EP0827388A1 - Cosmetic make-up compositions - Google Patents

Cosmetic make-up compositions

Info

Publication number
EP0827388A1
EP0827388A1 EP96912982A EP96912982A EP0827388A1 EP 0827388 A1 EP0827388 A1 EP 0827388A1 EP 96912982 A EP96912982 A EP 96912982A EP 96912982 A EP96912982 A EP 96912982A EP 0827388 A1 EP0827388 A1 EP 0827388A1
Authority
EP
European Patent Office
Prior art keywords
mixtures
monomers
carboxylic acids
unsaturated carboxylic
water
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP96912982A
Other languages
German (de)
French (fr)
Other versions
EP0827388A4 (en
Inventor
Padraig Hugh Mcdermott
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
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 Procter and Gamble Co filed Critical Procter and Gamble Co
Publication of EP0827388A1 publication Critical patent/EP0827388A1/en
Publication of EP0827388A4 publication Critical patent/EP0827388A4/en
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A61K8/894Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
    • 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
    • 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
    • A61K8/06Emulsions
    • 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
    • A61K8/06Emulsions
    • A61K8/062Oil-in-water emulsions
    • 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
    • A61K8/06Emulsions
    • A61K8/064Water-in-oil emulsions, e.g. Water-in-silicone emulsions
    • 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
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • 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
    • A61K8/8105Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • A61K8/8111Homopolymers or copolymers of aliphatic olefines, e.g. polyethylene, polyisobutene; 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
    • A61K8/8147Homopolymers 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
    • 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
    • A61K8/817Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A61K8/8182Copolymers of vinyl-pyrrolidones. 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
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • A61Q1/10Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara
    • 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
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/594Mixtures of polymers

Definitions

  • the present invention relates to cosmetic make-up compositions, particularly eye make-ups and mascaras, comprising water-insoluble polymeric material in the form of an aqueous emulsion or latex.
  • Said compositions have improved wear benefits compared to compositions known in the art and are easily removed with soap and water.
  • Eye make-up compositions including mascara, are significant products in the cosmetics market. Mascara enhances the beauty of the wearer by coating the eye lashes, or in some instances eyebrows, with color.
  • Eye makeup compositions comprising polymeric emulsions in order to eliminate smudging are well known in the art and typically include water- insoluble polymers, also referred to as latexes.
  • Such compositions including eye shadows as disclosed in U.S. Patent 3,639,572, Henrich, issued February 1 , 1972; and mascaras as disclosed in U.S. Patent 4,423,031 , Murui et al., issued December 27, 1983; and European Patent Application (EPA) 0568035, published November 3, 1993.
  • These compositions include plasticizers or solvents to assist in forming films using said latexes.
  • These compositions are known to contain thickeners to adjust the viscosity of the composition.
  • Said thickeners include water-soluble and water-swellable polymers, typically known for such use in the cosmetic art.
  • the invention disclosed therein includes mascara compositions comprising water-based silicone elastomeric latex, emulsions as opposed to "water- based" acrylic polymers. Longer wear and durability is attributed to the used of the elastomeric latex as it is more compatible with the rest of the compositional matrix than the acrylic polymers.
  • compositions known in the art which seek to avoid the combination of plasticizers and insoluble-polymer are exemplified in EPO 0530084, published March 3, 1993.
  • This application discloses compositions comprising a dispersed phase and a dispersant phase , the dispersant phase containing at least one water-soluble polymer and the dispersed phase containing at least 50% wax.
  • Said composition may contain other materials routinely used in cosmetic compositons including water-insoluble polymers.
  • compositions of the present invention are water-in-oil and oil-in-water emulsions.
  • a cosmetic make-up composition suitable for use as a mascara or the like and which comprises:
  • a cosmetic make-up composition suitable for use as a mascara or the like and which comprises:
  • X is a hydrogen atom or a C-
  • Y is C8-C22 alkoxy or alkyl radical
  • n from about 0 to about 200
  • m from about 1 to about 40
  • q from about 1 to about 100
  • the molecular weight of the residue (C2H4 ⁇ -) x (C 3 H6 ⁇ -) y X being from about 250 to about 2000
  • x and y being selected so that the weight ratio of the oxyethylene/oxypropylene groups is from about 100:0 to about 20:80.
  • compositions of the invention exhibit improved wear, increased resistance to water and are easily removed with soap and water.
  • a first essential component of the make-up composition of the present invention is an insoluble polymeric material in an aqueous emulsion.
  • Said materials disclosed in the art as latexes, are aqueous emulsions or dispersions of polymeric materials comprising polymerized monomers, mixtures of monomers, derivatives of said monomers and mixtures of said monomers and mixtures thereof.
  • These polymeric materials disclosed herein also include chemically modified (derivatives) of said polymeric material disclosed above.
  • the polymerization process for making said polymeric material of the present invention is well known in the art. Such processes are disclosed in Kirk Othmer, Encyclopedia of Chemical Technology. Volume 14, "Latex Technology” 3rd Ed. 1981 ; incorporated herein by reference.
  • These insoluble polymeric materials of the present invention comprise from about 0.1% to about 60%; preferably from about 2% to about 40% and most preferably from about 3% to about 30% by weight of the composition.
  • These insoluble polymeric materials comprise polymerized monomers, mixtures of monomers, derivatives of said monomers and mixtures of said monomers and mixtures thereof selected from the group consisting of aromatic vinyls, dienes, vinyl cyanides, vinyl halides, vinylidene halides, vinyl esters, olefins and their isomers, vinyl pyrrolidone, unsaturated carboxylic acids, alkyl esters of unsaturated carboxylic acids, hydroxy derivatives of alkyl esters of unsaturated carboxylic acids, amides of unsaturated carboxylic acids, amine derivatives of unsaturated carboxylic acids, glycidyl derivatives of alkyl esters of unsaturated carboxylic acids, olefinic diamines and isomers, aromatic diamines, terephthaloyl
  • the insoluble polymeric material preferably comprise polymerized monomers, mixtures of monomers, derivatives of said monomers and mixtures of said monomers and mixtures thereof preferably selected from the group consisting of aromatic vinyls, dienes, vinyl esters, olefins and their isomers, unsaturated carboxylic acids, alkyl esters of unsaturated carboxylic acids, hydroxy derivatives of alkyl esters of unsaturated carboxylic acids, amides of unsaturated carboxylic acids and mixtures thereof.
  • the insoluble polymeric material comprise polymerized monomers, mixtures of monomers, derivatives of said monomers and mixtures of said monomers and mixtures thereof most preferably selected from the group consisting of aromatic vinyls, dienes, vinyl esters, alkyl esters of unsaturated carboxylic acids, hydroxy derivatives of alkyl esters of unsaturated carboxylic acids and mixtures thereof.
  • Specific polymeric material useful in the present invention include, but, are not necessarily limited to the Syntran Series (of latexes) from Interpolymer Corporation, for example Syntran 5170 and Syntran 5130 (acrylates copolymers formulated with added ammonia, propylene glycol, preservative and surfactant) and Syntran 5002 (styrene/acrylates/methacrylate copolymer formulated with added ammonia, propylene glycol, preservative and surfactant); the Primal Series (acrylic latexes) from Rohm & Hass; Appretan V (styrene/acrylic ester copolymer latexes) from Hoechst; Vinac (polyvinylacetate latex) from Air Products; UCAR latex resin 130 (polyvinylacetate latex) from Union Carbide; Rhodopas A Series (polyvinylacetate latexes) from Rhone Poulenc; Appretan MB, EM, TV (vinyl
  • the make-up compositions of the present invention also preferably comprise from about 0.1% to about 10% by weight of a first surfactant or mixture of surfactants having an average HLB of from about 3 to about 6 and from about 0.1% to about 10% by weight of a second surfactant or mixture of surfactants having an weight average HLB of from about 8 to about 15.
  • the first surfactant comprises an alkyl- or alkoxy-dimethicone copolyol having the general formula:
  • X is a hydrogen atom or a C-
  • Y is C8-C22 alkoxy or alkyl radical
  • n from about 0 to about 200
  • m from about 1 to about 40.
  • q from about 1 to about 100
  • the molecular weight of the residue (C2H4 ⁇ -) x (C3H6 ⁇ -) v X being from about 250 to about 2000
  • x and y being selected so that the weight ratio of the oxyethylene/oxypropylene groups is from about 100:0 to about 20:80.
  • Y is C16-C20 a
  • a make-up composition comprising:
  • X is a hydrogen atom or a C1 to C-j ⁇ alkyl, alkoxy or acyl radical
  • Y is C8-C22 alkoxy or alkyl radical
  • n from about 0 to about 200
  • m from about 1 to about 40
  • q from about 1 to about 100
  • the molecular weight of the residue (C2H4 ⁇ -) x (C HeO-)yX being from about 250 to about 2000
  • x and y being selected so that the weight ratio of the oxyethylene/oxypropylene groups is from about 100:0 to about 20:80.
  • the second surfactant herein preferably comprises an organic base neutralized C12 -C24 fatty acid.
  • a preferred organic base herein is triethanolamine.
  • a preferred fatty acid herein is stearic acid.
  • compositions herein additionally comprise from about 0.1 % to about 10% of polyvinylpyrrolidone hexadecene copolymer.
  • This copolymer is useful in combination with the insoluble polymeric material in an aqueous emulsion and surfactants for improving water resistance and wear of the compositions.
  • a cosmetic make-up composition suitable for use as a mascara or the like and which is in the form of an emulsion comprising:
  • Optional ingredients useful in the present invention are selected based on either the various forms or attributes the composition is to have.
  • the most preferred embodiments of the present invention are water-in-oil or oil-in- water emulsions.
  • Some of the most common optional ingredients include oils and fats, emulsifiers, waxes, pigments and mixtures thereof.
  • Make-up compositions of the present invention can take the form of oil-in- water or water-in-oil emulsion compositions. These compositions are based on a combination of lipophilic materials optionally with one or more solvents. Said lipophilic materials typically comprise oils and fats generally known for use in the cosmetic art and are generally utilized herein in a level of from about 0% to about 70%, preferably from about 20 % to about 60% by weight.
  • Oils typically used in cosmetics include those selected from the group consisting of polar oils, non-polar oils, volatile oils, non-volatile oils and mixtures thereof. These oils may be saturated or unsaturated, straight or branched chained, aliphatic or aromatic hydrocarbons. Preferred oils include non-polar volatile hydrocarbons including isodecane (such as Permethyl-99A®, available from Presperse Inc.) and the C7-C8 through C12-C15 isoparaffins (such as the Isopar® Series available from Exxon Chemicals).
  • isodecane such as Permethyl-99A®, available from Presperse Inc.
  • C7-C8 through C12-C15 isoparaffins such as the Isopar® Series available from Exxon Chemicals.
  • Fats employed according to the invention are selected from the group consisting of fats derived from animals, vegetables, synthetically derived fats, and mixtures thereof wherein said fats have a melting point from about 55°C to about 100°C and a needle penetration, as measured according to the American standard ASTM D5, from about 3 to about 40 at 25°C.
  • the fats selected for use in the present invention are fatty acid esters which are solids at room temperature and exhibit crystalline structure.
  • fatty acid esters useful in the present invention include the glyceryl esters of higher fatty acids such as stearic and palmitic such as glyceryl monostearate, glyceryl distearate, glyceryl tristearate, palmitate esters of glycerol, C-
  • Waxes are defined as lower-melting organic mixtures or compounds of high molecular weight, solid at room temperature and generally similar in composition to fats and oils except that they contain no glycerides. Some are hydrocarbons, others are esters of fatty acids and alcohols. Waxes useful in the present invention are selected from the group consisting of animal waxes, vegetable waxes, mineral waxes, various fractions of natural waxes, synthetic waxes, petroleum waxes, ethylenic polymers, hydrocarbon types such as Fischer-Tropsch waxes, silicone waxes, and mixtures thereof wherein the waxes have a melting point between 55° and 100°C and a needle penetration, as measured according to the American standard ASTM D5, of 3 to 40 at 25°C.
  • the principle of the measurement of the needle penetration according to the standards ASTM D5 consists in measuring the depth, expressed in tenths of a millimeter, to which a standard needle (weighing 2.5 g and placed in a needle holder weighing 47.5 g, i.e. a total of 50 g) penetrates when placed on the wax for 5 seconds.
  • the specific waxes useful in the present invention are selected from the group consisting of beeswax, lanolin wax, shellac wax (animal waxes); camauba, candelilla, bayberry (vegetable waxes); ozokerite, ceresin, (mineral waxes); paraffin, microcrystalline waxes (petroleum waxes); polyethylene, (ethylenic polymers); polyethylene homopolymers (Fischer- Tropsch waxes); C24-45 alkyl methicones (silicone waxes); and mixtures thereof. Most preferred are beeswax, lanolin wax, camauba, candelilla, ozokerite, ceresin, paraffins, microcrystalline waxes, polyethylene, C24-45 alkyl methicones, and mixtures thereof.
  • Inorganic pigments useful in the present invention include those selected from the group consisting of rutile or anatase titanium dioxide, coded in the Color Index under the reference Cl 77,891; black, yellow, red and brown iron oxides, coded under references Cl 77,499, 77, 492 and, 77,491; manganese violet (Cl 77,742); ultramarine blue (Cl 77,007); chromium oxide (Cl 77,288); chromium hydrate (Cl 77,289); and ferric blue (Cl 77,510) and mixtures thereof.
  • the organic pigments and lakes useful in the present invention include those selected from the group consisting of D&C Red No. 19 (Cl 45,170), D&C Red No. 9 (Cl 15,585),D&C Red NO. 21 (Cl 45,380), D&C Orange No. 4 (Cl 15,510), D&C Orange No. 5 (Cl 45,370), D&C Red No. 27 (Cl 45,410), D&C Red No. 13 (Cl 15,630), D&C Red No. 7 (Cl 15,850), D&C Red No. 6 (Cl 15,850), D&C Yellow No. 5 (Cl 19,140), D&C Red No. 36 (Cl 12,085), D&C Orange No. 10 (Cl 45,425), D&C Yellow No. 6 (Cl 15,985), D&C Red No. 30 (Cl 73,360), D&C Red No. 3 (Cl 45,430) and the dye or lakes based on Cochineal Carmine (Cl 75,570) and mixtures thereof.
  • the pearlescent pigments useful in the present invention include those selected from the group consisting of the white pearlescent pigments such as mica coated with titanium oxide, bismuth oxychloride, colored pearlescent pigments such as titanium mica with iron oxides, titanium mica with ferric blue. chromium oxide and the like, titanium mica with an organic pigment of the above-mentioned type as well as those based on bismuth oxychloride and mixtures thereof.
  • composition of the present invention contain a preservative system to inhibit microbiological growth and maintain the integrity of the product.
  • the preservative system does not have a detrimental effect on the composition.
  • Water dispersible and oil dispersible clays may also be useful in the invention to thicken the water or the oil phase.
  • the water dispersible clays comprise bentonite and hectorite, such as Bentone EW, LT from Rheox; magnesium aluminum silicate, such as Veegum from Vanderbilt Co.; attapulgite such as Attasorb or Pharamasorb from Engelhard, Inc.; laponite and montmorrilonite, such as Gelwhite from ECC America; and mixtures thereof.
  • the oil dispersible clays comprise quaternium-18 bentonite, such as Bentone 34 and 38 from Rheox; the Claytone Series from ECC America; quaternium-18 hectorite, such as Bentone gels from Rheox; and mixtures thereof.
  • compositions of the invention can be prepared as follows. 1. Oil-in-Water Emulsion
  • the waxes and fats are placed in a vessel equipped with heating and mixing.
  • the waxes and fats are heated to about 85°C with low speed mixing until liquefied and homogeneous.
  • pigments any oil dispersible or soluble components are added.
  • the mixing rate is increased to high and mixed until the pigments are uniformly dispersed throughout the lipid mixture; about 30-35 minutes.
  • the emulsifiers are added to said lipid mixture while continuing to mix .
  • aqueous mixture is mixed with heating until this aqueous mixture is about 85°C. Q.S. for any water loss from said aqueous mixture.
  • the two mixtures are slowly combined and mixed with a high speed dispersator type mixer.
  • the heat source is removed and the mixing is continued until the temperature of said combined mixture is from about 65°C- 70°C.
  • Q.S. said combined mixture for any water loss.
  • the preservatives and insoluble polymer component are added and mixed until homogeneous.
  • Said combined mixture is cooled to about 45°C-47°C and any remaining components are added. Cooling and mixing is continued until said combined mixture is about 27°C to about 30°C.
  • Said combined mixture is transfered to suitable storage containers for subsequent filling of retail size packaging.
  • phase A The components of phase A are premixed for 30 minutes at room temperature with high shear.
  • the phase A premix is then heated to 85-90°C with high shear.
  • the wax phase B ingredients are premixed and heated to 90°C with slow stirring for one hour.
  • the wax phase is added to the phase A premix at 90°C and mixed for 20 minutes with high shear. Cooling is commenced and the water phase ingredients are added. Mixing is continued with high shear. The mixture is cooled to 45°C and the remaining ingredients are added.
  • QS for paraffin loss.
  • Examples l-V Water-in-oil emulsions) l/% ll/% HI/% IV/% V/%
  • Paraffin wax 1.5 2.2 2.0 2.5 1.8
  • Syntran 5170 containing 41% by weight insoluble polymer solids, available from Inte ⁇ olymer Co ⁇ .

Landscapes

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

Abstract

A cosmetic make-up composition suitable for use as a mascara or the like and which is in the form of an emulsion comprising an insoluble polymeric material in an aqueous emulsion; and lipophilic oil components including a polyvinylpyrrolidone hexadecane copolymer. The compositions exhibit improved wear and water resistance and are removable with soap and water.

Description

COSMETIC MAKE-UP COMPOSITIONS
Technical Field
The present invention relates to cosmetic make-up compositions, particularly eye make-ups and mascaras, comprising water-insoluble polymeric material in the form of an aqueous emulsion or latex. Said compositions have improved wear benefits compared to compositions known in the art and are easily removed with soap and water.
Background of the Invention
Eye make-up compositions, including mascara, are significant products in the cosmetics market. Mascara enhances the beauty of the wearer by coating the eye lashes, or in some instances eyebrows, with color.
In spite of their beauty enhancing characteristics, conventional eye make-up preparations have been criticized for their failure to produce the desired effects during long periods of wear. Problems such as staining and smearing, commonly referred to as smudging, and flaking of the mascara from the eyelashes are well known. Even where longevity has been improved, such compositions also are known to be difficult to completely remove from the delicate eye area. An eye makeup composition conceptually having significantly superior wear life, yet, easy removability with soap and water would be very desirable.
Eye makeup compositions comprising polymeric emulsions in order to eliminate smudging are well known in the art and typically include water- insoluble polymers, also referred to as latexes. Such compositions including eye shadows as disclosed in U.S. Patent 3,639,572, Henrich, issued February 1 , 1972; and mascaras as disclosed in U.S. Patent 4,423,031 , Murui et al., issued December 27, 1983; and European Patent Application (EPA) 0568035, published November 3, 1993. These compositions include plasticizers or solvents to assist in forming films using said latexes. These compositions are known to contain thickeners to adjust the viscosity of the composition. Said thickeners include water-soluble and water-swellable polymers, typically known for such use in the cosmetic art. In a different embodiment of the above concept is disclosed in Patent Cooperation Treaty application WO 94/17775, published August 18, 1994. The invention disclosed therein includes mascara compositions comprising water-based silicone elastomeric latex, emulsions as opposed to "water- based" acrylic polymers. Longer wear and durability is attributed to the used of the elastomeric latex as it is more compatible with the rest of the compositional matrix than the acrylic polymers.
Other compositions known in the art which seek to avoid the combination of plasticizers and insoluble-polymer are exemplified in EPO 0530084, published March 3, 1993. This application discloses compositions comprising a dispersed phase and a dispersant phase , the dispersant phase containing at least one water-soluble polymer and the dispersed phase containing at least 50% wax. Said composition may contain other materials routinely used in cosmetic compositons including water-insoluble polymers.
Surprisingly, it has been found that the combination of water-insoluble polymeric materials in an aqueous emulsion and particular surfactants provides mascara and other cosmetic make-up compositions that have superior wear and are removable with soap and water. These make-up compositions can be fabricated in a multitude of forms, such as creams, pastes and solids. Preferably the compositions of the present invention are water-in-oil and oil-in-water emulsions.
Summary of the Invention
According to one aspect of the present invention there is provided a cosmetic make-up composition suitable for use as a mascara or the like and which comprises:
(a) from about 0.1% to about 60% by weight of insoluble polymeric material in an aqueous emulsion;
(b) from about 0.1% to about 10% by weight of a first surfactant or mixture of surfactants having a weight averaged HLB of from about 3 to about 6; and (c) from about 0.1% to about 10% by weight of a second surfactant or mixture of surfactants having a weight averaged HLB of from about 8 to about 15.
According to a second aspect of the present invention there is provided a cosmetic make-up composition suitable for use as a mascara or the like and which comprises:
(a) from about 0.1% to about 60% by weight of insoluble polymeric material in an aqueous emulsion; and
(b) from about 0.1% to about 10% by weight of an alkyl- or alkoxy- dimethicone copolyol having the general formula:
wherein X is a hydrogen atom or a C-| to C-iβ alkyl, alkoxy or acyl radical, Y is C8-C22 alkoxy or alkyl radical, n = from about 0 to about 200, m = from about 1 to about 40, q = from about 1 to about 100, the molecular weight of the residue (C2H4θ-)x(C3H6θ-)yX being from about 250 to about 2000, x and y being selected so that the weight ratio of the oxyethylene/oxypropylene groups is from about 100:0 to about 20:80. According to a third aspect of the present invention there is provided a cosmetic make-up composition suitable for use as a mascara or the like and which is in the form of an emulsion comprising:
(a) from about 0.1% to about 60% by weight of insoluble polymeric material in an aqueous emulsion; and
(b) from about 0.1% to about 80% by weight of lipophilic oil components including from about 0.1% to about 10% by weight of polyvinylpyrrolidone hexadecene copolymer.
The compositions of the invention exhibit improved wear, increased resistance to water and are easily removed with soap and water.
All percentages are by weight of composition unless otherwise indicated. All solutions are on a weight/weight concentration unless otherwise indicated.
Detailed Description of the Invention
A first essential component of the make-up composition of the present invention is an insoluble polymeric material in an aqueous emulsion. Said materials, disclosed in the art as latexes, are aqueous emulsions or dispersions of polymeric materials comprising polymerized monomers, mixtures of monomers, derivatives of said monomers and mixtures of said monomers and mixtures thereof. These polymeric materials disclosed herein also include chemically modified (derivatives) of said polymeric material disclosed above. The polymerization process for making said polymeric material of the present invention is well known in the art. Such processes are disclosed in Kirk Othmer, Encyclopedia of Chemical Technology. Volume 14, "Latex Technology" 3rd Ed. 1981 ; incorporated herein by reference. These insoluble polymeric materials of the present invention comprise from about 0.1% to about 60%; preferably from about 2% to about 40% and most preferably from about 3% to about 30% by weight of the composition. These insoluble polymeric materials comprise polymerized monomers, mixtures of monomers, derivatives of said monomers and mixtures of said monomers and mixtures thereof selected from the group consisting of aromatic vinyls, dienes, vinyl cyanides, vinyl halides, vinylidene halides, vinyl esters, olefins and their isomers, vinyl pyrrolidone, unsaturated carboxylic acids, alkyl esters of unsaturated carboxylic acids, hydroxy derivatives of alkyl esters of unsaturated carboxylic acids, amides of unsaturated carboxylic acids, amine derivatives of unsaturated carboxylic acids, glycidyl derivatives of alkyl esters of unsaturated carboxylic acids, olefinic diamines and isomers, aromatic diamines, terephthaloyl halides, olefinic polyols and mixtures thereof.
The insoluble polymeric material preferably comprise polymerized monomers, mixtures of monomers, derivatives of said monomers and mixtures of said monomers and mixtures thereof preferably selected from the group consisting of aromatic vinyls, dienes, vinyl esters, olefins and their isomers, unsaturated carboxylic acids, alkyl esters of unsaturated carboxylic acids, hydroxy derivatives of alkyl esters of unsaturated carboxylic acids, amides of unsaturated carboxylic acids and mixtures thereof.
In highly preferred embodiments the insoluble polymeric material comprise polymerized monomers, mixtures of monomers, derivatives of said monomers and mixtures of said monomers and mixtures thereof most preferably selected from the group consisting of aromatic vinyls, dienes, vinyl esters, alkyl esters of unsaturated carboxylic acids, hydroxy derivatives of alkyl esters of unsaturated carboxylic acids and mixtures thereof.
Specific polymeric material useful in the present invention include, but, are not necessarily limited to the Syntran Series (of latexes) from Interpolymer Corporation, for example Syntran 5170 and Syntran 5130 (acrylates copolymers formulated with added ammonia, propylene glycol, preservative and surfactant) and Syntran 5002 (styrene/acrylates/methacrylate copolymer formulated with added ammonia, propylene glycol, preservative and surfactant); the Primal Series (acrylic latexes) from Rohm & Hass; Appretan V (styrene/acrylic ester copolymer latexes) from Hoechst; Vinac (polyvinylacetate latex) from Air Products; UCAR latex resin 130 (polyvinylacetate latex) from Union Carbide; Rhodopas A Series (polyvinylacetate latexes) from Rhone Poulenc; Appretan MB, EM, TV (vinyl acetate / ethylene copolymer latexes) from Hoechst; 200 Series (styrene/butadiene copolymer latexes) from Dow Chemical; Rhodopas SB Series (styrene/butadiene copolymer latexes) from Rhone Poulenc; Witcobond (polyurethane latexes) from Witco; Hycar Series (butadiene/acrylonitrile copolymer latexes) from Goodrich; Chemigum Series (butadiene/acrylonitrile copolymer latexes) from Goodyear; and Neo Cryl (styrene/acrylates/acrylonitrile copolymer latex) from ICI Resins.
The make-up compositions of the present invention also preferably comprise from about 0.1% to about 10% by weight of a first surfactant or mixture of surfactants having an average HLB of from about 3 to about 6 and from about 0.1% to about 10% by weight of a second surfactant or mixture of surfactants having an weight average HLB of from about 8 to about 15.
Preferably the first surfactant comprises an alkyl- or alkoxy-dimethicone copolyol having the general formula:
wherein X is a hydrogen atom or a C-| to C<|6 alkyl, alkoxy or acyl radical, Y is C8-C22 alkoxy or alkyl radical, n = from about 0 to about 200, m = from about 1 to about 40. q = from about 1 to about 100, the molecular weight of the residue (C2H4θ-)x(C3H6θ-)vX being from about 250 to about 2000, x and y being selected so that the weight ratio of the oxyethylene/oxypropylene groups is from about 100:0 to about 20:80. Preferably Y is C16-C20 a|kv| Especially preferred herein in combination with the insoluble polymer emulsion from the viewpoint of increasing resistance to water is cetyl dimethicone copolyol. Hence according to a second aspect of the present invention there is provided a make-up composition comprising:
(a) from about 0.1% to about 60% by weight of insoluble polymeric material in an aqueous emulsion; and
(b) from about 0.1% to about 10% by weight of an alkyl- or alkoxy- dimethicone copolyol having the general formula:
wherein X is a hydrogen atom or a C1 to C-jø alkyl, alkoxy or acyl radical, Y is C8-C22 alkoxy or alkyl radical, n = from about 0 to about 200, m = from about 1 to about 40, q = from about 1 to about 100, the molecular weight of the residue (C2H4θ-)x(C HeO-)yX being from about 250 to about 2000, x and y being selected so that the weight ratio of the oxyethylene/oxypropylene groups is from about 100:0 to about 20:80.
The second surfactant herein preferably comprises an organic base neutralized C12 -C24 fatty acid. A preferred organic base herein is triethanolamine. A preferred fatty acid herein is stearic acid.
Preferably the compositions herein additionally comprise from about 0.1 % to about 10% of polyvinylpyrrolidone hexadecene copolymer. This copolymer is useful in combination with the insoluble polymeric material in an aqueous emulsion and surfactants for improving water resistance and wear of the compositions. Hence according to a further aspect of the present invention there is provided a cosmetic make-up composition suitable for use as a mascara or the like and which is in the form of an emulsion comprising:
(a) from about 0.1% to about 60% by weight of insoluble polymeric material in an aqueous emulsion; and
(b) from about 0.1% to about 80% by weight of lipophilic oil components including from about 0.1% to about 10% by weight of polyvinylpyrrolidone hexadecene copolymer.
Optional ingredients useful in the present invention are selected based on either the various forms or attributes the composition is to have. The most preferred embodiments of the present invention are water-in-oil or oil-in- water emulsions. Some of the most common optional ingredients include oils and fats, emulsifiers, waxes, pigments and mixtures thereof.
A. Oils and Fats
Make-up compositions of the present invention can take the form of oil-in- water or water-in-oil emulsion compositions. These compositions are based on a combination of lipophilic materials optionally with one or more solvents. Said lipophilic materials typically comprise oils and fats generally known for use in the cosmetic art and are generally utilized herein in a level of from about 0% to about 70%, preferably from about 20 % to about 60% by weight.
Oils typically used in cosmetics include those selected from the group consisting of polar oils, non-polar oils, volatile oils, non-volatile oils and mixtures thereof. These oils may be saturated or unsaturated, straight or branched chained, aliphatic or aromatic hydrocarbons. Preferred oils include non-polar volatile hydrocarbons including isodecane (such as Permethyl-99A®, available from Presperse Inc.) and the C7-C8 through C12-C15 isoparaffins (such as the Isopar® Series available from Exxon Chemicals). Fats employed according to the invention are selected from the group consisting of fats derived from animals, vegetables, synthetically derived fats, and mixtures thereof wherein said fats have a melting point from about 55°C to about 100°C and a needle penetration, as measured according to the American standard ASTM D5, from about 3 to about 40 at 25°C. Preferably the fats selected for use in the present invention are fatty acid esters which are solids at room temperature and exhibit crystalline structure. Examples of fatty acid esters useful in the present invention include the glyceryl esters of higher fatty acids such as stearic and palmitic such as glyceryl monostearate, glyceryl distearate, glyceryl tristearate, palmitate esters of glycerol, C-|8-36 triglycerides, glyceryl tribehenate and mixtures thereof.
B. Waxes
Waxes are defined as lower-melting organic mixtures or compounds of high molecular weight, solid at room temperature and generally similar in composition to fats and oils except that they contain no glycerides. Some are hydrocarbons, others are esters of fatty acids and alcohols. Waxes useful in the present invention are selected from the group consisting of animal waxes, vegetable waxes, mineral waxes, various fractions of natural waxes, synthetic waxes, petroleum waxes, ethylenic polymers, hydrocarbon types such as Fischer-Tropsch waxes, silicone waxes, and mixtures thereof wherein the waxes have a melting point between 55° and 100°C and a needle penetration, as measured according to the American standard ASTM D5, of 3 to 40 at 25°C. The principle of the measurement of the needle penetration according to the standards ASTM D5 consists in measuring the depth, expressed in tenths of a millimeter, to which a standard needle (weighing 2.5 g and placed in a needle holder weighing 47.5 g, i.e. a total of 50 g) penetrates when placed on the wax for 5 seconds.
The specific waxes useful in the present invention are selected from the group consisting of beeswax, lanolin wax, shellac wax (animal waxes); camauba, candelilla, bayberry (vegetable waxes); ozokerite, ceresin, (mineral waxes); paraffin, microcrystalline waxes (petroleum waxes); polyethylene, (ethylenic polymers); polyethylene homopolymers (Fischer- Tropsch waxes); C24-45 alkyl methicones (silicone waxes); and mixtures thereof. Most preferred are beeswax, lanolin wax, camauba, candelilla, ozokerite, ceresin, paraffins, microcrystalline waxes, polyethylene, C24-45 alkyl methicones, and mixtures thereof.
C. Pigments
The solids component of the make-up compositions of the present invention contain cosmetically acceptable pigments selected from the group consisting of inorganic pigments, organic pigments, and pearlescent pigments. When employed, the pigments are present in proportions depending on the color and the intensity of the color which it is intended to produce. The level of pigments in the solid portion of the composition of present invention is from about 3% to about 30%, preferably from about 5% to about 20%. Pigments are selected from the group consisting of inorganic pigments, organic lake pigments, pearlesent pigments, and mixtures thereof. Said pigments may optionally be surface-treated within the scope of the present invention but are not limited to treatments such as silicones, perfluorinated compounds, lecithin, and amino acids.
Inorganic pigments useful in the present invention include those selected from the group consisting of rutile or anatase titanium dioxide, coded in the Color Index under the reference Cl 77,891; black, yellow, red and brown iron oxides, coded under references Cl 77,499, 77, 492 and, 77,491; manganese violet (Cl 77,742); ultramarine blue (Cl 77,007); chromium oxide (Cl 77,288); chromium hydrate (Cl 77,289); and ferric blue (Cl 77,510) and mixtures thereof.
The organic pigments and lakes useful in the present invention include those selected from the group consisting of D&C Red No. 19 (Cl 45,170), D&C Red No. 9 (Cl 15,585),D&C Red NO. 21 (Cl 45,380), D&C Orange No. 4 (Cl 15,510), D&C Orange No. 5 (Cl 45,370), D&C Red No. 27 (Cl 45,410), D&C Red No. 13 (Cl 15,630), D&C Red No. 7 (Cl 15,850), D&C Red No. 6 (Cl 15,850), D&C Yellow No. 5 (Cl 19,140), D&C Red No. 36 (Cl 12,085), D&C Orange No. 10 (Cl 45,425), D&C Yellow No. 6 (Cl 15,985), D&C Red No. 30 (Cl 73,360), D&C Red No. 3 (Cl 45,430) and the dye or lakes based on Cochineal Carmine (Cl 75,570) and mixtures thereof.
The pearlescent pigments useful in the present invention include those selected from the group consisting of the white pearlescent pigments such as mica coated with titanium oxide, bismuth oxychloride, colored pearlescent pigments such as titanium mica with iron oxides, titanium mica with ferric blue. chromium oxide and the like, titanium mica with an organic pigment of the above-mentioned type as well as those based on bismuth oxychloride and mixtures thereof.
D. Miscellaneous
In the present invention numerous optional ingredients may be added to provide additional benefits other than that attributed to the invention as defined above. For example, it is preferred that the composition of the present invention contain a preservative system to inhibit microbiological growth and maintain the integrity of the product. In the present invention, the preservative system does not have a detrimental effect on the composition.
Any optional ingredients known to those skilled in the art may also be used in the invention. Examples of optional ingredients are cosmetic fillers including, but not limited to, mica, talc, nylon, polyethylene, silica, polymethacrylate, kaolin, teflon; cosmetic preservatives including, but not limited to, methylparaben, propylparaben, butylparaben, ethylparaben, potassium sorbate, trisodium EDTA, phenoxyethanol, ethyl alcohol, diazolidinyl urea, imidazolidinyl urea, quaternium-15. Also, additives such as tall oil glycerides are easily incorporated into emulsion forms of the composition.
Water dispersible and oil dispersible clays may also be useful in the invention to thicken the water or the oil phase. The water dispersible clays comprise bentonite and hectorite, such as Bentone EW, LT from Rheox; magnesium aluminum silicate, such as Veegum from Vanderbilt Co.; attapulgite such as Attasorb or Pharamasorb from Engelhard, Inc.; laponite and montmorrilonite, such as Gelwhite from ECC America; and mixtures thereof. The oil dispersible clays comprise quaternium-18 bentonite, such as Bentone 34 and 38 from Rheox; the Claytone Series from ECC America; quaternium-18 hectorite, such as Bentone gels from Rheox; and mixtures thereof.
Methods of Manufacture
The compositions of the invention can be prepared as follows. 1. Oil-in-Water Emulsion
The waxes and fats are placed in a vessel equipped with heating and mixing. The waxes and fats are heated to about 85°C with low speed mixing until liquefied and homogeneous. At 85-90°C, pigments, any oil dispersible or soluble components are added. The mixing rate is increased to high and mixed until the pigments are uniformly dispersed throughout the lipid mixture; about 30-35 minutes. The emulsifiers are added to said lipid mixture while continuing to mix .
In a second vessel equipped with mixing and heating, the water and the remainder of the water dispersible components are added. The aqueous mixture is mixed with heating until this aqueous mixture is about 85°C. Q.S. for any water loss from said aqueous mixture.
The two mixtures are slowly combined and mixed with a high speed dispersator type mixer. The heat source is removed and the mixing is continued until the temperature of said combined mixture is from about 65°C- 70°C. Q.S. said combined mixture for any water loss. The preservatives and insoluble polymer component are added and mixed until homogeneous. Said combined mixture is cooled to about 45°C-47°C and any remaining components are added. Cooling and mixing is continued until said combined mixture is about 27°C to about 30°C. Said combined mixture is transfered to suitable storage containers for subsequent filling of retail size packaging.
2. Water-in-Oil Emulsions (Examples l-V)
The components of phase A are premixed for 30 minutes at room temperature with high shear. The phase A premix is then heated to 85-90°C with high shear. The wax phase B ingredients are premixed and heated to 90°C with slow stirring for one hour. The wax phase is added to the phase A premix at 90°C and mixed for 20 minutes with high shear. Cooling is commenced and the water phase ingredients are added. Mixing is continued with high shear. The mixture is cooled to 45°C and the remaining ingredients are added. QS for paraffin loss. Examples l-V (Water-in-oil emulsions) l/% ll/% HI/% IV/% V/%
Petroleum Distillates —to 100 -
Quaternium-18 Hectorite 4 3.5 4.2 4.0 3.8 Black Iron Oxide 7.5 8.5 9.0 9.5 8.6
B.
PVP/Hexadecene 1.7 2.5 2.2 1.9 2.0
Copolymer
Polybutene 1.9 2.75 2.0 2.5 1.8
Beeswax 2.8 3.5 4.4 4.0 3.0
Camauba wax 2.5 4.4 3.5 3.3 4.0
Paraffin wax 1.5 2.2 2.0 2.5 1.8
C18- 36 Acid triglycerides 1.5 3.0 3.3 2.5 2.8
Ethyl paraben 0.15 0.15 0.15 0.15 0.15
Methyl paraben 0.2 0.2 0.2 0.2 0.2
Propyl paraben 0.2 0.2 0.2 0.2 0.2
Zinc stearate 2.5 2.0 2.1 2.3 1.9
Cetyl dimethicone copolyol 0.5 0.6 0.3 0.5 0.8
Stearic acid 0.9 1.0 1.8 1.9 1.5 propylene glycol 1.0 1.5 1.4 1.3 0.9 propylene carbonate 1.5 1.0 1.3 1.2 1.4
l/% ll/% lll/% IV/% V/%
Triethanolamine 0.4 0.5 0.25 0.3 0.5
Water 2.5 2.65 1.4 1.8 2.0 D.
Ammonium Acrylate 9.0 12.5 10.5 12.0 10.0
Copolymer1
E.
Panthenol 0.2 0.5 0.3 0.25 0.2
Water 1.0 1.0 1.5 0.8 1.2
Quaternium-15 94% 0.05 0.06 0.07 0.08 0.07
Trisodium EDTA 0.1 0.1 0.1 0.1 0.1
F. phenoxyethanol 0.8 1.0 0.75 1.1 0.85
1. Syntran 5170, containing 41% by weight insoluble polymer solids, available from Inteφolymer Coφ.

Claims

What is claimed is:
1. A cosmetic make-up composition suitable for use as a mascara or the like and which is in the form of an emulsion comprising:
(a) from about 0.1% to about 60% by weight of insoluble polymeric material in an aqueous emulsion; and
(b) from about 0.1% to about 80% by weight of lipophilic oil components including from about 0.1% to about 10% by weight of polyvinylpyrrolidone hexadecane copolymer.
2. A composition according to Claim 1 wherein said water-insoluble polymeric material comprises polymerized monomers, mixtures of monomers, derivatives of said monomers and mixtures of said monomers and mixtures thereof selected from aromatic vinyls, dienes, vinyl cyanides, vinyl halides, vinylidene halides, vinyl esters, olefins and their isomers, vinyl pyrrolidone, unsaturated carboxylic acids, alkyl esters of unsaturated carboxylic acids, hydroxy derivatives of alkyl esters of unsaturated carboxylic acids, amides of unsaturated carboxylic acids, amine derivatives of unsaturated carboxylic acids, glycidyl derivatives of alkyl esters of unsaturated carboxylic acids, olefinic diamines and isomers, aromatic diamines, terephthaloyl halides, olefinic polyols, and mixtures thereof.
3. A composition according to Claim 1 comprising from about 2% to about 40% by weight of water-insoluble polymeric material comprising polymerized monomers, mixtures of monomers, derivatives of said monomers and mixtures of said monomers and mixtures thereof selected from aromatic vinyls, dienes, vinyl esters, olefins and their isomers, unsaturated carboxylic acids, alkyl esters of unsaturated carboxylic acids, hydroxy derivatives of alkyl esters of unsaturated carboxylic acids, amides of unsaturated carboxylic acids and mixtures thereof.
4. A composition according to Claim 1 comprising from about 3% to about 30% water-insoluble polymeric material comprising polymerized monomers, mixtures of monomers, derivatives of said monomers and mixtures of said monomers and mixtures thereof selected from aromatic vinyls, dienes, vinyl esters, alkyl esters of unsaturated carboxylic acids, hydroxy derivatives of alkyl esters of unsaturated carboxylic acids and mixtures thereof.
5. A composition according to any of Claims 1 to 4 comprising from about 2% to about 40% by weight of the insoluble polymeric material in an aqueous emulsion.
6. A composition according to any of Claims 1 to 5 wherein the composition is in the form of a water-in-oil emulsion.
EP96912982A 1995-05-20 1996-04-23 Cosmetic make-up compositions Withdrawn EP0827388A4 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB9510229 1995-05-20
GBGB9510229.9A GB9510229D0 (en) 1995-05-20 1995-05-20 Cosmetic make-up compositions
PCT/US1996/005535 WO1996036308A1 (en) 1995-05-20 1996-04-23 Cosmetic make-up compositions

Publications (2)

Publication Number Publication Date
EP0827388A1 true EP0827388A1 (en) 1998-03-11
EP0827388A4 EP0827388A4 (en) 1999-08-11

Family

ID=10774771

Family Applications (1)

Application Number Title Priority Date Filing Date
EP96912982A Withdrawn EP0827388A4 (en) 1995-05-20 1996-04-23 Cosmetic make-up compositions

Country Status (5)

Country Link
EP (1) EP0827388A4 (en)
JP (1) JPH11505543A (en)
CA (1) CA2221410A1 (en)
GB (1) GB9510229D0 (en)
WO (1) WO1996036308A1 (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2751212B1 (en) * 1996-07-17 1998-11-06 Oreal COMPOSITION COMPRISING THE ASSOCIATION OF A VOLATILE COMPOUND AND A COPOLYMER OF POLYVINYLPYRROLIDONE AND ALPHA-OLEFINS AND USE OF SAID ASSOCIATION
US6503495B1 (en) * 1996-10-31 2003-01-07 The Procter & Gamble Company Cosmetic compositions having improved wear and beauty
WO1998023251A1 (en) * 1996-11-27 1998-06-04 The Procter & Gamble Company Mascara compositions having improved wear and beauty benefits
FR2782918B1 (en) * 1998-09-04 2001-09-07 Oreal COSMETIC COMPOSITION COMPRISING A FILM-FORMING POLYMER, AN ALPHA-OLEFIN POLY AND A FATTY LIQUID PHASE
FR2811547B1 (en) * 2000-07-13 2003-09-26 Oreal LONG-LASTING COSMETIC COMPOSITION COMPRISING A PARTICULAR PRO-ADHESIVE MATERIAL
FR2824267B1 (en) * 2001-05-04 2008-06-27 Oreal COSMETIC COMPOSITION FILMOGENE
US6726900B2 (en) 2001-05-18 2004-04-27 Revlon Consumer Products Corporation Long wearing composition for making up eyes, skin, and lips
US20030017123A1 (en) * 2001-05-29 2003-01-23 Scancarella Neil D. Long wearing emulsion composition for making up eyes and skin
US7270828B2 (en) 2001-06-20 2007-09-18 The Procter & Gamble Company Personal care composition comprising hydrophobic gel
JP2005501022A (en) * 2001-06-20 2005-01-13 ザ プロクター アンド ギャンブル カンパニー Personal care composition comprising a polyol-in-silicone emulsion
CA2390952C (en) 2001-07-02 2006-07-11 Rohm And Haas Company Compositions and process for retaining active ingredients comprising networked structured polymers
FR2917609B1 (en) * 2007-06-22 2012-11-16 Oreal MAKE UP COMPOSITION COMPRISING A HYDROXYL COMPOUND.
DE202016008030U1 (en) * 2016-12-28 2018-04-01 Schwan-Stabilo Cosmetics Gmbh & Co. Kg wax conditioning
FR3130134B1 (en) * 2021-12-14 2023-12-22 Oreal Water-in-oil emulsions comprising a surfactant, an acrylic polymer and an organosiloxane

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4795631A (en) * 1986-03-26 1989-01-03 Chesebrough-Pond's, Inc. Water based lip color comprising an alkali soluble film-forming agent
US5389363A (en) * 1993-04-23 1995-02-14 Revlon Consumer Products Corporation Cosmetic compositions for lengthening, coloring and curling eyelashes

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5041281A (en) * 1989-03-16 1991-08-20 Amway Corporation Oil in water emulsion sunscreen composition
US4917883A (en) * 1989-03-16 1990-04-17 Amway Corporation Oil in water emulsion sunscreen composition

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4795631A (en) * 1986-03-26 1989-01-03 Chesebrough-Pond's, Inc. Water based lip color comprising an alkali soluble film-forming agent
US5389363A (en) * 1993-04-23 1995-02-14 Revlon Consumer Products Corporation Cosmetic compositions for lengthening, coloring and curling eyelashes

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO9636308A1 *

Also Published As

Publication number Publication date
WO1996036308A1 (en) 1996-11-21
MX9708972A (en) 1998-03-31
CA2221410A1 (en) 1996-11-21
GB9510229D0 (en) 1995-07-19
EP0827388A4 (en) 1999-08-11
JPH11505543A (en) 1999-05-21

Similar Documents

Publication Publication Date Title
EP0824339B2 (en) Mascara compositions comprising water-insoluble polymeric material and water-soluble, film-forming polymers
US6248336B1 (en) Cosmetic make-up compositions
US6503495B1 (en) Cosmetic compositions having improved wear and beauty
US7871634B2 (en) Cosmetic compositions useful for lengthening lashes
EP0942708B2 (en) Mascara compositions having improved wear and beauty benefits
US5985258A (en) Mascara compositions comprising water-insoluble polymeric material and water-soluble, film-forming polymers
US20030165451A1 (en) Composition containing a semicrystalline polymer, uses thereof, and method for making
US6395262B1 (en) Cosmetic composition comprising a copolymer and utilization of the copolymer in a cosmetic composition
EP0827388A1 (en) Cosmetic make-up compositions
WO1996036323A1 (en) Cosmetic make-up compositions
WO1996036309A1 (en) Cosmetic make-up compositions
MXPA97008280A (en) Compositions of rimel comprising polymeric insoluble material in water and hydrosoluble polymers pelic formators
MXPA97008972A (en) Cosmetic compositions for makeup
WO2021177326A1 (en) Composition suitable for eyelashes
MXPA97008969A (en) Cosmetic compositions for makeup
MXPA97008968A (en) Cosmetic compositions for makeup
MXPA99004127A (en) Cosmetic compositions comprising an insoluble polymer, a film-forming polymer and an organophilic clay

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19971106

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LI LU NL PT SE

A4 Supplementary search report drawn up and despatched

Effective date: 19990624

AK Designated contracting states

Kind code of ref document: A4

Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LI LU NL PT SE

RIC1 Information provided on ipc code assigned before grant

Free format text: 6A 61K 7/48 A, 6A 61K 7/02 B, 6A 61K 7/032 B

17Q First examination report despatched

Effective date: 20020430

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20020911