WO1992019218A2 - Cosmetic compositions - Google Patents

Cosmetic compositions Download PDF

Info

Publication number
WO1992019218A2
WO1992019218A2 PCT/US1992/003347 US9203347W WO9219218A2 WO 1992019218 A2 WO1992019218 A2 WO 1992019218A2 US 9203347 W US9203347 W US 9203347W WO 9219218 A2 WO9219218 A2 WO 9219218A2
Authority
WO
WIPO (PCT)
Prior art keywords
composition according
cps
weight
viscosity
gelling agent
Prior art date
Application number
PCT/US1992/003347
Other languages
French (fr)
Other versions
WO1992019218A3 (en
Inventor
Richard John Cooke
Robert Francis Date
Nigel Geoffrey Barrington
Eric George Spengler
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
Publication of WO1992019218A2 publication Critical patent/WO1992019218A2/en
Publication of WO1992019218A3 publication Critical patent/WO1992019218A3/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/042Gels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/736Chitin; Chitosan; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions 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
    • A61K8/8147Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions 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
    • A61K8/8152Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/30Characterized by the absence of a particular group of ingredients
    • A61K2800/33Free of surfactant
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/594Mixtures of polymers

Definitions

  • the present invention relates to skin- and hair-care cosmetic compositions.
  • cosmetic compositions in the form of aqueous gels which provide improved skin feel and skin care benefits, reduced tack and residue characteristics together with excellent visual clarity, moisturising, rub-in and absorption characteristics.
  • Skin is made up of several layers of cells which coat and protect the keratin and collagen fibrous proteins that form the skeleton of its structure.
  • the outermost of these layers referred to as the stratum corneum, is known to be composed of 250 A protein bundles surrounded by 80 A thick layers.
  • Anionic surfactants and organic solvents typically penetrate the stratum corneum membrane and, by delipidization (i.e. removal of the lipids from the stratum corneum), destroy its integrity. This destruction of the skin surface topography leads to a rough feel and may eventually permit the surfactant or solvent to interact with the keratin, creating irritation.
  • Hair consists of many of the same constituents as the stratum corneum.
  • the outermost region of cells forms a rather thick chemically resistant protective coating enclosing the hair fibre which is called the cuticle.
  • the surface of the cuticle is covered with a thin layer called the epicuticle which is thought to contain lipids and protein.
  • the cuticle envelopes the cortex cells which comprise the major part of the fibre mass. Keratinization takes place in the cortex to build stability into the hair structure.
  • compositions which will assist the stratum corneum and hair cuticle in maintaining their barrier and water retention functions at optimum performance in spite of deleterious interactions which the skin and hair may encounter in washing, work, and recreation.
  • the present invention therefore provides skin- and hair-care cosmetic compositions which provide improvements in absorption, residue, tackiness, skin-feel and skin care characteristics without detriment to either short or longer term moisturizing effectiveness.
  • a skin or hair care composition in the form of an aqueous gel comprising:
  • compositions of this aspect of the present invention contain three essential ingredients as well as various optional components as indicated below. All levels and ratios are by weight of total composition, unless otherwise indicated.
  • a first essential ingredient is carboxymethylchitin.
  • Chitin is a polysaccharide which is present in the integument of lobsters and crabs and is a mucopolysaccharide having beta (1-4) linkages of N-acetyl-D- glucosamine.
  • Carboxymethylchitin is prepared by treating the purified chitin material with alkali followed by monochloracetic acid. It is sold commercially in the form of a dilute (approximately 0.1 % to 0.5% by weight) aqueous solution under the name Chitin Liquid available from A & E Connock Ltd., Fordingbridge, Hampshire, England.
  • carboxymethylchitin is present at a level of from about 0.001 % to about 0.5%, preferably from about 0.002% to about 0.05%, more preferably from about 0.005% to about 0.02% by weight of composition.
  • a second essential component is a water soluble polyglycerylmethacrylate lubricant.
  • This generally should have a viscosity (10% aqueous solution, 20°C, Brookfield RVT) of less than about 4000 cps, preferably less than about 1000 cps and more preferably less than about 500 cps.
  • the polyglycerylmethacrylate lubricant preferably also has a viscosity (neat) in the range of from about 200 to about 5000 cps (Brookfield RVT, 20°C), more preferably from about 500 to about 2000 cps and especially from about 700 to about 900 cps.
  • Lubragel The polyglycerylmethacrylate lubricants which can be used in the compositions of this invention are available under the trademark Lubragel (RTM) from Guardian Chemical Corporation, 230 Marcus Blvd., Hauppage, N.Y. 1 1787.
  • Lubragels can be described as hydrates or clathrates which are formed by the reaction of sodium glycerate with a methacrylic acid polymer. Thereafter, the hydrate or clathrate is stabilized with a small amount of propylene glycol, followed by controlled hydration of the resulting product.
  • Lubragels are marketed in a number of grades of varying glycerate: polymer ratio and viscosity. Preferred for use herein, however, is so-called Lubragel Oil which has a typical viscosity of about 800 cps.
  • Other suitable Lubragels include Lubrigel TW, Lubragel CG and Lubragel MS.
  • the polyglycerylmethacrylate lubricant is incorporated at a level of from about 0.1 % to about 10%, preferably from about 0.2% to about 2%, and more preferably from about 0.3% to about 1 % by weight of composition.
  • compositions of the invention also contain a hydrophilic gelling agent at a level preferably from about 0.1 % to about 20%, more preferably from about 0.2% to about 2%, and especially from about 0.3% to about 1 %.
  • the gelling agent preferably has a viscosity (1 % aqueous solution, 20°C, Brookfield RVT) of at least about 4000 cps, more preferably at least about 10,000 cps, and especially at least 50,000.
  • Suitable hydrophilic gelling agents can generally be described as water- soluble or colloidally water-soluble polymers, and include cellulose ethers (e.g. hydroxyethyl cellulose, methyl cellulose, hydroxy propylmethyl cellulose), polyvinylpyrrolidone, polyvinylalcohol, guar gum, hydroxypropyl guar gum and xanthan gum.
  • cellulose ethers e.g. hydroxyethyl cellulose, methyl cellulose, hydroxy propylmethyl cellulose
  • polyvinylpyrrolidone polyvinylalcohol
  • guar gum hydroxypropyl guar gum
  • xanthan gum xanthan gum
  • Preferred hydrophilic gelling agents herein are acrylic acid/ethyl acrylate copolymers and the carboxy vinyl polymers sold by the B.F. Goodrich Company under the trade mark of Carbopol resins. These resins consist essentially of a colloidally water-soluble polyalkenyl polyether crosslinked polymer of acrylic acid crosslinked with from 0.75% to 2.00% of a crosslinking agent such as for example polyallyl sucrose or polyallyl pentaerythritol. Examples include Carbopol 934, Carbopol 940, Carbopol 950 and Carbopol 980.
  • Carbopol 934 is a water-soluble polymer of acrylic acid crosslinked with about 1 % of a polyallyl ether of sucrose having an average of about 5.8 allyl groups for each sucrose molecule.
  • a most preferred polymer is Carbopol 980 which has an average molecular weight of about 4,000,000.
  • Highly preferred from the viewpoint of tack reduction is a combination of the polyalkenyl polyether cross-linked acrylic acid polymer and the hydrophobically modified cross-linked acrylic acid polymer.
  • Neutralizing agents suitable for use in neutralizing acidic group containing hydrophilic gelling agents herein include sodium hydroxide, potassium hydroxide, ammonium hydroxide, monoethanolamine, diethanolamine and triethanolamine.
  • the compositions of the invention also contain from about 0.1 % to about 10%, preferably from about 1 % to about 5% of a panthenol moisturiser.
  • the panthenol moisturiser can be selected from D-panthenol ⁇ [R]-2,4-dihydroxy-N-[3-hydroxypropyl]-3,3- dimethylbutarriide), DL-panthenol, calcium pantothenate, royal jelly, panthetine, pantotheine, panthenyl ethyl ether, pangamic acid, pyridoxin, pantoyl lactose and Vitamin B complex.
  • Highly preferred from the viewpoint of skin care and tack reduction is D-panthenol.
  • compositions of the invention are in aqueous gel form and are preferably formulated so as to have a product viscosity of at least about 4,000 and preferably in the range from about 4,000 to about 300,000 cps, more preferably from about 20,000 to about 200,000 cps amd especially from about 80,000 to about 150,000 cps (20°C, neat, Brookfield RVT).
  • the compositions are visually clear.
  • the compositions are also preferably substantially free of oil, i.e. contain less than about 1 %, and preferably less than about 0.1 % of materials which are insoluble or which are not colloidally-soluble in the aqueous gel matrix at 20°C.
  • Colloidally-soluble herein refers to particles in the usual colloidal size range, typically from 1 to 1000 nm, especially from 1 to 500 nm. In highly preferred embodiments, the compositions are substantially free of materials which are insoluble or not colloidally soluble in distilled water at 20°C.
  • Such materials include many conventional emollient materials such as hydrocarbon oils and waxes, glyceride esters, alkyl esters, alkenyl esters, fatty alcohols, certain fatty alcohol ethers and fatty acid esters of ethoxylated fatty alcohols, sterols extracted from lanolin, lanolin esters, wax esters, beeswax derivatives, vegetable waxes, phospholipids, sterols and amides.
  • the compositions can, however, contain low levels of insoluble Ingredients added, for example for visual-effect purposes, e.g.
  • thermochromic liquid crystalline materials such as the microencapsulated cholesteryl esters and chiral nematic (non-sterol) based chemicals such as the ⁇ 2-methylbutyl)phenyl 4-alkyl(oxy)benzoates available from Hallcrest, Glenview, Illinois 60025, U.S.A.
  • compositions of the invention have no need of and are preferably also substantially free of surfactant materials which are conventionally added to cosmetic cream and lotion compositions in order to emulsify a water-insoluble oily phase.
  • substantially free means less than about 1 %, preferably less than about 0.1 % of the indicated materials.
  • emulsifiers include ethoxylated fatty acids, ethoxylated esters, phosphated esters, ethoxylated fatty alcohols, polyoxyethylene fatty ether phosphates, fatty acid amides, acyl lactylates, soaps, etc.
  • a further optional but preferred component of the compositions herein added for the purpose of skin feel and tack reduction is a fluid copolymer of ethylene oxide and propylene oxide having a viscosity in the range of from about 55 to about 300,000 Saybolt Universal Seconds [S.U.S.], preferably from about 100 to about 2,000 S.U.S. at 100°F, for example Ucon Fluid 75-H 450.
  • compositions of the invention can be supplemented by other humectants, especially polyhydric alcohol humectants, although preferably they are substantially free (contain less than 0.5%) of glycerol.
  • Polyhydric alcohol humectants other than glycerol which can be added herein include sorbitol, propylene glycol, butylene glycol, hexylene glycol, ethoxylated glucose and hexanetriol.
  • compositions of the invention can be added to the compositions of the invention.
  • An optional but preferred ingredient of the compositions of the invention is trimethylglycine, otherwise sometimes known as betaine. Trimethylglycine is valuable herein from the viewpoint of providing improved skin feel and tack reduction.
  • trimethylglycine is preferably present at a level of from about 1 % to about 10% by weight, preferably from about 3% to about 7% by weight.
  • keratolytic agents such as salicylic acid; proteins and polypeptides and derivatives thereof; water-soluble or solubilizable preservatives such as Germall 115, methyl, ethyl, propyl and butyl esters of hydroxybenzoic acid, EDTA, Euxyl(RTM)K400, Bromopol (2-bromo-2-nitropropane-1 ,3-diol) and phenoxypropanol; anti-bacterials such as Irgasan (RTM) and phenoxyethanol (preferably at levels of from 0.5% to about 5%); soluble or colloidally-soluble moisturising agents such as hylaronic acid, and starch-grafted sodium polyacrylates such as Sanwet (RTM) IM-1000, IM-1500 and IM-2500 available from Celanese Superabsorbent Materials, Portsmith, VA, USA and described in USA-A- 4,076,663; colouring agents; perfumes and perfume solubilizers
  • the pH of the compositions is preferably from about 4 to about 9, more preferably from about 4.5 to about 7.
  • compositions are made by mixing at ambient temperature.
  • compositions display improved skin feel, skin care, tackiness and residue characteristics together with excellent moisturizing, emolliency, rub-in and absorption characteristics.

Abstract

A skin or hair care composition in the form of an aqueous gel comprising carboxymethylchitin, a water-soluble polyglycerylmethacrylate lubricant having a viscosity of less than 4000 cps, and a hydrophilic gelling agent. The compositions provide improved skin feel and skin care benefits, reduced tack and residue characteristics together with excellent visual clarity, moisturising, rub-in and absorption characteristics.

Description

Cosmetic Compositions
Technical Field The present invention relates to skin- and hair-care cosmetic compositions. In particular it relates to cosmetic compositions in the form of aqueous gels which provide improved skin feel and skin care benefits, reduced tack and residue characteristics together with excellent visual clarity, moisturising, rub-in and absorption characteristics.
Background of the Invention Skin is made up of several layers of cells which coat and protect the keratin and collagen fibrous proteins that form the skeleton of its structure. The outermost of these layers, referred to as the stratum corneum, is known to be composed of 250 A protein bundles surrounded by 80 A thick layers. Anionic surfactants and organic solvents typically penetrate the stratum corneum membrane and, by delipidization (i.e. removal of the lipids from the stratum corneum), destroy its integrity. This destruction of the skin surface topography leads to a rough feel and may eventually permit the surfactant or solvent to interact with the keratin, creating irritation.
It is now recognised that maintaining the proper water gradient across the statum corneum is important to its functionality. Most of this water, which is sometimes considered to be the stratum corneum's plasticizer, comes from inside the body. If the humidity is too low, such as in a cold climate, insufficient water remains in the outer layers of the stratum corneum to properly plasticize the tissue; and the skin begins to scale and becomes itchy. Skin permeability is also decreased somewhat when there is inadequate water across the stratum corneum. On the other hand, too much water on the outside of the skin causes the stratum corneum to ultimately sorb three to five times its own weight of bound water. This swells and puckers the skin and results in approximately a two to three fold increase in the permeability of the skin to water and other polar molecules.
Hair consists of many of the same constituents as the stratum corneum. The outermost region of cells forms a rather thick chemically resistant protective coating enclosing the hair fibre which is called the cuticle. The surface of the cuticle is covered with a thin layer called the epicuticle which is thought to contain lipids and protein. The cuticle envelopes the cortex cells which comprise the major part of the fibre mass. Keratinization takes place in the cortex to build stability into the hair structure.
Thus, a need exists for compositions which will assist the stratum corneum and hair cuticle in maintaining their barrier and water retention functions at optimum performance in spite of deleterious interactions which the skin and hair may encounter in washing, work, and recreation.
Conventional cosmetic cream and lotion compositions as described, for example, in Sagarin, Cosmetics Science and Technology, 2nd Edition, Vol. I, Wiley Interscience (1972) and Encyclopaedia of Chemical Technology, Third Edition, Volume 7 are known to provide varying degrees of emolliency, barrier and water-retention (moisturising) benefits. However, they can also suffer serious negatives in terms of skin feel (i.e. they often feel very greasy on the skin) as well as having poor rub-in, absorption and residue characteristics. In the case of hair-care compositions they can also suffer from resoiling negatives.
The present invention therefore provides skin- and hair-care cosmetic compositions which provide improvements in absorption, residue, tackiness, skin-feel and skin care characteristics without detriment to either short or longer term moisturizing effectiveness.
Summary of the Invention Accordingly, in one aspect of the present invention, there is provided a skin or hair care composition in the form of an aqueous gel comprising:
(a) from about 0.001 % to about 0.5% by weight of carboxymethylchitin,
(b) from about 0.1 % to about 10% by weight of a water polyglycerylmethacrylate lubricant having a viscosity (10% aqueous solution, 20°C, Brookfield RVT) of less than 4000 cps, and (c) from about 0.1 % to about 20% by weight of a hydrophilic gelling agent.
The compositions of this aspect of the present invention contain three essential ingredients as well as various optional components as indicated below. All levels and ratios are by weight of total composition, unless otherwise indicated.
A first essential ingredient is carboxymethylchitin. Chitin is a polysaccharide which is present in the integument of lobsters and crabs and is a mucopolysaccharide having beta (1-4) linkages of N-acetyl-D- glucosamine. Carboxymethylchitin is prepared by treating the purified chitin material with alkali followed by monochloracetic acid. It is sold commercially in the form of a dilute (approximately 0.1 % to 0.5% by weight) aqueous solution under the name Chitin Liquid available from A & E Connock Ltd., Fordingbridge, Hampshire, England.
In the present compositions, carboxymethylchitin is present at a level of from about 0.001 % to about 0.5%, preferably from about 0.002% to about 0.05%, more preferably from about 0.005% to about 0.02% by weight of composition.
A second essential component is a water soluble polyglycerylmethacrylate lubricant. This generally should have a viscosity (10% aqueous solution, 20°C, Brookfield RVT) of less than about 4000 cps, preferably less than about 1000 cps and more preferably less than about 500 cps. In addition, the polyglycerylmethacrylate lubricant preferably also has a viscosity (neat) in the range of from about 200 to about 5000 cps (Brookfield RVT, 20°C), more preferably from about 500 to about 2000 cps and especially from about 700 to about 900 cps.
The polyglycerylmethacrylate lubricants which can be used in the compositions of this invention are available under the trademark Lubragel (RTM) from Guardian Chemical Corporation, 230 Marcus Blvd., Hauppage, N.Y. 1 1787. In general, Lubragels can be described as hydrates or clathrates which are formed by the reaction of sodium glycerate with a methacrylic acid polymer. Thereafter, the hydrate or clathrate is stabilized with a small amount of propylene glycol, followed by controlled hydration of the resulting product. Lubragels are marketed in a number of grades of varying glycerate: polymer ratio and viscosity. Preferred for use herein, however, is so-called Lubragel Oil which has a typical viscosity of about 800 cps. Other suitable Lubragels include Lubrigel TW, Lubragel CG and Lubragel MS.
In the present compositions, the polyglycerylmethacrylate lubricant is incorporated at a level of from about 0.1 % to about 10%, preferably from about 0.2% to about 2%, and more preferably from about 0.3% to about 1 % by weight of composition.
The compositions of the invention also contain a hydrophilic gelling agent at a level preferably from about 0.1 % to about 20%, more preferably from about 0.2% to about 2%, and especially from about 0.3% to about 1 %. The gelling agent preferably has a viscosity (1 % aqueous solution, 20°C, Brookfield RVT) of at least about 4000 cps, more preferably at least about 10,000 cps, and especially at least 50,000.
Suitable hydrophilic gelling agents can generally be described as water- soluble or colloidally water-soluble polymers, and include cellulose ethers (e.g. hydroxyethyl cellulose, methyl cellulose, hydroxy propylmethyl cellulose), polyvinylpyrrolidone, polyvinylalcohol, guar gum, hydroxypropyl guar gum and xanthan gum.
Preferred hydrophilic gelling agents herein, however, are acrylic acid/ethyl acrylate copolymers and the carboxy vinyl polymers sold by the B.F. Goodrich Company under the trade mark of Carbopol resins. These resins consist essentially of a colloidally water-soluble polyalkenyl polyether crosslinked polymer of acrylic acid crosslinked with from 0.75% to 2.00% of a crosslinking agent such as for example polyallyl sucrose or polyallyl pentaerythritol. Examples include Carbopol 934, Carbopol 940, Carbopol 950 and Carbopol 980. Carbopol 934 is a water-soluble polymer of acrylic acid crosslinked with about 1 % of a polyallyl ether of sucrose having an average of about 5.8 allyl groups for each sucrose molecule. A most preferred polymer is Carbopol 980 which has an average molecular weight of about 4,000,000. Also preferred for use herein are hydrophobically-modified cross-linked polymers of acrylic acid having amphipathic properties available under the Trade Name Carbopol 1342 and Pemulen TR-1 (CTFA Designation: Acrylates/10-30 Alkyl Acrylate Crosspolymer.) Highly preferred from the viewpoint of tack reduction is a combination of the polyalkenyl polyether cross-linked acrylic acid polymer and the hydrophobically modified cross-linked acrylic acid polymer.
Neutralizing agents suitable for use in neutralizing acidic group containing hydrophilic gelling agents herein include sodium hydroxide, potassium hydroxide, ammonium hydroxide, monoethanolamine, diethanolamine and triethanolamine.
In preferred embodiments, the compositions of the invention also contain from about 0.1 % to about 10%, preferably from about 1 % to about 5% of a panthenol moisturiser. The panthenol moisturiser can be selected from D-panthenol {[R]-2,4-dihydroxy-N-[3-hydroxypropyl]-3,3- dimethylbutarriide), DL-panthenol, calcium pantothenate, royal jelly, panthetine, pantotheine, panthenyl ethyl ether, pangamic acid, pyridoxin, pantoyl lactose and Vitamin B complex. Highly preferred from the viewpoint of skin care and tack reduction is D-panthenol.
The compositions of the invention are in aqueous gel form and are preferably formulated so as to have a product viscosity of at least about 4,000 and preferably in the range from about 4,000 to about 300,000 cps, more preferably from about 20,000 to about 200,000 cps amd especially from about 80,000 to about 150,000 cps (20°C, neat, Brookfield RVT). Preferably the compositions are visually clear. The compositions are also preferably substantially free of oil, i.e. contain less than about 1 %, and preferably less than about 0.1 % of materials which are insoluble or which are not colloidally-soluble in the aqueous gel matrix at 20°C. "Colloidally-soluble" herein refers to particles in the usual colloidal size range, typically from 1 to 1000 nm, especially from 1 to 500 nm. In highly preferred embodiments, the compositions are substantially free of materials which are insoluble or not colloidally soluble in distilled water at 20°C. Such materials include many conventional emollient materials such as hydrocarbon oils and waxes, glyceride esters, alkyl esters, alkenyl esters, fatty alcohols, certain fatty alcohol ethers and fatty acid esters of ethoxylated fatty alcohols, sterols extracted from lanolin, lanolin esters, wax esters, beeswax derivatives, vegetable waxes, phospholipids, sterols and amides. The compositions can, however, contain low levels of insoluble Ingredients added, for example for visual-effect purposes, e.g. thermochromic liquid crystalline materials such as the microencapsulated cholesteryl esters and chiral nematic (non-sterol) based chemicals such as the {2-methylbutyl)phenyl 4-alkyl(oxy)benzoates available from Hallcrest, Glenview, Illinois 60025, U.S.A.
The compositions of the invention have no need of and are preferably also substantially free of surfactant materials which are conventionally added to cosmetic cream and lotion compositions in order to emulsify a water-insoluble oily phase. Again, "substantially free" means less than about 1 %, preferably less than about 0.1 % of the indicated materials. Such emulsifiers include ethoxylated fatty acids, ethoxylated esters, phosphated esters, ethoxylated fatty alcohols, polyoxyethylene fatty ether phosphates, fatty acid amides, acyl lactylates, soaps, etc.
A further optional but preferred component of the compositions herein added for the purpose of skin feel and tack reduction is a fluid copolymer of ethylene oxide and propylene oxide having a viscosity in the range of from about 55 to about 300,000 Saybolt Universal Seconds [S.U.S.], preferably from about 100 to about 2,000 S.U.S. at 100°F, for example Ucon Fluid 75-H 450.
The compositions of the invention can be supplemented by other humectants, especially polyhydric alcohol humectants, although preferably they are substantially free (contain less than 0.5%) of glycerol. Polyhydric alcohol humectants other than glycerol which can be added herein include sorbitol, propylene glycol, butylene glycol, hexylene glycol, ethoxylated glucose and hexanetriol.
A number of additional water-soluble materials can be added to the compositions of the invention. An optional but preferred ingredient of the compositions of the invention is trimethylglycine, otherwise sometimes known as betaine. Trimethylglycine is valuable herein from the viewpoint of providing improved skin feel and tack reduction. In the present compositions, trimethylglycine is preferably present at a level of from about 1 % to about 10% by weight, preferably from about 3% to about 7% by weight.
Other optional ingredients include keratolytic agents such as salicylic acid; proteins and polypeptides and derivatives thereof; water-soluble or solubilizable preservatives such as Germall 115, methyl, ethyl, propyl and butyl esters of hydroxybenzoic acid, EDTA, Euxyl(RTM)K400, Bromopol (2-bromo-2-nitropropane-1 ,3-diol) and phenoxypropanol; anti-bacterials such as Irgasan (RTM) and phenoxyethanol (preferably at levels of from 0.5% to about 5%); soluble or colloidally-soluble moisturising agents such as hylaronic acid, and starch-grafted sodium polyacrylates such as Sanwet (RTM) IM-1000, IM-1500 and IM-2500 available from Celanese Superabsorbent Materials, Portsmith, VA, USA and described in USA-A- 4,076,663; colouring agents; perfumes and perfume solubilizers etc. Water is also present at a level of from about 50% to about 99.2%, preferably from about 80% to about 95% by weight of the compositions herein.
The pH of the compositions is preferably from about 4 to about 9, more preferably from about 4.5 to about 7.
The invention is illustrated to the following limiting examples.
Figure imgf000010_0001
The compositions are made by mixing at ambient temperature.
The compositions display improved skin feel, skin care, tackiness and residue characteristics together with excellent moisturizing, emolliency, rub-in and absorption characteristics.

Claims

1. A skin or hair care composition in the form of an aqueous gel comprising:
(a) from about 0.001 % to about 0.5% by weight of carboxymethylchitin,
(b) from about 0.1 % to about 10% by weight of a water-soluble polyglycerylmethacrylate lubricant having a viscosity (10% aqueous solution, 20°C, Brookfield RVT) of less than 4000 cps, and
(c) from about 0.1 % to about 20% by weight of a hydrophilic gelling agent.
2. A composition according to claim 1 comprising from about 0.002% to about 0.5%, preferably from about 0.005% to about 0.02% by weight of carboxymethylchitin.
3. A composition according to claim 1 or 2 wherein the polyglycerylmethacrylate lubricant is a hydrate or clathrate formed by the reaction of sodium glycerate with a methacrylic acid polymer.
4. A composition according to any of claims 1 to 3 wherein the polyglycerylmethacrylate lubricant has a viscosity (neat) in the range of from about 200 to about 5000 cps (Brookfield RVT, 20°C), preferably from about 500 to about 2000 cps, more preferably from about 700 to about 900 cps.
5. A composition according to any of claims 1 to 4 comprising from about 0.2% to about 2%, preferably from about 0.3% to about 1 % by weight of the polyglycerylmethacrylate lubricant.
6. A composition according to any of claims 1 to 5 having a viscosity (20°C, neat, Brookfield RVT) of from about 4000 to about 300,000 cps.
7. A composition according to any of claims 1 to 6 wherein the gelling agent has a viscosity (1 % aqueous solution, 20°C, Brookfield RVT) of at least about 4000 cps, preferably at least about 10,000 cps.
8. A composition according to any of claims 1 to 7 wherein the gelling agent comprises a carboxyvinyl polymer, preferably a colloidally water-soluble polymer of acrylic acid cross-linked with from about 0.75% to about 2.0% of a cross-linking agent selected from polyallyl sucrose and polyallyl pentaerythritol.
9. A composition according to any of claims 1 to 8 wherein the gelling agent comprises a hydrophobically-modified cross-linked polymer of acrylic acid having amphipathic properties.
10. A composition according to any of claims 1 to 9 comprising from about 0.2% to about 2%, preferably from about 0.3% to about 1 % of the gelling agent.
11. A composition according to any of claims 1 to 10 additionally comprising from about 0.1 % to about 10% of a panthenol moisturiser.
12. A composition according to any of Claims 1 to 1 1 additionally comprising from about 0.1 % to about 5% by weight of a fluid copolymer of ethylene oxide and propylene oxide having a viscosity in the range of from about 55 to about 300,000 Saybolt Universal Seconds.
13. A composition according to any of claims 1 to 12 additionally comprising from about 1 % to about 10% of trimethylglycine (betaine).
14. A composition according to any of claims 1 to 13 which is substantially oil-free.
PCT/US1992/003347 1991-05-04 1992-04-24 Cosmetic compositions WO1992019218A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9109757.6 1991-05-04
GB9109757A GB9109757D0 (en) 1991-05-04 1991-05-04 Cosmetic compositions

Publications (2)

Publication Number Publication Date
WO1992019218A2 true WO1992019218A2 (en) 1992-11-12
WO1992019218A3 WO1992019218A3 (en) 1993-01-07

Family

ID=10694509

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1992/003347 WO1992019218A2 (en) 1991-05-04 1992-04-24 Cosmetic compositions

Country Status (8)

Country Link
CN (1) CN1066387A (en)
AU (1) AU2315892A (en)
GB (1) GB9109757D0 (en)
IE (1) IE921416A1 (en)
MA (1) MA22517A1 (en)
MX (1) MX9202088A (en)
PT (1) PT100451A (en)
WO (1) WO1992019218A2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0610655A1 (en) * 1993-02-10 1994-08-17 Dr. GERHARD MANN chem.-pharm. Fabrik GmbH Medicament containing dexpanthenol for topical application
EP0780116A1 (en) * 1995-07-12 1997-06-25 Shiseido Company Limited External skin preparation
WO1999032071A2 (en) * 1997-12-22 1999-07-01 Henkel Kommanditgesellschaft Auf Aktien Hair treatment agent containing biopolymers and monosaccharides and/or dissacharides and/or panthenol

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4837019A (en) * 1986-08-11 1989-06-06 Charles Of The Ritz Group Ltd. Skin treatment composition and method for treating burned skin
US4973473A (en) * 1989-06-23 1990-11-27 Revlon, Inc. Skin care preparation
US4980155A (en) * 1989-09-11 1990-12-25 Revlon, Inc. Two phase cosmetic composition
US5030443A (en) * 1987-08-28 1991-07-09 Clairol Incorporated Alginate hair setting compositions
US5122598A (en) * 1988-05-13 1992-06-16 Fidia S.P.A. Polysaccharide esters

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4837019A (en) * 1986-08-11 1989-06-06 Charles Of The Ritz Group Ltd. Skin treatment composition and method for treating burned skin
US5030443A (en) * 1987-08-28 1991-07-09 Clairol Incorporated Alginate hair setting compositions
US5122598A (en) * 1988-05-13 1992-06-16 Fidia S.P.A. Polysaccharide esters
US4973473A (en) * 1989-06-23 1990-11-27 Revlon, Inc. Skin care preparation
US4980155A (en) * 1989-09-11 1990-12-25 Revlon, Inc. Two phase cosmetic composition

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0610655A1 (en) * 1993-02-10 1994-08-17 Dr. GERHARD MANN chem.-pharm. Fabrik GmbH Medicament containing dexpanthenol for topical application
EP0780116A1 (en) * 1995-07-12 1997-06-25 Shiseido Company Limited External skin preparation
EP0780116A4 (en) * 1995-07-12 1997-09-10 Shiseido Co Ltd External skin preparation
US6008246A (en) * 1995-07-12 1999-12-28 Shiseido Co., Ltd. External preparation for skin containing a low-molecular-weight betaine
WO1999032071A2 (en) * 1997-12-22 1999-07-01 Henkel Kommanditgesellschaft Auf Aktien Hair treatment agent containing biopolymers and monosaccharides and/or dissacharides and/or panthenol
WO1999032071A3 (en) * 1997-12-22 1999-09-30 Henkel Kgaa Hair treatment agent containing biopolymers and monosaccharides and/or dissacharides and/or panthenol

Also Published As

Publication number Publication date
IE921416A1 (en) 1992-11-04
CN1066387A (en) 1992-11-25
GB9109757D0 (en) 1991-06-26
PT100451A (en) 1993-08-31
MA22517A1 (en) 1992-12-31
AU2315892A (en) 1992-12-21
MX9202088A (en) 1993-07-01
WO1992019218A3 (en) 1993-01-07

Similar Documents

Publication Publication Date Title
US5420118A (en) Gel type cosmetic compositions
US5380528A (en) Silicone containing skin care compositions having improved oil control
US5858340A (en) Cosmetic compositions
EP0689456B1 (en) Cosmetic compositions
JPH07509177A (en) Cosmetic composition in the form of a water/oil/water ternary emulsion with a gelled external phase
CA2095721C (en) Gel type compositions having improved oil control
JPH08506583A (en) Cosmetic composition
EP0513183B1 (en) Cosmetic compositions
WO1992019216A1 (en) Skin and hair-care gel compositions
US5641493A (en) Cosmetic compositions
WO1992019275A2 (en) Cosmetic compositions
EP0641189A1 (en) Cosmetic compositions
WO1994008555A1 (en) Cosmetic composition comprising a silicone/polyglycerylmethacrylate lubricant
WO1992019217A1 (en) Cosmetic compositions
WO1992019218A2 (en) Cosmetic compositions
US5879689A (en) Cosmetic compositions

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): AU BB BG BR CA CS FI HU JP KP KR LK MG MN MW NO PL RO RU SD US

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): AT BE BF BJ CF CG CH CI CM DE DK ES FR GA GB GN GR IT LU MC ML MR NL SE SN TD TG

AK Designated states

Kind code of ref document: A3

Designated state(s): AU BB BG BR CA CS FI HU JP KP KR LK MG MN MW NO PL RO RU SD US

AL Designated countries for regional patents

Kind code of ref document: A3

Designated state(s): AT BE BF BJ CF CG CH CI CM DE DK ES FR GA GB GN GR IT LU MC ML MR NL SE SN TD TG

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase in:

Ref country code: CA