Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
  • A61K8/04—Dispersions; Emulsions
  • A61K8/042—Gels
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
  • A61K8/26—Aluminium; Compounds thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/55—Phosphorus compounds
  • A61K8/553—Phospholipids, e.g. lecithin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/63—Steroids; Derivatives thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
  • A61Q1/02—Preparations containing skin colorants, e.g. pigments
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
  • A61Q1/02—Preparations containing skin colorants, e.g. pigments
  • A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
  • A61Q1/06—Lipsticks

Definitions

• the present invention relates to personal care compositions comprising a hydrophobic gel.
• the composition is particularly useful for making lipsticks, foundations, and creams.
• Lipsticks are primarily made of lipophilic or hydrophobic materials. Lipsticks designed for providing a moisturizing benefit to the lips further contain water, polar solvents, or other moisturizing components which are more or less hydrophilic. The use of association structures have been suggested to bind such moisturizing components in the lipophilic matrix of the lipstick. While such lipstick compositions provide a favorable moisturizing benefit to the lips, they were not completely satisfactory in terms of physical stability, color stability, and sweat resistance.
• Physical stability relates to the stability of the stick during storage and upon use.
• a stable stick does not deform during storage at ambient temperature, and does not bend or break upon normal condition use.
• Color stability relates to the stability of color during storage and after applied on the lip. It has been known that lipsticks containing a high amount of moisturizing components have the tendency to change color over time after applied on the lip. Sweating is a phenomena seen on the surface of sticks, and is believed to be due to oils and/or solvents separating and leaking out of the lipophilic matrix of the stick. Sweating provides a negative appearance to the user.
• Emulsion compositions utilizing cholesteryl derivatives and swelling clay material are disclosed, for example, in Japanese publication A-8-20529. While such emulsion is believed to provide physical stability to the composition, further improvement is desired. Based on the foregoing, there is a need for a lipstick composition which has improved physical stability, improved color stability, and improved sweat resistance, while also providing moisturizing benefit to the lips. There is also a need for a personal care composition which has improved physical stability over a wide range of viscosity and/or hardness.
• the present invention is directed to a personal care composition comprising by weight:
• a hydrophobic gel comprising: (i) a cholesteryl derivative; (ii) an oil swelling clay material;
• the present invention is further directed to a lipstick composition which satisfies the need for improved physical stability, improved color stability, and improved sweat resistance, while also providing moisturizing benefit to the lips.
• the present invention is still further directed to suitable methods of preparing the compositions above.
• the composition of the present invention comprises a cholesteryl derivative having high water holding ability.
• the cholesteryl derivative useful herein provides the hydrophobic gel together with the oil swelling clay material, non-volatile liquid oil, and polar solvent. Without being bound by theory, it is believed that the cholesteryl derivative holds the polar solvent, thereby provides a stable gel.
• the amount of cholesteryl derivative included is adjusted depending on the amount of polar solvent. Namely, when a high amount of polar solvent is desired, a high amount of cholesteryl derivative is included to effectively hold the polar solvent.
• the cholesteryl derivative is comprised by weight of the entire composition at from about 2% to about 7%, preferably from about 3% to about 6%.
• Cholesteryl derivatives useful herein include cholesterol and a C12-22 fatty acid or hydroxy fatty acid having high water holding ability, preferably cholesteryl 12-hydroxystearate, cholesteryl macadamiate, Cholesteryl Stearate, and mixtures thereof.
• Commercially available cholesteryl derivatives include cholesteryl 12-hydroxystearate with tradename Salacos HS available from Nisshin Oil Mills, Ltd., and cholesteryl macadamiate with tradename YOFCO MAC available from Nippon Fine Chemical Co., Ltd. OIL SWELLING CLAY MATERIAL
• the composition of the present invention comprises an oil swelling clay material which was high oil swelling ability.
• the oil swelling clay material useful herein provides the hydrophobic gel together with the cholesteryl derivative, nonvolatile liquid oil, and polar solvent.
• the oil swelling clay material is first swelled with the non-volatile liquid oil prior to mixing with other components for making the hydrophobic gel. Without being bound by theory, it is believed that the oil swelling clay material, while absorbing the non-volatile liquid oil, further holds the closely bonded cholesteryl derivative and polar solvent within its structure.
• the oil swelling clay material functions as a thickener for the composition.
• the amount of oil swelling clay material included is adjusted depending on the desired viscosity and hardness of the composition.
• the oil swelling clay material is comprised by weight of the entire composition at from about 0.1 % to about 1%, preferably from about 0.2% to about 0.5%.
• Oil swelling clay materials useful herein include hectorite, bentonite, montmorillonite, and bentone clays which have been modified to be compatible with oil. Preferably, the modification is quatemization with an ammonium compound. Preferable oil swelling clay materials include quaternary ammonium modified hectorite. Commercially available oil swelling clay materials include benzyldimethyl stearyl ammonium hectorite with tradename Bentone 38 CG OR available from Rheox. Inc. NON-VOLATILE OIL
• the composition of the present invention comprises a non-volatile oil suitable for personal use.
• the non-volatile oil is comprised by weight of the entire composition at from about 2% to about 10%, preferably from about 4% to about 7%.
• the non-volatile oil useful herein may also be used in the carrier depending on the characteristics desired for the product.
• the non-volatile oil to be used for making the hydrophobic gel is independently mixed with the other components for making the hydrophobic gel.
• the non-volatile oil to be used for making the carrier would thus preferably be mixed with other components for making the carrier, if present; and the hydrophobic gel and carrier would be finally mixed together to make the composition of the present invention.
• Non-volatile oils useful herein are, for example, tridecyl isononanoate, isostearyl isostearate, isocetyl isosteatrate, isopropyl isostearate, isodecyl isonoanoate, cetyl octanoate, isononyl isononanoate, diisopropyl myristate, isocetyl myristate, isotridecyl myristate, isopropyl myristate, isostearyl palmitate, isocetyl palmitate, isodecyl palmitate, isopropyl palmitate, octyl palmitate, caprylic/capric acid triglyceride, glyceryl tri-2-ethylhexanoate, diglyceryl sebacate, neopentyl glycol di(2-ethyl hexanoate), diisopropyl dimerate, tocopherol
• oils include, for example, tridecyl isononanoate with tradename Crodamol TN available from Croda, Hexalan available from Nisshin Oil Mills, Ltd., and tocopherol acetates available from Eisai.
• Non-volatile oils useful herein also include polyalkyl or polyaryl siloxanes with the following
• R 93 is alkyl or aryl
• p is an integer from about 7 to about 8,000.
• Z 8 represents groups which block the ends of the silicone chains.
• the alkyl or aryl groups substituted on the siloxane chain (R 93 ) or at the ends of the siloxane chains Z 8 can have any structure as long as the resulting silicone remains fluid at room temperature, is dispersible, is neither irritating, toxic nor otherwise harmful when applied to the skin, is compatible with the other components of the composition, and is chemically stable under normal use and storage conditions.
• Suitable Z 8 groups include hydroxy, methyl, methoxy, ethoxy, propoxy, and aryloxy.
• the two R 93 groups on the silicon atom may represent the same group or different groups.
• the two R 93 groups represent the same group.
• Suitable R 93 groups include methyl, ethyl, propyl, phenyl, methylphenyl and phenylmethyl.
• the preferred silicone compounds are polydimethylsiloxane, polydiethylsiloxane, and polymethylphenylsiloxane. Polydimethylsiloxane, which is also known as dimethicone, is especially preferred.
• the polyalkylsiloxanes that can be used include, for example, polydimethylsiloxanes. These silicone compounds are available, for example, from the General Electric Company in their Viscasil® and SF 96 series, and from Dow Corning in their Dow Corning 200 series.
• Polyalkylaryl siloxane fluids can also be used and include, for example, polymethylphenylsiloxanes. These siloxanes are available, for example, from the General Electric Company as SF 1075 methyl phenyl fluid or from Dow Corning as 556 Cosmetic Grade Fluid.
• Non-volatile oils also useful herein are the various grades of mineral oils.
• Mineral oils are liquid mixtures of hydrocarbons that are obtained from petroleum. Specific examples of suitable hydrocarbons include paraffin oil, mineral oil, dodecane, isododecane, hexadecane, isohexadecane, eicosene, isoeicosene, tridecane, tetradecane, polybutene, polyisobutene, and mixtures thereof.
• suitable hydrocarbons include paraffin oil, mineral oil, dodecane, isododecane, hexadecane, isohexadecane, eicosene, isoeicosene, tridecane, tetradecane, polybutene, polyisobutene, and mixtures thereof.
• composition of the present invention comprises a polar solvent which is soluble in water.
• the polar solvent provides the moisturizing benefit to the skin.
• the polar solvent also serves as solvent for incorporating water-soluble humectants which otherwise would not be compatible in the lipophilic carrier base. Without being bound by theory, it is believed that the polar solvent is held in the cholesteryl derivative and further trapped in the oil swelling clay material, to provide a stable hydrophobic gel.
• the polar solvent is comprised by weight of the entire composition at from about 0.01% to about 10%, preferably from about 1 % to about 8%.
• Polar solvents useful herein include polyhydric alcohols such as glycerin, 1,3-butylene glycol, propylene glycol, hexylene glycol, propane diol, ethylene glycol, diethylene glycol, dipropylene glycol, diglycerin, sorbitol, and other sugars which are in liquid form at ambient temperature. Also useful herein are water soluble alkoxylated nonionic polymers such as polyethylene glycol.
• polar solvents herein include: glycerin available from Asahi Denka; propylene glycol with tradename LEXOL PG-865/855 available from Inolex, 1 ,2-PROPYLENE GLYCOL USP available from BASF; 1,3- butylene glycol available from Daisel Kagaku Kogyo; dipropylene glycol with the same tradename available from BASF; diglycerin with tradename DIGLYCEROL available from Solvay GmbH; sodium hyaluronate with tradenames ACTIMOIST available from Active Organics, AVIAN SODIUM HYALURONATE series available from Intergen, HYALURONIC ACID Na available from lchimaru Pharcos. Water-Soluble Humectant
• composition of the present invention may further comprise a water- soluble humectant in an amount soluble in the polar solvent above, preferably from about 0.1% to about 10%, more preferably from about 1% to about 5%.
• Water-soluble humectants useful herein in include niacinamide, panthenol, bacterial cultured mediums, allantoin, sodium lactate, PCA soda, amino acids, urea, sodium hyaluronate, chondroitin sulfate, collagen, elastin, pectin, carageenan, sodium alginate, trehalose, tuberose saccharide, chitin derivatives, chitosan derivatives, and mixtures thereof.
• Niacinamide and panthenol are commercially available, for example, by Roche.
• the hydrophobic gel can hold the polar and water-soluble material incorporated in the hydrophobic gel in a stable manner when contained in a lipophilic carrier.
• compositions containing the hydrophobic gel and having various viscosity and hardness can be made, ranging from firm sticks to thin creams.
• Personal care compositions containing the hydrophobic gel provide improved physical stability, such as in phase condition and viscosity. Without being bound by theory, it is believed that the hydrophobic gel herein possesses excellent thermal stability, thereby being stable under environments beyond ambient temperature.
• the hydrophobic gel herein is preferably made by a method comprising the steps of: (a) mixing the mixture of the cholesteryl derivative, the oil swelling clay material, and the non-volatile liquid oil at a speed of from about 1500 rpm to about 3000 rpm, preferably from about 1500 rpm to about 2500 rpm and at a temperature of from about 80°C to about 95°C, preferably from about 88°C to about 92°C ; and (b) mixing the polar solvent with the mixture obtained in step (a) at a speed of at least about 4000 rpm, preferably from about 4000 rpm to about 8000 rpm, more preferably from about 5000rpm to about 7000rpm, and at a temperature of from about 85°C to about 95°C, preferably from about 88°C to about 92°C.
• the mixing can be provided by any high shear mixer known in the art, such as those known as Homomixer or Disper.
• the hydrophobic gel herein is preferably made by mixing at a rotation speed higher than typically used for making personal care compositions, and in 2 steps. Without being bound by theory, it is believed that, in step (a), the mixture of components are mixed at a controlled rotation speed so that the oil swelling clay material is expanded to provide sufficient room for the cholesteryl hydroxystearate and subsequently added polar solvent to be entrapped within the oil swelling clay material, yet not too vigorous to destroy the structure of the oil swelling clay material. Without being bound by theory, it is further believed that, in step (b), the mixture of components are mixed at a high rotation speed so that the polar solvent is effectively entrapped in the oil swelling clay material. This is believed to provide the stability of the hydrophobic gel.
• the composition of the present invention comprises a carrier suitable for the desired use which is substantially free of water, surfactant, and lecithin.
• a carrier suitable for the desired use which is substantially free of water, surfactant, and lecithin.
• the hydrophobic gel provides the physical stability, color stability, and sweat resistance to the composition.
• surfactants a composition mild to the skin can be obtained.
• substantially free what is meant is that none of water, surfactant, or lecithin is actively included in the composition.
• the present invention does not exclude the use of components which may carry an insignificant amount of water, surfactant, or lecithin as an impurity or byproduct.
• the polar solvents mentioned above may carry a small percentage of water.
• any of water, surfactant or lecithin, respectively, should be included at a level of less than about 1 %, preferably less than about 0.5% of the entire composition.
• the carrier of the present composition is lipophilic in nature. Any component that is compatible with the hydrophobic gel can be used as a carrier.
• the carrier is selected to make various personal care compositions, including lipsticks, foundations, pigmented and non-pigmented creams for the skin or hair, antiperspirant sticks, and hair sticks.
• Solid waxes, gelling agents, non-volatile oils as mentioned above, powders, coloring pigments, and other lipophilic active components can be incorporated in the carrier.
• the non-volatile oils as mentioned above can be included in the carrier.
• the non-volatile oils used for the carrier can be the same or different from the non-volatile oils used for making the hydrophobic gel.
• the carrier is selected from one or more of a solid wax, a non-volatile oil, a powder, and a coloring pigment.
• the composition is particularly suitable for making lipstick compositions which contain a solid wax and a coloring pigment in the carrier.
• Solid Wax The composition of the present invention may contain a solid wax.
• the solid wax is comprised by weight of the entire composition at from about 10% to about 20%, preferably 12% to about 15%. The amount of the solid wax is controlled to provide the desired hardness and strength to the product.
• the solid waxes useful herein are paraffin wax, microcrystalline wax, ozokerite was, ceresin wax, carnauba wax, candelilla wax, eicosanyl behenate, and mixtures thereof. A mixture of waxes is preferably used.
• Solid waxes useful herein include: Candelilla wax NC-1630 available from Noda wax, Ozokerite wax SP-1021 available from Strahl & Pitsh, and Eicosanyl behenate available from Cas Chemical. Powders and Coloring Pigments
• the composition of the present invention may contain powders and color pigments.
• the powders and color pigments component is comprised by weight of the entire composition at from about 1 % to about 30%, preferably 2% to about 20%.
• the amount and type of powders and color pigments are selected depending on the desired characteristic of the product, for example, shade, coverage, UV protection benefit, and various skin feel.
• clay mineral powders such as talc, mica, sericite, silica, magnesium silicate, synthetic fluorphlogopite, calcium silicate, aluminum silicate, bentonite and montomorillonite
• pearl pigments such as alumina, barium sulfate, calcium secondary phosphate, calcium carbonate, titanium oxide, finely divided titanium oxide, zirconium oxide, zinc oxide, hydroxy apatite, iron oxide, iron titate, ultramarine blue, Prussian blue, chromium oxide, chromium hydroxide, cobalt oxide, cobalt titanate, titanium oxide coated mica
• organic powders such as polyester, polyethylene, polystyrene, methyl metharylate resin, cellulose, 12-nylon, 6-nylon, styrene-acrylic acid copolymers, poly proprylene, vinyl chloride polymer, tetrafluoroethylene polymer, boron nitride, fish scale guanine, laked tar color
• a certain percentage of spherical pigments can be used.
• the materials are selected depending on the oil absorbing capability of the pigments.
• pigments having high oil absorbing capability and those having low oil absorbing capability are combined.
• Hydrophobically treated pigments can also be used.
• Such hydrophobically treated pigments are made by treating the base material, as above, with a hydrophobical treatment agent, including: silicone such as Methicone, Dimethicone and perfluoroalkylsilane; fatty material such as stearic acid; metal soap such as aluminium dimyristate; aluminium hydrogenated tallow glutamate, hydrogenated lecithin, lauroyl lysine, aluminium salt of perfluoroalkyl phosphate, and mixtures thereof.
• silicone such as Methicone, Dimethicone and perfluoroalkylsilane
• fatty material such as stearic acid
• metal soap such as aluminium dimyristate
• aluminium hydrogenated tallow glutamate hydrogenated lecithin
• lauroyl lysine aluminium salt of perfluoroalkyl phosphate, and mixtures thereof.
• composition of the present invention may include other additional components, which may be selected by the artisan according to the desired characteristics of the final product and which are suitable for rendering the composition more cosmetically or aesthetically acceptable or to provide them with additional usage benefits.
• additional components generally are used individually at levels of no more than about 5% by weight of the composition.
• composition of the present invention may further contain a nonvolatile dispersed silicone usually referred to as silicone gum.
• silicone gum means a polyorganosiloxane material having a viscosity at 25°C of greater than or equal to 1 ,000,000 mPa » s. Silicone gums are believed to provide wearability improvement such as long-lasting effect.
• the "silicone gums” will typically have a mass molecular weight in excess of about 200,000, generally between about 200,000 and about 1 ,000,000.
• composition of the present invention may further contain a silicone resin, which are highly crosslinked polymeric siloxane systems. Silicone resins are believed to enhance spreadability and improve the feel to the skin.
• the crosslinking is introduced through the incorporation of tri-functional and tetra- functional silanes with mono-functional or di-functional, or both, silanes during manufacture of the silicone resin.
• the degree of crosslinking that is required in order to result in a silicone resin will vary according to the specific silane units incorporated into the silicone resin.
• silicone materials which have a sufficient level of trifunctional and tetrafunctional siloxane monomer units, and hence, a sufficient level of crosslinking, such that they dry down to a rigid, or hard, film are considered to be silicone resins.
• the ratio of oxygen atoms to silicon atoms is indicative of the level of crosslinking in a particular silicone material.
• Silicone materials which have at least about 1.1 oxygen atoms per silicon atom will generally be silicone resins herein.
• the ratio of oxyge silicon atoms is at least about 1.2:1.0.
• Silanes used in the manufacture of silicone resins include monomethyl-, dimethyl-, trimethyl-, monophenyl-, diphenyl-, methylphenyl-, monovinyl-, and methylvinylchlorosilanes, and tetrachlorosilane, with the methyl substituted silanes being most commonly utilized.
• silicone resin powders such as the material given the CTFA designation polymethylsilsequioxane, which is commercially available as TospearlTM from Toshiba Silicones.
• Silicone materials and silicone resins in particular can conveniently be identified according to a shorthand nomenclature system well known to those skilled in the art as the "MDTQ" nomenclature. Under this system, the silicone is described according to the presence of various siloxane monomer units which make up the silicone.
• M denotes the mono-functional unit (CH 3 ) 3 SiO 0 ,5; D denotes the difunctional unit (CH 3 ) 2 SiO; T denotes the trifunctional unit (CH 3 )SiOi.5; and Q denotes the quadri- or tetra-functional unit SiO2.
• Primes of the unit symbols, e.g., M', D', T', and Q' denote substituents other than methyl, and must be specifically defined for each occurrence. Typical alternate substituents include groups such as vinyl, phenyl, amino, hydroxyl, etc.
• the molar ratios of the various units either in terms of subscripts to the symbols indicating the total number of each type of unit in the silicone, or an average thereof, or as specifically indicated ratios in combination with molecular weight, complete the description .of the silicone material under the MDTQ system.
• Higher relative molar amounts of T, Q, T' and/or Q' to D, D', M and/or or M' in a silicone resin is indicative of higher levels of crosslinking.
• the overall level of crosslinking can also be indicated by the oxygen to silicon ratio.
• the silicone resins for use herein which are preferred are MQ, MT, MTQ, MQ and MDTQ resins.
• the preferred silicone substituent is methyl.
• MQ resins wherein the M:Q ratio is from about 0.5:1.0 to about 1.5:1.0 and the average molecular weight of the resin is from about 1000 to about 10,000.
• Commercially available MQ resins are, for example, trimethyl siloxy silicate with tradename BY11-018 available from Dow Corning.
• composition of the present invention may further contain a water- soluble polymer. It is believed that water-soluble polymers provide long-lasting effect.
• Useful water-soluble polymers include sodium carboxymethyl cellulose, polyvinyl pyrrolidone, polyvinyl alcohol, xanthan gum, agar, pulleran, bentonite, and mixtures thereof.
• Commercially available water-soluble polymers include the Carbopol series available from B. F. Goodrich Company, and PVP K-30 available from G.A.F. Chemicals.
• compositions of the present invention are; preservatives such as benzyl alcohol, methyl paraben, propyl paraben, imidazolidinyl area, and EDTA and its salts, perfumes, ultraviolet and infrared screening and absorbing agents such as ethylhexyl methoxycinnamate, and others.
• preservatives such as benzyl alcohol, methyl paraben, propyl paraben, imidazolidinyl area, and EDTA and its salts
• perfumes ultraviolet and infrared screening and absorbing agents such as ethylhexyl methoxycinnamate, and others.
• Candelilla wax Candelilla wax NC-1630 available from Noda wax *12 Paraffin : Paraffin wax FT-150 available from Sazole *13 Diglyceryl Sebacate/lsopalmitale : Salacos DGS-16 available from Nisshin
• the make-up compositions of Examples 1 - 5 are suitably prepared as follows: First, a mixture of component numbers 1 through 5 are heated to disperse at a speed of from 1500rpm to 2500rpm using a Homomixer at 90°C in a sealed tank. Separately, a mixture of component numbers 6 through 8 are dissolved at 90°C. This solution (component numbers 6-8) is added to the dispersion (component numbers 1-5), and the mixture is further dispersed at a speed of from 5000rpm to 7000rpm using a Homomixer to form a hydrophobic gel.
• component numbers 9 through 19, as present are heated to dissolve at 80°C in a sealed tank, followed by adding the above hydrophobic gel and component number 20, and the mixture is dispersed at 80°C using a disper to make a lipophilic dispersion. The obtained dispersion is adjusted to a temperature of 80°C. Finally, the dispersion is filled in an air-tight container and allowed to cool to room temperature.
• Examples 1 through 3 provide lipsticks which provide; improved lip suppleness, moisturization, and reduction of visible liplines and wrinkles to the lips.
• Example 4 provides a stick foundation.
• Example 5 provides a poured foundation. The foundations of Examples 4 and 5 provide; improved suppleness, moisturization, and reduction of visible lines and wrinkles to the skin, particularly facial skin.
• the make up compositions of Example 1 through 5 further have improved stability with regard to physical hardness, color, and sweat resistance.

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Citations (4)

• 2000
  • 2000-09-26 MX MXPA03002695A patent/MXPA03002695A/es unknown
  • 2000-09-26 KR KR10-2003-7004152A patent/KR20030036817A/ko not_active Application Discontinuation
  • 2000-09-26 EP EP00968424A patent/EP1320352A1/en not_active Ceased
  • 2000-09-26 AU AU7834100A patent/AU7834100A/xx active Pending
  • 2000-09-26 CZ CZ2003789A patent/CZ2003789A3/cs unknown
  • 2000-09-26 CN CN00819916A patent/CN1454072A/zh active Pending
  • 2000-09-26 WO PCT/US2000/026492 patent/WO2002026198A1/en not_active Application Discontinuation
  • 2000-09-26 JP JP2002530029A patent/JP2004509911A/ja active Pending
  • 2000-09-26 AU AU2000278341A patent/AU2000278341B2/en not_active Ceased
  • 2000-09-26 CA CA002422453A patent/CA2422453A1/en not_active Abandoned

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