US20010026811A1 - Stable topical composition comprising a solid elastomeric organopolysiloxane and spherical particles - Google Patents

Stable topical composition comprising a solid elastomeric organopolysiloxane and spherical particles Download PDF

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Publication number
US20010026811A1
US20010026811A1 US09/860,460 US86046001A US2001026811A1 US 20010026811 A1 US20010026811 A1 US 20010026811A1 US 86046001 A US86046001 A US 86046001A US 2001026811 A1 US2001026811 A1 US 2001026811A1
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particles
composition
organopolysiloxane
fatty phase
chosen
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US09/860,460
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Violaine Rouquet
Jean-Claude Contamin
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LOreal SA
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LOreal SA
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Priority to US09/860,460 priority Critical patent/US20010026811A1/en
Publication of US20010026811A1 publication Critical patent/US20010026811A1/en
Priority to US10/051,040 priority patent/US20020102284A1/en
Abandoned legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04—Polysiloxanes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A61K8/895—Polysiloxanes containing silicon bound to unsaturated aliphatic groups, e.g. vinyl dimethicone
    • 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
    • A61K8/0241—Containing particulates characterized by their shape and/or structure
    • A61K8/025—Explicitly spheroidal or spherical shape
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/58—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • A61K8/585—Organosilicon compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • A61K8/731—Cellulose; Quaternized cellulose derivatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • 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
    • A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products 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
    • A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/12—Polysiloxanes containing silicon bound to hydrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K7/00—Use of ingredients characterised by shape
    • C08K7/16—Solid spheres
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/41—Particular ingredients further characterized by their size
    • A61K2800/412—Microsized, i.e. having sizes between 0.1 and 100 microns
    • 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
    • A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations

Definitions

  • the invention relates to a stable topical composition
  • a stable topical composition comprising a liquid fatty phase in combination with a partially or completely crosslinked elastomeric organopolysiloxane.
  • This composition is more especially intended for the cosmetic or dermatological field. It can constitute in particular a composition for caring for, treating, making up or removing make-up from the skin of the face or of the body, keratinous fibres (hair, eyelashes, eyebrows) and mucous membranes, such as the lips and the inner surfaces of the eyelids, of human beings.
  • spherical particles such as silica particles
  • silica particles for the purpose of conferring a degree of consistency on these compositions.
  • these particles have the property of absorbing fatty substances, and conferring a non-greasy appearance on these compositions, even in the presence of a large amount of fatty substances.
  • This type of composition is much appreciated by consumers, in particular those with a skin with a greasy tendency.
  • the higher the amount of silica particles the greater the instability of the composition.
  • these particles confer a very rough and dry feel on the composition, thus limiting the use of this type of composition.
  • the inventors have developed a stable composition with a high level of spherical particles which does not exhibit the above disadvantages, while retaining the non-greasy property.
  • the invention relates to a composition
  • a composition comprising at least one liquid fatty phase associated with a solid phase comprising particles of at least one partially or completely crosslinked elastomeric organopolysiloxane, wherein the particles in the solid phase represent at least 10% of the total weight of the fatty phase and, in addition, the composition comprises spherical organic particles with a particle- diameter of less than 10 ⁇ m.
  • Another subject-matter of the invention is the use, in a composition comprising at least one liquid fatty phase associated with a solid phase containing particles, and further comprising spherical organic particles with a particle diameter of less than 10 ⁇ m, the particles in the solid phase representing at least 10% of the total weight of the fatty phase, of particles of one or more partially or completely crosslinked elastomeric organopolysiloxanes, in order to stabilize and/or to render homogeneous the said composition.
  • a further subject-matter of the invention is a process for the stabilization and/or homogenization of a composition comprising at least one liquid fatty phase associated with a solid phase containing particles, the particles in the solid phase representing at least 10% of the total weight of the fatty phase and further comprising spherical particles with a particle diameter of less than 10 ⁇ m, which process comprises using particles of at least one partially or completely crosslinked elastomeric organopolysiloxane in the solid phase.
  • compositions comprising a high amount of spherical organic particles which can represent up to 40% by weight (as active material) of the total fatty phase.
  • “Stable composition” should be understood as meaning maintenance of the homogeneous appearance of the composition, without demixing, precipitation or flocculation of the particles, for at least 2 months at 45° C.
  • “Elastomeric” is understood to mean a flexible and deformable material having viscoelastic properties and exhibiting in particular the consistency of a sponge or of a flexible sphere.
  • Liquid fatty phase should be understood as meaning a fatty phase which is liquid at room temperature, often known as oily phase.
  • composition of the invention is well suited to topical application.
  • the elastomeric organopolysiloxanes of the composition according to the invention exhibit a notable oil-gelling power. They are not desiccating to the skin and contribute good cosmetic properties. These novel elastomers result in compositions which are comfortable on application, soft and nonsticky to the touch. This softness is due in particular to the texture of the organopolysiloxanes.
  • the combination of the invention also makes it possible to obtain care or make-up products intended in particular for softening blemishes of the contours of the skin, while contributing a natural appearance to it.
  • the spherical organic particles have a particle diameter of less than 5 ⁇ m.
  • Particle diameter should be understood as meaning the diameter of the unit particles. This is because the spherical particles may have a tendency to agglomerate, resulting in aggregates which can have particle diameters of greater than 5 ⁇ m, or even greater than 10 ⁇ m.
  • representative spherical organic particles to which the invention applies are polymeric particles chosen from microbeads of methylsilsesquioxane resins, such as, for example, those sold by Toshiba Silicone under the name Tospearl 145A, microbeads of poly(methyl methacrylate)s, such as in particular those sold by Seppic under the name Micropearl M 100, spherical particles of crosslinked polydimethylsiloxanes, such as in particular those sold by Dow Corning Toray Silicone under the name Trefil E 506 C or Trefil E-505C, spherical particles of polyamide and more especially of Nylon 12, such as in particular those sold by Atochem under the name Orgasol 2002 D Nat C05, polystyrene microspheres, such as, for example, those sold by Dyno Particles under the name Dynospheres, and their mixtures.
  • microbeads of methylsilsesquioxane resins such as, for example, those sold by
  • the “Trefils” are in particular spherical particles of crosslinked polymers disclosed in Application EP-A-0,295,886 of Toray Silicone Company. According to this application, they are obtained by addition and crosslinking reaction, in the presence of a catalyst of the platinum type, of at least:
  • the elastomeric organopolysiloxanes of the composition of the invention exhibit a three-dimensional structure. Depending on the level of the liquid fatty phase used in combination with these organopolysiloxanes, the latter are converted from a product with a spongy appearance, when they are used in the presence of low contents of fatty phase, to a more or less homogeneous gel, in the presence of larger amounts of fatty phase.
  • the gelling of the liquid fatty phase by these elastomers can be complete or partial.
  • the elastomers of the composition of the invention are generally carried in the form of a gel composed of an elastomeric organopolysiloxane with a three-dimensional structure included in at least one hydrocarbon-comprising oil and/or one silicone oil.
  • elastomeric organopolysiloxanes of the composition according to the invention can also be chosen from those disclosed in U.S. Pat. No. 5,266,321 of Kobayashi Kose, the disclosure of which is specifically incorporated by reference herein. According to this patent, they are chosen in particular from:
  • organopolysiloxanes comprising R 2 SiO and RSiO 1.5 units and optionally R 3 SiO 0.5 and/or SiO 2 units in which the R radicals, independently of one another, represent a hydrogen, an alkyl, such as methyl, ethyl or propyl, an aryl, such as phenyl or tolyl, or an unsaturated aliphatic group, such as vinyl, the ratio by weight of the R 2 SiO units to the RSiO 1.5 units ranging from 1/1 to 30/1;
  • organopolysiloxanes which are insoluble and which can be swollen in a silicone oil, obtained by addition of an organohydropolysiloxane (1) and of an organopolysiloxane (2) having unsaturated aliphatic groups, so that the amount of hydrogen or of unsaturated aliphatic groups in (1) and (2) respectively is between 1 and 20 mol % when the organopolysiloxane is non-cyclic and between 1 and 50 mol % when the organopolysiloxane is cyclic.
  • the organopolysiloxanes which are the subject-matter of the invention are, for example, those sold under the names KSG6 of Shin-Etsu or Gransil of Grant Industries (SR-CYC, SR DMF10, SR-DC556) or those sold in the form of already constituted gels (KSG15, KSG17, KSG16, KSG18 of Shin-Etsu, Gransil SR 5CYC gel, Gransil SR DMF 10 gel, Gransil SR DC 556 gel, SF 1204 and JK 113 of General Electric. Use may also be made of a mixture of these commercial products.
  • the combined elastomeric organopolysiloxane particles and spherical particles represent at least 10% (as active material) of the total weight of the (liquid+solid) fatty phase and better still at least 20% (as active material). This combination can, in addition, represent up to 40% (as active material) of the total weight of the fatty phase.
  • the stability and the homogeneity of the composition depend on the amount of spherical particles and increase with the amount of elastomeric organopolysiloxane.
  • the ratio by weight of the spherical particles to the elastomeric organopolysiloxane particles (as active material) is chosen within the range from 0.25:1 to 1 and better still from 0.4 to 0.7.
  • the amount of spherical particles (as active material) preferably varies from 2% to 20% of the total weight of the composition and the amount of elastomeric organopolysiloxane particles (as active material) preferably varies from 2% to 20% of the total weight of the composition.
  • the composition advantageously comprises a continuous fatty phase.
  • this type of composition is neither greasy to the touch and on application, nor oily.
  • this composition has great softness.
  • the composition of the invention can advantageously be an anhydrous gel or a water-in-oil (W/O) emulsion.
  • W/O water-in-oil
  • it can be provided in the form of an oil-in-water emulsion.
  • it is provided in the form of a cream.
  • compositions which are more or less viscous, stable and homogeneous over time.
  • the composition can have a dynamic viscosity, measured at room temperature with a device of the Rheomat RM 180 (Mettler) type, ranging from 2 to 20 Pa ⁇ s.
  • the composition of the invention advantageously constitutes a care or make-up base to be applied to the skin or the lips before the care or make-up product.
  • it makes it possible to extend the hold over time of the care or make-up composition, which is particularly advantageous for foundation products, products for concealing rings under the eyes, lip glosses and sun protection products. It can also be used as a composition for rendering the skin matt which is suited to greasy skin.
  • the oily fatty phase used in combination with the elastomeric organopolysiloxanes of the invention can comprise hydrocarbon-comprising oils and/or silicone oils.
  • hydrocarbon-comprising oils which can be used in the invention, of:
  • hydrocarbon-comprising oils of animal origin such as perhydrosqualene
  • oils of plant origin such as liquid triglycerides of fatty acids containing 4 to 10 carbon atoms, such as triglycerides of heptanoic or octanoic acids, or alternatively sunflower, maize, soybean, hazelnut, apricot, macadamia, castor or avocado oils, triglycerides of caprylic/capric acids, such as those sold by the company Stéarineries Dubois or those sold under the names Miglyol 810, 812 and 818 by the company Dynamit Nobel, jojoba oil or karite butter;
  • oils of plant origin such as liquid triglycerides of fatty acids containing 4 to 10 carbon atoms, such as triglycerides of heptanoic or octanoic acids, or alternatively sunflower, maize, soybean, hazelnut, apricot, macadamia, castor or avocado oils, triglycerides of caprylic/capric acids, such as those
  • linear or branched hydrocarbons of mineral or synthetic origin such as liquid paraffins and their derivatives, hydrogenated isoparaffins, which may or may not be volatile, petrolatum, polydecenes, purcellin oil or hydrogenated polyisobutene, such as sesam;
  • esters and ethers such as oils of formula R 1 COOR 2 in which R 1 represents the residue of a higher fatty acid comprising from 6 to 29 carbon atoms and R 2 represents a hydrocarbon-comprising chain comprising from 3 to 30 carbon atoms, such as purcellin oil, isopropyl myristate, 2-ethylhexyl palmitate, 2-octyldodecyl stearate, isostearyl isostearate, arachidyl propionate or 2-octyldodecyl benzoate; hydroxylated esters, such as isostearyl lactate, octyl hydroxystearate, octyldodecyl hydroxystearate, diisostearyl malate or triisocetyl citrate; or polyol esters, such as propylene glycol dioctanoate, neopentyl glycol diheptanoate,
  • fatty alcohols having from 12 to 26 carbon atoms such as octyldodecanol, 2-butyloctanol, 2-hexyldecanol, 2-undecylpentadecanol, oleyl alcohol or cetyl alcohol;
  • the silicone oils which can be used in the invention are in particular polymethylsiloxanes with a linear or cyclic structure which are liquid or pasty at room temperature, such as polydimethylsiloxanes, such as hexamethyldisiloxane, octamethylcyclopentasiloxane or decamethylcyclopentasiloxane, phenyl dimethicones, phenyl trimethicones and polymethylphenylsiloxanes, or their mixtures.
  • polydimethylsiloxanes such as hexamethyldisiloxane, octamethylcyclopentasiloxane or decamethylcyclopentasiloxane
  • phenyl dimethicones phenyl trimethicones
  • polymethylphenylsiloxanes or their mixtures.
  • the solid or semi-solid fatty phase optionally present in the composition comprises in particular waxes and/or gums.
  • the waxes and the gums which can be used in the invention are in particular microcrystalline waxes and silicone gums.
  • the total fatty phase can represent from 5 to 90% of the total weight of the finished product and better still from 10 to 80%.
  • the composition of the invention advantageously comprises colouring materials and in particular a particulate phase generally present in a proportion of 0.05 (or even 0%) to 35% of the total weight of the composition, preferably of 2 to 25%, and which can comprise pigments and/or pearlescent agents commonly used in cosmetic products.
  • This phase can result in a coloured, white or colourless product.
  • pigment which can be used in the composition of the invention of titanium, zirconium or cerium oxides, as well as zinc, iron or chromium oxides, ferric blue, carbon black and barium, strontium, calcium or aluminium lakes.
  • composition according to the invention can comprise, in addition, the ingredients commonly used in cosmetics, chosen as a function of the activity or of the cosmetic effect desired for the final product, such as coverage, transparency, mattness and/or satin appearance. Mention may be made, without implied limitation, of:
  • lipophilic or hydrophilic thickeners such as modified clays known under the names of bentone; aluminium fatty salts; carboxymethylcellulose; or polyacrylamides;
  • vitamins such as tocopherols and their derivatives, including the acetate, vitamin A and its derivatives, or vitamin C and its derivatives, such as the fatty esters, including the palmitate;
  • sunscreening agents such as octyl methoxycinnamate (Parsol MCX), 3-benzophenone (Uvinul M40) or butylmethoxydibenzoylmethane (Parsol 1789);
  • lecithin e.g., lecithin, fragrances, essential oils, ceramides, preservatives or antioxidants;
  • moisturizing agents such as propylene glycol, glycerol or even ethanol
  • agents which act on greasy skin and/or antiseborrhoeic agents such as copper and/or zinc salts.
  • the composition can also comprise a surfactant, for example a conventional anionic or non-ionic surfactant.
  • the surfactant is preferably present in a proportion of 0.3 (or even 0%, in an anhydrous composition) to 8% of the total weight of the composition. Mention may be made, as surfactant which can be used in the composition of the invention, of polysorbate 40, glycerol monostearate or dimethicone copolyols with an oxypropylenated and/or oxyethylenated chain.
  • compositions according to the invention do not differ in any way from the processes conventionally used in cosmetics and are fully known to a person skilled in the art.
  • Phase 1a Tospearl 145 A 6
  • Phase 2a Gransil SR 5 CYC (containing 25% of crosslinked 40.0 siloxane)
  • Liquid fatty phase Cyclomethicone 44.0 Octyl methoxycinnamate 5.0 Plant perhydrosqualene 5.0 Fragrance q.s.
  • This composition is obtained by dispersing the phase 1a in the liquid phase at room temperature and with stirring and by then adding the phase 2a, still while stirring.
  • This composition has the appearance of a translucent, non-greasy and soft gel. It is stable for 2 months at 45° C.
  • W/O foundation Phase 1b Micropearl M 100 5 Phase 2b: KSG 16 (containing 24% of crosslinked siloxane) 25.0 Liquid fatty phase: Dimethicone copolyol 0.5 Cyclomethicone 45 Octyl methoxycinnamate 2.0 Liquid PDMS 30.0 Hydrogenated isoparaffin 5.0 Fragrance q.s. Colouring phase: TiO 2 4.0 Iron oxides 0.8 Aqueous phase: Glycerol 10.0 Demineralized water 15.0 Preservatives q.s.
  • This composition is obtained by successively dispersing the colouring phase, the phase 1b and then the phase 2b in the liquid phase at room temperature and with stirring.
  • the aqueous phase is subsequently emulsified in the fatty phase in a turbo mixer at room temperature.
  • This composition has the appearance of a tinted, non-greasy and soft cream. It is stable for 2 months at 45° C.
  • W/O care cream Phase 1c Trefil E 5060 (100% active material) 2 Phase 2c: Gransil SR 5 CYC (containing 25% of crosslinked 8.0 siloxane) Liquid fatty phase: Polysorbate 40 2.0 Glycerol monostearate 2.0 Cetyl alcohol 1.0 Cyclomethicone 2.0 Dimethicone 2.0 Avocado oil 2.0 Soybean oil 3.0 Antioxidant (vitamin E) 0.1 Aqueous phase: Glycerol 5.0 Polyacrylamide (hydrophilic gelling agent) 0.7 Carboxymethylcellulose 0.5 Demineralized water q.s. for 100 Preservative and fragrance q.s.
  • the starting point is the emulsification of the aqueous phase in the fatty phase in a turbo mixer at 65° C.
  • the phase 1c and then the phase 2c are successively added to the emulsion in a turbo mixer at 50° C. with stirring.
  • the mixture is allowed to cool.
  • This composition has the appearance of a white, non-greasy and soft cream. It is stable for 2 months at 45° C.
  • the make-up base is applied before the foundation and a comparison is made with and without make-up base.
  • composition of the invention confers, on the make-up, improved properties of hold over time, of comfort and of softness.

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  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A stable topical composition, which can be used in the cosmetic or dermatological fields, comprising at least one liquid fatty phase in combination with a solid phase representing at least 10% of the total weight of the fatty phase and further comprising a partially or completely crosslinked elastomeric organopolysiloxane and spherical polymeric particles with a particle diameter of less than 10 μm.

Description

  • The invention relates to a stable topical composition comprising a liquid fatty phase in combination with a partially or completely crosslinked elastomeric organopolysiloxane. This composition is more especially intended for the cosmetic or dermatological field. It can constitute in particular a composition for caring for, treating, making up or removing make-up from the skin of the face or of the body, keratinous fibres (hair, eyelashes, eyebrows) and mucous membranes, such as the lips and the inner surfaces of the eyelids, of human beings. [0001]
  • It is known to use, in cosmetic or dermatological compositions, spherical particles, such as silica particles, for the purpose of conferring a degree of consistency on these compositions. Reference may in particular be made to the document by Shiseido EP-A-765,656. In these compositions, the higher the amount of particles, the thicker the composition. In addition, these particles have the property of absorbing fatty substances, and conferring a non-greasy appearance on these compositions, even in the presence of a large amount of fatty substances. This type of composition is much appreciated by consumers, in particular those with a skin with a greasy tendency. Unfortunately, the higher the amount of silica particles, the greater the instability of the composition. In addition, these particles confer a very rough and dry feel on the composition, thus limiting the use of this type of composition. [0002]
  • The inventors have developed a stable composition with a high level of spherical particles which does not exhibit the above disadvantages, while retaining the non-greasy property. [0003]
  • More specifically, the invention relates to a composition comprising at least one liquid fatty phase associated with a solid phase comprising particles of at least one partially or completely crosslinked elastomeric organopolysiloxane, wherein the particles in the solid phase represent at least 10% of the total weight of the fatty phase and, in addition, the composition comprises spherical organic particles with a particle- diameter of less than 10 μm. [0004]
  • Another subject-matter of the invention is the use, in a composition comprising at least one liquid fatty phase associated with a solid phase containing particles, and further comprising spherical organic particles with a particle diameter of less than 10 μm, the particles in the solid phase representing at least 10% of the total weight of the fatty phase, of particles of one or more partially or completely crosslinked elastomeric organopolysiloxanes, in order to stabilize and/or to render homogeneous the said composition. [0005]
  • A further subject-matter of the invention is a process for the stabilization and/or homogenization of a composition comprising at least one liquid fatty phase associated with a solid phase containing particles, the particles in the solid phase representing at least 10% of the total weight of the fatty phase and further comprising spherical particles with a particle diameter of less than 10 μm, which process comprises using particles of at least one partially or completely crosslinked elastomeric organopolysiloxane in the solid phase. [0006]
  • By virtue of the presence of one or more solid elastomeric organopolysiloxanes, it is possible to obtain stable compositions comprising a high amount of spherical organic particles which can represent up to 40% by weight (as active material) of the total fatty phase. [0007]
  • “Stable composition” should be understood as meaning maintenance of the homogeneous appearance of the composition, without demixing, precipitation or flocculation of the particles, for at least 2 months at 45° C. [0008]
  • “Elastomeric” is understood to mean a flexible and deformable material having viscoelastic properties and exhibiting in particular the consistency of a sponge or of a flexible sphere. [0009]
  • “Liquid fatty phase” should be understood as meaning a fatty phase which is liquid at room temperature, often known as oily phase. [0010]
  • According to the invention, it is additionally possible to combine, with the liquid fatty phase, a fatty phase which is solid or semi-solid at room temperature, for the purpose of modifying the rheology of the composition. [0011]
  • Although the invention applies to any technical field, it is intended more especially for the cosmetic and dermatological fields. The composition of the invention is well suited to topical application. [0012]
  • The elastomeric organopolysiloxanes of the composition according to the invention exhibit a notable oil-gelling power. They are not desiccating to the skin and contribute good cosmetic properties. These novel elastomers result in compositions which are comfortable on application, soft and nonsticky to the touch. This softness is due in particular to the texture of the organopolysiloxanes. [0013]
  • The combination of the invention also makes it possible to obtain care or make-up products intended in particular for softening blemishes of the contours of the skin, while contributing a natural appearance to it. [0014]
  • Preferably, the spherical organic particles have a particle diameter of less than 5 μm. Particle diameter should be understood as meaning the diameter of the unit particles. This is because the spherical particles may have a tendency to agglomerate, resulting in aggregates which can have particle diameters of greater than 5 μm, or even greater than 10 μm. [0015]
  • In particular, representative spherical organic particles to which the invention applies are polymeric particles chosen from microbeads of methylsilsesquioxane resins, such as, for example, those sold by Toshiba Silicone under the name Tospearl 145A, microbeads of poly(methyl methacrylate)s, such as in particular those sold by Seppic under the name Micropearl M 100, spherical particles of crosslinked polydimethylsiloxanes, such as in particular those sold by Dow Corning Toray Silicone under the name Trefil E 506 C or Trefil E-505C, spherical particles of polyamide and more especially of Nylon 12, such as in particular those sold by Atochem under the name Orgasol 2002 D Nat C05, polystyrene microspheres, such as, for example, those sold by Dyno Particles under the name Dynospheres, and their mixtures. [0016]
  • The “Trefils” are in particular spherical particles of crosslinked polymers disclosed in Application EP-A-0,295,886 of Toray Silicone Company. According to this application, they are obtained by addition and crosslinking reaction, in the presence of a catalyst of the platinum type, of at least: [0017]
  • (a) one organopolysiloxane having at least two lower alkenyl groups per molecule; and [0018]
  • (b) one organopolysiloxane having at least two hydrogen atoms bonded to a silicon atom per molecule. [0019]
  • The elastomeric organopolysiloxanes of the composition of the invention exhibit a three-dimensional structure. Depending on the level of the liquid fatty phase used in combination with these organopolysiloxanes, the latter are converted from a product with a spongy appearance, when they are used in the presence of low contents of fatty phase, to a more or less homogeneous gel, in the presence of larger amounts of fatty phase. The gelling of the liquid fatty phase by these elastomers can be complete or partial. [0020]
  • The elastomers of the composition of the invention are generally carried in the form of a gel composed of an elastomeric organopolysiloxane with a three-dimensional structure included in at least one hydrocarbon-comprising oil and/or one silicone oil. [0021]
  • The elastomeric organopolysiloxanes of the composition according to the invention can also be chosen from those disclosed in U.S. Pat. No. 5,266,321 of Kobayashi Kose, the disclosure of which is specifically incorporated by reference herein. According to this patent, they are chosen in particular from: [0022]
  • i) organopolysiloxanes comprising R[0023] 2SiO and RSiO1.5 units and optionally R3SiO0.5 and/or SiO2 units in which the R radicals, independently of one another, represent a hydrogen, an alkyl, such as methyl, ethyl or propyl, an aryl, such as phenyl or tolyl, or an unsaturated aliphatic group, such as vinyl, the ratio by weight of the R2SiO units to the RSiO1.5 units ranging from 1/1 to 30/1;
  • ii) organopolysiloxanes which are insoluble and which can be swollen in a silicone oil, obtained by addition of an organohydropolysiloxane (1) and of an organopolysiloxane (2) having unsaturated aliphatic groups, so that the amount of hydrogen or of unsaturated aliphatic groups in (1) and (2) respectively is between 1 and 20 mol % when the organopolysiloxane is non-cyclic and between 1 and 50 mol % when the organopolysiloxane is cyclic. [0024]
  • The organopolysiloxanes which are the subject-matter of the invention are, for example, those sold under the names KSG6 of Shin-Etsu or Gransil of Grant Industries (SR-CYC, SR DMF10, SR-DC556) or those sold in the form of already constituted gels (KSG15, KSG17, KSG16, KSG18 of Shin-Etsu, Gransil SR 5CYC gel, Gransil SR DMF 10 gel, Gransil SR DC 556 gel, SF 1204 and JK 113 of General Electric. Use may also be made of a mixture of these commercial products. [0025]
  • The combined elastomeric organopolysiloxane particles and spherical particles represent at least 10% (as active material) of the total weight of the (liquid+solid) fatty phase and better still at least 20% (as active material). This combination can, in addition, represent up to 40% (as active material) of the total weight of the fatty phase. [0026]
  • The stability and the homogeneity of the composition depend on the amount of spherical particles and increase with the amount of elastomeric organopolysiloxane. By way of indication, the ratio by weight of the spherical particles to the elastomeric organopolysiloxane particles (as active material) is chosen within the range from 0.25:1 to 1 and better still from 0.4 to 0.7. The amount of spherical particles (as active material) preferably varies from 2% to 20% of the total weight of the composition and the amount of elastomeric organopolysiloxane particles (as active material) preferably varies from 2% to 20% of the total weight of the composition. [0027]
  • The composition advantageously comprises a continuous fatty phase. By virtue of the specific particles present in the composition, this type of composition is neither greasy to the touch and on application, nor oily. In addition, this composition has great softness. Thus, the composition of the invention can advantageously be an anhydrous gel or a water-in-oil (W/O) emulsion. However, it can be provided in the form of an oil-in-water emulsion. In addition, it is provided in the form of a cream. [0028]
  • Depending on the amount of particles used, it is possible to obtain compositions which are more or less viscous, stable and homogeneous over time. In particular, the composition can have a dynamic viscosity, measured at room temperature with a device of the Rheomat RM 180 (Mettler) type, ranging from 2 to 20 Pa·s. [0029]
  • The composition of the invention advantageously constitutes a care or make-up base to be applied to the skin or the lips before the care or make-up product. In particular, it makes it possible to extend the hold over time of the care or make-up composition, which is particularly advantageous for foundation products, products for concealing rings under the eyes, lip glosses and sun protection products. It can also be used as a composition for rendering the skin matt which is suited to greasy skin. [0030]
  • The oily fatty phase used in combination with the elastomeric organopolysiloxanes of the invention can comprise hydrocarbon-comprising oils and/or silicone oils. [0031]
  • Mention may in particular be made, as hydrocarbon-comprising oils which can be used in the invention, of: [0032]
  • hydrocarbon-comprising oils of animal origin, such as perhydrosqualene; [0033]
  • hydrocarbon-comprising oils of plant origin, such as liquid triglycerides of fatty acids containing 4 to 10 carbon atoms, such as triglycerides of heptanoic or octanoic acids, or alternatively sunflower, maize, soybean, hazelnut, apricot, macadamia, castor or avocado oils, triglycerides of caprylic/capric acids, such as those sold by the company Stéarineries Dubois or those sold under the names Miglyol 810, 812 and 818 by the company Dynamit Nobel, jojoba oil or karite butter; [0034]
  • linear or branched hydrocarbons of mineral or synthetic origin, such as liquid paraffins and their derivatives, hydrogenated isoparaffins, which may or may not be volatile, petrolatum, polydecenes, purcellin oil or hydrogenated polyisobutene, such as parleam; [0035]
  • synthetic esters and ethers, such as oils of formula R[0036] 1COOR2 in which R1 represents the residue of a higher fatty acid comprising from 6 to 29 carbon atoms and R2 represents a hydrocarbon-comprising chain comprising from 3 to 30 carbon atoms, such as purcellin oil, isopropyl myristate, 2-ethylhexyl palmitate, 2-octyldodecyl stearate, isostearyl isostearate, arachidyl propionate or 2-octyldodecyl benzoate; hydroxylated esters, such as isostearyl lactate, octyl hydroxystearate, octyldodecyl hydroxystearate, diisostearyl malate or triisocetyl citrate; or polyol esters, such as propylene glycol dioctanoate, neopentyl glycol diheptanoate, diethylene glycol diisononanoate and pentaerythritol esters;
  • fatty alcohols having from 12 to 26 carbon atoms, such as octyldodecanol, 2-butyloctanol, 2-hexyldecanol, 2-undecylpentadecanol, oleyl alcohol or cetyl alcohol; [0037]
  • their mixtures. [0038]
  • The silicone oils which can be used in the invention are in particular polymethylsiloxanes with a linear or cyclic structure which are liquid or pasty at room temperature, such as polydimethylsiloxanes, such as hexamethyldisiloxane, octamethylcyclopentasiloxane or decamethylcyclopentasiloxane, phenyl dimethicones, phenyl trimethicones and polymethylphenylsiloxanes, or their mixtures. [0039]
  • The solid or semi-solid fatty phase optionally present in the composition comprises in particular waxes and/or gums. The waxes and the gums which can be used in the invention are in particular microcrystalline waxes and silicone gums. [0040]
  • The total fatty phase can represent from 5 to 90% of the total weight of the finished product and better still from 10 to 80%. [0041]
  • The composition of the invention advantageously comprises colouring materials and in particular a particulate phase generally present in a proportion of 0.05 (or even 0%) to 35% of the total weight of the composition, preferably of 2 to 25%, and which can comprise pigments and/or pearlescent agents commonly used in cosmetic products. This phase can result in a coloured, white or colourless product. Mention may be made, as pigment which can be used in the composition of the invention, of titanium, zirconium or cerium oxides, as well as zinc, iron or chromium oxides, ferric blue, carbon black and barium, strontium, calcium or aluminium lakes. [0042]
  • The composition according to the invention can comprise, in addition, the ingredients commonly used in cosmetics, chosen as a function of the activity or of the cosmetic effect desired for the final product, such as coverage, transparency, mattness and/or satin appearance. Mention may be made, without implied limitation, of: [0043]
  • lipophilic or hydrophilic thickeners, such as modified clays known under the names of bentone; aluminium fatty salts; carboxymethylcellulose; or polyacrylamides; [0044]
  • vitamins, such as tocopherols and their derivatives, including the acetate, vitamin A and its derivatives, or vitamin C and its derivatives, such as the fatty esters, including the palmitate; [0045]
  • sunscreening agents, such as octyl methoxycinnamate (Parsol MCX), 3-benzophenone (Uvinul M40) or butylmethoxydibenzoylmethane (Parsol 1789); [0046]
  • lecithin, fragrances, essential oils, ceramides, preservatives or antioxidants; [0047]
  • moisturizing agents, such as propylene glycol, glycerol or even ethanol; [0048]
  • agents which act on greasy skin and/or antiseborrhoeic agents, such as copper and/or zinc salts. [0049]
  • The composition can also comprise a surfactant, for example a conventional anionic or non-ionic surfactant. The surfactant is preferably present in a proportion of 0.3 (or even 0%, in an anhydrous composition) to 8% of the total weight of the composition. Mention may be made, as surfactant which can be used in the composition of the invention, of polysorbate 40, glycerol monostearate or dimethicone copolyols with an oxypropylenated and/or oxyethylenated chain. [0050]
  • The processes for manufacturing the compositions according to the invention do not differ in any way from the processes conventionally used in cosmetics and are fully known to a person skilled in the art. [0051]
  • In the examples below, the amount of the ingredients is given as percentage by weight.[0052]
    • EXAMPLE 1
  • Anhydrous anti-sun care [0053]
    Phase 1a:
    Tospearl 145 A  6  
    Phase 2a:
    Gransil SR 5 CYC (containing 25% of crosslinked 40.0
    siloxane)
    Liquid fatty phase:
    Cyclomethicone 44.0
    Octyl methoxycinnamate  5.0
    Plant perhydrosqualene  5.0
    Fragrance q.s.
  • This composition is obtained by dispersing the phase 1a in the liquid phase at room temperature and with stirring and by then adding the phase 2a, still while stirring. This composition has the appearance of a translucent, non-greasy and soft gel. It is stable for 2 months at 45° C. [0054]
    • EXAMPLE 2
  • W/O foundation [0055]
    Phase 1b:
    Micropearl M 100  5  
    Phase 2b:
    KSG 16 (containing 24% of crosslinked siloxane) 25.0
    Liquid fatty phase:
    Dimethicone copolyol  0.5
    Cyclomethicone 45  
    Octyl methoxycinnamate  2.0
    Liquid PDMS 30.0
    Hydrogenated isoparaffin  5.0
    Fragrance q.s.
    Colouring phase:
    TiO2  4.0
    Iron oxides  0.8
    Aqueous phase:
    Glycerol 10.0
    Demineralized water 15.0
    Preservatives q.s.
  • This composition is obtained by successively dispersing the colouring phase, the phase 1b and then the phase 2b in the liquid phase at room temperature and with stirring. The aqueous phase is subsequently emulsified in the fatty phase in a turbo mixer at room temperature. This composition has the appearance of a tinted, non-greasy and soft cream. It is stable for 2 months at 45° C. [0056]
    • EXAMPLE 3
  • W/O care cream [0057]
    Phase 1c:
    Trefil E 5060 (100% active material) 2  
    Phase 2c:
    Gransil SR 5 CYC (containing 25% of crosslinked 8.0
    siloxane)
    Liquid fatty phase:
    Polysorbate 40 2.0
    Glycerol monostearate 2.0
    Cetyl alcohol 1.0
    Cyclomethicone 2.0
    Dimethicone 2.0
    Avocado oil 2.0
    Soybean oil 3.0
    Antioxidant (vitamin E) 0.1
    Aqueous phase:
    Glycerol 5.0
    Polyacrylamide (hydrophilic gelling agent) 0.7
    Carboxymethylcellulose 0.5
    Demineralized water q.s. for 100
    Preservative and fragrance q.s.
  • The starting point is the emulsification of the aqueous phase in the fatty phase in a turbo mixer at 65° C. The phase 1c and then the phase 2c are successively added to the emulsion in a turbo mixer at 50° C. with stirring. The mixture is allowed to cool. This composition has the appearance of a white, non-greasy and soft cream. It is stable for 2 months at 45° C. [0058]
    • EXAMPLE 4
  • Test of use of a make-up base [0059]
  • This composition is identical to the foundation of Example 2, without the colouring phase. [0060]
  • People in the test: 80 women, who are users of foundation [0061]
  • Duration of the test: 1 week [0062]
  • The make-up base is applied before the foundation and a comparison is made with and without make-up base. [0063]
  • The results are as follows: [0064]
    Without Base With Base
    (complete (complete
    agreement) agreement)
    The skin is matt 76% 94%
    The skin is soft 49% 88%
    The skin is smooth 40% 80%
    The make-up holds all day 74% 95%
  • From this test, it clearly emerges that the composition of the invention confers, on the make-up, improved properties of hold over time, of comfort and of softness. [0065]

Claims (44)

We claim:
1. A composition comprising:
(a) at least one liquid fatty phase associated with a solid phase comprising particles of at least one partially or completely crosslinked elastomeric organopolysiloxane, wherein said particles in the solid phase represent at least 10% of the total weight of the fatty phase and;
(b) spherical organic particles with a particle diameter of less than 10 μm.
2. A composition formed from:
(a) at least one liquid fatty phase associated with a solid phase comprising particles of at least one partially or completely crosslinked elastomeric organopolysiloxane, wherein said particles in the solid phase represent at least 10% of the total weight of the fatty phase and;
(b) spherical organic particles with a particle diameter of less than 10 μm.
3. A composition according to
claim 1
, wherein the organopolysiloxane is obtained by addition and crosslinking reaction, in the presence of a platinum type catalyst of:
(a) at least one organopolysiloxane having at least two lower alkenyl groups per molecule; and
(b) at least one organopolysiloxane having at least two hydrogen atoms bonded to a silicon atom per molecule.
4. A composition according to
claim 1
, wherein the organopolysiloxane is chosen from:
i) organopolysiloxanes comprising R2SiO and RSiO1.5 units and optionally R3SiO0.5 and/or SiO2 units in which the R radicals, independently of one another, denote a hydrogen, an alkyl, an aryl, or an unsaturated aliphatic group, and where the ratio by weight of the R2SiO units to the RSiO1.5 units varies from 1:1 to 30:1; and
ii) organopolysiloxanes which are insoluble and which can be swollen in a silicone oil, obtained by addition of an organohydropolysiloxane (1) and of an organopolysiloxane (2) having unsaturated aliphatic groups, so that the amount of hydrogen or of unsaturated aliphatic groups in (1) and (2) respectively ranges from 1 to 20 mol % when the organopolysiloxane is non-cyclic and from 1 to 50 mol % when the organopolysiloxane is cyclic.
5. A composition according to
claim 1
, wherein the spherical organic particles have a particle diameter of less than 5 μm.
6. A composition according to
claim 1
, wherein the spherical orgainic particles are chosen from microbeads of methylsilsesquioxane resins, microbeads of poly(methyl methacrylate)s, spherical particles of crosslinked polydimethylsiloxanes, spherical particles of polyamide, polystyrene microspheres and mixtures thereof.
7. A composition according to
claim 1
, wherein the spherical orgainic particles are chosen from polymeric organic particles.
8. A composition according to
claim 1
, wherein the particles in the solid phase represent at least 20% of the total weight of the fatty phase.
9. A composition according to
claim 1
, wherein the ratio by weight of the organic spherical particles to the elastomeric organopolysiloxane particles ranges from 0.25:1 to 1:1.
10. A composition according to
claim 9
, wherein the ratio by weight of the spherical organic particles to the elastomeric organopolysiloxane particles ranges from 0.4:1 to 0.7:1.
11. A composition according to
claim 1
, wherein the liquid fatty phase comprises at least one oil chosen from silicone oils and hydrocarbon-comprising oils.
12. A composition according to
claim 1
, wherein the liquid fatty phase comprises at least one oil chosen from hydrocarbon-comprising oils of animal, plant, mineral and synthetic origin, fatty alcohols and polymethylsiloxanes.
13. A composition according to
claim 1
, wherein the composition additionally comprises a solid or semi-solid fatty phase.
14. A composition according to
claim 1
, wherein the composition is in the form of an anhydrous gel or of a water-in-oil or oil-in-water emulsion.
15. A composition according to
claim 1
, wherein the composition comprises a continuous fatty phase.
16. A composition according to
claim 1
, wherein said composition is a cosmetic or dermatological composition.
17. A composition according to
claim 1
, wherein said composition is a composition for caring for, treating, making up or removing make-up from the skin, mucous membranes or keratinous fibres.
18. A composition according to
claim 1
, wherein said composition additionally comprises at least one ingredient chosen from sunscreening agents, essential oils, vitamins, antiseborrhoeic agents, marine extracts, emollients, antioxidants, hydrophilic thickeners, lipophilic thickeners, preservatives, fragrances, and colouring materials.
19. A composition according to
claim 1
, wherein said composition is a care or make-up base for the skin or the lips.
20. A method for softening blemishes of the contours of the skin comprising the step of applying to said blemishes an effective amount of a composition according to
claim 1
.
21. A method for rendering the skin matt comprising the step of applying to said skin an effective amount of a composition according to
claim 1
.
22. A method for extending the hold over time of a cosmetic or dermatological composition comprising the step of including in said composition an effective amount of a composition according to
claim 1
.
23. A method for stabilizing a composition comprising at least one liquid fatty phase and further comprising spherical organic particles with a particle diameter of less than 10 μm, comprising the step of associating with said at least one liquid fatty phase a solid phase containing particles of at least one partially or completely crosslinked elastomeric organopolysiloxane, said particles representing at least 10% of the total weight of the fatty phase.
24. A method for stabilizing a composition formed from at least one liquid fatty phase and from spherical organic particles with a particle diameter of less than 10 μm, comprising the step of further forming said composition by associating with said at least one liquid fatty phase a solid phase containing particles of at least one partially or completely crosslinked elastomeric organopolysiloxane, said particles representing at least 10% of the total weight of the fatty phase.
25. A method for rendering homogeneous a composition comprising at least one liquid fatty phase and further comprising spherical organic particles with a particle diameter of less than 10 μm, comprising the step of associating with said at least one liquid fatty phase a solid phase containing particles of at least one partially or completely crosslinked elastomeric organopolysiloxane, said particles representing at least 10% of the total weight of the fatty phase.
26. A method for rendering homogeneous a composition formed from at least one liquid fatty phase and from spherical organic particles with a particle diameter of less than 10 μm, comprising the step of further forming said composition by associating with said at least one liquid fatty phase a solid phase containing particles of at least one partially or completely crosslinked elastomeric organopolysiloxane, said particles representing at least 10% of the total weight of the fatty phase.
27. A method according to
claim 23
, wherein the organopolysiloxane is obtained by addition and crosslinking reaction, in the presence of a platinum type catalyst of:
(a) at least one organopolysiloxane having at least two lower alkenyl groups per molecule; and
(b) at least one organopolysiloxane having at least two hydrogen atoms bonded to a silicon atom per molecule.
28. A method according to
claim 25
, wherein the organopolysiloxane is obtained by addition and crosslinking reaction, in the presence of a platinum type catalyst of:
(a) at least one organopolysiloxane having at least two lower alkenyl groups per molecule; and
(b) at least one organopolysiloxane having at least two hydrogen atoms bonded to a silicon atom per molecule.
29. A method according to
claim 23
, wherein the organopolysiloxane is chosen from:
i) organopolysiloxanes comprising R2SiO and RSiO1.5 units and optionally R3SiO0.5 and/or SiO2 units in which the R radicals, independently of one another, denote a hydrogen, an alkyl, an aryl, or an unsaturated aliphatic group, and where the ratio by weight of the R2SiO units to the RSiO1.5 units varies from 1/1 to 30/1;
ii) organopolysiloxanes which are insoluble and which can be swollen in a silicone oil, obtained by addition of an organohydropolysiloxane (1) and of an organopolysiloxane (2) having unsaturated aliphatic groups, so that the amount of hydrogen or of unsaturated aliphatic groups in (1) and (2) respectively ranges from 1 to 20 mol % when the organopolysiloxane is non-cyclic and from 1 to 50 mol % when the organopolysiloxane is cyclic.
30. A method according to
claim 29
, wherein said alkyl R radical is chosen from methyl, ethyl and propyl, wherein said aryl radical is chosen from phenyl and tolyl, and wherein said unsaturated alkyl group radical is chosen from vinyl.
31. A method according to
claim 25
, wherein the organopolysiloxane is chosen from:
i) organopolysiloxanes comprising R2SiO and RSiO1.5 units and optionally R3SiO0.5 and/or SiO2 units in which the R radicals, independently of one another, denote a hydrogen, an alkyl, an aryl, or an unsaturated aliphatic group, and where the ratio by weight of the R2SiO units to the RSiO1.5 units varies from 1/1 to 30/1;
ii) organopolysiloxanes which are insoluble and which can be swollen in a silicone oil, obtained by addition of an organohydropolysiloxane (1) and of an organopolysiloxane (2) having unsaturated aliphatic groups, so that the amount of hydrogen or of unsaturated aliphatic groups in (1) and (2) respectively ranges from 1 to 20 mol % when the organopolysiloxane is non-cyclic and from 1 to 50 mol % when the organopolysiloxane is cyclic.
32. A method according to
claim 31
, wherein said alkyl R radical is chosen from methyl, ethyl and propyl, wherein said aryl radical is chosen from phenyl and tolyl, and wherein said unsaturated alkyl group radical is chosen from vinyl.
33. A method according to
claim 23
, wherein the ratio by weight of the spherical organic particles to the elastomeric organopolysiloxane is chosen within the range from 0.25:1 to 1:1.
34. A method according to
claim 25
, wherein the ratio by weight of the spherical organic particles to the elastomeric organopolysiloxane is chosen within the range from 0.25:1 to 1:1.
35. A method according to
claim 23
, wherein the ratio by weight of the spherical organic particles to the elastomeric organopolysiloxane is chosen within the range from 0.4:1 to 0.7:1.
36. A method according to
claim 25
, wherein the ratio by weight of the spherical organic particles to the elastomeric organopolysiloxane is chosen within the range from 0.4:1 to 0.7:1.
37. A method according to
claim 23
, wherein the liquid fatty phase comprises at least one oil selected from silicone oils andhydrocarbon-comprising oils.
38. A method according to
claim 25
, wherein the liquid fatty phase comprises at least one oil selected from silicone oils andhydrocarbon-comprising oils.
39. A method according to
claim 23
, wherein the composition is a care or make-up base for the skin or lips.
40. A method according to
claim 25
, wherein the composition is a care or make-up base for the skin or lips.
41. A method according to
claim 20
, wherein the particles in the solid phase represent at least 20% of the total weight of the fatty phase.
42. A method according to
claim 21
, wherein the particles in the solid phase represent at least 20% of the total weight of the fatty phase.
43. A method according to
claim 23
, wherein the particles in the solid phase represent at least 20% of the total weight of the fatty phase.
44. A method according to
claim 25
, wherein the particles in the solid phase represent at least 20% of the total weight of the fatty phase.
US09/860,460 1997-10-01 2001-05-21 Stable topical composition comprising a solid elastomeric organopolysiloxane and spherical particles Abandoned US20010026811A1 (en)

Priority Applications (2)

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US09/860,460 US20010026811A1 (en) 1997-10-01 2001-05-21 Stable topical composition comprising a solid elastomeric organopolysiloxane and spherical particles
US10/051,040 US20020102284A1 (en) 1997-10-01 2002-01-22 Stable topical composition comprising a solid elastomeric organopolysiloxane and spherical particles

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FR9712223A FR2768926B1 (en) 1997-10-01 1997-10-01 STABLE TOPICAL COMPOSITION CONTAINING A SOLID ORGANOPOLYSILOXANE ELASTOMERIC AND SPHERICAL PARTICLES
FR9712223 1997-10-01
US09/163,407 US6258345B1 (en) 1997-10-01 1998-09-30 Stable topical composition comprising a solid elastomeric organopolysiloxane and spherical particles
US09/860,460 US20010026811A1 (en) 1997-10-01 2001-05-21 Stable topical composition comprising a solid elastomeric organopolysiloxane and spherical particles

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US09/163,407 Continuation US6258345B1 (en) 1997-10-01 1998-09-30 Stable topical composition comprising a solid elastomeric organopolysiloxane and spherical particles

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US10/051,040 Continuation US20020102284A1 (en) 1997-10-01 2002-01-22 Stable topical composition comprising a solid elastomeric organopolysiloxane and spherical particles

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US20010026811A1 true US20010026811A1 (en) 2001-10-04

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US09/163,407 Expired - Fee Related US6258345B1 (en) 1997-10-01 1998-09-30 Stable topical composition comprising a solid elastomeric organopolysiloxane and spherical particles
US09/860,460 Abandoned US20010026811A1 (en) 1997-10-01 2001-05-21 Stable topical composition comprising a solid elastomeric organopolysiloxane and spherical particles
US10/051,040 Abandoned US20020102284A1 (en) 1997-10-01 2002-01-22 Stable topical composition comprising a solid elastomeric organopolysiloxane and spherical particles

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KR100294784B1 (en) 2001-10-26
FR2768926A1 (en) 1999-04-02
DE69821180T2 (en) 2004-11-25
KR19990036776A (en) 1999-05-25
US20020102284A1 (en) 2002-08-01
EP0908175A1 (en) 1999-04-14
FR2768926B1 (en) 2000-01-28
EP0908175B1 (en) 2004-01-21
US6258345B1 (en) 2001-07-10
DE69821180D1 (en) 2004-02-26
JPH11158030A (en) 1999-06-15
BR9804138A (en) 1999-12-14
ES2215282T3 (en) 2004-10-01
CA2245989A1 (en) 1999-04-01
PL328909A1 (en) 1999-04-12

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