AU2000254575B2 - Water-in-oil emulsified make-up composition - Google Patents
Water-in-oil emulsified make-up composition Download PDFInfo
- Publication number
- AU2000254575B2 AU2000254575B2 AU2000254575A AU2000254575A AU2000254575B2 AU 2000254575 B2 AU2000254575 B2 AU 2000254575B2 AU 2000254575 A AU2000254575 A AU 2000254575A AU 2000254575 A AU2000254575 A AU 2000254575A AU 2000254575 B2 AU2000254575 B2 AU 2000254575B2
- Authority
- AU
- Australia
- Prior art keywords
- oil
- water
- composition according
- composition
- volatile
- 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.)
- Ceased
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- 239000000203 mixture Substances 0.000 title claims description 92
- -1 isodecly isonoanoate Chemical compound 0.000 claims description 35
- 239000004094 surface-active agent Substances 0.000 claims description 33
- 239000003921 oil Substances 0.000 claims description 29
- 239000007787 solid Substances 0.000 claims description 26
- 239000000049 pigment Substances 0.000 claims description 25
- 239000000346 nonvolatile oil Substances 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- 229920002545 silicone oil Polymers 0.000 claims description 17
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 239000011570 nicotinamide Substances 0.000 claims description 10
- 229960003966 nicotinamide Drugs 0.000 claims description 10
- 235000005152 nicotinamide Nutrition 0.000 claims description 10
- 239000003906 humectant Substances 0.000 claims description 7
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 claims description 6
- 238000002844 melting Methods 0.000 claims description 6
- 230000008018 melting Effects 0.000 claims description 6
- NRLLZRJXDKUVHM-UHFFFAOYSA-N tridecyl 7-methyloctanoate Chemical compound CCCCCCCCCCCCCOC(=O)CCCCCC(C)C NRLLZRJXDKUVHM-UHFFFAOYSA-N 0.000 claims description 6
- ASKIVFGGGGIGKH-UHFFFAOYSA-N 2,3-dihydroxypropyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(O)CO ASKIVFGGGGIGKH-UHFFFAOYSA-N 0.000 claims description 5
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- CUNWUEBNSZSNRX-RKGWDQTMSA-N (2r,3r,4r,5s)-hexane-1,2,3,4,5,6-hexol;(z)-octadec-9-enoic acid Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O CUNWUEBNSZSNRX-RKGWDQTMSA-N 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- FGUZFFWTBWJBIL-XWVZOOPGSA-N [(1r)-1-[(2s,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)O[C@H](CO)[C@H]1OC[C@H](O)[C@H]1O FGUZFFWTBWJBIL-XWVZOOPGSA-N 0.000 claims description 4
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 claims description 4
- OQILCOQZDHPEAZ-UHFFFAOYSA-N octyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCCCCCC OQILCOQZDHPEAZ-UHFFFAOYSA-N 0.000 claims description 4
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- 229960005078 sorbitan sesquioleate Drugs 0.000 claims description 3
- DRAWQKGUORNASA-UHFFFAOYSA-N (2-hydroxy-3-octadec-9-enoyloxypropyl) octadec-9-enoate Chemical compound CCCCCCCCC=CCCCCCCCC(=O)OCC(O)COC(=O)CCCCCCCC=CCCCCCCCC DRAWQKGUORNASA-UHFFFAOYSA-N 0.000 claims description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 2
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- GLXBPZNFNSLJBS-UHFFFAOYSA-N 11-methyldodecyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCCCCCCCCCCC(C)C GLXBPZNFNSLJBS-UHFFFAOYSA-N 0.000 claims description 2
- OUZOBPPZPCBJAR-UHFFFAOYSA-N 14-methylpentadecyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCC(C)C OUZOBPPZPCBJAR-UHFFFAOYSA-N 0.000 claims description 2
- YICVJSOYNBZJAK-UHFFFAOYSA-N 14-methylpentadecyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCC(C)C YICVJSOYNBZJAK-UHFFFAOYSA-N 0.000 claims description 2
- ABEXEQSGABRUHS-UHFFFAOYSA-N 16-methylheptadecyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC(C)C ABEXEQSGABRUHS-UHFFFAOYSA-N 0.000 claims description 2
- SAMYFBLRCRWESN-UHFFFAOYSA-N 16-methylheptadecyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCC(C)C SAMYFBLRCRWESN-UHFFFAOYSA-N 0.000 claims description 2
- UIVPNOBLHXUKDX-UHFFFAOYSA-N 3,5,5-trimethylhexyl 3,5,5-trimethylhexanoate Chemical compound CC(C)(C)CC(C)CCOC(=O)CC(C)CC(C)(C)C UIVPNOBLHXUKDX-UHFFFAOYSA-N 0.000 claims description 2
- KUCCCVXLSQTKHH-UHFFFAOYSA-N 8-methylnonyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCCCCCC(C)C KUCCCVXLSQTKHH-UHFFFAOYSA-N 0.000 claims description 2
- ONJPCDHZCFGTSI-NJYHNNHUSA-N CC(C)CCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCC(C)C)[C@H]1OC[C@H](O)[C@H]1O Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCC(C)C)[C@H]1OC[C@H](O)[C@H]1O ONJPCDHZCFGTSI-NJYHNNHUSA-N 0.000 claims description 2
- NCHJGQKLPRTMAO-XWVZOOPGSA-N [(2R)-2-[(2R,3R,4S)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NCHJGQKLPRTMAO-XWVZOOPGSA-N 0.000 claims description 2
- TTZKGYULRVDFJJ-GIVMLJSASA-N [(2r)-2-[(2s,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-[(z)-octadec-9-enoyl]oxyethyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1O TTZKGYULRVDFJJ-GIVMLJSASA-N 0.000 claims description 2
- LDDUCKDUDZVHLN-UHFFFAOYSA-N [2-hydroxy-3-[2-hydroxy-3-(16-methylheptadecanoyloxy)propoxy]propyl] 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(O)COCC(O)COC(=O)CCCCCCCCCCCCCCC(C)C LDDUCKDUDZVHLN-UHFFFAOYSA-N 0.000 claims description 2
- GORMSINSWZJIKL-UHFFFAOYSA-N [3-(2-ethylhexanoyloxy)-2,2-dimethylpropyl] 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)OCC(C)(C)COC(=O)C(CC)CCCC GORMSINSWZJIKL-UHFFFAOYSA-N 0.000 claims description 2
- DWMMZQMXUWUJME-UHFFFAOYSA-N hexadecyl octanoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)CCCCCCC DWMMZQMXUWUJME-UHFFFAOYSA-N 0.000 claims description 2
- 229940078568 isocetyl myristate Drugs 0.000 claims description 2
- 229940100554 isononyl isononanoate Drugs 0.000 claims description 2
- 229940093629 isopropyl isostearate Drugs 0.000 claims description 2
- 229940074928 isopropyl myristate Drugs 0.000 claims description 2
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 claims description 2
- 229940060384 isostearyl isostearate Drugs 0.000 claims description 2
- 229940113915 isostearyl palmitate Drugs 0.000 claims description 2
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- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 claims description 2
- BFZNCPXNOGIELB-UHFFFAOYSA-N propan-2-yl 10-[5,6-dihexyl-2-(8-oxo-8-propan-2-yloxyoctyl)cyclohex-3-en-1-yl]dec-9-enoate Chemical compound CCCCCCC1C=CC(CCCCCCCC(=O)OC(C)C)C(C=CCCCCCCCC(=O)OC(C)C)C1CCCCCC BFZNCPXNOGIELB-UHFFFAOYSA-N 0.000 claims description 2
- NEOZOXKVMDBOSG-UHFFFAOYSA-N propan-2-yl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OC(C)C NEOZOXKVMDBOSG-UHFFFAOYSA-N 0.000 claims description 2
- 239000001593 sorbitan monooleate Substances 0.000 claims description 2
- 235000011069 sorbitan monooleate Nutrition 0.000 claims description 2
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- 239000000463 material Substances 0.000 description 13
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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
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
- A61K8/894—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
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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
-
- 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
- A61K8/064—Water-in-oil emulsions, e.g. Water-in-silicone 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
- A61K8/18—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
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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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
WO 01/91704 PCT/US00/15164 WATER-IN-OIL EMULSIFIED MAKE-UP COMPOSITION FIELD OF THE INVENTION The present invention relates to make-up compositions which have a water-in-oil emulsion phase type. Specifically, the present invention relates to make-up compositions which have specified levels of components which provide the benefits of both a solid foundation and a liquid foundation. The present invention also relates to make-up compositions containing water-soluble skin treatment agents such as niacinamide.
BACKGROUND
A foundation composition can be applied to the face and other parts of the body to even skin tone and texture and to hide pores imperfections, fine lines and the like. A foundation composition is also applied to moisturize the skin, to 2o balance the oil level of the skin, and to provide protection against the adverse effects of sunlight, wind, and other environmental factors.
Foundation compositions are generally available in the form of liquid or cream suspensions, emulsions, gels, pressed powders or anhydrous oil and wax compositions. Emulsion-type foundations in the form of liquid are suitable in that they provide moisturizing effects by the water and water-soluble skin treatment agents incorporated. These liquid form foundations, however, are less convenient to use- and carry for the consumer. On the other hand, solid foundations packaged in compacts are suitable for use by the consumer, however, are typically less efficient than liquid form foundations in terms of moisturizing the skin and coverage of the skin.
Foundation compositions in the form of solid, yet water-in-oil emulsion have been suggested. Such emulsion solid foundations can been filled in a wide variety of packaging, including compacts, and is increasing popularity among Asian consumers. References which disclose such foundation compositions are JPA 2-88511, 3-261707, and USP 5,362,482. While such emulsion solid foundations have been successful in meeting the drawbacks of conventional 1 2 liquid form foundations and solid foundations to a certain degree, further improvement is desired. For example, it is known that by increasing the level of water and components intended to moisturize the skin, the fresh and light feel to the skin may be deteriorated. In another example, it is known that, by increasing components which provide smoothness and good spreadability upon application, the appearance on the skin may become powdery. Further, while addressing the desired improvements, the foundation product must be stable during a typical shelf-life of these foundations, and capable of being manufactured at a reasonable cost.
Based on the foregoing, there is a need for a make-up composition which is solid in ambient temperature, provide improved moisturizing benefit to the skin, yet also provide good spreadability to the skin and leave the skin with a fresh and light feel.
The discussion of documents, acts, materials, devices, articles and the like is included in this specification solely for the purpose of providing a context for the present invention. It is not suggested or represented that any or all of these matters formed part of the prior art base or were common general knowledge in the field relevant to the present invention as it existed in Australia before the priority date of each claim of this application.
Throughout the description and claims of the specification, the word "comprise" and variations of the word, such as "comprising" and "comprises", is not intended to exlude other additives, components, integers or steps.
SUMMARY
The present invention is directed to a water-in-oil emulsified make-up composition comprising by weight: from about 25% to about 40% of a volatile silicone oil; from about 0.5% to about 8% of a non-volatile oil; from about 1% to about 5% of a solid wax; from about 1% to about 5% of a lipophilic surfactant having an HLB of less than about 8; from about 25% to about 35% of hydrophobically treated pigments; and water in an amount such that the total of the volatile silicone oil and water is at least about P:\UseNluieU2000254575 Amend Spec.doc 2a which satisfies the need for a make-up composition which is solid in ambient temperature, provide improved moisturizing benefit to the skin, yet also provide good spreadability to the skin and leave the skin with a fresh and light feel.
In one aspect, the present invention provides a water-in-oil emulsified make-up composition comprising by weight: from 25% to 40% of a volatile silicone oil; from 0.5% to 8% of a non-volatile oil; from 2% to 4% of a solid wax; from 1% to 5% of a lipophilic surfactant having an HLB of less than 8; from 25% to 35% of hydrophobically treated pigments; and water in an amount such that the total of the volatile silicone oil and water is at least These and other features, aspects, and advantages of the present invention will become evident to those skilled in the art from a reading of the present disclosure with the appended claims.
DETAILED DESCRIPTION The following is a list of definitions for terms used herein.
P:\UserJulie2000254575 Amend Speci.doc WO 01/91704 PCT/US00/15164 "Comprising" means that other steps and other ingredients which do not affect the end result can be added. This term encompasses the terms "consisting of" and "consisting essentially of'.
All percentages are by weight of total composition unless specifically stated otherwise.
All cited references are incorporated herein by reference in their entireties.
Citation of any reference is not an admission regarding any determination as to its availability as prior art to the claimed invention.
All ratios are weight ratios unless specifically stated otherwise.
The present invention, in its product and process aspects, is described in detail as follows.
VOLATILE SILICONE OIL The composition of the present invention comprises a volatile silicone oil by weight of the entire composition at from about 25% to about 40%, preferably 30% to about 40%. The amount of the volatile silicone oil is controlled so that the total of the volatile silicone oil and water is more than about 50% of the entire composition. Without being bound by theory, the species and levels of the volatile silicone oil herein is believed to provide improved refreshing and light feeling to the skin, without necessarily leaving a dried feeling to the skin.
The volatile silicone oil useful herein are selected from those having a boiling point of from about 60 to about 2600C, preferably those having from 2 to 7 silicon atoms.
The volatile silicone oils useful herein include polyalkyl or polyaryl siloxanes with the following structure R93 R 9 3 R93 1 I I I 8
Z
8 -Si-O Si-O Si-Z 193 L93 P 93 R R R (1) wherein R 9 3 is independently alkyl or aryl, and p is an integer from about 0 to about 5. Z a represents groups which block the ends of the silicone chains.
Preferably, R 9 3 groups include methyl, ethyl, propyl, phenyl, methylphenyl and phenylmethyl, Z 8 groups include hydroxy, methyl, methoxy, ethoxy, propoxy, and aryloxy. More preferably, R 9 3 groups and Z 8 groups are methyl groups. The preferred volatile silicone compounds are hexamethyldisiloxane, octamethyltrisiloxane, decamethyltetrasiloxane, hexadecamethylheptasiloxane.
WO 01/91704 PCT/US00/15164 Commercially available volatile silicone compounds useful herein include octamethyltrisiloxane with tradename SH200C-1cs, decamethyltetrasiloxane with tradename SH200C-1.5cs, hexadecamethylheptasiloxane with tradename SH200C-2cs, all available from Dow Corning.
The volatile silicone oils useful herein also include a cyclic silicone compound having the formula: 93
R
R
wherein R 9 3 is independently alkyl or aryl, and n is an integer of from 3 to 7.
Preferably, R93 groups include methyl, ethyl, propyl, phenyl, methylphenyl and phenylmethyl. More preferably, R 9 3 groups are methyl groups. The preferred volatile silicone compounds are octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, tetradecamethylcyclohexasiloxane.
Commercially available volatile silicone compounds useful herein include octamethylcyclotetrasiloxane with tradename SH244, decamethylcyclopentasiloxane with tradename DC245 and SH245, and dodeamethylcyclohexasiloxane with tradename DC246; all available from Dow Corning.
NON-VOLATILE OIL The composition of the present invention comprises a non-volatile oil by weight of the entire composition at from about 0.5% to about preferably 2% to about The amount of the non-volatile oil is controlled so that the ratio of 1) the total of the non-volatile oil, the solid wax, and the lipophilic surfactant; and 2) the hydrophobically treated pigments is from about 1 7 to about 1 preferably from about 1 5 to about 1 2, more preferably from about 1 5 to about 1 2.5. Without being bound by theory, the species and levels of the nonvolatile oil herein is believed to provide improved smoothness to the skin, and also alleviate the powdery look often found when pigments are included at a high level.
Non-volatile oils useful herein are, for example, tridecyl isononanoate, isostearyl isostearate, isocetyl isosteatrate, isopropyl isostearate, isodecyl isonoanoate, cetyl octanoate, isononyl isononanoate, diisopropyl myristate, WO 01/91704 PCT/US00/15164 isocetyl myristate, isotridecyl myristate, isopropyl myristate, isostearyl palmitate, isocetyl palmitate, isodecyl palmitate, isopropyl palmitate, octyl palmitate, caprylic/capric acid triglyceride, glyceryl tri-2-ethylhexanoate, neopentyl glycol di(2-ethyl hexanoate), diisopropyl dimerate, tocopherol, tocopherol acetate, avocado oil, camellia oil, turtle oil, macadamia nut oil, corn oil, mink oil, olive oil, rapeseed oil, eggyolk oil, sesame oil, persic oil, wheat germ oil, pasanqua oil, castor oil, linseed oil, safflower oil, cotton seed oil, perillic oil, soybean oil, peanut oil, tea seed oil, kaya oi., rice bran oil, china paulownia oi., Japanese paulownia oil, jojoba oil, rice germ oil, glycerol trioctanate, glycerol triisopalmiatate, trimethylolpropane triisostearate, isopropyl myristate, glycerol tri-2ethylhexanoate, pentaerythritol tetra-2-ethylhexanoate, lanolin, liquid lanolin, liquid paraffin, squalane, vaseline, and mixtures thereof. Commercially available oils include, for example, tridecyl isononanoate with tradename Crodamol TN available from Croda, Hexalan available from Nisshin Seiyu, and tocopherol acetates available from Eisai.
Non-volatile oils useful herein also include polyalkyl or polyaryl siloxanes with the following structure (I)
R
93
R
93
R
93 8 I 8 Z-Si- Si-O- Si- 193 193 p 93 R R R wherein R 93 is alkyl or aryl, and p is an integer from about 7 to about 8,000. Z 8 represents groups which block the ends of the silicone chains. The alkyl or aryl groups substituted on the siloxane chain (R 9 3 or at the ends of the siloxane chains Z 8 can have any structure as long as the resulting silicone remains fluid at room temperature, is dispersible, is neither irritating, toxic nor otherwise harmful when applied to the skin, is compatible with the other components of the composition, and is chemically stable under normal use and storage conditions.
Suitable Z 8 groups include hydroxy, methyl, methoxy, ethoxy, propoxy, and aryloxy. The two R 9 3 groups on the silicon atom may represent the same group or different groups. Preferably, the two R 9 3 groups represent the same group.
Suitable R 93 groups include methyl, ethyl, propyl, phenyl, methylphenyl and phenylmethyl. The preferred silicone compounds are polydimethylsiloxane, polydiethylsiloxane, and polymethylphenylsiloxane. Polydimethylsiloxane, which is also known as dimethicone, is especially preferred. The polyalkylsiloxanes that can be used include, for example, polydimethylsiloxanes. These silicone WO 01/91704 PCT/US00/15164 compounds are available, for example, from the General Electric Company in their Viscasil® and SF 96 series, and from Dow Coming in their Dow Corning 200 series.
Polyalkylaryl siloxane fluids can also be used and include, for example, polymethylphenylsiloxanes. These siloxanes are available, for example, from the General Electric Company as SF 1075 methyl phenyl fluid or from Dow Coming as 556 Cosmetic Grade Fluid.
Non-volatile oils also useful herein are the various grades of mineral oils.
Mineral oils are liquid mixtures of hydrocarbons that are obtained from petroleum. Specific examples of suitable hydrocarbons include paraffin oil, mineral oil, dodecane, isododecane, hexadecane, isohexadecane, eicosene, isoeicosene, tridecane, tetradecane, polybutene, polyisobutene, and mixtures thereof.
Non-volatile oils particularly useful herein are those which have relatively low viscosity. Such low viscosity non-volatile oils are believed to enhance the fresh and light feel when the composition is applied to the skin.
SOLID WAX The composition of the present invention comprises a solid wax by weight of the entire composition at from about 1% to about preferably 2% to about The amount of the solid wax is controlled so that the ratio of 1) the total of the non-volatile oil, the solid wax, and the lipophilic surfactant; and 2) the hydrophobically treated pigments is from about 1 7 to about 1 1.5, preferably from about 1 5 to about 1 2, more preferably from about 1 5 to about 1 Without being bound by theory, the species and levels of the solid wax herein is believed to provide consistency to the composition and coverage to the skin, while not negatively contributing to the spreadability upon application to the skin, and fresh and light feel of the skin.
The solid waxes useful herein are paraffin wax, microcrystalline wax, ozokerite was, ceresin wax, carnauba wax, candellila wax, eicosanyl behenate, and mixtures thereof. A mixture of waxes is preferably used.
Commercially available solid waxes useful herein include: Candelilla wax NC-1630 available from Noda wax, Ozokerite wax SP-1021 available from Strahl Pitsh, and Eicosanyl behenate available from Cas Chemical.
LIPOPHILIC SURFACTANT The composition of the present invention comprises a lipophilic surfactant by weight of the entire composition at from about 1% to about preferably 1% 6 WO 01/91704 PCT/US00/15164 to about The lipophilic surfactant herein has an HLB value of less than about 8.
The HLB value is a theoretical index value which describes the hydrophilicity-hydrophobicity balance of a specific compound. Generally, it is recognized that the HLB index ranges from 0 (very hydrophobic) to 40 (very hydrophilic). The HLB value of the lipophilic surfactants may be found in tables and charts known in the art, or may be calculated with the following general equation: HLB 7 (hydrophobic group values) (hydrophilic group values).
The HLB and methods for calculating the HLB of a compound are explained in detail in "Surfactant Science Series, Vol. 1: Nonionic Surfactants", pp 606-13, M.
J. Schick (Marcel Dekker Inc., New York, 1966).
The amount of the lipophilic surfactant is controlled so that the ratio of 1) the total of the non-volatile oil, the solid wax, and the lipophilic surfactant; and 2) the hydrophobically treated pigments is from about 1 7 to about 1 preferably from about 1 5 to about 1 2, more preferably from about 1 5 to about 1 2.5. Without being bound by theory, the species and levels of the lipophilic surfactant herein is believed to provide a stable water-in-oil emulsion in view of the other components of the present invention.
The lipophilic surfactant can be an ester-type surfactant. Ester-type surfactants useful herein include: sorbitan monoisostearate, sorbitan diisostearate, sorbitan sesquiisostearate, sorbitan monooleate, sorbitan dioleate, sorbitan sesquioleate, glyceryl monoisostearate, glyceryl diiostearate, glyceryl sesquiisostearate, glyceryl monooleate, glyceryl dioleate, glyceryl sesquioleate, diglyceryl diisostearate, diglyceryl dioleate, diglycerin monoisostearyl ether, diglycerin diisostearyl ether, and mixtures thereof.
Commercially available ester-type surfactants are, for example, sorbitan isostearate having a tradename Crill 6 available from Croda, and sorbitan sesquioleate with tradename Arlacel 83 available from Kao Atras.
The lipophilic surfactant can be a silicone-type surfactant. Silicone-type surfactants useful herein are as shown below, and mixtures thereof.
dimethicone copolyols having the structure: WO 01/91704 PCT/US00/15164
-CH
3
I
(CH3)3SiO Si(CHa)2Ux Si-O-- Si(CHa)3
I
03H6
(C
2 H40)a(C3H60)b- H wherein x is an integer from 5 to 100, y is an integer from 1 to 50, a is zero or greater, b is zero or greater, the average sum of a+b being 1-100.
(ii) dimethicone copolyols having the structure:
CH
3
CH
3
CH
3 R- 0-(C3H70)-(C2H40)-{CH2)3 Si- 0- Si 0- S CH 2 3 -(OCZH4OCH R
CH
3
CH
3 CH3 wherein R is selected from the group consisting of hydrogen, methyl, and combinations thereof, m is an integer from 5 to 100, x is independently zero or greater, y is independently zero or greater, the sum of x+y being 1-100.
Commercially available silicone-type surfactants are, for example, DC5225C, BY22-012, BY22-008, SH3746M, SH3771M, SH3772M, SH3773M, SH3775M, SH3748, SH3749, and DC5200, all available from Dow Corning.
In a preferred embodiment, the lipophilic surfactant is a mixture of at least one ester-type surfactant and at least one silicone-type surfactant to provide a stable emulsion for the other essential components of the present invention.
HYDROPHOBICALLY TREATED PIGMENTS The composition of the present invention comprises a hydrophobically treated pigment by weight of the entire composition at from about 25% to about preferably from about 25% to about 30%. The amount of the hydrophobically treated pigment is controlled so that the ratio of 1) the total of the non-volatile oil, the solid wax, and the lipophilic surfactant; and 2) the hydrophobically treated pigments is from about 1 7 to about 1 1.5, preferably from about 1 5 to about 1 2, more preferably from about 1 5 to about 1 Without being bound by theory, the species and levels of the hydrophobically treated pigment herein is believed to provide good wear performance, and is stable in the composition as being stable in the oily continuous phase.
WO 01/91704 PCT/US00/15164 The hydrophobically treated pigments are selected depending on the desired characteristic of the product, for example, shade, coverage, UV protection benefit, and various skin feel.
The base material useful for the hydrophobically treated pigments herein are clay mineral powders such as talc, mica, sericite, silica, magnesium silicate, synthetic fluorphlogopite, calcium silicate, aluminum silicate, bentonite and montomorilonite; pearl pigments such as alumina, barium sulfate, calcium secondary phosphate, calcium carbonate, titanium oxide, finely divided titanium oxide, zirconium oxide, zinc oxide, hydroxy apatite, iron oxide, iron titate, ultramarine blue, Prussian blue, chromium oxide, chromium hydroxide, cobalt oxide, cobalt titanate, titanium oxide coated mica; organic powders such as polyester, polyethylene, polystyrene, methyl metharylate resin, cellulose, 12nylon, 6-nylon, styrene-acrylic acid copolymers, poly proprylene, vinyl chloride polymer, tetrafluoroethylene polymer, boron nitride, fish scale guanine, laked tar color dyes, and laked natural color dyes. Such base material are treated with a hydrophobical treatment agent, including: silicone such as Methicone, Dimethicone and perfluoroalkylsilane; fatty material such as stearic acid; metal soap such as aluminium dimyristate; aluminium hydrogenated tallow glutamate, hydrogenated lecithin, lauroyl lysine, aluminium salt of perfluoroalkyl phosphate, and mixtures thereof.
A certain percentage of spherical pigments can be used. In a preferred embodiment, the hydrophobically treated pigments are also selected depending on the oil absorbing capability of the pigments. In one preferred embodiment, pigments having high oil absorbing capability and those having low oil absorbing capability are combined.
WATER
The composition of the present invention comprises water in an amount such that the total of the volatile silicone oil and water is more than about 50% of the entire composition, preferably from about 15% to about 25% by weight of the entire composition.
Without being bound by theory, the species and levels of water herein is believed to provide improved refreshing and light feeling to the skin, without necessarily leaving a dried feeling to the skin. Further, this amount of water allows the inclusion of water-soluble skin treatment agents such as niacinamide.
WO 01/91704 PCT/US00/15164 In the present invention, deionized water is typically used. Water from natural sources including mineral cations can also be used, depending on the desired characteristic of the product.
SKIN TREATMENT AGENT The composition of the present invention may further comprise a skin treatment agent by weight of the entire composition at from about 0.1% to about preferably from about 1% to about Skin treatment agents useful herein are niacinamide, panthenol, and mixtures thereof. Niacinamide is particularly preferred in that, when used in a pharmaceutically effective amount, is capable of reducing or alleviating the intensity of chronical spots. Niacinamide is suitably incorporated in the composition by first dissolving in water. Niacinamide and panthenol are commercially available, for example, by Roche.
HUMECTANT
The composition of the present invention may further comprise a humectant by weight of the entire composition at from about 1% to about preferably 2% to about 7%.
The humectants herein are selected from the group consisting of polyhydric alcohols, water soluble alkoxylated nonionic polymers, and mixtures thereof.
Polyhydric alcohols useful herein include glycerin, propylene glycol, 1,3butylene glycol, dipropylene glycol, diglycerin, sodium hyaluronate, and mixtures thereof.
Commercially available humectants herein include: glycerin available from Asahi Denka; propylene glycol with tradename LEXOL PG-865/855 available from Inolex, 1,2-PROPYLENE GLYCOL USP available from BASF; 1,3-butylene glycol available from Daisel Kagaku Kogyo; dipropylene glycol with the same tradename available from BASF; diglycerin with tradename DIGLYCEROL available from Solvay GmbH; sodium hyaluronate with tradenames ACTIMOIST available from Active Organics, AVIAN SODIUM HYALURONATE series available from Intergen, HYALURONIC ACID Na available from Ichimaru Pharcos.
ADDITIONAL COMPONENTS The composition of the present invention may include other additional components, which may be selected by the artisan according to the desired characteristics of the final product and which are suitable for rendering the WO 01/91704 PCT/US00/15164 composition more cosmetically or aesthetically acceptable or to provide them with additional usage benefits. Such additional components generally are used individually at levels of no more than about 5% by weight of the composition.
The composition of the present invention may further contain a nonvolatile dispersed silicone usually referred to as silicone gum. The term "silicone gum", as used herein, means a polyorganosiloxane material having a viscosity at of greater than or equal to 1,000,000 mPa*s. Silicone gums are believed to provide wearability improvement such as long-lasting effect. The "silicone gums" will typically have a mass molecular weight in excess of about 200,000, generally between about 200,000 and about 1,000,000. Specific examples include polydimethylsiloxane, poly(dimethylsiloxane methylvinylsiloxane) copolymer, poly(dimethylsiloxane diphenylsiloxane methylvinylsiloxane) copolymer and mixtures thereof. Commercially available silicone gums are described in General Electric Silicone Rubber Product Data Sheets as SE 30, SE 33, SE 54 and SE 76.
The composition of the present invention may further contain a silicone resin, which are highly crosslinked polymeric siloxane systems. Silicone resins are believed to enhance spreadability and improve the feel to the skin. The crosslinking is introduced through the incorporation of tri-functional and tetrafunctional silanes with mono-functional or di-functional, or both, silanes during manufacture of the silicone resin. As is well understood in the art, the degree of crosslinking that is required in order to result in a silicone resin will vary according to the specific silane units incorporated into the silicone resin. In general, silicone materials which have a sufficient level of trifunctional and tetrafunctional siloxane monomer units, and hence, a sufficient level of crosslinking, such that they dry down to a rigid, or hard, film are considered to be silicone resins. The ratio of oxygen atoms to silicon atoms is indicative of the level of crosslinking in a particular silicone material. Silicone materials which have at least about 1.1 oxygen atoms per silicon atom will generally be silicone resins herein. Preferably, the ratio of oxygen:silicon atoms is at least about 1.2:1.0. Silanes used in the manufacture of silicone resins include monomethyl-, dimethyl-, trimethyl-, monophenyl-, diphenyl-, methylphenyl-, monovinyl-, and methylvinylchlorosilanes, and tetrachlorosilane, with the methyl substituted silanes being most commonly utilized. Preferred are crosslinked silicone powders with tradenames Trefil E-505C, Trefil E-506C, and 9506 Powder; suspensions of silicone elastomer powders with tradenames BY29-119 and 11 WO 01/91704 PCT/US00/15164 BY29-122; and silicone compound emulsions with tradenames SH5500, SC5570, and SM 5571; all available from Dow Corning.
Other useful silicone resins are silicone resin powders such as the material given the CTFA designation polymethylsilsequioxane, which is commercially available as TospearlTM from Toshiba Silicones.
Silicone materials and silicone resins in particular, can conveniently be identified according to a shorthand nomenclature system well known to those skilled in the art as the "MDTQ" nomenclature. Under this system, the silicone is described according to the presence of various siloxane monomer units which make up the silicone. Briefly, the symbol M denotes the mono-functional unit
(CH
3 3 SiOo.r; D denotes the difunctional unit (CH 3 2 SIO; T denotes the trifunctional unit (CH 3 )SiOi and Q denotes the quadri- or tetra-functional unit SiO2. Primes of the unit symbols, and Q' denote substituents other than methyl, and must be specifically defined for each occurrence. Typical alternate substituents include groups such as vinyl, phenyl, amino, hydroxyl, etc.
The molar ratios of the various units, either in terms of subscripts to the symbols indicating the total number of each type of unit in the silicone, or an average thereof, or as specifically indicated ratios in combination with molecular weight, complete the description of the silicone material under the MDTQ system.
Higher relative molar amounts of T, Q, T' and/or Q' to D, M and/or or M' in a silicone resin is indicative of higher levels of crosslinking. As discussed before, however, the overall level of crosslinking can also be indicated by the oxygen to silicon ratio.
The silicone resins for use herein which are preferred are MQ, MT, MTQ, MQ and MDTQ resins. Thus, the preferred silicone substituent is methyl.
Especially preferred are MQ resins wherein the M:Q ratio is from about 0.5:1.0 to about 1.5:1.0 and the average molecular weight of the resin is from about 1000 to about 10,000. Commercially available MQ resins are, for example, trimethyl siloxy silicate with tradename BY11-018 available from Dow Corning.
The composition of the present invention may further contain a watersoluble polymer. It is believed that water-soluble polymers provide long-lasting effect. Useful water-soluble polymers include sodium carboxymethyl cellulose, polyvinyl pyrrolidone, polyvinyl alcohol, xanthan gum, agar, pulleran, bentonite, and mixtures thereof. Commercially available water-soluble polymers include the Carbopol series available from B. F. Goodrich Company, and PVP available from G.A.F. Chemicals.
WO 01/91704 PCT/US00/15164 Other components which can be formulated into the compositions of the present invention are; preservatives such as benzyl alcohol, methyl paraben, propyl paraben, imidazolidinyl area, and EDTA and its salts, perfumes, ultraviolet and infrared screening and absorbing agents, and others.
THE COMPOSITION The composition of the present invention may be made by a method well known in the art. In a suitable process, the composition is made by the steps of: 1) heating and dissolving the volatile silicone oil, non-volatile oil, solid wax, lipophilic surfactant, and any other hydrophobic material having a high melting point to about 80-850C in a sealed tank, to make a lipophilic mixture; 2) adding the hydrophobically treated pigments into such liphophilic mixture and dispersing with a homogenizer at about 75-80OC; 3) separate from 1) and heating and dissolving in water, skin treatment agents, humectants, when present, and any other hydrophilic material to about 75-80°C; 4) adding the product of step 2) to the product of step 3) to effect an emulsification; and cooling the obtained emulsion to a temperature of about 60-801C.
The obtained composition, which is still fluid at such temperature, is filled in an air-tight container and allowed to cool to room temperature typically using a cooling unit. The obtained composition is solid at ambient temperature, and thus can be poured into such container and left to solidify. The air-tight container is typically in a package form of a compact.
The obtained composition preferably has a melting point of less than about 500C, when measured by "General Tests, Melting Point Method 2" as stated in "The Japanese Standard of Cosmetic Ingredients". Without being bound by theory, it is believed that this relatively low melting point of the preferred embodiment composition of the present invention provides the improved spreadability and improved fresh and light feeling to the skin. In another preferred embodiment, the DSC thermogram of the composition of the present invention shows a relatively small enthalpy required for melting the composition. Without being bound by theory, it is believed that such small enthalpy leads to less energy required for the composition to be applied to the skin, thereby, also contributing to the improved spreadability and improved fresh and light feeling to the skin.
WO 01/91704 PCT/US00/15164
EXAMPLES
The following examples further describe and demonstrate the preferred embodiments within the scope of the present invention. The examples are given solely for the purpose of illustration, and are not to be construed as limitations of the present invention since many variations thereof are possible without departing from its spirit and scope.
EXAMPLES The following make-up compositions herein: are formed by the process described NO. Component Ex. 1 Ex. 2 Ex. 3 Ex. 4 Ex. 1 Cyclomethicone *1 35.9 30.95 32.95 33.3 32.8 2 Tridecyl isononanoate *2 2.0 2.0 2.0 2.0 3 Tocopherol acetate *3 0.5 0.5 0.5 4 Candelilla wax *4 0.4 0.4 0.4 0.3 Ozokerite wax *5 2.2 2.8 2.8 2.8 6 Eicosanyl Behenate *6 0.4 0.4 0.4 7 Sorbitan isostearate *7 2.0 2.0 2.0 1.0 8 Dimethicone copolyol *8 0.5 1.2 1.2 1.2 1.2 9 Crosslinked silicone powder *9 Trimethyl siloxy silicate *10 11 Hydrophobically Treated 28.75 30.00 28.00 30.00 25.00 Pigments *11 12 Deionized water 20 22 20 20 22 13 Niacinamide*12 2.0 2.0 2.0 2.0 14 Panthenol *13 0.25 0.25 0.25 Preservative 0.5 0.5 0.5 0.5 16 1,3 butylene glycol *14 5.0 5.0 5.0 17 Glycerin *15 18 Polyvinylpyrrolidone *16 Definitions of Components WO 01/91704 PCT/US00/15164 *1 Cyclomethicone: SH245 available from Dow Corning *2 Tridecyl isononanoate Crodamol TN available from Croda *3 Tocopheryl Acetate DL-a-Tocopheryl Acetate available from Eisai *4 Candelilla wax Candelilla wax NC-1630 available from Noda wax *5 Ozokerite wax Ozokerite wax SP-1021 available from Strahl Pitsh *6 Eicosanyl Behenate Eicosanyl Behenate available from Cas Chemical *7 Sorbitan isostearate Crill 6 available from Croda *8 Dimethicone copolyol DC5225C available from Dow Coming *9 Crosslinked silicone powder: Torayfil E-506C available from Dow Corning *10 Trimethylsiloxy silicate: BY11-018 available from Dow Corning *11 Hydrophobically treated pigments Component Level *Oil Absorbency Supplier level (ml/g) Methicone Treated Titanium 0 70 24.4 Miyoshi Kasei Dioxide and Talc Methicone Treated Mica 15 85 58.5 Miyoshi Kasei Dimethicone and Stearic Acid 0 25 23.0 Miyoshi Kasei Treated Micro Titanium Dioxide Dimethicone Treated Silica 5 35 130.4 Miyoshi Kasei Methicone Treated Synthetic 0 35 Topy Kougyou Mica (synthetic fluorphlogopite) Methicone Treated Iron Oxides 0 70 Daito Kasei Test Method for Oil Absorvency Level JIS K5101 No.21 *12 Niacinamide: Niacinamide available from Roche *13 Panthenol: DL-Panthenol available from Roche *14 1,3 Butylene Glycol 1,3 Butylene Glycol available from Daisel Kagakukougyou Glycerine: Glycerine USP available from Asahi Denka *16 Polyvinylpyrrolidone: PVP K-30 available from GAF Chemicals Method of Preparation WO 01/91704 PCT/US00/15164 The make-up compositions of Examples 1 5 are prepared as follows: component numbers I through 10, as present, are heated to dissolve at 820C in a sealed tank, followed by adding component number 11, and the mixture is dispersed at 800C using a homogenizer to make a lipophilic mixture. Separately, a mixture of component numbers 12 through 18, as present, are heated to dissolve at 800C and added to the lipophilic mixture to effect an emulsification.
The obtained emulsion is adjusted to a temperature of 700C. Finally, the emulsion is filled in an air-tight container and allowed to cool to room temperature using a cooling unit.
These embodiments represented by the previous examples have many advantages. For example, they can provide improved moisturizing benefit to the skin, yet also provide good spreadability to the skin and leave the skin with a fresh and light feel.
Claims (9)
1. A water-in-oil emulsified make-up composition comprising by weight: from 25% to 40% of a volatile silicone oil; from 0.5% to 8% of a non-volatile oil; from about 2% to 4% of a solid wax; from 1% to 5% of a lipophilic surfactant having an HLB of less than 8; from 25% to 35% of hydrophobically treated pigments; and water in an amount such that the total of the volatile silicone oil and water is at least
2. The water-in-oil emulsified make-up composition according to Claim 1 further comprising from 0.1% to 10% of a skin treatment agent comprising at least 0.1% niacinamide.
3. The water-in-oil emulsified make-up composition according to Claim 1 or 2 wherein the composition has a melting point of less than 50 0 C.
4. The water-in-oil emulsified make-up composition according to Claim 1 or 2 wherein the weight ratio of: the total amount of the non-volatile oil, the solid wax, and the lipophilic surfactant; to the amount of the hydrophobically treated pigments is from 1 7 to 1 The water-in-oil emulsified make-up composition according to Claim 1 or 2 wherein the non-volatile oil is selected from the group consisting of tridecyl isononanoate, tridecyl isononanoate, isostearyl isostearate, isocetyl isosteatrate, isopropyl isostearate, isodecly isonoanoate, cetyl octanoate, isononyl isononanoate, diisopropyl myristate, isocetyl myristate, isotridecyl myristate, isopropyl myristate, isostearyl palmitate, isocetyl palmitate, isodecyl palmitate, isopropyl palmitate, octyl palmitate, caprylic/capric acid triglyceride, glyceryl tri-2-ethylhexanoate, neopentyl glycol di(2-ethyl hexanoate), diisopropyl dimerate, and mixtures thereof.
P:\Userhulie\2000254575 Amend Speci.doc 18
6. The water-in-oil emulsified make-up composition according to Claim 1 or 2 wherein the lipophilic surfactant is selected from the group consisting of ester- type surfactants, silicone-type surfactants, and mixtures thereof.
7. The water-in-oil emulsified make-up composition according to Claim 6 wherein the ester-type surfactant is selected from the group consisting of sorbitan isostearate, sorbitan monoisostearate, sorbitan diisostearate, sorbitan sesquiisostearate, sorbitan monooleate, sorbitan dioleate, sorbitan sesquioleate, glyceryl monoisostearate, glyceryl diiostearate, glycerly sesquiisostearate, gylceryl monooleate, glyceryl dioleate, glycerly sesquioleate, diglyceryl diisostearate, diglycerly dioleate, diglycerin monoisostearyl ether diglycerin diisostearly ether, and mixtures thereof.
8. The water-in-oil emulsified make-up composition according to Claim 1 or 2 further comprising from 1% to 15% of a humectant.
9. The water-in-oil emulsified make-up composition according to Claim 1 or 2 comprising by weight: from 30% to 40% of the volatile silicone oil; from 2% to 5% of the non-volatile oil; from 2% to 4% of the solid wax; from 1% to 3% of the lipophilic surfactant; from 25% to 30% of hydrophobically treated pigments wherein the weight ratio of: the total amount of the non-volatile oil, the solid wax, and the lipophilic surfactant; the the amount of the hydrophobically treated pigments is 1 5 to 1 from 15% to 25% water; from 1% to 5% of the skin treatment agent; and from 2% to 7% of a humectant. P:%UserJuIie\2OOO254575 Amend Specidoc A water-in-oil emulsified make-up composition according to claim 1 substantially as hereinbefore described with reference to any of the examples. DATED: 15 July, 2004 PHILLIPS ORMONDE FITZPATRICK Attorneys for: THE PROCTER GAMBLE COMPANY @9"PB ^^s P:\UsedJulle2000254575 Amend Speci.doc
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| CA2409616C (en) * | 2000-06-01 | 2007-01-09 | The Procter & Gamble Company | Water-in-oil emulsified make-up composition |
| US6936241B2 (en) * | 2001-08-17 | 2005-08-30 | The Procter & Gamble Company | Sunscreen composition |
| WO2003015726A1 (en) * | 2001-08-17 | 2003-02-27 | The Procter & Gamble Company | Sunscreen composition |
| CA2476324A1 (en) * | 2002-03-12 | 2003-09-25 | The Procter & Gamble Company | Cosmetic composition comprising double coated pigment and a gelling agent |
| US20040086473A1 (en) * | 2002-06-17 | 2004-05-06 | The Procter & Gamble Company | Multi-step sebum and perspiration absorption foundation kit and associated methods |
| WO2004000333A1 (en) * | 2002-06-20 | 2003-12-31 | Astion Dermatology A/S | Novel complexes of fatty acid esters of polyhydroxyalkanes and pyridine carboxy derivatives |
| US20050191328A1 (en) * | 2004-02-26 | 2005-09-01 | Toshiya Taniguchi | Make-up composition |
| US20050191329A1 (en) * | 2004-02-26 | 2005-09-01 | Toshiya Taniguchi | Solid water-in-oil emulsion make-up composition |
| DE102005020583B4 (en) | 2004-09-06 | 2016-02-18 | Schwan-Stabilo Cosmetics Gmbh & Co. Kg | Preparation, in particular cosmetic preparation and its use |
| CN101115462B (en) * | 2005-09-09 | 2012-10-10 | 宝洁公司 | Solid skin care composition comprising multiple layers |
| WO2007032937A1 (en) * | 2005-09-09 | 2007-03-22 | The Procter & Gamble Company | Solid skin care composition comprising multiple layers based on water-in-oil emulsions |
| EP1922057A2 (en) * | 2005-09-09 | 2008-05-21 | The Procter and Gamble Company | Solid skin care composition comprising multiple layers |
| CA2589096C (en) * | 2005-09-09 | 2010-11-16 | The Procter & Gamble Company | Solid skin care composition comprising multiple layers |
| JP5266063B2 (en) * | 2006-01-03 | 2013-08-21 | ロレアル | Cosmetic composition containing oil |
| FR2895675B1 (en) * | 2006-01-03 | 2011-07-22 | Oreal | COSMETIC COMPOSITION COMPRISING AN OIL |
| FR2895673B1 (en) * | 2006-01-03 | 2012-08-24 | Oreal | COSMETIC COMPOSITION COMPRISING AN OIL |
| FR2895672B1 (en) * | 2006-01-03 | 2012-08-24 | Oreal | COSMETIC COMPOSITION COMPRISING AN OIL |
| CN101224174B (en) * | 2007-01-18 | 2011-11-02 | 株式会社太平洋 | Solid supplement cosmetics compound and preparing method thereof |
| JP2009269881A (en) * | 2008-05-09 | 2009-11-19 | Noevir Co Ltd | Water-in-oil emulsion type makeup cosmetic |
| CN102355883A (en) * | 2009-03-19 | 2012-02-15 | 株式会社资生堂 | Solvent composition for conversion to makeup cosmetic |
| JP4629799B2 (en) * | 2009-03-27 | 2011-02-09 | 株式会社資生堂 | Water-in-oil emulsion composition |
| FR2949954B1 (en) * | 2009-09-11 | 2012-10-05 | Oreal | COSMETIC SET OF MAKE-UP AND / OR CARE OF KERATINIC MATERIAL. |
| FR2954106B1 (en) * | 2009-12-18 | 2012-01-06 | Oreal | COLORED COMPOSITION FOR CAMOUFLING SKIN IMPERFECTIONS |
| WO2011137563A1 (en) | 2010-05-07 | 2011-11-10 | Unilever Plc | High solvent content emulsions |
| FR2976479B1 (en) * | 2011-06-16 | 2013-09-06 | Oreal | COSMETIC FILTER COMPOSITIONS COMPRISING AN ASSOCIATION OF TITANIUM OXIDE PARTICLES |
| JP6126846B2 (en) * | 2012-12-28 | 2017-05-10 | 花王株式会社 | Water-in-oil solid emulsified cosmetic |
| EP3099286A4 (en) * | 2014-01-30 | 2017-12-20 | Dow Corning Corporation | Compositions for application to the skin for reducing adhesion of pollution particles on skin and methods of preparing same |
| JP6574613B2 (en) * | 2015-05-29 | 2019-09-11 | 株式会社日本色材工業研究所 | Water-in-oil emulsified cosmetic |
| KR102610439B1 (en) * | 2016-09-20 | 2023-12-06 | (주)아모레퍼시픽 | Hair conditioning composition |
| WO2021222764A1 (en) * | 2020-04-30 | 2021-11-04 | L'oreal | Water-in-oil emulsions containing surfactant, silicone gum and/or latex, and siloxysilicate resin |
| FR3113588B1 (en) * | 2020-08-28 | 2023-06-09 | Oreal | WATER-IN-OIL EMULSIONS CONTAINING LOW HLB SURFACTANT, SILICONE GUM AND SILOXYSILICATE RESIN |
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| WO2001091704A1 (en) * | 2000-06-01 | 2001-12-06 | The Procter & Gamble Company | Water-in-oil emulsified make-up composition |
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| CA1322725C (en) * | 1986-12-19 | 1993-10-05 | Jane Hollenberg | Cosmetic compositions comprising water-in-oil emulsion containing pigment |
| JP2691729B2 (en) * | 1987-06-23 | 1997-12-17 | 株式会社資生堂 | Solid water-in-oil emulsified cosmetic |
| JP2665473B2 (en) * | 1988-09-27 | 1997-10-22 | 株式会社資生堂 | Solid water-in-oil emulsified cosmetic |
| JP2996410B2 (en) * | 1990-03-09 | 1999-12-27 | 株式会社資生堂 | Solid water-in-oil emulsified cosmetic |
| JP3099977B2 (en) * | 1991-05-02 | 2000-10-16 | 株式会社日本色材工業研究所 | Water-in-oil type emulsified cosmetic and method for producing the same |
| JPH05262617A (en) * | 1992-03-23 | 1993-10-12 | Shiseido Co Ltd | Make-up cosmetic |
| JPH07267819A (en) * | 1994-03-30 | 1995-10-17 | Shiseido Co Ltd | Water in oil type emulsion cosmetic |
| EP0951269B1 (en) * | 1996-12-18 | 2001-08-16 | The Procter & Gamble Company | Stable high spf foundation |
| JPH11209243A (en) * | 1998-01-20 | 1999-08-03 | Shiseido Co Ltd | Foundation |
| JP3562561B2 (en) * | 1998-02-20 | 2004-09-08 | 株式会社コーセー | Solid water-in-oil cosmetics |
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- 2000-06-01 MX MXPA02011924A patent/MXPA02011924A/en unknown
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- 2000-06-01 JP JP2001587720A patent/JP2003534361A/en active Pending
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001091704A1 (en) * | 2000-06-01 | 2001-12-06 | The Procter & Gamble Company | Water-in-oil emulsified make-up composition |
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| CA2409616A1 (en) | 2001-12-06 |
| CA2409616C (en) | 2007-01-09 |
| AU5457500A (en) | 2001-12-11 |
| AU2000254575A1 (en) | 2002-02-28 |
| CN1454071A (en) | 2003-11-05 |
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| FGA | Letters patent sealed or granted (standard patent) | ||
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Owner name: NOXELL CORPORATION Free format text: FORMER OWNER(S): THE PROCTER & GAMBLE COMPANY |
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| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |