WO2023275497A1 - Coloured solid cosmetic composition with a non-silicone elastomer and a phospholipid - Google Patents
Coloured solid cosmetic composition with a non-silicone elastomer and a phospholipid Download PDFInfo
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- WO2023275497A1 WO2023275497A1 PCT/FR2022/051306 FR2022051306W WO2023275497A1 WO 2023275497 A1 WO2023275497 A1 WO 2023275497A1 FR 2022051306 W FR2022051306 W FR 2022051306W WO 2023275497 A1 WO2023275497 A1 WO 2023275497A1
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- 239000000203 mixture Substances 0.000 title claims abstract description 197
- 150000003904 phospholipids Chemical class 0.000 title claims abstract description 18
- 239000007787 solid Substances 0.000 title claims abstract description 16
- 239000002537 cosmetic Substances 0.000 title claims description 23
- 229920002379 silicone rubber Polymers 0.000 title description 17
- 229920003225 polyurethane elastomer Polymers 0.000 claims abstract description 58
- 229920001971 elastomer Polymers 0.000 claims abstract description 34
- 239000000806 elastomer Substances 0.000 claims abstract description 34
- 239000000049 pigment Substances 0.000 claims abstract description 32
- 239000000787 lecithin Substances 0.000 claims abstract description 26
- 235000010445 lecithin Nutrition 0.000 claims abstract description 26
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims abstract description 22
- 229940067606 lecithin Drugs 0.000 claims abstract description 22
- 239000012948 isocyanate Substances 0.000 claims abstract description 21
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 21
- 239000002904 solvent Substances 0.000 claims abstract description 17
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 11
- 239000003921 oil Substances 0.000 claims description 33
- 150000002148 esters Chemical class 0.000 claims description 21
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 20
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 19
- 229920001577 copolymer Polymers 0.000 claims description 18
- 229920005862 polyol Polymers 0.000 claims description 18
- 150000003077 polyols Chemical class 0.000 claims description 18
- PJHKBYALYHRYSK-UHFFFAOYSA-N triheptanoin Chemical compound CCCCCCC(=O)OCC(OC(=O)CCCCCC)COC(=O)CCCCCC PJHKBYALYHRYSK-UHFFFAOYSA-N 0.000 claims description 18
- 239000000539 dimer Substances 0.000 claims description 16
- 239000012860 organic pigment Substances 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 16
- VJZWIFWPGRIJSN-XRHABHTOSA-N dilinoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O VJZWIFWPGRIJSN-XRHABHTOSA-N 0.000 claims description 15
- 239000004359 castor oil Substances 0.000 claims description 14
- 235000019438 castor oil Nutrition 0.000 claims description 14
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 14
- 239000000194 fatty acid Substances 0.000 claims description 14
- 229930195729 fatty acid Natural products 0.000 claims description 14
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 14
- 239000004615 ingredient Substances 0.000 claims description 14
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 claims description 13
- XJFGDLJQUJQUEI-UHFFFAOYSA-N dodecyl decanoate dodecyl octanoate Chemical compound CCCCCCCCCCCCOC(=O)CCCCCCC.CCCCCCCCCCCCOC(=O)CCCCCCCCC XJFGDLJQUJQUEI-UHFFFAOYSA-N 0.000 claims description 13
- 150000004665 fatty acids Chemical class 0.000 claims description 12
- 239000001023 inorganic pigment Substances 0.000 claims description 12
- 229940078561 triheptanoin Drugs 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- PZTQVMXMKVTIRC-UHFFFAOYSA-L chembl2028348 Chemical compound [Ca+2].[O-]S(=O)(=O)C1=CC(C)=CC=C1N=NC1=C(O)C(C([O-])=O)=CC2=CC=CC=C12 PZTQVMXMKVTIRC-UHFFFAOYSA-L 0.000 claims description 11
- 229940057946 d&c red no. 7 Drugs 0.000 claims description 11
- 235000010187 litholrubine BK Nutrition 0.000 claims description 11
- 235000014121 butter Nutrition 0.000 claims description 10
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical class CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 claims description 10
- 239000004408 titanium dioxide Substances 0.000 claims description 10
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 9
- 239000000945 filler Substances 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
- 239000000377 silicon dioxide Substances 0.000 claims description 9
- 239000001993 wax Substances 0.000 claims description 9
- 102000011782 Keratins Human genes 0.000 claims description 8
- 108010076876 Keratins Proteins 0.000 claims description 8
- OIQPTROHQCGFEF-UHFFFAOYSA-L chembl1371409 Chemical compound [Na+].[Na+].OC1=CC=C2C=C(S([O-])(=O)=O)C=CC2=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 OIQPTROHQCGFEF-UHFFFAOYSA-L 0.000 claims description 8
- 235000011837 pasties Nutrition 0.000 claims description 8
- 239000013638 trimer Substances 0.000 claims description 8
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 7
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 7
- 235000013980 iron oxide Nutrition 0.000 claims description 7
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 claims description 7
- 235000013311 vegetables Nutrition 0.000 claims description 7
- SGHZXLIDFTYFHQ-UHFFFAOYSA-L Brilliant Blue Chemical compound [Na+].[Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 SGHZXLIDFTYFHQ-UHFFFAOYSA-L 0.000 claims description 6
- 241000196324 Embryophyta Species 0.000 claims description 6
- 229940056316 d&c red no. 28 Drugs 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- GVKCHTBDSMQENH-UHFFFAOYSA-L phloxine B Chemical compound [Na+].[Na+].[O-]C(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 GVKCHTBDSMQENH-UHFFFAOYSA-L 0.000 claims description 6
- KVMUSGMZFRRCAS-UHFFFAOYSA-N sodium;5-oxo-1-(4-sulfophenyl)-4-[(4-sulfophenyl)diazenyl]-4h-pyrazole-3-carboxylic acid Chemical compound [Na+].OC(=O)C1=NN(C=2C=CC(=CC=2)S(O)(=O)=O)C(=O)C1N=NC1=CC=C(S(O)(=O)=O)C=C1 KVMUSGMZFRRCAS-UHFFFAOYSA-N 0.000 claims description 6
- 235000012751 sunset yellow FCF Nutrition 0.000 claims description 6
- 239000004173 sunset yellow FCF Substances 0.000 claims description 6
- 235000012756 tartrazine Nutrition 0.000 claims description 6
- 239000004149 tartrazine Substances 0.000 claims description 6
- IIYFAKIEWZDVMP-UHFFFAOYSA-N tridecane Chemical compound CCCCCCCCCCCCC IIYFAKIEWZDVMP-UHFFFAOYSA-N 0.000 claims description 6
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 claims description 6
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 5
- 239000012764 mineral filler Substances 0.000 claims description 5
- 230000008569 process Effects 0.000 claims description 5
- 125000005442 diisocyanate group Chemical group 0.000 claims description 4
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 4
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 claims description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims description 3
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims description 3
- 229940035437 1,3-propanediol Drugs 0.000 claims description 3
- 235000010654 Melissa officinalis Nutrition 0.000 claims description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 3
- 239000000865 liniment Substances 0.000 claims description 3
- 229920000166 polytrimethylene carbonate Polymers 0.000 claims description 3
- 150000003626 triacylglycerols Chemical class 0.000 claims description 3
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 claims description 3
- ZEMPKEQAKRGZGQ-VBJOUPRGSA-N triricinolein Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/C[C@H](O)CCCCCC)COC(=O)CCCCCCC\C=C/C[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-VBJOUPRGSA-N 0.000 claims description 3
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 2
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 2
- AEIJTFQOBWATKX-UHFFFAOYSA-N octane-1,2-diol Chemical compound CCCCCCC(O)CO AEIJTFQOBWATKX-UHFFFAOYSA-N 0.000 claims description 2
- UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 claims description 2
- 229960004063 propylene glycol Drugs 0.000 claims description 2
- 235000013772 propylene glycol Nutrition 0.000 claims description 2
- MAYCICSNZYXLHB-UHFFFAOYSA-N tricaproin Chemical compound CCCCCC(=O)OCC(OC(=O)CCCCC)COC(=O)CCCCC MAYCICSNZYXLHB-UHFFFAOYSA-N 0.000 claims description 2
- 241000021559 Dicerandra Species 0.000 claims 2
- -1 preferably anhydrous Substances 0.000 abstract description 6
- 235000019198 oils Nutrition 0.000 description 32
- 239000000499 gel Substances 0.000 description 23
- OSCJHTSDLYVCQC-UHFFFAOYSA-N 2-ethylhexyl 4-[[4-[4-(tert-butylcarbamoyl)anilino]-6-[4-(2-ethylhexoxycarbonyl)anilino]-1,3,5-triazin-2-yl]amino]benzoate Chemical compound C1=CC(C(=O)OCC(CC)CCCC)=CC=C1NC1=NC(NC=2C=CC(=CC=2)C(=O)NC(C)(C)C)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 OSCJHTSDLYVCQC-UHFFFAOYSA-N 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 11
- 229920001296 polysiloxane Polymers 0.000 description 9
- 235000015112 vegetable and seed oil Nutrition 0.000 description 9
- 239000008158 vegetable oil Substances 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 150000001335 aliphatic alkanes Chemical class 0.000 description 6
- 239000008407 cosmetic solvent Substances 0.000 description 6
- 239000010696 ester oil Substances 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 150000002191 fatty alcohols Chemical class 0.000 description 5
- LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 229930186217 Glycolipid Natural products 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- BTFJIXJJCSYFAL-UHFFFAOYSA-N arachidyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000008247 solid mixture Substances 0.000 description 4
- TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 description 3
- 244000020551 Helianthus annuus Species 0.000 description 3
- 235000003222 Helianthus annuus Nutrition 0.000 description 3
- SGVYKUFIHHTIFL-UHFFFAOYSA-N Isobutylhexyl Natural products CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000012178 vegetable wax Substances 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- DFPJRUKWEPYFJT-UHFFFAOYSA-N 1,5-diisocyanatopentane Chemical compound O=C=NCCCCCN=C=O DFPJRUKWEPYFJT-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- XMVBHZBLHNOQON-UHFFFAOYSA-N 2-butyl-1-octanol Chemical compound CCCCCCC(CO)CCCC XMVBHZBLHNOQON-UHFFFAOYSA-N 0.000 description 2
- BANXPJUEBPWEOT-UHFFFAOYSA-N 2-methyl-Pentadecane Chemical compound CCCCCCCCCCCCCC(C)C BANXPJUEBPWEOT-UHFFFAOYSA-N 0.000 description 2
- JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 235000019486 Sunflower oil Nutrition 0.000 description 2
- 241001135917 Vitellaria paradoxa Species 0.000 description 2
- 235000018936 Vitellaria paradoxa Nutrition 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 235000013871 bee wax Nutrition 0.000 description 2
- 239000012166 beeswax Substances 0.000 description 2
- 229910052797 bismuth Inorganic materials 0.000 description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
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- 239000007809 chemical reaction catalyst Substances 0.000 description 2
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- 239000003086 colorant Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical class OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 2
- 235000019197 fats Nutrition 0.000 description 2
- 150000002314 glycerols Chemical class 0.000 description 2
- 229940119170 jojoba wax Drugs 0.000 description 2
- 239000007934 lip balm Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 150000008104 phosphatidylethanolamines Chemical class 0.000 description 2
- 150000003905 phosphatidylinositols Chemical class 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
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- 229920006395 saturated elastomer Polymers 0.000 description 2
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- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 2
- NDDLLTAIKYHPOD-ISLYRVAYSA-N (2e)-6-chloro-2-(6-chloro-4-methyl-3-oxo-1-benzothiophen-2-ylidene)-4-methyl-1-benzothiophen-3-one Chemical compound S/1C2=CC(Cl)=CC(C)=C2C(=O)C\1=C1/SC(C=C(Cl)C=C2C)=C2C1=O NDDLLTAIKYHPOD-ISLYRVAYSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- NKJOXAZJBOMXID-UHFFFAOYSA-N 1,1'-Oxybisoctane Chemical compound CCCCCCCCOCCCCCCCC NKJOXAZJBOMXID-UHFFFAOYSA-N 0.000 description 1
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- XLTMWFMRJZDFFD-UHFFFAOYSA-N 1-[(2-chloro-4-nitrophenyl)diazenyl]naphthalen-2-ol Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC1=CC=C([N+]([O-])=O)C=C1Cl XLTMWFMRJZDFFD-UHFFFAOYSA-N 0.000 description 1
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 1
- ABEXEQSGABRUHS-UHFFFAOYSA-N 16-methylheptadecyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC(C)C ABEXEQSGABRUHS-UHFFFAOYSA-N 0.000 description 1
- RWKSBJVOQGKDFZ-UHFFFAOYSA-N 16-methylheptadecyl 2-hydroxypropanoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)C(C)O RWKSBJVOQGKDFZ-UHFFFAOYSA-N 0.000 description 1
- 229940043268 2,2,4,4,6,8,8-heptamethylnonane Drugs 0.000 description 1
- GFUCMNMXYOVTDJ-UHFFFAOYSA-N 2,4-diamino-6-butan-2-ylphenol Chemical compound CCC(C)C1=CC(N)=CC(N)=C1O GFUCMNMXYOVTDJ-UHFFFAOYSA-N 0.000 description 1
- FWIUBOWVXREPPL-UHFFFAOYSA-N 2-[2-(7-methyloctanoyloxy)ethoxy]ethyl 7-methyloctanoate Chemical compound CC(C)CCCCCC(=O)OCCOCCOC(=O)CCCCCC(C)C FWIUBOWVXREPPL-UHFFFAOYSA-N 0.000 description 1
- SFAAOBGYWOUHLU-UHFFFAOYSA-N 2-ethylhexyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC SFAAOBGYWOUHLU-UHFFFAOYSA-N 0.000 description 1
- XULHFMYCBKQGEE-UHFFFAOYSA-N 2-hexyl-1-Decanol Chemical compound CCCCCCCCC(CO)CCCCCC XULHFMYCBKQGEE-UHFFFAOYSA-N 0.000 description 1
- KMUBFTBPGVULKC-UHFFFAOYSA-N 2-hexyldecyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CCCCCC)CCCCCCCC KMUBFTBPGVULKC-UHFFFAOYSA-N 0.000 description 1
- GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 description 1
- PGJDCIDLMPSNPX-UHFFFAOYSA-N 2-octyldecyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CCCCCCCC)CCCCCCCC PGJDCIDLMPSNPX-UHFFFAOYSA-N 0.000 description 1
- HXVCOQUDJKMJQY-UHFFFAOYSA-N 2-octyldodecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CCCCCCCC)CCCCCCCCCC HXVCOQUDJKMJQY-UHFFFAOYSA-N 0.000 description 1
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- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- SEACYXSIPDVVMV-UHFFFAOYSA-L eosin Y Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 SEACYXSIPDVVMV-UHFFFAOYSA-L 0.000 description 1
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- 238000005886 esterification reaction Methods 0.000 description 1
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- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000008169 grapeseed oil Substances 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- YCOZIPAWZNQLMR-UHFFFAOYSA-N heptane - octane Natural products CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- XIRNKXNNONJFQO-UHFFFAOYSA-N hexadecanoic acid ethyl ester Natural products CCCCCCCCCCCCCCCC(=O)OCC XIRNKXNNONJFQO-UHFFFAOYSA-N 0.000 description 1
- 229940100463 hexyl laurate Drugs 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- DSAQQOXMBISFHK-UHFFFAOYSA-N icosan-10-yl benzoate Chemical compound CCCCCCCCCCC(CCCCCCCCC)OC(=O)C1=CC=CC=C1 DSAQQOXMBISFHK-UHFFFAOYSA-N 0.000 description 1
- LTYSCLBTUYRCBF-UHFFFAOYSA-N icosan-9-yl 2-hydroxyoctadecanoate Chemical compound CCCCCCCCCCCCCCCCC(O)C(=O)OC(CCCCCCCC)CCCCCCCCCCC LTYSCLBTUYRCBF-UHFFFAOYSA-N 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
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- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical class C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000011146 organic particle Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- ZYIBVBKZZZDFOY-UHFFFAOYSA-N phloxine O Chemical compound O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(Br)=C(O)C(Br)=C1OC1=C(Br)C(O)=C(Br)C=C21 ZYIBVBKZZZDFOY-UHFFFAOYSA-N 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-M pivalate Chemical compound CC(C)(C)C([O-])=O IUGYQRQAERSCNH-UHFFFAOYSA-M 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000008171 pumpkin seed oil Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 239000004170 rice bran wax Substances 0.000 description 1
- 235000019384 rice bran wax Nutrition 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229940057910 shea butter Drugs 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
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- 229910052725 zinc Inorganic materials 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0216—Solid or semisolid forms
- A61K8/0229—Sticks
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/25—Silicon; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/29—Titanium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/55—Phosphorus compounds
- A61K8/553—Phospholipids, e.g. lecithin
-
- 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
- A61K8/87—Polyurethanes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/30—Characterized by the absence of a particular group of ingredients
- A61K2800/34—Free of silicones
Definitions
- TITLE Solid cosmetic composition colored with a non-silicone elastomer and a phospholipid
- the present invention relates to the cosmetic field and in particular to solid, preferably anhydrous, colored cosmetic compositions comprising a non-silicone elastomer and a phospholipid, preferably a lecithin.
- the non-silicone elastomer is preferably biosourced.
- Silicone elastomers are widely used in cosmetics for their ability to impart sensoriality and mattness to care and makeup products in which they are incorporated.
- compositions preferably anhydrous, with ingredients of natural or bio-sourced origin, as an alternative to silicone ingredients, but without compromising on the stability (texture) of the composition and its sensory and matte properties at the app.
- This combination makes it possible to obtain an anhydrous solid colored composition with a uniform shade, comfort and a gummed and homogeneous effect on keratin materials and in particular the lips, and is advantageously an alternative to compositions for the lips comprising silicone elastomers.
- a first aspect of the invention is therefore a solid composition
- a solid composition comprising, in a physiologically acceptable medium: i) a crosslinked polyurethane elastomer gel comprising at least one solvent and a single crosslinked polyurethane elastomer or a mixture of at least two cross-linked polyurethane elastomers, said elastomer or said mixture of elastomers being obtained from a prepolymer having at least two hydroxyl groups and from a (poly)isocyanate, ii) a phospholipid, preferably a lecithin, and iii) a or more pigments.
- the composition of the invention is an anhydrous composition.
- the pigments are chosen from inorganic pigments, organic pigments and mixtures thereof.
- the composition comprises at least one organic pigment (lacquer) on an alumina or aluminum oxide support.
- the composition comprises at least white pigments, such as titanium dioxide, in particular in a content of at least 1% by weight relative to the total weight of the composition, and inorganic and/or organic pigments , in particular at least one organic pigment on an alumina or aluminum oxide support.
- white pigments such as titanium dioxide
- inorganic and/or organic pigments in particular at least one organic pigment on an alumina or aluminum oxide support.
- the composition will also comprise a fatty phase comprising one or more oils and at least one fatty substance chosen from pasty fatty substances, waxes, butters and mixtures thereof.
- the composition also comprises at least one filler, in particular a mineral filler, more preferably a silica.
- the composition according to the invention comprises at least 70%, 80%, 90%, or even at least 95% by weight of biobased ingredients.
- the invention also relates to a cosmetic process for caring for and/or making up keratin materials, in particular the skin and/or the lips and preferably the lips, comprising the application to the said keratin materials and preferably the lips of a composition according to the invention.
- a first aspect of the invention is therefore a solid cosmetic composition
- a solid cosmetic composition comprising, in a physiologically acceptable medium: i) a crosslinked polyurethane elastomer gel comprising at least one solvent and a single crosslinked polyurethane elastomer or a mixture of at least two cross-linked polyurethane elastomers, said elastomer or said mixture of elastomers being obtained from a prepolymer having at least two hydroxyl groups and from a (poly)isocyanate, ii) a phospholipid, preferably a lecithin, and iii) one or more pigments.
- composition of the invention is in solid form.
- the composition of the invention is an anhydrous composition.
- anhydrous is meant in particular that the water is preferably not deliberately added to the compositions but may be present in trace form in the various compounds used in the compositions.
- the composition according to the invention comprises less 4% by weight of water, preferably less than 3%, preferably less than 2%, more preferably less than 1%, even more preferably less than 0.5% by weight of water, relative to the total weight of said composition, or even is completely free of water.
- the ingredients present in the composition of the invention are biosourced ingredients.
- biosourced ingredients we mean ingredients obtained essentially from materials of natural origin. According to the definition given by ADEME (Ecological Transition Agency), biobased products are non-food industrial products obtained from renewable raw materials from biomass (plants for example).
- the composition will comprise at least 70% by weight of bio-based ingredients, in particular at least 80%, 90% or even at least 95% by weight of bio-based compounds, relative to the total weight of the composition.
- the composition of the invention contains less than 5%, preferably less than 1%, of silicone compounds. It is preferably free from it.
- silicone compound means a molecule comprising at least one silicon atom.
- the composition is preferably devoid of a compound chosen from crosslinked silicone polymers such as silicone elastomers, silicone resins, silicone surfactants, silicone gums, cyclic silicones of a volatile nature, and phenyl silicone oils, and dimethicones.
- elastomer we generally mean a cross-linked polymer with elastic properties.
- the crosslinked polyurethane elastomer is in particular in the form of a gel, in which the crosslinked polyurethane elastomer is dispersed in at least one solvent.
- the elastomer gel can comprise one or more cross-linked polyurethane elastomers.
- the composition of the invention comprises a crosslinked polyurethane elastomer gel comprising at least one solvent and a single crosslinked polyurethane elastomer or a mixture of at least two crosslinked polyurethane elastomers, said elastomer or said mixture of elastomers being obtained from a prepolymer having at least two hydroxyl groups and from a (poly)isocyanate.
- the polyurethane elastomer(s) are/is micronized (particle size of 1 to 100 microns, preferably 1 to 60 microns in diameter).
- the crosslinked polyurethane elastomer gel used in the invention may consist of a single crosslinked polyurethane elastomer or of a mixture of at least two crosslinked polyurethane elastomers, the elastomer or the mixture of elastomers being obtained by reacting a (poly)isocyanate with a prepolymer having at least two hydroxyl groups and a cosmetic solvent under conditions to form the crosslinked polyurethane elastomer.
- a urethanization reaction catalyst is used, such as a catalyst based on bismuth or zinc.
- the crosslinked polyurethane elastomer is advantageously biosourced, that is to say obtained from raw materials of natural origin (85%, better still 90%, or even 95% biosourced).
- the prepolymer, the (poly)isocyanate and the cosmetic solvent are of natural origin (for example vegetable) at more than 85%, even more than 95%.
- the prepolymer having at least two hydroxyl groups is a copolymer of a carboxylic acid dimer or trimer, and of a polyol.
- prepolymers mention may in particular be made of copolymers of a dimer or a trimer of a carboxylic acid, preferably C16-C20, and of a polyol.
- the carboxylic acid may comprise a linear carbon chain with at least one carbon-carbon double bond, as is the case with an unsaturated fatty acid.
- the carboxylic acid is a dimer of C12-C18 fatty acids, in particular dilinoleic acid.
- the polyol can be saturated or unsaturated, can include two or three -OH functions, and optionally include other functions such as one or more ester functions.
- the polyol is for example an aliphatic diol comprising 2 to 8 carbon atoms, in particular 3 or 4 carbon atoms, such as propanediol or butanediol.
- the polyol can also be a fatty acid triglyceride comprising at least two —OH groups, for example ricinoleic acid triglyceride, or a natural plant source containing it, such as castor oil.
- the polyol is chosen from the group consisting of an aliphatic diol comprising 2 to 8 carbon atoms, such as 1,2 ethanediol, propanediols such as 1,2 propanediol, 1,3 propanediol , butanediol, pentanediol, caprylyl glycol, preferably propanediols and butanediol; a fatty acid triglyceride comprising at least two -OH groups, such as ricinoleic acid triglyceride or a vegetable source containing it, such as castor oil.
- an aliphatic diol comprising 2 to 8 carbon atoms
- propanediols such as 1,2 propanediol, 1,3 propanediol , butanediol, pentanediol, caprylyl glycol, preferably propanediols and butanediol
- the prepolymer is a copolymer of dilinoleic acid and propanediol (DAPD) or a copolymer of dilinoleic acid and butanediol (DABP).
- DAPD dilinoleic acid and propanediol
- DABP dilinoleic acid and butanediol
- (Poly)isocyanates are compounds containing an isocyanate (-NCO) group. They react with prepolymers containing hydroxyl groups to produce polyurethane polymers.
- the (poly)isocyanate is advantageously a diisocyanate, preferably an aliphatic diisocyanate which may contain 5 or 6 carbon atoms (in its main chain or its cycle).
- the diisocyanate can be linear or cyclic.
- the (poly)isocyanate is a diisocyanate, in particular an aliphatic diisocyanate which may contain from 5 to 6 carbon atoms, preferably chosen from 1,6-hexamethylene diisocyanate (HDI), 1 ,5-pentamethylene diisocyanate (PDI) or isophorone diisocyanate (IPDI).
- HDI 1,6-hexamethylene diisocyanate
- PDI 1 ,5-pentamethylene diisocyanate
- IPDI isophorone diisocyanate
- cosmetic solvent As cosmetic solvents used in the synthesis of the crosslinked polyurethane elastomer and/or the formation of the crosslinked polyurethane elastomer gel, mention may be made of esters, ethers, alkanes and their mixtures.
- triglycerides of plant origin such as glycerol trihexanoate, glycerol triheptanoate (triheptanoin), glycerol trioctanoate, coco-caprylate/caprate, C9-C22 alkanes such as undecane, tridecane; esters of natural origin and mixtures thereof, preferably glycerol triheptanoate (triheptanoin), coco-caprylate/caprate, C9-C22 alkanes, esters of natural origin and mixtures thereof.
- Crosslinked polyurethane elastomers which can be used according to the invention are described in the application published under the number W0202141046 in the name of Grant Industries Inc.
- the preparation of a crosslinked polyurethane elastomer and the subsequent formation of a crosslinked polyurethane elastomer gel as used according to the invention may comprise the following steps:
- the concentrated elastomer can then optionally be diluted with a secondary solvent, volatile or non-volatile, to obtain the desired viscosity for the cross-linked polyurethane elastomer gel.
- the prepolymer which contains 2 hydroxyl groups, represents a content ranging from 5 to 25% by weight of the crosslinked polyurethane elastomer.
- the preferably bio-based (poly)isocyanate contains 15 to 38%, or 15 to 28% -NCO group.
- the total molar ratio of the -NCO groups of the isocyanate to the -OH groups of the polyol can range from 2:1 to 1:2, and is preferably 1:1.
- the content of cosmetic solvent(s) will generally be 70 to 95% by weight relative to the weight of cross-linked polyurethane elastomer.
- the catalyst content may be from 0.1 to 2.5% by weight.
- the elastomer gel can comprise at least one solvent and a crosslinked polyurethane elastomer or a mixture of crosslinked polyurethane elastomers.
- the crosslinked polyurethane elastomer gel used in the compositions according to the invention may comprise from 5 to 30% by weight, in particular from 5 to 17% by weight of active material of elastomer(s) of cross-linked polyurethane(s), and from 70 to 95% by weight, in particular from 83 to 95% by weight of solvent(s).
- the crosslinked polyurethane elastomer gel used according to the invention is the crosslinked polyurethane elastomer gel prepared in Example 6 or in Example 9 of application WO202141046 from Grant Industries Inc.
- the pre -polymer is a copolymer of C8 dimer acid and 1,3 propanediol (DAPD) or 1,4 butanediol (DABD)
- the polyisocyanate is a pentylene diisocyanate (PDT) trimer
- the catalyst is bismuth neodecanoate
- the solvent is a mixture of coco-caprylate/caprate and glycerol triheptanoate.
- the concentrated gel is then formed by the micronization of said cross-linked polyurethane elastomer and the addition of glycerol triheptanoate.
- the concentrated gel is then diluted with the addition of C9-C12 alkanes (Vegelight 1214).
- Such crosslinked polyurethane elastomer gels are marketed under the name GransenseTM by Grant Industries.
- the prepolymer is a reaction product of a diol and a dimer acid, in particular of a dilinoleic acid and propanediol or butanediol and the (poly)isocyanate is a trimer of 1, 5-pentamethylene diisocyanate.
- the crosslinked polyurethane elastomer is obtained from dilinoleic acid, propanediol or butanediol and pentamethylene diisocyanate.
- This cross-linked polyurethane elastomer can be described as a non-silicone elastomer of a polyester nature and have the INCI name: polyurethane-10 Elastomer or polyurethane-100 Elastomer.
- GRANSENSE TC-8X with INCI name Coco-Caprylate/Caprate (and) Triheptanoin (and) C9-12 Alkane (and) Polyurethane-100 Elastomer.
- the gel of crosslinked polyurethane elastomers comprises a mixture of at least two crosslinked polyurethane elastomers, said mixture being obtained from prepolymers of dilinoleic acid/polyols and of isophorone diisocyanate, the two polyols being butanediol and castor oil.
- the mixture of these elastomers may have the following INCI names:
- Triheptanoin and) Coco-Caprylate/Caprate (and) Dilinoleic Acid/Butanediol Copolymer (and) Castor Oil/IPDI Copolymer Elastomer, or
- Coco-Caprylate/Caprate and) Triheptanoin (and) C9-12 Alkane (and) Dilinoleic Acid/Butanediol Copolymer (and) Castor Oil/IPDI Copolymer Elastomer.
- the crosslinked polyurethane elastomer (alone or mixture of two elastomers) according to the invention will generally be present in the composition in a total dry matter (active) content ranging from 0.5% to 5% by weight, in particular from 1 % to 3% and in particular from 2 to 3% by weight relative to the total weight of the composition.
- composition further comprises a phospholipid, preferably a phospholipid of plant origin.
- the phospholipids can be phosphatidylcholine, phosphatidylserine, phosphatidylethanolamine, phosphatidylserine, phosphatidylglycerol, phosphatidylinositol or mixtures thereof, preferably phosphatidylcholine.
- Lecithin is a mixture composed of choline, fatty acids, glycerol, glycolipids, triglycerides, carbohydrates and phospholipids (ex: phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine and phosphatidylinositol). It can be isolated from vegetable oils such as soybean oil, sunflower oil, corn oil, from which it is chemically or mechanically extracted.
- the composition of the invention comprises a lecithin (INCI name lecithin).
- Compliant lecithins are for example:
- EmulmetikTM - Lecithins marketed by Lucas Meyer Cosmetics under the brand names EmulmetikTM:
- EmulmetikTM 100 (INCI name: lecithin): 60% phospholipids and glycolipids and 12% phosphatidylcholine,
- EmulmetikTM 300 (INCI name: lecithin): 97% phospholipids and glycolipids and 23% phosphatidylcholine.
- EmulmetikTM 300 (INCI name: lecithin) is used: 97% phospholipids and glycolipids and 23% phosphatidylcholine.
- the composition of the invention comprises a total content of phospholipid(s), in particular a total content of lecithin(s) ranging from 0.1 to 2%, in particular from 0.2 to 1% and in particular from 0.4 at 0.8%, or even from 0.5 to 0.6% by weight relative to the total weight of the composition.
- composition of the invention comprises one or more pigments for coloring keratin materials, in particular the skin and/or the lips, in particular the lips.
- the pigment(s) are present in a total content ranging from 1% to 15% by weight, in particular from 2% to 12%, by weight relative to the total weight of the composition.
- pigments white or colored, mineral or organic particles, insoluble in an aqueous solution, intended to color and/or opacify the resulting deposit. Mention may be made of inorganic pigments (otherwise called mineral pigments), organic pigments, and composite pigments (that is to say pigments based on inorganic and/or organic materials).
- organic pigments mention may be made, by way of examples, of titanium dioxide; black, yellow, red and brown iron oxides and manganese violet.
- organic pigments mention may be made, for example, of the pigments D & C red No. 19; D & C red No. 9; D&C Red No. 22; D&C Red No. 21; D&C Red No. 28; D&C Yellow No. 6; D & C Orange No. 4; D & C Orange No. 5; D & C Red No. 27; D & C red No. 13; D&C Red No. 7; D&C Red No. 6; D&C Yellow No. 5; D&C Red No. 36; D&C Red No.
- the composition comprises an organic pigment consisting of a colorant on an alumina or aluminum hydroxide base, such as the pigments D&C Red No.7 lake (Cl 15850 (and) Aluminum Hydroxide), FD&C Yellow 5 Al Lake ( C69-4424); FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), and mixtures thereof.
- a colorant on an alumina or aluminum hydroxide base such as the pigments D&C Red No.7 lake (Cl 15850 (and) Aluminum Hydroxide), FD&C Yellow 5 Al Lake ( C69-4424); FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), and mixtures thereof.
- the composition of the invention comprises pigments chosen from inorganic pigments, organic pigments and mixtures thereof, in particular:
- inorganic pigments chosen from titanium dioxide, iron oxides (for example red, yellow, brown, black) and mixtures thereof, preferably a mixture of titanium dioxide and iron oxides, and
- one or more organic pigments chosen from the pigments D & C Red No. 7, D & C Red No.7 lake (Cl 15850), D & C Red No. 28 lake (Cl 45410); FD&C Yellow 5 Al Lake (C69-4424); FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), and mixtures thereof.
- the composition of the invention comprises at least inorganic pigments. According to a particular embodiment, the composition of the invention comprises at least inorganic pigments and organic pigments.
- the composition comprises at least titanium dioxide, one or more iron oxides (yellow, red, brown and/or black) and one or more organic pigments, in particular chosen from D & C Red no. 7, D&C Red No.7 lake (Cl 15850), D&C Red No.28 lake (Cl 45410); FD&C Yellow 5 Al Lake (C69-4424); FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), and mixtures thereof.
- the composition of the invention comprises titanium dioxide in a content of at least 0.5% by weight, in particular at least 0.8% by weight, or even at least 1% by weight with respect to by weight of the composition, one or more iron oxides (yellow, red, brown and/or black) and one or more organic pigments, in particular chosen from D & C Red No. 7, D & C Red No.7 lake (Cl 15850), D&C Red No.28 lake (Cl 45410); FD&C Yellow 5 Al Lake (C69-4424); FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), and mixtures thereof.
- one or more iron oxides yellow, red, brown and/or black
- organic pigments in particular chosen from D & C Red No. 7, D & C Red No.7 lake (Cl 15850), D&C Red No.28 lake (Cl 45410); FD&C Yellow 5 Al Lake (C69-4424); FD&C Yellow 6 Al Lake (C70-5270
- the total content of pigment(s) ranges from 1 to 15% by weight relative to the total weight of said composition.
- the inorganic pigments are present in a content ranging from 1 to 15% by weight, in particular from 2 to 12% by weight relative to the total weight of the composition.
- the organic pigments are present in a content ranging from 1 to 15% by weight, in particular from 2 to 12% by weight relative to the total weight of the composition.
- the composition of the invention comprises: a) A crosslinked polyurethane elastomer (alone or as a mixture) in a total dry matter content ranging from 0.5% to 5% by weight, in particular from 1% to 3% and in particular from 2 to 3% by weight, relative to the total weight of the composition, b) A lecithin in a content ranging from 0.4 to 0.8% by weight relative to the total weight of the composition and c) Inorganic and/or organic pigments in a total content ranging from 2 to 12% by weight per relative to the total weight of the composition.
- composition of the invention also comprises a fatty phase.
- This fatty phase comprises oils (identical to or distinct from the solvents present in the gel of the non-silicone elastomer) and at least one fatty substance chosen from waxes, pasty fatty substances, butters, and mixtures thereof.
- oil is meant a fatty substance, insoluble in water, liquid at 25° C. and atmospheric pressure.
- fat is meant a solid compound or comprising a solid fraction at 25°C. Mention may in particular be made of butters, waxes, pasty compounds, and mixtures thereof.
- wax within the meaning of the present invention, is meant to denote a solid compound at 25° C. which exhibits a reversible solid/liquid state change and a melting temperature greater than 30° C., preferably greater than 45° C. .
- pasty fatty substance denotes a non-crystalline fatty compound comprising, at a temperature of 25° C., a liquid fraction and a solid fraction.
- the additional oils and fatty substances that can be used according to the invention can be of animal, vegetable, mineral or synthetic origin. Preferably, biosourced oils and fatty substances will be used.
- fatty substances or vegetable oils that can be used, mention may be made in particular of the following vegetable oils and fatty substances:
- “vegetable oils” such as: deodorized oleic sunflower oil, virgin sweet almond oil, virgin muscat rose oil, avocado oil, safflower oil, camelina oil, jojoba oil, borage oil, grape seed oil, argan oil, nigella oils, pumpkin seed oil, perilla oil, castor oil and mixtures thereof,
- butters such as: Murumuru butter, Mango butter, Shea butter, cocoa butter and Cupuaçu butter, and mixtures thereof,
- “vegetable waxes” such as: carnauba wax, beeswax, candelilla wax, jojoba wax, sunflower wax, rice bran wax and mixtures thereof,
- esters of polyol(s) and of fatty acid diacid dimer or of one of its esters, hydrogenated castor oil esters, oligomeric glycerol esters, in particular diglycerol esters, and mixtures thereof,
- the composition of the invention will comprise, as pasty fatty substance, at least one ester of diol dimer and diacid dimer, where appropriate, esterified on their alcohol(s) or acid function(s). s) free(s) by acid or alcohol radicals, in particular dimer dilinoleate esters, such as those with the following INCI nomenclature:
- the total content of diol ester(s) and fatty acid diacid dimer, or one of its esters in the composition of the invention will generally range from 0.5% to 20% by weight, in particular from 1% to 10% by weight and preferably from 2% to 5% by weight relative to the total weight of said composition.
- the composition of the invention will comprise at least one vegetable oil and at least one vegetable fatty substance chosen from a vegetable wax, a vegetable butter and mixtures thereof.
- the composition further comprises, as additional oil distinct from the oils (solvents) present in the gel of the non-silicone elastomer, at least one polar hydrocarbon-based oil.
- polar oil within the meaning of the present invention, is meant an oil whose solubility parameter at 25° C., ⁇ a, is different from 0 (J/cm 3 ) 1/2 .
- the polar hydrocarbon-based oil or oils comprise at least one alcohol function (it is then an “alcohol oil”) or at least one ester function (it is then an “ester oil”).
- the “alcohol oils” mention may in particular be made of C10-C26, more particularly C10-C24, and preferably C12-C22 alcohols, saturated or not, branched or not, more particularly monoalcohols. More particularly, the C10-C26 alcohols are fatty monoalcohols, preferably branched when they comprise at least 16 carbon atoms. As examples of fatty alcohols which can be used according to the invention, mention may be made of linear or branched fatty alcohols, of synthetic or even natural origin.
- fatty alcohols which can be used on a preferred basis, mention may in particular be made of lauryl, isostearyl or oleic alcohol, 2-butyloctanol, 2-undecyl pentadecanol, 2-hexyldecyl alcohol, isocetyl alcohol , octyldodecanol and mixtures thereof.
- the fatty alcohol is octyldodecanol.
- ester oils mention may be made in particular of:
- esters preferably having a total carbon number ranging from 35 to 70, such as polyglycerol-2 triisostearate, isostearyl lactate, octyldodecyl hydroxystearate, diisostearyl malate, glycerol stearate; diethylene glycol diisononanoate;
- oils of formula R1COOR2 in which Ri represents the residue of a linear or branched fatty acid containing from 4 to 40 carbon atoms and R2 represents a hydrocarbon chain, in particular branched, containing from 4 to 40 carbon atoms at provided that R1+R2 is >16, such as isononyl isononanoate, 2-hexyl ethyl palmitate, octyledodecyl neopentanoate, 2-octyldodecyl stearate, isostearyl isostearate, octyl-2 dodecyl benzoate, isopropyl myristate, isopropyl palmitate, butyl stearate, hexyl laurate, 2-ethyl-hexyl palmitate, 2-hexyl-decyl laurate, 2-octyl-decyl palmitate, 2-octyldode
- esters of aromatic acids and alcohols comprising 4 to 22 atoms; - esters of fatty alcohol or of branched C24-C28 fatty acids;
- composition of the invention may also comprise at least one hydrocarbon oil chosen from: capric/caprylic triglyceride, dicaprylyl ether, dicaprylyl carbonate, coco-caprylate/caprate, triheptanoin, linear or branched C9-C22 alkanes , in particular: C8-C16 iso-alkanes (also called isoparaffins) such as isododecane, isodecane, isohexadecane, and for example the oils sold under the trade names ISOPAR® or PERMETYL®, linear or branched alkanes having hydrocarbon chains in
- VEGELIGHT® SILK INF-12 ALKANE
- VEGELIGHT® 1214LC VEGELIGHT® 1214LC
- C12 - n-dodecane
- C14 n-tetradecane
- the composition of the invention comprises oils chosen from the group consisting of vegetable oils, C10-C26 alcohol oils, preferably hydroxylated ester oils, and mixtures thereof.
- the composition of the invention comprises at least one vegetable oil and at least one polar hydrocarbon oil, in particular a C10-C26 alcohol oil, in particular octyldodecanol, and an ester oil chosen from hydroxylated esters. and in particular polyglycerol-2 triisostearate.
- polar hydrocarbon oil in particular a C10-C26 alcohol oil, in particular octyldodecanol
- ester oil chosen from hydroxylated esters. and in particular polyglycerol-2 triisostearate.
- the alcohol oils may be present in the composition in a content ranging from 1 to 20%, preferably from 5 to 15%, preferably from 8 to 12% by weight relative to the total weight of the composition.
- the ester oils may be present in the composition in a content ranging from 5 to 45%, preferably from 15 to 40%, preferably from 20 to 35% by weight relative to the total weight of the composition.
- the vegetable oils may be present in the composition in a content ranging from 1 to 20%, preferably from 5 to 15% and preferably from 7 to 13% by weight relative to the total weight of the composition.
- the total content of oil(s) in the composition of the invention may range, for example, from 30 to 90% by weight, in particular from 40 to 80%, preferably from 50 to 75% by weight relative to the total weight of the composition.
- This oil(s) content takes into account the oils (or solvents) present in the gel of the non-silicone elastomer.
- the total content of wax(es) in the composition of the invention may range, for example, from 5 to 20%, preferably from 8 to 18% by weight, in particular from 10 to 15% by weight relative to the total weight of the composition.
- the total content of butter(s) in the composition of the invention may range, for example, from 0.5 to 10% by weight, in particular from 1 to 5% by weight relative to the total weight of the composition.
- the composition may include other ingredients commonly used in cosmetic compositions. Such ingredients can be chosen from antioxidants, perfumes, preservatives, cosmetic active agents, fillers, pigments, and mixtures thereof.
- the fillers and pigments can be treated with a hydrophobic agent to facilitate their dispersion in the oily or fatty phase.
- the composition also comprises at least one filler.
- mineral fillers such as powders of alumina, silica, aluminum silicate, fumed silica, silica silylate, titanium dioxide or sericite.
- the composition of the invention comprises at least one filler, in particular a mineral filler, more preferably a silica, such as that marketed under the name Sunsphere H33.
- a filler in particular a mineral filler, more preferably a silica, such as that marketed under the name Sunsphere H33.
- the content of filler(s), in particular silica in the composition of the invention will range from 0.1 to 5% by weight relative to the total weight of the composition.
- the cosmetic active agents preferably biosourced (eg: plant extracts) can for example be advantageously chosen from those having an action on the care of the skin and/or the lips, such as moisturizing agents.
- composition of the invention comprises:
- filler(s) in particular mineral fillers, more preferably silica,
- the crosslinked polyurethane elastomer gel comprises at least one solvent and a single crosslinked polyurethane elastomer or a mixture of at least two crosslinked polyurethane elastomers, said elastomer or said mixture of elastomers being obtained from a prepolymer having at least two hydroxyl groups and a (poly)isocyanate.
- the prepolymer is a reaction product of a diol and a dimer acid, in particular of a dilinoleic acid and propanediol or butanediol and the (poly)isocyanate is a trimer of 1.5 -pentamethylene diisocyanate.
- the composition comprises a mixture of two crosslinked polyurethane elastomers, said mixture being obtained from acid prepolymers dilinoleic/polyols and isophorone diisocyanate, the two polyols being butanediol and castor oil.
- said composition further comprises:
- oil(s) in particular chosen from the group consisting of vegetable oils, C10-C26 alcohol oils, preferably octyldodecanol, preferably hydroxylated ester oils of preferably polyglycerol-2 triisostearate, and mixtures thereof,
- wax(es) in particular vegetable or animal waxes, preferably carnauba wax, sunflower wax, and/or beeswax and
- esters of polyol(s) and of fatty acid diacid dimer or of one of its esters
- esters of polyol(s) and of fatty acid diacid dimer or of one of its esters
- hydrogenated castor oil esters or of one of its esters
- oligomeric glycerol esters in particular diglycerol esters, and mixtures thereof, preferably esters of polyol(s) and fatty acid diacid dimer, or one of its esters.
- the total oil(s) content includes the content of oils present in the cross-linked polyurethane elastomer gel.
- the composition of the invention will comprise a content of biosourced compounds of at least 70%, 80%, 90%, 95%, 96%, 97%, 98%, 99%, 100% in weight relative to the total weight of the composition.
- composition according to the invention is a colored solid cosmetic composition for topical application to keratin materials, in particular the skin and/or the lips, preferably the lips. It is in particular a composition for caring for and/or making up the skin and/or the lips.
- It may in particular be in the form of a lip stick, a lip balm, poured into a dish, preferably a balm or a stick.
- the invention also relates to a cosmetic process for caring for and/or making up the skin and/or the lips, comprising at least the application to the skin and/or the lips of a composition according to the invention.
- a non-silicone elastomer and a phospholipid, in particular a lecithin, as described above, preferably biosourced makes it possible to obtain a homogeneous composition in shade with a very high natural origin and having an appeal desired cosmetic: melting, comfort, and a gummed and homogeneous effect on keratin materials and in particular the lips.
- the cosmetic process of the invention is intended in particular to obtain a matte and comfortable deposit on the lips.
- the invention will be illustrated by the following non-limiting examples.
- the percentages (%) are expressed as percentage by weight of raw material relative to the total weight of the composition, unless otherwise indicated.
- Example 1 Selection of an agent to stabilize the shade The following composition was prepared:
- composition is prepared according to the following protocol:
- phase A1 the ingredients of phase A1 are weighed and melted in a water bath at 95° C., then homogenized under Rayneri for 15 minutes;
- non-silicone elastomer (A2) is added and stirred for 15 minutes;
- the composition is then hot poured into a tool to obtain a stick (e.g.: silicone teat, metal mold or cup) or directly into the final packaging (bottle).
- a stick e.g.: silicone teat, metal mold or cup
- the appearance of the composition is inhomogeneous: a flow is observed in the bulk and/or on the surface of the composition.
- compositions identical to the one described above are prepared according to the same protocol, and 0.5% by weight of a wetting agent has been added (qsp on polyglycerol-2 Triisostearate).
- the wetting agent is pre-mixed in polyglycerol-2 Triisostearate and mixed with the phase B pigments (themselves pre-dispersed in polyglycerol-2 Triisostearate to form pigment dispersions).
- '-' inhomogeneous aspect, presence of flow
- '+/-' partially inhomogeneous aspect, slightly less important flow
- '+++' homogeneous aspect, absence of flow.
- Example 2 Colored lip balm [Table 3] The composition is prepared according to the following protocol:
- phase A1 the ingredients of phase A1 are weighed and melted in a water bath at 95° C., then homogenized under Rayneri for 15 minutes;
- non-silicone elastomer (A2) is added and stirred for 15 minutes;
- the lecithin is pre-mixed with polyglycerol-2 triisostearate, then mixed with the pigment dispersions (pigments of phase (B) themselves dispersed in polyglycerol-2 triisostearate); this mixture (lecithin and pigmentary dispersions) is then added and mixed for 15 minutes with Rayneri;
- the silica (C) is then dispersed, stirred for 5 minutes and passed through Turrax to obtain a homogeneous composition - the composition is then hot poured into a tool making it possible to obtain a stick (eg: silicone teat, metal mold or cup) or directly into the final packaging (bottle).
- a stick eg: silicone teat, metal mold or cup
- composition obtained is in the form of a stick that is homogeneous in shade, with a gummy and slightly colored matte finish (bitten lips effect) on the lips.
Abstract
The present invention relates to a solid, preferably anhydrous, composition comprising, in a physiologically acceptable medium: i) a crosslinked polyurethane elastomer gel comprising at least one solvent and a single crosslinked polyurethane elastomer or a mixture of at least two crosslinked polyurethane elastomers, said elastomer or said elastomer mixture being obtained from a prepolymer having at least two hydroxyl groups and from a (poly)isocyanate, ii) a phospholipid, preferably a lecithin, and iii) one or more pigments.
Description
DESCRIPTION DESCRIPTION
TITRE : Composition cosmétique solide colorée avec un élastomère non-siliconé et un phospholipide TITLE: Solid cosmetic composition colored with a non-silicone elastomer and a phospholipid
DOMAINE DE L'INVENTION FIELD OF THE INVENTION
La présente invention concerne le domaine cosmétique et en particulier des compositions cosmétiques solides colorées de préférence anhydres comprenant un élastomère non siliconé et un phospholipide, de préférence une lécithine. L’élastomère non siliconé est de préférence biosourcé. The present invention relates to the cosmetic field and in particular to solid, preferably anhydrous, colored cosmetic compositions comprising a non-silicone elastomer and a phospholipid, preferably a lecithin. The non-silicone elastomer is preferably biosourced.
ETAT DE LA TECHNIQUE STATE OF THE ART
Les élastomères siliconés sont très utilisés en cosmétique pour leur aptitude à conférer une sensorialité et une matité aux produits de soin et de maquillage dans lesquels ils sont incorporés. Silicone elastomers are widely used in cosmetics for their ability to impart sensoriality and mattness to care and makeup products in which they are incorporated.
Mais ils présentent cependant l’inconvénient d’une chimie siliconée que le consommateur délaisse, au profit de produits plus naturels, biodégradables. However, they have the disadvantage of a silicone chemistry that the consumer abandons, in favor of more natural, biodegradable products.
Il subsiste donc le besoin de développer de nouvelles compositions de préférence anhydres avec des ingrédients d’origine naturelle ou biosourcés, comme alternative aux ingrédients siliconés, mais sans compromis sur la stabilité (texture) de la composition et ses propriétés de sensorialité et de matité à l’application. There is therefore still a need to develop new compositions, preferably anhydrous, with ingredients of natural or bio-sourced origin, as an alternative to silicone ingredients, but without compromising on the stability (texture) of the composition and its sensory and matte properties at the app.
La demande internationale publiée sous le numéro W02021 /041046 au nom de GRANT INDUSTRIES INC. décrit un nouvel élastomère biosourcé, qui est commercialisé sous la dénomination Gransense™. Mais lorsque cet élastomère biosourcé est formulé dans une composition solide de préférence anhydre comprenant des pigments, telle que des sticks à lèvres, il peut conduire à des inhomogénéités de teinte (flux) dans le vrac ou en surface de la composition. Ce problème de teinte est encore plus visible à l’œil nu pour les teintes claires, comprenant des pigments blancs (ex : dioxyde de titane), notamment en une teneur d’au moins 1% en poids par rapport au poids total de la composition. On cherche donc à améliorer la stabilité et l’homogénéité de la teinte d’une telle composition solide de préférence anhydre comprenant ledit élastomère biosourcé et des pigments. La Demanderesse a justement montré que l’utilisation d’un phospholipide, en particulier une lécithine, dans une composition colorée solide anhydre, permettait de résoudre ce problème. The international application published under number W02021/041046 in the name of GRANT INDUSTRIES INC. describes a new biosourced elastomer, which is marketed under the name Gransense™. But when this biosourced elastomer is formulated in a solid composition, preferably anhydrous, comprising pigments, such as lip sticks, it can lead to color inhomogeneities (flow) in the bulk or on the surface of the composition. This color problem is even more visible to the naked eye for light colors, comprising white pigments (eg: titanium dioxide), in particular in a content of at least 1% by weight relative to the total weight of the composition . It is therefore sought to improve the stability and the homogeneity of the color of such a preferably anhydrous solid composition comprising said biosourced elastomer and pigments. The Applicant has precisely shown that the use of a phospholipid, in particular a lecithin, in an anhydrous solid colored composition, makes it possible to solve this problem.
Cette association permet d’obtenir une composition colorée solide anhydre avec une teinte homogène, du confort et un effet gommé et homogène sur les matières kératiniques et notamment les lèvres, et est avantageusement une alternative aux compositions pour les lèvres comprenant des élastomères siliconés. This combination makes it possible to obtain an anhydrous solid colored composition with a uniform shade, comfort and a gummed and homogeneous effect on keratin materials and in particular the lips, and is advantageously an alternative to compositions for the lips comprising silicone elastomers.
EXPOSE DE L'INVENTION DISCLOSURE OF THE INVENTION
Un premier aspect de l’invention est donc une composition solide comprenant, dans un milieu physiologiquement acceptable : i) un gel d 'élastomère de polyuréthane réticulé comprenant au moins un solvant et un seul élastomère de polyuréthane réticulé ou un mélange d’au moins deux élastomères de polyuréthane réticulé, ledit élastomère ou ledit mélange d’élastomères étant obtenu à partir d’un prépolymère ayant au moins deux groupes hydroxyles et d’un (poly)isocyanate, ii) un phospholipide, de préférence une lécithine, et iii) un ou plusieurs pigments.
Selon un mode particulier et préféré, la composition de l’invention est une composition anhydre. A first aspect of the invention is therefore a solid composition comprising, in a physiologically acceptable medium: i) a crosslinked polyurethane elastomer gel comprising at least one solvent and a single crosslinked polyurethane elastomer or a mixture of at least two cross-linked polyurethane elastomers, said elastomer or said mixture of elastomers being obtained from a prepolymer having at least two hydroxyl groups and from a (poly)isocyanate, ii) a phospholipid, preferably a lecithin, and iii) a or more pigments. According to a particular and preferred embodiment, the composition of the invention is an anhydrous composition.
Selon un mode particulier, les pigments sont choisis parmi les pigments inorganiques, les pigments organiques et leurs mélanges. According to a particular embodiment, the pigments are chosen from inorganic pigments, organic pigments and mixtures thereof.
Selon un mode particulier, la composition comprend au moins un pigment organique (laque) sur support alumine ou aluminium oxyde. According to a particular embodiment, the composition comprises at least one organic pigment (lacquer) on an alumina or aluminum oxide support.
Selon un mode particulier, la composition comprend au moins des pigments blancs, tels que du dioxyde de titane, notamment en une teneur d’au moins 1% en poids par rapport au poids total de la composition, et des pigments inorganiques et/ou organiques, en particulier au moins un pigment organique sur support alumine ou aluminium oxyde. According to one particular embodiment, the composition comprises at least white pigments, such as titanium dioxide, in particular in a content of at least 1% by weight relative to the total weight of the composition, and inorganic and/or organic pigments , in particular at least one organic pigment on an alumina or aluminum oxide support.
Selon un mode particulier, la composition comprendra en outre une phase grasse comprenant une ou plusieurs huiles et au moins un corps gras choisi parmi les corps gras pâteux, les cires, les beurres et leurs mélanges. According to a particular embodiment, the composition will also comprise a fatty phase comprising one or more oils and at least one fatty substance chosen from pasty fatty substances, waxes, butters and mixtures thereof.
Selon un mode particulier et préféré, la composition comprend en outre au moins une charge, en particulier une charge minérale, de préférence encore une silice. According to a particular and preferred embodiment, the composition also comprises at least one filler, in particular a mineral filler, more preferably a silica.
De préférence, la composition selon l’invention comprend au moins 70%, 80%, 90%, voire au moins 95% en poids d’ingrédients biosourcés. Preferably, the composition according to the invention comprises at least 70%, 80%, 90%, or even at least 95% by weight of biobased ingredients.
L’invention porte également sur un procédé cosmétique de soin et/ou de maquillage des matières kératiniques, en particulier de la peau et/ou des lèvres et de préférence des lèvres, comprenant l'application sur lesdites matières kératiniques et de préférence les lèvres d'une composition selon l’invention. The invention also relates to a cosmetic process for caring for and/or making up keratin materials, in particular the skin and/or the lips and preferably the lips, comprising the application to the said keratin materials and preferably the lips of a composition according to the invention.
DESCRIPTION DETAILLEE DE L'INVENTION DETAILED DESCRIPTION OF THE INVENTION
Un premier aspect de l’invention est donc une composition cosmétique solide comprenant, dans un milieu physiologiquement acceptable : i) un gel d’élastomère de polyuréthane réticulé comprenant au moins un solvant et un seul élastomère de polyuréthane réticulé ou un mélange d’au moins deux élastomères de polyuréthane réticulé, ledit élastomère ou ledit mélange d’élastomères étant obtenu à partir d’un prépolymère ayant au moins deux groupes hydroxyles et d’un (poly)isocyanate, ii) un phospholipide, de préférence une lécithine, et iii) un ou plusieurs pigments. A first aspect of the invention is therefore a solid cosmetic composition comprising, in a physiologically acceptable medium: i) a crosslinked polyurethane elastomer gel comprising at least one solvent and a single crosslinked polyurethane elastomer or a mixture of at least two cross-linked polyurethane elastomers, said elastomer or said mixture of elastomers being obtained from a prepolymer having at least two hydroxyl groups and from a (poly)isocyanate, ii) a phospholipid, preferably a lecithin, and iii) one or more pigments.
La composition de l’invention est sous forme solide. The composition of the invention is in solid form.
On entend par "solide" une composition présentant, à 20° C et à pression atmosphérique (1 atm = 105 Pa), une dureté supérieure à 0,5 N, de préférence supérieure à 1 ,5 N, ladite dureté étant de préférence mesurée à l'aide d'un texturomètre muni d'un socle hémisphérique de diamètre 11 ,6 mm. The term “solid” is understood to mean a composition exhibiting, at 20° C. and at atmospheric pressure (1 atm=105 Pa), a hardness greater than 0.5 N, preferably greater than 1.5 N, said hardness preferably being measured using a texturometer equipped with a hemispherical base with a diameter of 11.6 mm.
Selon un mode particulier et préféré, la composition de l’invention est une composition anhydre. According to a particular and preferred embodiment, the composition of the invention is an anhydrous composition.
Par ‘anhydre’, on entend notamment que l'eau n'est de préférence pas ajoutée délibérément dans les compositions mais peut être présente à l'état de trace dans les différents composés utilisés dans les compositions. En particulier, la composition selon l’invention comprend moins
de 4 % en poids d'eau, de préférence moins de 3 %, de préférence moins de 2 %, plus préférentiellement moins de 1 %, encore plus préférentiellement moins de 0,5 % en poids d'eau, par rapport au poids total de ladite composition, voire est totalement exempte d'eau. Avantageusement, les ingrédients présents dans la composition de l’invention sont des ingrédients biosourcés. By “anhydrous” is meant in particular that the water is preferably not deliberately added to the compositions but may be present in trace form in the various compounds used in the compositions. In particular, the composition according to the invention comprises less 4% by weight of water, preferably less than 3%, preferably less than 2%, more preferably less than 1%, even more preferably less than 0.5% by weight of water, relative to the total weight of said composition, or even is completely free of water. Advantageously, the ingredients present in the composition of the invention are biosourced ingredients.
Par ingrédients ‘biosourcés’ selon l’invention, on entend des ingrédients obtenus essentiellement à partir de matières d’origine naturelle. Selon la définition donnée par l’ADEME (Agence de la Transition Ecologique), les produits biosourcés sont des produits industriels non alimentaires obtenus à partir de matières premières renouvelables issues de la biomasse (végétaux par exemple). By “biosourced” ingredients according to the invention, we mean ingredients obtained essentially from materials of natural origin. According to the definition given by ADEME (Ecological Transition Agency), biobased products are non-food industrial products obtained from renewable raw materials from biomass (plants for example).
Ainsi selon un mode particulier et préféré, la composition comprendra au moins 70% en poids d’ingrédients biosourcés, notamment au moins 80%, 90% voire au moins 95% en poids de composés biosourcés, par rapport au poids total de la composition. Thus, according to a particular and preferred mode, the composition will comprise at least 70% by weight of bio-based ingredients, in particular at least 80%, 90% or even at least 95% by weight of bio-based compounds, relative to the total weight of the composition.
De façon avantageuse, la composition de l’invention contient moins de 5%, de préférence moins de 1% de composés siliconés. Elle en est de préférence exempte. On entend par composé siliconé, une molécule comprenant au moins un atome de silicium. La composition est de préférence dépourvue d’un composé choisi parmi les polymères siliconés réticulés tels que les élastomères siliconés, les résines siliconées, les surfactants siliconés, les gommes de silicone, les silicones cycliques à caractère volatile, et les huiles siliconées phénylées, et les diméthicones. Advantageously, the composition of the invention contains less than 5%, preferably less than 1%, of silicone compounds. It is preferably free from it. The term “silicone compound” means a molecule comprising at least one silicon atom. The composition is preferably devoid of a compound chosen from crosslinked silicone polymers such as silicone elastomers, silicone resins, silicone surfactants, silicone gums, cyclic silicones of a volatile nature, and phenyl silicone oils, and dimethicones.
ELASTOMERE NON SILICONE NON-SILICONE ELASTOMER
On parlera indifféremment d’élastomère non siliconé ou d’élastomère de polyuréthane réticulé de l’invention. We will speak indiscriminately of non-silicone elastomer or cross-linked polyurethane elastomer of the invention.
Par ‘élastomère’, on entend généralement un polymère réticulé ayant des propriétés élastiques. By ‘elastomer’ we generally mean a cross-linked polymer with elastic properties.
L’élastomère de polyuréthane réticulé est en particulier sous forme de gel, dans lequel l’élastomère de polyuréthane réticulé est dispersé dans au moins un solvant. Le gel d’élastomère peut comprendre un ou plusieurs élastomères de polyuréthane réticulés. The crosslinked polyurethane elastomer is in particular in the form of a gel, in which the crosslinked polyurethane elastomer is dispersed in at least one solvent. The elastomer gel can comprise one or more cross-linked polyurethane elastomers.
De préférence, la composition de l’invention comprend un gel d’élastomère de polyuréthane réticulé comprenant au moins un solvant et un seul élastomère de polyuréthane réticulé ou un mélange d’au moins deux élastomères de polyuréthane réticulé, ledit élastomère ou ledit mélange d’élastomères étant obtenu à partir d’un prépolymère ayant au moins deux groupes hydroxyles et d’un (poly)isocyanate. Preferably, the composition of the invention comprises a crosslinked polyurethane elastomer gel comprising at least one solvent and a single crosslinked polyurethane elastomer or a mixture of at least two crosslinked polyurethane elastomers, said elastomer or said mixture of elastomers being obtained from a prepolymer having at least two hydroxyl groups and from a (poly)isocyanate.
De préférence le ou les élastomères de polyuréthane sont/est micronisé(s) (taille de particules de 1 à 100 microns, de préférence 1 à 60 microns de diamètre). Preferably the polyurethane elastomer(s) are/is micronized (particle size of 1 to 100 microns, preferably 1 to 60 microns in diameter).
Le gel d’élastomère de polyuréthane réticulé utilisé dans l’invention peut être constitué d’un seul élastomère de polyuréthane réticulé ou d’un mélange d’au moins deux élastomères de polyuréthane réticulés, l’élastomère ou le mélange d’élastomères étant obtenus par réaction d’un (poly)isocyanate avec un pré-polymère ayant au moins deux groupes hydroxyles et d’un solvant cosmétique dans des conditions pour former l’élastomère de polyuréthane réticulé. En particulier, on utilise un catalyseur de réaction d’uréthanisation, tel qu’un catalyseur à base de bismuth ou de zinc. The crosslinked polyurethane elastomer gel used in the invention may consist of a single crosslinked polyurethane elastomer or of a mixture of at least two crosslinked polyurethane elastomers, the elastomer or the mixture of elastomers being obtained by reacting a (poly)isocyanate with a prepolymer having at least two hydroxyl groups and a cosmetic solvent under conditions to form the crosslinked polyurethane elastomer. In particular, a urethanization reaction catalyst is used, such as a catalyst based on bismuth or zinc.
L’élastomère de polyuréthane réticulé est avantageusement biosourcé, c’est-à-dire obtenu à partir de matières premières d’origine naturelle (à 85%, mieux 90%, voire 95% bio sourcées).
Ainsi, selon un mode préféré, le prépolymère, le (poly)isocyanate et le solvant cosmétique sont d’origine naturelle (par exemple végétale) à plus de 85%, voire plus de 95%. The crosslinked polyurethane elastomer is advantageously biosourced, that is to say obtained from raw materials of natural origin (85%, better still 90%, or even 95% biosourced). Thus, according to a preferred mode, the prepolymer, the (poly)isocyanate and the cosmetic solvent are of natural origin (for example vegetable) at more than 85%, even more than 95%.
Pré-polymères Pre-polymers
Selon un mode particulier, le prépolymère ayant au moins deux groupes hydroxyles est un copolymère d’un dimère ou d’un trimère d’acide carboxylique, et d’un polyol. According to a particular embodiment, the prepolymer having at least two hydroxyl groups is a copolymer of a carboxylic acid dimer or trimer, and of a polyol.
Comme pré-polymères, on peut citer notamment les copolymères d’un dimère ou d’un trimère d’acide carboxylique, de préférence en C16-C20 et d’un polyol. As prepolymers, mention may in particular be made of copolymers of a dimer or a trimer of a carboxylic acid, preferably C16-C20, and of a polyol.
Des exemples sont cités dans la demande publiée sous le numéro W0202141046 au nom de Grant Industries Inc. Examples are cited in the application published under the number WO202141046 in the name of Grant Industries Inc.
L’acide carboxylique peut comprendre une chaîne carbonée linéaire dotée d’au moins une double liaison carbone-carbone, comme c’est le cas d’un acide gras insaturé. The carboxylic acid may comprise a linear carbon chain with at least one carbon-carbon double bond, as is the case with an unsaturated fatty acid.
De préférence, l’acide carboxylique est un dimère d’acides gras en C12-C18, en particulier l’acide dilinoléique. Preferably, the carboxylic acid is a dimer of C12-C18 fatty acids, in particular dilinoleic acid.
Le polyol peut être saturé ou insaturé, peut comprendre deux ou trois fonctions -OH, et éventuellement comprendre d’autres fonctions telles qu’une ou plusieurs fonctions ester. Le polyol est par exemple un diol aliphatique comprenant 2 à 8 atomes de carbone, en particulier 3 ou 4 atomes de carbone, tels que le propanediol ou le butanediol. Le polyol peut être également un triglycéride d’acide gras comprenant au moins deux groupements -OH, par exemple le triglycéride de l'acide ricinoléique, ou une source naturelle végétale en contenant telle que l’huile de ricin. The polyol can be saturated or unsaturated, can include two or three -OH functions, and optionally include other functions such as one or more ester functions. The polyol is for example an aliphatic diol comprising 2 to 8 carbon atoms, in particular 3 or 4 carbon atoms, such as propanediol or butanediol. The polyol can also be a fatty acid triglyceride comprising at least two —OH groups, for example ricinoleic acid triglyceride, or a natural plant source containing it, such as castor oil.
Ainsi, selon un mode particulier, le polyol est choisi dans le groupe constitué par un diol aliphatique comprenant 2 à 8 atomes de carbone, tel que le 1 ,2 ethanediol, les propanediols tels que le 1 ,2 propanediol, le 1 ,3 propanediol, le butanediol, le pentanediol, le caprylyl glycol, de préférence les propanediols et le butanediol ; un triglycéride d’acide gras comprenant au moins deux groupements -OH, tel que le triglycéride de l'acide ricinoléique ou une source végétale en contenant, telle que l’huile de ricin. Thus, according to a particular embodiment, the polyol is chosen from the group consisting of an aliphatic diol comprising 2 to 8 carbon atoms, such as 1,2 ethanediol, propanediols such as 1,2 propanediol, 1,3 propanediol , butanediol, pentanediol, caprylyl glycol, preferably propanediols and butanediol; a fatty acid triglyceride comprising at least two -OH groups, such as ricinoleic acid triglyceride or a vegetable source containing it, such as castor oil.
Selon un mode particulier, le pré-polymère est un copolymère d’acide dilinoléique et de propanediol (DAPD) ou un copolymère d’acide dilinoléique et de butanediol (DABP). According to a particular embodiment, the prepolymer is a copolymer of dilinoleic acid and propanediol (DAPD) or a copolymer of dilinoleic acid and butanediol (DABP).
(Poly)isocyanates (Poly)isocyanates
Les (poly)isocyanates sont des composés contenant un groupe isocyanate (-NCO). Ils réagissent avec les pré-polymères contenant des groupes hydroxyles pour produire des polymères polyuréthanes. Le (poly)isocyanate est avantageusement un diisocyanate, de préférence un diisocyanate aliphatique pouvant contenir 5 ou 6 atomes de carbone (dans sa chaîne principale ou son cycle). Le diisocyanate peut être linéaire ou cyclique. (Poly)isocyanates are compounds containing an isocyanate (-NCO) group. They react with prepolymers containing hydroxyl groups to produce polyurethane polymers. The (poly)isocyanate is advantageously a diisocyanate, preferably an aliphatic diisocyanate which may contain 5 or 6 carbon atoms (in its main chain or its cycle). The diisocyanate can be linear or cyclic.
Ainsi, selon un mode de réalisation particulier, le (poly)isocyanate est un diisocyanate, en particulier un diisocyanate aliphatique pouvant contenir de 5 à 6 atomes de carbone, de préférence choisi parmi le 1 ,6-hexaméthylène diisocyanate (HDI), le 1 ,5-pentaméthylène diisocyanate (PDI) ou l’isophorone diisocyanate (IPDI). Thus, according to a particular embodiment, the (poly)isocyanate is a diisocyanate, in particular an aliphatic diisocyanate which may contain from 5 to 6 carbon atoms, preferably chosen from 1,6-hexamethylene diisocyanate (HDI), 1 ,5-pentamethylene diisocyanate (PDI) or isophorone diisocyanate (IPDI).
Comme (poly)isocyanate préféré, on peut citer le trimère diisocyanate de pentaméthylène 1 ,5. Solvant cosmétique
Comme solvants cosmétiques utilisés dans la synthèse de l’élastomère de polyuréthane réticulé et/ou la formation du gel d’élastomère de polyuréthane réticulé, on peut citer les esters, les éthers, les alcanes et leurs mélanges. Selon un mode particulier, on peut utiliser : des triglycérides d’origine végétale tels que le trihexanoate de glycérol, le triheptanoate de glycérol (triheptanoïne), le trioctanoate de glycérol, le coco-caprylate/caprate, les alcanes en C9-C22 tels que le undecane, le tridecane ; des esters d'origine naturelle et leurs mélanges, de préférence le triheptanoate de glycérol (triheptanoïne), le coco-caprylate/caprate, les alcanes en C9-C22, des esters d'origine naturelle et leurs mélanges. As preferred (poly)isocyanate, mention may be made of the 1,5-pentamethylene diisocyanate trimer. cosmetic solvent As cosmetic solvents used in the synthesis of the crosslinked polyurethane elastomer and/or the formation of the crosslinked polyurethane elastomer gel, mention may be made of esters, ethers, alkanes and their mixtures. According to a particular method, it is possible to use: triglycerides of plant origin such as glycerol trihexanoate, glycerol triheptanoate (triheptanoin), glycerol trioctanoate, coco-caprylate/caprate, C9-C22 alkanes such as undecane, tridecane; esters of natural origin and mixtures thereof, preferably glycerol triheptanoate (triheptanoin), coco-caprylate/caprate, C9-C22 alkanes, esters of natural origin and mixtures thereof.
Des élastomères de polyuréthane réticulés utilisables selon l’invention sont décrits dans la demande publiée sous le numéro W0202141046 au nom de Grant Industries Inc. Crosslinked polyurethane elastomers which can be used according to the invention are described in the application published under the number W0202141046 in the name of Grant Industries Inc.
La préparation d’un élastomère de polyuréthane réticulé et la formation subséquente d’un gel d’élastomère de polyuréthane réticulé tel qu’utilisé selon l’invention peut comprendre les étapes suivantes : The preparation of a crosslinked polyurethane elastomer and the subsequent formation of a crosslinked polyurethane elastomer gel as used according to the invention may comprise the following steps:
- Réaction d’un prépolymère biosourcé avec un (poly)isocyanate biosourcé en utilisant un catalyseur de réaction d’uréthanisation tel qu’un catalyseur de bismuth à une température adaptée et contrôlée, par exemple de 20° C à 100°C, dans un milieu de réaction comprenant un solvant biosourcé ou un mélange de solvants de préférence biosourcés pour former l’élastomère de polyuréthane réticulé ; alternativement la formation de l’élastomère de polyuréthane réticulé peut se réaliser sans agitation, à température ambiante, pendant environ 24 heures ; - Reaction of a biobased prepolymer with a biobased (poly)isocyanate using a urethanization reaction catalyst such as a bismuth catalyst at a suitable and controlled temperature, for example from 20° C. to 100° C., in a reaction medium comprising a bio-based solvent or a mixture of preferably bio-based solvents to form the crosslinked polyurethane elastomer; alternatively, the formation of the crosslinked polyurethane elastomer can take place without stirring, at room temperature, for about 24 hours;
- Formation d’un gel d’élastomère concentré sous forme d’une dispersion, en micronisant ledit élastomère de polyuréthane réticulé jusqu’à l’obtention d’une taille de particules allant de préférence de 1 à 100 microns et éventuellement l’ajout d’un solvant cosmétique avant ou après l’étape de micronisation ; - Formation of a concentrated elastomer gel in the form of a dispersion, by micronizing said crosslinked polyurethane elastomer until a particle size preferably ranging from 1 to 100 microns is obtained and optionally the addition of a cosmetic solvent before or after the micronization step;
- L’élastomère concentré peut ensuite éventuellement être dilué avec un solvant secondaire, volatile ou non volatile, pour obtenir la viscosité recherchée pour le gel d’élastomère de polyuréthane réticulé. - The concentrated elastomer can then optionally be diluted with a secondary solvent, volatile or non-volatile, to obtain the desired viscosity for the cross-linked polyurethane elastomer gel.
Selon un mode particulier, le pré-polymère, qui contient 2 groupes hydroxyles, représente une teneur allant de 5 à 25% en poids de l’élastomère de polyuréthane réticulé. Le (poly)isocyanate de préférence biosourcé contient de 15 à 38%, ou de 15 à 28% de groupe -NCO. Le ratio molaire total des groupes -NCO de l’isocyanate sur les groupes-OH du polyol peut aller de 2 :1 à 1 :2, et est de préférence de 1 :1 . According to a particular mode, the prepolymer, which contains 2 hydroxyl groups, represents a content ranging from 5 to 25% by weight of the crosslinked polyurethane elastomer. The preferably bio-based (poly)isocyanate contains 15 to 38%, or 15 to 28% -NCO group. The total molar ratio of the -NCO groups of the isocyanate to the -OH groups of the polyol can range from 2:1 to 1:2, and is preferably 1:1.
La teneur en solvant(s) cosmétique(s) sera généralement de 70 à 95% en poids par rapport au poids d’élastomère de polyuréthane réticulé. The content of cosmetic solvent(s) will generally be 70 to 95% by weight relative to the weight of cross-linked polyurethane elastomer.
La teneur en catalyseur pourra être de 0,1 à 2,5% en poids. The catalyst content may be from 0.1 to 2.5% by weight.
Le gel d’élastomère peut comprendre au moins un solvant et un élastomère de polyuréthane réticulé ou un mélange d 'élastomères de polyuréthane réticulés. The elastomer gel can comprise at least one solvent and a crosslinked polyurethane elastomer or a mixture of crosslinked polyurethane elastomers.
Selon un mode particulier, le gel d’élastomère de polyuréthane réticulé utilisé dans les compositions selon l’invention peut comprendre de 5 à 30% en poids, en particulier de 5 à 17% en poids de matière active d’élastomère(s) de polyuréthane réticulé(s), et de 70 à 95% en poids, en particulier de 83 à 95% en poids de solvant(s). According to one particular embodiment, the crosslinked polyurethane elastomer gel used in the compositions according to the invention may comprise from 5 to 30% by weight, in particular from 5 to 17% by weight of active material of elastomer(s) of cross-linked polyurethane(s), and from 70 to 95% by weight, in particular from 83 to 95% by weight of solvent(s).
Selon un mode particulier, le gel d’élastomère de polyuréthane réticulé utilisé selon l’invention est le gel d’élastomère de polyuréthane réticulé préparé à l’exemple 6 ou à l’exemple 9 de la demande W0202141046 de Grant Industries Inc. Le pré-polymère est un copolymère d’acide dimérique en C8 et de 1 ,3 propanediol (DAPD) ou de 1 ,4 butanediol (DABD), le polyisocyanate
est un trimère de diisocyanate de pentylène (PDT), le catalyseur est le neodecanoate de bismuth et le solvant un mélange de coco-caprylate/caprate et de triheptanoate de glycérol. Le gel concentré est ensuite formé par la micronisation dudit élastomère de polyuréthane réticulé et l’ajout de triheptanoate de glycérol. Le gel concentré est ensuite dilué avec l’ajout d’alcanes en C9-C12 (Vegelight 1214). According to a particular embodiment, the crosslinked polyurethane elastomer gel used according to the invention is the crosslinked polyurethane elastomer gel prepared in Example 6 or in Example 9 of application WO202141046 from Grant Industries Inc. The pre -polymer is a copolymer of C8 dimer acid and 1,3 propanediol (DAPD) or 1,4 butanediol (DABD), the polyisocyanate is a pentylene diisocyanate (PDT) trimer, the catalyst is bismuth neodecanoate and the solvent is a mixture of coco-caprylate/caprate and glycerol triheptanoate. The concentrated gel is then formed by the micronization of said cross-linked polyurethane elastomer and the addition of glycerol triheptanoate. The concentrated gel is then diluted with the addition of C9-C12 alkanes (Vegelight 1214).
De tels gels d’élastomères de polyuréthane réticulés sont commercialisés sous la dénomination Gransense™ par Grant Industries. Such crosslinked polyurethane elastomer gels are marketed under the name Gransense™ by Grant Industries.
Selon un mode de réalisation particulier, le prépolymère est un produit de réaction d'un diol et d'un acide dimère, en particulier d’un acide dilinoléique et de propanediol ou de butanediol et le (poly)isocyanate est un trimère de 1 ,5-pentaméthylène diisocyanate. According to a particular embodiment, the prepolymer is a reaction product of a diol and a dimer acid, in particular of a dilinoleic acid and propanediol or butanediol and the (poly)isocyanate is a trimer of 1, 5-pentamethylene diisocyanate.
Ainsi, selon un mode de réalisation particulier, l’élastomère de polyuréthane réticulé est obtenu à partir d’acide dilinoléique, de propanediol ou de butanediol et de diisocyanate de pentaméthylène. Cet élastomère de polyuréthane réticulé peut être qualifié d’élastomère non siliconé de nature polyester et avoir comme dénomination INCI : polyuréthane-10 Elastomer ou polyuréthane- 100 Elastomer. Thus, according to a particular embodiment, the crosslinked polyurethane elastomer is obtained from dilinoleic acid, propanediol or butanediol and pentamethylene diisocyanate. This cross-linked polyurethane elastomer can be described as a non-silicone elastomer of a polyester nature and have the INCI name: polyurethane-10 Elastomer or polyurethane-100 Elastomer.
On peut citer notamment les références commerciales suivantes de la société Grant Industries Inc. : The following commercial references of the company Grant Industries Inc. can be mentioned in particular:
GRANSENSE TC-11X de nom INCI Coco-Caprylate/Caprate (and) Triheptanoin (and) Polyurethane-10 Elastomer ; et GRANSENSE TC-11X with INCI name Coco-Caprylate/Caprate (and) Triheptanoin (and) Polyurethane-10 Elastomer; and
GRANSENSE TC-8X de nom INCI Coco-Caprylate/Caprate (and) Triheptanoin (and) C9-12 Alkane (and) Polyurethane-100 Elastomer. GRANSENSE TC-8X with INCI name Coco-Caprylate/Caprate (and) Triheptanoin (and) C9-12 Alkane (and) Polyurethane-100 Elastomer.
Selon un autre mode particulier de réalisation, le gel d’élastomères de polyuréthane réticulés comprend un mélange d’au moins deux élastomères de polyuréthane réticulé, ledit mélange étant obtenu à partir de prépolymères d’acide dilinoléique/ polyols et d’isophorone diisocyanate, les deux polyols étant le butanediol et l’huile de ricin. According to another particular embodiment, the gel of crosslinked polyurethane elastomers comprises a mixture of at least two crosslinked polyurethane elastomers, said mixture being obtained from prepolymers of dilinoleic acid/polyols and of isophorone diisocyanate, the two polyols being butanediol and castor oil.
Le mélange de ces élastomères peut avoir comme dénominations INCI : The mixture of these elastomers may have the following INCI names:
Triheptanoin (and) Coco-Caprylate/Caprate (and) Dilinoleic Acid/Butanediol Copolymer (and) Castor Oil/IPDI Copolymer Elastomer, ou Triheptanoin (and) Coco-Caprylate/Caprate (and) Dilinoleic Acid/Butanediol Copolymer (and) Castor Oil/IPDI Copolymer Elastomer, or
Coco-Caprylate/Caprate (and) Triheptanoin (and) C9-12 Alkane (and) Dilinoleic Acid/Butanediol Copolymer (and) Castor Oil/IPDI Copolymer Elastomer. Coco-Caprylate/Caprate (and) Triheptanoin (and) C9-12 Alkane (and) Dilinoleic Acid/Butanediol Copolymer (and) Castor Oil/IPDI Copolymer Elastomer.
On peut citer notamment les références commerciales suivantes de la société Grant Industries Inc. : The following commercial references of the company Grant Industries Inc. can be mentioned in particular:
GRANSENSE TC-18-X-C de nom INCI : Coco-Caprylate/Caprate (and) Triheptanoin (and) C9-12 Alkane (and) Dilinoleic Acid/Butanediol Copolymer (and) Castor Oil/IPDI Copolymer Elastomer GRANSENSE TC-21 -X-C de nom INCI : Triheptanoin (and) Coco-Caprylate/Caprate (and) Dilinoleic Acid/Butanediol Copolymer (and) Castor Oil/IPDI Copolymer Elastomer GRANSENSE TC-21X-SBC de nom INCI : Triheptanoin (and) Coco-caprylate/caprate (and) Dilinoleic Acid/Butanediol Copolymer (and) Castor Oil/IPDI Copolymer Elastomer (and) Butyrospermum Parkii (Shea Butter). GRANSENSE TC-18-X-C INCI name: Coco-Caprylate/Caprate (and) Triheptanoin (and) C9-12 Alkane (and) Dilinoleic Acid/Butanediol Copolymer (and) Castor Oil/IPDI Copolymer Elastomer GRANSENSE TC-21 -X-C INCI name: Triheptanoin (and) Coco-Caprylate/Caprate (and) Dilinoleic Acid/Butanediol Copolymer (and) Castor Oil/IPDI Copolymer Elastomer GRANSENSE TC-21X-SBC INCI name: Triheptanoin (and) Coco-caprylate/caprate (and ) Dilinoleic Acid/Butanediol Copolymer (and) Castor Oil/IPDI Copolymer Elastomer (and) Butyrospermum Parkii (Shea Butter).
L’élastomère de polyuréthane réticulé (seul ou mélange de deux élastomères) selon l’invention sera généralement présent dans la composition en une teneur totale en matière sèche (active) allant de 0,5% à 5% en poids, en particulier de 1% à 3% et notamment de 2 à 3% en poids par rapport au poids total de la composition. The crosslinked polyurethane elastomer (alone or mixture of two elastomers) according to the invention will generally be present in the composition in a total dry matter (active) content ranging from 0.5% to 5% by weight, in particular from 1 % to 3% and in particular from 2 to 3% by weight relative to the total weight of the composition.
PHOSPHOLIPIDE
La composition comprend en outre un phospholipide, de préférence un phospholipide d’origine végétale. PHOSPHOLIPID The composition further comprises a phospholipid, preferably a phospholipid of plant origin.
Les phospholipides peuvent être la phosphatidylcholine, phosphatidylsérine, la phosphatidyléthanolamine, la phosphatidylsérine, le phosphatidylglycérol, la phosphatidylinositol ou leurs mélanges, de préférence la phosphatidylcholine. The phospholipids can be phosphatidylcholine, phosphatidylserine, phosphatidylethanolamine, phosphatidylserine, phosphatidylglycerol, phosphatidylinositol or mixtures thereof, preferably phosphatidylcholine.
On peut citer en particulier la lécithine. Mention may in particular be made of lecithin.
La lécithine est un mélange composé de choline, acides gras, glycérol, glycolipides, triglycérides, carbohydrates et phospholipides (ex : phosphatidylcholine, phosphatidyléthanolamine, phosphatidylsérine et phosphatidylinositol). Elle peut être isolée à partir d’huiles végétales telles que l’huile de soja, l’huile de tournesol, l’huile de maïs, à partir desquelles elle est extraite chimiquement ou mécaniquement. Lecithin is a mixture composed of choline, fatty acids, glycerol, glycolipids, triglycerides, carbohydrates and phospholipids (ex: phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine and phosphatidylinositol). It can be isolated from vegetable oils such as soybean oil, sunflower oil, corn oil, from which it is chemically or mechanically extracted.
Selon un mode particulier, la composition de l’invention comprend une lécithine (nom INCI lecithin). According to a particular embodiment, the composition of the invention comprises a lecithin (INCI name lecithin).
Des lécithines conformes sont par exemple : Compliant lecithins are for example:
- Les lécithines d’origine végétale (tournesol, colza, soja) commercialisées sous la dénomination SOLEC® Lecithin par la société Dupont Nutrition & Bioscience ; - Lecithins of plant origin (sunflower, rapeseed, soya) marketed under the name SOLEC® Lecithin by the company Dupont Nutrition &Bioscience;
- Les lécithines de soja commercialisées sous la dénomination ALCOLEC® par la société American Lecithin Company ; - Soy lecithins marketed under the name ALCOLEC® by the American Lecithin Company;
- Les lécithines commercialisées par la société Lucas Meyer Cosmetics sous les noms de marque Emulmetik™ : - Lecithins marketed by Lucas Meyer Cosmetics under the brand names Emulmetik™:
• Emulmetik™ 100 (nom INCI : lecithin) : 60% phospholipids and glycolipids and 12% phosphatidylcholine, • Emulmetik™ 100 (INCI name: lecithin): 60% phospholipids and glycolipids and 12% phosphatidylcholine,
• Emulmetik™ 300 (nom INCI : lecithin) : 97% phospholipids and glycolipids and 23% phosphatidylcholine. • Emulmetik™ 300 (INCI name: lecithin): 97% phospholipids and glycolipids and 23% phosphatidylcholine.
Selon un mode particulier, on utilise la référence commerciale Emulmetik™ 300 (nom INCI : lecithin) : 97% phospholipids and glycolipids and 23% phosphatidylcholine. According to a particular mode, the commercial reference Emulmetik™ 300 (INCI name: lecithin) is used: 97% phospholipids and glycolipids and 23% phosphatidylcholine.
La composition de l’invention comprend une teneur totale en phospholipide(s), en particulier une teneur totale en lécithine(s) allant de 0,1 à 2%, notamment de 0,2 à 1% et en particulier de 0,4 à 0,8%, voire de 0,5 à 0,6% en poids par rapport au poids total de la composition. The composition of the invention comprises a total content of phospholipid(s), in particular a total content of lecithin(s) ranging from 0.1 to 2%, in particular from 0.2 to 1% and in particular from 0.4 at 0.8%, or even from 0.5 to 0.6% by weight relative to the total weight of the composition.
PIGMENTS PIGMENTS
La composition de l’invention comprend un ou plusieurs pigments pour colorer les matières kératiniques, en particulier la peau et/ou les lèvres, notamment les lèvres. The composition of the invention comprises one or more pigments for coloring keratin materials, in particular the skin and/or the lips, in particular the lips.
En particulier, le ou les pigments sont présents en une teneur totale allant de 1% à 15% en poids, notamment de 2% à 12%, en poids par rapport au poids total de la composition. In particular, the pigment(s) are present in a total content ranging from 1% to 15% by weight, in particular from 2% to 12%, by weight relative to the total weight of the composition.
Par « pigments » on entend des particules blanches ou colorées, minérales ou organiques, insolubles dans une solution aqueuse, destinées à colorer et/ou opacifier le dépôt résultant. On peut citer les pigments inorganiques (autrement nommés pigments minéraux), les pigments organiques, et les pigments composites (c'est-à-dire des pigments à base de matériaux inorganiques et/ou organiques). By “pigments” is meant white or colored, mineral or organic particles, insoluble in an aqueous solution, intended to color and/or opacify the resulting deposit. Mention may be made of inorganic pigments (otherwise called mineral pigments), organic pigments, and composite pigments (that is to say pigments based on inorganic and/or organic materials).
Parmi les « pigments inorganiques », on peut citer, à titre d'exemples le dioxyde de titane ; les oxydes de fer noir, jaune, rouge et brun et le violet de manganèse.
Parmi les « pigments organiques », on peut citer, par exemple, les pigments D & C red n° 19; D & C red n° 9; D & C Red n° 22 ; D & C Red n° 21 ; D & C Red n° 28 ; D & C Yellow n° 6 ; D & C orange n° 4 ; D & C orange n° 5 ; D & C Red n° 27; D & C red n° 13; D & C Red n° 7 ; D & C Red n° 6 ; D & C Yellow n° 5; D & C Red n° 36 ; D & C Red n° 33 ; D & C orange n° 10; D & C yellow n° 6 ; D & C Red n° 30 ; D &C red n° 3 ; D &C Blue 1 ; D &C Red No.7 lake ; D &C Red No.28 lake (Cl 45410) ; FD&C Yellow 5 Al Lake (C69-4424) ; FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433) ; le noir de carbone et les laques à base de carmin de cochenille. Among the “inorganic pigments”, mention may be made, by way of examples, of titanium dioxide; black, yellow, red and brown iron oxides and manganese violet. Among the "organic pigments", mention may be made, for example, of the pigments D & C red No. 19; D & C red No. 9; D&C Red No. 22; D&C Red No. 21; D&C Red No. 28; D&C Yellow No. 6; D & C Orange No. 4; D & C Orange No. 5; D & C Red No. 27; D & C red No. 13; D&C Red No. 7; D&C Red No. 6; D&C Yellow No. 5; D&C Red No. 36; D&C Red No. 33; D & C Orange No. 10; D & C yellow No. 6; D&C Red No. 30; D&C red No. 3; D&C Blue 1; D&C Red No.7 lake; D&C Red No.28 lake (Cl 45410); FD&C Yellow 5 Al Lake (C69-4424); FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433); carbon black and cochineal carmine-based lakes.
Selon un mode particulier, la composition comprend un pigment organique constitué d’un colorant sur une base alumine ou aluminium hydroxyde, tels que les pigments D&C Red No.7 lake (Cl 15850 (and) Aluminum Hydroxide), FD&C Yellow 5 Al Lake (C69-4424) ; FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), et leurs mélanges. According to a particular embodiment, the composition comprises an organic pigment consisting of a colorant on an alumina or aluminum hydroxide base, such as the pigments D&C Red No.7 lake (Cl 15850 (and) Aluminum Hydroxide), FD&C Yellow 5 Al Lake ( C69-4424); FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), and mixtures thereof.
Selon un mode particulier, la composition de l’invention comprend des pigments choisis parmi les pigments inorganiques, les pigments organiques et leurs mélanges, en particulier : According to a particular embodiment, the composition of the invention comprises pigments chosen from inorganic pigments, organic pigments and mixtures thereof, in particular:
- un ou plusieurs pigments inorganiques choisis parmi le dioxyde de titane, les oxydes de fer (par exemple rouge, jaune, brun, noir) et leurs mélanges, de préférence un mélange de dioxyde de titane et d’oxydes de fer, et - one or more inorganic pigments chosen from titanium dioxide, iron oxides (for example red, yellow, brown, black) and mixtures thereof, preferably a mixture of titanium dioxide and iron oxides, and
- un ou plusieurs pigments organiques choisis parmi les pigments D & C Red n° 7, D&C Red No.7 lake (Cl 15850), D &C Red No.28 lake (Cl 45410) ; FD&C Yellow 5 Al Lake (C69-4424) ; FD&C Yellow 6 Al Lake (C70-5270) ; FD&C Blue 1 Al Lake (C39-4433), et leurs mélanges. - one or more organic pigments chosen from the pigments D & C Red No. 7, D & C Red No.7 lake (Cl 15850), D & C Red No. 28 lake (Cl 45410); FD&C Yellow 5 Al Lake (C69-4424); FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), and mixtures thereof.
Selon un mode particulier, la composition de l’invention comprend au moins des pigments inorganiques. Selon un mode particulier, la composition de l’invention comprend au moins des pigments inorganiques et des pigments organiques. According to a particular embodiment, the composition of the invention comprises at least inorganic pigments. According to a particular embodiment, the composition of the invention comprises at least inorganic pigments and organic pigments.
Ainsi selon un mode particulier, la composition comprend au moins du dioxyde de titane, un ou plusieurs oxydes de fer (jaune, rouge, brun et/ou noir) et un ou plusieurs pigments organiques, en particulier choisis parmi D & C Red n° 7, D&C Red No.7 lake (Cl 15850), D &C Red No.28 lake (Cl 45410) ; FD&C Yellow 5 Al Lake (C69-4424) ; FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), et leurs mélanges. Thus, according to a particular embodiment, the composition comprises at least titanium dioxide, one or more iron oxides (yellow, red, brown and/or black) and one or more organic pigments, in particular chosen from D & C Red no. 7, D&C Red No.7 lake (Cl 15850), D&C Red No.28 lake (Cl 45410); FD&C Yellow 5 Al Lake (C69-4424); FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), and mixtures thereof.
Selon un mode particulier, la composition de l’invention comprend du dioxyde de titane en une teneur d’au moins 0,5% en poids, en particulier au moins 0,8% en poids, voire au moins 1% en poids par rapport au poids de la composition, un ou plusieurs oxydes de fer (jaune, rouge, brun et/ou noir) et un ou plusieurs pigments organiques, en particulier choisis parmi D & C Red n° 7, D&C Red No.7 lake (Cl 15850), D &C Red No.28 lake (Cl 45410) ; FD&C Yellow 5 Al Lake (C69- 4424) ; FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), et leurs mélanges.According to a particular mode, the composition of the invention comprises titanium dioxide in a content of at least 0.5% by weight, in particular at least 0.8% by weight, or even at least 1% by weight with respect to by weight of the composition, one or more iron oxides (yellow, red, brown and/or black) and one or more organic pigments, in particular chosen from D & C Red No. 7, D & C Red No.7 lake (Cl 15850), D&C Red No.28 lake (Cl 45410); FD&C Yellow 5 Al Lake (C69-4424); FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), and mixtures thereof.
En particulier, la teneur totale en pigment(s) va de 1 à 15% en poids par rapport au poids total de ladite composition. In particular, the total content of pigment(s) ranges from 1 to 15% by weight relative to the total weight of said composition.
Selon un mode particulier, les pigments inorganiques sont présents en une teneur allant de 1 à 15 % en poids, notamment de 2 à 12% en poids par rapport au poids total de la composition.According to a particular embodiment, the inorganic pigments are present in a content ranging from 1 to 15% by weight, in particular from 2 to 12% by weight relative to the total weight of the composition.
Selon un mode particulier, les pigments organiques sont présents en une teneur allant de 1 à 15% en poids, notamment de 2 à 12% en poids par rapport au poids total de la composition.According to a particular embodiment, the organic pigments are present in a content ranging from 1 to 15% by weight, in particular from 2 to 12% by weight relative to the total weight of the composition.
Selon un mode particulier, la composition de l’invention comprend : a) Un élastomère de polyuréthane réticulé (seul ou en mélange) en une teneur totale en matière sèche allant de 0,5% à 5% en poids, en particulier de 1% à 3% et notamment de 2 à 3% en poids, par rapport au poids total de la composition,
b) Une lécithine en une teneur allant de 0,4 à 0,8% en poids par rapport au poids total de la composition et c) Des pigments inorganiques et/ou organiques en une teneur totale allant de 2 à 12% en poids par rapport au poids total de la composition. According to one particular embodiment, the composition of the invention comprises: a) A crosslinked polyurethane elastomer (alone or as a mixture) in a total dry matter content ranging from 0.5% to 5% by weight, in particular from 1% to 3% and in particular from 2 to 3% by weight, relative to the total weight of the composition, b) A lecithin in a content ranging from 0.4 to 0.8% by weight relative to the total weight of the composition and c) Inorganic and/or organic pigments in a total content ranging from 2 to 12% by weight per relative to the total weight of the composition.
PHASE GRASSE FAT PHASE
La composition de l’invention comprend également une phase grasse. The composition of the invention also comprises a fatty phase.
Cette phase grasse comprend des huiles (identiques ou distincts des solvants présents dans le gel de l’élastomère non siliconé) et au moins un corps gras choisi parmi les cires, les corps gras pâteux, les beurres, et leurs mélanges. This fatty phase comprises oils (identical to or distinct from the solvents present in the gel of the non-silicone elastomer) and at least one fatty substance chosen from waxes, pasty fatty substances, butters, and mixtures thereof.
Par « huile », on entend un corps gras, non soluble dans l'eau, liquide à 25° C et pression atmosphérique. By "oil" is meant a fatty substance, insoluble in water, liquid at 25° C. and atmospheric pressure.
Par « corps gras » selon l’invention, on entend un composé solide ou comprenant une fraction solide à 25 °C. On peut citer notamment les beurres, les cires, les composés pâteux, et leurs mélanges. By “fat” according to the invention, is meant a solid compound or comprising a solid fraction at 25°C. Mention may in particular be made of butters, waxes, pasty compounds, and mixtures thereof.
Par « cire », au sens de la présente invention, entend désigner un composé solide à 25° C qui présente un changement d'état solide/liquide réversible et une température de fusion supérieure à 30 °C, de préférence supérieure à 45° C. By “wax”, within the meaning of the present invention, is meant to denote a solid compound at 25° C. which exhibits a reversible solid/liquid state change and a melting temperature greater than 30° C., preferably greater than 45° C. .
Par « corps gras pâteux », on désigne un composé gras non cristallin comprenant à une température de 25° C, une fraction liquide et une fraction solide. The term “pasty fatty substance” denotes a non-crystalline fatty compound comprising, at a temperature of 25° C., a liquid fraction and a solid fraction.
Les huiles additionnelles et corps gras utilisables selon l’invention peuvent être d'origine animale, végétale, minérale ou synthétique. De préférence, on utilisera des huiles et corps gras biosourcés. The additional oils and fatty substances that can be used according to the invention can be of animal, vegetable, mineral or synthetic origin. Preferably, biosourced oils and fatty substances will be used.
Comme corps gras ou huiles végétales utilisables, on peut citer notamment les huiles végétales et corps gras suivants : As fatty substances or vegetable oils that can be used, mention may be made in particular of the following vegetable oils and fatty substances:
- des « huiles végétales » telles que : huile désodorisée Tournesol oléique, huile vierge Amande douce, huile vierge de Rosier muscat, huile d’avocat, huile de carthame, de cameline, de jojoba, huile de bourrache, huile de pépins de raisins, huile d’argan, huiles de nigelle, huile de pépins de courges, huile de perilla, huile de ricin et leurs mélanges, - "vegetable oils" such as: deodorized oleic sunflower oil, virgin sweet almond oil, virgin muscat rose oil, avocado oil, safflower oil, camelina oil, jojoba oil, borage oil, grape seed oil, argan oil, nigella oils, pumpkin seed oil, perilla oil, castor oil and mixtures thereof,
- des « beurres » tels que : beurre de Murumuru, beurre de Mangue, beurre de Karité, beurre de cacao et beurre de Cupuaçu, et leurs mélanges, - “butters” such as: Murumuru butter, Mango butter, Shea butter, cocoa butter and Cupuaçu butter, and mixtures thereof,
- des « cires végétales » telles que : cire de Carnauba, cire d’abeilles, cire de candellila, cire de jojoba, cire de tournesol, cire de son de riz et leurs mélanges, - “vegetable waxes” such as: carnauba wax, beeswax, candelilla wax, jojoba wax, sunflower wax, rice bran wax and mixtures thereof,
- des « corps gras pâteux » choisi(s) dans le groupe constitué par les esters de polyol(s) et de dimère diacide d’acide gras, ou d’un de ses esters, les esters d’huile de ricin hydrogénée, les esters oligomères de glycérol, notamment les esters de diglycérol, et leurs mélanges, - "pasty fatty substances" chosen from the group consisting of esters of polyol(s) and of fatty acid diacid dimer, or of one of its esters, hydrogenated castor oil esters, oligomeric glycerol esters, in particular diglycerol esters, and mixtures thereof,
- et leurs mélanges. - and mixtures thereof.
Selon un mode particulier, la composition de l’invention comprendra, comme corps gras pâteux, au moins un ester de dimère diol et dimère diacide, le cas échéant, estérifiés sur leur(s) fonction(s) alcool(s) ou acide(s) libre(s) par des radicaux acides ou alcools, notamment les esters dimer dilinoleate, tels que ceux de nomenclature INCI suivante : According to a particular embodiment, the composition of the invention will comprise, as pasty fatty substance, at least one ester of diol dimer and diacid dimer, where appropriate, esterified on their alcohol(s) or acid function(s). s) free(s) by acid or alcohol radicals, in particular dimer dilinoleate esters, such as those with the following INCI nomenclature:
- le copolymère d’isostéarate de polyglyceryl-2 /dimer dilinoléate (Hailucent ISDA de Estenity) ;
- le bis- béhényl/isostéaryl/phytostéryl dimerdilinoléyle dimerdilinoléate (Plandool G de Estenity), ou le phytostéryl/isostéryl / cétyl / stéaryl / béhényl dimerdilinoléate (Plandool H ou Plandool S), - the copolymer of polyglyceryl-2 isostearate/dimer dilinoleate (Hailucent ISDA from Estenity); - bis-behenyl/isostearyl/phytosteryl dimerdilinoleyl dimerdilinoleate (Plandool G from Estenity), or phytosteryl/isosteryl/cetyl/stearyl/behenyl dimerdilinoleate (Plandool H or Plandool S),
- le dimerdilinoleyl dimerdilinoléate (Lusplan DDA7 de Unipex), et leurs mélanges. - dimerdilinoleyl dimerdilinoleate (Lusplan DDA7 from Unipex), and mixtures thereof.
La teneur totale en ester(s) de diols et de dimère diacide d'acides gras, ou un de ses esters dans la composition de l’invention ira généralement de 0,5% à 20% en poids, en particulier de 1% à 10% en poids et de préférence de 2% à 5% en poids par rapport au poids total de ladite composition. The total content of diol ester(s) and fatty acid diacid dimer, or one of its esters in the composition of the invention will generally range from 0.5% to 20% by weight, in particular from 1% to 10% by weight and preferably from 2% to 5% by weight relative to the total weight of said composition.
Selon un mode particulier, la composition de l’invention comprendra au moins une huile végétale et au moins un corps gras végétal choisi parmi une cire végétale, un beurre végétal et leurs mélanges. According to a particular mode, the composition of the invention will comprise at least one vegetable oil and at least one vegetable fatty substance chosen from a vegetable wax, a vegetable butter and mixtures thereof.
Selon un mode particulier, la composition comprend en outre, comme huile additionnelle distincte des huiles(solvants) présentes dans le gel de l’élastomère non siliconé, au moins une huile hydrocarbonée polaire. According to one particular embodiment, the composition further comprises, as additional oil distinct from the oils (solvents) present in the gel of the non-silicone elastomer, at least one polar hydrocarbon-based oil.
Par « huile polaire » au sens de la présente invention, on entend une huile dont le paramètre de solubilité à 25 °C, ôa, est différent de 0 (J/cm3)1/2. By “polar oil” within the meaning of the present invention, is meant an oil whose solubility parameter at 25° C., Δa, is different from 0 (J/cm 3 ) 1/2 .
En particulier, la ou les huiles hydrocarbonées polaires comprennent au moins une fonction alcool (il s'agit alors d'une « huile alcool ») ou au moins une fonction ester (il s'agit alors d'une « huile ester »). In particular, the polar hydrocarbon-based oil or oils comprise at least one alcohol function (it is then an “alcohol oil”) or at least one ester function (it is then an “ester oil”).
Parmi les « huiles alcools », on peut citer notamment les alcools en C10-C26, plus particulièrement en C10-C24, et de préférence en C12-C22, saturés ou non, ramifiés ou non, plus particulièrement les monoalcools. Plus particulièrement, les alcools en C10-C26 sont des monoalcools gras, de préférence ramifiés lorsqu'ils comprennent au moins 16 atomes de carbone. A titre d'exemples d'alcools gras pouvant être utilisés selon l'invention, on peut citer les alcools gras linéaires ou ramifiés, d'origine synthétique, ou encore naturelle. A titre d'exemples particuliers d'alcools gras utilisables à titre préféré, on peut notamment citer l'alcool laurique, isostéarylique, oléique, le 2-butyloctanol, le 2-undécyl pentadécanol, l'alcool 2-hexyldécylique, l'alcool isocétylique, l'octyldodécanol et leurs mélanges. Selon un mode de réalisation avantageux de l'invention, l'alcool gras est l'octyldodécanol. Among the “alcohol oils”, mention may in particular be made of C10-C26, more particularly C10-C24, and preferably C12-C22 alcohols, saturated or not, branched or not, more particularly monoalcohols. More particularly, the C10-C26 alcohols are fatty monoalcohols, preferably branched when they comprise at least 16 carbon atoms. As examples of fatty alcohols which can be used according to the invention, mention may be made of linear or branched fatty alcohols, of synthetic or even natural origin. As specific examples of fatty alcohols which can be used on a preferred basis, mention may in particular be made of lauryl, isostearyl or oleic alcohol, 2-butyloctanol, 2-undecyl pentadecanol, 2-hexyldecyl alcohol, isocetyl alcohol , octyldodecanol and mixtures thereof. According to an advantageous embodiment of the invention, the fatty alcohol is octyldodecanol.
Parmi les huiles esters, on peut notamment citer : Among the ester oils, mention may be made in particular of:
- les esters hydroxylés, de préférence ayant un nombre total de carbone allant de 35 à 70, comme le triisostéarate de polyglycérol-2, le lactate d'isostéaryle, l'hydroxystéarate d'octyldodécyle, le malate de diisostéaryle, le stéarate de glycérine ; le diisononanoate de diéthylèneglycol ; - hydroxylated esters, preferably having a total carbon number ranging from 35 to 70, such as polyglycerol-2 triisostearate, isostearyl lactate, octyldodecyl hydroxystearate, diisostearyl malate, glycerol stearate; diethylene glycol diisononanoate;
- les esters d'acide gras, en particulier de 4 à 22 atomes de carbone, - fatty acid esters, in particular with 4 to 22 carbon atoms,
- les esters de synthèse comme les huiles de formule R1COOR2 dans laquelle Ri représente le reste d'un acide gras linéaire ou ramifié comportant de 4 à 40 atomes de carbone et R2 représente une chaîne hydrocarbonée notamment ramifiée contenant de 4 à 40 atomes de carbone à condition que R1+R2 soit >16, comme par exemple l'isononanoate d'isononyle, le palmitate d'éthyle 2-hexyle, le néopentanoate d'octyledodécyle, le stéarate d'octyl-2 dodécyle, l'isostéarate d'isostéaryle, le benzoate d'octyl-2 dodécyle, le myristate d'isopropyle, le palmitate d'isopropyle, le stéarate de butyle, le laurate d'hexyle, le palmitate de 2-éthyl- hexyle, le laurate de 2-hexyl-décyle, le palmitate de 2-octyl-décyle, le myristate de 2- octyldodécyle, le succinate de 2-diéthyl- hexyle; - synthetic esters such as oils of formula R1COOR2 in which Ri represents the residue of a linear or branched fatty acid containing from 4 to 40 carbon atoms and R2 represents a hydrocarbon chain, in particular branched, containing from 4 to 40 carbon atoms at provided that R1+R2 is >16, such as isononyl isononanoate, 2-hexyl ethyl palmitate, octyledodecyl neopentanoate, 2-octyldodecyl stearate, isostearyl isostearate, octyl-2 dodecyl benzoate, isopropyl myristate, isopropyl palmitate, butyl stearate, hexyl laurate, 2-ethyl-hexyl palmitate, 2-hexyl-decyl laurate, 2-octyl-decyl palmitate, 2-octyldodecyl myristate, 2-diethylhexyl succinate;
- les esters d'acides gras linéaires ayant un nombre total de carbone allant de 35 à 70 ; - linear fatty acid esters having a total carbon number ranging from 35 to 70;
- les esters d'acides aromatiques et d'alcools comprenant 4 à 22 atomes ;
- les esters d'alcool gras ou d'acides gras ramifiés en C24-C28 ; - esters of aromatic acids and alcohols comprising 4 to 22 atoms; - esters of fatty alcohol or of branched C24-C28 fatty acids;
- les polyesters résultant de l'estérification d'au moins un triglycéride d'acide(s) carboxylique(s) hydroxylé(s) par un acide monocarboxylique aliphatique et par un acide dicarboxylique aliphatique, éventuellement insaturé ; et leurs mélanges. - polyesters resulting from the esterification of at least one triglyceride of hydroxylated carboxylic acid(s) with an aliphatic monocarboxylic acid and with an optionally unsaturated aliphatic dicarboxylic acid; and their mixtures.
La composition de l’invention peut comprendre également au moins une huile hydrocarbonée choisie parmi : le triglycéride caprique/caprylique, le dicaprylyl éther, le dicaprylyl carbonate, le coco- caprylate/caprate, la triheptanoïne, les alcanes linéaires ou ramifiés en C9-C22, en particulier : les iso-alcanes (appelées aussi isoparaffines) en C8-C16 tels que l'isododécane, l'isodécane, l'isohexadécane, et par exemple les huiles vendues sous les noms commerciaux d'ISOPAR® ou de PERMETYL®, les alcanes linéaires ou ramifiés ayant des chaînes hydrocarbonées en The composition of the invention may also comprise at least one hydrocarbon oil chosen from: capric/caprylic triglyceride, dicaprylyl ether, dicaprylyl carbonate, coco-caprylate/caprate, triheptanoin, linear or branched C9-C22 alkanes , in particular: C8-C16 iso-alkanes (also called isoparaffins) such as isododecane, isodecane, isohexadecane, and for example the oils sold under the trade names ISOPAR® or PERMETYL®, linear or branched alkanes having hydrocarbon chains in
- C9-C17, C10-C14, tel qu'un mélange de l’undécane et de tridécane, commercialisé par BASF Care Créations sous la dénomination Cetiol® Ultimate, - C9-C17, C10-C14, such as a mixture of undecane and tridecane, marketed by BASF Care Créations under the name Cetiol® Ultimate,
- C15-C19, tel que ceux commercialisés par Seppic sous la dénomination EMOGREEN® L15,- C15-C19, such as those marketed by Seppic under the name EMOGREEN® L15,
- C9-C12, C12-C14, tel que ceux commercialisés par BIOSYNTHIS sous la dénomination VEGELIGHT® SILK (nom INCI C9-12 ALKANE), VEGELIGHT® 1214LC, - C9-C12, C12-C14, such as those marketed by BIOSYNTHIS under the name VEGELIGHT® SILK (INCI name C9-12 ALKANE), VEGELIGHT® 1214LC,
- le n-dodécane (C12) et le n-tétradécane (C14), notamment vendus par Sasol respectivement sous les références PARAFOL® 12-97 et PARAFOL® 14-97, et leurs mélanges. - n-dodecane (C12) and n-tetradecane (C14), in particular sold by Sasol respectively under the references PARAFOL® 12-97 and PARAFOL® 14-97, and mixtures thereof.
Selon un mode particulier, la composition de l’invention comprend des huiles choisies dans le groupe constitué par les huiles végétales, les huiles alcools en C10-C26, les huiles esters de préférence hydroxylés, et leurs mélanges. According to a particular embodiment, the composition of the invention comprises oils chosen from the group consisting of vegetable oils, C10-C26 alcohol oils, preferably hydroxylated ester oils, and mixtures thereof.
Selon un mode particulier et préféré, la composition de l’invention comprend au moins une huile végétale et au moins une huile hydrocarbonée polaire, en particulier une huile alcool en C10-C26 en particulier l’octyldodecanol et une huile ester choisie parmi les esters hydroxylés et en particulier le triisostearate de polyglycerol-2. According to a particular and preferred embodiment, the composition of the invention comprises at least one vegetable oil and at least one polar hydrocarbon oil, in particular a C10-C26 alcohol oil, in particular octyldodecanol, and an ester oil chosen from hydroxylated esters. and in particular polyglycerol-2 triisostearate.
Les huiles alcools pourront être présentes dans la composition en une teneur allant de 1 à 20 %, de préférence de 5 à 15%, de manière préférée de 8 à 12 %en poids par rapport au poids total de la composition. The alcohol oils may be present in the composition in a content ranging from 1 to 20%, preferably from 5 to 15%, preferably from 8 to 12% by weight relative to the total weight of the composition.
Les huiles esters pourront être présentes dans la composition en une teneur allant de 5 à 45 %, de préférence de 15 à 40 %, de manière préférée de 20 à 35 en poids par rapport au poids total de la composition. The ester oils may be present in the composition in a content ranging from 5 to 45%, preferably from 15 to 40%, preferably from 20 to 35% by weight relative to the total weight of the composition.
Les huiles végétales pourront être présentes dans la composition en une teneur allant de 1 à 20% de préférence de 5 à 15% et de manière préférée de 7 à 13 % en poids par rapport au poids total de la composition. The vegetable oils may be present in the composition in a content ranging from 1 to 20%, preferably from 5 to 15% and preferably from 7 to 13% by weight relative to the total weight of the composition.
La teneur totale en huile(s) dans la composition de l’invention pourra aller par exemple de 30 à 90% en poids, notamment de 40 à 80%, de préférence de 50 à 75 % en poids par rapport au poids total de la composition. Cette teneur en huile(s) tient compte des huiles (ou solvants) présentes dans le gel de l’élastomère non siliconé. The total content of oil(s) in the composition of the invention may range, for example, from 30 to 90% by weight, in particular from 40 to 80%, preferably from 50 to 75% by weight relative to the total weight of the composition. This oil(s) content takes into account the oils (or solvents) present in the gel of the non-silicone elastomer.
La teneur totale en cire(s) dans la composition de l’invention pourra aller par exemple de 5 à 20% de manière préférée de 8 à 18% en poids, notamment de 10 à 15 % en poids par rapport au poids total de la composition.
La teneur totale en beurre(s) dans la composition de l’invention pourra aller par exemple de 0,5 à 10% en poids, notamment de 1 à 5% en poids par rapport au poids total de la composition. The total content of wax(es) in the composition of the invention may range, for example, from 5 to 20%, preferably from 8 to 18% by weight, in particular from 10 to 15% by weight relative to the total weight of the composition. The total content of butter(s) in the composition of the invention may range, for example, from 0.5 to 10% by weight, in particular from 1 to 5% by weight relative to the total weight of the composition.
AUTRES INGREDIENTS OTHER INGREDIENTS
La composition peut comprendre d'autres ingrédients utilisés couramment dans les compositions cosmétiques. De tels ingrédients peuvent être choisis parmi les antioxydants, les parfums, les conservateurs, les actifs cosmétiques, les charges, les pigments, et leurs mélanges. The composition may include other ingredients commonly used in cosmetic compositions. Such ingredients can be chosen from antioxidants, perfumes, preservatives, cosmetic active agents, fillers, pigments, and mixtures thereof.
Les charges et pigments peuvent être traités par un agent hydrophobe pour faciliter leur dispersion dans la phase huileuse ou grasse. The fillers and pigments can be treated with a hydrophobic agent to facilitate their dispersion in the oily or fatty phase.
Avantageusement, la composition comprend en outre au moins une charge. Advantageously, the composition also comprises at least one filler.
Parmi les charges, on peut citer notamment les charges minérales, telles que des poudres d’alumine, de silice, de silicate d'aluminium, de silice pyrogénée, de silylate de silice, de dioxyde de titane ou de séricite. Among the fillers, mention may in particular be made of mineral fillers, such as powders of alumina, silica, aluminum silicate, fumed silica, silica silylate, titanium dioxide or sericite.
Selon un mode particulier, la composition de l’invention comprend au moins une charge, en particulier une charge minérale, de préférence encore une silice, telle que celle commercialisée sous la dénomination Sunsphere H33. Avantageusement, la teneur en charge(s), en particulier en silice dans la composition de l’invention ira de 0,1 à 5% en poids par rapport au poids total de la composition. According to a particular embodiment, the composition of the invention comprises at least one filler, in particular a mineral filler, more preferably a silica, such as that marketed under the name Sunsphere H33. Advantageously, the content of filler(s), in particular silica in the composition of the invention will range from 0.1 to 5% by weight relative to the total weight of the composition.
Les actifs cosmétiques, de préférence biosourcés (ex : extraits végétaux) peuvent être par exemple choisis avantageusement parmi ceux ayant une action sur le soin de la peau et/ou des lèvres tels que des agents hydratants. The cosmetic active agents, preferably biosourced (eg: plant extracts) can for example be advantageously chosen from those having an action on the care of the skin and/or the lips, such as moisturizing agents.
Selon un mode particulier, la composition de l’invention comprend : According to a particular embodiment, the composition of the invention comprises:
- une teneur en matière sèche de 0,5% à 5%, en particulier de 1% à 3% et notamment de 2 à 3% en poids, d’un élastomère de polyuréthane réticulé (seul ou en mélange), - a dry matter content of 0.5% to 5%, in particular from 1% to 3% and in particular from 2 to 3% by weight, of a crosslinked polyurethane elastomer (alone or as a mixture),
- une teneur de 0,4% à 0,8% en poids de lécithine, - a content of 0.4% to 0.8% by weight of lecithin,
- une teneur de 2 à 12% en poids de pigments, et avantageusement en outre - a content of 2 to 12% by weight of pigments, and advantageously in addition
- une teneur totale de 1 à 5% en poids de charge(s), en particulier en charges minérales, de préférence encore de silice, - a total content of 1 to 5% by weight of filler(s), in particular mineral fillers, more preferably silica,
- par rapport au poids total de la composition. - relative to the total weight of the composition.
Selon un mode particulier, le gel d’élastomère de polyuréthane réticulé comprend au moins un solvant et un seul élastomère de polyuréthane réticulé ou un mélange d’au moins deux élastomères de polyuréthane réticulé, ledit élastomère ou ledit mélange d’élastomères étant obtenu à partir d’un prépolymère ayant au moins deux groupes hydroxyles et d’un (poly)isocyanate. According to a particular embodiment, the crosslinked polyurethane elastomer gel comprises at least one solvent and a single crosslinked polyurethane elastomer or a mixture of at least two crosslinked polyurethane elastomers, said elastomer or said mixture of elastomers being obtained from a prepolymer having at least two hydroxyl groups and a (poly)isocyanate.
Selon un premier mode préféré, le prépolymère est un produit de réaction d'un diol et d'un acide dimère, en particulier d’un acide dilinoléique et de propanediol ou de butanediol et le (poly)isocyanate est un trimère de 1 ,5-pentaméthylène diisocyanate. According to a first preferred mode, the prepolymer is a reaction product of a diol and a dimer acid, in particular of a dilinoleic acid and propanediol or butanediol and the (poly)isocyanate is a trimer of 1.5 -pentamethylene diisocyanate.
Selon un autre mode préféré, la composition comprend un mélange de deux élastomères de polyuréthane réticulé, ledit mélange étant obtenu à partir de prépolymères d’acide
dilinoléique/ polyols et d’isophorone diisocyanate, les deux polyols étant le butanediol et l’huile de ricin. According to another preferred embodiment, the composition comprises a mixture of two crosslinked polyurethane elastomers, said mixture being obtained from acid prepolymers dilinoleic/polyols and isophorone diisocyanate, the two polyols being butanediol and castor oil.
Selon un mode particulier, ladite composition comprend en outre : According to a particular embodiment, said composition further comprises:
- une teneur totale de 50 à 70% en poids d’huile(s), en particulier choisies parmi le groupe constitué par les huiles végétales, les huiles alcools en C10-C26 de préférence l’octyldodecanol, les huiles esters de préférence hydroxylés de préférence le triisostearate de polyglycérol-2, et leurs mélanges, - a total content of 50 to 70% by weight of oil(s), in particular chosen from the group consisting of vegetable oils, C10-C26 alcohol oils, preferably octyldodecanol, preferably hydroxylated ester oils of preferably polyglycerol-2 triisostearate, and mixtures thereof,
- une teneur totale de 10 à 20% en poids de cire(s), en particulier en cires végétales ou animales, de préférence en cire de carnauba, cire de tournesol, et/ou cire d’abeille et - a total content of 10 to 20% by weight of wax(es), in particular vegetable or animal waxes, preferably carnauba wax, sunflower wax, and/or beeswax and
- une teneur totale de 3 à 15% en poids de corps gras pâteux choisi(s) dans le groupe constitué par (i) les esters de polyol(s) et de dimère diacide d’acide gras, ou d’un de ses esters, (ii) les esters d’huile de ricin hydrogénée, (iii) les esters oligomères de glycérol, notamment les esters de diglycérol, et leurs mélanges, de préférence les esters de polyol(s) et de dimère diacide d’acide gras, ou d’un de ses esters. - a total content of 3 to 15% by weight of pasty fatty substances chosen from the group consisting of (i) esters of polyol(s) and of fatty acid diacid dimer, or of one of its esters , (ii) hydrogenated castor oil esters, (iii) oligomeric glycerol esters, in particular diglycerol esters, and mixtures thereof, preferably esters of polyol(s) and fatty acid diacid dimer, or one of its esters.
La teneur totale en huile(s) comprend la teneur en huiles présentes dans le gel d’élastomère de polyuréthane réticulé. The total oil(s) content includes the content of oils present in the cross-linked polyurethane elastomer gel.
Ainsi, selon un mode particulier, la composition de l’invention comprendra une teneur en composés biosourcés d’au moins 70%, 80%, 90%, 95%, 96%, 97%, 98%, 99%, 100% en poids par rapport au poids total de la composition. Thus, according to a particular mode, the composition of the invention will comprise a content of biosourced compounds of at least 70%, 80%, 90%, 95%, 96%, 97%, 98%, 99%, 100% in weight relative to the total weight of the composition.
GALENIQUE GALENIC
La composition selon l’invention est une composition cosmétique solide colorée pour application topique sur les matières kératiniques, en particulier la peau et/ou les lèvres, de préférence les lèvres. Il s’agit en particulier d’une composition de soin et/ou de maquillage de la peau et/ou des lèvres. The composition according to the invention is a colored solid cosmetic composition for topical application to keratin materials, in particular the skin and/or the lips, preferably the lips. It is in particular a composition for caring for and/or making up the skin and/or the lips.
Elle peut se présenter en particulier sous la forme d’un stick pour les lèvres, d’un baume pour les lèvres, d’un coulé dans une coupelle, de préférence d’un baume ou d’un stick. It may in particular be in the form of a lip stick, a lip balm, poured into a dish, preferably a balm or a stick.
PROCEDE COSMETIQUE COSMETIC PROCESS
L’invention porte encore sur un procédé cosmétique de soin et/ou de maquillage de la peau et/ou des lèvres, comprenant au moins l'application sur la peau et/ou les lèvres d'une composition selon l’invention. The invention also relates to a cosmetic process for caring for and/or making up the skin and/or the lips, comprising at least the application to the skin and/or the lips of a composition according to the invention.
L’association d’un élastomère non siliconé et d’un phospholipide, en particulier d’une lécithine, tel que décrit précédemment, de préférence biosourcés, permet d’obtenir une composition homogène en teinte avec une origine naturelle très élevée et ayant un attrait cosmétique recherché : fondant, confort, et un effet gommé et homogène sur les matières kératiniques et notamment les lèvres. The combination of a non-silicone elastomer and a phospholipid, in particular a lecithin, as described above, preferably biosourced, makes it possible to obtain a homogeneous composition in shade with a very high natural origin and having an appeal desired cosmetic: melting, comfort, and a gummed and homogeneous effect on keratin materials and in particular the lips.
Ainsi le procédé cosmétique de l’invention est destiné notamment à obtenir un dépôt mat et confortable sur les lèvres. Thus the cosmetic process of the invention is intended in particular to obtain a matte and comfortable deposit on the lips.
L’invention va être illustrée par les exemples non limitatifs suivants. Les pourcentages (%) sont exprimés en pourcentage en poids de matière première par rapport au poids total de la composition sauf indication contraire. The invention will be illustrated by the following non-limiting examples. The percentages (%) are expressed as percentage by weight of raw material relative to the total weight of the composition, unless otherwise indicated.
EXEMPLES EXAMPLES
Exemple 1 : Sélection d’un agent pour stabiliser la teinte
On a préparé la composition suivante : Example 1: Selection of an agent to stabilize the shade The following composition was prepared:
La composition est préparée selon le protocole suivant : The composition is prepared according to the following protocol:
- les ingrédients de la phase A1 sont pesés et mis à fondre dans un bain-marie à 95° C, puis homogénéisés sous Rayneri pendant 15 minutes ; - the ingredients of phase A1 are weighed and melted in a water bath at 95° C., then homogenized under Rayneri for 15 minutes;
- l’élastomère non siliconé (A2) est ajouté et mis sous agitation pendant 15 minutes ; - the non-silicone elastomer (A2) is added and stirred for 15 minutes;
- les pigments (B), préalablement dispersés dans le Triisostearate de polyglycerol-2, sont ajoutés et mélangés pendant 15 minutes au Rayneri ; - the pigments (B), previously dispersed in polyglycerol-2 Triisostearate, are added and mixed for 15 minutes with Rayneri;
- la silice (C) est ensuite dispersée, mise sous agitation pendant 5 minutes et passée au Turrax pour obtenir une composition homogène - the silica (C) is then dispersed, stirred for 5 minutes and passed through Turrax to obtain a homogeneous composition
- la composition est ensuite coulée à chaud dans un outil permettant d’obtenir un stick (ex : tétine en silicone, moule métal ou godet) ou directement dans le packaging final (flaconette).- the composition is then hot poured into a tool to obtain a stick (e.g.: silicone teat, metal mold or cup) or directly into the final packaging (bottle).
L’aspect de la composition est inhomogène : on observe un flux dans le vrac et/ou en surface de la composition. The appearance of the composition is inhomogeneous: a flow is observed in the bulk and/or on the surface of the composition.
Différentes compositions identiques à celle décrite ci-dessus sont préparées selon le même protocole, et 0,5% en poids d’un agent mouillant a été ajouté (qsp sur le Triisostearate de polyglycerol-2). L’agent mouillant est pré-mélangé dans du Triisostearate de polyglycerol-2 et mis avec les pigments de la phase B (eux-mêmes pré-dispersés dans du Triisostearate de polyglycerol-2 pour former des dispersions pigmentaires). Different compositions identical to the one described above are prepared according to the same protocol, and 0.5% by weight of a wetting agent has been added (qsp on polyglycerol-2 Triisostearate). The wetting agent is pre-mixed in polyglycerol-2 Triisostearate and mixed with the phase B pigments (themselves pre-dispersed in polyglycerol-2 Triisostearate to form pigment dispersions).
Différents agents mouillants ont ainsi été testés et l’aspect des compositions, en particulier l’homogénéité et la stabilité de la teinte (absence de flux), est observé (dans le vrac avant mise en forme de la composition et en surface de la composition mise en forme). Various wetting agents have thus been tested and the appearance of the compositions, in particular the homogeneity and stability of the color (absence of flow), is observed (in the bulk before shaping the composition and on the surface of the composition formatting).
Les résultats sont présentés dans le tableau 2 ci-dessous, avec la légende suivante : The results are presented in Table 2 below, with the following legend:
‘-‘ = aspect inhomogène, présence de flux,
‘+/-‘ = aspect partiellement inhomogène, flux légèrement moins important, ‘+++’ = aspect homogène, absence de flux. '-' = inhomogeneous aspect, presence of flow, '+/-' = partially inhomogeneous aspect, slightly less important flow, '+++' = homogeneous aspect, absence of flow.
Ces résultats mettent donc en évidence que la lécithine permet d’obtenir, dans une composition solide colorée selon l’invention comprenant un élastomère non siliconé, une composition dont l’aspect (teinte) est homogène et stable (absence de flux). These results therefore demonstrate that lecithin makes it possible to obtain, in a colored solid composition according to the invention comprising a non-silicone elastomer, a composition whose appearance (colour) is homogeneous and stable (absence of flux).
Exemple 2 : Baume coloré pour les lèvres [Table 3]
La composition est préparée selon le protocole suivant : Example 2: Colored lip balm [Table 3] The composition is prepared according to the following protocol:
- les ingrédients de la phase A1 sont pesés et mis à fondre dans un bain-marie à 95° C, puis homogénéisés sous Rayneri pendant 15 minutes ; - the ingredients of phase A1 are weighed and melted in a water bath at 95° C., then homogenized under Rayneri for 15 minutes;
- l’élastomère non siliconé (A2) est ajouté et mis sous agitation pendant 15 minutes ; - the non-silicone elastomer (A2) is added and stirred for 15 minutes;
- la lécithine est pré-mélangée avec le triisostearate de polyglycerol-2 , puis mélangée avec les dispersions pigmentaires (pigments de la phase (B) eux-mêmes dispersés dans du triisostearate de polyglycerol-2) ; ce mélange (lécithine et dispersions pigmentaires) est ensuite ajouté et mélangé pendant 15 minutes au Rayneri ; - the lecithin is pre-mixed with polyglycerol-2 triisostearate, then mixed with the pigment dispersions (pigments of phase (B) themselves dispersed in polyglycerol-2 triisostearate); this mixture (lecithin and pigmentary dispersions) is then added and mixed for 15 minutes with Rayneri;
- la silice (C) est ensuite dispersée, mise sous agitation pendant 5 minutes et passée au Turrax pour obtenir une composition homogène
- la composition est ensuite coulée à chaud dans un outil permettant d’obtenir un stick (ex : tétine en silicone, moule métal ou godet) ou directement dans le packaging final (flaconette).- the silica (C) is then dispersed, stirred for 5 minutes and passed through Turrax to obtain a homogeneous composition - the composition is then hot poured into a tool making it possible to obtain a stick (eg: silicone teat, metal mold or cup) or directly into the final packaging (bottle).
La composition obtenue se présente sous la forme d’un stick homogène dans la teinte, avec un fini mat gommeux et légèrement coloré (effet lèvres mordues) sur les lèvres.
The composition obtained is in the form of a stick that is homogeneous in shade, with a gummy and slightly colored matte finish (bitten lips effect) on the lips.
Claims
1. Composition cosmétique solide anhydre comprenant, dans un milieu physiologiquement acceptable : i) un gel d’élastomère de polyuréthane réticulé comprenant au moins un solvant et un seul élastomère de polyuréthane réticulé ou un mélange d’au moins deux élastomères de polyuréthane réticulé, ledit élastomère ou ledit mélange d’élastomères étant obtenu à partir d’un prépolymère ayant au moins deux groupes hydroxyles et d’un (poly)isocyanate, ii) un phospholipide, de préférence une lécithine, et iii) un ou plusieurs pigments. 1. Anhydrous solid cosmetic composition comprising, in a physiologically acceptable medium: i) a crosslinked polyurethane elastomer gel comprising at least one solvent and a single crosslinked polyurethane elastomer or a mixture of at least two crosslinked polyurethane elastomers, said elastomer or said mixture of elastomers being obtained from a prepolymer having at least two hydroxyl groups and from a (poly)isocyanate, ii) a phospholipid, preferably a lecithin, and iii) one or more pigments.
2. Composition selon la revendication 1 , caractérisée en ce que le prépolymère ayant au moins deux groupes hydroxyles est un copolymère d’un dimère ou d’un trimère d’acide carboxylique, et d’un polyol. 2. Composition according to claim 1, characterized in that the prepolymer having at least two hydroxyl groups is a copolymer of a carboxylic acid dimer or trimer, and of a polyol.
3. Composition selon la revendication 2, caractérisée en ce que l’acide carboxylique est un dimère d’acides gras en C12-C18, en particulier l’acide dilinoléique. 3. Composition according to claim 2, characterized in that the carboxylic acid is a dimer of C12-C18 fatty acids, in particular dilinoleic acid.
4. Composition selon la revendication 2, caractérisée en ce que le polyol est choisi dans le groupe constitué par un diol aliphatique comprenant 2 à 8 atomes de carbone, tel que le 1 ,2 ethanediol, les propanediols tels que le 1 ,2 propanediol, le 1 ,3 propanediol, le butanediol, le pentanediol, le caprylyl glycol, de préférence les propanediols et le butanediol ; un triglycéride d’acide gras comprenant au moins deux groupements -OH, tel que le triglycéride de l'acide ricinoléique ou une source végétale en contenant, telle que l’huile de ricin. 4. Composition according to claim 2, characterized in that the polyol is chosen from the group consisting of an aliphatic diol comprising 2 to 8 carbon atoms, such as 1,2 ethanediol, propanediols such as 1,2 propanediol, 1,3 propanediol, butanediol, pentanediol, caprylyl glycol, preferably propanediols and butanediol; a fatty acid triglyceride comprising at least two -OH groups, such as ricinoleic acid triglyceride or a vegetable source containing it, such as castor oil.
5. Composition selon l’une quelconque des revendications 1 à 4, caractérisée en ce que (poly)isocyanate est un diisocyanate, en particulier un diisocyanate aliphatique pouvant contenir de 5 à 6 atomes de carbone, de préférence choisi parmi le 1 ,6-hexaméthylène diisocyanate (HDI), le 1 ,5-pentaméthylène diisocyanate (PDI) ou l’isophorone diisocyanate (I PDI ). 5. Composition according to any one of claims 1 to 4, characterized in that (poly)isocyanate is a diisocyanate, in particular an aliphatic diisocyanate which may contain from 5 to 6 carbon atoms, preferably chosen from 1,6- hexamethylene diisocyanate (HDI), 1,5-pentamethylene diisocyanate (PDI) or isophorone diisocyanate (I PDI).
6. Composition selon l’une quelconque des revendications 1 à 5, caractérisé en ce que le prépolymère est un copolymère d’acide dilinoléique et de propanediol ou de butanediol et le (poly)isocyanate est un trimère de 1 ,5-pentaméthylène diisocyanate. 6. Composition according to any one of claims 1 to 5, characterized in that the prepolymer is a copolymer of dilinoleic acid and propanediol or butanediol and the (poly)isocyanate is a trimer of 1,5-pentamethylene diisocyanate.
7. Composition selon l’une quelconque des revendications 1 à 5, caractérisée en ce qu’elle comprend un mélange de deux élastomères de polyuréthane réticulé, ledit mélange étant obtenu à partir de prépolymères d’acide dilinoléique/ polyols et d’isophorone diisocyanate (I PDI ), les deux polyols étant le butanediol et l’huile de ricin. 7. Composition according to any one of claims 1 to 5, characterized in that it comprises a mixture of two crosslinked polyurethane elastomers, said mixture being obtained from prepolymers of dilinoleic acid/polyols and isophorone diisocyanate ( I PDI), the two polyols being butanediol and castor oil.
8. Composition selon l’une quelconque des revendications 1 à 7, caractérisée en ce que le gel d’élastomère de polyuréthane comprend au moins un solvant choisi dans le groupe constitué par des triglycérides d’origine végétale tels que le trihexanoate de glycérol, le triheptanoate de glycérol (triheptanoïne), le trioctanoate de glycérol, le coco-caprylate/caprate, les alcanes en C9-C22 tels que le undecane, le tridecane ; des esters d'origine naturelle et leurs mélanges, de préférence le triheptanoate de glycérol (triheptanoïne), le coco-caprylate/caprate, les alcanes en C9-C22, des esters d'origine naturelle et leurs mélanges. 8. Composition according to any one of claims 1 to 7, characterized in that the polyurethane elastomer gel comprises at least one solvent chosen from the group consisting of triglycerides of plant origin such as glycerol trihexanoate, glycerol triheptanoate (triheptanoin), glycerol trioctanoate, coco-caprylate/caprate, C9-C22 alkanes such as undecane, tridecane; esters of natural origin and mixtures thereof, preferably glycerol triheptanoate (triheptanoin), coco-caprylate/caprate, C9-C22 alkanes, esters of natural origin and mixtures thereof.
9. Composition cosmétique selon l’une quelconque des revendications 1 à 8, caractérisée en ce que la teneur totale en matière sèche (active) en élastomère(s) de polyuréthane réticulé(s) dans la composition va de 0,5% à 5% en poids, en particulier de 1% à 3% et notamment de 2 à 3% en poids par rapport au poids total de la composition.
9. Cosmetic composition according to any one of claims 1 to 8, characterized in that the total dry (active) matter content of crosslinked polyurethane elastomer(s) in the composition ranges from 0.5% to 5 % by weight, in particular from 1% to 3% and in particular from 2 to 3% by weight relative to the total weight of the composition.
10. Composition cosmétique selon l’une quelconque des revendications 1 à 9, caractérisée en ce que les pigments sont choisis parmi les pigments inorganiques, les pigments organiques et leurs mélanges, en particulier : 10. Cosmetic composition according to any one of claims 1 to 9, characterized in that the pigments are chosen from inorganic pigments, organic pigments and mixtures thereof, in particular:
- un ou plusieurs pigments inorganiques choisis parmi le dioxyde de titane, les oxydes de fer et leurs mélanges, de préférence un mélange de dioxyde de titane et d’oxydes de fer, et- one or more inorganic pigments chosen from titanium dioxide, iron oxides and mixtures thereof, preferably a mixture of titanium dioxide and iron oxides, and
- un ou plusieurs pigments organiques choisis parmi les pigments D & C Red n° 7, D&C Red No.7 lake (Cl 15850), D &C Red No.28 lake (Cl 45410) ; FD&C Yellow 5 Al Lake (C69-4424) ; FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), et leurs mélanges. - one or more organic pigments chosen from the pigments D & C Red No. 7, D & C Red No.7 lake (Cl 15850), D & C Red No. 28 lake (Cl 45410); FD&C Yellow 5 Al Lake (C69-4424); FD&C Yellow 6 Al Lake (C70-5270); FD&C Blue 1 Al Lake (C39-4433), and mixtures thereof.
11. Composition cosmétique selon l’une quelconque des revendications 1 à 10, caractérisée en ce que la teneur totale en pigment(s) va de 1 à 15% en poids par rapport au poids total de la composition. 11. Cosmetic composition according to any one of claims 1 to 10, characterized in that the total content of pigment(s) ranges from 1 to 15% by weight relative to the total weight of the composition.
12. Composition cosmétique selon l’une quelconque des revendications 1 à 11 , caractérisée en ce qu’elle comprend une phase grasse comprenant une ou plusieurs huile(s) et au moins un corps gras choisi parmi les corps gras pâteux, les cires, les beurres et leurs mélanges. 12. Cosmetic composition according to any one of claims 1 to 11, characterized in that it comprises a fatty phase comprising one or more oil(s) and at least one fatty substance chosen from pasty fatty substances, waxes, butters and their mixtures.
13. Composition selon l’une quelconque des revendications 1 à 12, caractérisée en ce qu’elle comprend en outre au moins une charge, en particulier une charge minérale, de préférence encore une silice. 13. Composition according to any one of claims 1 to 12, characterized in that it further comprises at least one filler, in particular a mineral filler, more preferably a silica.
14. Composition selon l’une quelconque des revendications 1 à 13, caractérisé en ce qu’elle comprend au moins 70%, 80%, 90%, 95% en poids d’ingrédients biosourcés. 14. Composition according to any one of claims 1 to 13, characterized in that it comprises at least 70%, 80%, 90%, 95% by weight of biosourced ingredients.
15. Composition cosmétique selon l’une quelconque des revendications 1 à 14, caractérisée en ce qu’il s’agit d’un stick pour les lèvres, d’un baume pour les lèvres, d’un coulé dans une coupelle, de préférence d’un baume ou d’un stick. 15. Cosmetic composition according to any one of claims 1 to 14, characterized in that it is a stick for the lips, a balm for the lips, poured into a dish, preferably a balm or a stick.
16. Procédé cosmétique de soin et/ou de maquillage des matières kératiniques, en particulier de la peau et/ou des lèvres et de préférence des lèvres, caractérisé en ce qu’il comprend l'application sur lesdites matières kératiniques et de préférence les lèvres d'une composition telle que définie dans l'une quelconque des revendications 1 à 15.
16. Cosmetic process for caring for and/or making up keratin materials, in particular the skin and/or the lips and preferably the lips, characterized in that it comprises the application to the said keratin materials and preferably the lips of a composition as defined in any one of claims 1 to 15.
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FRFR2107074 | 2021-06-30 | ||
FR2107074A FR3124728A1 (en) | 2021-06-30 | 2021-06-30 | Solid cosmetic composition colored with a non-silicone elastomer and a phospholipid |
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WO2023275497A1 true WO2023275497A1 (en) | 2023-01-05 |
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WO2021007489A1 (en) * | 2019-07-10 | 2021-01-14 | Nanometics Llc (D.B.A. Phd Biosciences) | Polyurethane gels |
WO2021041046A1 (en) | 2019-08-30 | 2021-03-04 | Grant Industries, Inc. | Bio-based and biodegradable elastomer for cosmetic and personal care |
-
2021
- 2021-06-30 FR FR2107074A patent/FR3124728A1/en active Pending
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Patent Citations (2)
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WO2021007489A1 (en) * | 2019-07-10 | 2021-01-14 | Nanometics Llc (D.B.A. Phd Biosciences) | Polyurethane gels |
WO2021041046A1 (en) | 2019-08-30 | 2021-03-04 | Grant Industries, Inc. | Bio-based and biodegradable elastomer for cosmetic and personal care |
Non-Patent Citations (1)
Title |
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TANIA ALEXANDRA VIANA ET AL: "GRANSENSE", IP.COM, IP.COM INC., WEST HENRIETTA, NY, US, 4 May 2021 (2021-05-04), XP013189955, ISSN: 1533-0001 * |
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