CA2180942C - Personal washing compositions - Google Patents
Personal washing compositions Download PDFInfo
- Publication number
- CA2180942C CA2180942C CA002180942A CA2180942A CA2180942C CA 2180942 C CA2180942 C CA 2180942C CA 002180942 A CA002180942 A CA 002180942A CA 2180942 A CA2180942 A CA 2180942A CA 2180942 C CA2180942 C CA 2180942C
- Authority
- CA
- Canada
- Prior art keywords
- composition according
- silicone
- esters
- oils
- group
- 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 - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 71
- 238000005406 washing Methods 0.000 title claims abstract description 12
- 229920000642 polymer Polymers 0.000 claims abstract description 55
- 230000008021 deposition Effects 0.000 claims abstract description 38
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 20
- 239000004094 surface-active agent Substances 0.000 claims abstract description 16
- 125000002091 cationic group Chemical group 0.000 claims abstract description 15
- 239000002453 shampoo Substances 0.000 claims description 32
- 229920001577 copolymer Polymers 0.000 claims description 18
- 239000003921 oil Substances 0.000 claims description 18
- 229920002545 silicone oil Polymers 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 11
- 239000003945 anionic surfactant Substances 0.000 claims description 11
- 229920002125 Sokalan® Polymers 0.000 claims description 10
- 230000000475 sunscreen effect Effects 0.000 claims description 10
- 239000000516 sunscreening agent Substances 0.000 claims description 10
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 9
- 239000011734 sodium Substances 0.000 claims description 9
- 229910052708 sodium Inorganic materials 0.000 claims description 9
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 8
- 230000003750 conditioning effect Effects 0.000 claims description 8
- 239000000178 monomer Substances 0.000 claims description 7
- QTDIEDOANJISNP-UHFFFAOYSA-N 2-dodecoxyethyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOCCOS(O)(=O)=O QTDIEDOANJISNP-UHFFFAOYSA-N 0.000 claims description 6
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 150000002430 hydrocarbons Chemical class 0.000 claims description 6
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 239000000344 soap Substances 0.000 claims description 5
- 229930003231 vitamin Natural products 0.000 claims description 5
- 239000011782 vitamin Substances 0.000 claims description 5
- 235000013343 vitamin Nutrition 0.000 claims description 5
- 229940088594 vitamin Drugs 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 229920003118 cationic copolymer Polymers 0.000 claims description 4
- 229940106189 ceramide Drugs 0.000 claims description 4
- 239000003925 fat Substances 0.000 claims description 4
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 3
- BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical compound [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 229920006037 cross link polymer Polymers 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 150000002191 fatty alcohols Chemical class 0.000 claims description 3
- 150000002632 lipids Chemical class 0.000 claims description 3
- 239000000375 suspending agent Substances 0.000 claims description 3
- 239000000341 volatile oil Substances 0.000 claims description 3
- 239000001993 wax Substances 0.000 claims description 3
- BIHQJMSIEXRWPS-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;dodecyl dihydrogen phosphate Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCOP(O)(O)=O BIHQJMSIEXRWPS-UHFFFAOYSA-N 0.000 claims description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims description 2
- 239000004141 Sodium laurylsulphate Substances 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 239000003093 cationic surfactant Substances 0.000 claims description 2
- 150000001783 ceramides Chemical class 0.000 claims description 2
- JZKFHQMONDVVNF-UHFFFAOYSA-N dodecyl sulfate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCOS(O)(=O)=O JZKFHQMONDVVNF-UHFFFAOYSA-N 0.000 claims description 2
- 230000002209 hydrophobic effect Effects 0.000 claims description 2
- 238000012986 modification Methods 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 claims description 2
- 150000003445 sucroses Chemical class 0.000 claims description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 6
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 229940049964 oleate Drugs 0.000 claims 1
- 229920000151 polyglycol Polymers 0.000 claims 1
- 239000010695 polyglycol Substances 0.000 claims 1
- 229920001296 polysiloxane Polymers 0.000 description 34
- -1 polydimethylsiloxanes Polymers 0.000 description 27
- 125000000217 alkyl group Chemical group 0.000 description 22
- 210000003491 skin Anatomy 0.000 description 15
- 238000009472 formulation Methods 0.000 description 12
- 125000004432 carbon atom Chemical group C* 0.000 description 11
- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 description 10
- 241000282372 Panthera onca Species 0.000 description 9
- 239000000839 emulsion Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 229920002401 polyacrylamide Polymers 0.000 description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- 230000014759 maintenance of location Effects 0.000 description 8
- 125000002252 acyl group Chemical group 0.000 description 6
- 229920006317 cationic polymer Polymers 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 101100112225 Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) cpa-1 gene Proteins 0.000 description 5
- 102220549062 Low molecular weight phosphotyrosine protein phosphatase_C13S_mutation Human genes 0.000 description 5
- 150000001768 cations Chemical class 0.000 description 5
- 238000012790 confirmation Methods 0.000 description 5
- FLEHQRTTWKDNGI-XTJILODYSA-N (1s,3r)-5-[(2e)-2-[(7ar)-1-[(2s)-5-(cyclopropylamino)pentan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1h-inden-4-ylidene]ethylidene]-2-methylidenecyclohexane-1,3-diol Chemical compound C([C@H](C)C1[C@]2(CCCC(/C2CC1)=C\C=C1C[C@@H](O)C(=C)[C@@H](O)C1)C)CCNC1CC1 FLEHQRTTWKDNGI-XTJILODYSA-N 0.000 description 4
- 102100030613 Carboxypeptidase A1 Human genes 0.000 description 4
- 244000303965 Cyamopsis psoralioides Species 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 101000772551 Homo sapiens Carboxypeptidase A1 Proteins 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 4
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 210000000245 forearm Anatomy 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 229910021653 sulphate ion Inorganic materials 0.000 description 4
- 244000060011 Cocos nucifera Species 0.000 description 3
- 235000013162 Cocos nucifera Nutrition 0.000 description 3
- FPVVYTCTZKCSOJ-UHFFFAOYSA-N Ethylene glycol distearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCCCC FPVVYTCTZKCSOJ-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- YBGZDTIWKVFICR-JLHYYAGUSA-N Octyl 4-methoxycinnamic acid Chemical compound CCCCC(CC)COC(=O)\C=C\C1=CC=C(OC)C=C1 YBGZDTIWKVFICR-JLHYYAGUSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 229920001282 polysaccharide Polymers 0.000 description 3
- 239000005017 polysaccharide Substances 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 238000004876 x-ray fluorescence Methods 0.000 description 3
- DUMAFWZFOOOEPH-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;dodecyl benzenesulfonate Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 DUMAFWZFOOOEPH-UHFFFAOYSA-N 0.000 description 2
- OYINQIKIQCNQOX-UHFFFAOYSA-M 2-hydroxybutyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCC(O)C[N+](C)(C)C OYINQIKIQCNQOX-UHFFFAOYSA-M 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 102100030621 Carboxypeptidase A4 Human genes 0.000 description 2
- 239000004150 EU approved colour Substances 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 108091006629 SLC13A2 Proteins 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 239000002390 adhesive tape Substances 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 239000003242 anti bacterial agent Substances 0.000 description 2
- 239000006172 buffering agent Substances 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 239000004064 cosurfactant Substances 0.000 description 2
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229940094506 lauryl betaine Drugs 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- DVEKCXOJTLDBFE-UHFFFAOYSA-N n-dodecyl-n,n-dimethylglycinate Chemical compound CCCCCCCCCCCC[N+](C)(C)CC([O-])=O DVEKCXOJTLDBFE-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229940079776 sodium cocoyl isethionate Drugs 0.000 description 2
- 210000000434 stratum corneum Anatomy 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- JKVBWACRUUUEAR-UHFFFAOYSA-N (4-chlorophenyl)sulfanyl-(2,4,5-trichlorophenyl)diazene Chemical compound C1=CC(Cl)=CC=C1SN=NC1=CC(Cl)=C(Cl)C=C1Cl JKVBWACRUUUEAR-UHFFFAOYSA-N 0.000 description 1
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical class C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- CHHHXKFHOYLYRE-UHFFFAOYSA-M 2,4-Hexadienoic acid, potassium salt (1:1), (2E,4E)- Chemical compound [K+].CC=CC=CC([O-])=O CHHHXKFHOYLYRE-UHFFFAOYSA-M 0.000 description 1
- JVTIXNMXDLQEJE-UHFFFAOYSA-N 2-decanoyloxypropyl decanoate 2-octanoyloxypropyl octanoate Chemical compound C(CCCCCCC)(=O)OCC(C)OC(CCCCCCC)=O.C(=O)(CCCCCCCCC)OCC(C)OC(=O)CCCCCCCCC JVTIXNMXDLQEJE-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical class CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- KNUPSOXBESCJLY-UHFFFAOYSA-N 2-methoxy-1-phenylhexan-1-one Chemical compound CCCCC(OC)C(=O)C1=CC=CC=C1 KNUPSOXBESCJLY-UHFFFAOYSA-N 0.000 description 1
- WLAMNBDJUVNPJU-UHFFFAOYSA-N 2-methylbutyric acid Chemical compound CCC(C)C(O)=O WLAMNBDJUVNPJU-UHFFFAOYSA-N 0.000 description 1
- RWYMBUBQZGZFES-UHFFFAOYSA-N 4-[4-(3-fluoro-2-methoxyphenyl)-1,3-thiazol-2-yl]morpholine Chemical compound COC1=C(C=CC=C1F)C1=CSC(=N1)N1CCOCC1 RWYMBUBQZGZFES-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
- ULPWBLHOWJRDBH-UHFFFAOYSA-N 5-amino-2-methylidenepentanamide Chemical compound NCCCC(=C)C(N)=O ULPWBLHOWJRDBH-UHFFFAOYSA-N 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 1
- 102100030614 Carboxypeptidase A2 Human genes 0.000 description 1
- RKWGIWYCVPQPMF-UHFFFAOYSA-N Chloropropamide Chemical compound CCCNC(=O)NS(=O)(=O)C1=CC=C(Cl)C=C1 RKWGIWYCVPQPMF-UHFFFAOYSA-N 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical class OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 101000772572 Homo sapiens Carboxypeptidase A4 Proteins 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 108091006675 Monovalent cation:proton antiporter-2 Proteins 0.000 description 1
- 108091006676 Monovalent cation:proton antiporter-3 Proteins 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- IZWSFJTYBVKZNK-UHFFFAOYSA-O N-dodecyl-N,N-dimethyl-3-ammonio-1-propanesulfonic acid Chemical compound CCCCCCCCCCCC[N+](C)(C)CCCS(O)(=O)=O IZWSFJTYBVKZNK-UHFFFAOYSA-O 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 244000044822 Simmondsia californica Species 0.000 description 1
- 235000004433 Simmondsia californica Nutrition 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical group 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- XNEFYCZVKIDDMS-UHFFFAOYSA-N avobenzone Chemical compound C1=CC(OC)=CC=C1C(=O)CC(=O)C1=CC=C(C(C)(C)C)C=C1 XNEFYCZVKIDDMS-UHFFFAOYSA-N 0.000 description 1
- ZWXYEWJNBYQXLK-UHFFFAOYSA-N azanium;4-dodecoxy-4-oxo-3-sulfobutanoate Chemical compound [NH4+].CCCCCCCCCCCCOC(=O)C(S(O)(=O)=O)CC([O-])=O ZWXYEWJNBYQXLK-UHFFFAOYSA-N 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 238000000237 capillary viscometry Methods 0.000 description 1
- 125000004181 carboxyalkyl group Chemical group 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 229940114081 cinnamate Drugs 0.000 description 1
- 229940073507 cocamidopropyl betaine Drugs 0.000 description 1
- 229940018562 coco monoisopropanolamide Drugs 0.000 description 1
- 229940079840 cocoyl isethionate Drugs 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical class C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 239000004815 dispersion polymer Substances 0.000 description 1
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 235000008524 evening primrose extract Nutrition 0.000 description 1
- 229940089020 evening primrose oil Drugs 0.000 description 1
- 239000010475 evening primrose oil Substances 0.000 description 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 150000008131 glucosides Chemical class 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 231100000640 hair analysis Toxicity 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-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
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000867 polyelectrolyte Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 235000010241 potassium sorbate Nutrition 0.000 description 1
- 239000004302 potassium sorbate Substances 0.000 description 1
- 229940069338 potassium sorbate Drugs 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- NPSSWQJHYLDCNV-UHFFFAOYSA-N prop-2-enoic acid;hydrochloride Chemical compound Cl.OC(=O)C=C NPSSWQJHYLDCNV-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 108700004121 sarkosyl Proteins 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 229940083542 sodium Drugs 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- ADWNFGORSPBALY-UHFFFAOYSA-M sodium;2-[dodecyl(methyl)amino]acetate Chemical compound [Na+].CCCCCCCCCCCCN(C)CC([O-])=O ADWNFGORSPBALY-UHFFFAOYSA-M 0.000 description 1
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- AGGIJOLULBJGTQ-UHFFFAOYSA-N sulfoacetic acid Chemical class OC(=O)CS(O)(=O)=O AGGIJOLULBJGTQ-UHFFFAOYSA-N 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- PUVAFTRIIUSGLK-UHFFFAOYSA-M trimethyl(oxiran-2-ylmethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1CO1 PUVAFTRIIUSGLK-UHFFFAOYSA-M 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 238000004846 x-ray emission Methods 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8158—Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing 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
- 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
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5426—Polymers characterized by specific structures/properties characterized by the charge cationic
-
- 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
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/594—Mixtures of polymers
Abstract
Personal washing compositions which contain a cationic deposition polymer of charge density in the range 0.0001 to 0.005 eq/g and average molecular weight greater than 2 x 106 daltons in combination with a surfactant to increase deposition of a benefit agent dispersed in the composition onto the skin or hair.
Description
~1~~94~
PERSONAL WASHING COMPOSITIONS
. This invention relates to personal washing compositions which contain a cationic deposition polymer to increase deposition -- 5 of a benefit agent onto the skin or hair.
For many years it has been known that hair can be conditioned by incorporation of silicone in a shampoo composition. US 2 826 551 (Geen) is typical of an early disclosure of such 2 in 1 shampoos. Various attempts have been made to improve the efficiency of use of the expensive silicone component. This would provide better conditioning and the option of reducing the level of expensive benefit agent in the shampoo, with consequent cost saving.
Deposition polymers with a cationic charge have been proposed to enhance the amount of benefit agent deposited from the shampoo. For example cationic guar gum has been described for the enhancement of the deposition of antidandruff particles in US 5 037 818 and for the enhanced deposition of insoluble non-volatile silicone in US 5 085 857. The use of cationic polymers in shower gels to enhance deposition of silicone oil is also known from EP-A-457 688 (L~Oreal).
Deposition polymers have also been proposed to enhance the deposition of sunscreen materials from a shampoo composition.
In EP 386 898 a cationic polygalactomannan gum derivative is used.
Polyacrylamides have been proposed for use in shampoos in EP
0 231 997. These polymers are not charged and do not assist in the deposition of benefit agents.
When washing with any of the prior art systems a considerable amount of the benefit agent will be rinsed away with the CONFIRMATION COPY
PERSONAL WASHING COMPOSITIONS
. This invention relates to personal washing compositions which contain a cationic deposition polymer to increase deposition -- 5 of a benefit agent onto the skin or hair.
For many years it has been known that hair can be conditioned by incorporation of silicone in a shampoo composition. US 2 826 551 (Geen) is typical of an early disclosure of such 2 in 1 shampoos. Various attempts have been made to improve the efficiency of use of the expensive silicone component. This would provide better conditioning and the option of reducing the level of expensive benefit agent in the shampoo, with consequent cost saving.
Deposition polymers with a cationic charge have been proposed to enhance the amount of benefit agent deposited from the shampoo. For example cationic guar gum has been described for the enhancement of the deposition of antidandruff particles in US 5 037 818 and for the enhanced deposition of insoluble non-volatile silicone in US 5 085 857. The use of cationic polymers in shower gels to enhance deposition of silicone oil is also known from EP-A-457 688 (L~Oreal).
Deposition polymers have also been proposed to enhance the deposition of sunscreen materials from a shampoo composition.
In EP 386 898 a cationic polygalactomannan gum derivative is used.
Polyacrylamides have been proposed for use in shampoos in EP
0 231 997. These polymers are not charged and do not assist in the deposition of benefit agents.
When washing with any of the prior art systems a considerable amount of the benefit agent will be rinsed away with the CONFIRMATION COPY
composition, and there is scope for substantially improving the deposition efficiency.
It is an object of the present invention to provide a more efficient deposition polymer than the previously described polygalactomannan polymers.
According to the present invention there is provided a personal washing composition comprising: a surface active agent selected from anionic, nonionic, zwitterionic and cationic surfactants, soap and mixtures thereof, water, a non-volatile insoluble benefit agent dispersed in the composition and from 0.001 to 1~ by weight of a deposition polymer which is a cationic copolymer wherein the charge density of the copolymer is in the range 0.0001 to 0.005 eq/g, preferably 0.0008 to 0.0025 eq/g; and the average molecular weight of the copolymer is more than 2x10 daltons.
Preferably the amount of deposition polymer lies in the range 0.05 to 0.2~ by weight. Preferably the cationic copolymer is a copolymer of acrylamide and a cationic monomer having the formula:
R
I
- ( CHZ-C ) -T
I
It is an object of the present invention to provide a more efficient deposition polymer than the previously described polygalactomannan polymers.
According to the present invention there is provided a personal washing composition comprising: a surface active agent selected from anionic, nonionic, zwitterionic and cationic surfactants, soap and mixtures thereof, water, a non-volatile insoluble benefit agent dispersed in the composition and from 0.001 to 1~ by weight of a deposition polymer which is a cationic copolymer wherein the charge density of the copolymer is in the range 0.0001 to 0.005 eq/g, preferably 0.0008 to 0.0025 eq/g; and the average molecular weight of the copolymer is more than 2x10 daltons.
Preferably the amount of deposition polymer lies in the range 0.05 to 0.2~ by weight. Preferably the cationic copolymer is a copolymer of acrylamide and a cationic monomer having the formula:
R
I
- ( CHZ-C ) -T
I
3 0 R' where: T is -O- or -C-II
O , R is H or CH3 and R' i s -NH- ( CHz ) ~-N' ( CH3 ) 3 X- or -O- ( CHZ ) ~-N' ( CH3 ) 3 X-ManoN coy 2)~~9~~
r.- WO 95/22311 PCTIEP95/00582 in which n is an integer from 1 to 4 and X is selected from C1, Br, I and CH3S03.
The composition is suitable for cleansing and conditioning of the skin or hair. The term "conditioning" is intended to cover "moisturising" and "protection".
Throughout this specification reference to average molecular weight (Mw) means a molecular weight calculated as follows.
The intrinsic viscosity of a polymer may be determined by standard capillary viscometry. The viscosity of a series of low polymer concentrations in a given solvent is determined relative to the pure solvent. The relative viscosity Nr is defined as:
Npolymez sol/N solvent The specific viscosity Nsp is:
Nz - 1 If Nsp/c, where c is the polymer concentration, is plotted against c, a straight line is usually obtained. The point at which the straight line crosses the y intercept is the intrinsic viscosity (N;n). This is related to the coil size of the polymer.
The intrinsic viscosity can also be related to the molecular weight of the polymer if the Mark-Houwink parameters are known. Thus, Nin = K(MW)a Where K and a are the Mark-Houwink parameters.
CONF1RMAT~ON COPY
r These have been determined for polyacrylamide, and also for a number of copolymers of acrylamide and N,N,N
trimethylaminoethyl chloride acrylate. These polymers are in accordance with those found useful in the present invention.
The parameters can be found in Mabire et al, Polymer 1984 (25) 1984.
For CPA1, CPA2 and CPAS to 10 we used the MH parameters for 30~ cationic polymer. For CPA 3 and CPA 4 we used MH
parameters for acrylamide homopolymer. Whichever is used, the Mw figure is approximately the same. Thus, if the MH
parameters for acrylamide are used for CPA 1, the Mw figure becomes 5,000,000 rather than 8,000,000.
There is a precedent in the scientific literature where an estimate of Mw has been made for cationic polyacrylamides by using the MH parameters for acrylamide homopolymer: Hubbe, M.A, Colloids and Surfaces 1987 25 p. 325.
The MH parameters are generated for 1 M NaCl, so, in accordance with normal practice for polyelectrolytes, 1M NaCl was used as a solvent for our measurements. Intrinsic viscosity of some of the polymers used is given below:
pONFIRMATION COPY
~,..
O , R is H or CH3 and R' i s -NH- ( CHz ) ~-N' ( CH3 ) 3 X- or -O- ( CHZ ) ~-N' ( CH3 ) 3 X-ManoN coy 2)~~9~~
r.- WO 95/22311 PCTIEP95/00582 in which n is an integer from 1 to 4 and X is selected from C1, Br, I and CH3S03.
The composition is suitable for cleansing and conditioning of the skin or hair. The term "conditioning" is intended to cover "moisturising" and "protection".
Throughout this specification reference to average molecular weight (Mw) means a molecular weight calculated as follows.
The intrinsic viscosity of a polymer may be determined by standard capillary viscometry. The viscosity of a series of low polymer concentrations in a given solvent is determined relative to the pure solvent. The relative viscosity Nr is defined as:
Npolymez sol/N solvent The specific viscosity Nsp is:
Nz - 1 If Nsp/c, where c is the polymer concentration, is plotted against c, a straight line is usually obtained. The point at which the straight line crosses the y intercept is the intrinsic viscosity (N;n). This is related to the coil size of the polymer.
The intrinsic viscosity can also be related to the molecular weight of the polymer if the Mark-Houwink parameters are known. Thus, Nin = K(MW)a Where K and a are the Mark-Houwink parameters.
CONF1RMAT~ON COPY
r These have been determined for polyacrylamide, and also for a number of copolymers of acrylamide and N,N,N
trimethylaminoethyl chloride acrylate. These polymers are in accordance with those found useful in the present invention.
The parameters can be found in Mabire et al, Polymer 1984 (25) 1984.
For CPA1, CPA2 and CPAS to 10 we used the MH parameters for 30~ cationic polymer. For CPA 3 and CPA 4 we used MH
parameters for acrylamide homopolymer. Whichever is used, the Mw figure is approximately the same. Thus, if the MH
parameters for acrylamide are used for CPA 1, the Mw figure becomes 5,000,000 rather than 8,000,000.
There is a precedent in the scientific literature where an estimate of Mw has been made for cationic polyacrylamides by using the MH parameters for acrylamide homopolymer: Hubbe, M.A, Colloids and Surfaces 1987 25 p. 325.
The MH parameters are generated for 1 M NaCl, so, in accordance with normal practice for polyelectrolytes, 1M NaCl was used as a solvent for our measurements. Intrinsic viscosity of some of the polymers used is given below:
pONFIRMATION COPY
~,..
Polymer Intrinsic Viscosity (dl/g) 1M NaCl CPA 1 11.1*
CPA 2 1.1*
CPA 3 11.8 CPA 4 1.2 CPA 5 12.5 CPA 6 8.0 CPA 7 2.8 CPA 8 10 . 4 CPA 9 6.9 CPA 10 8.25 JR 400 4.8 JR 30M 12.0 Jaguar C13S 9.8 Merquat 550 2.7 "CPA" polymers are copolymers of acrylamide and N,N,N-trimethyl aminopropylacrylamide. CPA 1, 2, 5, 7, 9 and 10 have cationic charge densities of 0.00145 eq/g. CPA 3 and CPA
4 have cationic charge densities of 0.0004 eq/g. CPA 6 and CPA 8 have respective cationic charge densities 0.00194 and 0.0009 eq/g. All CPA copolymers were ex Allied colloids.
The Intrinsic viscosities for CPA 1, 2 and 5 to 10 is data from Allied Colloids. The data for CPA3 and CPA4 was produced by the above method and corresponds closely with the data supplied by Allied Colloids for these materials.
co~r~anorv ~
218Q94~
CPA 2 1.1*
CPA 3 11.8 CPA 4 1.2 CPA 5 12.5 CPA 6 8.0 CPA 7 2.8 CPA 8 10 . 4 CPA 9 6.9 CPA 10 8.25 JR 400 4.8 JR 30M 12.0 Jaguar C13S 9.8 Merquat 550 2.7 "CPA" polymers are copolymers of acrylamide and N,N,N-trimethyl aminopropylacrylamide. CPA 1, 2, 5, 7, 9 and 10 have cationic charge densities of 0.00145 eq/g. CPA 3 and CPA
4 have cationic charge densities of 0.0004 eq/g. CPA 6 and CPA 8 have respective cationic charge densities 0.00194 and 0.0009 eq/g. All CPA copolymers were ex Allied colloids.
The Intrinsic viscosities for CPA 1, 2 and 5 to 10 is data from Allied Colloids. The data for CPA3 and CPA4 was produced by the above method and corresponds closely with the data supplied by Allied Colloids for these materials.
co~r~anorv ~
218Q94~
Preferred "CPA" polymers have an intrinsic viscosity of at least 7.
By "benefit agent" is meant a protective and/or softening substance that maintains softness by retarding the decrease in water content from the skin (stratum corneum) or hair.
Normally the benefit agent is an oil. For skin, preferred benefit agents include a) silicone oils, gums and modifications thereof such as linear and cyclic polydimethylsiloxanes; amino, alkyl alkylaryl and aryl silicone oils;
b) fats and oils including natural fats and oils such as jojoba and beef tallow;
c) waxes such as beeswax and lanolin;
d) hydrocarbons such as petrolatum and mineral oil;
e) higher fatty acids and higher fatty alcohols, both saturated and unsaturated, having a carbon chain length in the range C1; to Czz;
f) esters such as isopropyl myristate and isopropyl palmitate;
g) essential oils such as evening primrose oil;
h) lipids such as cholesterol, ceramides, sucrose esters and pseudo-ceramides as described in European Patent Specification No. 556 957;
i) vitamins such as vitamin A and E, and vitamin alkyl esters, including those vitamin C alkyl esters;
j) sunscreens such as octyl methoxyl cinnamate (Parsol MCX) and butyl methoxy benzoylmethane (Parsol 1789); and k) mixtures of any of the foregoing components.
For hair, the oil may take the form of a sunscreen, a styling or bodying agent or a conditioning oil. Among suitable CONFIRMATION COPY
~180~42 sunscreens and other benefit agents there may be mentioned:
the group of branched hydrocarbon materials of high molecular weight referred to elsewhere as peralk(en)yl hydrocarbons.
These may be either in an organic solvent or directly emulsified in the shampoo composition to give styling or bodying effects. Polyisobutene is a preferred branched hydrocarbon material. Also oil soluble sunscreens partitioned into emulsified oil droplets. Among the oils suitable for this purpose are phenyl silicones and among the suitable sunscreens are, benzophenone compounds, dibenzoyl methane derivatives and camphor derivatives. A preferred sunscreen material is a UV absorber such as 2-ethyl hexyl methoxy cinnamate sold under the trade name Parsol MCX by Givaudan.
Silicone oil is a preferred conditioning oil for skin or hair. The silicone may be in the form of a low viscosity oil which may contain a high viscosity oil or gum in solution.
Alternatively the high viscosity material may be in the form of an emulsion in water. The emulsion may be of high viscosity oil or of a solution of gum in a lower viscosity oil. The particle size of the oil phase may be anywhere in the range from 30 nanometres to up to 20 microns average size.
When the oil is a silicone it may be a polydimethylsiloxane with an average particle size of less than 20 microns and preferably less than 2 microns. Small particle size enables a more uniform distribution of silicone conditioning agent for the same concentration of silicone in the composition.
Advantageously a silicone with a viscosity in the range 1-20 million cst is used. The silicone can be cross-linked.
The personal washing composition may further comprise from 0.1 to 5 0 of a suspending agent selected from polyacrylic co~wanoN coy ~. ~ WO 95/22311 PCT/EP95/00582 _ g _ acids, cross linked polymers of acrylic acid, copolymers of acrylic acid with a hydrophobic monomer, copolymers of carboxylic acid- containing monomers and acrylic esters, cross-linked copolymers of acrylic acid and acrylate esters, heteropolysaccharide gums and crystalline long chain aryl derivatives. The long chain acyl derivative is desirably selected from ethylene glycol stearates, alkanolamides of fatty acids having from 16 to 22 carbon atoms and mixtures thereof. Ethylene glycol distearate and Polyethylene glycol 3 distearate are preferred long chain acyl derivatives.
Polyacrylic acid is available commercially as Carbopol 420, Carbopol 488 or Carbopol 493. Polymers of acrylic acid cross-linked with a polyfunctional agent may also be used, they are available commercially as Carbopol 910, Carbopol 934, Carbopol 940, Carbopol 941 and Carbopol 980. An example of a suitable copolymer of a carboxylic acid containing a monomer and acrylic acid esters is Carbopol 1342. All " Carbopol materials are available from Goodrich and Carbopol is a trade mark. The suspending agent is particularly preferred when silicone is present .
Suitable cross linked polymers of acrylic acid and acrylate esters are Pemulen TR1 or Pemulen TR2. A suitable heteropolysaccharide gum is xanthan gum, for example that available as Kelzan Mmu.
In skin washing compositions of the invention, the surface active agent can be selected from any known surfactant suitable for topical application to the human body. Mild surfactants, ie. surfactants which do not damage the stratum corneum, the outer layer of skin, are particularly preferred.
One preferred anionic surfactant is fatty acyl isethionate of formula:
3 5 RCO~CH,CHzSO,M
1.
..... fr-,.1. . . _. _ . _ _ - g _ where R is an alkyl or alkenyl group of 7 to 21 carbon atoms and M is a solubilising cation such as sodium, potassium, ammonium or substituted ammonium. Preferably at least three quarters of the RCO groups have 12 to 18 carbon atoms and may be derived from coconut, palm or a coconut/palm blend.
Another preferred anionic surfactant is alkyl ether sulphate of formula:
RO ( CHZCH~O ) ~S03M
where R is an alkyl group of 8 to 22 carbon atoms, n ranges from 0.5 to 10 especially 1.5 to 8, and M is a solubilising cation as before.
Other possible anionic surfactants include alkyl glyceryl ether sulphate, sulphosuccinates, taurates, sarcosinates, sulphoacetates, alkyl phosphate, alkyl phosphate esters and acyl lactylate, alkyl glutamates and mixtures thereof.
Sulphosuccinates may be monoalkyl sulphosuccinates having the formula : RSOZCCH~CH ( S03M) CO~M; and amido-MEA sulphosuccinates of the formula: RCONCH~CH202CCH~CH ( SO~M) CO~M; wherein RS ranges from C8-CZO alkyl, preferably C1~-C1; alkyl and M is a solubilising cation.
Sarcosinates are generally indicated by the formula:
RSCON ( CHj ) CHZCOzM, wherein R ranges f rom C8-Czo alkyl , preferably Clt-C1; alkyl and M is a solubilising cation.
Taurates are generally identified by the formula:
RSCONR°CH~CH.,S03M, wherein R'-' ranges from CQ-Czo alkyl, preferably C1~-Cl, alkyl, R'' ranges from C;-C~ alkyl, and M is a solubilising cation.
WO 95122311 , PCT/EP95I00582 Harsh surfactants such as primary alkane sulphonate or alkyl benzene sulphonate will generally be avoided.
Suitable nonionic surface active agents include alkyl polysaccharides, lactobionamides, ethyleneglycol esters, glycerol monoethers, polyhydroxyamides (glucamide), primary and secondary alcohol ethoxylates, especially the CB_2o aliphatic alcohols ethoxylated with an average of from 1 to 20 moles of ethylene oxide per mole of alcohol.
If the surface active agent comprises soap, the soap is preferably derived from materials with a C8 to C2a substantially saturated carbon chain and, preferably, is a potassium soap with a C12 to C18 carbon chain.
Mixtures of any of the foregoing surface active agents may also be used.
It is also preferable that the composition includes at least one cosurfactant agent with skin-mildness benefits. Suitable materials are zwitterionic detergents which have an alkyl or alkenyl group of 7 to 18 carbon atoms and comply with an overall structural formula II I
Rl - ~ -C-NH ( CH2 ) n,-~ ~-N'-X-Y
R-where R1 is alkyl or alkenyl of 7 to 18 carbon atoms R' and R' are each independently alkyl, hydroxyalkyl or carboxyalkyl of 1 to 3 carbon atoms m is 2 to 4 n is 0 or 1 con~Rn~non cvPy X is alkylene of 1 to 3 carbon atoms optionally substituted with hydroxyl, and Y is -COz- or -SO~,-Zwitterionic detergents within the above general formula include simple betaines of formula:
R' R1 ~'--CH2COz Rs and amido betaines of formula:
Rz R1 - CONH ( CHz ) m-N'-CHzCOz 2 0 R' where m is 2 or 3.
In both formulae R1, Rz and R3 are as defined previously.
R1 may, in particular, be a mixture of Clz and C1Q alkyl groups derived from coconut so that at least half, preferably at least three quarters of the groups R1 have 10 to 14 carbon atoms. Rz and R~ are preferably methyl.
A further possibility is a sulphobetaine of formula:
Rz R1-N'- ( CH._, ) -_,SO_;
R
CONFIf~L4TIDN CdPY
21809~~ --or R' R1-CONH ( CHZ ) m ~'- ( CH2 ) 3503-R=' where m is 2 or 3, or variants of these in which - (CHZ) 3SO3- is replaced by OH
-CHZCHCHzS03 Rl, R2 and R3 in these formulae are as defined previously.
The surface active agent is preferably present in amount of from 2 to 40~ by weight, and preferably from 5 to 30~ by weight. The cosurfactant, is present, is preferably present at a level of 0.5 to 15o by weight.
The skin washing composition according to the invention may also include minor amounts of other ingredients such as antibacterial agents, foam boosters, pearlescers, perfumes, dyes, colouring agents, preservatives, thickeners, proteins, other polymers, phosphate esters and buffering agents.
Shampoo compositions of the invention contain anionic surfactant together with optional nonionic and amphoteric surfactant.
Suitable anionic surfactants are the alkyl sulphates, alkyl ether sulphates, alkaryl sulphonates, alkyl succinates, alkyl sulphosuccinates, N-alkoyl sarcosinates, alkyl phosphates, alkyl ether phosphates, alkyl ether carboxylates, and alpha-olefin sulphonates, especially their sodium, magnesium, ammonium and mono-, di- and triethanolamine salts. The alkyl groups generally contains from 8 to 18 carbon atoms and may be unsaturated. The alkyl ether sulphates, alkyl ether phosphates and alkyl ether carboxylates may contain from one cvn~r~nvnr coy WO 95/22311 2 i 8 0 9 4 2 pCT~~S/00582 to 10 ethylene oxide or propylene oxide unites per molecule, and preferably contain an average of 2 to 3 ethylene oxide units per molecule.
Further examples of suitable anionic surfactants include sodium oleyl succinate, ammonium lauryl sulphosuccinate, ammonium lauryl sulphate, sodium dodecylbenzene sulphonate, triethanolamine dodecylbenzene sulphonate, triethanolamine dodecylbenzene sulphonate and sodium N-lauryl sarcosinate.
The most preferred anionic surfactants are sodium lauryl sulphate, triethanolamine lauryl sulphate, triethanolamine monolauryl phosphate, sodium lauryl ether sulphate 1E0, 2E0 and 3E0, ammonium lauryl sulphate and ammonium lauryl ether sulphate 1E0, 2E0 and 3E0.
The nonionic surfactants suitable for use in the shampoo compositions of the invention include condensation products of aliphatic (C8-C,8) primary or secondary linear or branched chain alcohols or phenols with alkylene oxides, usually ethylene oxide and generally 6-30 EO.
Other suitable nonionics include mono or di alkyl alkanolamides or alkyl polyglucosides. Examples include coco mono or diethanolamide, coco mono isopropanolamide, and coco di glucoside.
The amphoteric surfactants suitable for use in the composition of the invention may include alkyl amine oxides, alkyl betaines, alkyl amidopropyl betaines, alkyl sulphobetaines, alkyl glycinates, alkyl carboxyglycinates, alkyl amphopropionates, alkyl amidopropyl hydroxysultaines, acyl taurates and acyl glutameates wherein the alkyl and acyl groups have from 8 to 18 carbon atoms. Examples include lauryl amine oxide, cocodimethyl sulphopropyl betaine and corv~~anorv coy -,WO 95/22311 PCTIEP95/00582 preferably lauryl betaine, cocamidopropyl betaine and sodium cocamphopropionate.
The surfactants are present in the shampoo compositions of S the invention in an amount of from 2 to 40% by weight, and preferably from 5 to 30% by weight.
The shampoo may also include minor amounts of other ingredients such as antibacterial agents, foam boosters, pearlescers, perfumes, dyes, colouring agents, preservatives, thickeners, proteins, other polymers, phosphate esters and buffering agents.
The invention will now be described, with reference to the following non-limiting examples:
[A~ Skin Washing Compo i inns Examples In the examples:- w Coco amidopropyl betaine was Tergobetaine F ex Goldschmidt or Amonyl BA 380 ex Seppic.
Guar hydroxypropyl trimonium chloride was Jaguar C-13-S ex Meyhall.
rM
Silicone oil emulsion was BC 89/138 ex Basildon.
Sodium cocoyl isethionate was either Jordapon CI ex PPG/Mazer or Hostapan SCI ex Hoechst.
TM
Sodium lauzyl ether sulphate was Genapol ZRO ex Hoechst.
Compositions according to the invention and comparative compositions were tested by the following method.
A number of tests were carried out by human volunteers. The experimental procedure employed was as follows:
rnn rnrn ~ ~ T,n. , n.v ... , The volunteers washed their forearms with a shower gel. The procedure involved wetting the arm and also the volunteer's free hand with warm water then using the free hand to lather the arm with 0.5 grams of the shower gel, next rinsing for 10 seconds while rubbing with the free hand and then drying the arm with a single pass with a paper towel.
minutes after drying the forearm a strip of adhesive tape is pressed onto the areas on the forearms keeping it in place 10 for 30 seconds using a spring loaded device bearing on a rubber bung to press the tape onto the skin with a repeatable pressure of 85g.crri~. The adhesive tape employed was J-Lar Superclear (TM) tape having a width of 25mm. Two strips of tape are applied to each forearm in this way to adjacent areas of the skin.
In this test procedure silicone which has deposited on the skin is transferred to the tape along with some of the outer layer of the volunteer's skin.
The amounts of silicon and skin adhering to the tape are determined by means of X-ray fluorescence spectroscopy. The tape strips are placed in an X-ray fluorescence spectrometer with the adhesive side facing the beam of this machine. A
mask is applied over the tape to define a standardised area in the middle of the tape which is exposed to the X-ray beam.
The sample chamber of the machine is placed under vacuum before making measurements and the spectrometer is then used to measure the quantities of silicon and sulphur. The sulphur is representative of the amount of skin which has transferred to the tape. Results are presented in terms of the ratio of Si:S.
C~OIVFIRMATION COPY
Example 1 In this example deposition of silicone from compositions containing a range of polymers according to the invention was compared with deposition from a composition containing a polymer which is a commercially available shower gel, namely, guar hydroxypropyl trimonium chloride (comparison).
The base formulation was:-cwt Sodium lauryl ether sulphate ISLES) 13.00 Coco amidopropyl betaine (CAPB) 2.00 Silicone oil emulsion 5.00 Sorbic acid 0.37 Sodium citrate dehydrate 0.49 Sodium chloride 2.0 Citric acid 0.01 Water + minors to 100 Polymers were added to the base formulation at a level of 0.1 cwt.
Each composition was prepared by forming a 1o dispersion of the polymer by adding it to water at ~50°C. SLES and CAPB
were added to the excess water of the formulation with gentle stirring. Thereafter the silicone oil emulsion was added with stirring to the surfactant mixture. This was followed ' by the polymer dispersion and finally the minors.
CONFIRMATION COPY
~1~~~~~
Deposition of silicone was determined according to the procedure described above. The Si:S ratio for the comparison . was normalised to 1 and the values for the compositions according to the invention expressed relative to the comparison.
The following results were obtained:-Polymer Si:S
Comparison 1 CPA 6 4.19 CPA 1 2.42 CPA 7 1.90 The results demonstrate the improved deposition obtained with the compositions according to the invention.
In a further set of experiment with the same base formulation but with different polymers the following results were obtained.
Polymer Si:S
Comparison 1 CPA 9 1.83 CPA 10 2.10 CPA 5 2.81 ' CPA 8 1 . 72 These results also demonstrate the improved deposition obtained with the compositions according to the invention.
Exams 1 a 2 In this example the variation of silicone deposition with the amount of polymer added to the base formulation was examined and compared with that from a composition containing no polymer.
The base formulation was:-%wt Sodium lauryl ether sulphate 2.00 Coco amidopropyl betaine (CAPB) 8.00 Sodium cocoyl isethionate 5.00 Silicone oil emulsion 5.00 Water + minors to 100 It was prepared by forming a premix of the cocoyl isethionate (25% dispersion) by adding it to water at 45°C. The SLES and isethionate premix were then added to the excess water of the formulation with gentle stirring, followed by the CAPB.
Thereafter the silicone oil emulsion was added with stirring.
A 1% dispersion of the polymer was prepared by adding it to water at ~50°C. This was then added to the surfactant/silicone mixture to the required level followed by the minors.
Deposition of silicone was determined according to the procedure described above.
The following results were obtained:-I Polymer owt Si:S
/
Comparison 0 0.41 CPA 5 0.05 1.02 0.1 2.43 0.2 3.28 Comparison 0 0.36 CPA 6 0.05 2.95 0.1 4.28 0.2 4.16 The results demonstrate that silicone deposition increases as the amount of polymer present in the composition increases.
[B] Shampoo Compositions Test of Conventional Cationic Polymers Many of the commercially available cationic polymers designed for use in cosmetics show no ability to deposit silicone on to hair during the course of the hair washing/rinsing cycle.
Table 1 details the performance of a range of cationic polymers promoted by their manufacturers as suitable for use in shampoo applications. The polymers were tested as silicone deposition and retention aids in one of the shampoo formulations (A,B,C or D) given below in Table 3.
CONFIRMATION COPY
Table 1 Eg Polymer shampoo silicone o polymer retention aepositionMw on hair ppm C C15 A 142 3 <100 000 J Quat- A 0 - 125 000 PVA
A figure of zero for silicone retention indicates that the amount detected was negligible and could not accurately be measured.
C13S is JAGUAR (trade mark) C13S, a cationic guar derivative ex Meyhall °-'W 0.95122311 PCT/EP95100582 C15 is JAGUAR C15, also a cationic guar derivative ex Meyhall JR400 is POLYMER JR400, a polysaccharide derivative ex Union Carbide JR30M is POLYMER JR30M, a polysaccharide derivative ex Union Carbide FC370 is Luviquat FC 370(trade mark), ex BASF
Quat-pva is a copolymer prepared by reacting glycidyltrimethylammonium chloride with a commercial PVA;
Mowiol 40-88,~ ex Hoeschst. The molecular weight (Mw) is 127,000 (supplier's data). The final charge density (from ( NMR) is 1.2 meq/g.
rM
550 is Merquat 550 ex Croxton and Garry.
Of these examples, only example K is polyacrylamide based.
The value given for polymer Mw in the table is suppliers data for all examples except Example K. According to Croxton +
Garry, Merquat 550 has a weight average molecular weight of 2.8 million, however, when measured using our Intrinsic viscosity method a value for Mw of 700 000 is obtained.
All retention figures were obtained direct from hair switches washed twice for 30s, and rinsed twice for 30s, in running ' 25 tap water. Shampoo application was at the level of 0.12g/g hair. Silicone levels were determined from X-Ray Fluorescence count rates by comparison with known standards.
Silicone retention efficiency from formulations containing these low Mw polymers does not exceed 250.
examples 3-8 High Molecular Weight Cationic Polvacrvlamides Using high molecular weight polyacrylamides (Mw>3,000,000) gives previously unattainable levels of silicone retention, '.
typically far in excess of 50% efficiency. The results are shown in Table 2.
Table 2 -Example Polymer Shampoo Silicone EfficiencyMol wt retention $
ppm 3 CPA1 D >5000 >70 8 000 000 8 '703 A 2500 55 >5 000 000 Thus, although most commercially available cationic polymers with Mw below 1,000,000 intended for use in cosmetic products show little or no activity as deposition aids from conventional shampoo formulations, use of very high Mw (>
3,000,000) cationic polyacrylamides in shampoo formulations gives surprisingly increased levels of silicone retention.
::Oiv~RMATIDN COPY
Table 3 . SHAMPOO A:
~ 5 16 SLES 2E0 2 Lauryl Betaine 2.25 Ethylene glycol distearate 4 BY22-026 (50~ silicone emulsion) ex Toray silicone 0.1 Deposition Polymer as specified SHAMPOO B:
4 cocoamido propylbetaine 1.5 NaC1 0.3 Deposition Polymer as specified SHAMPOO C:
0.1 Deposition Polymer as specified SHAMPOO D:
2 cocoamido propylbetaine 1.5 ethylene glycol distearate 0.5 Potassium sorbate 0.25 Citric Acid 4.8 X2-1766 (60% Silicone emulsion)ex Dow Corning 0.3 NaC1 0.1 Deposition Polymer as specified CONFlRMAnON COPY
v Combarative Exambles N and O
Because we believed that the higher charge density Jaguar C17 might outperform the Jaguar C13S tested in Examples A, B and D, we made a comparison between C17 and other polymers in shampoo A as follows:
Example N: Shampoo A with Jaguar C13S 983 ppm 20~ efficiency Example O: Shampoo A with Jaguar C171 413 ppm 29~ efficiency The polyacrylamides with high molecular weight (Examples 1,2,4 and 6) clearly outperform Jaguar C17.
The silicone level in these shampoos was 2$ by weight.
Example 9 and Comparative Exam,Hles P and O
To show that the deposition polymers according to the invention can give benefit when added to a commercial shampoo we tested "Wash and Go" Dry Sensitive, (Comparative Example P
believed to be without deposition polymer) and "Wash and Go"
Extra Conditioning (Comparative Example Q, believed to be with Jaguar C17) against the "Dry Sensitive" formulation with 0.2o CPA1 added, (Example 7). CPA1 is a copolymer of acrylamide and N,N,N-trimethylaminopropylacrylamide. "Wash and Go" is a range of 2 in 1 shampoos sold by Procter &
Gamble based on an alkyl sulphate and ether sulphate anionic surfactant mixture. The increased deposition from use of the deposition polymer according to the invention is readily apparent.
Deposition of silicone (ppm silicone) was measured by X-Ray Fluorescence:
CONFIRMATION COPY
Example P 562 +/- 289 ppm Example Q 468 +/- 103 ppm Example 7 1630 +/- 635 ppm All figures are an average from 5 hair samples. It can be seen that addition of the Polymer according to the invention trebles the efficiency of silicone deposition.
CON~7RMAT10N COPY
By "benefit agent" is meant a protective and/or softening substance that maintains softness by retarding the decrease in water content from the skin (stratum corneum) or hair.
Normally the benefit agent is an oil. For skin, preferred benefit agents include a) silicone oils, gums and modifications thereof such as linear and cyclic polydimethylsiloxanes; amino, alkyl alkylaryl and aryl silicone oils;
b) fats and oils including natural fats and oils such as jojoba and beef tallow;
c) waxes such as beeswax and lanolin;
d) hydrocarbons such as petrolatum and mineral oil;
e) higher fatty acids and higher fatty alcohols, both saturated and unsaturated, having a carbon chain length in the range C1; to Czz;
f) esters such as isopropyl myristate and isopropyl palmitate;
g) essential oils such as evening primrose oil;
h) lipids such as cholesterol, ceramides, sucrose esters and pseudo-ceramides as described in European Patent Specification No. 556 957;
i) vitamins such as vitamin A and E, and vitamin alkyl esters, including those vitamin C alkyl esters;
j) sunscreens such as octyl methoxyl cinnamate (Parsol MCX) and butyl methoxy benzoylmethane (Parsol 1789); and k) mixtures of any of the foregoing components.
For hair, the oil may take the form of a sunscreen, a styling or bodying agent or a conditioning oil. Among suitable CONFIRMATION COPY
~180~42 sunscreens and other benefit agents there may be mentioned:
the group of branched hydrocarbon materials of high molecular weight referred to elsewhere as peralk(en)yl hydrocarbons.
These may be either in an organic solvent or directly emulsified in the shampoo composition to give styling or bodying effects. Polyisobutene is a preferred branched hydrocarbon material. Also oil soluble sunscreens partitioned into emulsified oil droplets. Among the oils suitable for this purpose are phenyl silicones and among the suitable sunscreens are, benzophenone compounds, dibenzoyl methane derivatives and camphor derivatives. A preferred sunscreen material is a UV absorber such as 2-ethyl hexyl methoxy cinnamate sold under the trade name Parsol MCX by Givaudan.
Silicone oil is a preferred conditioning oil for skin or hair. The silicone may be in the form of a low viscosity oil which may contain a high viscosity oil or gum in solution.
Alternatively the high viscosity material may be in the form of an emulsion in water. The emulsion may be of high viscosity oil or of a solution of gum in a lower viscosity oil. The particle size of the oil phase may be anywhere in the range from 30 nanometres to up to 20 microns average size.
When the oil is a silicone it may be a polydimethylsiloxane with an average particle size of less than 20 microns and preferably less than 2 microns. Small particle size enables a more uniform distribution of silicone conditioning agent for the same concentration of silicone in the composition.
Advantageously a silicone with a viscosity in the range 1-20 million cst is used. The silicone can be cross-linked.
The personal washing composition may further comprise from 0.1 to 5 0 of a suspending agent selected from polyacrylic co~wanoN coy ~. ~ WO 95/22311 PCT/EP95/00582 _ g _ acids, cross linked polymers of acrylic acid, copolymers of acrylic acid with a hydrophobic monomer, copolymers of carboxylic acid- containing monomers and acrylic esters, cross-linked copolymers of acrylic acid and acrylate esters, heteropolysaccharide gums and crystalline long chain aryl derivatives. The long chain acyl derivative is desirably selected from ethylene glycol stearates, alkanolamides of fatty acids having from 16 to 22 carbon atoms and mixtures thereof. Ethylene glycol distearate and Polyethylene glycol 3 distearate are preferred long chain acyl derivatives.
Polyacrylic acid is available commercially as Carbopol 420, Carbopol 488 or Carbopol 493. Polymers of acrylic acid cross-linked with a polyfunctional agent may also be used, they are available commercially as Carbopol 910, Carbopol 934, Carbopol 940, Carbopol 941 and Carbopol 980. An example of a suitable copolymer of a carboxylic acid containing a monomer and acrylic acid esters is Carbopol 1342. All " Carbopol materials are available from Goodrich and Carbopol is a trade mark. The suspending agent is particularly preferred when silicone is present .
Suitable cross linked polymers of acrylic acid and acrylate esters are Pemulen TR1 or Pemulen TR2. A suitable heteropolysaccharide gum is xanthan gum, for example that available as Kelzan Mmu.
In skin washing compositions of the invention, the surface active agent can be selected from any known surfactant suitable for topical application to the human body. Mild surfactants, ie. surfactants which do not damage the stratum corneum, the outer layer of skin, are particularly preferred.
One preferred anionic surfactant is fatty acyl isethionate of formula:
3 5 RCO~CH,CHzSO,M
1.
..... fr-,.1. . . _. _ . _ _ - g _ where R is an alkyl or alkenyl group of 7 to 21 carbon atoms and M is a solubilising cation such as sodium, potassium, ammonium or substituted ammonium. Preferably at least three quarters of the RCO groups have 12 to 18 carbon atoms and may be derived from coconut, palm or a coconut/palm blend.
Another preferred anionic surfactant is alkyl ether sulphate of formula:
RO ( CHZCH~O ) ~S03M
where R is an alkyl group of 8 to 22 carbon atoms, n ranges from 0.5 to 10 especially 1.5 to 8, and M is a solubilising cation as before.
Other possible anionic surfactants include alkyl glyceryl ether sulphate, sulphosuccinates, taurates, sarcosinates, sulphoacetates, alkyl phosphate, alkyl phosphate esters and acyl lactylate, alkyl glutamates and mixtures thereof.
Sulphosuccinates may be monoalkyl sulphosuccinates having the formula : RSOZCCH~CH ( S03M) CO~M; and amido-MEA sulphosuccinates of the formula: RCONCH~CH202CCH~CH ( SO~M) CO~M; wherein RS ranges from C8-CZO alkyl, preferably C1~-C1; alkyl and M is a solubilising cation.
Sarcosinates are generally indicated by the formula:
RSCON ( CHj ) CHZCOzM, wherein R ranges f rom C8-Czo alkyl , preferably Clt-C1; alkyl and M is a solubilising cation.
Taurates are generally identified by the formula:
RSCONR°CH~CH.,S03M, wherein R'-' ranges from CQ-Czo alkyl, preferably C1~-Cl, alkyl, R'' ranges from C;-C~ alkyl, and M is a solubilising cation.
WO 95122311 , PCT/EP95I00582 Harsh surfactants such as primary alkane sulphonate or alkyl benzene sulphonate will generally be avoided.
Suitable nonionic surface active agents include alkyl polysaccharides, lactobionamides, ethyleneglycol esters, glycerol monoethers, polyhydroxyamides (glucamide), primary and secondary alcohol ethoxylates, especially the CB_2o aliphatic alcohols ethoxylated with an average of from 1 to 20 moles of ethylene oxide per mole of alcohol.
If the surface active agent comprises soap, the soap is preferably derived from materials with a C8 to C2a substantially saturated carbon chain and, preferably, is a potassium soap with a C12 to C18 carbon chain.
Mixtures of any of the foregoing surface active agents may also be used.
It is also preferable that the composition includes at least one cosurfactant agent with skin-mildness benefits. Suitable materials are zwitterionic detergents which have an alkyl or alkenyl group of 7 to 18 carbon atoms and comply with an overall structural formula II I
Rl - ~ -C-NH ( CH2 ) n,-~ ~-N'-X-Y
R-where R1 is alkyl or alkenyl of 7 to 18 carbon atoms R' and R' are each independently alkyl, hydroxyalkyl or carboxyalkyl of 1 to 3 carbon atoms m is 2 to 4 n is 0 or 1 con~Rn~non cvPy X is alkylene of 1 to 3 carbon atoms optionally substituted with hydroxyl, and Y is -COz- or -SO~,-Zwitterionic detergents within the above general formula include simple betaines of formula:
R' R1 ~'--CH2COz Rs and amido betaines of formula:
Rz R1 - CONH ( CHz ) m-N'-CHzCOz 2 0 R' where m is 2 or 3.
In both formulae R1, Rz and R3 are as defined previously.
R1 may, in particular, be a mixture of Clz and C1Q alkyl groups derived from coconut so that at least half, preferably at least three quarters of the groups R1 have 10 to 14 carbon atoms. Rz and R~ are preferably methyl.
A further possibility is a sulphobetaine of formula:
Rz R1-N'- ( CH._, ) -_,SO_;
R
CONFIf~L4TIDN CdPY
21809~~ --or R' R1-CONH ( CHZ ) m ~'- ( CH2 ) 3503-R=' where m is 2 or 3, or variants of these in which - (CHZ) 3SO3- is replaced by OH
-CHZCHCHzS03 Rl, R2 and R3 in these formulae are as defined previously.
The surface active agent is preferably present in amount of from 2 to 40~ by weight, and preferably from 5 to 30~ by weight. The cosurfactant, is present, is preferably present at a level of 0.5 to 15o by weight.
The skin washing composition according to the invention may also include minor amounts of other ingredients such as antibacterial agents, foam boosters, pearlescers, perfumes, dyes, colouring agents, preservatives, thickeners, proteins, other polymers, phosphate esters and buffering agents.
Shampoo compositions of the invention contain anionic surfactant together with optional nonionic and amphoteric surfactant.
Suitable anionic surfactants are the alkyl sulphates, alkyl ether sulphates, alkaryl sulphonates, alkyl succinates, alkyl sulphosuccinates, N-alkoyl sarcosinates, alkyl phosphates, alkyl ether phosphates, alkyl ether carboxylates, and alpha-olefin sulphonates, especially their sodium, magnesium, ammonium and mono-, di- and triethanolamine salts. The alkyl groups generally contains from 8 to 18 carbon atoms and may be unsaturated. The alkyl ether sulphates, alkyl ether phosphates and alkyl ether carboxylates may contain from one cvn~r~nvnr coy WO 95/22311 2 i 8 0 9 4 2 pCT~~S/00582 to 10 ethylene oxide or propylene oxide unites per molecule, and preferably contain an average of 2 to 3 ethylene oxide units per molecule.
Further examples of suitable anionic surfactants include sodium oleyl succinate, ammonium lauryl sulphosuccinate, ammonium lauryl sulphate, sodium dodecylbenzene sulphonate, triethanolamine dodecylbenzene sulphonate, triethanolamine dodecylbenzene sulphonate and sodium N-lauryl sarcosinate.
The most preferred anionic surfactants are sodium lauryl sulphate, triethanolamine lauryl sulphate, triethanolamine monolauryl phosphate, sodium lauryl ether sulphate 1E0, 2E0 and 3E0, ammonium lauryl sulphate and ammonium lauryl ether sulphate 1E0, 2E0 and 3E0.
The nonionic surfactants suitable for use in the shampoo compositions of the invention include condensation products of aliphatic (C8-C,8) primary or secondary linear or branched chain alcohols or phenols with alkylene oxides, usually ethylene oxide and generally 6-30 EO.
Other suitable nonionics include mono or di alkyl alkanolamides or alkyl polyglucosides. Examples include coco mono or diethanolamide, coco mono isopropanolamide, and coco di glucoside.
The amphoteric surfactants suitable for use in the composition of the invention may include alkyl amine oxides, alkyl betaines, alkyl amidopropyl betaines, alkyl sulphobetaines, alkyl glycinates, alkyl carboxyglycinates, alkyl amphopropionates, alkyl amidopropyl hydroxysultaines, acyl taurates and acyl glutameates wherein the alkyl and acyl groups have from 8 to 18 carbon atoms. Examples include lauryl amine oxide, cocodimethyl sulphopropyl betaine and corv~~anorv coy -,WO 95/22311 PCTIEP95/00582 preferably lauryl betaine, cocamidopropyl betaine and sodium cocamphopropionate.
The surfactants are present in the shampoo compositions of S the invention in an amount of from 2 to 40% by weight, and preferably from 5 to 30% by weight.
The shampoo may also include minor amounts of other ingredients such as antibacterial agents, foam boosters, pearlescers, perfumes, dyes, colouring agents, preservatives, thickeners, proteins, other polymers, phosphate esters and buffering agents.
The invention will now be described, with reference to the following non-limiting examples:
[A~ Skin Washing Compo i inns Examples In the examples:- w Coco amidopropyl betaine was Tergobetaine F ex Goldschmidt or Amonyl BA 380 ex Seppic.
Guar hydroxypropyl trimonium chloride was Jaguar C-13-S ex Meyhall.
rM
Silicone oil emulsion was BC 89/138 ex Basildon.
Sodium cocoyl isethionate was either Jordapon CI ex PPG/Mazer or Hostapan SCI ex Hoechst.
TM
Sodium lauzyl ether sulphate was Genapol ZRO ex Hoechst.
Compositions according to the invention and comparative compositions were tested by the following method.
A number of tests were carried out by human volunteers. The experimental procedure employed was as follows:
rnn rnrn ~ ~ T,n. , n.v ... , The volunteers washed their forearms with a shower gel. The procedure involved wetting the arm and also the volunteer's free hand with warm water then using the free hand to lather the arm with 0.5 grams of the shower gel, next rinsing for 10 seconds while rubbing with the free hand and then drying the arm with a single pass with a paper towel.
minutes after drying the forearm a strip of adhesive tape is pressed onto the areas on the forearms keeping it in place 10 for 30 seconds using a spring loaded device bearing on a rubber bung to press the tape onto the skin with a repeatable pressure of 85g.crri~. The adhesive tape employed was J-Lar Superclear (TM) tape having a width of 25mm. Two strips of tape are applied to each forearm in this way to adjacent areas of the skin.
In this test procedure silicone which has deposited on the skin is transferred to the tape along with some of the outer layer of the volunteer's skin.
The amounts of silicon and skin adhering to the tape are determined by means of X-ray fluorescence spectroscopy. The tape strips are placed in an X-ray fluorescence spectrometer with the adhesive side facing the beam of this machine. A
mask is applied over the tape to define a standardised area in the middle of the tape which is exposed to the X-ray beam.
The sample chamber of the machine is placed under vacuum before making measurements and the spectrometer is then used to measure the quantities of silicon and sulphur. The sulphur is representative of the amount of skin which has transferred to the tape. Results are presented in terms of the ratio of Si:S.
C~OIVFIRMATION COPY
Example 1 In this example deposition of silicone from compositions containing a range of polymers according to the invention was compared with deposition from a composition containing a polymer which is a commercially available shower gel, namely, guar hydroxypropyl trimonium chloride (comparison).
The base formulation was:-cwt Sodium lauryl ether sulphate ISLES) 13.00 Coco amidopropyl betaine (CAPB) 2.00 Silicone oil emulsion 5.00 Sorbic acid 0.37 Sodium citrate dehydrate 0.49 Sodium chloride 2.0 Citric acid 0.01 Water + minors to 100 Polymers were added to the base formulation at a level of 0.1 cwt.
Each composition was prepared by forming a 1o dispersion of the polymer by adding it to water at ~50°C. SLES and CAPB
were added to the excess water of the formulation with gentle stirring. Thereafter the silicone oil emulsion was added with stirring to the surfactant mixture. This was followed ' by the polymer dispersion and finally the minors.
CONFIRMATION COPY
~1~~~~~
Deposition of silicone was determined according to the procedure described above. The Si:S ratio for the comparison . was normalised to 1 and the values for the compositions according to the invention expressed relative to the comparison.
The following results were obtained:-Polymer Si:S
Comparison 1 CPA 6 4.19 CPA 1 2.42 CPA 7 1.90 The results demonstrate the improved deposition obtained with the compositions according to the invention.
In a further set of experiment with the same base formulation but with different polymers the following results were obtained.
Polymer Si:S
Comparison 1 CPA 9 1.83 CPA 10 2.10 CPA 5 2.81 ' CPA 8 1 . 72 These results also demonstrate the improved deposition obtained with the compositions according to the invention.
Exams 1 a 2 In this example the variation of silicone deposition with the amount of polymer added to the base formulation was examined and compared with that from a composition containing no polymer.
The base formulation was:-%wt Sodium lauryl ether sulphate 2.00 Coco amidopropyl betaine (CAPB) 8.00 Sodium cocoyl isethionate 5.00 Silicone oil emulsion 5.00 Water + minors to 100 It was prepared by forming a premix of the cocoyl isethionate (25% dispersion) by adding it to water at 45°C. The SLES and isethionate premix were then added to the excess water of the formulation with gentle stirring, followed by the CAPB.
Thereafter the silicone oil emulsion was added with stirring.
A 1% dispersion of the polymer was prepared by adding it to water at ~50°C. This was then added to the surfactant/silicone mixture to the required level followed by the minors.
Deposition of silicone was determined according to the procedure described above.
The following results were obtained:-I Polymer owt Si:S
/
Comparison 0 0.41 CPA 5 0.05 1.02 0.1 2.43 0.2 3.28 Comparison 0 0.36 CPA 6 0.05 2.95 0.1 4.28 0.2 4.16 The results demonstrate that silicone deposition increases as the amount of polymer present in the composition increases.
[B] Shampoo Compositions Test of Conventional Cationic Polymers Many of the commercially available cationic polymers designed for use in cosmetics show no ability to deposit silicone on to hair during the course of the hair washing/rinsing cycle.
Table 1 details the performance of a range of cationic polymers promoted by their manufacturers as suitable for use in shampoo applications. The polymers were tested as silicone deposition and retention aids in one of the shampoo formulations (A,B,C or D) given below in Table 3.
CONFIRMATION COPY
Table 1 Eg Polymer shampoo silicone o polymer retention aepositionMw on hair ppm C C15 A 142 3 <100 000 J Quat- A 0 - 125 000 PVA
A figure of zero for silicone retention indicates that the amount detected was negligible and could not accurately be measured.
C13S is JAGUAR (trade mark) C13S, a cationic guar derivative ex Meyhall °-'W 0.95122311 PCT/EP95100582 C15 is JAGUAR C15, also a cationic guar derivative ex Meyhall JR400 is POLYMER JR400, a polysaccharide derivative ex Union Carbide JR30M is POLYMER JR30M, a polysaccharide derivative ex Union Carbide FC370 is Luviquat FC 370(trade mark), ex BASF
Quat-pva is a copolymer prepared by reacting glycidyltrimethylammonium chloride with a commercial PVA;
Mowiol 40-88,~ ex Hoeschst. The molecular weight (Mw) is 127,000 (supplier's data). The final charge density (from ( NMR) is 1.2 meq/g.
rM
550 is Merquat 550 ex Croxton and Garry.
Of these examples, only example K is polyacrylamide based.
The value given for polymer Mw in the table is suppliers data for all examples except Example K. According to Croxton +
Garry, Merquat 550 has a weight average molecular weight of 2.8 million, however, when measured using our Intrinsic viscosity method a value for Mw of 700 000 is obtained.
All retention figures were obtained direct from hair switches washed twice for 30s, and rinsed twice for 30s, in running ' 25 tap water. Shampoo application was at the level of 0.12g/g hair. Silicone levels were determined from X-Ray Fluorescence count rates by comparison with known standards.
Silicone retention efficiency from formulations containing these low Mw polymers does not exceed 250.
examples 3-8 High Molecular Weight Cationic Polvacrvlamides Using high molecular weight polyacrylamides (Mw>3,000,000) gives previously unattainable levels of silicone retention, '.
typically far in excess of 50% efficiency. The results are shown in Table 2.
Table 2 -Example Polymer Shampoo Silicone EfficiencyMol wt retention $
ppm 3 CPA1 D >5000 >70 8 000 000 8 '703 A 2500 55 >5 000 000 Thus, although most commercially available cationic polymers with Mw below 1,000,000 intended for use in cosmetic products show little or no activity as deposition aids from conventional shampoo formulations, use of very high Mw (>
3,000,000) cationic polyacrylamides in shampoo formulations gives surprisingly increased levels of silicone retention.
::Oiv~RMATIDN COPY
Table 3 . SHAMPOO A:
~ 5 16 SLES 2E0 2 Lauryl Betaine 2.25 Ethylene glycol distearate 4 BY22-026 (50~ silicone emulsion) ex Toray silicone 0.1 Deposition Polymer as specified SHAMPOO B:
4 cocoamido propylbetaine 1.5 NaC1 0.3 Deposition Polymer as specified SHAMPOO C:
0.1 Deposition Polymer as specified SHAMPOO D:
2 cocoamido propylbetaine 1.5 ethylene glycol distearate 0.5 Potassium sorbate 0.25 Citric Acid 4.8 X2-1766 (60% Silicone emulsion)ex Dow Corning 0.3 NaC1 0.1 Deposition Polymer as specified CONFlRMAnON COPY
v Combarative Exambles N and O
Because we believed that the higher charge density Jaguar C17 might outperform the Jaguar C13S tested in Examples A, B and D, we made a comparison between C17 and other polymers in shampoo A as follows:
Example N: Shampoo A with Jaguar C13S 983 ppm 20~ efficiency Example O: Shampoo A with Jaguar C171 413 ppm 29~ efficiency The polyacrylamides with high molecular weight (Examples 1,2,4 and 6) clearly outperform Jaguar C17.
The silicone level in these shampoos was 2$ by weight.
Example 9 and Comparative Exam,Hles P and O
To show that the deposition polymers according to the invention can give benefit when added to a commercial shampoo we tested "Wash and Go" Dry Sensitive, (Comparative Example P
believed to be without deposition polymer) and "Wash and Go"
Extra Conditioning (Comparative Example Q, believed to be with Jaguar C17) against the "Dry Sensitive" formulation with 0.2o CPA1 added, (Example 7). CPA1 is a copolymer of acrylamide and N,N,N-trimethylaminopropylacrylamide. "Wash and Go" is a range of 2 in 1 shampoos sold by Procter &
Gamble based on an alkyl sulphate and ether sulphate anionic surfactant mixture. The increased deposition from use of the deposition polymer according to the invention is readily apparent.
Deposition of silicone (ppm silicone) was measured by X-Ray Fluorescence:
CONFIRMATION COPY
Example P 562 +/- 289 ppm Example Q 468 +/- 103 ppm Example 7 1630 +/- 635 ppm All figures are an average from 5 hair samples. It can be seen that addition of the Polymer according to the invention trebles the efficiency of silicone deposition.
CON~7RMAT10N COPY
Claims (9)
1. A personal washing composition comprising:-a) a surface active agent selected from the group consisting of anionic, nonionic, xwitterionic and cationic surfactants, soap and mixtures thereof;
b) water;
c) a non-volatile insoluble benefit agent dispersed in the composition and selected from the group consisting of silicone oils, gums and modifications thereof, fats and oils, waxes, hydrocarbons, higher fatty acids and higher fatty alcohols, both saturated and unsaturated, having a carbon chain length in the range C12 to C22, esters, essential oils, lipids, ceramides, sucrose esters and pseudo-ceramides, vitamins and vitamin alkyl esters, sunscreens and mixtures of any of the forgoing components; and d) from 0.001 to 1% by weight of a deposition polymer which is a cationic copolymer wherein the charge density of the copolymer is in the range 0.0001 to 0.005 eq/g; and the average molecular weight of the copolymer is more than 2x10 6 daltons, and in which the cationic copolymer is a copolymer of acrylamide and a cationic monomer having the formula:
where: R is H or CH3 and R' is -NH-(CH2)n-N+(CH3)3 X- or -O-(CH2)n-N+(CH3)3 X- in which n is an integer from 1 to 4 and X is selected from Cl, Br, I and CH3SO3.
b) water;
c) a non-volatile insoluble benefit agent dispersed in the composition and selected from the group consisting of silicone oils, gums and modifications thereof, fats and oils, waxes, hydrocarbons, higher fatty acids and higher fatty alcohols, both saturated and unsaturated, having a carbon chain length in the range C12 to C22, esters, essential oils, lipids, ceramides, sucrose esters and pseudo-ceramides, vitamins and vitamin alkyl esters, sunscreens and mixtures of any of the forgoing components; and d) from 0.001 to 1% by weight of a deposition polymer which is a cationic copolymer wherein the charge density of the copolymer is in the range 0.0001 to 0.005 eq/g; and the average molecular weight of the copolymer is more than 2x10 6 daltons, and in which the cationic copolymer is a copolymer of acrylamide and a cationic monomer having the formula:
where: R is H or CH3 and R' is -NH-(CH2)n-N+(CH3)3 X- or -O-(CH2)n-N+(CH3)3 X- in which n is an integer from 1 to 4 and X is selected from Cl, Br, I and CH3SO3.
2. A composition according to claim 1 in which the amount of deposition polymer lies in the range 0.05 to 0.2% by weight.
3. A composition according to any preceding claim in which the charge density of the deposition polymer lies in the range 0.0008 to 0.0025 eq/g.
4. A composition according to any preceding claim in which the benefit agent is selected from the group consisting of silicone oils and gums; fats; oils; waxes;
hydrocarbons; higher fatty acids; higher fatty alcohols;
esters; essential oils; lipids; vitamins; sunscreens;
and mixtures thereof.
hydrocarbons; higher fatty acids; higher fatty alcohols;
esters; essential oils; lipids; vitamins; sunscreens;
and mixtures thereof.
5. A composition according to claim 4 in which the benefit agent is a silicone oil.
6. A composition according to claim 5 in which the composition further comprises from 0.1 to 5 % of a suspending agent for the silicone oil selected from the group consisting of polyacrylic acids; cross linked polymers of acrylic acid; copolymers of acrylic acid with a hydrophobic monomer; copolymers of carboxylic acid- containing monomers and acrylic esters; cross-linked copolymers of acrylic acid and acrylate esters;
heteropolysaccharide gums; crystalline long chain aryl derivatives; fatty acid monoglyceride polyglycol ethers;
propylene glycol and propylene glycol oleate; and mixtures thereof.
heteropolysaccharide gums; crystalline long chain aryl derivatives; fatty acid monoglyceride polyglycol ethers;
propylene glycol and propylene glycol oleate; and mixtures thereof.
7. A composition according to any preceding claim which is a shampoo composition and in which the surface active agent is an anionic surfactant.
8. A shampoo composition according to claim 7 in which the anionic surfactant is selected from the group consisting of sodium lauryl sulphate, triethanolamine lauryl sulphate, triethanolamine monolauryl phosphate, sodium lauryl ether sulphate 1EO, 2EO and 3EO, ammonium lauryl sulphate and ammonium lauryl ether sulphate 1EO, 2EO and 3EO and mixtures thereof.
9. A shampoo composition according to claim 7 or 8 in which the benefit agent is selected from the group consisting of sunscreens, styling or bodying agents and conditioning oils.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9403156A GB9403156D0 (en) | 1994-02-18 | 1994-02-18 | Hair shampoo |
GB9414332.8 | 1994-07-15 | ||
GB9414332A GB9414332D0 (en) | 1994-07-15 | 1994-07-15 | Detergent composition |
GB9403156.4 | 1994-07-15 | ||
PCT/EP1995/000582 WO1995022311A1 (en) | 1994-02-18 | 1995-02-16 | Personal washing compositions |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2180942A1 CA2180942A1 (en) | 1995-08-24 |
CA2180942C true CA2180942C (en) | 2001-12-04 |
Family
ID=26304353
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002180942A Expired - Lifetime CA2180942C (en) | 1994-02-18 | 1995-02-16 | Personal washing compositions |
Country Status (9)
Country | Link |
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US (1) | US5543074A (en) |
EP (1) | EP0744935B2 (en) |
JP (1) | JP2746758B2 (en) |
AU (1) | AU1809795A (en) |
BR (1) | BR9506797A (en) |
CA (1) | CA2180942C (en) |
DE (1) | DE69519372T3 (en) |
ES (1) | ES2153026T5 (en) |
WO (1) | WO1995022311A1 (en) |
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1995
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- 1995-02-16 JP JP7521593A patent/JP2746758B2/en not_active Expired - Lifetime
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- 1995-02-16 AU AU18097/95A patent/AU1809795A/en not_active Abandoned
- 1995-02-16 CA CA002180942A patent/CA2180942C/en not_active Expired - Lifetime
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EP0744935A1 (en) | 1996-12-04 |
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DE69519372T3 (en) | 2004-06-09 |
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