WO2017000050A1 - Oil controlling sunscreen composition - Google Patents
Oil controlling sunscreen composition Download PDFInfo
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- WO2017000050A1 WO2017000050A1 PCT/BR2015/050083 BR2015050083W WO2017000050A1 WO 2017000050 A1 WO2017000050 A1 WO 2017000050A1 BR 2015050083 W BR2015050083 W BR 2015050083W WO 2017000050 A1 WO2017000050 A1 WO 2017000050A1
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
- A61K8/062—Oil-in-water emulsions
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/29—Titanium; Compounds thereof
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- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
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- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
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- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
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- 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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
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- 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4966—Triazines or their condensed derivatives
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- 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
Definitions
- the present invention is directed to a composition in the form of an oil- in-water emulsion comprising (a) one or more oil-soluble organic sunscreen ingredient; (b) one or more water-soluble organic sunscreen ingredient; (c) one or more silica-coated titanium dioxide sunscreen ingredient; (d) one or more mattifying powder; (e) one or more fatty compound; (f) an emulsifier system comprising: (i) one or more anionic surfactant, (ii) one or more non-ionic surfactant, (iii) one or more co- emulsifying ingredient; and (g) water.
- the compositions are particularly useful for preventing and/or controlling skin oiliness.
- the compositions are also useful for protecting the skin from damage caused by ultraviolet radiation.
- UV-filter compounds and/or particulate UV-screening compounds (collectively, “sunscreen ingredients”) that are solubilized, emulsified, or dispersed in a cosmetically or physiologically acceptable carrier, which is topically applied to the skin.
- sunscreen ingredients typically through the aid of polymers and other ingredients included in the vehicle, form a thin, protective, and often water-resistant layer on the skin. Sunscreens can be used to protect against UV damage and delay the signs of aging.
- Human skin contains sebaceous glands which secrete an oily or waxy substance known as sebum. A build-up of sebum on the surface of skin can cause the skin to appear shiny and/or oily. Shiny and/or oily skin is both uncomfortable and unappealing to many consumers. Shiny and/or oily skin can also highlight skin imperfections and reduce the wearability of other cosmetic compositions.
- organic sunscreen ingredients are oil-like and/or oil-soluble materials.
- the degree of UV protection afforded by a sunscreen composition is related to the amount and type of sunscreen ingredients it contains. For example, compositions with higher amounts of sunscreen ingredients may provide a higher degree of UV protection.
- Sunscreen compositions which may prevent and control skin oiliness are disclosed, for example, in WO 2013/1022848.
- the disclosed compositions contain an emulsifying agent, a water-soluble sunscreen ingredient, an oil-soluble sunscreen ingredient, and up to 7% oil absorbing particles.
- Oil-soluble sunscreen ingredients tend to contribute to the greasy feel of sunscreen compositions.
- the compositions disclosed in WO 2013/1022848 contain a greater amount of water-soluble sunscreen ingredients compared to oil-soluble sunscreen ingredients by weight, relative to the total weight of the composition.
- Example 1 discloses a sunscreen composition comprising 9% water-soluble sunscreen ingredients and 7% oil-soluble sunscreen ingredients by weight, relative to the total weight of the composition. Without wishing to be bound by theory, the composition disclosed in example 1 may be expected to be less greasy and prevent and/or control skin oiliness better than a composition containing a greater amount of oil-soluble sunscreen ingredients compared to water-soluble sunscreen ingredients by weight, relative to the total weight of the composition.
- the present invention is directed to a composition in the form of an oil- in-water emulsion comprising:
- the invention is also directed to a method of preventing and/or controlling skin oiliness involving applying the above-disclosed composition onto a surface of the human skin.
- the invention is also directed to a method of protecting the skin from damage caused by ultraviolet radiation involving applying the above- disclosed composition onto a surface of the human skin.
- Oil-in-water emulsion or "O/W emulsion” as used herein, means an oil phase dispersed in an water phase, where the water phase is a continuous phase.
- One or more as used herein means at least one and thus includes individual components as well as mixtures/combinations.
- Substituted means comprising one or more substituents.
- substituents include atoms, such as oxygen atoms and nitrogen atoms, as well as functional groups, such as hydroxyl groups, ether groups, alkoxy groups, acyloxyalkyl groups, oxyalkylene groups, polyoxyalkylene groups, carboxylic acid groups, amine groups, acylamino groups, amide groups, halogen containing groups, ester groups, thiol groups, sulphonate groups, thiosulphate groups, siloxane groups, and polysiloxane groups.
- the substituent(s) may be further substituted.
- compositions and methods of the present invention can comprise, consist of, or consist essentially of the essential elements and limitations of the invention described herein, as well as any additional or optional ingredients, components, or limitations described herein or otherwise useful.
- ranges provided are meant to include every specific range within, and combination of subranges between, the given ranges.
- a range from 1 -5 includes specifically 1 , 2, 3, 4 and 5, as well as subranges such as 2- 5, 3-5, 2-3, 2-4, 1 -4, etc.
- a range of ratios is meant to include every specific ratio within, and combination of subranges between, the given ranges.
- the expression “at least one” means one or more and thus includes individual components as well as mixtures/combinations.
- Cosmetically acceptable means that the item in question is compatible with any keratinous substrate.
- cosmetically acceptable carrier means a carrier that is compatible with any keratinous substrate.
- composition in the form of an oil-in-water emulsion comprising:
- composition in the form of an oil-in-water emulsion comprising:
- composition in the form of an oil-in-water emulsion comprising:
- compositions of the present invention have a a pH of from about 5.0 to about 9.0, preferably from about 6.0 to about 8.0, and most preferably from about 7.0 to about 7.6.
- the invention is also directed to a method of preventing and/or controlling skin oiliness involving applying the above-disclosed composition onto a surface of the human skin.
- the invention is also directed to a method of protecting the skin from damage caused by ultraviolet radiation involving applying the above- disclosed composition onto a surface of the human skin.
- oil-soluble organic sunscreen ingredient means any organic compound for screening out UV radiation, which can be fully dissolved in molecular form or miscible in an oil phase or which can be dissolved in colloidal form (for example in micellar form) in an oil fatty phase.
- Non-limiting examples of oil-soluble organic sunscreen ingredients useful in the invention include, for example, cinnamic derivatives; anthranilates; salicylic derivatives; dibenzoylmethane derivatives; camphor derivatives; benzophenone derivatives; diphenylacrylate derivatives; triazine derivatives; benzotriazole derivatives; benzalmalonate derivatives, especially those cited in patent US5624663; benzimidazole derivatives; imidazolines; bis-benzoazolyl derivatives as described in patents EP669323 and US2463264; p-aminobenzoic acid (PABA) derivatives; methylene bis(hydroxyphenylbenzotriazole) derivatives as described in applications US5237071 , US5166355, GB2303549, DE19726184 and EP8931 19; benzoxazole derivatives as described in patent applications EP0832642, EP1027883, EP1300137 and DE10162844; screening polymers and screening silicones such as
- Cinnamic derivatives examples include, but are not limited to, ethylhexyl methoxycinnamate sold in particular under the trade name "Parsol ® MCX” by DSM Nutritional Products, isopropyl methoxycinnamate, isoamyl methoxycinnamate sold under the trade name "Neo Heliopan ® E 1000" by Symrise, DEA methoxycinnamate, diisopropyl methylcinnamate, glyceryl ethylhexanoate dimethoxycinnamate.
- ethylhexyl methoxycinnamate sold in particular under the trade name "Parsol ® MCX” by DSM Nutritional Products
- isopropyl methoxycinnamate isoamyl methoxycinnamate sold under the trade name "Neo Heliopan ® E 1000" by Symrise
- DEA methoxycinnamate diisopropyl methyl
- dibenzoylmethane derivatives include, but are not limited to, butyl methoxydibenzoylmethane sold especially under the trade name "Parsol ® 1789” by DSM, isopropyl dibenzoylmethane.
- suitable salicylic derivatives include, but are not limited to, homosalate sold under the name “Eusolex ® HMS” by Rona/EM Industries, ethylhexyl salicylate sold under the name “Neo Heliopan ® OS” by Symrise, dipropylene glycol salicylate sold under the name “DipsalTM” by Scher, TEA salicylate sold under the name “Neo Heliopan ® TS” by Symrise.
- beta, beta -Diphenylacrylate derivatives examples include, but are not limited to, octocrylene sold in particular under the trade name "Uvinul ® N539" by BASF, etocrylene sold in particular under the trade name "Uvinul ® N35” by BASF.
- benzophenone derivatives examples include, but are not limited to, benzophenone-1 sold under the trade name "Uvinul ® 400" by BASF, benzophenone-2 sold under the trade name “Uvinul ® D50” by BASF, benzophenone-
- Benzylidenecamphor derivatives examples include, but are not limited to, 3-Benzylidene camphor manufactured under the name “MexorylTM SD” by Chimex, 4-methylbenzylidene camphor sold under the name “Eusolex ® 6300” by Merck, polyacrylamidomethyl benzylidene camphor manufactured under the name “MexorylTM SW” by Chimex.
- Suitable phenylbenzotriazole derivatives include, but are not limited to, drometrizole trisiloxane sold under the name “silatrizole” by Rhodia Chimie, methylene bis-benzotriazolyl tetramethylbutyl-phenol sold in solid form under the trade name "MIXXIM BB/100” by Fairmount Chemical, or in micronized form as an aqueous dispersion under the trade name "Tinosorb ® M” by Ciba Specialty Chemicals.
- triazine derivatives include, but are not limited to, bis-Ethylhexyloxyphenol methoxyphenyl triazine sold under the trade name "Tinosorb ® S" by BASF, ethylhexyl triazone sold in particular under the trade name "Uvinul ® T150" by BASF, diethylhexyl butamido triazone sold under the trade name "Uvasorb ® HEB” by Sigma 3V, 2,4,6-tris(dineopentyl 4'-aminobenzalmalonate)-s- triazine, 2,4,6-tris(diisobutyl 4'-aminobenzalmalonate)-iS triazine, 2,4-bis(dineopentyl 4'-aminobenzalmalonate)-6-(n-butyl 4'-aminobenzoate)-s-triazine, symmetrical triazine screening agents described in patent US 6,225,
- An example of a suitable anthranilic derivative includes, but is not limited to, menthyl anthranilate sold under the trade name "Neo Heliopan ® MA" by Symrise.
- imidazoline derivative includes, but is not limited to, ethylhexyl dimethoxybenzylidene dioxoimidazoline propionate.
- Benzalmalonate derivatives include, but is not limited to, ethylhexyl dimethoxybenzylidene dioxoimidazoline propionate.
- Benzalmalonate derivative includes, but is not limited to, polyorganosiloxane containing benzalmalonate functions, for instance polysilicone-15, sold under the trade name "Parsol ® SLX" by DSM Nutritional Products.
- An examples of a suitable 4,4-diarylbutadiene derivative includes, but is not limited to, 1 -Dicarboxy(2,2'-dimethylpropyl)-4,4-diphenyl-butadiene.
- benzoxazole derivative includes, but is not limited to, 2,4-bis[5-(1 -dimethylpropyl)benzoxazol-2-yl-(4-phenyl)imino]-6-(2- ethylhexyl)imino-1 ,3,5-triazine sold under the name Uvasorb ® K2A by Sigma 3V, and mixtures thereof.
- the oil-soluble organic sunscreen ingredient will be chosen from butyl methoxydibenzoylmethane, ethylhexyl salicylate, ethylhexyl triazone, octocrylene, drometrizole trisiloxane, bis-ethylhexyloxyphenol methoxyphenyl triazine, and mixtures thereof.
- the oil-soluble organic sunscreen ingredient is preferably present in the composition according to the invention in an amount of from about 3% to about 25% by weight, preferably in an amount of from about 5% to about 20% by weight, and most preferably about 7% to about 18% by weight, based on the total weight of the composition.
- water-soluble organic sunscreen ingredient means any organic compound for screening out UV radiation, which can be fully dissolved in molecular form or miscible in a liquid aqueous phase or which can be dissolved in colloidal form (for example in micellar form) in a liquid aqueous phase.
- Non-limiting examples of water-soluble organic sunscreen ingredients useful in the invention include, for example, terephthalylidene dicamphor sulfonic acid (Ecamsule), phenylbenzimidazole sulfonic acid (Ensulizole), benzophenone-4, aminobenzoic acid (PABA), 4-Bis(polyethoxy)-para-aminobenzoic acid polyethoxyethyl ester (PEG-25 PABA), camphor benzalkonium methosulfate, methylene bis-benzotriazolyl tetramethylbutylphenol (Bisoctrizole), disodium phenyl dibenzimidazole tetrasulfonate (Bisdisulizole disodium), and tris-biphenyl triazine; their derivatives and corresponding salts; naphthalene bisimide derivatives such as those described in European patent application EP1990372 A2, the entire contents of which is hereby incorporated
- the salts of the compounds that may be used according to the invention are chosen in particular from salts of alkali metals, for example sodium or potassium; salts of alkaline-earth metals, for example calcium, magnesium or strontium; metal salts, for example zinc, aluminium, manganese or copper; salts of ammonium of formula NH4+; quaternary ammonium salts; salts of organic amines, for instance salts of methylamine, dimethylamine, trimethylamine, triethylamine, ethylamine, 2-hydroxyethylamine, bis(2-hydroxyethyl)amine or tris(2- hydroxyethyl)amine; lysine or arginine salts.
- Salts chosen from sodium, potassium, magnesium, strontium, copper, manganese or zinc salts are preferably used.
- the sodium salt is prefereably used.
- the water-soluble organic sunscreen ingredient will be chosen from terephthalylidene dicamphor sulfonic acid, methylene bis-benzotriazolyl tetramethylbutylphenol, and mixtures thereof.
- the water-soluble organic sunscreen ingredient is preferably present in the composition according to the invention in an amount of from about 0.1 % to about 10% by weight, preferably in an amount of from about 0.5% to about 8% by weight, and most preferably about 1 % to about 7% by weight, based on the total weight of the composition.
- silicon-coated titanium dioxide sunscreen ingredient means spherical beads which are formed by encapsulating titanium dioxide particles in silica.
- Non-limiting examples of silica coated titanium dioxide sunscreen ingredients useful in the invention include, for example, titanium dioxide coated with silica, such as the product "Sunsil Tin50" from Sunjin Chemical known under the INCI name silica (and) titanium dioxide having a composition of silica:titanium dioxide of about 55:45 and having a particle size from about 2 microns to about 7 microns.
- silica coated titanium dioxide sunscreen ingredients useful in the invention include, for example, titanium dioxide coated with silica, such as the product "Sunsil Tin50" from Sunjin Chemical known under the INCI name silica (and) titanium dioxide having a composition of silica:titanium dioxide of about 55:45 and having a particle size from about 2 microns to about 7 microns.
- the silica-coated titanium dioxide sunscreen ingredient is preferably present in the composition according to the invention in an amount of from about 1 % to about 10% by weight, preferably in an amount of from about 2% to about 10% by weight, and most preferably about 5% to about 10% by weight, based on the total weight of the composition.
- mattifying powder means a powder which absorbs sebum and provides a mattifying effect to the skin.
- Non-limiting examples of mattifying powders useful in the invention include, for example, modified starches, polyamide powders, hydrophobic silica aerogel particles, acrylic polymer powders, elastomeric silicone powders, clays, and mixtures thereof.
- Modified starches useful in the invention include, for example, those known under the INCI names aluminum starch octenylsuccinate, sodium starch octenylsuccinate, calcium starch octenylsuccinate, and mixtures thereof.
- Modified starches are preferably present in the composition according to the invention in an amount of from about 0.01 % to about 10% by weight, preferably in an amount of from about 0.1 % to about 5% by weight, and most preferably about 0.5% to about 4% by weight, based on the total weight of the composition.
- Polyamide powders useful in the invention include, for example, those known under the INCI name nylon-12, nylon-6, and mixtures thereof.
- Polyamide powders are preferably present in the composition according to the invention in an amount of from about 0.01 % to about 10% by weight, preferably in an amount of from about 0.1 % to about 5% by weight, and most preferably about 0.5% to about 4% by weight, based on 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 Si-Rn, for example trimethylsilyl groups.
- silylating agents for example halogenated silanes such as alkylchlorosilanes, siloxanes, in particular dimethylsiloxanes such as hexamethyldisiloxane, or silazanes
- Hydrophobic silica aerogel particles useful in the invention are preferably particles surface-modiified with trimethylsilyl groups known under the INCI name silica silylate and include, for example, the aerogel sold under the trade name "VM-2260” or “VM-2270” by the company Dow Corning, the particles of which have a mean size of about 1000 microns and a specific surface area per unit of mass ranging from 600 to 800 m 2 /g.
- a preferred hydrophobic silica aerogel particle is the aerogel sold under the name "VM-2270", by the company Dow Corning, the particles of which have a mean size ranging from 5-15 microns and a specific surface area per unit of mass ranging from 600 to 800 m 2 /g.
- Hydrophobic silica aerogel particles are preferably present in the composition according to the invention in an amount of from about 0.01 % to about 5% by weight, preferably in an amount of from about 0.1 % to about 5% by weight, and most preferably about 0.3% to 4% by weight, based on the total weight of the composition.
- Acrylic polymer powders useful in the invention include, for example, acrylic polymer powders such as the product "Covabead” LH85 from Sensient known under the INCI name methyl methacrylate crosspolymer.
- the acrylic polymer powder is preferably present in the composition according to the invention in an amount of from about 0.01 % to about 10% by weight, preferably in an amount of from about 0.1 % to about 5% by weight, and most preferably about 0.5% to about 4% by weight, based on the total weight of the composition.
- Elastomeric silicone powders useful in the invention include, for example, a powders such as the products DC-9509 and DC-9506 sold by Dow Corning known under the INCI name dimethicone/vinyl dimethicone crosspolymer.
- Clays useful in the invention include, for example, clays of the smectite family such as montmorillonites, hectorites, bentonites, beidellites and saponites, and also of the vermiculite, stevensite and chlorite families.
- Non-limiting examples of clays usefil in the invention include, for example, synthetic hectorites (also known as laponites), for instance the products sold by the company Laporte under the name Laponite XLG, Laponite RD and Laponite RDS (these products are sodium magnesium silicates and in particular sodium lithium magnesium silicates); bentonites, for instance the product sold under the name Bentone HC by the company Rheox; magnesium aluminium silicates, especially hydrated, for instance the product sold by the Vanderbilt Company under the name Veegum Ultra, or calcium silicates and especially the product in synthetic form sold by the company under the name Micro-cel C.
- synthetic hectorites also known as laponites
- laponites for instance the products sold by the company Laporte under the name Laponite XLG, Laponite RD and Laponite RDS (these products are sodium magnesium silicates and in particular sodium lithium magnesium silicates)
- bentonites for instance the product sold under the name Bentone HC by the company Rheox
- the mattifying powders will be chosen from aluminum starch octenylsuccinate, nylon-12, silica silylate, methyl methacrylate crosspolymer, and mixtures thereof.
- the mattifying powders are preferably present in the composition according to the invention in an amount of from about 0.1 % to about 10% by weight, preferably in an amount of from about 0.5% to about 8% by weight, and most preferably about 2% to about 6% by weight, based on the total weight of the composition.
- fatty compound means a lipophilic compound which is in the form of a liquid or solid room temperature (25°C) under atmospheric pressure (760 mmHg).
- the fatty compound may be a non-polar oil such as a hydrocarbon oil, a silicone oil; a polar oil such as a plant or animal oil and an ester oil or an ether oil; a fatty alcohol, or a mixture thereof.
- Non-limiting examples of plant oils useful in the invention include, for example, linseed oil, camellia oil, macadamia nut oil, corn oil, mink oil, olive oil, avocado oil, sasanqua oil, castor oil, safflower oil, jojoba oil, sunflower oil, almond oil, rapeseed oil, sesame oil, soybean oil, peanut oil, and mixtures thereof.
- Non-limiting examples of animal oils useful in the invention include, for example, squalene, squalane, and mixtures thereof.
- Non-limiting examples of synthetic oils useful in the invention include, for example, alkane oils such as isododecane and isohexadecane, ester oils, ether oils, and artificial triglycerides.
- Ester oils are preferably liquid esters of saturated or unsaturated, linear or branched C1 -C26 aliphatic monoacids or polyacids and of saturated or unsaturated, linear or branched C1 -C26 aliphatic monoalcohols or polyalcohols, the total number of carbon atoms of the esters being greater than or equal to 10.
- At least one from among the alcohol and the acid from which the esters of the invention are derived is branched.
- ester oils useful in the invention include C12-C15 alkyl benzoate, ethyl palmitate, ethyl hexyl palmitate, isopropyl palmitate, dicaprylyl carbonate, alkyl myristates such as isopropyl myristate or ethyl myristate, isocetyl stearate, 2-ethylhexyl isononanoate, isononyl isononanoate, isodecyl neopentanoate, isostearyl neopentanoate, diethyl sebacate, isopropyl lauroyl sarcosinate, diisopropyl sebacate, bis(2-ethylhexyl) sebacate, diisopropyl adipate, di- n-propyl adipate, dioctyl adipate, bis(2-ethylhexyl)
- Non-limiting examples of silicone oils useful in the invention include, for example, volatile or non-volatile silicone oils, such as volatile or non-volatile polydimethylsiloxanes (PDMS) containing a linear or cyclic silicone chain, that are liquid or pasty at ambient temperature, in particular cyclopolydimethylsiloxanes (cyclomethicones) such as cyclohexasiloxane; polydimethylsiloxanes containing alkyl, alkoxy or phenyl groups that are pendent or at the end of the silicone chain, which groups have from 2 to 24 carbon atoms; phenyl silicones such as phenyl trimethicones, phenyl dimethicones, phenyltrimethylsiloxydiphenylsiloxanes, diphenyl dimethicones, diphenylmethyldiphenyltrisiloxanes, 2-phenylethyltrimethyl siloxysilicates, polymethylphenylsilox
- hydrocarbon oils useful in the invention include, for example, undecane, dodecane, tridecane, isoparaffins, isohexadecane, isododecane and isodecane, liquid paraffins, liquid petroleum jelly, polydecenes hydrogenated polyisobutenes, synthetic wax, and mixtures thereof.
- Non-limiting examples of fatty alcohols useful in the invention include, for example, fatty alcohols containing from 8 to 26 carbon atoms, such as cetyl alcohol, stearyl alcohol and a mixture thereof (cetylstearyl alcohol), octyldodecanol, 2-butyloctanol, 2- hexyldecanol, 2-undecylpentadecanol, oleyl alcohol linoleyl alcohol, and mixtures thereof.
- the fatty compounds will be chosen from C12-15 alkyl benzoate, isopropyl sarcosinate, stearyl alcohol, synthetic wax, dimethicone, and mixtures thereof.
- the fatty compounds are preferably present in the composition according to the invention in an amount of from about 3% to about 15% by weight, preferably in an amount of from about 5% to about 13% by weight, and most preferably about 8% to about 12% by weight, based on the total weight of the composition.
- the emulsifier system of a composition according to the invention comprises one or more anionic surfactant, one or more non-ionic surfactant, and one or more co-emulsifying ingredient.
- anionic surfactants useful in the invention include, for example, carboxylates (sodium 2-(2-hydroxyalkyloxy)acetate), amino acid derivatives (N-acylglutamates, N-acylglycinates or acylsarcosinates), alkyl sulfates, alkyl ether sulfates and oxyethylenated derivatives thereof, sulfonates, isethionates and N-acylisethionates, taurates and N-acyl N-methyltaurates, sulfosuccinates, alkyl sulfoacetates, phosphates and alkyl phosphates, anionic derivatives of alkyl polyglycoside (acyl-D-galactoside uronate), and mixtures thereof.
- carboxylates sodium 2-(2-hydroxyalkyloxy)acetate
- amino acid derivatives N-acylglutamates, N-acylglycinates or acylsarco
- the phosphate surfactant may be selected from monoalkyl phosphates, dialkyl phosphates, salts of monoalkyl phosphates, salts of dialkyl phosphates, and mixtures thereof. More preferably, the monoalkyl phosphates and dialkyl phosphates comprise one or more linear or branched and aliphatic and/or aromatic alkyl chains having from 8 to 22 carbon atoms. According to preferred embodiments, the phosphate surfactant(s) can be neutralized with organic or inorganic bases such as, for example, potassium hydroxide, sodium hydroxide, triethanolamine, arginine, lysine and N-methylglucamine to form the aforementioned salts.
- organic or inorganic bases such as, for example, potassium hydroxide, sodium hydroxide, triethanolamine, arginine, lysine and N-methylglucamine to form the aforementioned salts.
- Suitable examples of phosphate surfactants include, but are not limited to, monolauryl phosphate, such as the product sold under the name MAP 20 ® by Kao Chemicals, the potassium salt of dodecyl phosphate, such as the mixture of mono- and diester (predominantly diester) sold under the name Crafol AP-31 ® by Cognis, the octyl monoester and the octyl diester of phosphoric acid, such as the mixture sold under the name Crafol AP-20 ® by Cognis, the ethoxylated (7 mol. of EO) 2- butyloctanol monoester and the ethoxylated (7 mol.
- monolauryl phosphate such as the product sold under the name MAP 20 ® by Kao Chemicals
- the potassium salt of dodecyl phosphate such as the mixture of mono- and diester (predominantly diester) sold under the name Crafol
- the anionic surfactant is postassium cetyl phosphate.
- the anionic surfactant is preferably present in the composition according to the invention in an amount of from about 0.1 % to about 10% by weight, preferably in an amount of from about 0.3% to about 8% by weight, and most preferably about 0.5% to about 4% by weight, based on the total weight of the composition.
- Non-limiting examples of non-ionic surfactants useful in the invention include, for example, oxyalkylenated (more particularly polyoxyethylenated) fatty acid esters of glycerol; oxyalkylenated fatty acid esters of sorbitan; oxyalkylenated (oxyethylenated and/or oxypropylenated) fatty acid esters, for instance the mixture PEG-100 Stearate and glyceryl stearate sold, for example, by the company ICI under the name ArlacelTM 165; oxyalkylenated (oxyethylenated and/or oxypropylenated) fatty alcohol ethers; sugar esters, for instance sucrose stearate; fatty alcohol ethers of sugars, especially alkyl polyglucosides (APGs) such as decyl glucoside and lauryl glucoside sold, for example, by the company Henkel under the respective names Plantaren ® 2000 and Plant
- the mixture of the alkyl polyglucoside as defined above with the corresponding fatty alcohol may be in the form of a self-emulsifying composition as described, for example, in document WO-A-92/06778. Mention may also be made of lecithins and derivatives (e.g. Biophilic), sugar esters and sodium stearoyl lactylate.
- the non-ionic surfactant is the mixture of PEG-100 stearate and glyceryl stearate.
- the non-ionic surfactant is preferably present in the composition according to the invention in an amount of from about 0.1 % to about 10% by weight, preferably in an amount of from about 0.5% to about 8% by weight, and most preferably about 0.75% to about 4% by weight, based on the total weight of the composition.
- co-emulsifying ingredient useful in the invention include, for example, fatty acids chosen from C12-C22 higher fatty acids, such as stearic acid, myristic acid, oleic acid, linoleic acid, linolenic acid, lauric acid, palmitic acid, and mixtures thereof. Most preferably, the co-emulsifying ingredient is stearic acid.
- the co-emulsifying ingredient is preferably present in the composition according to the invention in an amount of from about 0.2% to about 6% by weight, preferably in an amount of from about 0.5% to about 5% by weight, and most preferably about 1 % to about 2% by weight, based on the total weight of the composition.
- the composition according to the invention comprises water.
- the water used may be sterile demineralized water and/or a floral water such as rose water, cornflower water, chamomile water or lime water, and/or a natural thermal or mineral water such as, for example: water from Vittel, water from the Vichy basin, water from Uriage, water from La Roche Posay, water from La Bourboule, water from Enghien- les-Bains, water from Saint Gervais-les-Bains, water from Neris-les-Bains, water from Allevar-les-Bains, water from Digne, water from Maizieres, water from Neyrac-les- Bains, water from Lons-le-Saunier, water from Eaux Bonnes, water from Rochefort, water from Saint Christau, water from Les Fumades, water from Tercis-les-Bains or water from Avene.
- Water may also comprise reconstituted thermal water, that is to say a water comprising trace elements such as zinc, copper, magnesium, etc., reconsti
- Water is preferably present in the composition according to the invention in an amount of from about 20% to about 60% by weight, preferably in an amount of from about 25% to about 50% by weight, and most preferably about 30% to about 40% by weight, based on the total weight of the composition.
- compositions according to the invention optionally may comprise one or more water-soluble solvent.
- water-soluble solvent means a compound that is liquid at room temperature and water-miscible (miscibility with water of greater than 50% by weight at 25°C and atmospheric pressure).
- Non-limiting examples of water-soluble solvents useful in the invention include, for example, lower monoalcohols containing from 1 to 5 carbon atoms, such as ethanol and isopropanol, glycols containing from 2 to 8 carbon atoms, such as ethylene glycol, propylene glycol, 1 ,3-butylene glycol, hexylene glycol, and dipropylene glycol, glycerin, and mixtures thereof.
- lower monoalcohols containing from 1 to 5 carbon atoms such as ethanol and isopropanol
- glycols containing from 2 to 8 carbon atoms such as ethylene glycol, propylene glycol, 1 ,3-butylene glycol, hexylene glycol, and dipropylene glycol, glycerin, and mixtures thereof.
- the water-soluble solvent is preferably present in the composition according to the invention in an amount of from about 0.5% to about 20% by weight, preferably in an amount of from about 1 % to about 15% by weight, and most preferably about 5% to about 10% by weight, based on the total weight of the composition.
- compositions according to the invention may additionally comprise cosmetic adjuvants chosen from fragrances, pigments, chelating agents, softeners, antioxidants, opacifiers, stabilizers, moisturizing agents, vitamins, bactericides, preservatives, polymers, thickening agents, pH adjusters, or any other ingredient commonly used in cosmetics for this type of application.
- cosmetic adjuvants chosen from fragrances, pigments, chelating agents, softeners, antioxidants, opacifiers, stabilizers, moisturizing agents, vitamins, bactericides, preservatives, polymers, thickening agents, pH adjusters, or any other ingredient commonly used in cosmetics for this type of application.
- composition ingredients serve to illustrate the invention without however exhibiting a limiting character.
- amounts of the composition ingredients are given as weight percentages relative to the total weight of the composition.
- phase C1 The ingredients of phase C1 were combined in the main kettle and heated to 75°C with stirring. Phases C2 and C3 were added to the main kettle and stirring was continued until titanium dioxide (and) aluminum hydroxide (and) stearic acid was completely dispersed.
- the ingredients of phases A and B were combined in the annex and heated to 75°C with stirring. The contents of the annex were added to the main kettle and emulsified. The ingredients of phase D were added to the main kettle. Cooling of the main kettle was begun. When the contents of the main kettle reached, 40°C, the ingredients of phase E were added. The ingredients of phase F and phase H were added to the main kettle. When the contents of the main kettle reached 30°C, the ingredients of phase G were added. The contents of the kettle were homongenized.
- Example 1 significantly reduced the sebum level of the skin 10 minutes after product application.
- Dry touch has been identified as a key attribute for consumer perception of oil control.
- Brazilian consumers associate oil control as being a combination of both dry touch and shine. Even without a difference in shine, consumers perceive lower performance when they experience oily feel.
- compositions of Examples 1 and 2 were evaluated for the sensorial attributes of dry touch and shine. The results of this test are provided below in table 3.
- a trained expert beautician evaluated samples applied to the face of subjects having oily skin. Evaluation was performed after initial application (TO) and after 4 hours (T4h). The attributes of dry touch and shine were evaluated by touch and/or by view and quantified using a 6-point non-structured scale with 0 representing the least and 6 representing the most.
- inventive Example 1 containing silica (and) titanium dioxide (Sunsil Tin50 from Sunjin Chemical) had a dryer touch at both TO and T4 compared to comparative Example 2 having no silica (and) titanium dioxide (Sunsil Tin50 from Sunjin Chemical). Therefore, inventive Example 1 has superior oil control performance compared to comparative Example 2.
Abstract
Description
Claims
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PCT/BR2015/050083 WO2017000050A1 (en) | 2015-06-29 | 2015-06-29 | Oil controlling sunscreen composition |
BR112017026169A BR112017026169A2 (en) | 2015-06-29 | 2015-06-29 | oil-in-water emulsion composition and method for preventing and / or controlling skin oils |
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PCT/BR2015/050083 WO2017000050A1 (en) | 2015-06-29 | 2015-06-29 | Oil controlling sunscreen composition |
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Cited By (3)
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WO2020163928A1 (en) * | 2019-02-13 | 2020-08-20 | L'oreal | Sunscreen composition, use of the sunscreen composition and process of manufacturing the sunscreen composition |
WO2020220099A1 (en) * | 2019-04-30 | 2020-11-05 | L'oreal | Cosmetic compositions in a soft-solid format comprising a hydrophobic powder selected from silica aerogel and polylactic acid, starch and an uv-filter system |
WO2021132532A1 (en) * | 2019-12-24 | 2021-07-01 | L'oreal | Cosmetic composition comprising spherical hydrophobic silica aerogel and composite silica particles and/or hollow silica particles |
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Cited By (5)
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WO2020163928A1 (en) * | 2019-02-13 | 2020-08-20 | L'oreal | Sunscreen composition, use of the sunscreen composition and process of manufacturing the sunscreen composition |
WO2020220099A1 (en) * | 2019-04-30 | 2020-11-05 | L'oreal | Cosmetic compositions in a soft-solid format comprising a hydrophobic powder selected from silica aerogel and polylactic acid, starch and an uv-filter system |
CN113766906A (en) * | 2019-04-30 | 2021-12-07 | 欧莱雅 | Cosmetic composition in the form of a soft solid comprising a hydrophobic powder selected from silica aerogel and polylactic acid, starch and a UV filter system |
WO2021132532A1 (en) * | 2019-12-24 | 2021-07-01 | L'oreal | Cosmetic composition comprising spherical hydrophobic silica aerogel and composite silica particles and/or hollow silica particles |
CN114641271A (en) * | 2019-12-24 | 2022-06-17 | 莱雅公司 | Cosmetic composition comprising spherical hydrophobic silica aerogel and composite silica particles and/or hollow silica particles |
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