WO2013072488A2 - Even deposition and low rub-off compositions - Google Patents
Even deposition and low rub-off compositions Download PDFInfo
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- WO2013072488A2 WO2013072488A2 PCT/EP2012/072894 EP2012072894W WO2013072488A2 WO 2013072488 A2 WO2013072488 A2 WO 2013072488A2 EP 2012072894 W EP2012072894 W EP 2012072894W WO 2013072488 A2 WO2013072488 A2 WO 2013072488A2
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- 229940106025 phenylethyl resorcinol Drugs 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920013639 polyalphaolefin Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000059 polyethylene glycol stearate Polymers 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920003226 polyurethane urea Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- NEOZOXKVMDBOSG-UHFFFAOYSA-N propan-2-yl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OC(C)C NEOZOXKVMDBOSG-UHFFFAOYSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- ZUFQODAHGAHPFQ-UHFFFAOYSA-N pyridoxine hydrochloride Chemical compound Cl.CC1=NC=C(CO)C(CO)=C1O ZUFQODAHGAHPFQ-UHFFFAOYSA-N 0.000 description 1
- NPCOQXAVBJJZBQ-UHFFFAOYSA-N reduced coenzyme Q9 Natural products COC1=C(O)C(C)=C(CC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C(O)=C1OC NPCOQXAVBJJZBQ-UHFFFAOYSA-N 0.000 description 1
- 235000021283 resveratrol Nutrition 0.000 description 1
- 229940016667 resveratrol Drugs 0.000 description 1
- 229940108325 retinyl palmitate Drugs 0.000 description 1
- 235000019172 retinyl palmitate Nutrition 0.000 description 1
- 239000011769 retinyl palmitate Substances 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 235000002020 sage Nutrition 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229940057910 shea butter Drugs 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 230000037075 skin appearance Effects 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 235000019259 sodium dehydroacetate Nutrition 0.000 description 1
- 229940079839 sodium dehydroacetate Drugs 0.000 description 1
- DSOWAKKSGYUMTF-GZOLSCHFSA-M sodium;(1e)-1-(6-methyl-2,4-dioxopyran-3-ylidene)ethanolate Chemical compound [Na+].C\C([O-])=C1/C(=O)OC(C)=CC1=O DSOWAKKSGYUMTF-GZOLSCHFSA-M 0.000 description 1
- GOJYXPWOUJYXJC-UHFFFAOYSA-M sodium;2-[1-(2-hydroxyethyl)-2-undecyl-4,5-dihydroimidazol-1-ium-1-yl]acetate;hydroxide Chemical compound [OH-].[Na+].CCCCCCCCCCCC1=NCC[N+]1(CCO)CC([O-])=O GOJYXPWOUJYXJC-UHFFFAOYSA-M 0.000 description 1
- 229960002920 sorbitol Drugs 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000012177 spermaceti Substances 0.000 description 1
- 229940084106 spermaceti Drugs 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 229940116199 stearamide amp Drugs 0.000 description 1
- 229960004274 stearic acid Drugs 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000020238 sunflower seed Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- 229960002663 thioctic acid Drugs 0.000 description 1
- 239000001585 thymus vulgaris Substances 0.000 description 1
- AQWHMKSIVLSRNY-UHFFFAOYSA-N trans-Octadec-5-ensaeure Natural products CCCCCCCCCCCCC=CCCCC(O)=O AQWHMKSIVLSRNY-UHFFFAOYSA-N 0.000 description 1
- HTJNEBVCZXHBNJ-XCTPRCOBSA-H trimagnesium;(2r)-2-[(1s)-1,2-dihydroxyethyl]-3,4-dihydroxy-2h-furan-5-one;diphosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.OC[C@H](O)[C@H]1OC(=O)C(O)=C1O HTJNEBVCZXHBNJ-XCTPRCOBSA-H 0.000 description 1
- 229940035936 ubiquinone Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 239000011716 vitamin B2 Substances 0.000 description 1
- 239000011708 vitamin B3 Substances 0.000 description 1
- 239000011726 vitamin B6 Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 150000003700 vitamin C derivatives Chemical class 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 150000003712 vitamin E derivatives Chemical class 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 235000019386 wax ester Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
- A61K8/062—Oil-in-water emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0241—Containing particulates characterized by their shape and/or structure
- A61K8/0283—Matrix particles
- A61K8/0287—Matrix particles the particulate containing a solid-in-solid dispersion
-
- 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
-
- 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
- A61K8/31—Hydrocarbons
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/87—Polyurethanes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
Definitions
- the present invention is directed to an even deposition and low rub-off compositions.
- the invention is directed to a composition that comprises both particle comprising hydrophobic material and optionally active, as well as a film forming resin.
- the composition unexpectedly results in excellent active deposition and is not easy to rub-off.
- the composition surprisingly does not result in a topical film that easily separates and peels from skin after being applied, notwithstanding the fact that aqueous-based film forming resin within the water phase of an emulsion is used with particle comprising hydrophobic material within the oil phase of the emulsion.
- Skin appearance is a major indicia of looking healthy. Skin color, the lack of wrinkles and a complexion free of blemishes certainly makes one look and feel better.
- Make-up formulas for example, have been designed to mimic a person's skin tones.
- High loadings of colorants are optical ingredients necessary for such formulae. While formulae loaded with colorants achieve a covering purpose, high levels of colorants can negatively interfere with sensory attributes and active deposition. Moreover, formulae high in colorants can often, and undesirably, rub-off on clothing as well as other fabrics, including upholstery.
- Other formulae that provide good coverage of skin imperfections rely on the soft focus effect and utilize metal oxides, like titanium dioxide. These formulas whiten skin and hide blemishes but are easy to rub-off after application and usually result in an undesirable ashen appearance.
- compositions that are suitable to effectively deposit active on skin while at the same time being low rub-off and deplete of separation and peeling characteristics often associated with compositions classified as low rub-off.
- This invention is directed to a low rub-off composition comprising both a particle comprising hydrophobic material and optionally active, as well as a film forming resin.
- the composition unexpectedly results in excellent active deposition and is low rub-off after application notwithstanding the fact that aqueous-based film forming resin within the water phase of an emulsion is used along with particle comprising hydrophobic material within the oil phase of the emulsion.
- cosmetic compositions and a method to impart a healthy appearance to skin are described.
- cosmetic compositions comprising at least one continuous liquid fatty phase containing at least one hydrocarbon- based oil are described whereby the same are structured with at least one polymer chosen from polyurethanes, polyurethaneureas and polyureas. Still other efforts have been disclosed for making compositions suitable for topical application.
- compositions with encapsulated coloring agents are described.
- composition comprising a hydrophobic particle comprising hydrophobic material and optionally an active, as well as a film forming resin as claimed in this invention.
- the present invention is directed to an improved deposition and low rub-off composition, the composition being an emulsion comprising:
- the present invention is directed to a method for improving a skin characteristic by applying topically the composition of the first aspect of this invention.
- Skin as used herein, is meant to include skin on the face, neck, chest, back, arms
- Particle comprising hydrophobic material is meant to mean a particle (or bead) that has a diameter from 75 to 525 microns where diameter is meant to mean the longest measurable (cross-sectional) distance in the event the particle is not a perfect sphere.
- Such a particle is, overall, hydrophobic.
- Active is meant to be embedded within the particle comprising hydrophobic material (like petrolatum) to form the preferred particle, and preferably, homogeneously mixed therein.
- Low rub-off as used herein, generally means a composition capable of remaining on skin after normal contact with clothing worn.
- Active is meant to include a component that improves a skin characteristic and/or benefits skin wherein the same can be, and preferably, is an active in a leave-on composition, and most preferably, a cream, lotion, balm, deodorant, or gel.
- the weight ratio m+a/r means the amount by weight of hydrophobic material in the particle plus the amount by weight active in the particle/weight of film forming resin in the composition of this invention.
- Weight of film forming resin means the weight of resin used in the aqueous phase of the composition where the amount of resin (i.e., non- water soluble polymer) does not include the weight of the aqueous phase.
- Particle as used herein, is meant to mean a single particle as well as an agglomerate of large particle made of smaller particles.
- Comprising is meant to include consisting essentially of and consisting of.
- the particle of this invention may consist essentially of or consist of hydrophobic material and optionally active.
- Emulsion means oil-in- water emulsion and may be interchanged with composition of this invention, where the composition of this invention is often one that is employed to evenly deposit active which is a colorant. All ranges identified herein are meant to include all ranges subsumed therein if, for example, reference to the same is not explicitly made.
- the particle comprising hydrophobic material and optional active used in this invention can be used in a topical composition and has a diameter from 75 to 525 microns, and preferably, from 100 to 450 microns, and most preferably, from 150 to 300 microns, including all ranges subsumed therein.
- the weight of hydrophobic material in the particle 5 makes up from 1.5 to 9 times, and most preferably, from 1 .5 to 7 times, and optimally, from 2 to 5 times more than the weight of active (i.e., when used) in the particle, based on total weight of the particle and including all ranges subsumed therein.
- the total weight of hydrophobic material in the composition is often from 0.75 to 10.0%, and preferably, from 1 .5 to 6.0%, and most preferably, from 1.5 to 4.0% by weight, based on total weight of the 10 composition of this invention and including all ranges subsumed herein.
- the total weight of optional active in the particle comprising hydrophobic material in the composition when used, is often from 0.02 to 7.5%, and preferably, from 0.05 to 6.5%, and most preferably, from 0.1 to 5.0% by weight, based on total weight of the composition and including all ranges subsumed therein.
- the hydrophobic material used for particle formation may comprise, for example, petrolatum, high molecular weight isoparaffins, polyalphaolefins, siliconized waxes like siliconized beeswax, shea butter, carnauba, silicones, silicone elastomer, glycerides (like sunflower seed oil, soybean oil, safflower oil), mixtures thereof or the like (consistent with the
- hydrophobic material or combination of hydrophobic material used for making particle of this invention is limited only to the extent that the materials may be topically applied, and preferably, has a melting point from 40° to 50°C, and preferably, from 42° to 48°C, including all ranges subsumed therein.
- the hydrophobic material of the particle comprises at least 50% by weight petrolatum, and
- the particle comprising hydrophobic material preferably, from 75 to 100% by weight petrolatum as the hydrophobic material, and most preferably, 100% by weight petrolatum based on total weight of the hydrophobic material in the particle and including all ranges subsumed therein. It is within the scope of this invention for the particle comprising hydrophobic material to consist of petrolatum as the hydrophobic material. Moreover, the particle comprising hydrophobic material preferably comprises from
- hydrophobic material with or without active.
- hydrophobic material is heated from 40° to 65°C, and preferably, from 42° to 60°C, and most preferably, from 48° to 55°C, 35 including all ranges subsumed therein.
- active is combined with hydrophobic material and mixed. Mixing and heating is controlled and should continue until a preferably homogeneous composition of active and hydrophobic material is produced.
- the resulting heated composition comprising hydrophobic material (and optionally but preferably active) is now suitable for addition to an oil phase on its own or already in the emulsion of this invention (i.e., composition of the invention) wherein the emulsion is one which is an oil-in-water emulsion.
- the heated composition with or without active i.e., the oil phase being used for emulsion formation or already in the emulsion
- the same should be added to the oil phase and mixed with moderate shear via conventional mixing techniques (e.g., mechanical paddle).
- the oil phase should typically be maintained at a temperature from 25° to 48°C, and preferably, from 30° to 45°C, and most preferably, from 30° to 40°C, including all ranges subsumed therein.
- Heated composition comprising hydrophobic material (and optionally active) should be maintained at a
- Stirring should be maintained at a rate and for a time that results in particle comprising hydrophobic material (and optionally active) having a diameter described herein within the oil phase.
- the (m+a/r) ratio is greater than 0.05 and less than 35, and most preferably, from 0.1 to 6, including all ranges subsumed therein.
- the (m+a/r) ratio is from 0.2 to 1.0, and most optimally, the (m+a/r) ratio is from 0.25 to 0.5, including all ranges subsumed therein.
- the active is one that can be mixed with particle comprising hydrophobic material (like, for example, petrolatum), and preferably, homogenously mixed within the hydrophobic particle.
- Such actives may be water or oil soluble or the actives used may be a mixture of water and oil soluble actives.
- the active when used, may be a particle itself having a diameter from 100 to 1200 nm, and preferably, from 280 to 1000 nm, and most preferably, from 300 to 650 nm, including all ranges subsumed therein. Consistent with the diameter for the particle comprising hydrophobic material, diameter for the active (if applicable) is meant to mean the longest measurable distance of a cross-section of the solid active in the event the same is not a perfect sphere.
- water soluble active is present within the particle comprising hydrophobic material and in the oil phase of the emulsion when slow release of the active is desired and/or when isolation from other actives in the water phase of the emulsion is desired.
- water soluble active is present in the water phase
- oil soluble active is present in the oil phase of the emulsion (and preferably carried in with the particle described in this invention). It is within the scope of this invention for active to be added to the water phase and/or oil phase of the emulsion without being carried by particle. Such active, not carried with particle, can be used with or in lieu of active carried with particle.
- Actives suitable for use in this invention are meant to include but not be limited to opacifiers, colorants, skin lightening agents, moisturizers, sunscreens, plant extracts, anti- inflammatories, surfactants, wrinkle reducing agents, mixtures thereof or the like.
- the aqueous-based film forming resin suitable for use in this invention can comprise acrylate, polymers of ether cellulose polyurethane, polyethylene glycols, polyvinyl pyrrolidone, polyvinyl alcohol, silicone polymer as well as mixtures, copolymers, ter-polymers and blends thereof.
- non-water soluble resin i.e., film forming resin
- Such dispersions are commercially available and may be made with or without emulsifiers.
- the most desired aqueous-based resin is an aqueous-based polyurethane resin sold under the name Baycusan® by Bayer Material Science.
- aqueous-based film forming resins are from 30 to 60%, and preferably, from 35 to 55%, and most preferably, from 40 to 50% by weight polymer or resin, based on total weight of the aqueous-based dispersion and including all ranges subsumed therein.
- the weight of resin (excluding the aqueous phase) used in this invention typically makes up from 0.5 to 12%, and preferably, from 1 to 10%, and most preferably from 2 to 9% by weight of the composition of the invention, based on total weight of the composition and including all ranges subsumed therein. Typically, therefore, from 1 .5 to 20% by weight aqueous-based resin in dispersion or aqueous phase is added to the composition of this invention, including all ranges subsumed therein.
- Traditional methods for making aqueous-based film forming resins are described, for example, in U.S. Patent Nos. 3,310,416, 3,388,087 and 3,905,929, the disclosures of which are incorporated herein by reference.
- compositions (or oil-in-water emulsions) of the present invention may typically include cosmetically acceptable carrier components in addition to the water, oil, particles and resins described herein.
- Water is the most preferred carrier. Amounts of water may range from 1 to 98%, and preferably, from 5 to 90%, and most preferably, from 35 to 80%, and optimally, from 40 to 75% by weight, based on total weight of the composition and including all ranges subsumed therein.
- Cosmetically acceptable carriers suitable for use in this invention may include mineral oils, silicone oils, synthetic or natural esters, and alcohols. Amounts of these materials may range from 0.1 to 50%, and preferably, from 0.1 to 30%, and most preferably, from 1 to 20% by weight of the composition, including all ranges subsumed therein.
- Silicone oils may be divided into the volatile and non-volatile variety. The term
- volatile refers to those materials which have a measurable vapor pressure at ambient temperature. Volatile silicone oils are preferably chosen from cyclic or linear polydimethylsiloxanes containing from 3 to 9, and preferably, from 4 to 5 silicon atoms.
- Linear volatile silicone materials generally have viscosities of less than 5 centistokes at 25°C while cyclic materials typically have viscosities of less than 10 centistokes.
- Nonvolatile silicone oils useful as carrier material include polyalkyl siloxanes, polyalkylaryl siloxanes and polyether siloxane copolymers.
- the essentially non-volatile polyalkyl siloxanes useful herein include, for example, polydimethylsiloxanes (like
- esters are:
- Ether-esters such as fatty acid esters of ethoxylated fatty alcohols
- Polyhydric alcohol esters such as ethylene glycol mono- and di-fatty acid esters, diethylene glycol mono- and di-fatty acid esters, polyethylene glycol (200-6000) mono- and di-fatty acid esters, propylene glycol mono- and di-fatty acid esters, polypropylene glycol 2000 monooleate, polypropylene glycol 2000 monostearate, ethoxylated propylene glycol monostearate, glyceryl mono- and di-fatty acid esters, polyglycerol poly-fatty esters, ethoxylated glyceryl monostearate, 1 ,3-butylene glycol monostearate, 1 ,3-butylene glycol distearate, polyoxyethylene polyol fatty acid ester, sorbitan fatty acid esters, and polyoxyethylene sorbitan fatty acid esters; (4) Wax esters such as bees
- Sterol esters of which soya sterol and cholesterol fatty acid esters are examples thereof.
- Emulsifiers may be present in the composition of the present invention. Total concentration of the emulsifier may range from 0.1 to 40%, and preferably, from 1 to 20%, and most preferably, from 1 to 5% by weight of the composition, including all ranges subsumed therein.
- the emulsifier may be selected from the group consisting of anionic, nonionic, cationic and amphoteric actives.
- nonionic actives are those with a Ci 0 -C 2 o fatty alcohol or acid hydrophobe condensed with from 2 to 100 moles of ethylene oxide or propylene oxide per mole of hydrophobe; C 2 -Ci 0 alkyl phenols condensed with from 2 to 20 moles of alkylene oxide; mono- and di- fatty acid esters of ethylene glycol; fatty acid monoglyceride; sorbitan, mono- and di- C 8 -C 2 o fatty acids; and polyoxyethylene sorbitan as well as combinations thereof.
- Alkyl polyglycosides and saccharide fatty amides are also suitable nonionic emulsifiers.
- Preferred anionic emulsifiers include alkyl ether sulfate and sulfonates, alkyl sulfates and sulfonates, alkylbenzene sulfonates, alkyl and dialkyl sulfosuccinates, C 8 -C 2 o acyl isethionates, C 8 -C 20 alkyl ether phosphates, alkylethercarboxylat.es and combinations thereof.
- Cationic emulsifiers that may be used include, for example,
- palmitamidopropyltrimonium chloride distearyldimonium chloride and mixtures thereof.
- Useful amphoteric emulsifiers include cocoamidopropyl betaine, Ci 2 -C 20 trialkyl betaines, sodium lauroamphoacetate, and sodium laurodiamphoacetate or a mixture thereof.
- Other generally preferred emulsifiers include glyceryl stearate, glycol stearate, stearamide AMP, PEG-100 stearate, cetyl alcohol as well as emulsifying/thickening additives like hydroxyethylacrylate/sodium acryloyldimethyl taurates copolymer/squalane and mixtures thereof.
- Emulsion stabilizers generally classified as vegetable based liquids may also be used. Preferred stabilizers are sold under the name Oilwax LC and made available commercially by Lotioncrafter.
- Preservatives can desirably be incorporated into the compositions of this invention to protect against the growth of potentially harmful microorganisms.
- Suitable traditional preservatives for compositions of this invention are alkyl esters of para-hydroxybenzoic acid.
- Other preservatives which have more recently come into use include hydantoin derivatives, propionate salts, and a variety of quaternary ammonium compounds.
- Cosmetic chemists are familiar with appropriate preservatives and routinely choose them to satisfy the preservative challenge test and to provide product stability.
- preservatives are iodopropynyl butyl carbamate, phenoxyethanol, methyl paraben, propyl paraben, imidazolidinyl urea, sodium dehydroacetate and benzyl alcohol.
- the preservatives should be selected having regard for the use of the composition and possible incompatibilities between the preservatives and other ingredients in the emulsion.
- Preservatives are preferably employed in amounts ranging from 0.01 % to 2% by weight of the composition, including all ranges subsumed therein.
- Thickening agents may optionally be included in compositions of the present invention. Particularly useful are the polysaccharides. Examples include starches, natural/synthetic gums and cellulosics. Representative of the starches are chemically modified starches such as sodium hydroxypropyl starch phosphate and aluminum starch octenylsuccinate. Tapioca starch is often preferred. Suitable gums include xanthan, sclerotium, pectin, karaya, arabic, agar, guar, carrageenan, alginate and combinations thereof. Suitable cellulosics include hydroxypropyl cellulose, hydroxypropyl methylcellulose, ethylcellulose and sodium carboxy methylcellulose.
- Synthetic polymers are yet another class of effective thickening agent.
- This category includes crosslinked polyacrylates such as the Carbomers, polyacrylamides such as Sepigel® 305 and taurate copolymers such as Simulgel EG® and Aristoflex® AVC, the copolymers being identified by respective I NCI nomenclature as Sodium Acrylate/Sodium Acryloyldimethyl Taurate and Acryloyl Dimethyltaurate/Vinyl Pyrrolidone Copolymer.
- Another preferred synthetic polymer suitable for thickening is an acrylate-based polymer made commercially available by Seppic and sold under the name Simulgel INS100.
- Amounts of the thickener when used, may range from 0.001 to 5%, and preferably, from 0.1 to 3%, and most preferably, from 0.2 to 1.5% by weight of the composition including all ranges subsumed therein.
- Conventional humectants may be employed in the present invention. These are generally polyhydric alcohol-type materials.
- Typical polyhydric alcohols include glycerol (i.e., glycerine or glycerin), propylene glycol, dipropylene glycol, polypropylene glycol, polyethylene glycol, sorbitol, hydroxypropyl sorbitol, hexylene glycol, 1 ,3-butylene glycol, isoprene glycol, 1 ,2,6-hexanetriol, ethoxylated glycerol, propoxylated glycerol and mixtures thereof. Most preferred is glycerin, propylene glycol or a mixture thereof.
- the amount of humectant employed may range anywhere from 0.5 to 20%, preferably between 1 and 15% by weight of the composition.
- Fragrances, colorants, fixatives and abrasives may optionally be included in compositions of the present invention.
- Each of these substances may range from 0.05 to 5%, preferably between 0.1 and 3% by weight.
- actives suitable for use herein can include opacifiers like Ti0 2 and ZnO and colorants like iron oxide red, yellow and black.
- opacifiers and colorants typically have a particle size from 50 to 1200 nm, and preferably, from 50 to 350 nm.
- actives classified as cationic ammonium compounds may optionally be used in the compositions of this invention.
- Such compounds include salts of hydroxypropyltri (CrC 3 alkyl) ammonium mono-substituted-saccharide, salts of
- the cationic ammonium compound employed in this invention is the quaternary ammonium compound 1 ,2-dihydroxypropyltrimonium chloride. If used, such compounds typically make up from 0.01 to 30%, and preferably, from 0.1 to 15% by weight of the composition.
- moisturizing agents such as substituted ureas like hydroxymethyl urea, hydroxyethyl urea, hydroxypropyl urea; bis(hydroxymethyl) urea; bis(hydroxyethyl) urea; bis(hydroxypropyl) urea; ⁇ , ⁇ '-dihydroxymethyl urea; N,N'-di-hydroxyethyl urea; N,N'-di- hydroxypropyl urea; ⁇ , ⁇ , ⁇ '-tri-hydroxyethyl urea; tetra(hydroxymethyl) urea;
- moisturizing agents such as substituted ureas like hydroxymethyl urea, hydroxyethyl urea, hydroxypropyl urea; bis(hydroxymethyl) urea; bis(hydroxyethyl) urea; bis(hydroxypropyl) urea; ⁇ , ⁇ '-dihydroxymethyl urea; N,N'-di-hydroxyethyl urea;
- hydroxyethyl urea tetra (hydroxyethyl) urea; tetra(hydroxypropyl) urea; N-methyl-N'-hydroxyethyl urea; N-ethyl- N,N-N'-hydroxyethyl urea; N-hydroxypropyl-N'-hydroxyethyl urea and N,N'-dimethyl-N- hydroxyethyl urea or mixtures thereof.
- hydroxypropyl appears, the meaning is generic for either 3-hydroxy-n-propyl, 2-hydroxy-n-propyl, 3-hydroxy-i-propyl or 2-hydroxy-i- propyl radicals. Most preferred is hydroxyethyl urea. The latter is available as a 50% aqueous liquid from the National Starch & Chemical Division of ICI under the trademark Hydrovance.
- Amounts of substituted urea, when used, in the composition of this invention range from 0.01 to 20%, and preferably, from 0.5 to 15%, and most preferably, from 2 to 10% based on total weight of the composition and including all ranges subsumed therein.
- cationic ammonium compound and substituted urea in a most especially preferred embodiment at least from 1 to 15% glycerin external to the particle is used, based on total weight of the composition and including all ranges subsumed therein.
- compositions of the present invention may include vitamins as the desired active.
- Illustrative vitamins are Vitamin A (retinol) as well as retinol esters like retinol palmitate and retinol propionate, Vitamin B 2 , Vitamin B 3 (niacinamide), Vitamin B 6 , Vitamin C, Vitamin E, Folic Acid and Biotin.
- Derivatives of the vitamins may also be employed.
- Vitamin C derivatives include ascorbyl tetraisopalmitate, magnesium ascorbyl phosphate and ascorbyl glycoside.
- Derivatives of Vitamin E include tocopheryl acetate, tocopheryl palmitate and tocopheryl linoleate. DL-panthenol and derivatives may also be employed.
- Total amount of vitamins when present in compositions according to the present invention may range from 0.001 to 10%, preferably from 0.01 % to 1 %, optimally from 0.1 to 0.5% by weight of the composition.
- Octadecenedioic acid, azelaic acid, ubiquinone, dihydroxyacetone (DHA) and mixtures thereof may also be used as actives in the composition of this invention.
- Such compounds when used, typically make up from 0.2 to 4.5%, and preferably, from 0.5 to 3% by weight of the composition, including all ranges subsumed therein.
- resveratrol resorcinols like 4-ethyl resorcinol, 4-hexyl resorcinol, 4-phenylethyl resorcinol, dimethoxytoluyl propyl resorcinol, 4-cyclopentyl resorcinol, 4-cyclohexylresorcinol, alpha-an/or beta-hydroxyacids, petroselinic acid, conjugated linoleic acid, octadecanoic acid, phenylethyl resorcinol
- Desquamation promoters may be present.
- Illustrative are the alpha-hydroxycarboxylic acids, beta-hydroxycarboxylic acids.
- the term "acid” is meant to include not only the free acid but also salts and Ci-C 30 alkyl or aryl esters thereof and lactones generated from removal of water to form cyclic or linear lactone structures.
- Representative acids are glycolic and its derivatives, lactic and malic acids.
- Salicylic acid is representative of the beta- hydroxycarboxylic acids. Amounts of these materials when present may range from 0.01 to 15% by weight of the composition.
- compositions of this invention may optionally be included as actives in compositions of this invention.
- the extracts may either be water soluble or water-insoluble carried in a solvent which respectively is hydrophilic or hydrophobic. Water and ethanol are the preferred extract solvents.
- Illustrative extracts include those from green tea, yarrow, chamomile, licorice, aloe vera, grape seed, citrus unshui, willow bark, sage, thyme and rosemary. Soy extracts may be used and especially when it is desirable to include retinol.
- Also optionally suitable for use include materials like chelators (e.g., EDTA), C 8- 22 fatty acid substituted saccharides, lipoic acid, retinoxytnmethylsilane (available from Clariant Corp. under the Silcare 1 M-75 trademark), dehydroepiandrosterone (DHEA) and combinations thereof.
- Ceramides including Ceramide 1 , Ceramide 3, Ceramide 3B and Ceramide 6) as well as pseudoceramides may also be useful.
- Occlusives like Oilwax LC are often desired. Amounts of these materials may range from 0.000001 to 10%, preferably from 0.0001 to 1 % by weight of the composition.
- Sunscreen actives may also be included in compositions of the present invention and carried by the particle comprising hydrophobic material as described herein. Particularly preferred are such materials as phenylbenzimidazole sulfonic acid (Ensulizole), ethylhexyl p- methoxycinnamate, available as Parsol MCX®, Avobenzene, available as Parsol 1789® and benzophenone-3, also known as Oxybenzone.
- Inorganic sunscreen actives may be employed such as microfine titanium dioxide, zinc oxide, polyethylene and various other polymers. Also suitable for use is octocrylene. Amounts of the sunscreen agents when present may generally range from 0.1 to 30%, preferably from 0.5 to 20%, optimally from 0.75 to 10% by weight.
- the pH of the composition of this invention is from 4 to 8, and preferably, from 4.25 to 7.75, and most preferably, from 6 to 7.5, including all ranges subsumed therein.
- the composition of this invention may be a solid stick or bar. Viscosity of the composition of this invention is, however, preferably from 1 ,000 to 120,000 cps, and most preferably, from 5,000 to 80,000 cps, taken at ambient temperature NS and a shear rate of 1 s "1 with a strain controlled parallel plate rheometer made
- actives like dihydroxyacetone, colorants such as metal oxides, vitamins (e.g., niacinamide) and/or substituted ureas are homogeneously mixed within the particle comprising hydrophobic material.
- the active homogeneously mixed within the particle comprising hydrophobic material is metal oxide like an iron oxide.
- Packaging can be employed to store and deliver the composition of this invention.
- Packaging is often dependent upon the type of personal care end-use.
- leave-on skin lotions and creams, shampoos, conditioners and shower gels generally employ plastic containers with an opening at a dispensing end covered by a closure.
- Typical closures are screw-caps, non-aerosol pumps and flip-top hinged lids.
- Packaging for antiperspirants, deodorants and depilatories may involve a container with a roll- on ball on a dispensing end.
- these types of personal care products may be delivered in a stick composition formulation in a container with propel-repel mechanism where the stick moves on a platform towards a dispensing orifice.
- Metallic cans pressurized by a propellant and having a spray nozzle serve as packaging for antiperspirants, shave creams and other personal care products.
- Toilette bars may have packaging constituted by a cellulosic or plastic wrapper or within a cardboard box or even encompassed by a shrink wrap plastic film.
- Baycusan-C1004 made available by Bayer Material Science.
- water and water soluble and dispersible ingredients were thoroughly mixed as were oil and oil soluble and dispersible ingredients to produce water phases and oil phases. Heat was used but no phases were heated above about 70°C and dihydroxyacetone and fragrance were not added until cooling to about 35°C was achieved.
- the oil phases for each sample were added to the water phases for each sample and thoroughly mixed in the presence of emulsifier. Produced were oil-in-water emulsions.
- Particles with optional active were made by combining petrolatum and active (i.e., iron oxide red, yellow and black). Moderate stirring was used and the particle/active phases were heated to about 50°C.
- homogeneous mixtures of petrolatum and iron oxide were obtained.
- the homogeneous mixtures of petrolatum and iron oxide were maintained at a temperature of about 48°C and the same were added to emulsion at a temperature of about 33°C.
- Conventional stirring was employed to combine emulsion and homogeneous mixture wherein the resulting emulsions having aqueous-based resin in the aqueous phase and particle comprising hydrophobic material and active in the oil phase were produced with particle having a diameter of about 200 microns.
- the control composition was deplete of aqueous-based film forming resin.
- Example 1 The samples of Example 1 were assessed for rub-off and visually observed for evenness of application. The surprising results obtained may be found in the table below.
- Delta E * color difference, was obtained after samples were applied to artificial skin substrates (23 cm x 7cm) with the finger and rubbed for 60 seconds.
- a film applicator (1 u) was run through the surface to make a 25 urn thick film.
- the substrate selected was solid grip liner, 2mm thick, soft, visco- elastic and hydrophobic.
- compositions made consistent with this invention unexpectedly resulted in even deposition and low rub-off characteristics, notwithstanding the fact that aqueous-based film forming resin was used in a water phase of an emulsion and particle comprising hydrophobic material was used in the oil phase of the emulsion. Moreover, subsequent to visual inspection the compositions made consistent with this invention were surprisingly easily washed off but did not peel off during normal activity.
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Priority Applications (3)
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JP2014541686A JP6349258B2 (ja) | 2011-11-18 | 2012-11-16 | 付着が均一で摩擦落ちが少ない組成物 |
CN201280056718.1A CN103945823B (zh) | 2011-11-18 | 2012-11-16 | 包含成膜树脂的均匀沉积和低擦除性乳液 |
IN857MUN2014 IN2014MN00857A (enrdf_load_stackoverflow) | 2011-11-18 | 2012-11-16 |
Applications Claiming Priority (4)
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US201161561307P | 2011-11-18 | 2011-11-18 | |
US61/561,307 | 2011-11-18 | ||
US13/622,636 US20140079744A1 (en) | 2012-09-19 | 2012-09-19 | Even Deposition and Low Rub-Off Compositions |
US13/622,636 | 2012-09-19 |
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WO2013072488A2 true WO2013072488A2 (en) | 2013-05-23 |
WO2013072488A3 WO2013072488A3 (en) | 2013-08-15 |
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PCT/EP2012/072894 WO2013072488A2 (en) | 2011-11-18 | 2012-11-16 | Even deposition and low rub-off compositions |
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JP (1) | JP6349258B2 (enrdf_load_stackoverflow) |
CN (1) | CN103945823B (enrdf_load_stackoverflow) |
IN (1) | IN2014MN00857A (enrdf_load_stackoverflow) |
WO (1) | WO2013072488A2 (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2024200959A1 (fr) * | 2023-03-30 | 2024-10-03 | Lvmh Recherche | Composition cosmetique comprenant un melange elastique a base d'amidon naturel, de polyurethane et de polyol |
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US20090155321A1 (en) | 2007-12-12 | 2009-06-18 | Conopco, Inc., D/B/A Unilever | Compositions with encapsulated coloring agents and method to impart a healthy skin appearance |
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JP4170106B2 (ja) * | 2003-02-04 | 2008-10-22 | 花王株式会社 | 多孔性粒子及び化粧料 |
JP4866066B2 (ja) * | 2005-11-18 | 2012-02-01 | 花王株式会社 | 化粧料 |
US20070231355A1 (en) * | 2006-01-23 | 2007-10-04 | L'oreal | Cosmetic composition comprising multiphasic particles |
US9993403B2 (en) * | 2007-12-20 | 2018-06-12 | Avon Products, Inc. | Cosmetic compositions for imparting superhydrophobic films |
US8772212B2 (en) * | 2008-08-07 | 2014-07-08 | Conopco, Inc. | Liquid personal cleansing composition |
JP5455168B2 (ja) * | 2009-01-15 | 2014-03-26 | コニシ株式会社 | 化粧料 |
ES2728959T3 (es) * | 2009-12-18 | 2019-10-29 | Oreal | Máscara de pestañas que contiene una dispersión acuosa de poliuretano y una cera dura |
EP2525772A4 (en) * | 2010-01-19 | 2015-04-01 | Elc Man Llc | COMPOSITE MATERIALS, COMPOSITIONS AND METHODS |
WO2011129804A1 (en) * | 2010-04-12 | 2011-10-20 | Cockerell Dermatology Development, Ltd. | Spf liquid cleansing compositions |
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2012
- 2012-11-16 IN IN857MUN2014 patent/IN2014MN00857A/en unknown
- 2012-11-16 WO PCT/EP2012/072894 patent/WO2013072488A2/en active Application Filing
- 2012-11-16 CN CN201280056718.1A patent/CN103945823B/zh not_active Expired - Fee Related
- 2012-11-16 JP JP2014541686A patent/JP6349258B2/ja not_active Expired - Fee Related
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US3388087A (en) | 1962-10-26 | 1968-06-11 | Bayer Ag | Aqueous dispersions of quaternized polyurethanes |
US3310416A (en) | 1963-02-27 | 1967-03-21 | Ciba Ltd | Aqueous dispersions |
US3905929A (en) | 1973-03-23 | 1975-09-16 | Bayer Ag | Aqueous dispersions of polyurethane having side chain polyoxyethylene units |
US20030021815A9 (en) | 2000-09-28 | 2003-01-30 | Jean Mondet | Cosmetic compositions comprising at least one continuous liquid fatty phase structured with polyurethanes, polyurethaneureas, and polyureas |
US20090155321A1 (en) | 2007-12-12 | 2009-06-18 | Conopco, Inc., D/B/A Unilever | Compositions with encapsulated coloring agents and method to impart a healthy skin appearance |
US20090155373A1 (en) | 2007-12-12 | 2009-06-18 | Conopco, Inc., D/B/A Unilever | Cosmetic compositions and method which impart a healthy appearance to skin |
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WO2024200959A1 (fr) * | 2023-03-30 | 2024-10-03 | Lvmh Recherche | Composition cosmetique comprenant un melange elastique a base d'amidon naturel, de polyurethane et de polyol |
FR3147105A1 (fr) * | 2023-03-30 | 2024-10-04 | Lvmh Recherche | Composition cosmétique comprenant un mélange élastique à base d’amidon naturel, de polyuréthane et de polyol |
Also Published As
Publication number | Publication date |
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CN103945823A (zh) | 2014-07-23 |
JP6349258B2 (ja) | 2018-06-27 |
IN2014MN00857A (enrdf_load_stackoverflow) | 2015-04-17 |
CN103945823B (zh) | 2017-10-20 |
JP2015502929A (ja) | 2015-01-29 |
WO2013072488A3 (en) | 2013-08-15 |
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