqueous composition for conditioning, styling and matifying hair.
  • matifying it is meant that the hair shine is reduced so that intensity of the light reflected is considerably less, preferably no light reflection takes place.
  • compositions of the present invention are used as leave in compositions, not rinsed off from hair after application.
  • another object of the present invention is process for conditioning and/or styling and/or mattifying hair wherein the composition of the present invention is applied onto dry hair and optionally hair is dried.
  • composition of the present invention is preferably provided to the users, consumers, in the form of a kit comprising more than one container, preferably 2 to 5, more preferably 2 to 4 and most preferably 2 to 3 containers wherein one of the containers comprises a composition of the present invention.
  • Aqueous composition of the present invention comprises at least 20% by weight water, calculated to total of the composition.
  • aqueous composition comprises water at a concentration of 20 to 80% by weight, more preferably 30 to 70% by weight and most preferably 35 to 60% by weight and in particular 35 to 55% by weight, calculated to total of the composition.
  • Composition of the present invention comprise at least one wax component at a concentration of 10 to 60% by weight, preferably 15 to 60% by weight, more preferably 15 to 50% by weight, most preferably 20 to 40% by weight calculated to total of the composition.
  • wax refers to any compound with a melting point above 20 °C preferably above 30°C and more preferably 40°C. Suitable ones petrolatum, ozokerit, carnauba wax, paraffin, lanolin wax, candelila wax, bees wax, microcrystalline wax, cocoglyceride, fatty alcohols and their ethoxylated derivatives.
  • glycerin fatty acid esters with an acyl chain length of 14 to 24 C atoms which may be straight or branched and may have one or more substitutions, with a melting point above 40 °C such as glyceryl stearate, palmitate, behenate etc. which may further be ethoxylted and/or propoxylated.
  • Suitable wax components are fatty alcohols such as cetyl alcohol, stearyl alcohol, myristyl alcohol, behenyl alcohol and their mixtures.
  • wax components are ethoxylated fatty acids with an acyl chain length of 14 to 24 C atoms with a melting point above 40 °C such as PEG-100 stearate.
  • Preferred wax components are beeswax, petrolatum, ozokerit, carnauba wax and their mixtures.
  • Composition of the present invention comprises at least one surfactant preferably selected from anionic and non-ionic surfactants.
  • Suitable sulphate surfactants are according to the general structure wherein R is an alkyl chain which may be saturated or unsaturated, straight or branched with 10 to 22 C atoms, preferably 12 to 20 and more preferably 12 to 18 and most preferably 1 2 to 16 C atoms, n is a number between 0 and 5 and M is a cation and preferably sodium, potassium or ammonium, more preferably sodium or ammonium.
  • alkyl sulphates such as sodium lauryl sulphate, sodium cetyl sulphate, sodium stearyl sulphate and alkyl ether sulphates such as sodium laureth sulphate, sodium myreth sulphate, sodium ceteth sulphate, sodium oleth sulphate, sodium steareth sulphate, ammonium laureth sulphate, ammonium myreth sulphate, ammonium oleth sulphate, ammonium ceteth sulphate, ammonium steareth sulphate.
  • alkyl sulphates such as sodium lauryl sulphate, sodium cetyl sulphate, sodium stearyl sulphate and alkyl ether sulphates such as sodium laureth sulphate, sodium myreth sulphate, sodium ceteth sulphate, sodium oleth sulphate, sodium steareth sulphate, ammonium laure
  • Suitable surfactants of the carboxylate type are alkyl polyether carboxylic acids and the salts thereof of the formula
  • R 2 - (C 2 H 4 0) n - O - CH 2 COOX wherein R 9 is a C 8 -C 20 -alkyl group, preferably a Ci 2 -Ci 4 -alkyl group, n is a number from 1 to 20, preferably 2 to 1 7, and X is H or preferably a cation of the group sodium, potassium, magnesium and ammonium, which can optionally be hyd roxyal ky I -s ubsti tuted .
  • Suitable anionic aminocarboxylate surfactants are also C 8 -C 22 -acyl aminocarboxylic acids or the water-soluble salts thereof, such as N-lauroyl glutamate, in particular as sodium salt, as well as, for example, N-lauroyl sarcosinate, N-Ci 2 -Ci 8 -acyl asparaginic acid, N-myristoyl sarcosinate, N-oleoyl sarcosinate, N-lauroyl methylalanine, N-lauroyl lysine and N-lauroyl aminopropyl glycine, preferably in form of the water-soluble alkali or ammonium, in particular the sodium salts thereof, preferably in mixture with the above-named anionic surfactants.
  • anionic surfactants to mention are a-olefin sulfonates or the salts thereof, and in particular alkali salts of sulfosuccinic acid semiesters, for example, the disodium salt of monooctyl sulfosuccinate and alkali salts of long-chain monoalkyl ethoxysulfosuccinates.
  • Particularly preferred anionic surfactants are phosphate surfactants and especially the ones according to general structure
  • R 3 is an alkyl chain which may be saturated or unsaturated branched or straight with 8 to 22 C atoms, preferably 10 to 18 C atoms and more preferably 1 2 to 16 C atoms, x and y are in the range of 0 to 10 with the condition x+y is more than 0.
  • Suitable and most preferred anionic phosphate surfactant is Trilaureth-4 phosphate and its salts.
  • Suitable non-ionic surfactants are alkyl polyglucosides of the general formula wherein R 12 is an alkyl group with 8 to 18 carbon atoms, R 13 is an ethylene or propylene group, Z is a saccharide group with 5 to 6 carbon atoms, n is a number from 0 to 10 and x is a number between 1 and 5. Examples are decyl polyglucoside, cocoyl polyglucoside both are commercially available.
  • nonionic surfactant components are, for example, long-chain fatty acid mono- and dialkanolamides, such as coco fatty acid monoethanolamide and myristic fatty acid monoethanolamide.
  • non-ionic surfactants are, for example, the various sorbitan esters, such as polyethylene glycol sorbitan stearic acid ester, fatty acid polyglycol esters or poly-condensates of ethyleneoxide and propyleneoxide, as they are on the market, for example, under the trade name "Pluronics R ".
  • Further nonionic surfactants as emulsifiers useful in the compositions according to invention are Ci 0 -C 2 2-fatty alcohol ethoxylates.
  • Ci 0 -C 2 2-fatty alcohol ethers the alkyl polyglycol ethers known by the generic terms “Laureth”, “Myristeth”, “Oleth”, “Ceteth”, “Deceth”, “Steareth” and “Ceteareth” according to the CTFA nomenclature, including addition of the number of ethylene oxide molecules, e.g., "Laureth-16":
  • the average degree of ethoxylation thereby ranges between about 2.5 and about 50, preferably about 10 and about 30.
  • non-ionic surfactants mentioned above fatty alcohol ethoxylates are the most preferred ones.
  • non-ionic surfactants can also be used as mixture of one category such as several ethoxylated fatty alcohols or several categories such as mixture of alkyl polyglucoside and ethoxylated fatty alcohol.
  • Total surfactant concentration varies between 2 and 25%, preferably 3 and 25%, and more preferably 5 and 20% and most preferably 7.5 and 15% by weight, calculated to total composition.
  • compositions suitably comprise at least one anionic and at least one non-ionic surfactants.
  • anionic surfactants and especially those anionic surfactants with sulphate and phosphate end groups.
  • compositions comprise at least one phosphate surfactant of the above structure, and in particular trilaureth-4 phosphate.
  • Composition of the present invention comprises dispersed particles with a size below 200 ⁇ measured with sieve analysis at a total concentration of 1 to 35% by weight, preferably 2 to 30%, more preferably 3 to 25% and most preferably 5 to 20% by weight, calculated to total composition.
  • composition comprises additional second dispersed particles with a size below 200 ⁇ measured with sieve analysis selected from inert, non-swelling inorganic powder compounds. Suitable ones are calcium salts and especially preferred is calcium sulphate.
  • Suitable examples to the first dispersed particles are silicium dioxide, starch such as wheat, rice, potato and corn, and titan dioxide and their mixtures.
  • composition comprises the second dispersed partciles at a concentration higher than the first dispersed particles.
  • the weight ratio of first to second dispersed partciles is at least 1 :1 .01 and more preferably at least 1 :1 .1 and most preferably at least 1 :1 .5 and in particular at least 1 :2.
  • compositions of the present invention may comprise additional compounds found customarily in the cosmetic compositions.
  • Compositions may comprise at least one hair styling polymer selected from anionic, cationic, non-ionic and amphoteric ones at a concentration of 0.1 to 25%, preferably 1 .5 to 20%, more preferably 2.5 to 1 5 and most preferably 4 to 15% by weight calculated to total composition.
  • Suitable non-ionic polymer is first of all vinylpyrrolidon polymers either homopolymers or copolymers with, especially, vinylacetate. Those are known with the trade name "Luviskol” as homopolymers Luviskol K 30, K 60 or K 90 as well copolymers Luviskol VA 55, VA 64, Plus from BASF AG.
  • Natural non-ionic polymers are as well suitable for the composition of the present invention. Those are such as cellulose, chitosan, guar gum and their derivatives.
  • amphoteric polymers which can be used alone or in mixture with at least one additional nonionic polymer, reference is here made in particular to copolymers of N- octyl acrylamide, (meth)acrylic acid and tert.-butyl aminoethyl methacrylate of the type "Amphomer®”; copolymers from methacryloyl ethyl betaine and alkyl meth- acrylates of the type "Yukaformer®", e.g.. the butyl methacrylate copolymer
  • Yukaformer® Am75 copolymers from monomers containing carboxyl groups and sulfonic groups, e.g.. (meth)acrylic acid and itaconic acid, with monomers such as mono- or dialkyl aminoalkyl (meth)acrylates or mono- or dialkyl aminoalkyl (meth)- acrylamides containing basic groups, in particular amino groups; copolymers from N- octyl acrylamide, methyl methacrylate, hydroxypropyl methacrylate, N-tert. -butyl aminoethyl methacrylate and acrylic acid, as well as the copolymers known from US- A 3,927,199.
  • Suitable anionic polymers alone or in combination with non-ionic polymers are vinyl - alkyl ether, in particular methyl vinyl ether/maleic acid copolymers, obtained by hydrolysis of vinyl ether/maleic anhydride copolymers, distributed under the trade name "Gantrez® AN or ES". These polymers may also be partly esterified, as for example, “Gantrez® ES 225" or “ES 435", the ethyl ester of an ethyl vinyl ether/maleic acid copolymer, or the butyl or isobutyl ester thereof.
  • anionic polymers are in particular vinyl acetate/crotonic acid or vinyl acetate/vinyl neodecanoate/crotonic acid copolymers of the type "Resyn®”; sodium aery I ate/vinyl alcohol copolymers of the type “Hydagen® F", sodium polystyrene sulfonate, e.g..
  • anionic polymers are Acrylate copolymers available under trade name Salcare SC 81 , PEG/PPG 25/25 dimethicone / acrylate copolymer available under trade name Luvigel Silk from BASF, Acrylates/t-butylacrylamide copolymer available under trade name Ultrahold Strong, Advantage LC-E which is
  • Composition of the present invention can comprise cationic polymers alone or in combination with non-ionic polymer.
  • cationic cellulose type polymers know as Polymer JR type from Amerchol such as Polyquaternium-1 0 or cationic guar gum known with trade name Jaguar from Rhone-Poulenc and chemically for example Guar hydroxypropyl trimonium chloride.
  • chitosan and chitin can also be included in the compositions as cationic natural polymers.
  • Polyquaternium may as well be added into the compositions of the present invention. Typical examples of those are Polyquaternium-6, Polyquaternium-7, Polyquaternium-
  • Polyquaternium-1 1 Polyquaternium-16, Polyquaternium-22 and Polyquaternium- 28, Polyquaternium-30, Polyquaternium-37, Polyquaternium-36, Polyquaternium-46, Polyquaternium-24, Polyquaternium-67, and Polyquaternium-72.
  • the cationic polymers also include the quaternized products of graft polymers from organopolysiloxanes and polyethyl oxazolines described in EP-A 524 612 and EP-A 640 643. Among these especially preferred is the compound know with the INCI name Polysilicone-9.
  • the composition can comprise at least one synthetic or natural oil.
  • any oil allowed for cosmetic use is suitable for the compositions of the present invention.
  • Oils are those of synthetic and of natural ones. Natural oils are in principal any triglyceride suitable for cosmetic use. Non-limiting examples are avocado oil, coconut
  • compositions of the present invention can contain mixture of one or more natural oils and mineral oil.
  • suitable synthetic oil components are in particular fatty alcohol fatty acid esters such as isopropyl myristate, palmitate, stearate and isostearate, oleyl oleate, isocetyl stearate, hexyl laurate, dibutyl adipate, dioctyl adipate, myristyl myristate, oleyl erucate, polyethylene glycol and polyglyceryl fatty acid esters, cetyl palmitate, etc.
  • fatty alcohol fatty acid esters such as isopropyl myristate, palmitate, stearate and isostearate, oleyl oleate, isocetyl stearate, hexyl laurate, dibutyl adipate, dioctyl adipate, myristyl myristate, oleyl erucate, polyethylene glycol and polyglyceryl fatty acid esters, cetyl palmitate
  • Synthetic ones are those of silicone oils.
  • any silicone oil either volatile and/or non-volatile is suitable for the compositions of the present invention.
  • Preferred silicone oils are non-volatile silicone oils known with their INCI name as dimethicone and dimethiconol.
  • Volatile silicone oils such as cyclomethicones may be used in combination with non-volatile silicones and/or other wax and/or oils mentioned above.
  • Commercially, they are available from various companies for example Dow Corning with the known DC series, Wacker Chemie and Toray silicones. All commercially available non volatile silicones are suitable in the compositions of the present invention. Examples to those are DC 200 series, DC1401 , DC 1403, DC 1501 and DC 1503.
  • aminated silicones such as amodimethicone and arylated silicones comprising at least one aryl group in its molecule such as phenyl methicone, phenyl trimethicone, diphenyl dimethicone, diphenylsiloxy phenyl trimethicone, tetramethyl tetraphenyl trisiloxane, triphenyl trimethicone, tetramethyl tetraphenyl trisiloxane and trimethyl pentaphenyl trisiloxane can be advantageously comprised in the compositions of the present invention.
  • Concentration of one or more oil in the compositions of the present invention may be between 1 and 25%, preferably 1 .5 and 20% and more preferably 2 and 15% by weight calculated to total composition.
  • composition of the present invention can comprise polyols at a concentration of 0.5 to 15%, preferably 1 to 10%, more preferably 2 to 5% by weight calculated to the total composition.
  • the most preferred ones are glycerine, propylene glycols, butylene glycol and hexylene glycol.
  • compositions according to the invention may also comprise further agents, such as proteins, for example bamboo protein, and protein hydrolyzates and polypeptides, e.g. keratin hydrolyzates, collagen hydrolyzates of the type “Nutrilan ® " or elastin hydrolyzates, as well as, in particular vegetable, optionally cationized protein hydrolyzates, for example "Gluadin ® " .
  • proteins for example bamboo protein
  • protein hydrolyzates and polypeptides e.g. keratin hydrolyzates, collagen hydrolyzates of the type “Nutrilan ® " or elastin hydrolyzates
  • collagen hydrolyzates of the type "Nutrilan ® " or elastin hydrolyzates
  • optionally cationized protein hydrolyzates for example "Gluadin ® " .
  • Additional natural plant extracts can as well form part of the compositions of the present invention. Those are incorporated usually in an amount of about 0.01 % to about 5 %, preferably 0.05 % to 3.5 %, in particular 0.1 % to 2 % by weight, calculated as dry residue thereof to the total composition .
  • Suitable aqueous e.g.
  • alcoholic or hydro-alcoholic plant extracts known per se are in particular extracts from leaves, fruits, blossoms, roots, rinds or stems of aloe, pineapple, artichoke, arnica, avocado, valerian, bamboo, henbane, birch, stinging nettle, echinacea, ivy, wild angelica, gentian, ferns, pine needles, silver weed, ginseng, broom, oat, rose hip, hamamelis, hay flowers, elderberry, hop, coltsfoot, currants, chamomile, carrots, chestnuts, clover, burr root, coconut, cornflower, lime blossom, lily of the valley, marine algae, balm, mistletoe, passion flower, ratanhia, marigold, rosemary, horse chestnut, pink hawthorn, sage, horsetail, yarrow, primrose, nettle, thyme, walnut, wine leaves, white hawthorn, etc.
  • Suitable trade products are, for example, the various "Extrapon®" products,
  • compositions of the present invention may contain UV filters either for stabilization of the product colour and/or for protection of hair from environmental influences such as loss of elasticity, loss of hair colour (bleaching effect of sun light).
  • Suitable UV- absorbing substance are Polysilicone-15, 4-Aminobenzoic acid and the esters and salts thereof, 2-phenyl benzimidazole-5-sulfonic acid and the alkali and amine salts thereof, 4-dimethyl aminobenzoic acid and the esters and salts thereof, cinnamic acid and the esters and salts thereof, 4-methoxycinnamic acid and the esters and salts thereof, salicylic acid and the esters and salts thereof, 2,4-dihydroxybenzophenone, 2,2',4,4'-tetrahydroxy- benzophenone, 2-hydroxy-4-methoxybenzophenone and its 5- sulfonic acid or the sodium salt thereof, 2,2'-dihydroxy-4,4'-dimethoxybenzophenone, 2-hydroxy-5
  • the suitable amount of the UV-absorber ranges from about 0.01 % to 1 % by weight, calculated to the total composition . Attention should be paid to the stability and solubility especially when using UV filter as salts, e.g. anionic UV filter salts.
  • compositions of the present invention can contain one or more organic solvents within the scope of the invention, Suitable ones are ethanol, propanol, isopropanol, isopentane, n-pentane, n.hexane, dimethoxymethane, benzyl alcohol,
  • benzyloxyethanol alkylene carbonates such as ethylene carbonate and propylene carbonate, phenoxyethanol, butanol, isobutanol, cyclohexane, cyclohexanol, ethylenecarbonate, ethyleneglycol monoethylether, ethylene glycol monobutyl ether, ethylene glycol monophenyl ether, 1 -phenylethylalcohol, 2-phenylethylalcohol, o- methoxyphenol.
  • the most preferred organic solvents are ethanol, isopropanol and propanol. Concentration of solvents is in the range of 0 to 20% and preferably 1 to 15%, more preferably 1 to 10% and most preferably 2 to 10% by weight calculated to total composition.
  • compositions comprise at least one direct dye for colouring hair.
  • Suitable direct dyes are cationic, anionic, neutral dyes and their mixtures as available commercially from various suppliers and used mainly in semipermanent hair coloration.
  • Non-limiting examples to cationic dyes are Basic Blue 6, Basic Blue 7, Basic Blue 9, Basic Blue 26, Basic Blue 41 , Basic Blue 99, Basic Brown 4, Basic Brown 16, Basic Brown 17, Basic Orange 31 , Natural Brown 7, Basic Green 1 , Basic Red 2, Basic Red 12 Basic Red 22, Basic Red 51 , Basic Red 76, Basic Violet 1 , Basic Violet 2, Basic Violet 3, Basic Violet 10, Basic Violet 14, Basic Yellow 57 and Basic Yellow 87.
  • Suitable direct dyes are anionic dye.
  • Suitable non-limiting examples are Acid Black 1 , Acid Blue 1 , Acid Blue 3, Food Blue 5, Acid Blue 7, Acid Blue 9, Acid Blue 74, Acid Orange 3, Acid Orange 6, Acid Orange 7, Acid Orange 10, Acid Red 1 , Acid Red 14, Acid Red 1 8, Acid Red 27, Acid Red 50, Acid Red 52, Acid Red 73, Acid Red 87, Acid Red 88, Acid Red 92, Acid Red 155, Acid Red 180, Acid Violet 9, Acid Violet 43, Acid Violet 49, Acid Yellow 1 , Acid Yellow 23, Acid Yellow 3, Food Yellow No. 8, D&C Brown No. 1 , D&C Green No. 5, D&C Green No. 8, D&C Orange No. 4, D&C Orange No. 10, D&C Orange No. 1 1 , D&C Red No.
  • Suitable dyes for colouring hair within the meaning of the present invention are those of neutral nitro dyes.
  • Suitable non-limiting examples are HC Blue No.2, HC Blue No.4, HC Blue No.5, HC Blue No.6, HC Blue No.7, HC Blue No.8, HC Blue No.9, HC Blue No.10, HC Blue No.1 1 , HC Blue No.12, HC Blue No.13, HC Brown No.1 , HC Brown No.2, HC Green No.1 , HC Orange No.1 , HC Orange No.2, HC Orange No.3, HC Orange No.5, HC Red BN, HC Red No.1 , HC Red No.3, HC Red No.7, HC Red No.8, HC Red No.9, HC Red No.10, HC Red No.1 1 , HC Red No.13, HC Red No.54, HC Red No.14, HC Violet BS, HC Violet No.1 , HC Violet No.2, HC
  • Plant dyestuffs may also be used as hair colorant within the meaning of the present invention for example henna (red or black), alkanna root, laccaic acid, indigo, logwood powder, madder root and rhubarb powder, etc.
  • Concentration of direct dyes in the compositions of the present invention is within the range of 0.001 to 5%, preferably 0.01 to 3% and more preferably 0.05 to 2%, and most preferably 0.1 to 1 % by weight calculated to total composition, calculated to total composition.
  • composition of the present invention comprises additionally at least one propellant.
  • compositions of the present invention may comprise at least one propellant at a concentration of 5 to 60%, preferably 5 to 50% more preferably 10 to 50% by weight calculated to total composition.
  • Suitable propellants are lower alkanes such as n- butane, i-butane, propane, butane or their mixtures, as well as dimethylether (DME) either alone or in mixture with lower alkanes.
  • Further suitable propellants are fluorinated hydrocarbons such as 1 , 1 -difluoro ethane or tetrafluoroethane or their mixtures with each other, carbon dioxide and nitogen or their mixtures with the above mentioned propellants.
  • Preferred are lower alkanes such as propane, butane, n- butane, i-butane, and their mixtures and their mixture with DME at a alkane to DME weight ratio 10:1 to 1 :1 0.
  • compositions of the present invention can comprise all substances customarily found in such preparations. Examples of such substances are
  • composition was prepared by emulsifying petrolatum at elevated temperature with the aid of the surfactant in water and afterwards silica and calcium sulphate were dispersed in the composition and the batch was cooled down to room temperature.
  • the above composition was applied onto dry hair. It was observed that hair feels soft and smooth and matified. No particles were observed on the hair surface with naked eye.
  • the concentration in the composition represents active matter.
  • the above composition was applied onto dry hair. It was observed that hair feels soft and smooth and matified and well texturized and structured. No particles were observed on the hair surface with naked eye.

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Abstract

La présente invention concerne une composition aqueuse comprenant des particules insolubles en suspension pour conditionner et matifier les cheveux. Le premier objet de la présente invention concerne une composition aqueuse pour cheveux comprenant au moins 20 % en poids d'eau, 10 à 60 % en poids d'au moins une cire qui est solide à 20 °C, au moins un tensioactif émulsifiant à une concentration comprise dans la fourchette de 2 à 25 % en poids et des particules dispersées avec une taille inférieure à 200 μm mesurée par une analyse granulométrique à une concentration de 1 à 35 % en poids, toutes les valeurs étant calculées par rapport à la composition totale.
PCT/EP2011/058952 2011-05-31 2011-05-31 Composition de traitement des cheveux Ceased WO2012163406A1 (fr)

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WO2012163406A1 true WO2012163406A1 (fr) 2012-12-06

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DE2521960A1 (de) 1974-05-16 1976-04-08 Oreal Neue kosmetische mittel auf der basis von quaternisierten polymeren
DE2811010A1 (de) 1977-03-15 1978-09-28 Oreal Mittel und verfahren zur behandlung von keratinmaterialien mit kationischen und anionischen polymeren
DE3044738A1 (de) 1979-11-28 1981-06-19 L'Oreal, 75008 Paris Mittel und verfahren zur behandlung von keratinfasern
DE3217059A1 (de) 1981-05-08 1982-11-25 Oreal Unter druck stehendes mittel auf der basis von kationischen und anionischen polymeren, verfahren zur schaumbildung sowie verfahren zur behandlung der haare
EP0337354A1 (fr) 1988-04-12 1989-10-18 Kao Corporation Composition détergente faiblement irritante
EP0524612A2 (fr) 1991-07-22 1993-01-27 Kao Corporation Composition cosmétique contenant du silicone modifié
EP0640643A2 (fr) 1993-08-10 1995-03-01 Kao Corporation Organopolysiloxanes et procédé de fixation de la chevelure les utilisant
US6045589A (en) * 1998-04-28 2000-04-04 Aveda Corporation Methods of coloring hair or eyelashes with compositions which contain metal containing pigments and a copaiba resin
WO2001074311A2 (fr) 2000-03-31 2001-10-11 The Procter & Gamble Company Compositions cosmetiques s'integrant a la chevelure pour en augmenter le gonflant
EP1203573A2 (fr) * 2000-11-02 2002-05-08 GOLDWELL GmbH Compositions pour soins de cheveux
EP1495749A2 (fr) * 2003-07-07 2005-01-12 Beiersdorf AG Composition cosmétique fixante permettant plusieurs mises en forme des cheveux
EP1927346A1 (fr) * 2006-11-16 2008-06-04 KPSS-Kao Professional Salon Services GmbH Composition de coiffage sous forme d'émulsion
WO2009056398A2 (fr) 2007-10-31 2009-05-07 Henkel Ag & Co. Kgaa Cire mate
EP2394631A1 (fr) * 2010-06-08 2011-12-14 KPSS-Kao Professional Salon Services GmbH Composition de traitement capillaire

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3927199A (en) 1972-04-14 1975-12-16 Nat Starch Chem Corp Hair fixing compositions containing N-alkyl acrylamide or methacrylamide interpolymer
DE2521960A1 (de) 1974-05-16 1976-04-08 Oreal Neue kosmetische mittel auf der basis von quaternisierten polymeren
DE2811010A1 (de) 1977-03-15 1978-09-28 Oreal Mittel und verfahren zur behandlung von keratinmaterialien mit kationischen und anionischen polymeren
DE3044738A1 (de) 1979-11-28 1981-06-19 L'Oreal, 75008 Paris Mittel und verfahren zur behandlung von keratinfasern
DE3217059A1 (de) 1981-05-08 1982-11-25 Oreal Unter druck stehendes mittel auf der basis von kationischen und anionischen polymeren, verfahren zur schaumbildung sowie verfahren zur behandlung der haare
EP0337354A1 (fr) 1988-04-12 1989-10-18 Kao Corporation Composition détergente faiblement irritante
EP0524612A2 (fr) 1991-07-22 1993-01-27 Kao Corporation Composition cosmétique contenant du silicone modifié
EP0640643A2 (fr) 1993-08-10 1995-03-01 Kao Corporation Organopolysiloxanes et procédé de fixation de la chevelure les utilisant
US6045589A (en) * 1998-04-28 2000-04-04 Aveda Corporation Methods of coloring hair or eyelashes with compositions which contain metal containing pigments and a copaiba resin
WO2001074311A2 (fr) 2000-03-31 2001-10-11 The Procter & Gamble Company Compositions cosmetiques s'integrant a la chevelure pour en augmenter le gonflant
EP1203573A2 (fr) * 2000-11-02 2002-05-08 GOLDWELL GmbH Compositions pour soins de cheveux
EP1495749A2 (fr) * 2003-07-07 2005-01-12 Beiersdorf AG Composition cosmétique fixante permettant plusieurs mises en forme des cheveux
EP1927346A1 (fr) * 2006-11-16 2008-06-04 KPSS-Kao Professional Salon Services GmbH Composition de coiffage sous forme d'émulsion
WO2009056398A2 (fr) 2007-10-31 2009-05-07 Henkel Ag & Co. Kgaa Cire mate
EP2394631A1 (fr) * 2010-06-08 2011-12-14 KPSS-Kao Professional Salon Services GmbH Composition de traitement capillaire

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ANONYMOUS: "Dow Corning 9701 Cosmetic Powder", INTERNET CITATION, 19 January 2005 (2005-01-19), XP002480470, Retrieved from the Internet <URL:http://www4.dowcorning.com/DataFiles/090007c880004b64.pdf> [retrieved on 20080516] *
ANONYMOUS: "Rona - Basics of success - Ingredients for Cosmetics", INTERNET CITATION, 9 December 2010 (2010-12-09), pages 1 - 16, XP002613481, Retrieved from the Internet <URL:http://www.mercury-ltd.co.il/admin/userfiles/image/Information/Merck_ Cosmetics_Catalogue.pdf> [retrieved on 20101209] *

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