CA2360494C - A combined insect repellent and sunscreen composition - Google Patents
A combined insect repellent and sunscreen composition Download PDFInfo
- Publication number
- CA2360494C CA2360494C CA002360494A CA2360494A CA2360494C CA 2360494 C CA2360494 C CA 2360494C CA 002360494 A CA002360494 A CA 002360494A CA 2360494 A CA2360494 A CA 2360494A CA 2360494 C CA2360494 C CA 2360494C
- Authority
- CA
- Canada
- Prior art keywords
- composition
- sunscreening
- water
- agent
- emulsifiers
- 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.)
- Expired - Fee Related
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 70
- 239000000516 sunscreening agent Substances 0.000 title claims abstract description 53
- 230000000475 sunscreen effect Effects 0.000 title claims abstract description 27
- 239000000077 insect repellent Substances 0.000 title claims abstract description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 23
- 239000000839 emulsion Substances 0.000 claims abstract description 18
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 17
- 150000002484 inorganic compounds Chemical class 0.000 claims abstract description 14
- 229910010272 inorganic material Inorganic materials 0.000 claims abstract description 14
- MMOXZBCLCQITDF-UHFFFAOYSA-N N,N-diethyl-m-toluamide Chemical compound CCN(CC)C(=O)C1=CC=CC(C)=C1 MMOXZBCLCQITDF-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000004408 titanium dioxide Substances 0.000 claims abstract description 8
- IITCWRFYJWUUPC-UHFFFAOYSA-N dipropyl pyridine-2,5-dicarboxylate Chemical compound CCCOC(=O)C1=CC=C(C(=O)OCCC)N=C1 IITCWRFYJWUUPC-UHFFFAOYSA-N 0.000 claims abstract description 7
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- 238000000034 method Methods 0.000 claims description 16
- GLDOVTGHNKAZLK-UHFFFAOYSA-N n-octadecyl alcohol Natural products CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 claims description 11
- 238000003756 stirring Methods 0.000 claims description 11
- 239000002562 thickening agent Substances 0.000 claims description 11
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 10
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims description 8
- 239000002738 chelating agent Substances 0.000 claims description 8
- 150000002191 fatty alcohols Chemical class 0.000 claims description 8
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical group OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 claims description 8
- 229960001173 oxybenzone Drugs 0.000 claims description 8
- -1 fatty acid glycerol esters Chemical class 0.000 claims description 7
- YBGZDTIWKVFICR-JLHYYAGUSA-N Octyl 4-methoxycinnamic acid Chemical compound CCCCC(CC)COC(=O)\C=C\C1=CC=C(OC)C=C1 YBGZDTIWKVFICR-JLHYYAGUSA-N 0.000 claims description 6
- 229940082500 cetostearyl alcohol Drugs 0.000 claims description 6
- 239000003755 preservative agent Substances 0.000 claims description 6
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 claims description 6
- 229960001673 diethyltoluamide Drugs 0.000 claims description 5
- 229960001679 octinoxate Drugs 0.000 claims description 5
- 230000002335 preservative effect Effects 0.000 claims description 5
- 239000011787 zinc oxide Substances 0.000 claims description 5
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 claims description 4
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 claims description 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 claims description 4
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 claims description 4
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 claims description 4
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 claims description 4
- 239000002304 perfume Substances 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 3
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 claims description 3
- AALXZHPCKJILAZ-UHFFFAOYSA-N (4-propan-2-ylphenyl)methyl 2-hydroxybenzoate Chemical compound C1=CC(C(C)C)=CC=C1COC(=O)C1=CC=CC=C1O AALXZHPCKJILAZ-UHFFFAOYSA-N 0.000 claims description 2
- KBKGPMDADJLBEM-UHFFFAOYSA-N 1-(4-pentylphenyl)ethanone Chemical compound CCCCCC1=CC=C(C(C)=O)C=C1 KBKGPMDADJLBEM-UHFFFAOYSA-N 0.000 claims description 2
- VHWSRELATOUTAG-UHFFFAOYSA-N 2,3-dihydroxypropyl 2-aminobenzoate Chemical compound NC1=CC=CC=C1C(=O)OCC(O)CO VHWSRELATOUTAG-UHFFFAOYSA-N 0.000 claims description 2
- WSSJONWNBBTCMG-UHFFFAOYSA-N 2-hydroxybenzoic acid (3,3,5-trimethylcyclohexyl) ester Chemical compound C1C(C)(C)CC(C)CC1OC(=O)C1=CC=CC=C1O WSSJONWNBBTCMG-UHFFFAOYSA-N 0.000 claims description 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 claims description 2
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 claims description 2
- 244000166675 Cymbopogon nardus Species 0.000 claims description 2
- 235000018791 Cymbopogon nardus Nutrition 0.000 claims description 2
- VZRKEAFHFMSHCD-UHFFFAOYSA-N Ethyl 3-(N-butylacetamido)propionate Chemical compound CCCCN(C(C)=O)CCC(=O)OCC VZRKEAFHFMSHCD-UHFFFAOYSA-N 0.000 claims description 2
- 239000005770 Eugenol Substances 0.000 claims description 2
- 239000005792 Geraniol Substances 0.000 claims description 2
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 claims description 2
- LMXFTMYMHGYJEI-UHFFFAOYSA-N Menthoglycol Natural products CC1CCC(C(C)(C)O)C(O)C1 LMXFTMYMHGYJEI-UHFFFAOYSA-N 0.000 claims description 2
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 claims description 2
- VXSIXFKKSNGRRO-MXOVTSAMSA-N [(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;[(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1.CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VXSIXFKKSNGRRO-MXOVTSAMSA-N 0.000 claims description 2
- 229960004050 aminobenzoic acid Drugs 0.000 claims description 2
- YEAYGXLRPMKZBP-KQGICBIGSA-N bis(2-hydroxyethyl)azanium;(e)-3-(4-methoxyphenyl)prop-2-enoate Chemical compound OCCNCCO.COC1=CC=C(\C=C\C(O)=O)C=C1 YEAYGXLRPMKZBP-KQGICBIGSA-N 0.000 claims description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- CMDKPGRTAQVGFQ-RMKNXTFCSA-N cinoxate Chemical compound CCOCCOC(=O)\C=C\C1=CC=C(OC)C=C1 CMDKPGRTAQVGFQ-RMKNXTFCSA-N 0.000 claims description 2
- 229960001063 cinoxate Drugs 0.000 claims description 2
- 239000001941 cymbopogon citratus dc and cymbopogon flexuosus oil Substances 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 claims description 2
- 229960001826 dimethylphthalate Drugs 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
- CBZHHQOZZQEZNJ-UHFFFAOYSA-N ethyl 4-[bis(2-hydroxypropyl)amino]benzoate Chemical compound CCOC(=O)C1=CC=C(N(CC(C)O)CC(C)O)C=C1 CBZHHQOZZQEZNJ-UHFFFAOYSA-N 0.000 claims description 2
- YSPVHAUJXLGZHP-UHFFFAOYSA-N ethyl piperidine-1-carboxylate Chemical compound CCOC(=O)N1CCCCC1 YSPVHAUJXLGZHP-UHFFFAOYSA-N 0.000 claims description 2
- 229960002217 eugenol Drugs 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 229940113087 geraniol Drugs 0.000 claims description 2
- 229960004881 homosalate Drugs 0.000 claims description 2
- SOXAGEOHPCXXIO-DVOMOZLQSA-N menthyl anthranilate Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(=O)C1=CC=CC=C1N SOXAGEOHPCXXIO-DVOMOZLQSA-N 0.000 claims description 2
- 229960002248 meradimate Drugs 0.000 claims description 2
- 239000007764 o/w emulsion Substances 0.000 claims description 2
- 229960003921 octisalate Drugs 0.000 claims description 2
- FMJSMJQBSVNSBF-UHFFFAOYSA-N octocrylene Chemical group C=1C=CC=CC=1C(=C(C#N)C(=O)OCC(CC)CCCC)C1=CC=CC=C1 FMJSMJQBSVNSBF-UHFFFAOYSA-N 0.000 claims description 2
- 229960000601 octocrylene Drugs 0.000 claims description 2
- WCJLCOAEJIHPCW-UHFFFAOYSA-N octyl 2-hydroxybenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1O WCJLCOAEJIHPCW-UHFFFAOYSA-N 0.000 claims description 2
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 claims description 2
- 229940070846 pyrethrins Drugs 0.000 claims description 2
- 239000002728 pyrethroid Substances 0.000 claims description 2
- 159000000000 sodium salts Chemical class 0.000 claims description 2
- LOIYMIARKYCTBW-OWOJBTEDSA-N trans-urocanic acid Chemical compound OC(=O)\C=C\C1=CNC=N1 LOIYMIARKYCTBW-OWOJBTEDSA-N 0.000 claims description 2
- LOIYMIARKYCTBW-UHFFFAOYSA-N trans-urocanic acid Natural products OC(=O)C=CC1=CNC=N1 LOIYMIARKYCTBW-UHFFFAOYSA-N 0.000 claims description 2
- WYWZRNAHINYAEF-AWEZNQCLSA-N [(2s)-2-ethylhexyl] 4-(dimethylamino)benzoate Chemical compound CCCC[C@H](CC)COC(=O)C1=CC=C(N(C)C)C=C1 WYWZRNAHINYAEF-AWEZNQCLSA-N 0.000 claims 1
- BBNYLDSWVXSNOQ-UHFFFAOYSA-N oxolane-2-carbaldehyde Chemical compound O=CC1CCCO1 BBNYLDSWVXSNOQ-UHFFFAOYSA-N 0.000 claims 1
- 229960002638 padimate o Drugs 0.000 claims 1
- 239000012071 phase Substances 0.000 description 19
- 239000010408 film Substances 0.000 description 6
- 230000037072 sun protection Effects 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 5
- 239000005871 repellent Substances 0.000 description 5
- 230000002940 repellent Effects 0.000 description 5
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical group OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- 239000003109 Disodium ethylene diamine tetraacetate Substances 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 235000019301 disodium ethylene diamine tetraacetate Nutrition 0.000 description 3
- 239000003974 emollient agent Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 229920002907 Guar gum Polymers 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000665 guar gum Substances 0.000 description 2
- 235000010417 guar gum Nutrition 0.000 description 2
- 229960002154 guar gum Drugs 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 229960002900 methylcellulose Drugs 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000036555 skin type Effects 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- WMZHDICSCDKPFS-UHFFFAOYSA-N triacont-1-ene Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCC=C WMZHDICSCDKPFS-UHFFFAOYSA-N 0.000 description 2
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 102100035115 Testin Human genes 0.000 description 1
- 101710070533 Testin Proteins 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229940114081 cinnamate Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002605 large molecules Chemical class 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 229950000516 padimate Drugs 0.000 description 1
- LXTZRIBXKVRLOA-UHFFFAOYSA-N padimate a Chemical compound CCCCCOC(=O)C1=CC=C(N(C)C)C=C1 LXTZRIBXKVRLOA-UHFFFAOYSA-N 0.000 description 1
- VYMDGNCVAMGZFE-UHFFFAOYSA-N phenylbutazonum Chemical compound O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 VYMDGNCVAMGZFE-UHFFFAOYSA-N 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 230000003019 stabilising effect Effects 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical compound [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- 238000002834 transmittance Methods 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
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4926—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/27—Zinc; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/29—Titanium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- 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
- A61K8/86—Polyethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/02—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings containing insect repellants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Cosmetics (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
A combined insect repellent and sunscreen composition is disclosed including 3- 9 % by weight in total of at least two emulsifiers, based on the total weight of the composition. The composition preferably comprises titanium dioxide as the inorganic compound and N, N-diethyl-m-toluamide and dipropyl pyridine-2,5-dicarboxylate as insect repellents. A method of manufacturing a sunscreen composition is also disclosed. The composition including one or more insect repellents a nd one or more sunscreening agents, is the form of an emulsion having an oil phase and a water phase and is manufactured by preparing the o il phase and the water phase and combining to form an emulsion prior to the addition of at least one inorganic compound used as a sunscreening agent.
Description
A Combined Insect Repellent and Sunscreen Composition-Technical Field This invention relates to insect repellent and sunscreen compositions and in particular to combined insect repellent and sunscreen compositions that have both effective repellency and sunscreening properties.
Backgrround Art The prior art is replete with insect repellent compositions and sunscreen compositions. Whilst these compositions are separately effective, it is desirable to provide an effective combined insect repellent and sunscreen composition.
Surprisingly, it has now been found that to produce a stable, effective combined insect repellent and sunscreen composition requires a carefully selected use of emulsifiers.
Disclosure of Invention Accordingly, the present invention consists in a sunscreen composition including one or more insect repellents and one or more UV sunscreening agents characterised in that the composition includes 3-9% by weight in total of at least two emulsifiers, based on the total weight of the composition. The inventors have found that with appropriate emulsifiers, the sunscreen agent in combination with insect repellent give a composition that is stable and effective with respect to SPF.
One or more inorganic compounds are incorporated in the composition of the invention as a sunscreening agent. The preferred inorganic compounds are titanium oxide and zinc oxide. For these compounds, the particle size can be selected to scatter light in the UV range whilst transmitting light in the visible range thereby remaining transparent on the skin. This is highly desirable from a cosmetic point of view.
Micronised particles, that is those particles less than 100 nm in size, give optimal performance. Micronised titanium dioxide is most preferred for the composition of the invention. The concentration of inorganic compound may be in the range of 1-5%
by weight based on the total weight of the composition, preferably 2-4% by weight and more preferably 3% by weight.
One or more insect repellents are included in the composition. The repellents are chosen for repellency of flying or biting insects and for low skin irritancy.
Suitable repellents include N,N-diethyl-m-toluamide (DEET), dipropyl pyridine-2,5-dicarboxylate, pyrethrins, dimethyl phthalate, 2,3:4,5-bis(2-butylene)tetrahydrofiufural, citronella, geraniol, lemon grass oil, eugenol, p-menthane-3,8-diol, ethylbutyl acetylamino propionate, 1-piperidinecarboxylic acid and 2-(2-hydroxyethyl)-esterl -methylpropyl-ester.
These can be combined with synergists such as piperonyl butoxide and N-(2-ethylhexyl)-8,9,10-trinorborn-5-ene-2,3 -dicarboximide.
DEET and dipropyl pyridine-2,5-dicarboxylate are the preferred repellents.
The total amount of insect repellent in the composition may be 4-20% by weight based on the total weight of the composition, preferably 4-15% by weight and more preferably 5-10% by weight.
The composition may include one or more other UV sunscreening agents. These are generally organic compounds which absorb a specific range of UV radiation.
Suitable sunscreening agents include octyl methoxycinnamate, oxybenzone, amino benzoic acid, Cinoxate, DEA-methoxycinnamate, Digalloyl, Dioxybenzene, Padimate 0, Ethyl dihydroxypropyl p-aminobenzoate, octyl salicylate, glyceryl aminobenzoate, Homosalate, Urocanic acid, isopropylbenzyl salicylate, menthyl anthranilate, octocrylene, Sulisbenzone and its sodium salt and triethanolamine salicylate.
A combination of octylmethoxycinnamate and oxybenzone is most preferred. Each sunscreening agent is preferably incorporated in the composition in an amount of 3-10%
by weight based on the total weight of the composition.
The composition is prepared in the form an emulsion. Accordingly, a second aspect of the invention consists in a sunscreen composition further including, by weight, based on the total weight of the composition, 7% in total emulsifier, up to 5%, preferably 1-5%, more preferably 3% film former, up to 0.25%, preferably 0.05-0.25%, more preferably 0.15% thickener, up to 0.3%, preferably 0.1-0.3%, more preferably 0.15% neutraliser, up to 0.3%, preferably 0.1-0.3%, more preferably 0.2% chelating agent and up to 2.5% of at least one of preservative, perfume and moisturiser.
The choice of emulsifier will depend on the insect repellents and sunscreening agents selected. More than two emulsifiers may be included. An emulsion is most accurately defined as a dispersion of liquid droplets in a second immiscible liquid.
Dispersions may be formed temporarily through agitation of the two immiscible liquids, however, resolution of the emulsion is usually rapid and complete unless a stabilising additive or emulsifier is used.
Emulsions usually consist of water or an aqueous solution as one immiscible phase and some organic liquid, or "oil", as the other phase. When the oil is dispersed in the aqueous phase the emulsion is called oil in water (o/w ) or alternatively, if the aqueous phase is dispersed in the oily phase the emulsion is described as water in oil ( w/o ). An emulsifying agent is usually required to stabilise the emulsion. Such agents are ordinarily large molecules of which the greatest part of the molecule is non-polar ( for solubility in the oil phase ) and a smaller part is polar ( for orientation and solubility into the water phase ).
Typical properties of oil in water emulsions include : creamy feel, mixing readily with water and high SPF efficacy. The composition of the invention is preferably in the form of an oil in water emulsion.
An example of a suitable emulsifying system includes fatty acid glycerol esters such as glycerol monostearate, fatty alcohol ethoxylates such as ethoxy (20 ) stearyl alcohol, fatty alcohols such as C16.18 fatty alcohols, and blends of fatty alcohol ethoxylates with alkyl phenol ethoxylates such as a blend of cetostearyl alcohol and PEG
stearate. A
wide range of other emulsifiers also appear useful for this purpose.
The composition optionally includes a film former. The preferred film former is Tricontanyl PVP.
The composition may include thickeners, chelating agents and pH adjusting agents as required. These are readily known to the person skilled in the art.
Suitable thickeners include acidic acrylates such as carboxyl polymethylene, and cellulose based thickeners such as methyl cellulose, guar gum, sodium alginate and sodium carboxymethyl cellulose. A suitable chelating agent is disodium EDTA.
Triethanolamine may be used as a neutraliser as if required.
The person skilled in the art will recognise that perfumes, emollients and moisturisers may be included to satisfy organoleptic requirements.
Preservatives may also be used as required. These are readily known to the person skilled in the art.
The inventors have found that in preparing an emulsion, the order of addition of ingredients affects the SPF of the fmal composition.
Accordingly, a third aspect of the invention consists in a method of manufacturing a sunscreen composition including one or more insect repellents and one or more LJV
sunscreening agents, the composition being in the form of an emulsion having a water phase and an oil phase characterised in that the water phase and oil phase are prepared and combined to form an emulsion prior to the addition of at least one inorganic compound which is used as a sunscreening agent.
Backgrround Art The prior art is replete with insect repellent compositions and sunscreen compositions. Whilst these compositions are separately effective, it is desirable to provide an effective combined insect repellent and sunscreen composition.
Surprisingly, it has now been found that to produce a stable, effective combined insect repellent and sunscreen composition requires a carefully selected use of emulsifiers.
Disclosure of Invention Accordingly, the present invention consists in a sunscreen composition including one or more insect repellents and one or more UV sunscreening agents characterised in that the composition includes 3-9% by weight in total of at least two emulsifiers, based on the total weight of the composition. The inventors have found that with appropriate emulsifiers, the sunscreen agent in combination with insect repellent give a composition that is stable and effective with respect to SPF.
One or more inorganic compounds are incorporated in the composition of the invention as a sunscreening agent. The preferred inorganic compounds are titanium oxide and zinc oxide. For these compounds, the particle size can be selected to scatter light in the UV range whilst transmitting light in the visible range thereby remaining transparent on the skin. This is highly desirable from a cosmetic point of view.
Micronised particles, that is those particles less than 100 nm in size, give optimal performance. Micronised titanium dioxide is most preferred for the composition of the invention. The concentration of inorganic compound may be in the range of 1-5%
by weight based on the total weight of the composition, preferably 2-4% by weight and more preferably 3% by weight.
One or more insect repellents are included in the composition. The repellents are chosen for repellency of flying or biting insects and for low skin irritancy.
Suitable repellents include N,N-diethyl-m-toluamide (DEET), dipropyl pyridine-2,5-dicarboxylate, pyrethrins, dimethyl phthalate, 2,3:4,5-bis(2-butylene)tetrahydrofiufural, citronella, geraniol, lemon grass oil, eugenol, p-menthane-3,8-diol, ethylbutyl acetylamino propionate, 1-piperidinecarboxylic acid and 2-(2-hydroxyethyl)-esterl -methylpropyl-ester.
These can be combined with synergists such as piperonyl butoxide and N-(2-ethylhexyl)-8,9,10-trinorborn-5-ene-2,3 -dicarboximide.
DEET and dipropyl pyridine-2,5-dicarboxylate are the preferred repellents.
The total amount of insect repellent in the composition may be 4-20% by weight based on the total weight of the composition, preferably 4-15% by weight and more preferably 5-10% by weight.
The composition may include one or more other UV sunscreening agents. These are generally organic compounds which absorb a specific range of UV radiation.
Suitable sunscreening agents include octyl methoxycinnamate, oxybenzone, amino benzoic acid, Cinoxate, DEA-methoxycinnamate, Digalloyl, Dioxybenzene, Padimate 0, Ethyl dihydroxypropyl p-aminobenzoate, octyl salicylate, glyceryl aminobenzoate, Homosalate, Urocanic acid, isopropylbenzyl salicylate, menthyl anthranilate, octocrylene, Sulisbenzone and its sodium salt and triethanolamine salicylate.
A combination of octylmethoxycinnamate and oxybenzone is most preferred. Each sunscreening agent is preferably incorporated in the composition in an amount of 3-10%
by weight based on the total weight of the composition.
The composition is prepared in the form an emulsion. Accordingly, a second aspect of the invention consists in a sunscreen composition further including, by weight, based on the total weight of the composition, 7% in total emulsifier, up to 5%, preferably 1-5%, more preferably 3% film former, up to 0.25%, preferably 0.05-0.25%, more preferably 0.15% thickener, up to 0.3%, preferably 0.1-0.3%, more preferably 0.15% neutraliser, up to 0.3%, preferably 0.1-0.3%, more preferably 0.2% chelating agent and up to 2.5% of at least one of preservative, perfume and moisturiser.
The choice of emulsifier will depend on the insect repellents and sunscreening agents selected. More than two emulsifiers may be included. An emulsion is most accurately defined as a dispersion of liquid droplets in a second immiscible liquid.
Dispersions may be formed temporarily through agitation of the two immiscible liquids, however, resolution of the emulsion is usually rapid and complete unless a stabilising additive or emulsifier is used.
Emulsions usually consist of water or an aqueous solution as one immiscible phase and some organic liquid, or "oil", as the other phase. When the oil is dispersed in the aqueous phase the emulsion is called oil in water (o/w ) or alternatively, if the aqueous phase is dispersed in the oily phase the emulsion is described as water in oil ( w/o ). An emulsifying agent is usually required to stabilise the emulsion. Such agents are ordinarily large molecules of which the greatest part of the molecule is non-polar ( for solubility in the oil phase ) and a smaller part is polar ( for orientation and solubility into the water phase ).
Typical properties of oil in water emulsions include : creamy feel, mixing readily with water and high SPF efficacy. The composition of the invention is preferably in the form of an oil in water emulsion.
An example of a suitable emulsifying system includes fatty acid glycerol esters such as glycerol monostearate, fatty alcohol ethoxylates such as ethoxy (20 ) stearyl alcohol, fatty alcohols such as C16.18 fatty alcohols, and blends of fatty alcohol ethoxylates with alkyl phenol ethoxylates such as a blend of cetostearyl alcohol and PEG
stearate. A
wide range of other emulsifiers also appear useful for this purpose.
The composition optionally includes a film former. The preferred film former is Tricontanyl PVP.
The composition may include thickeners, chelating agents and pH adjusting agents as required. These are readily known to the person skilled in the art.
Suitable thickeners include acidic acrylates such as carboxyl polymethylene, and cellulose based thickeners such as methyl cellulose, guar gum, sodium alginate and sodium carboxymethyl cellulose. A suitable chelating agent is disodium EDTA.
Triethanolamine may be used as a neutraliser as if required.
The person skilled in the art will recognise that perfumes, emollients and moisturisers may be included to satisfy organoleptic requirements.
Preservatives may also be used as required. These are readily known to the person skilled in the art.
The inventors have found that in preparing an emulsion, the order of addition of ingredients affects the SPF of the fmal composition.
Accordingly, a third aspect of the invention consists in a method of manufacturing a sunscreen composition including one or more insect repellents and one or more LJV
sunscreening agents, the composition being in the form of an emulsion having a water phase and an oil phase characterised in that the water phase and oil phase are prepared and combined to form an emulsion prior to the addition of at least one inorganic compound which is used as a sunscreening agent.
In a fourth aspect, the invention consists in a method of manufacturing a sunscreen composition including the steps of:
(a) preparing a water phase including water and thickener (b) preparing an oil phase including at least two emulsifiers, at least one insect repellent, at least one organic sunscreen and optionally, a film former, (c) combining said water phase and oil phase to form an emulsion; and (d) adding at least one inorganic compound as a sunscreening agent.
In a fifth aspect, the invention consists in a sunscreening composition manufactured according to the methods described above.
The invention will now be further described with reference to a number of examples.
Modes for carrying Out the Invention Formula 1 Formula 2 Formula 3 Ingredients w/w% w/w% w/w MGK 326 2:8 2.8 2,8 Parso~MCX 7.5 9.0 9.0 Ox benzone USP 3 5 5 Tioveil'A -G 7.5 10 7.5 Cithrol GMS A/S 1.5 1.5 1.5 Vol o S20 2 2 2 Crodaaol*CS70 1.75 1.75 1.75 Polawax GP 200 1.75 1.75 1.75 Antaronn WP-660 3 3 3 (Tricontanyl PVP
Silicone DC 200/500 0.3 0.3 0.3 Carbo o1940 0.15 0.15 0.15 Aloe Vera owder 1:200 0.01 0.01 0.01 Disolvine Na2 0.2 0.2 0.2 (disodium EDTA) Triethanolamine 85% 0.15 0.15 0.15 Germabeo II-E I 1 I
Perfume Kokoda 6463 0.3 0.3 0.3 Water 60.09 54.09 56.59 100 10.0 100 The ingredients listed above are further described below in Table 1.
*Trade-mark INGREDIENT (SUPPLIER) PURPOSE
DEET (MGK) Mosquito repellent N,N-dieth 1-m-toluamide MGK* 326 (MGK) Fly repellent di ro 1 p 'dine-2,5-dicarbo late 99%
*
Parsol MCX (Givaudan) UVB filter, organic sunscreen o l metho cinnamate 98%
Benzophenone -3 (Aceto Corp.) UVA/B filter, organic sunscreen oxybenzone 98%
Tioveil AQ LNA/B filter, inorganic sunscreen micronised titanium dioxide 40%
Cithrol GMS A/S (Croda) emulsifier glycerol monostearate Volpo S20 (Croda) emulsifier ethox (20) s I alcohol ~
Crodacol CS70 (Croda) emulsifier cetostearyl alcohol 35/65 Polawax GP 200 (Croda) emulsifier blend of cetostearyl alcohol and PEG stearate AntaroriWP-660 (ISP) film former 2-pyrrolidinone, 1-ethenyl oI er with 1-triacontene Silicone DC 200/500 (Dow Corning) emollient silicone oil 200/500 *
Carbopo1940 (B F Goodrich) thickener carbo 1 ol eth lene Aloe Vera powder 1:200 moisturiser Sequestrene NA2 chelating agent disodium EDTA
Triethamolamine H/H (Union Carbide neutraliser Germaben II-E preservative Kokoda 6463 erfume Water diluent *Trade-mark Preparation A water phase is prepared by adding water to a clean, dry mixing vessel and stirring to create a vortex. Carbopol powder is sprinkled into the vortex and the mixture heated to 75-80 C. .
In a separate vessel, an oil phase is prepared by adding emulsifiers, film former, mosquito and fly repellent i.e. Cithrol GMS A/S, Volpo S20, Crodacol CS70, Polawax GP 200, Antaron WP-660, DEET and MGK-326. The mixture is stirred and heated.
When all ingredients have melted, oxybenzone is added. Heating is continued to 80 C until the oxybenzone is melted then octyl methoxycinnamate is added.
Stirring is maintained until the mixture is homogenous and clear.
When both the water and the oil phases are at a temperature of 75-80 C, the oil phase is introduced into the water phase with stirring. When all the oil phase is added, stirring is stopped and the mixture is homogenised for five minutes. Stirring is recommenced and the chelating agent and half of the neutraliser are added followed by the addition of the titanium dioxide. The remaining neutraliser is then added.
Stirring is stopped and the mixture is homogenised for five minutes. Stirring is recommenced with addition of moisturiser, emollient and preservative.
If a zinc oxide inorganic sunscreen agent is used, a different thickening system would be appropriate. A cellulose-based thickener such as methyl cellulose, guar gum, sodium alginate and sodium carboxymethyl cellulose could be used, in which case a neutraliser would not be required.
Testin~
Formulae 1 and 3 were tested in two ways:
A. Determination of sun protection factor (SPF) and B. Broad spectrum test.
A. Determination of sun protection factor (SPF) Principle: The individual sun protection factor, SPF, of a sunscreen product is determined from the minimum erthemal dose (MED) of the skin that has been protected with the sunscreen product and from the MED of an adjacent area of unprotected skin, under specific conditions by means of the following relationship, where the UV
source has constant intensity:
Sun Protection Factor = MED for protected skin MED for unprotected skin The sun protection factor of a product is calculated as the arithmetical mean of the individual sun protection factors. MED is defined as the amount of energy from any source required to produce a minimally perceptible redness reaction of the skin.
Test procedure:
The MED of the (untreated) subject at the test site is first determined using a solar simulator. An experienced tester can often predict a MED for a particularlamp intensity and subject but, where necessary, one or more sets of exposures must be read 16h to 24h later to determine the approximate MED without exposing the subject to excessive radiation. Exposures are made on one or more small subsite areas at measured exposure times.
On the basis of this predicted or approximate value, the MED is determined more precisely by a set of exposures which span a dose range of approximately 0.6 to 1.5 of the MED. Usually, these doses are administered the day before the product is tested but they may be administered at the same time. When the doses are administered the day before, the result when read, not only provides the denominator for calculating the protection factor but, when multiplied by the expected or likely value of the product's protection factor, provides an estimate for the longer exposure needed to assess the product.
The product is assessed by exposing a set of small subsite areas adjacent to the untreated areas, after application of the product. Times of exposure are selected to bracket the above estimate. when read 16h to 24h later, the MED for the treated skin is divided by the MED for untreated skin to give the protection factor.
The results of the tests on formulae 1 and 3 are shown below in table 2.
Table 2 Subject Sex Skin Type MED. Protected SPF
sec MED sec Formula 1 A F III 16 496 31 B M II 10 >341 34.1 C M II 12 372 31.0 Formula 3 A F III 16 >496 >31.0 B M II 10 341 34.1 C M II 12 >450 >37.5 Skin Type = I - sensitive, always burns II - moderate, burns sometimes III - normal, bums and tans MED = minimal erythermal dose SPF over 30 was demonstrated in each case.
B. Broad Spectrum test.
There are three alternative test methods of sample preparation and transmittance measurement in the region 320 - 360nm of broad spectrum sunscreen products well known to those skilled in the art. The method used by the inventors is the thin film method.
Materials and equipment:
The following materials and equipment are required: A spectrophotometer capable of determining percentage transmission from 320 -360nm radiation. A quartz cell, with suitable lid, constructed to provide an 84m layer of sunscreen product for testing.
Procedure:
Fill the cell with the sunscreen product and determine the transmission of the product from 320 - 360nm inclusive. Record the percentage transmission of the product under test from 320 - 360nm inclusive.
Results:
The compositions of formulae 1 and 3 did not transmit more than 10% of UV
radiation at any wavelength between 320 nm and 360 nm inclusive.
(a) preparing a water phase including water and thickener (b) preparing an oil phase including at least two emulsifiers, at least one insect repellent, at least one organic sunscreen and optionally, a film former, (c) combining said water phase and oil phase to form an emulsion; and (d) adding at least one inorganic compound as a sunscreening agent.
In a fifth aspect, the invention consists in a sunscreening composition manufactured according to the methods described above.
The invention will now be further described with reference to a number of examples.
Modes for carrying Out the Invention Formula 1 Formula 2 Formula 3 Ingredients w/w% w/w% w/w MGK 326 2:8 2.8 2,8 Parso~MCX 7.5 9.0 9.0 Ox benzone USP 3 5 5 Tioveil'A -G 7.5 10 7.5 Cithrol GMS A/S 1.5 1.5 1.5 Vol o S20 2 2 2 Crodaaol*CS70 1.75 1.75 1.75 Polawax GP 200 1.75 1.75 1.75 Antaronn WP-660 3 3 3 (Tricontanyl PVP
Silicone DC 200/500 0.3 0.3 0.3 Carbo o1940 0.15 0.15 0.15 Aloe Vera owder 1:200 0.01 0.01 0.01 Disolvine Na2 0.2 0.2 0.2 (disodium EDTA) Triethanolamine 85% 0.15 0.15 0.15 Germabeo II-E I 1 I
Perfume Kokoda 6463 0.3 0.3 0.3 Water 60.09 54.09 56.59 100 10.0 100 The ingredients listed above are further described below in Table 1.
*Trade-mark INGREDIENT (SUPPLIER) PURPOSE
DEET (MGK) Mosquito repellent N,N-dieth 1-m-toluamide MGK* 326 (MGK) Fly repellent di ro 1 p 'dine-2,5-dicarbo late 99%
*
Parsol MCX (Givaudan) UVB filter, organic sunscreen o l metho cinnamate 98%
Benzophenone -3 (Aceto Corp.) UVA/B filter, organic sunscreen oxybenzone 98%
Tioveil AQ LNA/B filter, inorganic sunscreen micronised titanium dioxide 40%
Cithrol GMS A/S (Croda) emulsifier glycerol monostearate Volpo S20 (Croda) emulsifier ethox (20) s I alcohol ~
Crodacol CS70 (Croda) emulsifier cetostearyl alcohol 35/65 Polawax GP 200 (Croda) emulsifier blend of cetostearyl alcohol and PEG stearate AntaroriWP-660 (ISP) film former 2-pyrrolidinone, 1-ethenyl oI er with 1-triacontene Silicone DC 200/500 (Dow Corning) emollient silicone oil 200/500 *
Carbopo1940 (B F Goodrich) thickener carbo 1 ol eth lene Aloe Vera powder 1:200 moisturiser Sequestrene NA2 chelating agent disodium EDTA
Triethamolamine H/H (Union Carbide neutraliser Germaben II-E preservative Kokoda 6463 erfume Water diluent *Trade-mark Preparation A water phase is prepared by adding water to a clean, dry mixing vessel and stirring to create a vortex. Carbopol powder is sprinkled into the vortex and the mixture heated to 75-80 C. .
In a separate vessel, an oil phase is prepared by adding emulsifiers, film former, mosquito and fly repellent i.e. Cithrol GMS A/S, Volpo S20, Crodacol CS70, Polawax GP 200, Antaron WP-660, DEET and MGK-326. The mixture is stirred and heated.
When all ingredients have melted, oxybenzone is added. Heating is continued to 80 C until the oxybenzone is melted then octyl methoxycinnamate is added.
Stirring is maintained until the mixture is homogenous and clear.
When both the water and the oil phases are at a temperature of 75-80 C, the oil phase is introduced into the water phase with stirring. When all the oil phase is added, stirring is stopped and the mixture is homogenised for five minutes. Stirring is recommenced and the chelating agent and half of the neutraliser are added followed by the addition of the titanium dioxide. The remaining neutraliser is then added.
Stirring is stopped and the mixture is homogenised for five minutes. Stirring is recommenced with addition of moisturiser, emollient and preservative.
If a zinc oxide inorganic sunscreen agent is used, a different thickening system would be appropriate. A cellulose-based thickener such as methyl cellulose, guar gum, sodium alginate and sodium carboxymethyl cellulose could be used, in which case a neutraliser would not be required.
Testin~
Formulae 1 and 3 were tested in two ways:
A. Determination of sun protection factor (SPF) and B. Broad spectrum test.
A. Determination of sun protection factor (SPF) Principle: The individual sun protection factor, SPF, of a sunscreen product is determined from the minimum erthemal dose (MED) of the skin that has been protected with the sunscreen product and from the MED of an adjacent area of unprotected skin, under specific conditions by means of the following relationship, where the UV
source has constant intensity:
Sun Protection Factor = MED for protected skin MED for unprotected skin The sun protection factor of a product is calculated as the arithmetical mean of the individual sun protection factors. MED is defined as the amount of energy from any source required to produce a minimally perceptible redness reaction of the skin.
Test procedure:
The MED of the (untreated) subject at the test site is first determined using a solar simulator. An experienced tester can often predict a MED for a particularlamp intensity and subject but, where necessary, one or more sets of exposures must be read 16h to 24h later to determine the approximate MED without exposing the subject to excessive radiation. Exposures are made on one or more small subsite areas at measured exposure times.
On the basis of this predicted or approximate value, the MED is determined more precisely by a set of exposures which span a dose range of approximately 0.6 to 1.5 of the MED. Usually, these doses are administered the day before the product is tested but they may be administered at the same time. When the doses are administered the day before, the result when read, not only provides the denominator for calculating the protection factor but, when multiplied by the expected or likely value of the product's protection factor, provides an estimate for the longer exposure needed to assess the product.
The product is assessed by exposing a set of small subsite areas adjacent to the untreated areas, after application of the product. Times of exposure are selected to bracket the above estimate. when read 16h to 24h later, the MED for the treated skin is divided by the MED for untreated skin to give the protection factor.
The results of the tests on formulae 1 and 3 are shown below in table 2.
Table 2 Subject Sex Skin Type MED. Protected SPF
sec MED sec Formula 1 A F III 16 496 31 B M II 10 >341 34.1 C M II 12 372 31.0 Formula 3 A F III 16 >496 >31.0 B M II 10 341 34.1 C M II 12 >450 >37.5 Skin Type = I - sensitive, always burns II - moderate, burns sometimes III - normal, bums and tans MED = minimal erythermal dose SPF over 30 was demonstrated in each case.
B. Broad Spectrum test.
There are three alternative test methods of sample preparation and transmittance measurement in the region 320 - 360nm of broad spectrum sunscreen products well known to those skilled in the art. The method used by the inventors is the thin film method.
Materials and equipment:
The following materials and equipment are required: A spectrophotometer capable of determining percentage transmission from 320 -360nm radiation. A quartz cell, with suitable lid, constructed to provide an 84m layer of sunscreen product for testing.
Procedure:
Fill the cell with the sunscreen product and determine the transmission of the product from 320 - 360nm inclusive. Record the percentage transmission of the product under test from 320 - 360nm inclusive.
Results:
The compositions of formulae 1 and 3 did not transmit more than 10% of UV
radiation at any wavelength between 320 nm and 360 nm inclusive.
5 It will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to the invention as shown in the specific embodiments without departing from the spirit or scope of the invention as broadly described. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive.
Claims (17)
1. A method of manufacturing a sunscreen composition including one or more insect repellents, one or more organic UV sunscreening agents and one or more inorganic sunscreening agents, the composition being in the form of an emulsion having an oil phase and a water phase, which method comprises:
preparing the water phase and the oil phase, and combining the water and oil phases to form the emulsion prior to addition of at least one inorganic compound which is used as a sunsereening agent.
preparing the water phase and the oil phase, and combining the water and oil phases to form the emulsion prior to addition of at least one inorganic compound which is used as a sunsereening agent.
2. A method of manufacturing a sunscreen composition, comprising the steps of:
(a) preparing a water phase including water and a thickener;
(b) preparing an oil phase including at least two emulsifiers, at least one insect repellent and at least one organic UV sunscreening agent;
(c) combining the water phase and the oil phase to form an emulsion; and (d) adding at least one inorganic compound which is used as a sunscreening agent.
(a) preparing a water phase including water and a thickener;
(b) preparing an oil phase including at least two emulsifiers, at least one insect repellent and at least one organic UV sunscreening agent;
(c) combining the water phase and the oil phase to form an emulsion; and (d) adding at least one inorganic compound which is used as a sunscreening agent.
3. A method of manufacturing a sunscreen composition in the form of an oil-in-water emulsion, comprising the steps of:
(a) preparing a water phase by combining water and a thickener while stirring and heating;
(b) preparing an oil phase by combining at least two emulsifiers, at least one insect repellent, at least one organic UV sunscreening agent and optionally a film former while stirring and heating;
(c) adding the oil phase to the water phase while stirring;
(d) optionally adding a chelating agent and a neutraliser to the combined water and oil phases; and (e) adding at least one inorganic compound which is used as a sunscreening agent to the combined water and oil phases while stirring.
(a) preparing a water phase by combining water and a thickener while stirring and heating;
(b) preparing an oil phase by combining at least two emulsifiers, at least one insect repellent, at least one organic UV sunscreening agent and optionally a film former while stirring and heating;
(c) adding the oil phase to the water phase while stirring;
(d) optionally adding a chelating agent and a neutraliser to the combined water and oil phases; and (e) adding at least one inorganic compound which is used as a sunscreening agent to the combined water and oil phases while stirring.
4. The method of claim 3, wherein the water phase of step (a) and the oil phase of step (b) are heated to a temperature in the range of 75-80°C, respectively, before combining in step (c).
5. The method of any one of claims 2 to 4, wherein the emulsifiers are selected from the group consisting of fatty acid glycerol esters, fatty alcohol ethoxylates, fatty alcohols and blends of fatty alcohol ethoxylates with alkyl phenol ethoxylates.
6. The method of any one of claims 2 to 4, wherein the emulsifiers are selected from the group consisting of glycerol monostearate, ethoxy stearyl alcohol, C16-18 fatty alcohols and blends of cetostearyl alcohol and PEG stearate.
7. The method of any one of claims 1 to 6, wherein the inorganic compound is zinc oxide or titanium dioxide.
8. The method of any one of claims 1 to 6, wherein the inorganic compound is micronised zinc oxide or micronised titanium dioxide.
9. The method of any one of claims 1 to 6, wherein the inorganic compound is micronised titanium dioxide.
10. The method of any one of claims 1 to 9, wherein the insect repellent is N,N-diethyl-m-toluamide, dipropylpyridine-2,5-dicarboxylate or a mixture thereof.
11. The method of any one of claims 1 to 10, wherein the organic UV sunscreening agent is oxybenzone, octylmethoxycinnamate or a mixture thereof.
12. The method of any one of claims 1 to 11, wherein the composition includes 3-9% by weight in total of the emulsifiers, based on the total weight of the composition.
13. The method of claim 12, wherein the composition includes by weight, based on the total weight of the composition:
(a) 1-5% of the inorganic compound sunscreening agent, (b) 4-20% of the insect repellent, and (c) 3-10% each of the organic UV sunscreening agents.
(a) 1-5% of the inorganic compound sunscreening agent, (b) 4-20% of the insect repellent, and (c) 3-10% each of the organic UV sunscreening agents.
14. The method of claim 12 or 13, wherein the composition further includes:
(e) up to 5% of a film former, (f) up to 0.25% of a thickener, (g) up to 0.3% of a neutraliser, (h) up to 0.3% of a chelating agent, and (i) up to 2.5% of at least one of a preservative, a perfume and a moisturiser, all based on the total weight of the composition.
(e) up to 5% of a film former, (f) up to 0.25% of a thickener, (g) up to 0.3% of a neutraliser, (h) up to 0.3% of a chelating agent, and (i) up to 2.5% of at least one of a preservative, a perfume and a moisturiser, all based on the total weight of the composition.
15. A sunscreen composition which is in the form of an emulsion having an oil phase and a water phase and which comprises:
(i) at least one insect repellent;
(ii) at least one organic UV sunscreening agent;
(iii) at least one inorganic sunscreening agent;
and (iv) at least two emulsifiers selected from the group consisting of glycerol monostearate, ethoxy (20) stearyl alcohol, cetostearyl alcohol 35/65 and a blend of cetostearyl alcohol and PEG stearate.
(i) at least one insect repellent;
(ii) at least one organic UV sunscreening agent;
(iii) at least one inorganic sunscreening agent;
and (iv) at least two emulsifiers selected from the group consisting of glycerol monostearate, ethoxy (20) stearyl alcohol, cetostearyl alcohol 35/65 and a blend of cetostearyl alcohol and PEG stearate.
16. The sunscreen composition of claim 15, wherein:
the insect repellent is selected from the group consisting of N,N-diethyl-m-toluamide (DEET), dipropyl pyridine-2,5-dicarboxylate, pyrethrins, dimethyl phthalate, 2,3:4,5-bis(2-butylene)tetrahydrofurfural, citronella, geraniol, lemon grass oil, eugenol, p-menthane-3,8-diol, ethylbutyl acetylamino propionate, 1-piperidinecarboxylic acid and 2-(2-hydroxyethyl)-ester1-methylpropyl-ester and is contained in a total amount of 4-20% by weight based on the total weight of the composition;
the organic UV sunscreening agent is selected from the group consisting of octyl methoxycinnamate, oxybenzone, amino benzoic acid, cinoxate, DEA-methoxycinnamate, digalloyl, dioxybenzene, padimate O, ethyl dihydroxypropyl p-aminobenzoate, octyl salicylate, glyceryl aminobenzoate, homosalate, urocanic acid, isopropylbenzyl salicylate, menthyl anthranilate, octocrylene, sulisbenzone and its sodium salt and triethanolamine salicylate and each is contained in an amount of 3-10% by weight based on the total weight of the composition;
the inorganic UV sunscreening agent is selected from the group consisting of micronized titanium dioxide and micronized zinc oxide and is contained in an amount of 1-5%
by weight based on the total weight of the composition; and the emulsifiers are contained in a total amount of 3-9% by weight based on the total weight of the composition.
the insect repellent is selected from the group consisting of N,N-diethyl-m-toluamide (DEET), dipropyl pyridine-2,5-dicarboxylate, pyrethrins, dimethyl phthalate, 2,3:4,5-bis(2-butylene)tetrahydrofurfural, citronella, geraniol, lemon grass oil, eugenol, p-menthane-3,8-diol, ethylbutyl acetylamino propionate, 1-piperidinecarboxylic acid and 2-(2-hydroxyethyl)-ester1-methylpropyl-ester and is contained in a total amount of 4-20% by weight based on the total weight of the composition;
the organic UV sunscreening agent is selected from the group consisting of octyl methoxycinnamate, oxybenzone, amino benzoic acid, cinoxate, DEA-methoxycinnamate, digalloyl, dioxybenzene, padimate O, ethyl dihydroxypropyl p-aminobenzoate, octyl salicylate, glyceryl aminobenzoate, homosalate, urocanic acid, isopropylbenzyl salicylate, menthyl anthranilate, octocrylene, sulisbenzone and its sodium salt and triethanolamine salicylate and each is contained in an amount of 3-10% by weight based on the total weight of the composition;
the inorganic UV sunscreening agent is selected from the group consisting of micronized titanium dioxide and micronized zinc oxide and is contained in an amount of 1-5%
by weight based on the total weight of the composition; and the emulsifiers are contained in a total amount of 3-9% by weight based on the total weight of the composition.
17. The sunscreening composition of claim 15 or 16, wherein the composition further includes:
(e) up to 5% of a film former, (f) up to 0.25% of a thickener, (g) up to 0.3% of a neutraliser, (h) up to 0.3% of a chelating agent, and (i) up to 2.5% of at least one of a preservative, a perfume and a moisturiser, all based on the total weight of the composition.
(e) up to 5% of a film former, (f) up to 0.25% of a thickener, (g) up to 0.3% of a neutraliser, (h) up to 0.3% of a chelating agent, and (i) up to 2.5% of at least one of a preservative, a perfume and a moisturiser, all based on the total weight of the composition.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9900663 | 1999-01-14 | ||
| GB9900663.7 | 1999-01-14 | ||
| PCT/GB2000/000068 WO2000041672A1 (en) | 1999-01-14 | 2000-01-11 | A combined insect repellent and sunscreen composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2360494A1 CA2360494A1 (en) | 2000-07-20 |
| CA2360494C true CA2360494C (en) | 2007-10-23 |
Family
ID=10845892
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002360494A Expired - Fee Related CA2360494C (en) | 1999-01-14 | 2000-01-11 | A combined insect repellent and sunscreen composition |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP1146849A1 (en) |
| JP (1) | JP2002534453A (en) |
| CN (1) | CN1172655C (en) |
| AR (1) | AR022280A1 (en) |
| AU (1) | AU770861B2 (en) |
| BR (1) | BR0007497A (en) |
| CA (1) | CA2360494C (en) |
| GB (1) | GB2345636A (en) |
| MX (1) | MXPA01007172A (en) |
| WO (1) | WO2000041672A1 (en) |
| ZA (1) | ZA200106589B (en) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6436377B1 (en) | 2001-02-26 | 2002-08-20 | Societe L'oreal S.A. | Enhanced SPF sunscreen (sprayable) formulations comprising interpolymers of PVP/dimethiconylacrylate/polycarbamyl/polyglycol ester |
| US6436376B1 (en) * | 2001-02-26 | 2002-08-20 | Societe L'oreal S.A. | Enhanced SPF UV-sunscreen/tricontanyl PVP photoprotecting (sprayable) formulations |
| WO2004071479A1 (en) | 2003-02-12 | 2004-08-26 | Connetics Australia Pty Ltd | Film foaming hydroalcoholic foam |
| US8512721B2 (en) * | 2004-11-19 | 2013-08-20 | Illinois Tool Works Inc. | Water resistant sunscreen and insect repellant towel |
| DE102006007547A1 (en) * | 2006-02-16 | 2007-08-30 | Lanxess Deutschland Gmbh | Gel formulation for arthropod and platelet defenses |
| CN101215782B (en) * | 2008-01-08 | 2010-06-09 | 上海大学 | Anti-light aging finishing method of aromatic polyamide fiber fabric |
| US8362077B2 (en) * | 2008-08-15 | 2013-01-29 | Pibed Limited | Chemical compositions for skin care emulsions and heavy duty hand cleansers |
| US8580861B2 (en) | 2008-08-15 | 2013-11-12 | Pibed Limited | Chemical composition for skin care formulations |
| KR101637185B1 (en) * | 2008-10-22 | 2016-07-07 | 다우 글로벌 테크놀로지스 엘엘씨 | Sunscreen compositions incorporating methylcellulose as an SPF booster and methods |
| CN101779627A (en) * | 2009-01-16 | 2010-07-21 | 岑绍辉 | Invisible mosquito-prevention mosquito-repellent combination |
| CN103356410A (en) * | 2012-03-29 | 2013-10-23 | 威玛精密化学科技股份有限公司 | Catalpa bungei extract composition with mosquito-proof and sun-proof effects |
| CA2879468A1 (en) * | 2012-07-26 | 2014-01-30 | Riemann Trading Aps | Improved sunscreen composition |
| CN102860960A (en) * | 2012-09-22 | 2013-01-09 | 南京正亮医药科技有限公司 | Insect repelling emulsifiable paste |
| CN105708863A (en) * | 2016-03-21 | 2016-06-29 | 江南大学 | Composition capable of achieving sun protection and preventing infection of mosquito-borne viruses such as Zika virus |
| MY199207A (en) * | 2016-07-15 | 2023-10-19 | Lec Kk | Pest repellent composition, and method for repelling pests |
| CN109769538A (en) * | 2019-03-08 | 2019-05-21 | 珠海市润农科技有限公司 | Utilize the method for photosynthetic film prevention and control balsam pear drosophila high in fat |
| CN110638675A (en) * | 2019-09-17 | 2020-01-03 | 江西农业大学 | Terpenoid repellent R2 microemulsion and preparation method thereof |
| CN110934780B (en) * | 2019-12-31 | 2021-07-27 | 威莱(广州)日用品有限公司 | Health care bath foam for pet dogs and preparation method thereof |
| US20230095618A1 (en) * | 2020-03-31 | 2023-03-30 | Firmenich Sa | Oil-in-water emulsion comprising a solid lipid material |
| CN112618434A (en) * | 2020-12-29 | 2021-04-09 | 广东岭南职业技术学院 | Mosquito-repelling sunscreen cream and preparation method thereof |
| CN116270270A (en) * | 2023-04-18 | 2023-06-23 | 深圳杉海创新技术有限公司 | Preparation method and application of supramolecular liposome sunscreen and mosquito repellent emulsion |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5518712A (en) * | 1992-06-25 | 1996-05-21 | Stewart; Ernest | Water resistant sunscreen protection and insect repellent compound |
| US5916541A (en) * | 1992-06-25 | 1999-06-29 | Stewart; Ernest G. | Water resistant sunscreen and insect repellent composition |
| GB2279007B (en) * | 1993-06-11 | 1997-04-02 | Tioxide Specialties Ltd | Compositions containing sunscreens |
| JPH0859447A (en) * | 1994-08-12 | 1996-03-05 | Kanebo Ltd | Skin protective agent |
| JPH08183720A (en) * | 1994-12-28 | 1996-07-16 | Kose Corp | Skin external medicine |
| EP0831766B2 (en) * | 1995-06-08 | 2009-11-11 | Johnson & Johnson Consumer Companies, Inc. | Sunscreen compositions |
| US5716602A (en) * | 1996-06-26 | 1998-02-10 | S. C. Johnson & Sons, Inc. | Insect repellent sunscreen |
| JP3518218B2 (en) * | 1996-12-26 | 2004-04-12 | 株式会社コーセー | Oil-in-water skin external preparation |
-
2000
- 2000-01-11 JP JP2000593286A patent/JP2002534453A/en active Pending
- 2000-01-11 CA CA002360494A patent/CA2360494C/en not_active Expired - Fee Related
- 2000-01-11 AU AU19932/00A patent/AU770861B2/en not_active Ceased
- 2000-01-11 BR BR0007497-7A patent/BR0007497A/en not_active IP Right Cessation
- 2000-01-11 CN CNB008027765A patent/CN1172655C/en not_active Expired - Fee Related
- 2000-01-11 EP EP00900269A patent/EP1146849A1/en not_active Withdrawn
- 2000-01-11 MX MXPA01007172A patent/MXPA01007172A/en unknown
- 2000-01-11 GB GB0000425A patent/GB2345636A/en not_active Withdrawn
- 2000-01-11 WO PCT/GB2000/000068 patent/WO2000041672A1/en not_active Ceased
- 2000-01-13 AR ARP000100151 patent/AR022280A1/en unknown
-
2001
- 2001-08-10 ZA ZA200106589A patent/ZA200106589B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2000041672A1 (en) | 2000-07-20 |
| AR022280A1 (en) | 2002-09-04 |
| CN1172655C (en) | 2004-10-27 |
| CA2360494A1 (en) | 2000-07-20 |
| ZA200106589B (en) | 2002-08-12 |
| JP2002534453A (en) | 2002-10-15 |
| CN1336816A (en) | 2002-02-20 |
| GB0000425D0 (en) | 2000-03-01 |
| GB2345636A (en) | 2000-07-19 |
| BR0007497A (en) | 2001-10-23 |
| EP1146849A1 (en) | 2001-10-24 |
| AU770861B2 (en) | 2004-03-04 |
| AU1993200A (en) | 2000-08-01 |
| MXPA01007172A (en) | 2002-07-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2360494C (en) | A combined insect repellent and sunscreen composition | |
| DE69716429T2 (en) | INSECT REPELLENT SUN PROTECT | |
| DE69620364T2 (en) | Light stabilizers | |
| US6485713B1 (en) | Sunscreen compositions and methods and materials for producing the same | |
| DE60319727T2 (en) | METHOD OF RESOLVING LIPOPHILER COMPOUNDS, AND COSMETIC COMPOSITION. | |
| US6770270B2 (en) | Methods of making and selling a sunscreen composition | |
| US20070189993A1 (en) | Stabilized photoprotective composition | |
| JP2001072531A (en) | Additive for improving water resistance of coscmetic formulations or formulations for skin care | |
| JPH0660092B2 (en) | Sunscreen composition | |
| JPH07304644A (en) | Anti-sunburn composition | |
| US20190290560A1 (en) | High SPF, Photo-protective Zinc Oxide Sunscreen Emulsions | |
| AU2009206363A1 (en) | Enhanced photoprotective compositions | |
| JPH06305949A (en) | Composition containing sunscreen | |
| GB2562134A (en) | Sunscreen compositions | |
| US20030072782A1 (en) | Combined insec repellent and suncreen composition | |
| DE69703676T2 (en) | SUBSTITUTED O-AMINOCARBONYLBENZOIC ACID SALTS AND THEIR USE AS LIGHT PROTECTION AGENTS | |
| ZA200600851B (en) | Metal oxide formulations | |
| KR20210139333A (en) | Efficient sunscreen composition with diethylamino hydroxybenzoyl hexyl benzoate and butyl methoxydibenzoylmethane and free of octocrylene | |
| CA2470622C (en) | Sunscreen composition comprising chlorphenesin | |
| JPS61215311A (en) | External agent for skin | |
| CA2270669A1 (en) | Sunscreen having disappearing color indicator | |
| KR100681705B1 (en) | Water-in-oil cosmetic composition containing fatty alcohol and cellulose alkyl ether as active ingredients | |
| US12533304B2 (en) | Waterproof mineral sunscreen compositions | |
| WO2003075878A2 (en) | Methods of making and selling a sunscreen composition | |
| JPS61215319A (en) | External agent for skin |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed |