US20180369095A1 - Cosmetic composition comprising a specific filler combination and a film-forming polymer to increase long-lasting effects - Google Patents

Cosmetic composition comprising a specific filler combination and a film-forming polymer to increase long-lasting effects Download PDF

Info

Publication number
US20180369095A1
US20180369095A1 US16/061,158 US201416061158A US2018369095A1 US 20180369095 A1 US20180369095 A1 US 20180369095A1 US 201416061158 A US201416061158 A US 201416061158A US 2018369095 A1 US2018369095 A1 US 2018369095A1
Authority
US
United States
Prior art keywords
composition
composition according
film
weight
moisturizer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US16/061,158
Other languages
English (en)
Inventor
Mariko Okamoto
Tomofumi Yoshida
Yuka KAMIDOI
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
LOreal SA
Original Assignee
LOreal SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by LOreal SA filed Critical LOreal SA
Assigned to L'OREAL reassignment L'OREAL ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KAMIDOI, Yuka, OKAMOTO, MARIKO, YOSHIDA, TOMOFUMI
Publication of US20180369095A1 publication Critical patent/US20180369095A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/25Silicon; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/26Aluminium; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8152Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/87Polyurethanes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin

Definitions

  • the present invention relates to a cosmetic composition for a keratin substance, preferably in liquid emulsion form, in particular a makeup base or a liquid foundation, which provides long-lasting effects without inducing any dry feeling.
  • WO 2013/190112 discloses a fluid cosmetic skin makeup composition with improved color retention, which comprises at least one continuous oil phase, at least one sebum-pump filler, at least one hydrophobic film-forming polymer, and at least one lipophilic gelling agent.
  • An objective of the present invention is to provide a cosmetic composition for the skin, preferably in liquid emulsion form, in particular a makeup base or a liquid foundation, which can achieve “long-lasting” effects without creating any dry feeling.
  • a cosmetic composition for a keratin substance for example the skin such as that of the face, comprising:
  • the (i) moisturizer may be selected from emollients, humectants and their mixtures.
  • the (i) moisturizer may be selected from emollients and in particular may be selected from non-volatile oils.
  • the (i) moisturizer may be selected from ester oils and lipophilic amino acid derivatives.
  • the amount of the (i) moisturizer in the composition may be from 0.001 to less than 20.0% by weight, preferably from 0.01 to less than 15.0% by weight, and more preferably from 0.05% by weight to 10.0% by weight, relative to the total weight of the composition.
  • the (ii) film-forming polymer may be silicone resins, preferably selected from MQ resins.
  • the amount of the (ii) film-forming polymer in the composition may be from 0.01 to less than 20.0% by weight, preferably from 0.1 to less than 15.0% by weight, and more preferably from 1.0% by weight to 10.0% by weight, relative to the total weight of the composition.
  • hydrophobic silica may be silica particles modified at the surface by silylation.
  • urethane polymer powder may be a cross-linked polyurethane powder, preferably hexamethylene diisocyanate(HDI)/trimethylol hexyllactone crosspolymer.
  • acrylic polymer powder may be a crosspolymer or copolymer powder, preferably lauryl methacrylate/glycol dimethacrylate crosspolymer or acrylonitrile/methacrylate/vinylidene chloride copolymer.
  • the amount of each of the (iii) fillers in the composition may be from 0.001 to less than 10.0% by weight, preferably from 0.01 to less than 8% by weight, and more preferably from 0.05% by weight to 5.0% by weight, relative to the total weight of the composition.
  • composition according to the present invention may further comprise at least one UV filter, preferably at least one organic UV filter.
  • composition according to the present invention may be a makeup base or a liquid foundation.
  • composition according to the present invention may be in the form of an emulsion, in particular of liquid or semi-liquid consistency, of the O/W, W/O or multiple type.
  • the present invention also relates to a cosmetic process for a keratin substance, for example the skin such as that of the face, comprising the step of: applying the composition according to the present invention onto the keratin substance.
  • one aspect of the present invention is a cosmetic composition for a keratin substance, for example the skin such as that of the face, comprising:
  • Another aspect of the present invention is a cosmetic process for a keratin substance, for example the skin such as that of the face, comprising the step of: applying the composition according to the present invention onto the keratin substance.
  • composition according to the present invention comprises at least one moisturizer.
  • Two or more moisturizers may be used in combination.
  • a single type of moisturizer or a combination of different types of moisturizers may be used.
  • Moisturizers are substances which impart external lubricant behavior, such as to soften and soothe the skin because they promote skin water retention. They may be selected from emollients which are able to remain on the skin surface or in the stratum corneum to act as lubricants, to reduce flaking, and to improve the skin's appearance.
  • Moisturizers may be also selected from humectants intended to increase the water content of the top layers of skin. This group of ingredients includes primarily hygroscopic agents employed for this specific purpose.
  • the moisturizer is selected from emollients, humectants and their mixtures.
  • the moisturizer is selected from emollients and more particularly from non-volatile oils.
  • oil is understood to mean any fatty substance which is in liquid form at ambient temperature (25° C.) and at atmospheric pressure.
  • non-volatile oil is understood to mean an oil having a vapor pressure of less than 0.13 Pa (0.01 mmHg).
  • non-volatile oils can be chosen in particular from non-volatile hydrocarbon oils, if appropriate fluorinated, and/or non-volatile silicone oils.
  • non-volatile oil suitable for use in the invention, mention may be made of:
  • ester oils mention may be made of fatty acid esters, such as, for example:
  • ester oils mention may also be made of esters formed between aliphatic or aromatic polycarboxylic acid and C 1 -C 10 aliphatic or aromatic alcohol.
  • the aliphatic and aromatic alcohol may comprise from 1 to 10 carbon atoms, for example, 1 to 8, preferably 1 to 6 carbon atoms, and may be selected from alcohol, ROH, in which R is selected from optionally-substituted methyl, ethyl, propyl, isopropyl, butyl, hexyl, ethylhexyl, decyl, isodecyl, and benzyl.
  • the aliphatic and aromatic polycarboxylic acid may comprise, for example, 3 to 12 carbon atoms, preferably 3 to 10 carbon atoms, more preferably, 3 to 8 carbon atoms, even more preferably 6 or 8 carbon atoms.
  • the aliphatic and aromatic polycarboxylic acid may be a dicarboxylic acid or tricarboxylic acid.
  • n ranges from 1 to 10, preferably from 2 to 8, more preferably, 2, 4, 6 or 8.
  • the dicarboxylic acid may be selected from succinic, adipic and sebacic acids.
  • the dicarboxylic acid may also be chosen from phthalic acid and its derivatives, for example, butyl benzyl phthalate, dibutyl phthalate, diethylhexyl phthalate, diethyl phthalate and dimethyl phthalate.
  • R is a hydrocarbon radical, for example H, —OH or —OCOR′ wherein R′ is alkyl such as alkyl comprising from 1 to 6 carbon atoms.
  • the tricarboxylic acid may be selected from acetylcitric acid and its derivatives.
  • citrates mention may be made of tributyl acetylcitrate, triethyl acetylcitrate, triethylhexyl acetylcitrate, trihexyl acetylcitrate, trihexyl butyryl citrate, isodecyl citrate, isopropyl citrate, tributyl citrate and triethylhexyl citrate.
  • adipates mention may be made of dibutyl adipate and di-2-ethylhexyl adipate.
  • sebacates mention may be made of dibutyl sebacate, diethylhexyl sebacate, diethyl sebacate and diisopropyl sebacate.
  • succinates mention may be made of diethylhexyl succinate and diethyl succinate.
  • the ester is formed between a dicarboxylic acid selected from succinic acid, adipic acid and sebacic acid, and an alcohol selected from methanol, ethanol, propanol, isopropanol, butanol, hexanol and ethylhexanol.
  • the ester may be diisopropyl sebacate, for example, sold by the company Stearinerie Dubois under the name Dub Dis.
  • non-volatile oil mention may also be made of:
  • the moisturizer mention may also be made of lipophilic amino acid derivatives.
  • the lipophilic amino acid derivatives are especially C 6 -C 22 N-acylamino acid esters, which can also be defined as the non-volatile oil, in particular the ester oils.
  • N-acylamino acid ester(s) are generally of the following formula:
  • the group R′ 1 (CO)— is an acyl group of an acid chosen from the group formed by capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, linoleic acid, linolenic acid, oleic acid, isostearic acid, 2-ethylhexanoic acid, coconut oil fatty acids and palm kernel oil fatty acids. These fatty acids may also contain a hydroxyl group. Even more preferably, it will be lauric acid.
  • the —N(R′ 2 )CH(R′ 3 )(CH 2 )—(CO)— part of the amino acid ester is preferably chosen from the following amino acids: glycine, alanine, valine, leucine, isoleucine, serine, threonine, proline, hydroxyproline, ⁇ -alanine, aminobutyric acid, aminocaproic acid, sarcosine, N-methyl- ⁇ -alanine.
  • the part of the amino acid esters corresponding to the group OR′ 4 may be obtained from alcohols chosen from the group formed by methanol, ethanol, propanol, isopropanol, butanol, tert-butanol, isobutanol, 3-methyl-1-butanol, 2-methyl-1-butanol, fusel oil, pentanol, hexanol, cyclohexanol, octanol, 2-ethylhexanol, decanol, lauryl alcohol, myristyl alcohol, cetyl alcohol, cetostearyl alcohol, stearyl alcohol, oleyl alcohol, behenyl alcohol, jojoba alcohol, 2-hexadecyl alcohol, 2-octyldodecanol and isostearyl alcohol.
  • amino acid esters may be obtained in particular from natural sources of amino acids.
  • the amino acids originate from the hydrolysis of natural plant proteins (oat, wheat, soybean, palm or coconut) and then necessarily lead to mixtures of amino acids that subsequently need to be esterified and then N-acylated.
  • the preparation of such amino acids is more particularly described in patent application FR 2 796 550.
  • amino acid ester more particularly preferred for its use in the present invention is isopropyl N-lauroylsarcosinate of formula:
  • amino acid esters preferably used for the purposes of the present invention, and the synthesis thereof, are described in patent applications EP 1 044 676 and EP 0 928 608 from the company Ajinomoto Co.
  • humectants examples include sorbitol, polyhydric alcohols, preferably of C 2 -C 8 and more preferably C 3 -C 6 , preferably such as glycerol, propylene glycol, 1,3-butylene glycol, pentylene glycol, hexylene glycol, dipropylene glycol, diethylene glycol and diglycerol, and derivatives and mixtures thereof, glycol ethers (especially containing from 3 to 16 carbon atoms) such as mono-, di- or tripropylene glycol (C 1 -C 4 )alkyl ethers, mono-, di- or triethylene glycol (C 1 -C 4 )alkyl ethers, urea and derivatives thereof, especially Hydrovance (2-hydroxyethylurea) sold by the company National Starch, lactic acids, hyaluronic acid, AHAs, BHAs, sodium pidolate, xylitol, serine, sodium lactitol, poly
  • the amount of the moisturizer in the composition may be from 0.001 to less than 20.0% by weight, preferably from 0.01 to less than 15.0% by weight, and more preferably from 0.05% by weight to 10.0% by weight, relative to the total weight of the composition.
  • composition according to the present invention comprises at least one film-forming polymer.
  • Two or more film-forming polymers may be used in combination.
  • a single type of film-forming polymer or a combination of different types of film-forming polymers may be used.
  • polymer means a compound corresponding to the repetition of one or more units (these units being derived from compounds known as monomers). This or these units(s) are repeated at least twice and preferably at least three times.
  • film-forming polymer means a polymer that is capable of forming, by itself or in the presence of an auxiliary film-forming agent, a macroscopically continuous film that adheres to a support, especially to keratin materials, preferably a cohesive film, and better still a film whose cohesion and mechanical properties are such that the said film may be isolable and manipulable in isolation, for example, when the said film is prepared by pouring onto a non-stick surface, for instance, a Teflon-coated or silicone-coated surface.
  • the film-forming polymer may be selected from the group comprising:
  • the amount of the film-forming polymer in the composition may be from 0.01 to less than 20.0% by weight, preferably from 0.1 to less than 15.0% by weight, and more preferably from 1.0% by weight to 10.0% by weight, relative to the total weight of the composition.
  • the film-forming polymer is selected from the group consisting of polyamide-silicone block polymers, block ethylenic polymers, vinyl polymers comprising at least one carboxiloxane dendrimer derivative, copolymers comprising carboxylate groups and polydimethylsilixane groups, silicone resins, lipodispersible polymers in the form of a non-aqueous dispersion of polymer particles, olefin copolymers selected from amorphous olefin copolymers and olefin copolymers with controlled and moderate crystallization, hydrocarbon-based resins having a number-average molecular weight of less than or equal to 10,000 g/ml, and a mixture thereof, more preferably from silicone resins.
  • the film-forming silicone resin may be any silicone resin which has film-forming properties.
  • the film-forming silicone resin may be selected from silsesquioxane, siloxysilicate and a resin obtained by hydroxysilylation.
  • silicone resin is known in the art under the name of “MDTQ” nomenclature, by which a silicone resin is described according to the various repeating siloxane monomer moieties which constitute the polymer. Each letter of “MDTQ” corresponds to a different type of moiety.
  • M corresponds to the monofunctional moiety (CH 3 ) 3 SiO 1/2 . This moiety is regarded as monofunctional because the silicon atom shares only one oxygen for the formation of the chain.
  • the “M” moiety can be represented by the following structure:
  • At least one of the methyl groups can be replaced so as, for example, to produce a moiety with the following formula: [R(CH 3 ) 2 ] SiO 1/2 , such as represented by the following structure:
  • R is other than a methyl group.
  • the symbol “D” corresponds to the difunctional moiety (CH 3 )SiO 2/2 in which two of the available bonds on the silicon atom are used to bond with oxygen for the formation of the polymer chain.
  • the “D” moiety which is the essential component element of the dimethicone oils, can be represented by the following formula:
  • T corresponds to the trifunctional moiety (CH 3 )SiO 3/2 , in which three of the available bonds on the silicon atom are used to bond with oxygen for the formation of the polymer chain.
  • the “T” moiety can be represented by the following structure:
  • any one of the methyl groups can be replaced in “D” or “T” by an R group which is other than methyl.
  • Q corresponds to a quadrifunctional moiety SiO 4/2 , in which all four available bonds on the silicon atom are used to bond with oxygen for the formation of the polymer chain.
  • the “Q” moiety can be represented by the following structure:
  • the film-forming silicone resin may be selected from the siloxysilicate, silsesquioxane and a resin obtained by hydroxysililation. Any siloxysilicate, silsesquioxane or resin obtained by hydroxysilylation, which acts as a film-forming agent, can be used in the composition of the present invention.
  • the film-forming silicone resin preferably is crosslinked.
  • the film-forming silicone resin may be selected from substituted siloxysilicate, silsesquioxane and resin obtained by hydroxysilylation.
  • a substituted siloxysilicate or a substituted silsesquioxane may be, for example, a siloxysilicate or a silsesquioxane in which a methyl group has been replaced by a longer carbon chain, such as an ethane, propane or butane chain.
  • the carbon chain may be saturated or nonsaturated.
  • the film-forming silicone resin may be selected from siloxysilicate, such as MQ resins represented by the following formula:
  • x and y may have values ranging from 20 to 100, preferably 50 to 80.
  • siloxysilicate may be selected from all the combinations of M and of Q moieties such as, for example, [(R) 3 Si] x (SiO 4/2 ) y , in which R is selected from a methyl group and a longer carbon chain
  • the film-forming silicone resin may be selected from silsesquioxane represented by the following formula:
  • x has a value which can range up to several thousands and the CH 3 can be replaced by an R, such as described hereinabove for the T moieties.
  • the film-forming silicone resin is trimethylsiloxysilicate, for example, sold by the company Momentive Performance Materials under the name SR 1000 MQ Resin.
  • composition according to the present invention comprises a filler combination of (a) hydrophobic silica, (b) perlite, (c) urethane polymer powder, and (d) acrylic polymer powder.
  • fillers mean colorless or white, mineral or synthetic particles of any shape, which are insoluble in the medium of the composition, irrespective of the temperature at which the composition is manufactured.
  • the amount of each of the (a) to (d) fillers in the composition may be from 0.001 to less than 10.0% by weight, preferably from 0.01 to less than 8% by weight, and more preferably from 0.05% by weight to 5.0% by weight, relative to the total weight of the composition.
  • hydrophobic silica means any silica whose surface is treated with silylating agents, for example halogenated silanes such as alkylchlorosilanes, siloxanes, in particular dimethylsiloxanes such as hexamethyldisiloxane, or silazanes, so as to functionalize the OH groups with silyl groups, for example trimethylsilyl groups.
  • silylating agents for example halogenated silanes such as alkylchlorosilanes, siloxanes, in particular dimethylsiloxanes such as hexamethyldisiloxane, or silazanes, so as to functionalize the OH groups with silyl groups, for example trimethylsilyl groups.
  • the silica may also be treated with dimethyldichlorosilane or alternatively with a polydimethylsiloxane.
  • silica suitable for the present invention mention may be made of the silicas sold under the references Silica Beads SB 150 and SB 700 from Miyoshi, having a mean size of 5 microns, and the Sunspheres H33, H51 and H53 from Asahi Glass, having respective sizes of about 3, 5 and 5 microns.
  • hydrophobic fumed silica As the hydrophobic silica, mention may also be made of hudrophobic fumed silica.
  • the hydrophobic fumed silicas can be obtained by modification of the surface of the silica by means of a chemical reaction that creates a decrease in the number of silanol groups, it being possible for these groups to be in particular substituted with hydrophobic groups.
  • the hydrophobic groups may be:
  • hydrophobic silica As preferred examples of the hydrophobic silica, mention may be made of
  • the hydrophobic silica is silica silylate, for example, sold by the company Dow Corning under the name Dow Corning VM-2270 Aerogel Fine Particles.
  • Perlite is generally obtained from natural glass of volcanic origin, of light-grey or glossy black color, resulting from the rapid cooling of lava, and which is in the form of small particles resembling pearls. When heated above 800° C., perlite has the particular feature of losing the water it contains and of adopting a porous expanded form (representing from four to twenty times its initial volume), enabling it to absorb large amounts of liquid, in particular oil and water. It then has a white color.
  • Perlite which is of mineral origin, is directly extracted from the ground and then finely ground to obtain a very fine white powder: perlite powder or perlite particles.
  • Perlite particles are thus particles of amorphous mineral materials, which are advantageously expanded, derived from at least one volcanic rock.
  • These particles may comprise at least two elements chosen from silicon, aluminum and magnesium.
  • these mineral materials may be obtained by thermal expansion of a volcanic or “effusive” rock comprising from 1% to 10% by weight of water and preferably 1% to 5% by weight of water and less than 10% by weight of crystalline rock relative to the total weight of the rock composition and preferably followed by grinding.
  • the temperature of the expansion process may range from 700 to 1500° C. and preferably from 800 to 1100° C.
  • Volcanic or “effusive” rocks are generally produced by the rapid cooling of liquid magma in contact with air or water (quenching phenomenon giving a hyaline rock).
  • the volcanic rocks that may be used according to the present invention may be selected from those defined according to the Streckeisen classification (1974). Among these volcanic rocks, mention may especially be made of trachytes, latites, andesites, basalts, rhyolites and dacites.
  • the perlite particles are aluminosilicates of volcanic origin. They advantageously have the following composition:
  • silica SiO 2
  • Al 2 O 3 aluminum oxide
  • Na 2 O sodium oxide
  • K 2 O potassium oxide
  • Fe 2 O 3 iron oxide
  • MgO magnesium oxide
  • CaO calcium oxide
  • TiO 2 titanium oxide
  • composition according to the present invention comprises perlite sold by the company Miyoshi Kasei under the name Perlite-M SZ12.
  • urethane polymer powder means fillers consisting of a material at least partly of polyurethane type.
  • the polyurethane material may advantageously be in crosslinked form.
  • the urethane polymer powder may generally be substantially spherical.
  • spherical means an essentially spherical shape, especially in the form of beads, preferably of a number-average size ranging from 1 to 15 ⁇ m, including 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, and 19 ⁇ m, and all subranges and values between stated values.
  • number-average size denotes the dimension given by the random particle size distribution to half the population, known as D50.
  • the urethane polymer powder may comprise a copolymer.
  • Said copolymer may comprise trimethylol hexyllactone, in particular a hexamethylene diisocyanate (HDI)/trimethylol hexyllactone crosspolymer.
  • HDI hexamethylene diisocyanate
  • the copolymer mention may be made of urethane polymer powder sold by the company Toshiki under the name Plastic Powder D-400® or Plastic Powder D-800® or sold by the company Shiki under the name Plastic Powder CS-400®.
  • the composition according to the present invention comprises hexamethylene diisocyanate (HDI)/trimethylol hexyllactone crosspolymer, for example, sold by the company Toshiki Pigment under the name Plastic Powder D 400.
  • HDI hexamethylene diisocyanate
  • acrylic polymer powder means fillers obtained by polymerization of an acrylate and/or methacrylate monomer(s) optionally-substituted with C 1 -C 20 alkyl, in the form of a homopolymer or of a copolymer.
  • acrylic polymer powder mention may be made of powder of polymethyl methacrylate, of polymethyl methacrylate/ethylene glycol dimethacrylate, of polyallyl methacrylate/ethylene glycol dimethacrylate, of lauryl methacrylate/ethylene glycol dimethacrylate, and of acrylonitrile/methacrylate/vinylidene chloride copolymer.
  • the acrylic polymer powder is generally preferably in the form of white-colored, hollow or solid, spherical particles of which the number-average size is generally preferably on the micrometer scale, and in particular ranges from 3 to 20 ⁇ m, and generally ranges from 7 to 15 ⁇ m, including 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, and 19 ⁇ m, and all subranges and values between stated values.
  • acrylic polymer powder mention may be made of:
  • the acrylic polymer powder is lauryl methacrylate/ethylene glycol dimethacrylate crosspolymer, for example, sold by the company Amcol Health & Beauty Solutions under the name Polytrap 6603 Adsorber, and/or acrylonitrile/methacrylate/vinylidine chloride copolymer, for example, sold by the company Akzo Nobel under the name Expancel 551 DE 40 D42.
  • composition according to the present invention may comprise at least one additional filler other than (a) hydrophobic silica, (b) perlite, (c) urethane polymer powder, and (d) acrylic polymer powder.
  • the additional filler may be selected from fillers such as:
  • the composition according to the present invention may comprise polyamide powder, for example that listed under the CTFA name of “Nylon 12” or “Nylon 6”.
  • a mixture of polyamide powder and, for example, a mixture of Nylon-6 and Nylon-12 may be used.
  • the polyamide powder includes that sold by the company Toray Industries under the name SP-500.
  • the amount of the additional filler in the composition may be from 0.01 to less than 10.0% by weight, and preferably from 0.1 to less than 5.0% by weight, relative to the total weight of the composition.
  • composition according to the present invention may include at least one UV filter. If two or more UV filters are used, they may be the same or different.
  • the UV filter may be solid or liquid, preferably liquid.
  • the terms “solid” and “liquid” mean solid and liquid, respectively, at 25° C. under 1 atm.
  • the UV filter may be made from at least one organic or inorganic material, preferably at least one organic material.
  • the UV filter is preferably an organic UV filter.
  • the organic UV filter may be selected from the group consisting of anthranilic derivatives; dibenzoylmethane derivatives; cinnamic derivatives; salicylic derivatives; camphor derivatives; benzophenone derivatives; ⁇ , ⁇ -diphenylacrylate derivatives; triazine derivatives; benzotriazole derivatives; benzalmalonate derivatives; benzimidazole derivatives; imidazoline derivatives; bis-benzoazolyl derivatives; p-aminobenzoic acid (PABA) and derivatives thereof benzoxazole derivatives; screening polymers and screening silicones; dimers derived from ⁇ -alkylstyrene; 4,4-diarylbutadienes; octocrylene and derivatives thereof, guaiazulene and derivatives thereof, rutin and derivatives thereof, flavonoids, biflavonoids, oryzanol and derivatives thereof, quinic acid and derivatives thereof, phenols, retin
  • Rutin and derivatives thereof Rutin and glucosylrutin.
  • Flavonoids Robustin (isoflavonoid), genistein (flavonoid), tectochrysin (flavonoid), and hispidone (flavonoid).
  • the preferred organic UV filter may be selected from:
  • the UV filter is an organic liquid UV filter.
  • the material of the organic liquid UV filter is not limited as long as it is organic. If two or more organic liquid UV filters are used, the material(s) of the organic liquid UV filters may be the same as or different from each other.
  • the preferred organic liquid UV filter(s) may be selected from methoxycinnamate, homosalate, ethylhexyl salicylate, ethylhexyl triazone, octocrylene, drometrizole trisiloxane, n-hexyl 2-(4-diethylamino-2-hydroxybenzoyl)benzoate, terephthalylidene dicamphor sulfonic acid, and bis-ethylhexyloxyphenol methoxyphenyl triazine.
  • the UV filter(s) may be present in the composition used for the present invention in a content ranging from 0.1 to 40% by weight, preferably ranging from 1 to 20% by weight, and more preferably from 3 to 10% by weight, relative to the total weight of the composition.
  • the composition according to the present invention further comprises at least one compound selected from water, hydrophilic solvents, lipophilic solvents, volatile oils, and mixtures thereof.
  • hydrophilic solvents such as ethanol, propanol, butanol, isopropanol or isobutanol; polyethylene glycols; polyols, such as propylene glycol, isoprene glycol, butylene glycol, glycerol or sorbitol; mono- or dialkyl derivatives of isosorbide, such as dimethyl isosorbide; glycol ethers, such as diethylene glycol monomethyl or monoethyl ether, and propylene glycol ethers, such as dipropylene glycol methyl ether.
  • monoalcohol such as ethanol, propanol, butanol, isopropanol or isobutanol
  • polyethylene glycols such as propylene glycol, isoprene glycol, butylene glycol, glycerol or sorbitol
  • mono- or dialkyl derivatives of isosorbide such as dimethyl isosorbide
  • glycol ethers such as
  • composition according to the present invention may also comprise any additive usually used in the field under consideration, chosen, for example, from gums, anionic, cationic, amphoteric, or nonionic surfactants, silicone surfactants, resins, thickeners, structuring agents such as waxes, dispersants, antioxidants, essential oils, preserving agents, fragrances, neutralizers, antiseptics, cosmetic active agents, such as vitamins, emollients, or pigments, and mixtures thereof.
  • additive usually used in the field under consideration, chosen, for example, from gums, anionic, cationic, amphoteric, or nonionic surfactants, silicone surfactants, resins, thickeners, structuring agents such as waxes, dispersants, antioxidants, essential oils, preserving agents, fragrances, neutralizers, antiseptics, cosmetic active agents, such as vitamins, emollients, or pigments, and mixtures thereof.
  • thickeners preferably selected from hydrophilic thickeners, lipophilic thickeners, or a mixture thereof. More preferably the thickener is selected from polysaccharide biopolymers, lipophilic clays, hydrophobic silicas, or a mixture thereof, even more preferably the thickener is chosen from xanthan gum, disteardimonium hectorite, silica silylate, or a mixture thereof. Most preferably, the thickeners are disteardimonium hectorite.
  • pigments mention may be made of white or colored, mineral or organic particles that are insoluble in an aqueous solution, for example titanium oxide, zirconium oxide or cerium oxide, and also zinc oxide, iron oxide or chromium oxide, ferric blue, manganese violet, ultramarine blue, and chromium hydrate.
  • the cosmetic composition according to the present invention may be in the form of a skin makeup product, in particular a makeup base, a foundation, a hot-cast foundation product, a body makeup product, a concealer, an eyeshadow, a lipstick, or a body deodorant.
  • the cosmetic composition may be a makeup base or a liquid foundation.
  • composition according to the present invention may be in any of the formulation forms conventionally used, preferably in the form of an emulsion, in particular of liquid or semi-liquid consistency, of the O/W, W/O or multiple type.
  • the present invention also relates to a method for improving “long-lasting” effects without creating any dry feeling, characterized by adding at least one film-forming polymer and a combination of the following fillers: (a) hydrophobic silica, (b) perlite, (c) urethane polymer powder, and (d) acrylic polymer powder to a cosmetic composition for a keratin substance, for example the skin such as that of the face, in particular a makeup base or a liquid foundation, the cosmetic composition comprising at least one moisturizer.
  • the present invention relates to use of at least one film-forming polymer and a combination of the following fillers: (a) hydrophobic silica, (b) perlite, (c) urethane polymer powder, and (d) acrylic polymer powder for providing “long-lasting” effects with a cosmetic composition for a keratin substance comprising at least one moisturizer without creating any dry feeling.
  • the present invention also relates to cosmetic process for a keratin substance, for example the skin such as that of the face, comprising the step of: applying the composition according to the present invention onto the keratin substance.
  • Simultaneous use of a film-forming polymer and a combination of the following fillers: (a) hydrophobic silica, (b) perlite, (c) urethane polymer powder, and (d) acrylic polymer powder can improve “long-lasting” effects for a cosmetic composition for a keratin substance comprising a moisturizer without creating any dry feeling.
  • the makeup base compositions according to Example 1 and Comparative Examples 1-6 shown in Table 1 were prepared by mixing the ingredients shown in Table 1 as follows: (1) adding phases A1 and A2 to a main beaker; (2) adding phase A3 and dissolving it completely; (3) adding phase A4 and dispersing it homogenously; (4) adding phase B and dispersing it homogenously; (5) adding phase C and dispersing it homogenously; (6) adding phase D and emulsifying the resultant mixture; and (7) adding phase E and dispersing it homogenously.
  • the numerical values for the amounts of the ingredients shown in Table 1 are all based on “% by weight” as active raw materials.
  • liquid foundation compositions according to Examples 2 and 3 and Comparative Examples 7 and 8 shown in Table 2 were prepared by mixing the ingredients shown in Table 2 in the same manner as described in the “Makeup Base Example” above.
  • the numerical values for the amounts of the ingredients shown in Table 2 are all based on “% by weight” as active raw materials.
  • compositions according to Examples 1 to 3 were applied onto half of the face of a user in the appropriate amount, while those according to Comparative Examples 1 to 8 were applied onto the other half of the face of the user in the same amount. After that, the compositions were spread with the fingers to form a cosmetic film. Five users participated in the evaluation test.
  • the composition according to Example 1 which comprised at least one moisturizer (dipentaerythrityl tetrahydroxystearate/tetraisostearate), a film-forming polymer (trimethylsiloxysilicate) and a filler combination of the present invention (silica silylate, perlite, HDI/trimethylol hexyllactone crosspolymer, and lauryl methcrylate/glycol dimethacrylate crosspolymer), was able to provide a moisturizing feeling and had “long-lasting” effects.
  • moisturizer dipentaerythrityl tetrahydroxystearate/tetraisostearate
  • a film-forming polymer trimethylsiloxysilicate
  • a filler combination of the present invention sica silylate, perlite, HDI/trimethylol hexyllactone crosspolymer, and lauryl methcrylate/glycol dimethacrylate crosspolymer
  • composition according to Comparative Example 1 which comprised the film-forming polymer and the filler combination of the present invention but did not comprise moisturizers, was not able to provide a moisturizing feeling.
  • composition according to Comparative Example 2 which comprised the moisturizer and the filler combination of the present invention but did not comprise the film-forming polymer, did not have “long-lasting” effects.
  • compositions according to Comparative Examples 3 to 6 comprised the moisturizer and the film-forming polymer but did not comprise one of the essential fillers of the present invention. These compositions did not have “long-lasting” effects.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Birds (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Emergency Medicine (AREA)
  • Dispersion Chemistry (AREA)
  • Dermatology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Cosmetics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
US16/061,158 2015-12-21 2014-12-14 Cosmetic composition comprising a specific filler combination and a film-forming polymer to increase long-lasting effects Abandoned US20180369095A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2015248359A JP6732444B2 (ja) 2015-12-21 2015-12-21 特定のフィラーの組合せ及び皮膜形成性ポリマーを含む、持続効果を向上させるための化粧用組成物
JP2015-248359 2015-12-21
PCT/JP2016/088599 WO2017111149A1 (en) 2015-12-21 2016-12-14 Cosmetic composition comprising a specific filler combination and a film-forming polymer to increase long-lasting effects

Publications (1)

Publication Number Publication Date
US20180369095A1 true US20180369095A1 (en) 2018-12-27

Family

ID=57882116

Family Applications (2)

Application Number Title Priority Date Filing Date
US16/061,158 Abandoned US20180369095A1 (en) 2015-12-21 2014-12-14 Cosmetic composition comprising a specific filler combination and a film-forming polymer to increase long-lasting effects
US16/930,666 Active 2037-01-24 US11771631B2 (en) 2015-12-21 2020-07-16 Cosmetic composition comprising a specific filler combination and a film-forming polymer to increase long-lasting effects

Family Applications After (1)

Application Number Title Priority Date Filing Date
US16/930,666 Active 2037-01-24 US11771631B2 (en) 2015-12-21 2020-07-16 Cosmetic composition comprising a specific filler combination and a film-forming polymer to increase long-lasting effects

Country Status (8)

Country Link
US (2) US20180369095A1 (zh)
EP (1) EP3393428B1 (zh)
JP (1) JP6732444B2 (zh)
KR (1) KR102230447B1 (zh)
CN (1) CN108366924B (zh)
BR (1) BR112018010984B1 (zh)
ES (1) ES2764730T3 (zh)
WO (1) WO2017111149A1 (zh)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108888524B (zh) * 2018-08-10 2021-06-18 广州市科能化妆品科研有限公司 遮瑕组合物及其制备方法
KR20210009125A (ko) 2019-07-16 2021-01-26 코스맥스 주식회사 유분산 아이 메이크업 화장료 조성물
FR3121044B1 (fr) * 2021-03-26 2024-04-19 Oreal Emulsion avec filtre hydrosoluble neutralisé, huile siliconée non volatile non phénylée, polymère filmogène et émulsionnant polydiméthylméthylsiloxane polyoxyalkyléné linéaire
CN113520916A (zh) * 2021-07-02 2021-10-22 上海永熙信息科技有限公司 一种高成膜性的化妆品定妆组合物
WO2023189392A1 (en) * 2022-03-29 2023-10-05 L'oreal Composition suitable for eyebrows
FR3134991B1 (fr) * 2022-04-29 2024-05-03 Oreal composition convenable pour les sourcils

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120014888A1 (en) * 2009-01-29 2012-01-19 Amcol International Corporation Matte Skin Finish Compositions
US20120035512A1 (en) * 2010-08-04 2012-02-09 Fong-Chin Su Upper limbs rehabilitation device
WO2013190102A2 (en) * 2012-06-21 2013-12-27 L'oreal Matt-effect composition comprising hydrophobic aerogel particles and perlite particles

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2463264A (en) 1942-12-23 1949-03-01 Ciba Ltd Derivatives of cyclic amidines and process of making same
JPS61277611A (ja) * 1985-06-03 1986-12-08 Kao Corp 弱酸性入浴剤
DE3760959D1 (en) 1986-01-10 1989-12-14 Ciba Geigy Ag Lubricant additives containing sulphur and nitrogen
US5240975A (en) 1988-04-11 1993-08-31 Ciba-Geigy Corporation Liquid substituted 2H-benzotriazole mixtures, stabilized compositions
JPH0753646B2 (ja) 1989-01-31 1995-06-07 東レ・ダウコーニング・シリコーン株式会社 化粧料
US5237071A (en) 1991-01-22 1993-08-17 Fairmount Chemical Company, Inc. Process for preparing 2,2'-methylene-bis(6-(2H-benzotriazol-2-yl)-4-hydrocarbyl phenols)
US5166355A (en) 1991-02-04 1992-11-24 Fairmount Chemical Co., Inc. Process for preparing substituted 2,2'-methylene-bis-[6-(2H-benzotriazol-2-yl)-4-hydrocarbyl-phenols]
FR2680683B1 (fr) 1991-08-29 1993-11-12 Oreal Composition cosmetique filtrante contenant un polymere filtre a structure hydrocarbonee et une silicone filtre.
JP3552741B2 (ja) * 1993-12-28 2004-08-11 株式会社コーセー アイメークアップ化粧料
JPH07196473A (ja) * 1994-01-07 1995-08-01 Earth Chem Corp Ltd 入浴剤
DE59509233D1 (de) 1994-02-24 2001-06-13 Haarmann & Reimer Gmbh Kosmetische und dermatologische zubereitungen, enthaltend phenylen-1,4-bisbenzimidiazolesulfonsäuren
GB9515048D0 (en) 1995-07-22 1995-09-20 Ciba Geigy Ag Sunscreen compositions
DE19648798C2 (de) 1996-11-26 1998-11-19 Hoechst Ag Verfahren zur Herstellung von organisch modifizierten Aerogelen durch Oberflächenmodifikation des wäßrigen Gels (ohne vorherigen Lösungsmitteltausch) und anschließender Trocknung
DE19726184A1 (de) 1997-06-20 1998-12-24 Beiersdorf Ag Kosmetische und dermatologische Lichtschutzformulierungen in Form von Emulsionen, insbesondere O/W-Makroemulsionen, O/W-Mikroemulsionen oder O/W/O-Emulsionen, mit einem Gehalt an lichtschutzwirksamen Benzotriazolderivaten
GB9715751D0 (en) 1997-07-26 1997-10-01 Ciba Geigy Ag Formulations
TWI225793B (en) 1997-12-25 2005-01-01 Ajinomoto Kk Cosmetic composition
DE19855649A1 (de) 1998-12-03 2000-06-08 Basf Ag Dimere alpha-Alkyl-Styrolderivate als photostabile UV-Filter in kosmetischen und pharmazeutischen Zubereitungen
JP3802288B2 (ja) 1999-04-16 2006-07-26 味の素株式会社 油性原料組成物
FR2796550B1 (fr) 1999-07-21 2003-05-09 Asepta Lab Preparations et applications d'esters de n-acylaminoacides
FR2818547B1 (fr) 2000-12-22 2006-11-17 Oreal Nouveaux derives c-glycosides et utilisation
JP2002226328A (ja) * 2001-01-31 2002-08-14 Sanyo Chem Ind Ltd 毛髪処理剤および毛髪処理方法
ES2320103T3 (es) 2001-06-26 2009-05-19 L'oreal Composiciones que comprenden un compuesto de baja solubilidad y un derivado lipofilo de acido aminado, utilizaciones y procedimientos correspondientes.
JP3756484B2 (ja) * 2002-12-27 2006-03-15 花王株式会社 凹凸部隠し用化粧料
US20050191328A1 (en) * 2004-02-26 2005-09-01 Toshiya Taniguchi Make-up composition
FR2870116B1 (fr) * 2004-05-13 2006-07-28 Oreal Poudre cosmetique comprenant du sulfate de baryum
FR2870114B1 (fr) * 2004-05-13 2008-10-31 Oreal Poudre cosmetique comprenant un organopolysiloxane elastomere
FR2870115B1 (fr) * 2004-05-13 2006-11-24 Oreal Poudre cosmetique comprenant une poudre acrylique
JP5705449B2 (ja) * 2010-03-31 2015-04-22 株式会社コーセー オーバーコート化粧料
FR2964871B1 (fr) * 2010-09-17 2012-10-19 Oreal Composition cosmetique solide de maquillage
FR2967350B1 (fr) * 2010-11-15 2015-05-01 Oreal Composition cosmetique solide sous forme de poudre compacte
US9949475B2 (en) * 2011-08-16 2018-04-24 Vandana Kurkal-Siebert Composition comprising active ingredient, oil and ionic liquid
FR2982159B1 (fr) * 2011-11-03 2013-11-29 Oreal Composition cosmetique solide sous forme de poudre compacte
FR2982148B1 (fr) * 2011-11-07 2014-08-01 Oreal Composition solide solaire a base de filtre uv organique lipophile et de particules d'aerogel de silice hydrophobes
JP5893896B2 (ja) * 2011-11-10 2016-03-23 株式会社コーセー 凹凸補正化粧料
FR2992203B1 (fr) 2012-06-21 2014-10-24 Oreal Composition cosmetique de maquillage de la peau
JP6543575B2 (ja) * 2013-05-14 2019-07-10 ロレアル 化粧用組成物
FR3015251B1 (fr) * 2013-12-20 2016-01-22 Oreal Composition cosmetique comprenant un polymere a motif dendrimere carbosiloxane et des particules de polymeres expanses
EP3139900B1 (fr) * 2014-05-07 2018-12-26 L'Oréal Préparation d'une composition pulvérulente / pâteuse comprenant un gel d'élastomère de silicone, des particules solides et une phase liante et procédé de traitement des lèvres

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120014888A1 (en) * 2009-01-29 2012-01-19 Amcol International Corporation Matte Skin Finish Compositions
US20120035512A1 (en) * 2010-08-04 2012-02-09 Fong-Chin Su Upper limbs rehabilitation device
WO2013190102A2 (en) * 2012-06-21 2013-12-27 L'oreal Matt-effect composition comprising hydrophobic aerogel particles and perlite particles

Also Published As

Publication number Publication date
EP3393428B1 (en) 2019-10-02
EP3393428A1 (en) 2018-10-31
KR102230447B1 (ko) 2021-03-19
BR112018010984B1 (pt) 2021-06-08
CN108366924A (zh) 2018-08-03
ES2764730T3 (es) 2020-06-04
WO2017111149A1 (en) 2017-06-29
JP6732444B2 (ja) 2020-07-29
KR20180074791A (ko) 2018-07-03
JP2017114773A (ja) 2017-06-29
US20210007955A1 (en) 2021-01-14
US11771631B2 (en) 2023-10-03
BR112018010984A2 (pt) 2018-12-04
CN108366924B (zh) 2021-03-02

Similar Documents

Publication Publication Date Title
US11771631B2 (en) Cosmetic composition comprising a specific filler combination and a film-forming polymer to increase long-lasting effects
US11389379B2 (en) Combination of polyion complex particle and non-polymeric acid having two or more acid dissociation constants
US20200390683A1 (en) Pore hiding cosmetic composition comprising a plate type filler, a silicon elastomer and an oil absorbing filler
US9233056B2 (en) Solid anti-sun composition based on lipophilic organic UV screening agent and aerogel particles of hydrophobic silica
ES2843515T3 (es) Composición que contiene partículas de material compuesto para filtrar la radiación UV, con un tamaño medio superior a 0,1 micras, y partículas de aerogel de sílice hidrofóbicas
ES2687296T3 (es) Composición antisol no pulverulenta que comprende una fase aceitosa polar y partículas de aerogel de sílice hidrófoba
ES2690019T3 (es) Crema contra el sol anhidra que comprende un organopolisiloxano elastómero no emulsionante, un agente deslustrante y un espesante oleoso orgánico no silicónico
US11642297B2 (en) Combination of polyion complex particle and hydrophilic or water-soluble UV filter
US11452676B2 (en) Combination of polyion complex particle and non-polymeric base having two or more dissociation constants
EP3197563B1 (en) Composition based on a lipophilic organic uv-screening agent and a filler
BR112016011640B1 (pt) Composição cosmética em pó, processo cosmético e processo de fabricação da composição cosmética em pó
CN109069366B (zh) 具有哑光效果和优异质地的uv屏蔽组合物
CN113840592A (zh) 包含浅绿色粘土和来源于益生菌的活性成分的防水化妆品组合物
KR20220103775A (ko) 분말 화장료 조성물

Legal Events

Date Code Title Description
AS Assignment

Owner name: L'OREAL, FRANCE

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:OKAMOTO, MARIKO;YOSHIDA, TOMOFUMI;KAMIDOI, YUKA;SIGNING DATES FROM 20180424 TO 20180426;REEL/FRAME:046558/0392

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE AFTER FINAL ACTION FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: ADVISORY ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION