CA1269015A - Exothermic stable foam compositions - Google Patents
Exothermic stable foam compositionsInfo
- Publication number
- CA1269015A CA1269015A CA000503882A CA503882A CA1269015A CA 1269015 A CA1269015 A CA 1269015A CA 000503882 A CA000503882 A CA 000503882A CA 503882 A CA503882 A CA 503882A CA 1269015 A CA1269015 A CA 1269015A
- Authority
- CA
- Canada
- Prior art keywords
- composition
- oil
- foaming agent
- propellant
- mixture
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 98
- 239000006260 foam Substances 0.000 title claims abstract description 39
- 239000004088 foaming agent Substances 0.000 claims abstract description 32
- 239000007787 solid Substances 0.000 claims abstract description 32
- 239000000443 aerosol Substances 0.000 claims abstract description 31
- 239000003380 propellant Substances 0.000 claims abstract description 27
- 239000007788 liquid Substances 0.000 claims abstract description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical group CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 36
- 239000003921 oil Substances 0.000 claims description 36
- 235000019198 oils Nutrition 0.000 claims description 36
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 20
- 239000001294 propane Substances 0.000 claims description 18
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims description 17
- 235000010445 lecithin Nutrition 0.000 claims description 17
- 239000000787 lecithin Substances 0.000 claims description 17
- 229940067606 lecithin Drugs 0.000 claims description 17
- 239000002245 particle Substances 0.000 claims description 17
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 16
- 239000000194 fatty acid Substances 0.000 claims description 16
- 229930195729 fatty acid Natural products 0.000 claims description 16
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims description 12
- 150000004665 fatty acids Chemical class 0.000 claims description 11
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical group CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 claims description 10
- 239000001587 sorbitan monostearate Substances 0.000 claims description 10
- 235000011076 sorbitan monostearate Nutrition 0.000 claims description 10
- 229940035048 sorbitan monostearate Drugs 0.000 claims description 10
- 239000003549 soybean oil Substances 0.000 claims description 10
- 235000012424 soybean oil Nutrition 0.000 claims description 10
- NGHUOSKIZOQGBY-PMDAXIHYSA-N [3-[3-[3-[3-[3-[3-[3-[3-[3-[2,3-bis[[(Z)-octadec-9-enoyl]oxy]propoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-[(Z)-octadec-9-enoyl]oxypropyl] (Z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(COC(=O)CCCCCCC\C=C/CCCCCCCC)OC(=O)CCCCCCC\C=C/CCCCCCCC)OC(=O)CCCCCCC\C=C/CCCCCCCC NGHUOSKIZOQGBY-PMDAXIHYSA-N 0.000 claims description 9
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical class O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 9
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 7
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 6
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 claims description 6
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 claims description 6
- 229920000223 polyglycerol Polymers 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000002430 hydrocarbons Chemical group 0.000 claims description 5
- 239000007921 spray Substances 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- 235000019483 Peanut oil Nutrition 0.000 claims description 4
- 235000012343 cottonseed oil Nutrition 0.000 claims description 4
- 239000002385 cottonseed oil Substances 0.000 claims description 4
- 150000002314 glycerols Chemical class 0.000 claims description 4
- 239000000312 peanut oil Substances 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 239000005639 Lauric acid Substances 0.000 claims description 3
- 235000019486 Sunflower oil Nutrition 0.000 claims description 3
- 239000004359 castor oil Substances 0.000 claims description 3
- 235000019438 castor oil Nutrition 0.000 claims description 3
- 229910052681 coesite Inorganic materials 0.000 claims description 3
- 235000005687 corn oil Nutrition 0.000 claims description 3
- 239000002285 corn oil Substances 0.000 claims description 3
- 229910052906 cristobalite Inorganic materials 0.000 claims description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 3
- 239000000944 linseed oil Substances 0.000 claims description 3
- 235000021388 linseed oil Nutrition 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 239000004006 olive oil Substances 0.000 claims description 3
- 235000008390 olive oil Nutrition 0.000 claims description 3
- 239000011236 particulate material Substances 0.000 claims description 3
- 235000019271 petrolatum Nutrition 0.000 claims description 3
- 235000012239 silicon dioxide Nutrition 0.000 claims description 3
- 229910052682 stishovite Inorganic materials 0.000 claims description 3
- 239000002600 sunflower oil Substances 0.000 claims description 3
- 229910052905 tridymite Inorganic materials 0.000 claims description 3
- AGNTUZCMJBTHOG-UHFFFAOYSA-N 3-[3-(2,3-dihydroxypropoxy)-2-hydroxypropoxy]propane-1,2-diol Chemical group OCC(O)COCC(O)COCC(O)CO AGNTUZCMJBTHOG-UHFFFAOYSA-N 0.000 claims description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical group FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims description 2
- 239000008173 hydrogenated soybean oil Substances 0.000 claims 2
- 235000021313 oleic acid Nutrition 0.000 claims 2
- 150000002889 oleic acids Chemical class 0.000 claims 2
- 229920005573 silicon-containing polymer Polymers 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 1
- 241000195940 Bryophyta Species 0.000 description 19
- 235000011929 mousse Nutrition 0.000 description 19
- 238000009472 formulation Methods 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 11
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 239000004615 ingredient Substances 0.000 description 9
- INJRKJPEYSAMPD-UHFFFAOYSA-N aluminum;silicic acid;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O INJRKJPEYSAMPD-UHFFFAOYSA-N 0.000 description 8
- -1 polyol fatty acid esters Chemical class 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 229920001296 polysiloxane Polymers 0.000 description 7
- 229910000323 aluminium silicate Inorganic materials 0.000 description 6
- 230000003750 conditioning effect Effects 0.000 description 6
- 230000004048 modification Effects 0.000 description 6
- 238000012986 modification Methods 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000010457 zeolite Substances 0.000 description 6
- 239000000084 colloidal system Substances 0.000 description 5
- 239000002537 cosmetic Substances 0.000 description 5
- 210000003128 head Anatomy 0.000 description 5
- 239000002453 shampoo Substances 0.000 description 5
- RXGUIWHIADMCFC-UHFFFAOYSA-N 2-Methylpropyl 2-methylpropionate Chemical compound CC(C)COC(=O)C(C)C RXGUIWHIADMCFC-UHFFFAOYSA-N 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 239000003974 emollient agent Substances 0.000 description 4
- 239000003205 fragrance Substances 0.000 description 4
- 229910021485 fumed silica Inorganic materials 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 239000000118 hair dye Substances 0.000 description 4
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 239000003981 vehicle Substances 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 3
- 230000000699 topical effect Effects 0.000 description 3
- 239000008256 whipped cream Substances 0.000 description 3
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 2
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 2
- XSEOYPMPHHCUBN-FGYWBSQSSA-N hydroxylated lecithin Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(COP([O-])(=O)OCC[N+](C)(C)C)COC(=O)CCCCCCC[C@@H](O)[C@H](O)CCCCCCCC XSEOYPMPHHCUBN-FGYWBSQSSA-N 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical compound [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 description 2
- 229960002026 pyrithione Drugs 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- IIZBNUQFTQVTGU-PTTKHPGGSA-N (z)-octadec-9-enoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O IIZBNUQFTQVTGU-PTTKHPGGSA-N 0.000 description 1
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- RFCAUADVODFSLZ-UHFFFAOYSA-N 1-Chloro-1,1,2,2,2-pentafluoroethane Chemical compound FC(F)(F)C(F)(F)Cl RFCAUADVODFSLZ-UHFFFAOYSA-N 0.000 description 1
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
- LVOGXJMCDAOKSQ-UHFFFAOYSA-N 10-oxo-10-propan-2-yloxydecanoic acid Chemical compound CC(C)OC(=O)CCCCCCCCC(O)=O LVOGXJMCDAOKSQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- WOKDXPHSIQRTJF-UHFFFAOYSA-N 3-[3-[3-[3-[3-[3-[3-[3-[3-(2,3-dihydroxypropoxy)-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]propane-1,2-diol Chemical compound OCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)CO WOKDXPHSIQRTJF-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- 208000001840 Dandruff Diseases 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 description 1
- 229910000503 Na-aluminosilicate Inorganic materials 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
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- 239000003082 abrasive agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
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- 150000001298 alcohols Chemical class 0.000 description 1
- 238000006136 alcoholysis reaction Methods 0.000 description 1
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- 229910052783 alkali metal Inorganic materials 0.000 description 1
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- 229960001231 choline Drugs 0.000 description 1
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- 150000002334 glycols Chemical class 0.000 description 1
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- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 1
- 229960000367 inositol Drugs 0.000 description 1
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- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- SJOXEWUZWQYCGL-DVOMOZLQSA-N menthyl salicylate Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(=O)C1=CC=CC=C1O SJOXEWUZWQYCGL-DVOMOZLQSA-N 0.000 description 1
- 229960004665 menthyl salicylate Drugs 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 229940035363 muscle relaxants Drugs 0.000 description 1
- 239000003158 myorelaxant agent Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 150000008104 phosphatidylethanolamines Chemical class 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- SJOXEWUZWQYCGL-UHFFFAOYSA-N salicylic acid menthyl ester Natural products CC(C)C1CCC(C)CC1OC(=O)C1=CC=CC=C1O SJOXEWUZWQYCGL-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical group 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 239000000429 sodium aluminium silicate Substances 0.000 description 1
- 235000012217 sodium aluminium silicate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- 229940034610 toothpaste Drugs 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
Classifications
-
- 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
- A61K9/12—Aerosols; Foams
- A61K9/122—Foams; Dry foams
-
- 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
-
- 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
- A61K8/046—Aerosols; Foams
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/24—Thermal properties
- A61K2800/242—Exothermic; Self-heating; Heating sensation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/30—Characterized by the absence of a particular group of ingredients
- A61K2800/31—Anhydrous
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/006—Antidandruff preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Dispersion Chemistry (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
EXOTHERMIC STABLE FOAM COMPOSITIONS
ABSTRACT
A stable, anhydrous aerosol foam capable of suspending up to 50% by weight of dispersed anhydrous particulate solids capable of absorbing water exothermically is prepared from such solids and a foamable liquid oil, a foaming agent and a propellant.
ABSTRACT
A stable, anhydrous aerosol foam capable of suspending up to 50% by weight of dispersed anhydrous particulate solids capable of absorbing water exothermically is prepared from such solids and a foamable liquid oil, a foaming agent and a propellant.
Description
Description of the Invention The use of anhydrous particulate absorbant materials capable of sorbing water exothermically in autoheatir,g cos~etic and similar compositions is well knowrl. Menkart, et al., in Canadian Patent No. 748,049, disclose liquids, creams, gels and pastes which utilize materials such as silica gel, activated alumina, and alkali rnetal alumino silicate molecular sieves (Zeolites) in non-aqueou~- vehicles which warm automatically on contact with moisture in or on the skin. Analgesic preparations containing Zeolite in an anhydrous liquid are disclosed in r).s. Patent ~Jo. 4,379,143. Cosmetic vehicles comprising a carboxy vinyl polymer and Zeolites are disclosed in U.S. Patent No. 4,362.715. A toothpaste containing Zeolite is disclosed in U;S. Patent No.
4,349,533.
Despite the foregoing cdisclosures, no products based on such formulations have been successfully marketed because such formulations are cosmetically inelegant, i.e., they are very oily, greasy and pasty in consistency;
spread poorly on the skin, and leave the skin with a greasy feel and appearance. ~hese undesirable characteristics result from the fact that water or hydroxylated solvents such as alcohols or glycols must ~6~ S
normally be omitted in order to preserve the exothermic reactivity of the particulate absorbants.
U.S. Patent No. 4,639,367 issued on January 27 ,1987 describes and claims novel annydrous aerosol foams which are capable of suspending up to 50~ by weight of a dispersed solid without causing malfunction of an aerosol valve. The novel properties of these aerosol foams make them suitable for use as delivery systems for a wide range of therapeutic agents and provide ~n alternative to tablets or capsules, which are difficult to swallow or bad tasti~g llquid medications.
It has now been unexpectedly discovered that the aerosol foam delivery system described and claimed in U.S. Patent No. 4,639,367 is capable of functioning to provide a cosmetically elegant delivery system for formulations containing particulate absorbant mat~rials capable of sorbing water exothermically alone or in combination with other therapeutic or cosmetic 2a ingredients. Specifically, it ha~ now been found that a stable, anhydrouc aerosol fo,am or whip capable of suspending up to 50% by weight of a dispersed solid can be prepared from a foamable anhydrous liquid oil; a foaming agent; and controlled amounts of a propellant which are sufficient to produce a stable foam rather than a spray.
~he foam, as delivered from an aerosol canister, has the consistency of whipped cream~ is stable for extended ~z~ p~
periods and i.s hostile to the growth of micro-organisms.
While not wishing to be limited to any particular theor~, it is presently believed that the expansion of the formulations caused by the presence of a propellant causes the product to spread in the form of a thin Lilm on the skin, thereby giving a soft, silky, and co~rnetically elegant feel. The observed effect is analogous to a comparison between whipped cream and bu~ter. ~Ihile both of these products are produced from cream, butter is a dense, yreasy water in oil emulsion, whereas whipped cream is a liyht air in oil emulsion in which the oil is extended over a ouch yreater volume, thereby masking its greasy properties to a substantial extent. In the present invention, by foaming the oils ~Jith a propellant to produce a low density aerated whip or mousse, the greasy property of the oil in the forrnulation is eliminated. The invention rnakes it possible to achieve the foregoing results without valve clogging due to a novel combination of ingredients that produces a high viscosity formulation capable of keeping the small solid~
particles dispersed and of lubricating the aerosol valve.
The foamable, anhydrous liquid oils utilized in the present invention are varied and of no great critical significance. Typical among the organic oils useful for the present invention are those such as .soybean oil, partially hydrogerlated soybean oil, linseed oil, corn oil, peanut oil, sun10wer oil, cottonseed oil, olive oil, ~Z~ Y~
castor oil, liquid petrolatum, oleic acid, lauric acid, and mono- and diglyceride oils. As indicated above, the basic criterion for a liquid oil utilizable in the present invention is that it is foamable.
Typically, the oils utilized in the present invention are present in the formulation in a percentage of 40 to 95~ by weight of the total composition. A
pre~erred range is 50 to 70% by weight of the total composition. The amount of oil may be varied based upon the nature and arnount of the other ingredients in the formulation, such as the amount of dispersed solids.
Ordinarily, the percentaye amount of each other ingredient in the formulation is first selected and the oil is the ingredient added to bring the formulation to 100~.
Foaming agents utilizable in the prescnt invention are selected from the yroup consisting of lecithin, various polyol fatty acid esters and mixtures thereof, or solid silicone copolymers as disclosed in U.S.
Patent No. 3,770,648. Lecithin is the commercial name for a clas of naturally occurring cornpounds derived from soybeans. These compounds are phosphatides and phospholipids. The principal components of lecithin are a naturally occurring mixture of phosphatidyl choline, phosphatidyl ethanolamine, inositol phosphatides and related phosphorous containing lipids. Chemically, lecithin is described as phosphatidyl choline and is a mixture of the diglyceride~ of stearic, palmitic and oleic 3~
acids lirlked to the choline ester of phosphoric acid. It is available commercially as a 60% solution in soybean oil or as a granular powder essentially free of soybean oil.
A hydroxylated lecithin, modified to increase the hydrophilic properties is also commercially available.
This hydroxylated lecithin is commonly supplied as a 60%
solution in soybean oil.
The polyol fatty acid esters utilizable in the pre.~ent invention are commercial products and are comprised of three types:
l. Glycerol esters of fatty acids.
4,349,533.
Despite the foregoing cdisclosures, no products based on such formulations have been successfully marketed because such formulations are cosmetically inelegant, i.e., they are very oily, greasy and pasty in consistency;
spread poorly on the skin, and leave the skin with a greasy feel and appearance. ~hese undesirable characteristics result from the fact that water or hydroxylated solvents such as alcohols or glycols must ~6~ S
normally be omitted in order to preserve the exothermic reactivity of the particulate absorbants.
U.S. Patent No. 4,639,367 issued on January 27 ,1987 describes and claims novel annydrous aerosol foams which are capable of suspending up to 50~ by weight of a dispersed solid without causing malfunction of an aerosol valve. The novel properties of these aerosol foams make them suitable for use as delivery systems for a wide range of therapeutic agents and provide ~n alternative to tablets or capsules, which are difficult to swallow or bad tasti~g llquid medications.
It has now been unexpectedly discovered that the aerosol foam delivery system described and claimed in U.S. Patent No. 4,639,367 is capable of functioning to provide a cosmetically elegant delivery system for formulations containing particulate absorbant mat~rials capable of sorbing water exothermically alone or in combination with other therapeutic or cosmetic 2a ingredients. Specifically, it ha~ now been found that a stable, anhydrouc aerosol fo,am or whip capable of suspending up to 50% by weight of a dispersed solid can be prepared from a foamable anhydrous liquid oil; a foaming agent; and controlled amounts of a propellant which are sufficient to produce a stable foam rather than a spray.
~he foam, as delivered from an aerosol canister, has the consistency of whipped cream~ is stable for extended ~z~ p~
periods and i.s hostile to the growth of micro-organisms.
While not wishing to be limited to any particular theor~, it is presently believed that the expansion of the formulations caused by the presence of a propellant causes the product to spread in the form of a thin Lilm on the skin, thereby giving a soft, silky, and co~rnetically elegant feel. The observed effect is analogous to a comparison between whipped cream and bu~ter. ~Ihile both of these products are produced from cream, butter is a dense, yreasy water in oil emulsion, whereas whipped cream is a liyht air in oil emulsion in which the oil is extended over a ouch yreater volume, thereby masking its greasy properties to a substantial extent. In the present invention, by foaming the oils ~Jith a propellant to produce a low density aerated whip or mousse, the greasy property of the oil in the forrnulation is eliminated. The invention rnakes it possible to achieve the foregoing results without valve clogging due to a novel combination of ingredients that produces a high viscosity formulation capable of keeping the small solid~
particles dispersed and of lubricating the aerosol valve.
The foamable, anhydrous liquid oils utilized in the present invention are varied and of no great critical significance. Typical among the organic oils useful for the present invention are those such as .soybean oil, partially hydrogerlated soybean oil, linseed oil, corn oil, peanut oil, sun10wer oil, cottonseed oil, olive oil, ~Z~ Y~
castor oil, liquid petrolatum, oleic acid, lauric acid, and mono- and diglyceride oils. As indicated above, the basic criterion for a liquid oil utilizable in the present invention is that it is foamable.
Typically, the oils utilized in the present invention are present in the formulation in a percentage of 40 to 95~ by weight of the total composition. A
pre~erred range is 50 to 70% by weight of the total composition. The amount of oil may be varied based upon the nature and arnount of the other ingredients in the formulation, such as the amount of dispersed solids.
Ordinarily, the percentaye amount of each other ingredient in the formulation is first selected and the oil is the ingredient added to bring the formulation to 100~.
Foaming agents utilizable in the prescnt invention are selected from the yroup consisting of lecithin, various polyol fatty acid esters and mixtures thereof, or solid silicone copolymers as disclosed in U.S.
Patent No. 3,770,648. Lecithin is the commercial name for a clas of naturally occurring cornpounds derived from soybeans. These compounds are phosphatides and phospholipids. The principal components of lecithin are a naturally occurring mixture of phosphatidyl choline, phosphatidyl ethanolamine, inositol phosphatides and related phosphorous containing lipids. Chemically, lecithin is described as phosphatidyl choline and is a mixture of the diglyceride~ of stearic, palmitic and oleic 3~
acids lirlked to the choline ester of phosphoric acid. It is available commercially as a 60% solution in soybean oil or as a granular powder essentially free of soybean oil.
A hydroxylated lecithin, modified to increase the hydrophilic properties is also commercially available.
This hydroxylated lecithin is commonly supplied as a 60%
solution in soybean oil.
The polyol fatty acid esters utilizable in the pre.~ent invention are commercial products and are comprised of three types:
l. Glycerol esters of fatty acids.
2. Polyglycerol esters of fatty acids.
3. Sorbitan esters of fatty acids.
The glycerol esters which have been found to be advantageous in generating a suitable anhydrous aerosol foam are prepared by standard esterification mettlods and have a HLB of bet~leen 2.5 and ~.5. Among the preferable glycerol fatty ester~ utilizable in the present invention are those ~uch a glycerol monostearate (HLB 3.2) and glycerol monooleate (HLB 3.4).
The polyglycerol esters utilizable itl the present invention are cornmercial products prepared by first polymerizing glycerine under alkaline conditions.
The polymerization is controlled to yield the particular desired average rnolecular weight. Investigations indicate that the polymerization of glycerol proyresses predominateJy in a straight-chairl marlrler, The ester~ are prepared by reactiny the polyglycerols with a specific fatty acid or by the alcoholysis of a triglyceride. By this method, it is possible to prepare esters ranging anywhere from hydrophilic monoesters such as decaglycerol monolaurate to a lipophilic decaglycerol decaoleate.
The polyglycerol esters preferably used in the present invention have an HLB value of between 4.0 and 13Ø Tnese have been iound to be most advantayeous in yeneratirly a suitable anhydrous aerosol foam. Among the preferable polyyly-erol esters utilizatle in the present invention are those such as: hexaylycerol distearate ( HLB
The glycerol esters which have been found to be advantageous in generating a suitable anhydrous aerosol foam are prepared by standard esterification mettlods and have a HLB of bet~leen 2.5 and ~.5. Among the preferable glycerol fatty ester~ utilizable in the present invention are those ~uch a glycerol monostearate (HLB 3.2) and glycerol monooleate (HLB 3.4).
The polyglycerol esters utilizable itl the present invention are cornmercial products prepared by first polymerizing glycerine under alkaline conditions.
The polymerization is controlled to yield the particular desired average rnolecular weight. Investigations indicate that the polymerization of glycerol proyresses predominateJy in a straight-chairl marlrler, The ester~ are prepared by reactiny the polyglycerols with a specific fatty acid or by the alcoholysis of a triglyceride. By this method, it is possible to prepare esters ranging anywhere from hydrophilic monoesters such as decaglycerol monolaurate to a lipophilic decaglycerol decaoleate.
The polyglycerol esters preferably used in the present invention have an HLB value of between 4.0 and 13Ø Tnese have been iound to be most advantayeous in yeneratirly a suitable anhydrous aerosol foam. Among the preferable polyyly-erol esters utilizatle in the present invention are those such as: hexaylycerol distearate ( HLB
4.0), lecaylycerol tetraoleate (~LB 6.0), triylycerol morlostearate (Ill.B 7.0), triglycerol monooleate (HLB 7.0), octaylycerol monostearate (~ILB 12.0) and octaglycerol monooleate ( HLB 13 . O ) .
Ttle sorbitan fatty acid esters which have been found to be advantageous in generatin~ a suitable anhydrous aerosol foam are cormmercial pro~ucts prepared by standard esterification methods and have an ~ILB of bet 3.0 and 7.0 Amony the preferable sorbitan esters utilizable in the present inventiorl are tho;e suctl as sorbitan rnonostearate (IILB 4.7), sorbitan monooleate (HLB
4.3), and sorbitan rnono palmitate (HLB 6.7).
Additionally, a combination of any of the polyol fatty acid esters may be utilized in the present invention.
The polyol fatty acid esters are somewhat more hydrophilic than lecithin ;o that tneir use allows ttle ~2~
foamable, anhydrous liquid oil to be more easily dispersed when contacted with an aqueous medium. Additionally, they may be used in conjunction with lecithin in the same system which causes the lecithin to become more hydrophilic and therefore more water miscible than the lecithin alone.
qhe solid silicone copolymers which are useful as foaming agents in this invention are fully disclosed in U.S. Patent No. 3,770,648.
1~
The foaming agent utilized in the present invention i8 present in an amount of from 2 to 40~ by weigh~. The amount of foaming agent utilized depends upon the particular foaming agent being utilized, the particular foamable, anhydrous liquid oil being utilized and the propellant ~y~tem. A preferred range of foaming agent i~ from about 3 tO 15% by weight of the composition, with 4 to 6S being especially prefer~ed. It i8 a particularly desirable additional feature of the foaming agent~ that they pos~ess surfactant properties and, therefore, affect the rate ~t which the insoluble solid active ingredient of the foam is released. Accordingly, some variations in the amount of foaming agent in a particular formulation may be purposely chosen based on the nature of the solid active ingredient in order to control the rate of release.
The propellant can be selected from the class of ,, , --..
hydrocarbons that are gaseous under atmospheric pressures and liquefy when compressed, or certain fluorocarbons such as ~REON 115; monochloropentafluorethane; FREON 12, dichlorodifluoromethane; Dymel 22; chlorodifluoromethane;
Dymel 152; 1, 1, difluoroethaane; and dirnethylether.
Propellants other than the liquefied hydrocarbon or fluorocarbon gases can be used including compressed gases like nitrogen, nitrous oxide and carbon dioxide, but they do not produce the most desirable foams over the life of the product in use. The most commorlly used propellants are propane, butane and isobutane. Since these liquefied yases are soluble in the oil vehicle oE the composition, there is a resulting reduction in their vapor pressure.
There~ore, it is most advantageous to use propane since it has the hi~hest pressure of the three hydrocarbon propellants and, everl when dissolved in the low concentrations normally employed in this invention, produces a product with a pressure of 30-40 pounds per ~quare inch over atrnospheric pressure. This pressure is required to eject the foam frorn the container and produce a stable, dense foam. ~lowever, since propane is soluble in the oil base, there is very little pressure drop from the first to the last actuation of the aerosol valve and a satisfactory foam is produced when each dose is expelled.
The amount of propellant used is critical since too much will produce an undesirable spray rather than the desired stable "neasurable foam. Arnourlts of propellant in ~Z~
the range of from l-10 wt. % are operative, but 4-6 wt. %
is the preferred concentration based upon the total weight of the contents of the aerosol container. The amount of propellant used may vary somewhat, depending upon the nature and amount of the other ingredients in the composition but, in all cases, the lowest amount sufficient to forrn a stable, measurable foam without forrning an unmeasurable spray will be selected.
The anhydrous solid particulate matter capable of sorbiny water exothermally whicil can constitute between lU ana 5~% by weight of the basic composition, includes any materials irl this class which are physiologically compatible with hair and skin and which are further compatible with any pharmaceutically active agents to be added to ~aid basic composition In this general category may be included calcillm chloride, silica gel, activated alumina and alkali metal alumino silicate molecular BieVes. The latter generally beiny know as Zeolites. Of particular interest, are the 7,eolites, especially those of the general formula Mx/n[~L2)x(SiO2)yJ, wherein X
and Y are integers greater than ~, the molecular ratio of X to Y is 0.1 to l.l and M is a metal with a valence of n. These Zeolites are preferably in the activated foam which effectively means that they have been pretreated in 25 SUCtl a manner that they contain not in excess of 5~ by weight of water.
~he anhydrous aerosol ioam oi the present ~ Z~ ~} .3 ~
invention may be used as a vehicle for any of a large variety of active pharmaceutical materials or cosmetic inyredients in addition to the exothermic material.
The foam itself may be used as a carrier for a large variety of additional hair or skin modifying agents. Such modifying agents may be cosmetics or pharmaceuticals and may include both prescription and non-prescription agents. Thus, there may be incorporated hair dyes and hair conditioning agents, shampoos, shaving ~oaps, skin emollients, anti-darldruff agents, anti-seborrheic agents, anti-inflammatory agents, muscle relaxants, and any other generally accepted agents for modifyill~ the condition of hair, the surface of the skin and subdermal areas generally treated by topical application of physiologically active materials. As eY.amples of conditioning agents, there may be mentioned the quaternary salts of fatty acids having a carbon content of 12 to 18 carbon atoms, yenerally accepted conditioniny oils such as i~opropyl myristat~, isopropyl palmitate, isopropyl sebacate and the like may be used; as anti-dandru~f ayents, there may be utili~ed ~inc pyrithione or selenium 5ulfide; as anti-seborrheic or anti-inflarnmatory agents there may be mentioned hydrocortisone; as hair dyes any of the conventionally used hair dyes may be employed. This list is to be considered as merely illustrative and in no way lirniting.
Additional ayents not listed hereirl would be apparent to ~L2~
those skilled in the art.
rrhe amount of these added agents will depend upon the required effective concentration and whether they are solid or liquid. If they are liquid, they may constitute up to 95% of the total composition by weight, although 20 to 65~ is to be preferred. If they are solids, they may constitute up to 40~ of the total conlposition, provided that the combined proportion of the anhydrous solid particulate material and said solid agent rJoes not excee~ 50% of the entire composition.
A particularly important and surprising feature of the foams o~ this invention is their ability to suspend high concentrations, i.e., up to 50~ by weight, of solids. Preferably, the suspended particles are ground to a very fine particle size since this facilitates the formation and maintenance of a uniforrn dispersion and prevents clocJging. Particle sizes less than 100 microns, preferably in the range of 50 to 100 microns in diameter, ~re empioyed.
rrhe foam of the present invention can contain up to 50 wt. % of suspended solid particles without any appreciable valve malfunctiorlirlc3, and will usually contain in excess of 15 wt. % of such solid particles since a primary purpose of the foam system is to deliver a high concentration of the active ingredient in the solid particles in a relatively small dose. This ability to suspend higtl percentayes of solids WittlOUt valve s malfunctioning enables the aerosol foam system of the present invention to be utilized for a wide variety of formulations. The reasons for the unique ability of the foams to suspend such a high concentration of solids without valve clogging are not fully understood, but it is believed to result from a combination of the small particle size, the high viscosity of the foam formulation due tv its low propellant content which aids in keeping the particles dispersed and reduces agylomeration and settling, and the lubricating effect of the oil on the valve.
The foarns of the present invention are prepared by conventional formulating techniques. Thus, typically, the foamable anhydrous liquid oil and the foaming agent are mixed together alony with any other soluble ingredients of the composition. The solid to be dispersed is then added and the resultant mixture passed through an appropriate mill to ensure uniform particle size. The batch is then submitted for aerosol filling to an aerosol can. An aerosol valve is placed on the can and the can is crimped. The propellant is;then added by pressure filling.
In addition to the active solid to be dispersed in the foam and the essential ingredients of the foam, there may also be incorporated in the foams of the present invention any of a variety of additives or a combination thereof, commonly added to aerosol compositions or to toiletries, cosmetics, or pharmaceuticals. Typically, ~ 2~ ~t~.S
such additives are those such as emollients, lubricants, humectants, abrasives, perfumes and colorants.
It will be apparent to those skilled in the art that many modifications, both of materials and methods, may be practiced without departing from the purpose and intent of the disclosure.
Hot Oil Hair Mousse Foa~l 1. *Valfor 950, anhydrous sod.
1~ aluminosilicate (P.Q. Corp.) 35.00%
*
2~ Cabosil M-5, Fumed Silica .50 3. Decaglycerol Tetra Oleate 6.00 4. Polyethylene glycol 400 dioleate 2.00
Ttle sorbitan fatty acid esters which have been found to be advantageous in generatin~ a suitable anhydrous aerosol foam are cormmercial pro~ucts prepared by standard esterification methods and have an ~ILB of bet 3.0 and 7.0 Amony the preferable sorbitan esters utilizable in the present inventiorl are tho;e suctl as sorbitan rnonostearate (IILB 4.7), sorbitan monooleate (HLB
4.3), and sorbitan rnono palmitate (HLB 6.7).
Additionally, a combination of any of the polyol fatty acid esters may be utilized in the present invention.
The polyol fatty acid esters are somewhat more hydrophilic than lecithin ;o that tneir use allows ttle ~2~
foamable, anhydrous liquid oil to be more easily dispersed when contacted with an aqueous medium. Additionally, they may be used in conjunction with lecithin in the same system which causes the lecithin to become more hydrophilic and therefore more water miscible than the lecithin alone.
qhe solid silicone copolymers which are useful as foaming agents in this invention are fully disclosed in U.S. Patent No. 3,770,648.
1~
The foaming agent utilized in the present invention i8 present in an amount of from 2 to 40~ by weigh~. The amount of foaming agent utilized depends upon the particular foaming agent being utilized, the particular foamable, anhydrous liquid oil being utilized and the propellant ~y~tem. A preferred range of foaming agent i~ from about 3 tO 15% by weight of the composition, with 4 to 6S being especially prefer~ed. It i8 a particularly desirable additional feature of the foaming agent~ that they pos~ess surfactant properties and, therefore, affect the rate ~t which the insoluble solid active ingredient of the foam is released. Accordingly, some variations in the amount of foaming agent in a particular formulation may be purposely chosen based on the nature of the solid active ingredient in order to control the rate of release.
The propellant can be selected from the class of ,, , --..
hydrocarbons that are gaseous under atmospheric pressures and liquefy when compressed, or certain fluorocarbons such as ~REON 115; monochloropentafluorethane; FREON 12, dichlorodifluoromethane; Dymel 22; chlorodifluoromethane;
Dymel 152; 1, 1, difluoroethaane; and dirnethylether.
Propellants other than the liquefied hydrocarbon or fluorocarbon gases can be used including compressed gases like nitrogen, nitrous oxide and carbon dioxide, but they do not produce the most desirable foams over the life of the product in use. The most commorlly used propellants are propane, butane and isobutane. Since these liquefied yases are soluble in the oil vehicle oE the composition, there is a resulting reduction in their vapor pressure.
There~ore, it is most advantageous to use propane since it has the hi~hest pressure of the three hydrocarbon propellants and, everl when dissolved in the low concentrations normally employed in this invention, produces a product with a pressure of 30-40 pounds per ~quare inch over atrnospheric pressure. This pressure is required to eject the foam frorn the container and produce a stable, dense foam. ~lowever, since propane is soluble in the oil base, there is very little pressure drop from the first to the last actuation of the aerosol valve and a satisfactory foam is produced when each dose is expelled.
The amount of propellant used is critical since too much will produce an undesirable spray rather than the desired stable "neasurable foam. Arnourlts of propellant in ~Z~
the range of from l-10 wt. % are operative, but 4-6 wt. %
is the preferred concentration based upon the total weight of the contents of the aerosol container. The amount of propellant used may vary somewhat, depending upon the nature and amount of the other ingredients in the composition but, in all cases, the lowest amount sufficient to forrn a stable, measurable foam without forrning an unmeasurable spray will be selected.
The anhydrous solid particulate matter capable of sorbiny water exothermally whicil can constitute between lU ana 5~% by weight of the basic composition, includes any materials irl this class which are physiologically compatible with hair and skin and which are further compatible with any pharmaceutically active agents to be added to ~aid basic composition In this general category may be included calcillm chloride, silica gel, activated alumina and alkali metal alumino silicate molecular BieVes. The latter generally beiny know as Zeolites. Of particular interest, are the 7,eolites, especially those of the general formula Mx/n[~L2)x(SiO2)yJ, wherein X
and Y are integers greater than ~, the molecular ratio of X to Y is 0.1 to l.l and M is a metal with a valence of n. These Zeolites are preferably in the activated foam which effectively means that they have been pretreated in 25 SUCtl a manner that they contain not in excess of 5~ by weight of water.
~he anhydrous aerosol ioam oi the present ~ Z~ ~} .3 ~
invention may be used as a vehicle for any of a large variety of active pharmaceutical materials or cosmetic inyredients in addition to the exothermic material.
The foam itself may be used as a carrier for a large variety of additional hair or skin modifying agents. Such modifying agents may be cosmetics or pharmaceuticals and may include both prescription and non-prescription agents. Thus, there may be incorporated hair dyes and hair conditioning agents, shampoos, shaving ~oaps, skin emollients, anti-darldruff agents, anti-seborrheic agents, anti-inflammatory agents, muscle relaxants, and any other generally accepted agents for modifyill~ the condition of hair, the surface of the skin and subdermal areas generally treated by topical application of physiologically active materials. As eY.amples of conditioning agents, there may be mentioned the quaternary salts of fatty acids having a carbon content of 12 to 18 carbon atoms, yenerally accepted conditioniny oils such as i~opropyl myristat~, isopropyl palmitate, isopropyl sebacate and the like may be used; as anti-dandru~f ayents, there may be utili~ed ~inc pyrithione or selenium 5ulfide; as anti-seborrheic or anti-inflarnmatory agents there may be mentioned hydrocortisone; as hair dyes any of the conventionally used hair dyes may be employed. This list is to be considered as merely illustrative and in no way lirniting.
Additional ayents not listed hereirl would be apparent to ~L2~
those skilled in the art.
rrhe amount of these added agents will depend upon the required effective concentration and whether they are solid or liquid. If they are liquid, they may constitute up to 95% of the total composition by weight, although 20 to 65~ is to be preferred. If they are solids, they may constitute up to 40~ of the total conlposition, provided that the combined proportion of the anhydrous solid particulate material and said solid agent rJoes not excee~ 50% of the entire composition.
A particularly important and surprising feature of the foams o~ this invention is their ability to suspend high concentrations, i.e., up to 50~ by weight, of solids. Preferably, the suspended particles are ground to a very fine particle size since this facilitates the formation and maintenance of a uniforrn dispersion and prevents clocJging. Particle sizes less than 100 microns, preferably in the range of 50 to 100 microns in diameter, ~re empioyed.
rrhe foam of the present invention can contain up to 50 wt. % of suspended solid particles without any appreciable valve malfunctiorlirlc3, and will usually contain in excess of 15 wt. % of such solid particles since a primary purpose of the foam system is to deliver a high concentration of the active ingredient in the solid particles in a relatively small dose. This ability to suspend higtl percentayes of solids WittlOUt valve s malfunctioning enables the aerosol foam system of the present invention to be utilized for a wide variety of formulations. The reasons for the unique ability of the foams to suspend such a high concentration of solids without valve clogging are not fully understood, but it is believed to result from a combination of the small particle size, the high viscosity of the foam formulation due tv its low propellant content which aids in keeping the particles dispersed and reduces agylomeration and settling, and the lubricating effect of the oil on the valve.
The foarns of the present invention are prepared by conventional formulating techniques. Thus, typically, the foamable anhydrous liquid oil and the foaming agent are mixed together alony with any other soluble ingredients of the composition. The solid to be dispersed is then added and the resultant mixture passed through an appropriate mill to ensure uniform particle size. The batch is then submitted for aerosol filling to an aerosol can. An aerosol valve is placed on the can and the can is crimped. The propellant is;then added by pressure filling.
In addition to the active solid to be dispersed in the foam and the essential ingredients of the foam, there may also be incorporated in the foams of the present invention any of a variety of additives or a combination thereof, commonly added to aerosol compositions or to toiletries, cosmetics, or pharmaceuticals. Typically, ~ 2~ ~t~.S
such additives are those such as emollients, lubricants, humectants, abrasives, perfumes and colorants.
It will be apparent to those skilled in the art that many modifications, both of materials and methods, may be practiced without departing from the purpose and intent of the disclosure.
Hot Oil Hair Mousse Foa~l 1. *Valfor 950, anhydrous sod.
1~ aluminosilicate (P.Q. Corp.) 35.00%
*
2~ Cabosil M-5, Fumed Silica .50 3. Decaglycerol Tetra Oleate 6.00 4. Polyethylene glycol 400 dioleate 2.00
5. Soybean Oil, partially hydrogenated 51.20
6. Propane 5.00
7. Fragrance 0.30 100. 0096 Procedure-The items #3, 4, 5,and 7 are mixed at ambient temperature until uniform. The powders #1 and #2 are added and mixed until uniform. The batch is passed though a colloid mill and then submitted for aerosol filling during which the propane is added.
Use When used as a hot oil hair mousse foam, it is * Trade-mark ~L2~
preferred, but not essential, that the hair be washed and touch dried with a towel so as to leave the hair moist but not dripping. A sufficent amount of mousse is applied to the hair to cover the entire area and worked into the hair. The contact with moist hair will cause the mousse to heat up giving rise to the desired heat conditioning.
The composition can be left on the hair as long as desired. In one modification of its use, a towel may be wrapped around the head in order to preserve the heat factor ~or somewhat longer.
While it i8 not totally necessary to do so, it is generally preferred to wash the composition out of the hair with a mild shampoo in the conventional manner.
The essential ingredients are:
1. The heat generating solid (Va;for 950) which is exothermic upon contact with water on the hair and scalp. Other heat generating anhydrous solids can be u ed in placé of the Valfor 950 in the same preparation, e.g., anhydrous calcium chloride, dried magnesium sulfate.
2Q 2. The foaming agent can be replaced by lecithin or the sorbitan monp esters or mixtures thereof or silicone #1252.
3. The foamable oil is any liquid anhydrous oily material.
The propellant is propane or any high pressure aerosol propellant.
~,2~
Hot Oil Anti-dandruff Mousse Foam -l. Valfor 950, anhydrous sod.
aluminosilicate (P.~. Corp) 35.00%
2. Cabosil M-5, ~umed Silica .50 ~. Sorbitan Mono stearate 4.00 4. Polyethylene glycol 400 dioleate 2.00 5. ~oy~ean Oil, partially hydrogenated 51.20 ~0 6. L'ropane 5.~0 7. ~inc Pyrithione 2.00 . Fragrance 0.30 100 . 00%
Procedure:
The i~em~ #3, 4, 5, 7 and ~ are mixed at 60C.
temperature until uniform. The powders #1 and ~2 are added and rnixed until uniform. The ~atch is cooled and passed through a colloid mill and then submitted for aerosol filliny during which the propane is added.
Use r 2~ It is preferred, but not essential, that the hair be washed and touch dried with a towel so as to leave the hair moist but not dripping. A sufficient arnount of mousse is applied to the hair to cover the entire area and worked into the hair. The contact with moist hair will cause the mousse to heat up givirlg risc to the desired 126~
heat conditioning. The composition can be left on the hair as long as desired. In one modification of its use, a towel may be wrapped around the head in order to preserve the heat factor for somewhat longer.
While it is not totally necessary to do so, it is generally preferred to wash the composition out of the hair with a mild shampoo in the conventional manner Hot Oil Halr Conditioninq Mousse Foam 1. Valfor ~50, anhydrous sod.
alurninosilicate (P.Q. Corp)35.00%
2~ Cabosil M-5, Fumed Silica .50 3. Lecithin, Powdered 3.00 4. Glycerol Mono Stereate 4.00 15 5. Poiyethylene glycol 400 dioleate2.00 6. Cotton Seed Oil 46.20 7. Propane 5,00
Use When used as a hot oil hair mousse foam, it is * Trade-mark ~L2~
preferred, but not essential, that the hair be washed and touch dried with a towel so as to leave the hair moist but not dripping. A sufficent amount of mousse is applied to the hair to cover the entire area and worked into the hair. The contact with moist hair will cause the mousse to heat up giving rise to the desired heat conditioning.
The composition can be left on the hair as long as desired. In one modification of its use, a towel may be wrapped around the head in order to preserve the heat factor ~or somewhat longer.
While it i8 not totally necessary to do so, it is generally preferred to wash the composition out of the hair with a mild shampoo in the conventional manner.
The essential ingredients are:
1. The heat generating solid (Va;for 950) which is exothermic upon contact with water on the hair and scalp. Other heat generating anhydrous solids can be u ed in placé of the Valfor 950 in the same preparation, e.g., anhydrous calcium chloride, dried magnesium sulfate.
2Q 2. The foaming agent can be replaced by lecithin or the sorbitan monp esters or mixtures thereof or silicone #1252.
3. The foamable oil is any liquid anhydrous oily material.
The propellant is propane or any high pressure aerosol propellant.
~,2~
Hot Oil Anti-dandruff Mousse Foam -l. Valfor 950, anhydrous sod.
aluminosilicate (P.~. Corp) 35.00%
2. Cabosil M-5, ~umed Silica .50 ~. Sorbitan Mono stearate 4.00 4. Polyethylene glycol 400 dioleate 2.00 5. ~oy~ean Oil, partially hydrogenated 51.20 ~0 6. L'ropane 5.~0 7. ~inc Pyrithione 2.00 . Fragrance 0.30 100 . 00%
Procedure:
The i~em~ #3, 4, 5, 7 and ~ are mixed at 60C.
temperature until uniform. The powders #1 and ~2 are added and rnixed until uniform. The ~atch is cooled and passed through a colloid mill and then submitted for aerosol filliny during which the propane is added.
Use r 2~ It is preferred, but not essential, that the hair be washed and touch dried with a towel so as to leave the hair moist but not dripping. A sufficient arnount of mousse is applied to the hair to cover the entire area and worked into the hair. The contact with moist hair will cause the mousse to heat up givirlg risc to the desired 126~
heat conditioning. The composition can be left on the hair as long as desired. In one modification of its use, a towel may be wrapped around the head in order to preserve the heat factor for somewhat longer.
While it is not totally necessary to do so, it is generally preferred to wash the composition out of the hair with a mild shampoo in the conventional manner Hot Oil Halr Conditioninq Mousse Foam 1. Valfor ~50, anhydrous sod.
alurninosilicate (P.Q. Corp)35.00%
2~ Cabosil M-5, Fumed Silica .50 3. Lecithin, Powdered 3.00 4. Glycerol Mono Stereate 4.00 15 5. Poiyethylene glycol 400 dioleate2.00 6. Cotton Seed Oil 46.20 7. Propane 5,00
8. Stearyl dimethyl benzyl ammonium chloride 4,00 29 g. Fragrance 0,30 100 . 00 Procedure:
The items #3, 4, 5, 6 and 8 are mixed at 60 C.
temperature until uniform. The powders #1 and #2 are added and mixed until uniform. The batch is cooled and passed throu~h a colloid mill and then submitted for ~L2~3~
aerosol filling during which the propane is added.
Use It is preferred, but not essential, that the hair be washed and touch dried with a towel so as to leave the hair moist but not dripping. A sufficient amount of mousse is applied to the hair to cover the entire area and worked into the hair. The contact with moist hair will cause the mousse to heat up giving rise to the desired heat conditioning. The compositiorl can be left on the hair as lony as desired. In one modification of its use, a towel may be wrapped around the head irl order to preserve the heat factor for somewhat longer.
While it is not totally necessary to do so, it is generally preferred to wash the composition out of the hair with a mild shampoo in the conventional manner.
Hot Oil Anti-Seborrheic Emollient Mo~sse Foam l. Valfor 950, anhydrous sod.
aluminosilicate (P.Q. Corp) 35.00 2. Cabosil M-5, Fumed Silica .50 3. Dow Corning Silicone #1252 (50~ silicone copolymer, 50% isobutyl isobutyrate) 4.00 4. Polyethylene glycol 400 dioleate 2.00 5. Sunflower Oil 50.00 6. Propane 5.00 7. Hydrocor~isone Acetat~ 3.00 8. Fragrance 0.30 10 0 . 00%
Procedure:
The items #3, 4, 5, 7 and 8 are mixed at ambient temperature until uniform. The powders #l and #2 are added and mixed until uniform. The batch is passed through a colloid mill and then submitted for aerosol filling duriny which the propane is added.
Use The composition may be used as a skin emollient. In this use the affected area is washed, the ~urplus water shaken off, and the mousse applied to the affected area.
This mousse may be used as an anti-seborrheic hair mousse foam. It is preferred, but not essential, that the hair be washed and touch dried with a towel so as to leave the hair moist but not dripping. A sufficient amount of mousse is applied to the hair to cover the entire area and worked into the hair. The contact with 29 moist hair will cause the mousse to heat up yiviny rise to the desired heat conditioning. The composition can be left on the hair as long as desired. In one modification of its use, a towel may be wrapped around the head in order to preserve the heat factor for somewhat longer.
~ZG~ 5 Hot Oil Hair Dye Mousse Foam 1. Valfor g50, anhydrous sod.
alurninosilicate ~P.Q. Corp) 35.00 2. Cabosil M-5, Fumed Silica .50 3. Dow Corning Silicone #1252 (50% silicone copolymer, 50% isobutyl isobutyrate) 4.00 ~. Polyethylene glycol 400 dioleate 2 00 5. Peanut Oil 50.06 6. Propane 5.00 7. Maxilon Blue GRL(500%) 0.3 Deorlene Orange 7GL 1.2 Deorlene Orange 2GL 0.3 Basacryl Red FB 1.0 8. Pragrance 0. 30 100 . 00%
Procedure:
The items #3, 4, 5, 7 and 8 are mixed at ambient temperature until uniform. ,The powders #1 and #2 are added and mixed until uniform. The batch is passed through a colloid mill and then submitted for aerosol filling during which the propane is added.
Use When used as a hair dye, it i8 preferred, but not essential, that the hair be washed and touch dried 5 ~r~
with a towel so as to leave the hair moist but not dripping. A sufficient amount of mousse is applied to the hair to cover the entire area and worked into the hair.
The contact wit~ moist hair will cause the mousse to heat up giviny rise to the desired heat conditioniny. The composition can be left on the hair as long as desired.
In one modification of its use, a towel may be wrapped around the head in order to preserve the heat factor for sornewhat lonyer.
]o WhiLe it is not totally necessary to do so, it is generally preferred to wash the compositiorl out oE the hair with a mil~ shampoo in the conventional manner.
~XAMPLE 6 Warm Topical Analqesic Mousse l. Menthol l0.0%
2. Sodium Alumino Silicate (Valfor 950) - 35.0 3. Cabosil M-5 1.0 4. Sorbitan Monostearate 4.0 5. Decaglycerol Tetraoleate 6.0 6. Soybean Oil 10.0 7. Isopropyl Myristate 30.0 8. Propane 4.0 100 . U%
Procedure:
Items 4, 5, 6 and 7 are mixed at 60 C.
~L2~ a temperature until uniform. Items 2 and 3 are ad~ed and mixed until uniform. The mixture is cooled to 40 C. and item 1 is added and mixed until uniform. The mixture is then submitted for aerosol filling during which the propane is added.
Warm ToPical Anal~esic Mousse 1. Menthyl Salicylate 15.0%
2. ~odium Alumino Silicate (Valfor 950) 35.0 3. Cabo~il M-5 1.0 4. Sorbitan Monostearate 4.0 5. Decaglycerol Tetraoleate 6.0 6. Soybean Oil 34,0 7. Propane 5,0 100 . 0%
Procedure:
o Items 4, 5, and 6 are mixed at 60 C.
temperature until uniform. Items 2 and 3 are added and mixed until uniform. The mixture is cooled to 40C. and item 1 is added and mixed until uniform. The mixture is then submitted for aerosol filling during which the propane is added.
The items #3, 4, 5, 6 and 8 are mixed at 60 C.
temperature until uniform. The powders #1 and #2 are added and mixed until uniform. The batch is cooled and passed throu~h a colloid mill and then submitted for ~L2~3~
aerosol filling during which the propane is added.
Use It is preferred, but not essential, that the hair be washed and touch dried with a towel so as to leave the hair moist but not dripping. A sufficient amount of mousse is applied to the hair to cover the entire area and worked into the hair. The contact with moist hair will cause the mousse to heat up giving rise to the desired heat conditioning. The compositiorl can be left on the hair as lony as desired. In one modification of its use, a towel may be wrapped around the head irl order to preserve the heat factor for somewhat longer.
While it is not totally necessary to do so, it is generally preferred to wash the composition out of the hair with a mild shampoo in the conventional manner.
Hot Oil Anti-Seborrheic Emollient Mo~sse Foam l. Valfor 950, anhydrous sod.
aluminosilicate (P.Q. Corp) 35.00 2. Cabosil M-5, Fumed Silica .50 3. Dow Corning Silicone #1252 (50~ silicone copolymer, 50% isobutyl isobutyrate) 4.00 4. Polyethylene glycol 400 dioleate 2.00 5. Sunflower Oil 50.00 6. Propane 5.00 7. Hydrocor~isone Acetat~ 3.00 8. Fragrance 0.30 10 0 . 00%
Procedure:
The items #3, 4, 5, 7 and 8 are mixed at ambient temperature until uniform. The powders #l and #2 are added and mixed until uniform. The batch is passed through a colloid mill and then submitted for aerosol filling duriny which the propane is added.
Use The composition may be used as a skin emollient. In this use the affected area is washed, the ~urplus water shaken off, and the mousse applied to the affected area.
This mousse may be used as an anti-seborrheic hair mousse foam. It is preferred, but not essential, that the hair be washed and touch dried with a towel so as to leave the hair moist but not dripping. A sufficient amount of mousse is applied to the hair to cover the entire area and worked into the hair. The contact with 29 moist hair will cause the mousse to heat up yiviny rise to the desired heat conditioning. The composition can be left on the hair as long as desired. In one modification of its use, a towel may be wrapped around the head in order to preserve the heat factor for somewhat longer.
~ZG~ 5 Hot Oil Hair Dye Mousse Foam 1. Valfor g50, anhydrous sod.
alurninosilicate ~P.Q. Corp) 35.00 2. Cabosil M-5, Fumed Silica .50 3. Dow Corning Silicone #1252 (50% silicone copolymer, 50% isobutyl isobutyrate) 4.00 ~. Polyethylene glycol 400 dioleate 2 00 5. Peanut Oil 50.06 6. Propane 5.00 7. Maxilon Blue GRL(500%) 0.3 Deorlene Orange 7GL 1.2 Deorlene Orange 2GL 0.3 Basacryl Red FB 1.0 8. Pragrance 0. 30 100 . 00%
Procedure:
The items #3, 4, 5, 7 and 8 are mixed at ambient temperature until uniform. ,The powders #1 and #2 are added and mixed until uniform. The batch is passed through a colloid mill and then submitted for aerosol filling during which the propane is added.
Use When used as a hair dye, it i8 preferred, but not essential, that the hair be washed and touch dried 5 ~r~
with a towel so as to leave the hair moist but not dripping. A sufficient amount of mousse is applied to the hair to cover the entire area and worked into the hair.
The contact wit~ moist hair will cause the mousse to heat up giviny rise to the desired heat conditioniny. The composition can be left on the hair as long as desired.
In one modification of its use, a towel may be wrapped around the head in order to preserve the heat factor for sornewhat lonyer.
]o WhiLe it is not totally necessary to do so, it is generally preferred to wash the compositiorl out oE the hair with a mil~ shampoo in the conventional manner.
~XAMPLE 6 Warm Topical Analqesic Mousse l. Menthol l0.0%
2. Sodium Alumino Silicate (Valfor 950) - 35.0 3. Cabosil M-5 1.0 4. Sorbitan Monostearate 4.0 5. Decaglycerol Tetraoleate 6.0 6. Soybean Oil 10.0 7. Isopropyl Myristate 30.0 8. Propane 4.0 100 . U%
Procedure:
Items 4, 5, 6 and 7 are mixed at 60 C.
~L2~ a temperature until uniform. Items 2 and 3 are ad~ed and mixed until uniform. The mixture is cooled to 40 C. and item 1 is added and mixed until uniform. The mixture is then submitted for aerosol filling during which the propane is added.
Warm ToPical Anal~esic Mousse 1. Menthyl Salicylate 15.0%
2. ~odium Alumino Silicate (Valfor 950) 35.0 3. Cabo~il M-5 1.0 4. Sorbitan Monostearate 4.0 5. Decaglycerol Tetraoleate 6.0 6. Soybean Oil 34,0 7. Propane 5,0 100 . 0%
Procedure:
o Items 4, 5, and 6 are mixed at 60 C.
temperature until uniform. Items 2 and 3 are added and mixed until uniform. The mixture is cooled to 40C. and item 1 is added and mixed until uniform. The mixture is then submitted for aerosol filling during which the propane is added.
Claims (31)
1. An anhydrous aerosol foam composition comprising a foamable liquid oil, a foaming agent and a propellant, said propellant being present in an amount sufficient to produce a stable, measurable foam but insufficient to produce a spray when said composition is ejected through an aerosol valve, and dispersed solid particles, said particles comprising substantially anhydrous particulate material capable of absorbing water exothermically.
2. The composition of claim 1 wherein said propellant comprises 1 to 10 wt. % of said composition.
3. The composition of claim 2 wherein said particles comprise 10 to 50 wt. % % of said composition.
4. The composition of claim 3 wherein the average size of said solid particles is in the range of 50 to 100 microns.
5. A composition of claim 1 containing 10 to 50% of activated Zeolite of the formula Mx/n [AlO2)x)SiO2)y]
wherein x and y are integers greater than 6, the molar ratio of x to y is 0.1 to 1.1 and M is a metal with the valence of n.
wherein x and y are integers greater than 6, the molar ratio of x to y is 0.1 to 1.1 and M is a metal with the valence of n.
6. The composition of claim 1 wherein said propellant comprises 1 to 10 wt. % of said composition, said foaming agent comprises 2 to 40 wt. % of said composition, said solid particles comprise 10 to 50 wt. %
of said composition and the balance of said composition is said liquid oil.
of said composition and the balance of said composition is said liquid oil.
7. The composition of claim 6 wherein said propellant is a hydrocarbon.
8. The composition of claim 6 wherein said propellant is a fluorocarbon.
9. The composition of claim 6 wherein said liquid oil is selected from the group consisting of soybean oil, partially hydrogenated soybean oil, linseed oil, corn oil, peanut oil, sunflower oil, cottonseed oil, olive oil, castor oil, liquid petrolatums, oleic acids, lauric acid and mono- and diglyceride oils.
10. The composition of claim 6 wherein the foaming agent is selected from the group consisting of solid silicone polymers, lecithin, polyglycerol esters of fatty acids having an HLB value of between 4.0 and 13.0, glycerol esters of fatty acids having an HLB value of between 2.5 and 4.5, sorbitan esters of fatty acids having an HLB value of between 3.0 and 7.0 and mixtures thereof.
11. The composition of claim 10 wherein said foaming agent comprises 2 to 40 wt. % of said composition.
12. The composition of claim 10 wherein the foaming agent is a mixture of lecithin and glycerol monostearate.
13. The composition of claim 10 wherein the foaming agent is a mixture of lecithin and decaglycerol tetraoleate.
14. The composition of claim 10 wherein the foaming agent is triglycerol monooleate.
15. The composition of claim 10 wherein the foaming agent is decaglycerol tetraoleate.
16. The composition of claim 10 wherein the foaming agent is sorbitan monostearate.
17. The composition of claim 10 wherein the foaming agent is a mixture of decaglycerol tetraoleate and sorbitan monostearate.
18. The composition of claim 10 wherein the foaming agent is a mixture of decaglycerol tetraoleate and glycerol monostearate.
19. The composition of claim 10 wherein the foaming agent is a mixture of decaglycerol tetraoleate, sorbitan monostearate and glycerol monostearate.
20. The composition of claim 10 wherein the foaming agent is a mixture of sorbitan monostearate and glycerol monostearate.
21. The composition of claim 10 wherein the foaming agent is from about 3 to 15 wt. % of the composition.
22. The composition of claim 10 wherein the foaming agent is a mixture of lecithin, sorbitan monostearate and glycerol monostearate.
23. The composition of claim 10 wherein the foaming agent is a mixture of lecithin, sorbitan monostearate and decaglycerol tetraoleate.
24. The composition of claim 10 wherein the foaming agent is a mixture of lecithin and sorbitan monostearate.
25. As an article of manufacture, a pressurized aerosol container, said container having therein an anhydrous aerosol foam composition comprising a foamable liquid oil, a foaming agent and a propellant, said propellant being present in an amount sufficient to produce a stable, measurable foam but insufficient to produce a spray when said composition is ejected through an aerosol valve, and dispersed solid particles, said particles comprising substantially anhydrous particulate material capable of absorbing water exothermically.
26. The composition of claim 25 wherein said propellant comprises 1 to 10 wt. % of said composition, said foaming agent comprises 2 to 40 wt. % of said composition, said solid particles comprise at least 10 wt. % of said composition and the balance of said composition is said liquid oil.
27. The composition of claim 25 wherein said propellant is a hydrocarbon.
28. The composition of claim 25 wherein said propellant is propane.
29. The composition of claim 25 wherein said liquid oil is selected from the group consisting of soybean oil, partially hydrogenated soybean oil, linseed oil, corn oil, peanut oil, sunflower oil, cottonseed oil, olive oil, castor oil, liquid petrolatums, oleic acids, lauric acid and mono- and diglyceride oils.
30. The composition of claim 25 wherein the foaming agent is selected from the group consisting of solid silicone polymers, lecithin, polyglycerol esters of fatty acids having an HLB value of between 4.0 and 13.0, glycerol esters of fatty acids having an HLB value of between 2.5 and 4.5. sorbitan esters of fatty acids having an HLB value of between 3.0 and 7.0 and mixtures thereof.
31. A composition of claim 25 containing 10 to 50% of activated Zeolite of the formula Mx/n [AlO2)x)SiO2)y]
wherein x and y are integers greater than 6, the molar ratio of x to y is 0.1 to 1.1 and M is a metal with the valence of n.
wherein x and y are integers greater than 6, the molar ratio of x to y is 0.1 to 1.1 and M is a metal with the valence of n.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA000503882A CA1269015A (en) | 1985-03-18 | 1986-03-12 | Exothermic stable foam compositions |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71329385A | 1985-03-18 | 1985-03-18 | |
| US713,293 | 1985-03-18 | ||
| US79768785A | 1985-11-13 | 1985-11-13 | |
| US797,687 | 1985-11-13 | ||
| CA000503882A CA1269015A (en) | 1985-03-18 | 1986-03-12 | Exothermic stable foam compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA1269015C CA1269015C (en) | 1990-05-15 |
| CA1269015A true CA1269015A (en) | 1990-05-15 |
Family
ID=27108963
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000503882A Expired CA1269015A (en) | 1985-03-18 | 1986-03-12 | Exothermic stable foam compositions |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP0215903A1 (en) |
| AU (1) | AU5549486A (en) |
| CA (1) | CA1269015A (en) |
| WO (1) | WO1986005389A1 (en) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2888292A (en) * | 1991-10-30 | 1993-06-07 | Boots Company Plc, The | Toiletries composition |
| HRP20000029C1 (en) * | 2000-01-18 | 2005-02-28 | Mustapi Marina | Cosmetic preparations for the skin and hair care |
| MXPA03006890A (en) * | 2001-02-01 | 2003-11-13 | Procter & Gamble | Anhydrous self-heating cosmetic compositions, especially anhydrous hair conditioning compositions. |
| US6843983B2 (en) * | 2001-06-07 | 2005-01-18 | Virgie Bright-Ellington | Shaving preparations and methods for the prevention and treatment of pseudofolliculitis barbae |
| US7255869B2 (en) | 2001-10-30 | 2007-08-14 | The Procter & Gamble Company | Anhydrous cosmetic compositions containing polyols |
| IL152486A0 (en) | 2002-10-25 | 2003-05-29 | Meir Eini | Alcohol-free cosmetic and pharmaceutical foam carrier |
| US9211259B2 (en) | 2002-11-29 | 2015-12-15 | Foamix Pharmaceuticals Ltd. | Antibiotic kit and composition and uses thereof |
| US9668972B2 (en) | 2002-10-25 | 2017-06-06 | Foamix Pharmaceuticals Ltd. | Nonsteroidal immunomodulating kit and composition and uses thereof |
| US7704518B2 (en) | 2003-08-04 | 2010-04-27 | Foamix, Ltd. | Foamable vehicle and pharmaceutical compositions thereof |
| EP1556009B2 (en) | 2002-10-25 | 2021-07-21 | Foamix Pharmaceuticals Ltd. | Cosmetic and pharmaceutical foam |
| US10117812B2 (en) | 2002-10-25 | 2018-11-06 | Foamix Pharmaceuticals Ltd. | Foamable composition combining a polar solvent and a hydrophobic carrier |
| US7820145B2 (en) | 2003-08-04 | 2010-10-26 | Foamix Ltd. | Oleaginous pharmaceutical and cosmetic foam |
| US7700076B2 (en) | 2002-10-25 | 2010-04-20 | Foamix, Ltd. | Penetrating pharmaceutical foam |
| US8900554B2 (en) | 2002-10-25 | 2014-12-02 | Foamix Pharmaceuticals Ltd. | Foamable composition and uses thereof |
| US9265725B2 (en) | 2002-10-25 | 2016-02-23 | Foamix Pharmaceuticals Ltd. | Dicarboxylic acid foamable vehicle and pharmaceutical compositions thereof |
| US20080138296A1 (en) | 2002-10-25 | 2008-06-12 | Foamix Ltd. | Foam prepared from nanoemulsions and uses |
| DE10253304A1 (en) * | 2002-11-15 | 2004-05-27 | Beiersdorf Ag | Self-warming cosmetic or dermatological composition, useful as mask for cleaning face, neck and decolletage, comprises emulsion of polyol, oil and emulsifier, plus zeolite |
| KR100938577B1 (en) | 2002-12-23 | 2010-01-26 | 주식회사 엘지생활건강 | Non-emulsifying pyrogenic cosmetic composition |
| DE10302096B4 (en) * | 2003-01-16 | 2005-03-17 | Coty B.V. | Cosmetic self-heating products and their use |
| US8795693B2 (en) | 2003-08-04 | 2014-08-05 | Foamix Ltd. | Compositions with modulating agents |
| US20080260655A1 (en) | 2006-11-14 | 2008-10-23 | Dov Tamarkin | Substantially non-aqueous foamable petrolatum based pharmaceutical and cosmetic compositions and their uses |
| US8636982B2 (en) | 2007-08-07 | 2014-01-28 | Foamix Ltd. | Wax foamable vehicle and pharmaceutical compositions thereof |
| WO2009069006A2 (en) | 2007-11-30 | 2009-06-04 | Foamix Ltd. | Foam containing benzoyl peroxide |
| WO2009072007A2 (en) | 2007-12-07 | 2009-06-11 | Foamix Ltd. | Carriers, formulations, methods for formulating unstable active agents for external application and uses thereof |
| FR2930433A1 (en) * | 2008-04-25 | 2009-10-30 | Oreal | COSMETIC COMPOSITION HAVING HEATING EFFECT IN AEROSOL. |
| CA2739920C (en) | 2008-10-07 | 2017-12-12 | Ross Technology Corporation | Spill-resistant surfaces having hydrophobic and oleophobic borders |
| WO2010125470A2 (en) | 2009-04-28 | 2010-11-04 | Foamix Ltd. | Foamable vehicle and pharmaceutical compositions comprising aprotic polar solvents and uses thereof |
| WO2011013008A2 (en) | 2009-07-29 | 2011-02-03 | Foamix Ltd. | Non surface active agent non polymeric agent hydro-alcoholic foamable compositions, breakable foams and their uses |
| WO2011013009A2 (en) | 2009-07-29 | 2011-02-03 | Foamix Ltd. | Non surfactant hydro-alcoholic foamable compositions, breakable foams and their uses |
| FR2949972B1 (en) * | 2009-09-14 | 2011-12-09 | Oreal | LIP RED IN THE FORM OF ANHYDROUS FOAM. |
| US8871184B2 (en) | 2009-10-02 | 2014-10-28 | Foamix Ltd. | Topical tetracycline compositions |
| US9849142B2 (en) | 2009-10-02 | 2017-12-26 | Foamix Pharmaceuticals Ltd. | Methods for accelerated return of skin integrity and for the treatment of impetigo |
| CA2796305A1 (en) | 2010-03-15 | 2011-09-22 | Ross Technology Corporation | Plunger and methods of producing hydrophobic surfaces |
| WO2012115986A1 (en) | 2011-02-21 | 2012-08-30 | Ross Technology Corporation | Superhydrophobic and oleophobic coatings with low voc binder systems |
| WO2013090939A1 (en) | 2011-12-15 | 2013-06-20 | Ross Technology Corporation | Composition and coating for superhydrophobic performance |
| MX2015000119A (en) | 2012-06-25 | 2015-04-14 | Ross Technology Corp | ELASTOMERIC COATINGS WITH HYDROPHOBIC AND / OR OLEOPHOBIC PROPERTIES. |
| US10398641B2 (en) | 2016-09-08 | 2019-09-03 | Foamix Pharmaceuticals Ltd. | Compositions and methods for treating rosacea and acne |
| WO2018167956A1 (en) | 2017-03-17 | 2018-09-20 | 東洋エアゾール工業株式会社 | Warming aerosol composition and aerosol formulation including same |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA758049A (en) * | 1960-07-19 | 1967-05-02 | The Gillette Company | Heat-generating cosmetic composition |
| US3770648A (en) * | 1971-07-12 | 1973-11-06 | Bristol Myers Co | Anhydrous aerosol foam |
| US4379143A (en) * | 1980-12-05 | 1983-04-05 | Pq Corporation | Topical liquid or ointment |
-
1986
- 1986-03-10 WO PCT/US1986/000488 patent/WO1986005389A1/en not_active Ceased
- 1986-03-10 AU AU55494/86A patent/AU5549486A/en not_active Abandoned
- 1986-03-10 EP EP86902145A patent/EP0215903A1/en not_active Withdrawn
- 1986-03-12 CA CA000503882A patent/CA1269015A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| WO1986005389A1 (en) | 1986-09-25 |
| CA1269015C (en) | 1990-05-15 |
| EP0215903A1 (en) | 1987-04-01 |
| AU5549486A (en) | 1986-10-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKLA | Lapsed | ||
| MKLA | Lapsed |
Effective date: 19921117 |