SK133799A3 - Oil-in-water emulsions for reconstituting lamellarity of the lipid structure of damaged skin - Google Patents
Oil-in-water emulsions for reconstituting lamellarity of the lipid structure of damaged skin Download PDFInfo
- Publication number
- SK133799A3 SK133799A3 SK1337-99A SK133799A SK133799A3 SK 133799 A3 SK133799 A3 SK 133799A3 SK 133799 A SK133799 A SK 133799A SK 133799 A3 SK133799 A3 SK 133799A3
- Authority
- SK
- Slovakia
- Prior art keywords
- oil
- emulsifier
- lipophilic
- lipid
- fatty
- Prior art date
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- 239000000839 emulsion Substances 0.000 title abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title abstract description 19
- 125000003473 lipid group Chemical group 0.000 title 1
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 25
- 150000002632 lipids Chemical class 0.000 claims abstract description 18
- 239000007957 coemulsifier Substances 0.000 claims abstract description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 14
- 239000002537 cosmetic Substances 0.000 claims abstract description 13
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 claims abstract description 13
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 12
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 10
- 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 8
- 125000002252 acyl group Chemical group 0.000 claims abstract description 7
- 239000001257 hydrogen Substances 0.000 claims abstract description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
- 229960000735 docosanol Drugs 0.000 claims abstract description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 3
- 239000012071 phase Substances 0.000 claims description 31
- 239000007764 o/w emulsion Substances 0.000 claims description 9
- 239000008346 aqueous phase Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 2
- 239000012875 nonionic emulsifier Substances 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 30
- 235000019198 oils Nutrition 0.000 description 30
- -1 sucrose fatty acid esters Chemical class 0.000 description 19
- 239000000194 fatty acid Substances 0.000 description 16
- 235000014113 dietary fatty acids Nutrition 0.000 description 15
- 229930195729 fatty acid Natural products 0.000 description 15
- 239000006071 cream Substances 0.000 description 12
- 210000003491 skin Anatomy 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 150000004665 fatty acids Chemical class 0.000 description 8
- 239000004094 surface-active agent Substances 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 239000002304 perfume Substances 0.000 description 5
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- 235000010493 xanthan gum Nutrition 0.000 description 5
- 235000019489 Almond oil Nutrition 0.000 description 4
- 239000008168 almond oil Substances 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 150000002191 fatty alcohols Chemical class 0.000 description 4
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 150000003626 triacylglycerols Chemical class 0.000 description 4
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 3
- 239000005662 Paraffin oil Substances 0.000 description 3
- NWGKJDSIEKMTRX-BFWOXRRGSA-N [(2r)-2-[(3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)C1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-BFWOXRRGSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000010374 citricidal Substances 0.000 description 3
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 3
- 239000008103 glucose Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 210000000434 stratum corneum Anatomy 0.000 description 3
- 229940042585 tocopherol acetate Drugs 0.000 description 3
- 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 description 2
- SSCYWBFGEPBPAK-UHFFFAOYSA-N 2,2,3,3,4,4-hexamethyldecane Chemical compound CCCCCCC(C)(C)C(C)(C)C(C)(C)C SSCYWBFGEPBPAK-UHFFFAOYSA-N 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 235000019486 Sunflower oil Nutrition 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 235000013871 bee wax Nutrition 0.000 description 2
- 239000012166 beeswax Substances 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- 229960003237 betaine Drugs 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004945 emulsification Methods 0.000 description 2
- 235000008524 evening primrose extract Nutrition 0.000 description 2
- 229940089020 evening primrose oil Drugs 0.000 description 2
- 239000010475 evening primrose oil Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 210000000245 forearm Anatomy 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- BTFJIXJJCSYFAL-UHFFFAOYSA-N icosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 2
- 229940093629 isopropyl isostearate Drugs 0.000 description 2
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
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- WTVHAMTYZJGJLJ-UHFFFAOYSA-N (+)-(4S,8R)-8-epi-beta-bisabolol Natural products CC(C)=CCCC(C)C1(O)CCC(C)=CC1 WTVHAMTYZJGJLJ-UHFFFAOYSA-N 0.000 description 1
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- CFOQKXQWGLAKSK-KTKRTIGZSA-N (13Z)-docosen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCCO CFOQKXQWGLAKSK-KTKRTIGZSA-N 0.000 description 1
- NKJOXAZJBOMXID-UHFFFAOYSA-N 1,1'-Oxybisoctane Chemical compound CCCCCCCCOCCCCCCCC NKJOXAZJBOMXID-UHFFFAOYSA-N 0.000 description 1
- UKIARGZKGOGJNE-UHFFFAOYSA-N 1-(16-methylheptadecanoyloxy)butyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OC(CCC)OC(=O)CCCCCCCCCCCCCCC(C)C UKIARGZKGOGJNE-UHFFFAOYSA-N 0.000 description 1
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- DHGISFWHDBPFBJ-UHFFFAOYSA-N 2-(11-methyldodecanoyloxy)ethyl 11-methyldodecanoate Chemical compound CC(C)CCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCC(C)C DHGISFWHDBPFBJ-UHFFFAOYSA-N 0.000 description 1
- RYKSMKFLIHUEBL-UHFFFAOYSA-N 2-(2-ethylhexanoyloxy)propyl 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)OCC(C)OC(=O)C(CC)CCCC RYKSMKFLIHUEBL-UHFFFAOYSA-N 0.000 description 1
- NDHKAEBPGBKCIO-UHFFFAOYSA-N 2-(hexadecylamino)propanoic acid Chemical compound CCCCCCCCCCCCCCCCNC(C)C(O)=O NDHKAEBPGBKCIO-UHFFFAOYSA-N 0.000 description 1
- QVRMIJZFODZFNE-UHFFFAOYSA-N 2-[dimethyl-[3-(octadecanoylamino)propyl]azaniumyl]acetate Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O QVRMIJZFODZFNE-UHFFFAOYSA-N 0.000 description 1
- DHVLDKHFGIVEIP-UHFFFAOYSA-N 2-bromo-2-(bromomethyl)pentanedinitrile Chemical compound BrCC(Br)(C#N)CCC#N DHVLDKHFGIVEIP-UHFFFAOYSA-N 0.000 description 1
- LWLRMRFJCCMNML-UHFFFAOYSA-N 2-ethylhexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CC)CCCC LWLRMRFJCCMNML-UHFFFAOYSA-N 0.000 description 1
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- 230000034659 glycolysis Effects 0.000 description 1
- 229940107702 grapefruit seed extract Drugs 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 210000000003 hoof Anatomy 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229940100554 isononyl isononanoate Drugs 0.000 description 1
- 229940089456 isopropyl stearate Drugs 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000010690 paraffinic oil Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- PZQSQRCNMZGWFT-QXMHVHEDSA-N propan-2-yl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC(C)C PZQSQRCNMZGWFT-QXMHVHEDSA-N 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
- ZPWFUIUNWDIYCJ-UHFFFAOYSA-N propan-2-yl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(C)C ZPWFUIUNWDIYCJ-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 210000000582 semen Anatomy 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 230000008591 skin barrier function Effects 0.000 description 1
- 230000037380 skin damage Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000002569 water oil cream Substances 0.000 description 1
- 235000019386 wax ester Nutrition 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 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
- A61K8/0295—Liquid crystals
-
- 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
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
- A61K9/1274—Non-vesicle bilayer structures, e.g. liquid crystals, tubules, cubic phases, cochleates; Sponge phases
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Dispersion Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Crystallography & Structural Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Colloid Chemistry (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19713793A DE19713793A1 (de) | 1997-04-03 | 1997-04-03 | Öl-in-Wasser-Emulsionen zur Wiederherstellung der Lamellarität der Lipidstruktur geschädigter Haut |
| PCT/EP1997/006639 WO1998044896A1 (de) | 1997-04-03 | 1997-11-28 | Öl-in-wasser-emulsionen zur wiederherstellung der lamellarität der lipidstruktur geschädigter haut |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK133799A3 true SK133799A3 (en) | 2000-02-14 |
Family
ID=7825359
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK1337-99A SK133799A3 (en) | 1997-04-03 | 1997-11-28 | Oil-in-water emulsions for reconstituting lamellarity of the lipid structure of damaged skin |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6379681B1 (no) |
| EP (1) | EP0973484B1 (no) |
| JP (1) | JP2001518886A (no) |
| CN (1) | CN1248904A (no) |
| AT (1) | ATE270537T1 (no) |
| CA (1) | CA2285216A1 (no) |
| DE (2) | DE19713793A1 (no) |
| ES (1) | ES2226010T3 (no) |
| HU (1) | HUP0000501A3 (no) |
| NO (1) | NO994786D0 (no) |
| PL (1) | PL335902A1 (no) |
| SK (1) | SK133799A3 (no) |
| WO (1) | WO1998044896A1 (no) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19857349A1 (de) * | 1998-12-11 | 2000-06-15 | Wolfgang Schnizer | Hautpflege-System |
| FR2816852B1 (fr) * | 2000-11-21 | 2005-08-26 | Nuxe Lab | Association stabilisee d'un colorant et d'un emulsionnant, composition cosmetique et/ou dermatologique la contenant et procede de preparation |
| JP2002265347A (ja) * | 2001-03-13 | 2002-09-18 | Shiseido Co Ltd | コーニファイドエンベロープの成熟を促す化粧料 |
| US6608011B2 (en) | 2001-06-11 | 2003-08-19 | Colgate-Palmolive Company | Shampoos with behenyl-alcohol |
| US7758636B2 (en) * | 2002-09-20 | 2010-07-20 | Innovational Holdings Llc | Expandable medical device with openings for delivery of multiple beneficial agents |
| CN100455193C (zh) * | 2003-03-11 | 2009-01-28 | 科宁公司 | 用作农用化学品佐剂的微乳液 |
| JP4592347B2 (ja) * | 2003-07-14 | 2010-12-01 | 株式会社ヤクルト本社 | 外用剤組成物 |
| CN1874752A (zh) * | 2003-11-04 | 2006-12-06 | 宝洁公司 | 个人清洁组合物 |
| WO2005044206A1 (en) | 2003-11-04 | 2005-05-19 | The Procter & Gamble Company | Fragrances comprising residual accords |
| GB0403879D0 (en) * | 2004-02-21 | 2004-03-24 | Unilever Plc | Hair conditioning compositions and methods of manufacture |
| JP4854194B2 (ja) * | 2004-07-05 | 2012-01-18 | 株式会社ファンケル | ラメラ構造再生剤及び皮膚外用剤 |
| WO2006018149A1 (de) * | 2004-08-13 | 2006-02-23 | Henkel Kommanditgesellschaft Auf Aktien | Kosmetische zusammensetzungen zur behandlung gestresster haut enthaltend taurin und langkettige fettalkohole |
| DE102005063178A1 (de) * | 2005-12-30 | 2007-07-05 | Henkel Kgaa | Kosmetische Lichtschutzzusammensetzungen auf der Basis lamellarer Emulsionen |
| DE102006015544A1 (de) * | 2006-03-31 | 2007-10-04 | Kuhs Gmbh | Topisch zu applizierende Zusammensetzung |
| GB0714817D0 (en) * | 2007-07-31 | 2007-09-12 | Croda Int Plc | Polyglycerol derivatives |
| DE102010046931A1 (de) * | 2010-09-29 | 2012-03-29 | Sanderstrothmann Gmbh | Verfahren zur Herstellung eines kosmetischen Mittels |
| FR2991171B1 (fr) | 2012-06-01 | 2014-05-23 | Galderma Res & Dev | Procede de preparation d'une composition dermatologique comprenant des oleosomes |
| DE102013217316A1 (de) * | 2013-08-30 | 2015-03-05 | Henkel Ag & Co. Kgaa | Hautpflegeöl |
| WO2017182264A1 (en) | 2016-04-21 | 2017-10-26 | Unilever Plc | Novel nanoemulsions comprising fatty acid and n-acyl derivatives of amino acid salt |
| EA037099B1 (ru) | 2016-04-21 | 2021-02-05 | Юнилевер Н.В. | Способ получения композиции масел в виде наноэмульсии |
| WO2018108530A1 (de) | 2016-12-13 | 2018-06-21 | Basf Se | Texturierte zusammensetzungen |
| US20200375854A1 (en) * | 2019-05-31 | 2020-12-03 | L'oreal | Compositions and methods for treating keratinous substrates |
| CN113476346A (zh) * | 2021-06-16 | 2021-10-08 | 西安德诺海思医疗科技有限公司 | 一种皮肤屏障修复组合物 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4400295A (en) * | 1979-03-24 | 1983-08-23 | Loire Cosmetics Co., Ltd. | Emulsifier composition |
| JPS61158909A (ja) * | 1984-12-29 | 1986-07-18 | Pola Chem Ind Inc | パツク料 |
| US4767625A (en) * | 1985-09-02 | 1988-08-30 | Kao Corporation | Lamella type single phase liquid crystal composition and oil-base cosmetic compositions using the same |
| GB8724254D0 (en) * | 1987-10-15 | 1987-11-18 | Unilever Plc | Hair treatment product |
| GB9302492D0 (en) | 1993-02-09 | 1993-03-24 | Procter & Gamble | Cosmetic compositions |
| JP3250877B2 (ja) * | 1993-07-08 | 2002-01-28 | 株式会社資生堂 | 撥水性水中油型乳化組成物 |
| JP2855057B2 (ja) * | 1993-07-09 | 1999-02-10 | 株式会社資生堂 | 増粘ゲル化剤及び増粘ゲル状組成物 |
| FR2709666B1 (fr) | 1993-09-07 | 1995-10-13 | Oreal | Composition cosmétique ou dermatologique constituée d'une émulsion huile dans eau à base de globules huileux pourvus d'un enrobage cristal liquide lamellaire. |
| DE4337041A1 (de) * | 1993-10-29 | 1995-05-04 | Henkel Kgaa | Verfahren zur Herstellung in Öl-in-Wasser-Emulsionen |
| FR2714382B1 (fr) * | 1993-12-27 | 1996-02-02 | Roussel Uclaf | Phospholipides vecteur de molécule active, leur préparation et leur utilisation dans des compositions cosmétiques ou dermatologiques. |
| GB9408259D0 (en) | 1994-04-26 | 1994-06-15 | Procter & Gamble | Cosmetic compositions |
| GB9414572D0 (en) * | 1994-07-19 | 1994-09-07 | Unilever Plc | Soap composition |
| JPH08268877A (ja) * | 1995-03-31 | 1996-10-15 | Shiseido Co Ltd | 撥水撥油性水中油型乳化組成物 |
| JPH08337513A (ja) * | 1995-06-13 | 1996-12-24 | Shiseido Co Ltd | 撥水性水中油型乳化組成物 |
| US5948416A (en) * | 1995-06-29 | 1999-09-07 | The Procter & Gamble Company | Stable topical compositions |
| JP3549336B2 (ja) * | 1995-10-12 | 2004-08-04 | 株式会社資生堂 | 水中油型乳化組成物 |
| US5738856A (en) * | 1995-11-03 | 1998-04-14 | Ocular Research Of Boston, Inc. | Skin care preparation and method |
| JPH09301847A (ja) * | 1996-03-15 | 1997-11-25 | Shiseido Co Ltd | 低粘度水中油型乳化組成物及びこれを用いた皮膚外用剤 |
| ATE220893T1 (de) * | 1996-08-21 | 2002-08-15 | Childrens Hosp Medical Center | Hautaufhellungszusammensetzungen |
-
1997
- 1997-04-03 DE DE19713793A patent/DE19713793A1/de not_active Withdrawn
- 1997-11-28 CN CN97182084A patent/CN1248904A/zh active Pending
- 1997-11-28 HU HU0000501A patent/HUP0000501A3/hu unknown
- 1997-11-28 AT AT97953710T patent/ATE270537T1/de not_active IP Right Cessation
- 1997-11-28 SK SK1337-99A patent/SK133799A3/sk unknown
- 1997-11-28 DE DE59711769T patent/DE59711769D1/de not_active Expired - Lifetime
- 1997-11-28 US US09/402,301 patent/US6379681B1/en not_active Expired - Lifetime
- 1997-11-28 EP EP97953710A patent/EP0973484B1/de not_active Revoked
- 1997-11-28 JP JP54228598A patent/JP2001518886A/ja not_active Ceased
- 1997-11-28 WO PCT/EP1997/006639 patent/WO1998044896A1/de active IP Right Grant
- 1997-11-28 CA CA002285216A patent/CA2285216A1/en not_active Abandoned
- 1997-11-28 PL PL97335902A patent/PL335902A1/xx unknown
- 1997-11-28 ES ES97953710T patent/ES2226010T3/es not_active Expired - Lifetime
-
1999
- 1999-10-01 NO NO994786A patent/NO994786D0/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| US6379681B1 (en) | 2002-04-30 |
| DE59711769D1 (de) | 2004-08-12 |
| ES2226010T3 (es) | 2005-03-16 |
| JP2001518886A (ja) | 2001-10-16 |
| CN1248904A (zh) | 2000-03-29 |
| PL335902A1 (en) | 2000-05-22 |
| WO1998044896A1 (de) | 1998-10-15 |
| HUP0000501A3 (en) | 2001-11-28 |
| DE19713793A1 (de) | 1998-10-08 |
| ATE270537T1 (de) | 2004-07-15 |
| EP0973484B1 (de) | 2004-07-07 |
| EP0973484A1 (de) | 2000-01-26 |
| HUP0000501A2 (en) | 2000-07-28 |
| NO994786L (no) | 1999-10-01 |
| NO994786D0 (no) | 1999-10-01 |
| CA2285216A1 (en) | 1998-10-15 |
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