Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/58—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
  • A61K8/585—Organosilicon compounds
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
  • A61K8/04—Dispersions; Emulsions
  • A61K8/06—Emulsions
• • 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
  • A61K8/06—Emulsions
  • A61K8/064—Water-in-oil emulsions, e.g. Water-in-silicone emulsions
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
  • A61K8/41—Amines
  • A61K8/416—Quaternary ammonium compounds
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
  • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
  • A61K8/89—Polysiloxanes
  • A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
  • A61K8/894—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
• • 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
  • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
  • A61K8/89—Polysiloxanes
  • A61K8/896—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
  • A61K8/898—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
• • 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

Definitions

• the present invention relates to a cosmetic treatment composition for keratin materials, of the water-in-oil emulsion type, comprising in a cosmetically acceptable medium, at least one volatile silicone, at least one silicone surfactant and at least one cationic surfactant, and to a cosmetic treatment process for keratin materials.
• the Applicant has surprisingly discovered that by introducing a cationic surfactant in a concentration strictly greater than 0.5% by weight, into a mixture of volatile silicone and silicone surfactant, the cosmetic properties of the hair are markedly improved, for example, detangling and softness.
• the present invention therefore relates to a composition for treating keratin materials, of the water-in-oil emulsion type, comprising in a cosmetically acceptable medium, at least one volatile silicone, at least one silicone surfactant and at least one cationic surfactant in one concentration strictly greater than 0.5% by weight relative to the total weight of the composition.
• Another subject of the invention consists of a cosmetic treatment process for keratin materials using a composition according to the invention as described below.
• the subject of the invention is also a use of the composition according to the invention as a conditioner.
• the composition for cosmetic treatment of keratin materials, of the water-in-oil emulsion type comprises, in a cosmetically acceptable medium, at least one volatile silicone, at least one silicone surfactant and at least one cationic surfactant as defined below, in a concentration strictly greater than
• composition according to the invention comprises a total amount of oils comprising at least said volatile silicone, less than or equal to 20% by weight, preferably between 5 and 20% by weight relative to the total weight of the composition.
• oil is meant in the present invention any fatty substance immiscible with water, which is liquid at room temperature.
• oils which can be used in the present invention can also comprise at least one of the compounds chosen from vegetable oils, animal oils, mineral oils, synthetic oils, fatty acid esters, and mixtures thereof.
• sweet almond oil there may be mentioned in particular sweet almond oil, avocado oil, castor oil, olive oil, jojoba oil, sunflower oil, wheat germ oil, sesame oil, peanut oil, grape seed oil, soybean oil, rapeseed oil, safflower oil, coconut oil , corn oil, hazelnut oil, shea butter, palm oil, apricot kernel oil, calophyllum oil.
• mineral oil mention may in particular be made of paraffin oil and petrolatum oil.
• synthetic oil examples include squalane, poly ( ⁇ -olefins) such as isododecane or isohexadecane, transesterified vegetable oils, fluorinated oils, and mixtures thereof.
• R a COOR b As fatty acid esters, mention may be made, for example, of the compounds of formula R a COOR b in which R a represents the remainder of a higher fatty acid containing from 6 to 29 carbon atoms and R b represents a hydrocarbon chain containing 3 to 30 carbon atoms, such as Purcellin oil (stearyl octanoate), isopropyl myristate, isopropyl palmitate, butyl stearate, hexyl laurate, diisopropyl adipate , isononyl isononanoate, 2-ethylhexyl palmitate, 2-hexyldecyl laurate, 2-octyldecyl palmitate, myristate or 2-octyldodecyl lactate.
• Purcellin oil stearyl octanoate
• isopropyl myristate isopropyl palmitate
• composition according to the invention has in particular a minimum penetration resistance force of 0.075 N, as measured by penetrometry.
• the penetration measurements were carried out with a TA-TX2 texture analyzer (Rhéo). They correspond to compression force measurements under the following conditions:
• the cationic surfactants which can be used in the composition according to the invention are chosen from the salts of primary, secondary or tertiary fatty amines, optionally polyoxyalkylenated, quaternary ammonium salts, and their mixtures.
• R 8 represents a C 12 alkyl group. 30 , preferably C, 4 _ 22 , C 12 alkenyl. 30 , (C 12 -C 22 ) alkyl (C 2 -C 6 ) amidoalkyl, (C 12 -C 22 ) alkyl - acetate, or an aromatic group such as aryl or C 6 -C 12 alkylaryl,
• R 9 to R ⁇ which may be the same or different, represent a C 1 alkyl group. 8 , C 8 alkenyl, 8 alkoxy, hydroxy alkyyl
• VS,. 8 polyoxyalkylene (C 2 -C 6 ) or C 6 alkylamide. 8 ;
• X is an anion chosen from the group of halides, phosphates, acetates, lactates, (C 2 -C 6 ) alkyl sulfates, alkyl- or alkylaryl sulfonates;
• R 12 represents an alkenyl or alkyl radical containing from 8 to 30 carbon atoms, for example derived from tallow fatty acids
• R 13 represents a hydrogen atom, a C ⁇ -C 4 alkyl radical or an alkenyl radical or alkyl having from 8 to 30 carbon atoms
• R 14 represents an alkyl radical in C, -C 4
• R 15 represents a hydrogen atom, an alkyl radical in C ⁇ -C 4
• X " is an anion chosen from the group halides, phosphates, acetates, lactates, alkylsulfates, alkyl- or alkylaryl-sulfonates.
• R 12 and R 13 denote a mixture of alkenyl or alkyl radicals containing from 12 to 21 carbon atoms, for example derived from fatty acids of tallow, R 14 denotes a methyl radical, R 15 denotes a hydrogen atom.
• R 12 and R 13 denote a mixture of alkenyl or alkyl radicals containing from 12 to 21 carbon atoms, for example derived from fatty acids of tallow
• R 14 denotes a methyl radical
• R 15 denotes a hydrogen atom.
• Such a product is for example sold under the name Rewoquat ® W 75 by Rewo;
• R 16 denotes an aliphatic radical comprising approximately
• R 16 to 30 carbon atoms, R 17 , R 18 , R 19 , R 20 and R 21 , identical or different, are chosen from hydrogen or an alkyl radical containing from 1 to 4 carbon atoms, and X is a chosen anion in the group of halides, acetates, phosphates, nitrates and methylsulfates.
• Such quaternary diammonium salts include in particular propane diammonium dichloride; - quaternary ammonium salts containing at least one ester function, such as those of formula (IX) below:
• R 22 is selected from alkyl C, -C 6 hydroxyalkyl or dihydroxyalkyl radicals C, -C 6 alkyl;
• R 23 is chosen from:
• R 25 is chosen from:
• R 24 , R 26 and R 28 are chosen from C 7 -C 21 hydrocarbon radicals, linear or branched, saturated or unsaturated; r, s and t, identical or different, are integers ranging from 2 to 6; y is an integer from 1 to 10; x and z, identical or different, are integers ranging from 0 to 10; X " is a simple or complex, organic or inorganic anion; provided that the sum x + y + z is from 1 to 15, that when x is 0 then R 23 is R 27 and that when z is 0 then R 25 is R 29.
• the alkyl radicals R 22 can be linear or branched and more particularly linear.
• R 22 denotes a methyl, ethyl, hydroxyethyl or dihydroxypropyl radical, and more particularly a methyl or ethyl radical.
• the sum x + y + z is worth from 1 to 10.
• R 23 is a hydrocarbon radical R 27 , it can be long and have from 12 to 22 carbon atoms, or short and have from 1 to 3 carbon atoms.
• R 25 is a hydrocarbon radical R 29 , it preferably has 1 to 3 carbon atoms.
• R 24 , R 26 and R 28 are chosen from C, -C 21 hydrocarbon radicals, linear or branched, saturated or unsaturated, and more particularly from C, alkenyl and alkyl radicals, -C 21 , linear or branched, saturated or unsaturated.
• x and z are worth 0 or 1.
• y is equal to 1.
• r, s and t are worth 2 or 3, and even more particularly are equal to 2.
• the anion is preferably a halide (chloride, bromide or iodide) or an alkyl sulfate, more particularly methyl sulfate. It is however possible to use methanesulfonate, phosphate, nitrate, tosylate, an anion derived from organic acid such as acetate or lactate or any other anion compatible with ammonium having an ester function.
• anion X is even more particularly the chloride or the methyl sulphate. Use is more particularly made, in the composition according to the invention, of the ammonium salts of formula (IX) in which:
• R 22 denotes a methyl or ethyl radical
• - z is 0 or 1; - r, s and t are equal to 2;
• R 24 , R 26 and R 28 are chosen from C 13 -C 17 hydrocarbon radicals, linear or branched, saturated or unsaturated, and preferably from alkyl and alkenyl radicals in
• hydrocarbon radicals are linear.
• acyl radicals preferably have 14 to 18 carbon atoms and more particularly come from a vegetable oil such as palm or sunflower oil. When the compound contains several acyl radicals, these can be identical or different.
• Such compounds are for example marketed under the names DEHYQUART ® by the company Henkel, Stepanquat® ® by the company Stepan, Noxamium ® by CECA Rewoquat ® WE 18 by Rewo-Witco.
• composition according to the invention preferably contains a mixture of mono-, di- and triester quaternary ammonium salts with a majority by weight of diester salts.
• acyloxyethyl-dihydroxyethyl-methylammonium methyl sulfate use may be made, for example, of a mixture containing 15 to 30% by weight of acyloxyethyl-dihydroxyethyl-methylammonium methyl sulfate, 45 to 60% of diacyloxyethyl-hydroxyethyl-methylammonium methyl sulfate and 15 to 30% of triacyloxyethyl-methylammonium methyl sulphate, the acyl radicals having from 14 to 18 carbon atoms and originating from palm oil which may be partially hydrogenated.
• ammonium salts containing at least one ester function described in patents US-A-4,874,554 and US-A-4,137,180.
• quaternary ammonium salts of formula (NI) preference is given, on the one hand, to alkyltrimethylammonium chlorides in which the alkyl radical contains approximately from 14 to 22 carbon atoms, in particular behenyltrimethylammonium and arachidyltrimethylammonium chlorides.
• the cationic surfactants which are particularly preferred in the composition of the invention are chosen from quaternary ammonium salts, and in particular from behenyltrimethylammonium chloride and palmitylamidopropyltrimethylammonium chloride.
• composition for cosmetic treatment of keratin materials preferably comprises the cationic surfactant (s) in an amount of between 0.5 and 10% by weight, better still between 0.8 and 8% by weight, and even more preferably between 1 and 5 % by weight relative to the total weight of the composition.
• the volatile silicones which can be used in the invention are linear or cyclic silicones, having a viscosity at ambient temperature and under atmospheric pressure, less than 8 mm 2 / s (8 cSt).
• the viscosity is preferably measured by capillary viscometry, for example, using a capillary viscometer, in particular of the Ubbelohde type, at a temperature of 25 ° C., according to standard ASTM D445-97. You can also use the so-called ball drop method.
• Volatile silicones generally have a boiling point between 60 ° C and 260 ° C, and are more particularly chosen from: (i) cyclic volatile silicones containing from 3 to 7 silicon atoms and, preferably, 4 to 5 It is, for example, octamethylcyclotetrasiloxane marketed in particular under the name of "VOLATILE SILICONE 7207" by UNION CARBIDE or "SILBIONE ® 70045 V 2" by RHODIA, decamethylcyclopenta- siloxane marketed under the name of "NOLATILE SILICONE 7158" by UNION CARBIDE, "SILBIONE ® 70045 N 5" by RHODIA or under the name DC245 Fluid by DOW COR ⁇ I ⁇ G, as well as their mixtures.
• linear volatile silicones having 2 to 9 silicon atoms and having a viscosity less than or equal to 5 mm 2 / s at 25 ° C. It is, for example, decamethyltetrasiloxane marketed in particular under the name "SH 200" by the company TORAY SILICONE. Silicones included in this class are also described in the article published in Cosmetics and toiletries, Vol. 91, Jan. 76, p. 27-32 - TODD & BYERS "Volatile Silicone fluids for cosmetics".
• composition according to the invention preferably comprises volatile silicones in an amount of between 5 and 20% by weight, and even more preferably between 8 and 15% by weight relative to the total weight of the composition.
• silicone surfactants which can be used in the present invention are those well known to those skilled in the art. They can be hydro- soluble, spontaneously water-dispersible or not water-soluble. Preferably, they are water-soluble or spontaneously water-dispersible.
• silicone surfactants are, for example, chosen from the compounds of general formulas (I), (II), (III), (IV) and (V):
• - R represents an alkyl group, linear or branched, C, -C 30 , or phenyl;
• - R 2 identical or different, represents -C c H 2c -O- (C 2 H 4 O) a - (C 3 H 6 O) b -R 5 or -C c H 2c -O- (C 4 H 8 O) a -R 5 ;
• - R 3 and R 4 identical or different, each denote an alkyl group, linear or branched, in -C ⁇ , and preferably a methyl group;
• R 5 is chosen from a hydrogen atom, an alkyl group, linear or branched, comprising from 1 to 12 carbon atoms, an alkoxy group, linear or branched, comprising from 1 to 6 carbon atoms , an acyl group, linear or branched, comprising from 2 to 12 carbon atoms, a hydroxyl group, -SO 3 M, -OCOR 6 , C 1 -C 6 aminoalkoxy optionally substituted on the amine, C 2 aminoacyl - C 6 optionally substituted on the amine, -NHCH 2 CH 2 COOM, -N (CH 2 CH 2 COOM) 2 , aminoalkyl in -C ⁇ optionally substituted on the amine and on the alkyl chain, carboxyacyl in C, -C 30 , a phosphono group optionally substituted by one or two substituted C 12 -C 12 aminoalkyl groups, -CO (CH 2 ) d COOM, -OCOC
• R 6 denotes an alkyl group, linear or branched, in -C ⁇ ,
• R 7 denotes a hydrogen atom or an SO 3 M group
• - d varies from 1 to 10;
• - m varies from 0 to 20;
• - n varies from 0 to 500;
• - c varies from 0 to 4.
• - w varies from 1 to 100;
• - Y represents a mineral or organic monovalent anion such as a halide (chloride, bromide), a sulfate, or a carboxylate (acetate, lactate, citrate).
• silicone surfactants corresponding to the general formulas (I) or (II) as defined above are used, and more in particular, those corresponding to formulas (I) or (II) in which at least one of, and preferably all of the following conditions are satisfied:
• - c is equal to 2 or 3;
• - R denotes the methyl group;
• R 5 represents a hydrogen atom, a methyl group or an acetyl group and preferably a hydrogen atom
• - a varies from 1 to 25 and more particularly from 2 to 25;
• - b varies from 0 to 25, preferably from 10 to 20;
• - n varies from 0 to 100;
• silicone surfactants are, for example, those sold under the trade names FLUID DC 193 and DC 5225C by DOW CORNING, Silwet ® L 77 by OSI and MAZIL ® 756 by the company Mazer PPG.
• the silicone surfactants are contained in the present invention in an amount between 0.01 and 3% by weight, better still between 0.2 and 3% by weight relative to the total weight of the composition for treating keratin materials.
• cosmetically acceptable medium is meant a medium compatible with all ketatin materials such as the skin, hair, nails, eyelashes, eyebrows, lips and any other area of the body and face, but also of pleasant smell, appearance and touch.
• the cosmetically acceptable aqueous medium comprises water or a mixture of water and a cosmetically acceptable solvent chosen from lower alcohols, C 4 -C 4 , such as ethanol, isopropanol, tert-butanol or n-butanol; polyols such as propylene glycol; polyol ethers; C 5 -C 10 alkanes; C 3 ketones. 4 such as acetone and methyl ethyl ketone; C 1 -C 4 alkyl acetates such as methyl acetate, ethyl acetate and butyl acetate; dimethoxyethane, diethoxyethane; and their mixtures.
• the proportion of water in the composition according to the invention is preferably between 30 and 90% by weight relative to the total weight of the composition.
• the pH of the compositions of the invention is between 4 and 8, preferably between 5 and 7.
• compositions according to the invention can also contain additives such as cationic, anionic, nonionic or amphoteric polymers, non-volatile silicones, modified or not, natural or synthetic polymeric thickeners, anionic, amphoteric, zwitterionic, nonionic or cationic , associative or not, non-polymeric thickeners such as electrolytes, sugars, pearlescent agents, opacifiers, sun filters, perfumes, dyes, organic or mineral particles, preservatives, pH stabilizers.
• additives such as cationic, anionic, nonionic or amphoteric polymers, non-volatile silicones, modified or not, natural or synthetic polymeric thickeners, anionic, amphoteric, zwitterionic, nonionic or cationic , associative or not, non-polymeric thickeners such as electrolytes, sugars, pearlescent agents, opacifiers, sun filters, perfumes, dyes, organic or mineral particles, preservatives, pH stabilize
• additives are present in the composition according to the invention in an amount ranging from 0 to 50% by weight relative to the total weight of the composition.
• compositions according to the invention can be in the form of fluid or thickened liquids, gels, creams, or single or multiple emulsions.
• compositions can be used, for example, as shampoos, coloring or bleaching or perming products, styling products, rinsed care, deep care masks, shower gels, scalp treatment lotions or creams, shaving products or hair removal products.
• the present invention also relates to a process for the cosmetic treatment of keratin materials which consists in applying an effective amount of a composition as described above, to the keratin materials, in effecting a possible rinsing after a possible exposure time.
• the composition can be used as a conditioner.
• Conditioner compositions were prepared from the ingredients shown in the table below. The contents indicated are expressed in% by weight relative to the total weight of the composition.
• compositions were applied to the hair and rinsed after an exposure time of one minute, rinsing being easy. The hair was then dried.
• the dried hair is soft and untied to the touch, and without unpleasant residues.

Landscapes

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

Priority Applications (5)

Applications Claiming Priority (2)

Publications (1)

Family

ID=8858473

Family Applications (1)

Country Status (8)

Cited By (1)

Families Citing this family (14)

Citations (7)

Family Cites Families (2)

• 2001
  • 2001-01-02 FR FR0100015A patent/FR2818902B1/fr not_active Expired - Fee Related
• 2002
  • 2002-01-02 ES ES02711916T patent/ES2349893T3/es not_active Expired - Lifetime
  • 2002-01-02 DE DE60235521T patent/DE60235521D1/de not_active Expired - Lifetime
  • 2002-01-02 US US10/250,362 patent/US7833516B2/en not_active Expired - Fee Related
  • 2002-01-02 JP JP2002554063A patent/JP2004526688A/ja active Pending
  • 2002-01-02 ES ES02710936T patent/ES2340986T3/es not_active Expired - Lifetime
  • 2002-01-02 AT AT02710936T patent/ATE459330T1/de active
  • 2002-01-02 WO PCT/FR2002/000003 patent/WO2002053112A1/fr not_active Ceased
  • 2002-01-02 EP EP02710936A patent/EP1347737B1/fr not_active Revoked

Patent Citations (7)

Also Published As

Similar Documents

Legal Events