WO2000048555A2 - Compositions cosmétiques - Google Patents

Compositions cosmétiques Download PDF

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Publication number
WO2000048555A2
WO2000048555A2 PCT/US2000/004082 US0004082W WO0048555A2 WO 2000048555 A2 WO2000048555 A2 WO 2000048555A2 US 0004082 W US0004082 W US 0004082W WO 0048555 A2 WO0048555 A2 WO 0048555A2
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WO
WIPO (PCT)
Prior art keywords
mixtures
skin
composition according
composition
compositions
Prior art date
Application number
PCT/US2000/004082
Other languages
English (en)
Other versions
WO2000048555A3 (fr
Inventor
Michael David Bell
Richard George Albert Rolls
Russell Philip Elliott
Roland Philip Duke
Original Assignee
The Procter & Gamble Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to EP00914614A priority Critical patent/EP1152747A2/fr
Priority to BR0008335-6A priority patent/BR0008335A/pt
Priority to CA002362349A priority patent/CA2362349A1/fr
Priority to AU35981/00A priority patent/AU771906B2/en
Priority to JP2000599349A priority patent/JP2002537236A/ja
Priority to KR1020017010593A priority patent/KR20010102282A/ko
Publication of WO2000048555A2 publication Critical patent/WO2000048555A2/fr
Publication of WO2000048555A3 publication Critical patent/WO2000048555A3/fr

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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
    • A61K8/60—Sugars; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8194—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds; 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
    • A61K8/30—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
    • A61K8/34—Alcohols
    • A61K8/345—Alcohols containing more than one hydroxy 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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/67—Vitamins
    • A61K8/673—Vitamin B group
    • A61K8/675—Vitamin B3 or vitamin B3 active, e.g. nicotinamide, nicotinic acid, nicotinyl aldehyde
    • 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
    • A61K8/731—Cellulose; Quaternized cellulose derivatives
    • 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
    • A61K8/737—Galactomannans, e.g. guar; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8158—Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • 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
    • A61K8/86—Polyethers
    • 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
    • A61K8/88—Polyamides
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54—Polymers characterized by specific structures/properties
    • A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5422—Polymers characterized by specific structures/properties characterized by the charge nonionic
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54—Polymers characterized by specific structures/properties
    • A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5424—Polymers characterized by specific structures/properties characterized by the charge anionic
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54—Polymers characterized by specific structures/properties
    • A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5426—Polymers characterized by specific structures/properties characterized by the charge cationic
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54—Polymers characterized by specific structures/properties
    • A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5428—Polymers characterized by specific structures/properties characterized by the charge amphoteric or zwitterionic
    • 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
    • A61K2800/59—Mixtures
    • A61K2800/594—Mixtures of polymers

Definitions

  • Prefe ⁇ ed polyhydric alcohols of the present invention are selected from glycerine, butylene glycol, propylene glycol, dipropylene glycol, polyethylene glycol and derivatives thereof, hexane triol, ethoxylated glycerine and propoxylated glycerine, or mixtures thereof.
  • the oil phase components of the compositions herein comprise an emollient material or mixtures thereof, a polyol carboxylic acid ester and a silicone oil, or mixtures thereof.
  • Suitable ester emollient materials of Formula I above include, but are not limited to, methyl isostearate, isopropyl isostearate, isostearyl neopentanoate. isononyl isononanoate, isodecyl octanoate, isodecyl isononanoate, tridecyl isononanoate, myristyl octanoate, octyl pelargonate, octyl isononanoate, myristyl myristate, myristyl neopentanoate, myristyl octanoate, myristyl propionate, isopropyl myristate and mixtures thereof.
  • Suitable ester emollient materials of Formula (U) include but are not limited to C 12- 15 alkyl benzoates.
  • Prefe ⁇ ed emollients for use herein are isohexadecane, isooctacontane, isononyl isononanoate, isodecyl octanoate, isodecyl isononanoate, tridecyl isononanoate, myristyl octanoate, octyl isononanoate, myristyl myristate, methyl isostearate, isopropyl isostearate, C12-15 alkyl benzoates and mixtures thereof.
  • Particularly prefe ⁇ ed emollients for use herein are isohexadecane, isononyl isononanoate, methyl isostearate, isopropyl isostearate, or mixtures thereof.
  • compositions of the present invention may further comprise as an additional emollient, a polyol carboxylic acid ester.
  • the prefe ⁇ ed polyol polyesters useful in this invention are C1 -C30 mono- and polyesters of sugars and related materials. These esters are derived from a sugar or polyol moiety and one or more carboxylic acid moieties. Depending on the constituent acid and sugar, these esters can be in either liquid or solid form at room temperature.
  • Suitable silicone fluids useful herein include silicones inclusive of polyalkyl siloxane fluids, polyaryl siloxane fluids, cyclic and linear polyalkylsiloxanes, polyalkoxylated silicones, amino and quaternary ammonium modified silicones, polyalkylaryl siloxanes or a polyether siloxane copolymer and mixtures thereof.
  • the silicone fluids can be volatile or non- volatile.
  • Silicone fluids generally have a weight average molecular weight of less than about 200,000. Suitable silicone fluids have a molecular weight of about 100,000 or less, preferably about 50,000 or less, most preferably about 10,000 or less.
  • essentially non-volatile polyalkylarylsiloxanes for example, polymethylphenylsiloxanes, having viscosities of about 0.65 to 30,000 mm ⁇ .s ' l at 25°C.
  • These siloxanes are available, for example, from the General Electric Company as SF 1075 methyl phenyl fluid or from Dow Coming as 556 Cosmetic Grade Fluid.
  • Cyclic polydimethylsiloxanes suitable for use herein are those having a ring structure inco ⁇ orating from about 3 to about 7 (CH3)2SiO moieties.
  • Silicone gums can also be used herein.
  • the term "silicone gum” herein means high molecular weight silicones having a weight average molecular weight in excess of about 200,000 and preferably from about 200,000 to about 4,000,000. Iincluded are nonvolatile polyalkyl and polyaryl siloxane gums.
  • a silicone oil phase comprises a silicone gum or a mixture of silicones including the silicone gum.
  • silicone gums include polydimethylsiloxane, (polydimethylsiloxane)(methylvinylsiloxane) copolymer, poly(dimethylsiloxane)- (diphenyl)(methylvinylsiloxane) copolymer and mixtures thereof.
  • Prefe ⁇ ed silicone gums for use herein are silicone gums having a molecular weight of from about 200,000 to about 4,000,000 selected from dimethiconol, and dimethicone and mixtures thereof.
  • An especially prefe ⁇ ed silicone-gum fluid blend based component for use in the compositions herein is a dimethiconol gum having a molecular weight of from about 200,000 to about 4,000,000 along with a silicone fluid carrier with a viscosity of about
  • the assigned LNCI names for KSG-15, KSG- 16, KSG-17 and KSG-18 are cyclomethicone dimethicone/vinyl dimethicone crosspolymer, dimethicone dimethicone/vinyl dimethicone crosspolymer, cyclomethicone dimethicone/vinyl dimethicone crosspolymer and phenyl trimethicone dimethicone/phenyl vinyl dimethicone crosspolymer, respectively.
  • a particularly prefe ⁇ ed copolymer fluid blend for use herein includes Dow Coming DC3225C which has the CTFA designation Dimethicone/Dimethicone copolyol.
  • Prefe ⁇ ed classes of non-ionic amphiphilic surfactants suitable herein and their properties are disclosed in WO98/22085, inco ⁇ orated herein by reference.
  • Preferred herein are the mono-, di- and tri-acyl sugar esters and mixtures thereof wherein the acyl substituents contain from about 8 to about 24, preferably from about 8 to about 20 carbon atoms and 0,1 or 2 unsaturated moieties and polyethylene glycol derivatives, or mixtures thereof.
  • High prefe ⁇ ed herein is a fatty acid ester blend based on a mixture of sorbitan or sorbitol fatty acid ester and sucrose fatty acid ester, the fatty acid in each instance being preferably Cg-C24, more preferably C10-C20
  • the prefe ⁇ ed fatty acid ester emulsifier from the viewpoint of moisturisation is a blend of sorbitan or sorbitol C16-C20 f att y a cid ester with sucrose C I Q-C J ⁇ fatty acid ester, especially sorbitan stearate and sucrose cocoate. This is commercially available from ICI under the trade name Arlatone 2121.
  • compositions of the present invention may comprise additional humectants which are preferably present at a level of from about 0.01%> to about 20%>, more preferably from about 0.1%) to about 15% and especially from about 0.5%> to about 15%>.
  • humectants are selected from urea, panthenol and mixtures thereof.
  • suitable pigments are titanium dioxide, predispersed titanium dioxide from Kobo e.g. Kobo GWL75CAP, iron oxides, acyglutamate iron oxides, ultramarine blue, D&C dyes, carmine, and mixtures thereof. Depending upon the type of composition, a mixture of pigments will normally be used.
  • the prefe ⁇ ed pigments for use herein from the viewpoint of moisturisation, skin feel, skin appearance and emulsion compatibility are treated pigments.
  • the pigments can be treated with compounds such as amino acids, silicones, lecithin and ester oils.
  • Suitable esters of nicotinic acid include nicotinic acid esters of C [-C22 > preferably C1 - C ⁇ , more preferably C ⁇ -Cg alcohols.
  • the alcohols are suitably straight-chain or branched chain, cyclic or acyclic, saturated or unsaturated (including aromatic), and substituted or unsubstituted.
  • the esters are preferably non-vasodilating. As used herein, "non-vasodilating" means that the ester does not commonly yield a visible flushing response after application to the skin in the subject compositions (the majority of the general population would not experience a visible flushing response, although such compounds may cause vasodilation not visible to the naked eye).
  • compositions of the present invention may also contain a retinoid.
  • retinoid includes all natural and/or synthetic analogs of Vitamin A or retinol-like compounds which possess the biological activity of Vitamin A in the skin as well as the geometric isomers and stereoisomers of these compounds.
  • vitamin B3 compound may provide benefits in regulating skin condition, as described in WO98/22085, herein inco ⁇ orated by reference.
  • the pH of the compositions herein is greater than 4.25, preferably greater than 4.5 and more preferably greater than 4.75, also preferably less than 9, more preferably less than 8 and even more preferably less than 7.
  • the water content of the compositions herein is generally from about 30% to about 98.89%>, preferably from about 50% to about 95%o and especially from about 60% to about 90% by weight.
  • compositions are made as follows:
  • Sepigel 305 (polyacrylamide) is not added until the mixture is cooled to 60°C.
  • the Sepigel 305 is added under shear and then the NaOH solution added.
  • EDTA, silicone oil, and then urea solution (lg dissolved in 1ml of water) are then added to the resulting oil-in-water emulsion and the mixture is cooled before adding minor ingredients.
  • the composition is ready for packaging.
  • compositions display low levels of tack, as well as good rheological, abso ⁇ tion and insulation properties, in addition to skin feel, skin softness and skin smoothness benefits.

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

Abstract

L'invention concerne une composition cosmétique durable conçue pour l'application topique à la peau et qui comprend: a) un agent d'épaississement polymère, sélectionné parmi des agents d'épaississement non ioniques et anioniques ou leurs mélanges et qui possède un poids moléculaire moyen supérieur à 20 000 et b) un polymère contenant des cations (ou ses mélanges), ladite composition comprenant moins de 4 % d'un surfactant anionique, zwittérionique ou amphotérique. Cette composition possède un faible degré de collage ainsi que de bonnes propriétés rhéologiques, d'absorption et d'isolation, outre les bénéfices de sensation agréable, de douceur et de caractère lisse au contact avec la peau.
PCT/US2000/004082 1999-02-19 2000-02-17 Compositions cosmétiques WO2000048555A2 (fr)

Priority Applications (6)

Application Number Priority Date Filing Date Title
EP00914614A EP1152747A2 (fr) 1999-02-19 2000-02-17 Compositions cosm tiques
BR0008335-6A BR0008335A (pt) 1999-02-19 2000-02-17 Composição cosmética de deixar ficar, processo de tratamento, utilização de um polìmero que contém cátions e utilização de uma composição
CA002362349A CA2362349A1 (fr) 1999-02-19 2000-02-17 Compositions cosmetiques pour application renfermant un polymere cationique
AU35981/00A AU771906B2 (en) 1999-02-19 2000-02-17 Cosmetic compositions
JP2000599349A JP2002537236A (ja) 1999-02-19 2000-02-17 化粧品組成物
KR1020017010593A KR20010102282A (ko) 1999-02-19 2000-02-17 화장용 조성물

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP99039257 1999-02-19
GB9903925.7 1999-02-19

Publications (2)

Publication Number Publication Date
WO2000048555A2 true WO2000048555A2 (fr) 2000-08-24
WO2000048555A3 WO2000048555A3 (fr) 2001-01-11

Family

ID=8237298

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2000/004082 WO2000048555A2 (fr) 1999-02-19 2000-02-17 Compositions cosmétiques

Country Status (7)

Country Link
EP (1) EP1152747A2 (fr)
KR (1) KR20010102282A (fr)
CN (1) CN1196470C (fr)
AU (1) AU771906B2 (fr)
BR (1) BR0008335A (fr)
CA (1) CA2362349A1 (fr)
WO (1) WO2000048555A2 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000071093A1 (fr) * 1999-05-25 2000-11-30 The Procter & Gamble Company Compositions a base de niacinamide et a pouvoir poisseux reduit
WO2010039291A1 (fr) * 2008-10-02 2010-04-08 Trutek Corp. Produits antistatiques pour la peau et procédé

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2701844A1 (fr) * 1993-02-23 1994-09-02 Oreal Association épaississante à base de gomme de guar ou de cellulose non ionique, sans groupe hydrophobe et d'un polymère réticulé, et application pour le traitement des cheveux ou de la peau contenant une telle association.
WO1996003967A1 (fr) * 1994-07-29 1996-02-15 The Procter & Gamble Company Compositions cosmetiques pour cheveux
DE19727508A1 (de) * 1996-07-01 1998-01-08 Schwarzkopf Gmbh Hans Verwendung von Hydrogelbildnern und Mittel zur Behandlung keratinischer Fasern
WO2000006093A1 (fr) * 1998-07-30 2000-02-10 The Procter & Gamble Company Compositions pour cheveux

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2701844A1 (fr) * 1993-02-23 1994-09-02 Oreal Association épaississante à base de gomme de guar ou de cellulose non ionique, sans groupe hydrophobe et d'un polymère réticulé, et application pour le traitement des cheveux ou de la peau contenant une telle association.
WO1996003967A1 (fr) * 1994-07-29 1996-02-15 The Procter & Gamble Company Compositions cosmetiques pour cheveux
DE19727508A1 (de) * 1996-07-01 1998-01-08 Schwarzkopf Gmbh Hans Verwendung von Hydrogelbildnern und Mittel zur Behandlung keratinischer Fasern
WO2000006093A1 (fr) * 1998-07-30 2000-02-10 The Procter & Gamble Company Compositions pour cheveux

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE PROMT [Online] STN; AN 92:300040, MARY T. CLARKE: "Water-soluble Cellulose Ethers for Hair Care Products." XP002143416 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000071093A1 (fr) * 1999-05-25 2000-11-30 The Procter & Gamble Company Compositions a base de niacinamide et a pouvoir poisseux reduit
WO2010039291A1 (fr) * 2008-10-02 2010-04-08 Trutek Corp. Produits antistatiques pour la peau et procédé
AU2009300281B2 (en) * 2008-10-02 2013-09-05 Trutek Corp. Anti-static skin products and method

Also Published As

Publication number Publication date
EP1152747A2 (fr) 2001-11-14
CA2362349A1 (fr) 2000-08-24
AU771906B2 (en) 2004-04-08
CN1345227A (zh) 2002-04-17
CN1196470C (zh) 2005-04-13
WO2000048555A3 (fr) 2001-01-11
KR20010102282A (ko) 2001-11-15
AU3598100A (en) 2000-09-04
BR0008335A (pt) 2002-01-29

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