US20030007935A1 - Stable pressurized antiperspirant compositions containing dimethylether propellant and a low polarity solvent - Google Patents
Stable pressurized antiperspirant compositions containing dimethylether propellant and a low polarity solvent Download PDFInfo
- Publication number
- US20030007935A1 US20030007935A1 US09/864,012 US86401201A US2003007935A1 US 20030007935 A1 US20030007935 A1 US 20030007935A1 US 86401201 A US86401201 A US 86401201A US 2003007935 A1 US2003007935 A1 US 2003007935A1
- Authority
- US
- United States
- Prior art keywords
- composition
- pressurized
- low polarity
- antiperspirant
- aluminum
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 164
- 230000001166 anti-perspirative effect Effects 0.000 title claims abstract description 120
- 239000003213 antiperspirant Substances 0.000 title claims abstract description 120
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 title claims abstract description 80
- 239000002904 solvent Substances 0.000 title claims abstract description 57
- 239000003380 propellant Substances 0.000 title claims description 47
- 239000007788 liquid Substances 0.000 claims abstract description 38
- 229920005862 polyol Polymers 0.000 claims abstract description 31
- 150000003077 polyols Chemical class 0.000 claims abstract description 30
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 26
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 6
- 229920001296 polysiloxane Polymers 0.000 claims description 42
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 30
- 229930195733 hydrocarbon Natural products 0.000 claims description 20
- 150000002430 hydrocarbons Chemical class 0.000 claims description 20
- 239000004215 Carbon black (E152) Substances 0.000 claims description 19
- -1 acetic acid glycerol ester Chemical class 0.000 claims description 18
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 13
- 229960004063 propylene glycol Drugs 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 229910052782 aluminium Inorganic materials 0.000 claims description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 9
- LVYZJEPLMYTTGH-UHFFFAOYSA-H dialuminum chloride pentahydroxide dihydrate Chemical compound [Cl-].[Al+3].[OH-].[OH-].[Al+3].[OH-].[OH-].[OH-].O.O LVYZJEPLMYTTGH-UHFFFAOYSA-H 0.000 claims description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 8
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- 239000002202 Polyethylene glycol Substances 0.000 claims description 6
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 229920001223 polyethylene glycol Polymers 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 239000001273 butane Substances 0.000 claims description 5
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- ARXKVVRQIIOZGF-UHFFFAOYSA-N 1,2,4-butanetriol Chemical compound OCCC(O)CO ARXKVVRQIIOZGF-UHFFFAOYSA-N 0.000 claims description 4
- SZNYYWIUQFZLLT-UHFFFAOYSA-N 2-methyl-1-(2-methylpropoxy)propane Chemical compound CC(C)COCC(C)C SZNYYWIUQFZLLT-UHFFFAOYSA-N 0.000 claims description 4
- AGNTUZCMJBTHOG-UHFFFAOYSA-N 3-[3-(2,3-dihydroxypropoxy)-2-hydroxypropoxy]propane-1,2-diol Chemical compound OCC(O)COCC(O)COCC(O)CO AGNTUZCMJBTHOG-UHFFFAOYSA-N 0.000 claims description 4
- JHWQMXKQJVAWKI-UHFFFAOYSA-N 3-phenylpropane-1,2-diol Chemical compound OCC(O)CC1=CC=CC=C1 JHWQMXKQJVAWKI-UHFFFAOYSA-N 0.000 claims description 4
- UNFGWQUDDQBNLD-UHFFFAOYSA-N 3-propan-2-yloxypropane-1,2-diol Chemical compound CC(C)OCC(O)CO UNFGWQUDDQBNLD-UHFFFAOYSA-N 0.000 claims description 4
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 claims description 4
- FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 claims description 4
- 239000001282 iso-butane Substances 0.000 claims description 4
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 claims description 4
- WCVRQHFDJLLWFE-UHFFFAOYSA-N pentane-1,2-diol Chemical compound CCCC(O)CO WCVRQHFDJLLWFE-UHFFFAOYSA-N 0.000 claims description 4
- 239000001294 propane Substances 0.000 claims description 4
- ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 claims description 2
- 229940015975 1,2-hexanediol Drugs 0.000 claims description 2
- XERGTCWVYOKNAV-UHFFFAOYSA-N 2-methylpentane-1,2-diol Chemical compound CCCC(C)(O)CO XERGTCWVYOKNAV-UHFFFAOYSA-N 0.000 claims description 2
- AIOHBDYXYKMBIF-UHFFFAOYSA-N 3-(3-methylbutoxy)propane-1,2-diol Chemical compound CC(C)CCOCC(O)CO AIOHBDYXYKMBIF-UHFFFAOYSA-N 0.000 claims description 2
- PSJBSUHYCGQTHZ-UHFFFAOYSA-N 3-Methoxy-1,2-propanediol Chemical compound COCC(O)CO PSJBSUHYCGQTHZ-UHFFFAOYSA-N 0.000 claims description 2
- JCYHHICXJAGYEL-UHFFFAOYSA-N 3-butoxypropane-1,2-diol Chemical compound CCCCOCC(O)CO JCYHHICXJAGYEL-UHFFFAOYSA-N 0.000 claims description 2
- LOSWWGJGSSQDKH-UHFFFAOYSA-N 3-ethoxypropane-1,2-diol Chemical compound CCOCC(O)CO LOSWWGJGSSQDKH-UHFFFAOYSA-N 0.000 claims description 2
- HJJZIMFAIMUSBW-UHFFFAOYSA-N 3-methylbutane-1,2-diol Chemical compound CC(C)C(O)CO HJJZIMFAIMUSBW-UHFFFAOYSA-N 0.000 claims description 2
- ZTKZJXGLCCVMLJ-UHFFFAOYSA-N 3-propoxypropane-1,2-diol Chemical compound CCCOCC(O)CO ZTKZJXGLCCVMLJ-UHFFFAOYSA-N 0.000 claims description 2
- AMOCOBXCNIBDMC-UHFFFAOYSA-N 4-Methyl-1,2-dihydroxypentane Chemical compound CC(C)CC(O)CO AMOCOBXCNIBDMC-UHFFFAOYSA-N 0.000 claims description 2
- IMHLMIRSHNHXBC-UHFFFAOYSA-N 4-methylhexane-1,2-diol Chemical compound CCC(C)CC(O)CO IMHLMIRSHNHXBC-UHFFFAOYSA-N 0.000 claims description 2
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 claims description 2
- YCLAMANSVUJYPT-UHFFFAOYSA-L aluminum chloride hydroxide hydrate Chemical compound O.[OH-].[Al+3].[Cl-] YCLAMANSVUJYPT-UHFFFAOYSA-L 0.000 claims description 2
- 229940053431 aluminum sesquichlorohydrate Drugs 0.000 claims description 2
- SJXYSRSHDPPYIU-UHFFFAOYSA-L aluminum;propane-1,2-diol;chloride;hydroxide;hydrate Chemical compound O.[OH-].[Al+3].[Cl-].CC(O)CO SJXYSRSHDPPYIU-UHFFFAOYSA-L 0.000 claims description 2
- YXZZLAMCXFHTTE-UHFFFAOYSA-N aluminum;propane-1,2-diol;trihypochlorite;hydrate Chemical compound O.[Al+3].Cl[O-].Cl[O-].Cl[O-].CC(O)CO YXZZLAMCXFHTTE-UHFFFAOYSA-N 0.000 claims description 2
- BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 claims description 2
- XILPPDQAWPSZIL-UHFFFAOYSA-H dialuminum;dichloride;tetrahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[Al+3].[Al+3].[Cl-].[Cl-] XILPPDQAWPSZIL-UHFFFAOYSA-H 0.000 claims description 2
- KNXDJTLIRRQLBE-UHFFFAOYSA-H dialuminum;propane-1,2-diol;chloride;pentahydroxide;hydrate Chemical compound O.[OH-].[OH-].[OH-].[OH-].[OH-].[Al+3].[Al+3].[Cl-].CC(O)CO KNXDJTLIRRQLBE-UHFFFAOYSA-H 0.000 claims description 2
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 claims description 2
- 125000001033 ether group Chemical group 0.000 claims description 2
- GCXZDAKFJKCPGK-UHFFFAOYSA-N heptane-1,2-diol Chemical compound CCCCCC(O)CO GCXZDAKFJKCPGK-UHFFFAOYSA-N 0.000 claims description 2
- 239000003125 aqueous solvent Substances 0.000 abstract description 4
- 239000000463 material Substances 0.000 description 23
- 238000009472 formulation Methods 0.000 description 21
- 239000000047 product Substances 0.000 description 17
- 239000000243 solution Substances 0.000 description 13
- 239000004615 ingredient Substances 0.000 description 11
- 239000000443 aerosol Substances 0.000 description 7
- 239000007921 spray Substances 0.000 description 7
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 6
- 239000002537 cosmetic Substances 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 5
- 239000000969 carrier Substances 0.000 description 5
- 229940008099 dimethicone Drugs 0.000 description 5
- 239000004205 dimethyl polysiloxane Substances 0.000 description 5
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 239000002781 deodorant agent Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000003205 fragrance Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 3
- 239000002798 polar solvent Substances 0.000 description 3
- 0 *C(O)CO Chemical compound *C(O)CO 0.000 description 2
- 150000000180 1,2-diols Chemical class 0.000 description 2
- BANXPJUEBPWEOT-UHFFFAOYSA-N 2-methyl-Pentadecane Chemical compound CCCCCCCCCCCCCC(C)C BANXPJUEBPWEOT-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000004471 Glycine Substances 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 150000001408 amides Chemical group 0.000 description 2
- 239000006172 buffering agent Substances 0.000 description 2
- 230000000536 complexating effect Effects 0.000 description 2
- 239000008139 complexing agent Substances 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 150000002148 esters Chemical group 0.000 description 2
- HXYCHJFUBNTKQR-UHFFFAOYSA-N heptane-1,2,3-triol Chemical compound CCCCC(O)C(O)CO HXYCHJFUBNTKQR-UHFFFAOYSA-N 0.000 description 2
- 229940073561 hexamethyldisiloxane Drugs 0.000 description 2
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000000699 topical effect Effects 0.000 description 2
- 229910009112 xH2O Inorganic materials 0.000 description 2
- 150000003754 zirconium Chemical class 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- BOSAWIQFTJIYIS-UHFFFAOYSA-N 1,1,1-trichloro-2,2,2-trifluoroethane Chemical compound FC(F)(F)C(Cl)(Cl)Cl BOSAWIQFTJIYIS-UHFFFAOYSA-N 0.000 description 1
- 229940083957 1,2-butanediol Drugs 0.000 description 1
- 229940043268 2,2,4,4,6,8,8-heptamethylnonane Drugs 0.000 description 1
- AXPZGEVHEBDDHX-UHFFFAOYSA-N C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C.[H][Si](C)(O[Si](C)(C)C)O[Si](C)(C)C Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C.[H][Si](C)(O[Si](C)(C)C)O[Si](C)(C)C AXPZGEVHEBDDHX-UHFFFAOYSA-N 0.000 description 1
- CWUHERHJSPPFHQ-UHFFFAOYSA-N C[Si]1(C)CCCCO1 Chemical compound C[Si]1(C)CCCCO1 CWUHERHJSPPFHQ-UHFFFAOYSA-N 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
- 229920004511 Dow Corning® 200 Fluid Polymers 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical class [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- WWHZEXDIQCJXSV-UHFFFAOYSA-N aluminum;trihypochlorite Chemical compound [Al+3].Cl[O-].Cl[O-].Cl[O-] WWHZEXDIQCJXSV-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000013011 aqueous formulation Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002333 glycines Chemical class 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229940060367 inert ingredients Drugs 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- KUVMKLCGXIYSNH-UHFFFAOYSA-N isopentadecane Natural products CCCCCCCCCCCCC(C)C KUVMKLCGXIYSNH-UHFFFAOYSA-N 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- ADGFKRMKSIAMAI-UHFFFAOYSA-L oxygen(2-);zirconium(4+);chloride;hydroxide Chemical compound [OH-].[O-2].[Cl-].[Zr+4] ADGFKRMKSIAMAI-UHFFFAOYSA-L 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229940113116 polyethylene glycol 1000 Drugs 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229910052725 zinc Chemical class 0.000 description 1
- 239000011701 zinc Chemical class 0.000 description 1
- 229910052726 zirconium Inorganic materials 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/345—Alcohols 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/26—Aluminium; 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
- A61K8/37—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
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
Definitions
- the present invention relates to pressurized antiperspirant compositions comprising solubilized antiperspirant active, a dimethylether propellant, and a low polarity solvent.
- the compositions can be formulated as stable single phase or clear pressurized liquids without reliance upon ethanol, propylene glycol, or aqueous solvents.
- pressurized antiperspirant formulations known for use in controlling or inhibiting underarm perspiration and odor.
- Most of these formulations comprise an antiperspirant powder such as an aluminum salt, which is suspended in an anhydrous carrier and combined with a liquefied volatile propellant in a pressurized container. The formulation is then applied to the underarm as a pressurized spray which is generated by the rapid boiling of the propellant upon dispensing from an atomizing valve in association with the pressurized container.
- aerosol antiperspirants have been formulated with antiperspirant active dissolved or solubilized in a suitable aqueous or anhydrous carrier.
- Many of these formulations are also single phase systems without any dispersed or suspended solids, thus resulting in little or no visible residue on the applied areas that is attributable to the deposition of such dispersed or suspended solids on the skin.
- These single phase formulations often have a clear or translucent appearance, and apply neatly from an aerosolized spray without a dusty or powdery application.
- Many of these single phase aerosols however, contain ethanol, or water to help solubilize the antiperspirant active to allow for the formulation of a stable, single-phase system.
- the aqueous formulations tend to feel wet during application and the ethanol formulations tend to irritate or sting the sensitive underarm area of the skin during and after application.
- Single phase antiperspirant aerosols have also been described in the antiperspirant art in which single phase aerosols are formulated with dimethylether, solubilized antiperspirant active, and polyol solvents such as propylene glycol.
- These compositions contain dimethylether which allows for the formulation of a stable single-phase system, provided that the system also contains water, ethanol or relatively high propylene glycol concentrations to maintain the stability of the single phase system.
- Such compositions tend to be unstable when formulated with substantive low polarity solvents, thus resulting in precipitation of antiperspirant active from solution or phase separation shortly after formulation, unless the compositions are modified to contain relatively high ethanol, water or propylene glycol concentrations.
- high ethanol or propylene glycol concentrations can irritate or sting the sensitive underarm area of the skin and high water concentrations can result in an undesirably wet skin feel during and after application.
- pressurized antiperspirant products can be formulated as single phase or clear products, without reliance upon high ethanol, propylene glycol, or water concentrations to solubilize and couple antiperspirant active with the various other ingredients to form a single phase or clear system.
- single-phase, pressurized antiperspirants can be prepared without reliance upon such materials provided that it comprises an antiperspirant active solubilized in a polyol solvent having at least 4 carbon atoms and a hydroxyl group on each of the ⁇ and ⁇ carbon atoms of the polyol solvent, wherein the solubilized active and selected polyol solvent are combined with a dimethylether propellant in combination with a low polarity solvent having a solubility parameter of less than about 8.0, wherein the weight ratio of the dimethylether to the low polarity solvent is from about 0.1 to about 3.0.
- pressurized single-phase antiperspirant product will remain stable over prolonged periods, provided that the defined polyol solvent and dimethylether propellant are coupled with the low polarity solvent, and provided that the weight ratio of the dimethylether propellant to low polarity solvent is maintained within the range as defined here.
- low polarity solvents or materials can include materials such as volatile or non-volatile silicone fluids that provide additional benefits such as active substantivity, emolliency, improved skin feel during or after application, formulation flexibility, and similar other benefits.
- These low polarity solvents also include liquefied hydrocarbon propellants to provide a low cost option to more expensive propellant materials.
- the present invention is directed to pressurized anhydrous antiperspirant compositions comprising: (a) a polyol solvent having at least 4 carbon atoms and a hydroxyl group on each of the ⁇ and ⁇ carbon atoms of the polyol solvent; (b) solubilized antiperspirant active; (c) dimethylether; (d) a low polarity liquid having a solubility parameter of less than about 8.0, wherein the weight ratio of the dimethylether to low polarity solvent is from about 0.1 to about 3.0.
- compositions are especially useful in formulating clear or single-phase pressurized antiperspirant compositions that remain stable over prolonged periods and that can be formulated without high concentrations of ethanol, propylene glycol or aqueous solvents. It has also been found that these compositions can be maintained as single phase or clear formulations, even when formulated with low polarity solvents such as silicone oils, liquefied hydrocarbon propellants, and other similar materials.
- the pressurized antiperspirant compositions of the present invention comprise a selected polyol solvent, a solubilized antiperspirant active, a dimethylether propellant, and a low polarity solvent in a defined weight ratio relative to the dimethylether propellant.
- anhydrous refers to those compositions or materials containing less than about 5%, more preferably less than about 3%, even more preferably less than about 1%, even more preferably zero percent, by weight of free or added water.
- ambient conditions refers to surrounding conditions at about one atmosphere of pressure, at about 50% relative humidity, and at about 25° C.
- pressurized antiperspirant means any packaged antiperspirant composition that is pressurized from a gas or liquefied gas propellant to thus provide a means for pushing or moving the antiperspirant composition through an application device.
- pressurized antiperspirant compositions of the present invention can comprise, consist of, or consist essentially of the essential elements and limitations of the invention described herein, as well as any additional or optional ingredients, components, or limitations described herein or otherwise useful in pressurized antiperspirant applications.
- the pressurized antiperspirant compositions of the present invention comprise selected liquid polyols for solubilizing or helping to solubilize the antiperspirant active material in the composition.
- the antiperspirant composition preferably comprises from about 1% to about 80%, more preferably from about 2% to about 60%, even more preferably from about 3% to about 20%, by weight of the selected liquid polyols.
- liquid polyols for use in the pressurized antiperspirant composition of the present invention are selected to have at least 4 carbon atoms and adjacent hydroxy-substituted carbon atoms at the ⁇ and ⁇ positions of the liquid polyol.
- Preferred liquid polyols for use in the compositions are those that conform to the formula:
- R is an amide, ester, alkyl, ether or silicone-containing moiety, each moiety containing at least 2 carbon atoms.
- the R group is preferably an alkyl or ether group, more preferably an alkyl group having from about 2 to about 10 carbon atoms, more preferably from about 4 to about 6 carbon atoms.
- the liquid polyols preferably have either 2 or 3 hydroxyl groups in total.
- the R group on the liquid polyol can therefore be substituted or unsubstituted, branched or straight or cyclic, saturated or unsaturated.
- suitable substituents include hydroxyl groups, amines, amides, esters, ethers, alkoxylate groups (e.g., ethoxylates, propoxylates, etc.) and so forth.
- Non limiting examples of suitable liquid polyols for use in the pressurized compositions of the present invention include 1,2-butanediol; 1,2-pentanediol; 4-methyl-1,2-pentanediol; 2-methyl-1,2-pentanediol; 3,3-methyl-1 ,2-butanediol; 4-methyl-1 ,2-hexanediol; 1,2-heptanediol; 3-phenyl-1,2-propanediol; 1,2,6-hexanetriol; 1,2-hexandiol; 1,2,4-butanetriol; and combinations thereof.
- glycerol ethers such as glycerol isopropyl ether; glycerol propyl ether; glycerol ethyl ether; glycerol methyl ether; glycerol butyl ether; glycerol isopentyl ether; diglycerol isopropyl ether; diglycerol isobutyl ether; diglycerol; triglycerol; triglycerol isopropyl ether; and combinations thereof.
- glycerol ethers such as glycerol isopropyl ether; glycerol propyl ether; glycerol ethyl ether; glycerol methyl ether; glycerol butyl ether; glycerol isopentyl ether; diglycerol isopropyl ether; diglycerol isobutyl ether; diglycerol; triglycerol;
- liquid polyols include acetic acid glycerol ester; propanoic acid glycerol ester; butanoic acid glycerol ester; 3-methyl butanoic acid glycerol ester; and 3-trimethylsily-1,2-propane diol; silicone-containing 1,2-diols such as those described in U.S. Pat. No. 5,969,172 (Nye); and combinations thereof.
- These selected polyols are formulated into the antiperspirant composition alone or preferably in combination with one or more other anhydrous liquid carriers, examples of such other anhydrous liquid carriers include any known or otherwise effective carrier liquids suitable for topical application to the skin which are also compatible with the solubilized antiperspirant active and propellant components of the composition.
- the pressurized antiperspirant compositions of the present invention are preferably anhydrous, but will typically contain at least small amounts of water associated with the antiperspirant active during formulation.
- anhydrous means the antiperspirant compositions of the present invention preferably contain less than 10%, more preferably less than 5%, even more preferably less than 3%, most preferably less than 1%, of water by weight of the composition.
- the pressurized antiperspirant compositions of the present invention comprise a solubilized antiperspirant active suitable for application to human skin.
- concentration of antiperspirant active in the composition should be sufficient to provide the finished antiperspirant product with the desired perspiration wetness and odor control.
- the antiperspirant active is preferably solubilized by the liquid polyol component described hereinbefore.
- Solubilized antiperspirant active concentrations in the pressurized antiperspirant compositions preferably range from about 0.1% to about 26%, more preferably from about 1% to about 20%, even more preferably from about 2% to about 10%, by weight of the composition. All such weight percentages are calculated on an anhydrous metal salt basis exclusive of water and any complexing or buffering agent such as glycine, glycine salts, or other complexing or buffering agent.
- the solubilized antiperspirant active for use in the antiperspirant compositions of the present invention include any compound, composition or other material having antiperspirant activity.
- Preferred antiperspirant actives include astringent metallic salts, especially the inorganic and organic salts of aluminum, zirconium and zinc, as well as mixtures thereof. Particularly preferred are salts such as aluminum halides, aluminum chlorohydrate, aluminum hydroxyhalides, zirconyl oxyhalides, zirconyl hydroxyhalides, and mixtures thereof.
- Aluminum salts are most preferred for non-contact pressurized compositions.
- Preferred aluminum salts for use in the antiperspirant compositions include those that conform to the formula:
- a is from about 2 to about 5; the sum of a and b is about 6; x is from about 1 to about 6; and wherein a, b, and x may have non-integer values.
- Processes for preparing aluminum salts are disclosed in U.S. Pat. No. 3,887,692, Gilman, issued Jun. 3, 1975; U.S. Pat. No. 3,904,741, Jones et al., issued Sep. 9, 1975; U.S. Pat. No.
- Zirconium salts for use in the antiperspirant compositions, especially in pressurized contact forms include those which conform to the formula:
- a is any number having a value of from 0 to about 2; x is from about 1 to about 7; and wherein a and x may both have non-integer values.
- Preferred zirconium salts are those complexes which additionally contain aluminum and glycine, commonly known as ZAG complexes. These ZAG complexes contain aluminum chlorhydroxide and zirconyl hydroxy chloride conforming to the above described formulas. Such ZAG complexes are described in U.S. Pat. No. 3,679,068, Luedders et al., issued Feb. 12, 1974; Great Britain Patent Application 2,144,992, Callaghan et al., published Mar. 20, 1985; and U.S. Pat. No. 4,120,948, Shelton, issued Oct. 17, 1978.
- Preferred antiperspirant actives for use in the compositions include aluminum chlorohydrate, aluminum dichlorohydrate, aluminum sesquichlorohydrate, aluminum chlorohydrex propylene glycol complex, aluminum dichlorohydrex propylene glycol complex, aluminum sesquichlorohydrex propylene glycol complex, aluminum chlorohydrex polyethylene glycol complex, aluminum dichlorohydrex polyethylene glycol complex, aluminum sesquichlorohydrex polyethylene glycol complex, aluminum sulfate buffered, and combinations thereof.
- Non limiting examples of solubilized antiperspirant active for use in the pressurized antiperspirant compositions of the present invention, and methods of making the solubilized active are described in U.S. Pat. No. 6,149,897 (Swaile); U.S. Pat. No. 6,126,928 (Swaile); and U.S. Pat. No. 5,968,489 (Swaile et al.), which descriptions are incorporated herein by reference.
- Other non limiting examples of solubilized antiperspirant active and methods of making it are described in EP 0 404 533 (Smith et al.).
- the pressurized antiperspirant compositions of the present invention comprise a dimethylether propellant in combination with a low polarity solvent as defined hereinafter, wherein the weight ratio of the dimethylether to the low polarity solvent ranges from about 0.1 to 2.8, preferably from about 0.2 to about 1.0, more preferably from about 0.2 to about 0.5.
- the propellant component of the pressurized antiperspirant compositions of the present invention may contain only dimethylether or a combination of dimethylether and any other known or otherwise suitable propellant for application to the skin, preferably a combination of dimethylether and a hydrocarbon propellant.
- the dimethylether or total propellant concentration in the pressurized antiperspirant compositions of the present invention ranges from about 5% to about 99%, more typically from about 15% to about 90%, even more preferably from about 30% to about 70%, by weight of the composition.
- the combination of dimethylether and hydrocarbon propellant preferably represents from about 50% to 100%, more preferably 100%, by weight of the total propellant concentration.
- compositions may comprise minor amounts of other propellants such as nitrous oxide, carbon dioxide, and halogenated hydrocarbons such as triclorofluoromethane, diclorodifluoromethane, diclorotetrafluoroethane trichlorotrifluoroethane, trichlorotetrafluoroethane, and monochlorodifluoromethane, and combinations thereof.
- propellants such as nitrous oxide, carbon dioxide, and halogenated hydrocarbons such as triclorofluoromethane, diclorodifluoromethane, diclorotetrafluoroethane trichlorotrifluoroethane, trichlorotetrafluoroethane, and monochlorodifluoromethane, and combinations thereof.
- hydrocarbon propellants suitable for use in the pressurized antiperspirant compositions include any hydrocarbon propellant known for or otherwise suitable for application to human skin, non limiting examples of which include propane, butane, pentane, isobutane, and combinations thereof. These hydrocarbon propellants are generally in the form of liquefied gases when formulated into the antiperspirant compositions, and are characterized for purposes of defining the compositions of the present invention as a low polarity solvent having a solubility parameter less than about 8.0, which low polarity solvents are described in greater detail hereinafter.
- the pressurized antiperspirant compositions of the present invention comprise a low polarity solvent in combination with the above-described dimethylether propellant, wherein the weight ratio of the dimethylether and low polarity solvent is selected within the defined range as described hereinbefore.
- the low polarity solvent can be any material that is liquid under ambient conditions or which is otherwise in liquid form within the pressurized composition described herein, and which has a solubility parameter of less than about 8.0, preferably from about 1 to about 6, more preferably from about 1 to about 4.
- the low polarity solvent for use in the composition of the present invention is preferably a liquefied hydrocarbon propellant, non limiting examples of which include propane, butane, isopentane, pentane, isobutane, and combinations thereof.
- the liquefied hydrocarbon propellant acts as both a low polarity solvent and an additional propellant within the pressurized compositions.
- the hydrocarbon propellant as a low polarity solvent is preferably formulated in combination with the dimethylether propellant, wherein the weight ratio of dimethylether to hydrocarbon propellant in this preferred embodiment ranges from about 0.1 to 2.0, more preferably from about 0.1 to 1.0, even more preferably from about 0.2 to about 0.8.
- Other low polarity solvents suitable for use in the pressurized antiperspirant compositions of the present invention include any silicone or silicone-containing material that is known or otherwise suitable for topical application to the skin, provided that the silicone or silicone-containing material is a liquid under ambient conditions or is otherwise in liquid form within the pressurized antiperspirant compositions of the present invention, and provided that the silicone or silicone-containing material has the requisite solubility parameter as defined herein.
- the silicone or silicone-containing material as a low polarity solvent for use in the pressurized antiperspirant compositions of the present invention can be a volatile or non volatile, cyclic or linear or branched chain, substituted or unsubstituted.
- the concentration of the silicone liquid as a low polarity solvent in the composition preferably ranges from about 0.1% to about 50%, more preferably from about 1% to about 25%, more preferably from about 2% to about 15%, by weight of the pressurized antiperspirant composition.
- Non limiting examples of suitable volatile silicones are described in Todd et al., “Volatile Silicone Fluids for Cosmetics”, Cosmetics and Toiletries, 91:27-32 (1976), which descriptions are incorporated herein by reference.
- Preferred among these volatile silicones are the cyclic silicones having from about 3 to about 7, more preferably from about 4 to about 5, silicon atoms. Most preferably are those that conform to the formula:
- n is from about 3 to about 7, preferably from about 4 to about 5, most preferably 5.
- These volatile cyclic silicones generally have a viscosity value of less than about 10 centistokes as measured at 25° C.
- Suitable volatile silicones for use herein include, but are not limited to, Cyclomethicone D-5 (commercially available from G. E.
- Non limiting examples of non volatile silicone liquids for use in the pressurized antiperspirant compositions of the present invention include those which conform to either of the formulas:
- n is greater than or equal to 1.
- linear silicone materials will generally have viscosity values of from about 10 centistoke to about 100,000 centistoke, preferably less than about 500 centistoke, more preferably from about 20 centistoke to about 200 centistoke, even more preferably from about 20 centistoke to about 50 centistoke, as measured under ambient conditions.
- Non limiting examples of non-volatile, linear silicones suitable for use in the antiperspirant compositions include but are not limited to, Dow Corning 200, hexamethyldisiloxane, Rhodorsil Oils 70047 available from Rhone-Poulenc, Masil SF Fluid available from Mazer, Dow Corning 225, Dow Corning 1732, Dow Corning 5732, Dow Corning 5750 (available from Dow Corning Corp.); SF-96, SF-1066 and SF18(350) Silicone Fluids (available from G.E.
- silicone liquids as low polarity solvents for use in the pressurized antiperspirant compositions of the present invention include modified or organofunctional silicone carriers such as polyalkylsiloxanes, polyalkyarylsiloxanes, cross-linked silicone elastomers, polyestersiloxanes, polyethersiloxane copolymers, polyfluorosiloxanes, polyaminosiloxanes, and combinations thereof.
- modified or organofunctional silicone carriers such as polyalkylsiloxanes, polyalkyarylsiloxanes, cross-linked silicone elastomers, polyestersiloxanes, polyethersiloxane copolymers, polyfluorosiloxanes, polyaminosiloxanes, and combinations thereof.
- modified silicone carriers are typically liquid under ambient conditions, and have a preferred viscosity of less than about 100,000 centistokes, more preferably less than about 500 centistokes, even more preferably from about 1 centistoke to about 50 centistokes, and most more preferably from about 1 centistoke to about 20 centistokes.
- modified silicone carriers are generally known in the chemical arts, some examples of which are described in 1 Cosmetics, Science and Technology 27-104 (M. Balsam and E. Sagarin ed. 1972); U.S. Pat. No. 4,202,879, issued to Shelton on May 13, 1980; U.S. Pat. No. 5,069,897, issued to Orr on Dec. 3, 1991; which descriptions are incorporated herein by reference.
- the pressurized antiperspirant compositions of the present invention may further comprise many other materials for use as the low polarity solvent, provided that such other materials have the defined solubility parameter and are formulated into the composition such that the weight ratio of the dimethylether to low polarity solvent remains within the ranges described herein.
- Such other materials include volatile and non volatile hydrocarbons in addition to or other than the hydrocarbon propellants described hereinbefore.
- the pressurized antiperspirant compositions of the present invention may further comprise other optional components which may modify the physical, chemical, cosmetic or aesthetic characteristics of the compositions or serve as additional “active” components when deposited on the skin.
- the compositions may also further comprise optional inert ingredients. Many such optional ingredients are known for use in deodorants, antiperspirants or other personal care compositions, and may also be used in the antiperspirant compositions herein, provided that such optional materials are compatible with the essential materials described herein, or do not otherwise unduly impair product performance.
- Non limiting examples of optional ingredients include preservatives, deodorant antimicrobials, fragrances, deodorant perfumes, coloring agents or dyes, thickeners, pH modifiers, surfactants and other wash-off aids, co-solvents, emollients or residue masking liquids other than the silicone liquids described herein, pharmaceutical actives, vitamins, and combinations thereof.
- Preferred optional ingredients include dimethicone copolyols.
- the pressurized antiperspirant compositions may further comprise any organic or silicone-containing liquid carrier other than the selected polyols and silicone liquids described herein, the compositions are preferably substantially free of ethanol, and also preferably substantially free of propylene glycol or dipropylene glycol.
- substantially free means that the pressurized antiperspirant compositions preferably contain less than 5%, more preferably less than 3%, even more preferably less than 1%, most preferably zero percent, by weight of any of these materials individually.
- the pressurized antiperspirant compositions of the present invention are preferably anhydrous formulations, and are also preferably clear or single-single phase liquids, although the present invention is not limited to clear or single-phase systems.
- These pressurized antiperspirant compositions are packaged in any known or otherwise suitable pressurized container for use in delivering the combination of materials described herein for any selected pressurized formulation.
- the pressurized antiperspirant compositions are also preferably free of any suspended or dispersed solids, e.g., insufficient solid concentrations to visibly reduce the clarity of the composition.
- the pressurized antiperspirant composition may be packaged in conventional pressurized containers for use in contact or non-contact product forms.
- Non-contact products from pressurized containers are well known in the antiperspirant and personal care arts, non limiting examples of which are described in U.S. Pat. Nos. 3,082,917; U.S. Pat. No. 3,083,918; and U.S. Pat. No. 3,544,258, which descriptions are incorporated herein by reference.
- Pressurized contact antiperspirants are likewise known in the antiperspirant art, non limiting examples of which are described in U.S. Pat. No. 5,567,073 (de Laforcade et al.), which description is incorporated herein by reference.
- contact or “contact product form” refers to any known or otherwise suitable pressurized package that comprises an applicator surface to which the antiperspirant composition is delivered under pressure from within the pressurized package, and from which the antiperspirant composition is then applied directly to the underarm area of the skin.
- the applicator surface directly contacts the underarm during application, thus delivering or depositing the antiperspirant composition to the underarm area of the skin.
- non-contact or “non-contact product form” as used herein refers to pressurized packages from which the antiperspirant composition is delivered to the underarm through a product stream delivered under pressure from within the package to the skin. In this context, there is no direct contact between any surface of the pressurized package and the underarm.
- the pressurized antiperspirant compositions of the present invention may be prepared by any known or otherwise effective technique, suitable for making and formulating a clear or single phase pressurized antiperspirant formulation.
- These pressurized compositions are generally prepared by adding, individually or as a premix, all ingredients other than the dimethylether and any other selected propellant to a suitable container. The container is then sealed and residual air within the container is evacuated. The propellant is then added as a liquefied gas under appropriate pressures to the sealed container.
- Preferred compositions and methods of manufacture are described hereinafter in the following exemplified embodiments of the pressurized antiperspirant compositions of the present invention.
- the dimethylether propellant when used in combination with a hydrocarbon or other similar propellant, is preferably added to the composition after the hydrocarbon or other similar propellant has been added. It has been found that this particular manufacturing sequence helps stabilize the composition during formulation, and thus minimize or eliminate any active precipitation during the manufacturing process.
- This particular manufacturing process is preferably applied to the pressurized antiperspirant compositions of the present invention, but can also be applied to any pressurized antiperspirant composition known or otherwise disclosed in the antiperspirant art that contains a solubilized antiperspirant active and a combination of dimethylether and other propellants such as liquefied hydrocarbon gases.
- compositions described below in Examples A-P are anhydrous, pressurized antiperspirant compositions that are single-phase systems having a clear or translucent appearance.
- Each of the compositions is packaged in a pressurized contact container, as well as a non-contact pressurized spray container.
- the products are applied to the underarm area of the skin to provide antiperspirant and deodorant efficacy.
- the products during and after application to the underarm result in little or no visible residue.
- each of the compositions described below is formulated by combining and mixing together in a glass bottle (suitable for pressurized packaging) all of the listed ingredients in each composition that are in liquid form under otherwise ambient conditions.
- the glass bottle is then sealed with a delivery valve and evacuated to between 14 and 25 inches of mercury.
- the propellant in each formulation is then added to the glass bottle under appropriate pressure using a burette filler.
- the dimethylether is always added last.
- the resulting packaged composition is then heated in a water bath (150° F.) for 5 minutes to assure proper sealing of the valve.
- Each of the resulting compositions is a clear or single-phase pressurized antiperspirant composition that remains stable over prolonged periods of ambient storage without the use of solvents such as ethanol or aqueous solvents.
- compositions described below are formulated with solubilized antiperspirant active solution.
- the solution is prepared by co-spray drying an initial antiperspirant active solution with a moderately polar solvent to form a spray dried active powder, and then dissolving the spray dried active powder in the desired 1,2-diol solvent with simple agitation over a few hours and no added heat, to thus form an antiperspirant active solution for formulation into the pressurized antiperspirant compositions exemplified herein.
- the solubilized antiperspirant active for formulation into the pressurized antiperspirant compositions exemplified herein is prepared by making an aqueous mixture containing 40% by weight of either the aluminum chlorohydrate or aluminum zirconium chlorohydrate glycerin, 9% by weight of butylene glycol, and 2% by weight of polyethylene glycol 1000.
- the resulting aqueous mixture is then spray dried to provide a spray dried powder that contains about 65-75% by weight of anhydrous antiperspirant active and 20% by weight of the moderately polar solvent (solubility parameter of the moderately polar solvent being from about 9 to about 15).
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Abstract
Description
- The present invention relates to pressurized antiperspirant compositions comprising solubilized antiperspirant active, a dimethylether propellant, and a low polarity solvent. The compositions can be formulated as stable single phase or clear pressurized liquids without reliance upon ethanol, propylene glycol, or aqueous solvents.
- There are many different pressurized antiperspirant formulations known for use in controlling or inhibiting underarm perspiration and odor. Most of these formulations comprise an antiperspirant powder such as an aluminum salt, which is suspended in an anhydrous carrier and combined with a liquefied volatile propellant in a pressurized container. The formulation is then applied to the underarm as a pressurized spray which is generated by the rapid boiling of the propellant upon dispensing from an atomizing valve in association with the pressurized container.
- Although many consumers enjoy the convenience of an aerosol antiperspirant, many of these aerosols have highly undesirable application cosmetics. Activation of these aerosols often results in a dusty or powdery application, which then results in a heavy white residue on the applied areas of the skin. Moreover, the powdery residue on the skin tends to flake away or otherwise fall off relatively easily after application, especially when the applied surface comes in contact with clothing, thus resulting in an undesirable residue on the clothing itself and a loss or reduction of antiperspirant coverage on those areas of the skin from which the product has flaked away or otherwise fallen off.
- To improve application cosmetics, some aerosol antiperspirants have been formulated with antiperspirant active dissolved or solubilized in a suitable aqueous or anhydrous carrier. Many of these formulations are also single phase systems without any dispersed or suspended solids, thus resulting in little or no visible residue on the applied areas that is attributable to the deposition of such dispersed or suspended solids on the skin. These single phase formulations often have a clear or translucent appearance, and apply neatly from an aerosolized spray without a dusty or powdery application. Many of these single phase aerosols, however, contain ethanol, or water to help solubilize the antiperspirant active to allow for the formulation of a stable, single-phase system. The aqueous formulations tend to feel wet during application and the ethanol formulations tend to irritate or sting the sensitive underarm area of the skin during and after application.
- Single phase antiperspirant aerosols have also been described in the antiperspirant art in which single phase aerosols are formulated with dimethylether, solubilized antiperspirant active, and polyol solvents such as propylene glycol. These compositions contain dimethylether which allows for the formulation of a stable single-phase system, provided that the system also contains water, ethanol or relatively high propylene glycol concentrations to maintain the stability of the single phase system. Such compositions, however, tend to be unstable when formulated with substantive low polarity solvents, thus resulting in precipitation of antiperspirant active from solution or phase separation shortly after formulation, unless the compositions are modified to contain relatively high ethanol, water or propylene glycol concentrations. As noted throughout the antiperspirant art, high ethanol or propylene glycol concentrations can irritate or sting the sensitive underarm area of the skin and high water concentrations can result in an undesirably wet skin feel during and after application.
- It has now been found that pressurized antiperspirant products can be formulated as single phase or clear products, without reliance upon high ethanol, propylene glycol, or water concentrations to solubilize and couple antiperspirant active with the various other ingredients to form a single phase or clear system. It has been found that single-phase, pressurized antiperspirants can be prepared without reliance upon such materials provided that it comprises an antiperspirant active solubilized in a polyol solvent having at least 4 carbon atoms and a hydroxyl group on each of the α and β carbon atoms of the polyol solvent, wherein the solubilized active and selected polyol solvent are combined with a dimethylether propellant in combination with a low polarity solvent having a solubility parameter of less than about 8.0, wherein the weight ratio of the dimethylether to the low polarity solvent is from about 0.1 to about 3.0.
- It has been found that the pressurized single-phase antiperspirant product will remain stable over prolonged periods, provided that the defined polyol solvent and dimethylether propellant are coupled with the low polarity solvent, and provided that the weight ratio of the dimethylether propellant to low polarity solvent is maintained within the range as defined here.
- It has also been found that the above-described pressurized antiperspirant products remain stable over prolonged periods of time, and can be formulated as clear or single phase systems with low polarity solvents or materials. These low polarity solvents or materials can include materials such as volatile or non-volatile silicone fluids that provide additional benefits such as active substantivity, emolliency, improved skin feel during or after application, formulation flexibility, and similar other benefits. These low polarity solvents also include liquefied hydrocarbon propellants to provide a low cost option to more expensive propellant materials.
- The present invention is directed to pressurized anhydrous antiperspirant compositions comprising: (a) a polyol solvent having at least 4 carbon atoms and a hydroxyl group on each of the α and β carbon atoms of the polyol solvent; (b) solubilized antiperspirant active; (c) dimethylether; (d) a low polarity liquid having a solubility parameter of less than about 8.0, wherein the weight ratio of the dimethylether to low polarity solvent is from about 0.1 to about 3.0.
- It has been found that these compositions are especially useful in formulating clear or single-phase pressurized antiperspirant compositions that remain stable over prolonged periods and that can be formulated without high concentrations of ethanol, propylene glycol or aqueous solvents. It has also been found that these compositions can be maintained as single phase or clear formulations, even when formulated with low polarity solvents such as silicone oils, liquefied hydrocarbon propellants, and other similar materials.
- The pressurized antiperspirant compositions of the present invention comprise a selected polyol solvent, a solubilized antiperspirant active, a dimethylether propellant, and a low polarity solvent in a defined weight ratio relative to the dimethylether propellant. These and other essential elements or limitations of the pressurized antiperspirant compositions of the present invention are described in detail hereinafter.
- The term “anhydrous” as used herein, unless otherwise specified, refers to those compositions or materials containing less than about 5%, more preferably less than about 3%, even more preferably less than about 1%, even more preferably zero percent, by weight of free or added water.
- The term “ambient conditions” as used herein refers to surrounding conditions at about one atmosphere of pressure, at about 50% relative humidity, and at about 25° C.
- The term “pressurized antiperspirant” as used herein means any packaged antiperspirant composition that is pressurized from a gas or liquefied gas propellant to thus provide a means for pushing or moving the antiperspirant composition through an application device.
- All percentages, parts and ratios as used herein are by weight of the total composition, unless otherwise specified. All such weights as they pertain to listed ingredients are based on the active level and, therefore, do not include solvents or by-products that may be included in commercially available materials, unless otherwise specified.
- The pressurized antiperspirant compositions of the present invention can comprise, consist of, or consist essentially of the essential elements and limitations of the invention described herein, as well as any additional or optional ingredients, components, or limitations described herein or otherwise useful in pressurized antiperspirant applications.
- The pressurized antiperspirant compositions of the present invention comprise selected liquid polyols for solubilizing or helping to solubilize the antiperspirant active material in the composition. The antiperspirant composition preferably comprises from about 1% to about 80%, more preferably from about 2% to about 60%, even more preferably from about 3% to about 20%, by weight of the selected liquid polyols.
- The liquid polyols for use in the pressurized antiperspirant composition of the present invention are selected to have at least 4 carbon atoms and adjacent hydroxy-substituted carbon atoms at the α and β positions of the liquid polyol. Preferred liquid polyols for use in the compositions are those that conform to the formula:
- wherein R is an amide, ester, alkyl, ether or silicone-containing moiety, each moiety containing at least 2 carbon atoms. The R group is preferably an alkyl or ether group, more preferably an alkyl group having from about 2 to about 10 carbon atoms, more preferably from about 4 to about 6 carbon atoms. The liquid polyols preferably have either 2 or 3 hydroxyl groups in total.
- The R group on the liquid polyol can therefore be substituted or unsubstituted, branched or straight or cyclic, saturated or unsaturated. Non limiting examples of suitable substituents include hydroxyl groups, amines, amides, esters, ethers, alkoxylate groups (e.g., ethoxylates, propoxylates, etc.) and so forth.
- Non limiting examples of suitable liquid polyols for use in the pressurized compositions of the present invention include 1,2-butanediol; 1,2-pentanediol; 4-methyl-1,2-pentanediol; 2-methyl-1,2-pentanediol; 3,3-methyl-1 ,2-butanediol; 4-methyl-1 ,2-hexanediol; 1,2-heptanediol; 3-phenyl-1,2-propanediol; 1,2,6-hexanetriol; 1,2-hexandiol; 1,2,4-butanetriol; and combinations thereof. Other suitable liquid polyols include glycerol ethers such as glycerol isopropyl ether; glycerol propyl ether; glycerol ethyl ether; glycerol methyl ether; glycerol butyl ether; glycerol isopentyl ether; diglycerol isopropyl ether; diglycerol isobutyl ether; diglycerol; triglycerol; triglycerol isopropyl ether; and combinations thereof. Still other suitable liquid polyols include acetic acid glycerol ester; propanoic acid glycerol ester; butanoic acid glycerol ester; 3-methyl butanoic acid glycerol ester; and 3-trimethylsily-1,2-propane diol; silicone-containing 1,2-diols such as those described in U.S. Pat. No. 5,969,172 (Nye); and combinations thereof.
- These selected polyols are formulated into the antiperspirant composition alone or preferably in combination with one or more other anhydrous liquid carriers, examples of such other anhydrous liquid carriers include any known or otherwise effective carrier liquids suitable for topical application to the skin which are also compatible with the solubilized antiperspirant active and propellant components of the composition.
- The pressurized antiperspirant compositions of the present invention are preferably anhydrous, but will typically contain at least small amounts of water associated with the antiperspirant active during formulation. In this context, the term anhydrous means the antiperspirant compositions of the present invention preferably contain less than 10%, more preferably less than 5%, even more preferably less than 3%, most preferably less than 1%, of water by weight of the composition.
- The pressurized antiperspirant compositions of the present invention comprise a solubilized antiperspirant active suitable for application to human skin. The concentration of antiperspirant active in the composition should be sufficient to provide the finished antiperspirant product with the desired perspiration wetness and odor control. The antiperspirant active is preferably solubilized by the liquid polyol component described hereinbefore.
- Solubilized antiperspirant active concentrations in the pressurized antiperspirant compositions preferably range from about 0.1% to about 26%, more preferably from about 1% to about 20%, even more preferably from about 2% to about 10%, by weight of the composition. All such weight percentages are calculated on an anhydrous metal salt basis exclusive of water and any complexing or buffering agent such as glycine, glycine salts, or other complexing or buffering agent.
- The solubilized antiperspirant active for use in the antiperspirant compositions of the present invention include any compound, composition or other material having antiperspirant activity. Preferred antiperspirant actives include astringent metallic salts, especially the inorganic and organic salts of aluminum, zirconium and zinc, as well as mixtures thereof. Particularly preferred are salts such as aluminum halides, aluminum chlorohydrate, aluminum hydroxyhalides, zirconyl oxyhalides, zirconyl hydroxyhalides, and mixtures thereof. Aluminum salts are most preferred for non-contact pressurized compositions.
- Preferred aluminum salts for use in the antiperspirant compositions include those that conform to the formula:
- Al2(OH)aClb.xH2O
- wherein a is from about 2 to about 5; the sum of a and b is about 6; x is from about 1 to about 6; and wherein a, b, and x may have non-integer values. Particularly preferred are the aluminum chlorhydroxides referred to as “⅚ basic chlorhydroxide”, wherein a=5, and “⅔ basic chlorhydroxide” wherein a=4. Processes for preparing aluminum salts are disclosed in U.S. Pat. No. 3,887,692, Gilman, issued Jun. 3, 1975; U.S. Pat. No. 3,904,741, Jones et al., issued Sep. 9, 1975; U.S. Pat. No. 4,359,456, and Gosling et al., issued Nov. 16, 1982, all of which are incorporated herein by reference. Mixtures of aluminum salts are described in British Patent Specification 1,347,950, Shin et al., published Feb. 27, 1974.
- Zirconium salts for use in the antiperspirant compositions, especially in pressurized contact forms, include those which conform to the formula:
- ZrO(OH)2-aCla.xH2O
- wherein a is any number having a value of from 0 to about 2; x is from about 1 to about 7; and wherein a and x may both have non-integer values. Preferred zirconium salts are those complexes which additionally contain aluminum and glycine, commonly known as ZAG complexes. These ZAG complexes contain aluminum chlorhydroxide and zirconyl hydroxy chloride conforming to the above described formulas. Such ZAG complexes are described in U.S. Pat. No. 3,679,068, Luedders et al., issued Feb. 12, 1974; Great Britain Patent Application 2,144,992, Callaghan et al., published Mar. 20, 1985; and U.S. Pat. No. 4,120,948, Shelton, issued Oct. 17, 1978.
- Preferred antiperspirant actives for use in the compositions include aluminum chlorohydrate, aluminum dichlorohydrate, aluminum sesquichlorohydrate, aluminum chlorohydrex propylene glycol complex, aluminum dichlorohydrex propylene glycol complex, aluminum sesquichlorohydrex propylene glycol complex, aluminum chlorohydrex polyethylene glycol complex, aluminum dichlorohydrex polyethylene glycol complex, aluminum sesquichlorohydrex polyethylene glycol complex, aluminum sulfate buffered, and combinations thereof.
- Non limiting examples of solubilized antiperspirant active for use in the pressurized antiperspirant compositions of the present invention, and methods of making the solubilized active, are described in U.S. Pat. No. 6,149,897 (Swaile); U.S. Pat. No. 6,126,928 (Swaile); and U.S. Pat. No. 5,968,489 (Swaile et al.), which descriptions are incorporated herein by reference. Other non limiting examples of solubilized antiperspirant active and methods of making it are described in EP 0 404 533 (Smith et al.).
- The pressurized antiperspirant compositions of the present invention comprise a dimethylether propellant in combination with a low polarity solvent as defined hereinafter, wherein the weight ratio of the dimethylether to the low polarity solvent ranges from about 0.1 to 2.8, preferably from about 0.2 to about 1.0, more preferably from about 0.2 to about 0.5.
- The propellant component of the pressurized antiperspirant compositions of the present invention may contain only dimethylether or a combination of dimethylether and any other known or otherwise suitable propellant for application to the skin, preferably a combination of dimethylether and a hydrocarbon propellant. The dimethylether or total propellant concentration in the pressurized antiperspirant compositions of the present invention ranges from about 5% to about 99%, more typically from about 15% to about 90%, even more preferably from about 30% to about 70%, by weight of the composition. The combination of dimethylether and hydrocarbon propellant preferably represents from about 50% to 100%, more preferably 100%, by weight of the total propellant concentration. Although less preferred, the compositions may comprise minor amounts of other propellants such as nitrous oxide, carbon dioxide, and halogenated hydrocarbons such as triclorofluoromethane, diclorodifluoromethane, diclorotetrafluoroethane trichlorotrifluoroethane, trichlorotetrafluoroethane, and monochlorodifluoromethane, and combinations thereof.
- The hydrocarbon propellants suitable for use in the pressurized antiperspirant compositions include any hydrocarbon propellant known for or otherwise suitable for application to human skin, non limiting examples of which include propane, butane, pentane, isobutane, and combinations thereof. These hydrocarbon propellants are generally in the form of liquefied gases when formulated into the antiperspirant compositions, and are characterized for purposes of defining the compositions of the present invention as a low polarity solvent having a solubility parameter less than about 8.0, which low polarity solvents are described in greater detail hereinafter.
- The pressurized antiperspirant compositions of the present invention comprise a low polarity solvent in combination with the above-described dimethylether propellant, wherein the weight ratio of the dimethylether and low polarity solvent is selected within the defined range as described hereinbefore. The low polarity solvent can be any material that is liquid under ambient conditions or which is otherwise in liquid form within the pressurized composition described herein, and which has a solubility parameter of less than about 8.0, preferably from about 1 to about 6, more preferably from about 1 to about 4.
- The low polarity solvent for use in the composition of the present invention is preferably a liquefied hydrocarbon propellant, non limiting examples of which include propane, butane, isopentane, pentane, isobutane, and combinations thereof. In this context, the liquefied hydrocarbon propellant acts as both a low polarity solvent and an additional propellant within the pressurized compositions. The hydrocarbon propellant as a low polarity solvent is preferably formulated in combination with the dimethylether propellant, wherein the weight ratio of dimethylether to hydrocarbon propellant in this preferred embodiment ranges from about 0.1 to 2.0, more preferably from about 0.1 to 1.0, even more preferably from about 0.2 to about 0.8.
- Other low polarity solvents suitable for use in the pressurized antiperspirant compositions of the present invention include any silicone or silicone-containing material that is known or otherwise suitable for topical application to the skin, provided that the silicone or silicone-containing material is a liquid under ambient conditions or is otherwise in liquid form within the pressurized antiperspirant compositions of the present invention, and provided that the silicone or silicone-containing material has the requisite solubility parameter as defined herein. The silicone or silicone-containing material as a low polarity solvent for use in the pressurized antiperspirant compositions of the present invention can be a volatile or non volatile, cyclic or linear or branched chain, substituted or unsubstituted.
- The concentration of the silicone liquid as a low polarity solvent in the composition preferably ranges from about 0.1% to about 50%, more preferably from about 1% to about 25%, more preferably from about 2% to about 15%, by weight of the pressurized antiperspirant composition.
- Non limiting examples of suitable volatile silicones are described in Todd et al., “Volatile Silicone Fluids for Cosmetics”, Cosmetics and Toiletries, 91:27-32 (1976), which descriptions are incorporated herein by reference. Preferred among these volatile silicones are the cyclic silicones having from about 3 to about 7, more preferably from about 4 to about 5, silicon atoms. Most preferably are those that conform to the formula:
- wherein n is from about 3 to about 7, preferably from about 4 to about 5, most preferably 5. These volatile cyclic silicones generally have a viscosity value of less than about 10 centistokes as measured at 25° C. Suitable volatile silicones for use herein include, but are not limited to, Cyclomethicone D-5 (commercially available from G. E. Silicones); DC 1184, Dow Corning 344, and Dow Corning 345 (commercially available from Dow Corning Corp.); GE 7207, GE 7158 and Silicone Fluids SF-1202 and SF-1173 (available from General Electric Co.); SWS-03314, SWS-03400, F-222, F-223, F-250, F-251 (available from SWS Silicones Corp.); Volatile Silicones 7158, 7207, 7349 (available from Union Carbide); Masil SF-V (available from Mazer) and combinations thereof. Cyclopentasiloxane is most preferred among the volatile silicone liquids.
-
- wherein n is greater than or equal to 1. These linear silicone materials will generally have viscosity values of from about 10 centistoke to about 100,000 centistoke, preferably less than about 500 centistoke, more preferably from about 20 centistoke to about 200 centistoke, even more preferably from about 20 centistoke to about 50 centistoke, as measured under ambient conditions. Non limiting examples of non-volatile, linear silicones suitable for use in the antiperspirant compositions include but are not limited to, Dow Corning 200, hexamethyldisiloxane, Rhodorsil Oils 70047 available from Rhone-Poulenc, Masil SF Fluid available from Mazer, Dow Corning 225, Dow Corning 1732, Dow Corning 5732, Dow Corning 5750 (available from Dow Corning Corp.); SF-96, SF-1066 and SF18(350) Silicone Fluids (available from G.E. Silicones); Velvasil and Viscasil (available from General Electric Co.); and Silicone L-45, Silicone L530, Silicone L-531 (available from Union Carbide), and Siloxane F-221 and Silicone Fluid SWS-101 (available from SWS Silicones).
- Other silicone liquids as low polarity solvents for use in the pressurized antiperspirant compositions of the present invention include modified or organofunctional silicone carriers such as polyalkylsiloxanes, polyalkyarylsiloxanes, cross-linked silicone elastomers, polyestersiloxanes, polyethersiloxane copolymers, polyfluorosiloxanes, polyaminosiloxanes, and combinations thereof. These modified silicone carriers are typically liquid under ambient conditions, and have a preferred viscosity of less than about 100,000 centistokes, more preferably less than about 500 centistokes, even more preferably from about 1 centistoke to about 50 centistokes, and most more preferably from about 1 centistoke to about 20 centistokes. These modified silicone carriers are generally known in the chemical arts, some examples of which are described in 1Cosmetics, Science and Technology 27-104 (M. Balsam and E. Sagarin ed. 1972); U.S. Pat. No. 4,202,879, issued to Shelton on May 13, 1980; U.S. Pat. No. 5,069,897, issued to Orr on Dec. 3, 1991; which descriptions are incorporated herein by reference.
- The pressurized antiperspirant compositions of the present invention may further comprise many other materials for use as the low polarity solvent, provided that such other materials have the defined solubility parameter and are formulated into the composition such that the weight ratio of the dimethylether to low polarity solvent remains within the ranges described herein. Such other materials include volatile and non volatile hydrocarbons in addition to or other than the hydrocarbon propellants described hereinbefore.
- The pressurized antiperspirant compositions of the present invention may further comprise other optional components which may modify the physical, chemical, cosmetic or aesthetic characteristics of the compositions or serve as additional “active” components when deposited on the skin. The compositions may also further comprise optional inert ingredients. Many such optional ingredients are known for use in deodorants, antiperspirants or other personal care compositions, and may also be used in the antiperspirant compositions herein, provided that such optional materials are compatible with the essential materials described herein, or do not otherwise unduly impair product performance.
- Non limiting examples of optional ingredients include preservatives, deodorant antimicrobials, fragrances, deodorant perfumes, coloring agents or dyes, thickeners, pH modifiers, surfactants and other wash-off aids, co-solvents, emollients or residue masking liquids other than the silicone liquids described herein, pharmaceutical actives, vitamins, and combinations thereof. Preferred optional ingredients include dimethicone copolyols.
- Although the pressurized antiperspirant compositions may further comprise any organic or silicone-containing liquid carrier other than the selected polyols and silicone liquids described herein, the compositions are preferably substantially free of ethanol, and also preferably substantially free of propylene glycol or dipropylene glycol. In this context, the term “substantially free” means that the pressurized antiperspirant compositions preferably contain less than 5%, more preferably less than 3%, even more preferably less than 1%, most preferably zero percent, by weight of any of these materials individually.
- The pressurized antiperspirant compositions of the present invention are preferably anhydrous formulations, and are also preferably clear or single-single phase liquids, although the present invention is not limited to clear or single-phase systems. These pressurized antiperspirant compositions are packaged in any known or otherwise suitable pressurized container for use in delivering the combination of materials described herein for any selected pressurized formulation. The pressurized antiperspirant compositions are also preferably free of any suspended or dispersed solids, e.g., insufficient solid concentrations to visibly reduce the clarity of the composition.
- The pressurized antiperspirant composition may be packaged in conventional pressurized containers for use in contact or non-contact product forms. Non-contact products from pressurized containers are well known in the antiperspirant and personal care arts, non limiting examples of which are described in U.S. Pat. Nos. 3,082,917; U.S. Pat. No. 3,083,918; and U.S. Pat. No. 3,544,258, which descriptions are incorporated herein by reference. Pressurized contact antiperspirants are likewise known in the antiperspirant art, non limiting examples of which are described in U.S. Pat. No. 5,567,073 (de Laforcade et al.), which description is incorporated herein by reference.
- The term “contact” or “contact product form” refers to any known or otherwise suitable pressurized package that comprises an applicator surface to which the antiperspirant composition is delivered under pressure from within the pressurized package, and from which the antiperspirant composition is then applied directly to the underarm area of the skin. In this context, the applicator surface directly contacts the underarm during application, thus delivering or depositing the antiperspirant composition to the underarm area of the skin.
- The term “non-contact” or “non-contact product form” as used herein refers to pressurized packages from which the antiperspirant composition is delivered to the underarm through a product stream delivered under pressure from within the package to the skin. In this context, there is no direct contact between any surface of the pressurized package and the underarm.
- The pressurized antiperspirant compositions of the present invention may be prepared by any known or otherwise effective technique, suitable for making and formulating a clear or single phase pressurized antiperspirant formulation. These pressurized compositions are generally prepared by adding, individually or as a premix, all ingredients other than the dimethylether and any other selected propellant to a suitable container. The container is then sealed and residual air within the container is evacuated. The propellant is then added as a liquefied gas under appropriate pressures to the sealed container. Preferred compositions and methods of manufacture are described hereinafter in the following exemplified embodiments of the pressurized antiperspirant compositions of the present invention.
- It has been found that the dimethylether propellant, when used in combination with a hydrocarbon or other similar propellant, is preferably added to the composition after the hydrocarbon or other similar propellant has been added. It has been found that this particular manufacturing sequence helps stabilize the composition during formulation, and thus minimize or eliminate any active precipitation during the manufacturing process. This particular manufacturing process is preferably applied to the pressurized antiperspirant compositions of the present invention, but can also be applied to any pressurized antiperspirant composition known or otherwise disclosed in the antiperspirant art that contains a solubilized antiperspirant active and a combination of dimethylether and other propellants such as liquefied hydrocarbon gases.
- The following examples further describe and demonstrate specific embodiments within the scope of the present invention. The examples are given solely for the purpose of illustration and are not to be construed as limitations of the present invention, as many variations thereof are possible without departing from the spirit and scope of the invention. All exemplified amounts are concentrations by weight of the total composition, unless otherwise specified.
- The compositions described below in Examples A-P are anhydrous, pressurized antiperspirant compositions that are single-phase systems having a clear or translucent appearance. Each of the compositions is packaged in a pressurized contact container, as well as a non-contact pressurized spray container. The products are applied to the underarm area of the skin to provide antiperspirant and deodorant efficacy. The products during and after application to the underarm result in little or no visible residue.
- Each of the compositions described below (Examples A-P) is formulated by combining and mixing together in a glass bottle (suitable for pressurized packaging) all of the listed ingredients in each composition that are in liquid form under otherwise ambient conditions. The glass bottle is then sealed with a delivery valve and evacuated to between 14 and 25 inches of mercury. The propellant in each formulation is then added to the glass bottle under appropriate pressure using a burette filler. For those formulations containing more than one propellant material, the dimethylether is always added last. The resulting packaged composition is then heated in a water bath (150° F.) for 5 minutes to assure proper sealing of the valve. Each of the resulting compositions is a clear or single-phase pressurized antiperspirant composition that remains stable over prolonged periods of ambient storage without the use of solvents such as ethanol or aqueous solvents.
- Each of the compositions described below (Examples A-P) is formulated with solubilized antiperspirant active solution. The solution is prepared by co-spray drying an initial antiperspirant active solution with a moderately polar solvent to form a spray dried active powder, and then dissolving the spray dried active powder in the desired 1,2-diol solvent with simple agitation over a few hours and no added heat, to thus form an antiperspirant active solution for formulation into the pressurized antiperspirant compositions exemplified herein. More specifically, the solubilized antiperspirant active for formulation into the pressurized antiperspirant compositions exemplified herein is prepared by making an aqueous mixture containing 40% by weight of either the aluminum chlorohydrate or aluminum zirconium chlorohydrate glycerin, 9% by weight of butylene glycol, and 2% by weight of polyethylene glycol 1000. The resulting aqueous mixture is then spray dried to provide a spray dried powder that contains about 65-75% by weight of anhydrous antiperspirant active and 20% by weight of the moderately polar solvent (solubility parameter of the moderately polar solvent being from about 9 to about 15). About 30 parts of the resulting spray-dried powder is then mixed with 70 parts of 1,2-hexanediol under ambient conditions, with simple agitation, and without added heat over approximately 2 hours to form the final antiperspirant active solution for formulation into the pressurized antiperspirant compositions exemplified herein.
TABLE 1 Anhydrous Pressurized Antiperspirant Products Ingredient A B C D E F G H Dimethylether 20 15 20 20 10 20 20 40 Butane 60 45 25 40 60 60 Pentane 60 Isobutane 30 Propane 3 Aluminum chlorohydrate 15% 12 10 4 solution in 1,2-hexanediol Aluminum chlorohydrate 25% 25 solution in isopropyl glycerol ether Aluminum chlorohydrate 20% 10 25 solution in butyl glycerol ether Aluminum chlorohydrate 25% 13 20 solution in 1,2-pentanediol Dimethicone (10 cst) 7 14 3 5 10 Dimethicone copolyol 4 3 10 6 5 Cyclopentasiloxane 5 3 14 10 25 Fragrance 1 1 1 1 1 1 1 Weight ratio 0.29 0.30 0.28 0.30 0.19 0.27 0.30 1.14 Dimethylether to low polarity solvent -
TABLE 2 Anhydrous Pressurized Antiperspirant Products Ingredient I J K L M N O P Dimethylether 30 15 20 20 50 40 30 20 Butane 19 20 Isohexadecane 25 Mineral Oil 30 Aluminum chlorohydrate 20% 30 20 25 20 30 solution in 1,2-hexanediol Aluminum chlorohydrate 25% 25 solution in isopropyl glycerol ether Aluminum chlorohydrate 25% 20 25 solution in butyl glycerol ether Dimethicone (10 cst) 14 20 10 10 Dimethicone copolyol 10 10 Cyclopentasiloxane 39 20 49 14 9 9 10 Hexamethyl disiloxane 45 Fragrance 1 1 1 1 1 1 1 Weight ratio 0.76 0.25 0.28 0.33 2.6 1.2 1.4 0.4 Dimethylether to low polarity solvent
Claims (24)
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
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US09/864,012 US6485715B1 (en) | 2001-05-23 | 2001-05-23 | Stable pressurized antiperspirant compositions containing dimethylether propellant and a low polarity solvent |
AU2002259302A AU2002259302A1 (en) | 2001-05-23 | 2002-05-23 | Stable pressurized antiperspirant compositions containing dimethylether propellant and a polyol |
PCT/US2002/016405 WO2002094327A2 (en) | 2001-05-23 | 2002-05-23 | Stable pressurized antiperspirant compositions containing dimethylether propellant and a polyol |
CNA028101499A CN1509161A (en) | 2001-05-23 | 2002-05-23 | Stable pressurized antiperspirant composition coutaining dimethylether propellant and low polarity solvent |
HU0303858A HUP0303858A2 (en) | 2001-05-23 | 2002-05-23 | Stable pressurized antiperspirant compositions containing dimethylether propellant and a polyol |
JP2002591043A JP2004529964A (en) | 2001-05-23 | 2002-05-23 | Stable pressurized antiperspirant composition containing dimethyl ether propellant and polyol |
MXPA03010673A MXPA03010673A (en) | 2001-05-23 | 2002-05-23 | Stable pressurized antiperspirant compositions containing dimethylether propellant and a polyol. |
EP02729302A EP1390005A2 (en) | 2001-05-23 | 2002-05-23 | Stable pressurized antiperspirant compositions containing dimethylether propellant and a polyol |
CA002445462A CA2445462A1 (en) | 2001-05-23 | 2002-05-23 | Stable pressurized antiperspirant compositions containing dimethylether propellant and a polyol |
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US09/864,012 US6485715B1 (en) | 2001-05-23 | 2001-05-23 | Stable pressurized antiperspirant compositions containing dimethylether propellant and a low polarity solvent |
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US20210022983A1 (en) * | 2018-03-28 | 2021-01-28 | Conopco, Inc., D/B/A Unilever | Non-aluminium antiperspirant compositions |
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US7344707B2 (en) * | 2002-05-15 | 2008-03-18 | The Procter & Gamble Company | Low combustion aerosol products in plastic packages having a reduced fire hazard classification that subsequently reduces storage costs |
US7235229B2 (en) * | 2002-11-22 | 2007-06-26 | The Procter & Gamble Company | Clear, stable, dry-and-non-sticky antiperspirant having a select group of polar silicone emollients |
US8211449B2 (en) * | 2004-06-24 | 2012-07-03 | Dpt Laboratories, Ltd. | Pharmaceutically elegant, topical anhydrous aerosol foam |
JP5291460B2 (en) * | 2005-07-30 | 2013-09-18 | ユニリーバー・ナームローゼ・ベンノートシヤープ | Spray composition |
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ZA829387B (en) | 1981-12-30 | 1984-08-29 | Colgate Palmolive Co | Liquid deodorant |
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JP2898316B2 (en) * | 1989-11-01 | 1999-05-31 | 株式会社大阪造船所 | Eazole products for human body |
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- 2002-05-23 MX MXPA03010673A patent/MXPA03010673A/en active IP Right Grant
- 2002-05-23 JP JP2002591043A patent/JP2004529964A/en active Pending
- 2002-05-23 CA CA002445462A patent/CA2445462A1/en not_active Abandoned
- 2002-05-23 HU HU0303858A patent/HUP0303858A2/en unknown
- 2002-05-23 AU AU2002259302A patent/AU2002259302A1/en not_active Abandoned
- 2002-05-23 WO PCT/US2002/016405 patent/WO2002094327A2/en not_active Application Discontinuation
- 2002-05-23 CN CNA028101499A patent/CN1509161A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20210022983A1 (en) * | 2018-03-28 | 2021-01-28 | Conopco, Inc., D/B/A Unilever | Non-aluminium antiperspirant compositions |
Also Published As
Publication number | Publication date |
---|---|
EP1390005A2 (en) | 2004-02-25 |
AU2002259302A1 (en) | 2002-12-03 |
US6485715B1 (en) | 2002-11-26 |
CN1509161A (en) | 2004-06-30 |
HUP0303858A2 (en) | 2004-03-29 |
CA2445462A1 (en) | 2002-11-28 |
WO2002094327A2 (en) | 2002-11-28 |
WO2002094327A3 (en) | 2003-04-03 |
MXPA03010673A (en) | 2004-03-02 |
JP2004529964A (en) | 2004-09-30 |
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