EP3958986A1 - Compound comprising a functional agent and a waxy matrix including an organosilicon material, and associated manufacturing method - Google Patents
Compound comprising a functional agent and a waxy matrix including an organosilicon material, and associated manufacturing methodInfo
- Publication number
- EP3958986A1 EP3958986A1 EP20754313.3A EP20754313A EP3958986A1 EP 3958986 A1 EP3958986 A1 EP 3958986A1 EP 20754313 A EP20754313 A EP 20754313A EP 3958986 A1 EP3958986 A1 EP 3958986A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- compound
- solid particles
- cosmetic
- functional agent
- solid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000011159 matrix material Substances 0.000 title claims abstract description 117
- 150000001875 compounds Chemical class 0.000 title claims abstract description 84
- 239000000463 material Substances 0.000 title claims abstract description 57
- 238000004519 manufacturing process Methods 0.000 title claims description 33
- 239000007787 solid Substances 0.000 claims abstract description 129
- 239000000203 mixture Substances 0.000 claims abstract description 103
- 239000002245 particle Substances 0.000 claims abstract description 103
- 239000002537 cosmetic Substances 0.000 claims abstract description 91
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 62
- 238000005243 fluidization Methods 0.000 claims abstract description 20
- 238000005063 solubilization Methods 0.000 claims abstract description 20
- 230000007928 solubilization Effects 0.000 claims abstract description 20
- 239000012530 fluid Substances 0.000 claims description 28
- 238000004381 surface treatment Methods 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 26
- 238000010438 heat treatment Methods 0.000 claims description 18
- 238000000227 grinding Methods 0.000 claims description 17
- 238000011282 treatment Methods 0.000 claims description 16
- 229920003217 poly(methylsilsesquioxane) Polymers 0.000 claims description 14
- 230000008569 process Effects 0.000 claims description 13
- 239000008187 granular material Substances 0.000 claims description 11
- 239000006185 dispersion Substances 0.000 claims description 10
- 238000010521 absorption reaction Methods 0.000 claims description 9
- 239000008188 pellet Substances 0.000 claims description 9
- 238000002844 melting Methods 0.000 claims description 8
- 230000008018 melting Effects 0.000 claims description 8
- 238000001125 extrusion Methods 0.000 claims description 7
- 230000002209 hydrophobic effect Effects 0.000 claims description 7
- 229920001296 polysiloxane Polymers 0.000 claims description 7
- 230000007423 decrease Effects 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- 230000000475 sunscreen effect Effects 0.000 claims description 4
- 239000000516 sunscreening agent Substances 0.000 claims description 4
- 229910052719 titanium Inorganic materials 0.000 claims description 4
- 239000010936 titanium Substances 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 239000011173 biocomposite Substances 0.000 claims description 3
- 239000002131 composite material Substances 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 3
- 239000001023 inorganic pigment Substances 0.000 claims description 3
- 239000012766 organic filler Substances 0.000 claims description 3
- 239000012860 organic pigment Substances 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 230000001747 exhibiting effect Effects 0.000 claims description 2
- 229910003471 inorganic composite material Inorganic materials 0.000 claims description 2
- 239000011256 inorganic filler Substances 0.000 claims description 2
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 2
- 229920005615 natural polymer Polymers 0.000 claims description 2
- 239000010703 silicon Substances 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 230000003381 solubilizing effect Effects 0.000 claims 1
- 229920001059 synthetic polymer Polymers 0.000 claims 1
- 238000004018 waxing Methods 0.000 claims 1
- 238000009472 formulation Methods 0.000 abstract description 7
- 229940125904 compound 1 Drugs 0.000 description 84
- 239000000049 pigment Substances 0.000 description 33
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 24
- 239000003921 oil Substances 0.000 description 18
- 235000019198 oils Nutrition 0.000 description 18
- 239000000126 substance Substances 0.000 description 18
- 239000001993 wax Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 238000003860 storage Methods 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 235000008390 olive oil Nutrition 0.000 description 5
- 239000004006 olive oil Substances 0.000 description 5
- 229940024606 amino acid Drugs 0.000 description 4
- 150000001413 amino acids Chemical class 0.000 description 4
- 239000003925 fat Substances 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 239000013020 final formulation Substances 0.000 description 3
- 238000000265 homogenisation Methods 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 229920005573 silicon-containing polymer Polymers 0.000 description 3
- 229920002545 silicone oil Polymers 0.000 description 3
- 229940077092 sodium myristoyl glutamate Drugs 0.000 description 3
- FCBUGCHAVCFTHW-NTISSMGPSA-N sodium;(2s)-2-(tetradecanoylamino)pentanedioic acid Chemical compound [Na].CCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC(O)=O FCBUGCHAVCFTHW-NTISSMGPSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 238000004581 coalescence Methods 0.000 description 2
- 229940008099 dimethicone Drugs 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- MSRJTTSHWYDFIU-UHFFFAOYSA-N octyltriethoxysilane Chemical compound CCCCCCCC[Si](OCC)(OCC)OCC MSRJTTSHWYDFIU-UHFFFAOYSA-N 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- -1 sericite Substances 0.000 description 2
- 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 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 244000062730 Melissa officinalis Species 0.000 description 1
- 235000010654 Melissa officinalis Nutrition 0.000 description 1
- RGMZNZABJYWAEC-UHFFFAOYSA-N Methyltris(trimethylsiloxy)silane Chemical compound C[Si](C)(C)O[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C RGMZNZABJYWAEC-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229940051182 aluminum dimyristate Drugs 0.000 description 1
- YNQRLDQNSBVJGU-UHFFFAOYSA-K aluminum;tetradecanoate;hydroxide Chemical compound [OH-].[Al+3].CCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCC([O-])=O YNQRLDQNSBVJGU-UHFFFAOYSA-K 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000000732 arylene group Chemical group 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- SHFGJEQAOUMGJM-UHFFFAOYSA-N dialuminum dipotassium disodium dioxosilane iron(3+) oxocalcium oxomagnesium oxygen(2-) Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Na+].[Na+].[Al+3].[Al+3].[K+].[K+].[Fe+3].[Fe+3].O=[Mg].O=[Ca].O=[Si]=O SHFGJEQAOUMGJM-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229940079784 disodium stearoyl glutamate Drugs 0.000 description 1
- WODOUQLMOIMKAL-FJSYBICCSA-L disodium;(2s)-2-(octadecanoylamino)pentanedioate Chemical compound [Na+].[Na+].CCCCCCCCCCCCCCCCCC(=O)N[C@H](C([O-])=O)CCC([O-])=O WODOUQLMOIMKAL-FJSYBICCSA-L 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 229960002989 glutamic acid Drugs 0.000 description 1
- HNMCSUXJLGGQFO-UHFFFAOYSA-N hexaaluminum;hexasodium;tetrathietane;hexasilicate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].S1SSS1.S1SSS1.[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] HNMCSUXJLGGQFO-UHFFFAOYSA-N 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 229910052588 hydroxylapatite Inorganic materials 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000000865 liniment Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000007937 lozenge Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229940073663 methyl trimethicone Drugs 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000012764 mineral filler Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
- 239000007962 solid dispersion Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61K8/022—Powders; Compacted Powders
- A61K8/0225—Granulated powders
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- 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
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- A—HUMAN NECESSITIES
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- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0241—Containing particulates characterized by their shape and/or structure
- A61K8/0275—Containing agglomerated particulates
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- 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
- A61K8/0241—Containing particulates characterized by their shape and/or structure
- A61K8/0283—Matrix particles
- A61K8/0287—Matrix particles the particulate containing a solid-in-solid dispersion
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- 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
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- 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
- A61K8/28—Zirconium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
- A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
-
- 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
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- 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
- A61Q1/06—Lipsticks
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/0081—Composite particulate pigments or fillers, i.e. containing at least two solid phases, except those consisting of coated particles of one compound
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/0081—Composite particulate pigments or fillers, i.e. containing at least two solid phases, except those consisting of coated particles of one compound
- C09C1/0084—Composite particulate pigments or fillers, i.e. containing at least two solid phases, except those consisting of coated particles of one compound containing titanium dioxide
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/22—Compounds of iron
- C09C1/24—Oxides of iron
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/36—Compounds of titanium
- C09C1/3607—Titanium dioxide
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/36—Compounds of titanium
- C09C1/3607—Titanium dioxide
- C09C1/3669—Treatment with low-molecular organic compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/08—Treatment with low-molecular-weight non-polymer organic compounds
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- 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
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- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
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- A61K2800/61—Surface treated
- A61K2800/612—By organic compounds
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- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
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- C—CHEMISTRY; METALLURGY
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- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/62—Submicrometer sized, i.e. from 0.1-1 micrometer
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- C01P2004/64—Nanometer sized, i.e. from 1-100 nanometer
Definitions
- the present invention relates to the general technical field of substances and compounds used in the field of the formulation of cosmetic and / or dermatological compositions, in particular of the type of compound comprising a functional agent, for example of pigment type.
- the present invention relates more particularly to a compound comprising at least 50% by weight of a functional agent.
- the present invention also relates to a method of manufacturing such a compound.
- the present invention relates to a process for manufacturing a cosmetic and / or dermatological composition.
- grinding units are often specialized and very expensive, while the grinding process itself can prove to be particularly long and complex depending on the nature and desired size of the ground pigment particles, which may vary according to requirements. for example aesthetic, organoleptic and / or qualitative.
- These grinding units in most cases, due to their cost and complexity, are not dedicated specifically to the specific grinding of a pigment, and therefore require adjustments to grind a pigment to other specifications, such as different particle size, or to grind other types of pigments.
- these grinding units generally carry out different “batches” or batches of several types and sizes of ground pigments which must then be stored, transported and used at the level of different units for manufacturing cosmetic compositions.
- the invention therefore proposes to remedy the various drawbacks described above by proposing a new compound which not only proves capable of being easily integrated into a cosmetic and / or dermatological composition, but also exhibits great ease of use. works with regard to its management and in particular its transport, storage and handling.
- Another object of the invention aims to provide a new compound of extremely simple and inexpensive design.
- Another object of the invention aims to provide a new compound which is particularly easy to handle.
- Another object of the invention aims to provide a new compound which is particularly easy to transport and store.
- Another object of the invention aims to provide a new compound that is easy to integrate effectively into cosmetic and / or dermatological compositions.
- Another object of the invention aims to provide a new compound whose design allows it to obtain good repeatability as a component for the formulation of cosmetic and / or dermatological compositions.
- Another object of the invention aims to provide a new compound whose design allows it to be used in a very wide range of applications, in particular for a very wide variety of cosmetic and / or dermatological compositions.
- Another object of the invention aims to provide a new compound presenting a minimal risk to the safety of living beings and which does not degrade the installations.
- Another object of the invention aims to provide a novel compound which can be easily industrialized, using a minimum number of different substances.
- Another object of the invention aims to provide a new compound which degrades very little or not at all over time.
- Another object of the invention aims to provide a method of manufacturing a compound whose implementation is simple, easy and inexpensive, and has good repeatability and good safety for the user.
- Another object of the invention aims to provide a process for manufacturing a cosmetic and / or dermatological composition, the application of which is rapid, easy to control and easy, while ensuring optimum safety conditions.
- a compound comprising at least 50% by weight of a functional agent, characterized in that it also comprises a waxy matrix, comprising at least one organosilicon material, said organosilicon material forming the major part by weight, preferably all, of said waxy matrix, within which said functional agent, formed of solid particles, is dispersed, said compound being solid at room temperature and intended to be dispersed by fluidization and / or solubilization in a cosmetic and / or dermatological composition in order to integrate said functional agent therein.
- the objects assigned to the invention are also achieved using a process for the manufacture of a compound comprising at least 50% by weight of a functional agent, characterized in that it comprises at least: a step of heating a waxy matrix comprising at least one organosilicon material in order to obtain a fluid matrix, said organosilicon material forming the major part by weight, preferably all, of said waxy matrix, a step of dispersing said functional agent, formed of solid particles, within said fluid matrix, said compound being solid at room temperature and intended to be dispersed by fluidization and / or solubilization within a cosmetic and / or dermatological composition in order to integrate said functional agent therein.
- the objects assigned to the invention are further achieved using a process for manufacturing a cosmetic and / or dermatological composition comprising a redispersion step during which a compound as mentioned above is added to then mixed with one or more components acceptable in cosmetics and / or dermatology.
- FIG. 1 schematically illustrates, in a side view, an example of a compound according to the invention, which is in this case in the form of a rod obtained by extrusion.
- FIG. 2 schematically illustrates, on a microscopic or nanometric scale, a detail of the compound of FIG. 1.
- FIG. 3 schematically illustrates, in a side view, part of an example of production equipment allowing the implementation of a process for manufacturing a compound according to the invention, according to a particular embodiment including implementing an extrusion step.
- the invention relates to a compound 1.
- Said compound 1 is therefore preferably formed of several different elements, more precisely of a relatively homogeneous and stable mixture of several substances, materials, different materials together, all advantageously acceptable on the surface.
- cosmetic and / or dermatological plan that is to say suitable for being integrated within a cosmetic and / or dermatological composition.
- Compound 1 therefore advantageously exhibits a very low or even zero level of toxicity with regard to the use of a cosmetic and / or dermatological composition.
- compound 1 comprises at least 50% by weight of a functional agent.
- compound 1 comprises (strictly) more than 50%, preferably (strictly) more than 60%, more preferably at least 70%, more preferably still at least 80%, or even even more preferably at least. less 85%, more preferably still at least 90%, by weight, of said functional agent.
- Said functional agent is advantageously chosen in an appropriate manner, so as to form an element acceptable to be integrated within a cosmetic and / or dermatological composition.
- a high proportion of functional agent within compound 1 is particularly advantageous when the latter constitutes an intermediate (or possibly quasi-finished) product intended to be redispersed with other components to form a finished cosmetic and / or dermatological product. .
- said compound 1 advantageously serves as an intermediate “support” or “vehicle” for the functional agent, and it is therefore preferable that the proportion of functional agent in compound 1 is as high as possible on the one hand. so that the final formulation (that is to say the finished cosmetic and / or dermatological product) is not or only very little dependent on the nature of the substances other than said functional agent within said compound 1, and on the other hand for obvious reasons of cost, storage and transport, an intermediate compound having a low content of functional agent must by definition be used in greater quantity and therefore occupying a larger volume for an overall greater weight for a given quantity of functional agent, while the substances other than said functional agent within said compound 1, being in larger proportions, represent a significant cost which n 'is moreover not valued in the final formulation (or even "parasitizes said final formulation", or finished cosmetic and / or dermatological).
- said functional agent is intended to fulfill one or more very specific functions within a cosmetic and / or dermatological composition.
- said functional agent is intended to form a physical sunscreen, in particular within a cosmetic and / or dermatological composition of sunscreen type, that is to say it is intended to form a physical barrier, preferably opaque, between the ultraviolet rays of the sun and the skin of a user of said cosmetic and / or dermatological composition.
- said functional agent is formed of solid particles 2, that is to say which are preferably solid at least at room temperature, and even solid at higher temperatures, such as for example between 30 and 90 ° vs.
- said solid particles are insoluble in water.
- said solid particles have an average size of between 10 nm and 500 ⁇ m, preferably between 100 nm and 100 ⁇ m. Said average size therefore preferably denotes the average particle size of said particles 2, and in particular their average diameter or even an average maximum dimension of said particles, which can be measured in particular using only a sample of said particles.
- said solid particles 2 comprise at least organic and / or inorganic pigments (that is to say inorganic), organic and / or inorganic fillers, composite materials and / or biocomposites, or a mixture of these. this.
- said solid particles 2 are mainly, or even totally, formed of inorganic pigments, which may consist for example of sodium dioxide. titanium, iron oxide (s), chromium oxide (s), ultramarine pigment (s) (ultramarine blue or violet for example), tin oxide (s) and / or zinc oxide.
- Said organic pigments consist for example of carbon black and / or organic lakes.
- Said mineral fillers consist, for example, of talc, mica, sericite, kaolin, silica, hydroxyapatite, barium sulphate, perlite, calcium carbonate, and / or borosilicates.
- Said organic fillers consist for example of starch, cellulose, polymers of natural or synthetic origin, and / or silicone polymers and resins.
- Said composites and / or biocomposites include, for example, one or more nacres.
- the functional agent is for example intended to color a cosmetic and / or dermatological formulation, or to protect the skin from the sun (case of sunscreen mentioned above, the solid particles 2 forming in particular a solar filter).
- the functional agent may for example be intended to modify the organoleptic properties of a cosmetic and / or dermatological formulation.
- compound 1 also comprises a waxy matrix 3 within which said functional agent is dispersed.
- said functional agent, and more precisely said solid particles 2 is / are advantageously mixed with said waxy matrix 3 and scattered within the latter, preferably in a homogeneous manner, that is, that is to say according to a regular volume distribution.
- the waxy matrix 3 and said solid particles 2 form, from a macroscopic point of view, a single phase, and it is impossible to differentiate with the naked eye the waxy matrix 3 from said solid particles 2. .
- said waxy matrix 3 comprises at least one organosilicon (or organosilicon) material. It can also optionally comprise a plurality of different organosilicon materials.
- said organosilicon material forms the major part by weight, preferably all, of said waxy matrix 3.
- the organosilicon material forms at least 50% by weight, advantageously at least 75% by weight. , preferably at less 90% by weight, even more preferably substantially 100% by weight of said waxy matrix 3.
- said waxy matrix 3 is mainly formed by weight, preferably in totality, of a plurality of different organosilicon materials, that is to say that said organosilicon material is in this case formed of a plurality of different organosilicon compounds.
- Said waxy matrix 3 may optionally comprise, in addition to said organosilicon material, at least one other waxy material such as a natural, mineral and / or synthetic wax, a fatty substance which is solid at room temperature resulting from the fractionation of one or more oil (s). ) natural and / or synthetic (s), a natural and / or synthetic resin, a silicone wax or silicone polymer, or a mixture of these.
- a natural, mineral and / or synthetic wax such as a natural, mineral and / or synthetic wax, a fatty substance which is solid at room temperature resulting from the fractionation of one or more oil (s). ) natural and / or synthetic (s), a natural and / or synthetic resin, a silicone wax or silicone polymer, or a mixture of these.
- said organosilicon material (or the plurality of different organosilicon materials) is part of the silsesquioxane family, which have the general formula (RSi03 / 2) n, R representing a carbon group in particular of alkane, alkene, aryl or arylene, while usually Si represents a silicon atom, and O represents an oxygen atom, n representing an integer generally greater than 1, for example between 3 and 20, such as equal to 8. More advantageously further, said organosilicon material is a silsesquioxane polymer. Said organosilicon material is preferably an organosilicon material.
- said organosilicon material is polymethylsilsesquioxane.
- said waxy matrix 3 comprises polymethylsilsesquioxane, and preferably is mainly formed by the latter, or even almost completely or totally formed by the latter.
- Polymethylsilsesquioxane is thus, advantageously, a type of organosilicon material which is particularly effective when it is used as a waxy matrix 3, alone or optionally in admixture with another waxy material such as another organosilicon material or one of the waxy materials described above (natural wax, resin, etc.).
- the waxy matrix 3 also comprises, mainly (by weight) or not, cyclopentasiloxane, at least one alkyl (C30 to C45) -methicone and / or esters hydrogenated such as the hydrogenated esters of vegetable oils, for example a hydrogenated ester of olive oil of INCI name “Hydrogenated olive oil stearyl esters”.
- said waxy matrix 3 can optionally be formed from a mixture of several substances, in particular from those mentioned above, the polymethylsilsesquioxane advantageously remaining in the majority by weight.
- said waxy matrix 3 is substantially solid at room temperature, and in particular below 30 ° C, preferably below 45 ° C, more preferably below 55 ° C, more preferably still below 65 ° C.
- said waxy matrix 3 is advantageously substantially fluid at a temperature above ambient temperature, and for example a temperature equal to or greater than 30 ° C, preferably 45 ° C, more preferably 55 ° C, and even more preferably 65 ° C.
- said waxy matrix 3 has a melting point and / or a softening point of between 30 and 150 ° C inclusive, more preferably between 45 and 130 ° C inclusive, more preferably still between 55 and 130 ° C. included.
- said waxy matrix 3 has a melting point and / or a softening point of between 55 and 150 ° C inclusive, for example between 55 and 95 ° C inclusive or between 95 and 150 ° C included.
- Said waxy matrix 3 has for example a density of approximately between 0.80 and 1.5, preferably between 0.9 and 1.3, for example of 1.24 approximately in the case where the waxy matrix 3 is mainly, or even totally formed of polymethylsilsesquioxane.
- its softening point is advantageously between 55 and 150 ° C, or even between 75 and 90 ° C.
- Said waxy matrix 3 is preferably formed by a material having general physical characteristics similar or equivalent to those of waxes, and in particular a material which fluidizes significantly above a certain temperature, that is to say a material that loses its strength or changes from a very high viscosity to a much lower viscosity when heated to a certain temperature or above.
- said waxy matrix 3 is formed by a substantially hot-melt and / or thermoplastic material, and significantly softens and / or melts when heated to or above a certain temperature, for example 65 ° C. .
- Said waxy matrix 3 is therefore preferably solid at temperature ambient and preferably becomes substantially fluid when it is brought to a certain temperature above ambient temperature, in particular above its melting and / or softening point.
- the waxy matrix 3 can advantageously be formed, at ambient temperature, of solid granules which are distinct from each other, that is to say which are difficult to compact or which cannot be compacted by mechanical pressure.
- said compound 1 is solid at room temperature and intended to be dispersed by fluidization and / or solubilization within a cosmetic and / or dermatological composition in order to integrate said functional agent therein.
- compound 1 has, at room temperature or even below 30 ° C or even below 45 ° C for example, a relatively firm, non-flaccid consistency, that is to say a minimum mechanical strength, the clearly differentiating from a fluid and in particular from a liquid.
- said compound 1 is in the form of granules, for example pellets or rods 4, obtained by extrusion, as illustrated in FIGS. 1 and 3. Said compound 1 is preferably intended to be integrated or incorporated within d.
- compound 1 is advantageously intended to be mixed, preferably in a homogeneous manner, with components which are acceptable from a cosmetic and / or dermatological point of view, to form a cosmetic and / or dermatological composition.
- the incorporation of compound 1 within a cosmetic and / or dermatological composition is, as will be seen in more detail below with the process, carried out by one and / or the other of the actions following: with the aid of a fluidization, obtained by heating, of said compound 1, that is to say a loss of the solid character of said compound 1, generally via softening or melting (at least partially, since the particles solids advantageously do not fluidify) of the latter and / or of the waxy matrix 3.
- the mixture provided for the fluidized (“hot”) compound 1 with components which are acceptable from a cosmetic and / or dermatological point of view to form a cosmetic and / or dermatological composition can be facilitated because said other components are advantageously also mainly in fluid form (“hot” themselves or not).
- a solubilization of said compound 1 by one or more of the other components of a cosmetic and / or dermatological composition these other components preferably being mainly in fluid form, at least one of these components being capable of solubilize said compound 1, in particular even when the latter is “cold” (that is to say at room temperature, in particular around 20 ° C or below 30 ° C), said component 1 being able of course of course possibly be “hot” (in this case, we will rather speak of mixing by fluidization as described above, a combination of fluidization and solubilization obviously being possible).
- compound 1 comprises a waxy matrix 3 formed mainly from a silicone wax, which is easily dissolved by components which are acceptable from a cosmetic and / or dermatological point of view, in particular. of oil type, said compound 1 then also being advantageously easily soluble in said components which are acceptable from a cosmetic and / or dermatological point of view to form a cosmetic and / or dermatological composition.
- said waxy matrix 3 is designed to be able to be solubilized at room temperature, that is to say advantageously at a temperature below 30 ° C, more advantageously below 25 ° C (and optionally above 15 ° C). ), for example about 20 ° C (+/- 2 ° C), in a fatty phase (that is to say an oil phase) of said cosmetic and / or dermatological composition.
- Said organosilicon material is thus advantageously easily dissolved at room temperature in a fatty phase of a cosmetic and / or dermatological composition.
- Said compound 1 (therefore integrating said waxy matrix 3) can advantageously be solubilized at ambient temperature, that is to say preferably at a temperature below 30 ° C, more advantageously below 25 ° C (and optionally above 15 ° C).
- ° C for example approximately 20 ° C (+/- 2 ° C), in a fatty phase (that is to say an oil phase) of said cosmetic and / or dermatological composition.
- Such a configuration makes it possible to dissolve "cold", that is to say at room temperature (in practice generally between 18 and 25 ° C approximately), compound 1 in different types of oil which can be integrated into a composition.
- cosmetic and / or dermatological Such a configuration makes it possible to dissolve "cold", that is to say at room temperature (in practice generally between 18 and 25 ° C approximately), compound 1 in different types of oil which can be integrated into a composition. cosmetic and / or dermatological.
- Said cosmetic and / or dermatological composition may be intended directly for a user, or form an intermediate product itself intended to integrate a cosmetic and / or dermatological product itself final, intended for a user, or an intermediate.
- compound 1 When cold, that is to say at room temperature, compound 1 therefore advantageously constitutes a solid dispersion, in the manner of a set of solid particles 2 dispersed within the waxy matrix 3 which is also solid when cold.
- such a configuration makes it possible in particular to overcome the constraints linked to the often naturally pulverulent nature of said solid particles 2 alone.
- compound 1 is appreciably easier to manage, that is to say to store, transport and handle, than said particles 2 alone, in particular because the compound 1 is for example at temperature.
- ambient in the form of small solids (for example granules of the pellet or rod type 4), coherent, relatively inert, and easily handled, while said particles 2, when alone, on the contrary often have an extremely fractionated character , powdery, with high reactivity and high dispersibility in air.
- Compound 1 is advantageously formed, at room temperature, of solids which are distinct from one another, preferably of reduced size, such as granules, for example sticks of pellets 4, said distinct solids preferably being difficult or not compactable by mechanical pressure.
- said compound 1 is easy to store and easily transportable, in the form of said separate (small) solids packed in bulk in containers, for example bags, of several kilograms or several tens of kilograms (at least), without said separate solids not being become integral with each other, for example by agglomeration, by coalescence, by crushing, or by sedimentation.
- said compound 1 is preferably easy to store and transport in the form of said solids distinct from each other, and which remain distinct from each other during transport and / or storage, even when (s ) is / are carried out using containers of the bag type each weighing, with their contents (formed by said separate solids), several kilograms or tens of kilograms.
- the separate solids, formed of compound 1 preferably remain easy to handle even after having been stored and / or transported within said containers, and this thanks to the absence of joining of said separate solids even when they are packed in bulk, said solids distinct retaining their respective unitary character in spite of crowding.
- the transport described above is preferably carried out at room temperature or a temperature slightly warmer than room temperature, but which advantageously remains below the melting and / or softening point of said waxy matrix 3.
- compound 1 is not only practical to transport and store, but also to quantify when it has to be dispersed within a cosmetic and / or dermatological composition, said distinct solids, and in particular granules (for example lozenges or sticks 4). This makes it possible in particular to easily quantify the quantity of functional agent to be obtained in the final cosmetic and / or dermatological composition, which implies excellent repeatability as regards the formulation of the latter by virtue of the compound 1.
- said solid particles 2 have undergone a surface treatment resulting in a decrease in the absorption capacity of waxy matrix 3 by said solid particles 2 treated, compared to solid particles of the same nature that are untreated.
- said solid particles 2, which form the functional agent of compound 1 have advantageously undergone a surface treatment making it possible to “saturate” them more quickly with a waxy matrix 3, that is to say to 'using a smaller amount of waxy matrix 3 compared to an amount of solid particles 2 considered.
- the absorption limit (or “saturation”) of waxy matrix 3 by a quantity of solid particles 2 (treated or not) is tested as follows: a quantity (more than necessary) of waxy matrix 2 (preferably formed by an organosilicon material and in particular polymethylsilsesquioxane) is heated to be fluidized, for example heated to 65 °, and is added dropwise to a considered quantity of solid particles 2 (treated or not), which are preferably subjected at the same time to a mixing or triturating action; the mixture of solid particles 2 / drops of waxy matrix 3 mixed or triturated will first form an extremely viscous or even solid or almost solid paste, in the manner of modeling clay for example, then will, with the addition of 'an additional drop of waxy matrix 3, see its viscosity drop significantly and / or change from a solid or quasi-solid state to a fluid or quasi-fluid state (liquid or softened in particular).
- a quantity (more than necessary) of waxy matrix 2 preferably formed by an organosilicon material and
- Said surface treatment therefore advantageously makes it possible to reduce the quantity of fluidized waxy matrix 3 to be added to a considered quantity of solid particles 2 so that their mixture loses its consistency, that is to say passes from a very viscous, solid state. or near-solid, in a significantly less viscous, fluid or near-fluid state.
- the surface treatments making it possible to bring about a reduction in the absorption capacity of the waxy matrix are known as such and are available according to many alternatives, the invention obviously not being limited to a particular treatment.
- the surface treatment of the solid particles 2 implemented in the context of the invention may be based on a treatment based on amino acids, for example N-acylamino acids such as acid N-acyl-L-glutamic, and be advantageously in accordance with the teaching of US Pat. No. 4,606,914.
- the surface treatment is based on a treatment based on amino acids in the form of metal salts of N-acylamino acid, such as a salt made from sodium myristoyl glutamate and hydroxide d 'aluminum.
- the surface treatment can for example be based on: a treatment implementing disodium stearoyl glutamate, as well as advantageously aluminum dimyristate and triethoxycaprylylsilane; a treatment using an alkoxysilane such as triethoxycaprylylsilane; a treatment in accordance with the teaching of US Pat. No. 6482441, a treatment using a silicone polymer such as dimethicone, a treatment using a fatty acid, a treatment implementing one or more phospholipids, a treatment using a hydrogenated olive oil ester, etc.
- Said solid particles 2 having undergone a surface treatment are for example formed of crude pigments (preferably more than 90% by weight), sodium myristoyl glutamate (preferably less than 10% by weight) and a hydroxide of aluminum (preferably less than 10% by weight), according to a purely illustrative and non-limiting example.
- the surface treatment making it possible to bring about a reduction in the absorption capacity of the waxy matrix can also be formed by a combination of the various treatments listed above.
- the surface treatments making it possible to bring about a reduction in the absorption capacity of the waxy matrix also advantageously make it possible to increase the hydrophobic character of the solid particles 2 treated, and / or to improve their dispersibility in the oil phase, compared with solid particles of the same nature untreated.
- said functional agent forms (strictly) more than 50%, preferably more than 60%, more preferably at least 70%, more preferably still at least 80%, still more preferably at least 85% or even at least 90 %, by weight, of said compound 1.
- at least 70%, preferably at least 80%, or even at least 85%, by weight, of said compound 1 is formed by said solid particles 2.
- said waxy matrix preferably forms between 5 and 25%, preferably between 7 and 22%, more preferably between 15 and 20%, by weight, of compound 1.
- a relatively small amount of waxy matrix 3 is sufficient to serve as a support for a relatively large amount of solid particles 2.
- the compound 1, when it is fluidized and / or solubilized, and by extension the functional agent which it contains (and more precisely said solid particles 2), can be dispersed or mixed ( s) in a homogeneous and stable manner within a cosmetic and / or dermatological composition.
- the functional agent which it contains and more precisely said solid particles 2
- the waxy matrix 3, and by extension the compound 1, advantageously acts as a support for the functional agent before its redispersion in a cosmetic and / or dermatological composition.
- the redispersion of compound 1 can be carried out by fluidization and therefore heating of compound 1 until it becomes fluid, to mix it more easily with components which are acceptable from a cosmetic and / or dermatological point of view, themselves fluid. , or by dissolving compound 1, preferably in the form of small solids (granules in particular, for example pellets or rods 4), optionally cold (that is to say without heating), within acceptable components from a cosmetic and / or dermatological point of view also fluid.
- the relatively small or limited amount of waxy matrix 3 within said compound 1, as well as the nature of organosilicon material (such as polymethylsilsesquioxane) thereof, advantageously allows said compound 1 to be able to be integrated into a very wide range of cosmetic and / or dermatological compositions.
- the design of compound 1 advantageously makes it possible to integrate said functional agent which it contains within a cosmetic and / or dermatological composition, without constraint or practically without constraint vis-à-vis the others. components of the latter, that is to say without needing to modify these other components forming said cosmetic and / or dermatological composition in order to adapt them to said compound 1.
- compound 1 of the invention is advantageously capable of be integrated into a wide variety of cosmetic and / or dermatological compositions.
- the waxy matrix 3, and in particular the organosilicon material which forms it in part or in whole preferably consisting of polymethylsilsesquioxane
- has a high film-forming character which is particularly advantageous in cosmetic and / or dermatological compositions intended to be used on a user's hair.
- Compound 1 can thus be intended to be dispersed in a composition cosmetic and / or dermatological not only to integrate the functional agent therein but also to integrate therein a character specific to the waxy matrix 3, for example the film-forming character of the waxy matrix 3 mentioned above, in particular when the organosilicon material which forms it in part or in whole is polymethylsilsesquioxane.
- said waxy matrix 3 is liposoluble and / or insoluble or almost insoluble in water.
- the waxy matrix 3 which advantageously has physical characteristics close to or similar to those of natural or synthetic waxes (and in particular silicone waxes), preferably has a lipophilic, liposoluble and / or hydrophobic character.
- the waxy matrix 3 is dissolved in particular in the oil phases commonly used in the manufacture of cosmetic and / or dermatological compositions.
- the waxy matrix 3 is intended to relatively easily integrate the cosmetic and / or dermatological composition in which the compound is itself intended to be integrated, preferably without significantly modify the physical and / or chemical properties of said composition, and this all the more easily when said composition has a fatty or oil phase (and / or lipophilic) optionally in an emulsion of the water in oil, water in oil, for example of the water-in-silicone type, or alternatively of the oil-in-water type.
- Said compound 1 may optionally be intended to be redispersed to form part of a cosmetic and / or dermatological composition comprising only one anhydrous phase, preferably of the fatty / oil / silicone type, said composition being for example a balm, a red lip, etc.
- said surface treatment also makes it possible to increase the lipophilic and / or hydrophobic character of the solid particles 2 treated, compared to solid particles 2 of the same nature that are untreated.
- the surface treatment confers on said solid particles 2 or reinforces in the latter a chemical affinity for fats and fats and the like of which said waxy matrix 3 advantageously forms part.
- Such a characteristic makes it possible in particular to obtain a better dispersion. solid individuals 2 within said waxy matrix 3 and / or a better dispersion of said compound 1 (and therefore solid particles 2 themselves) within a cosmetic and / or dermatological composition (itself comprising in particular a oil phase or the like).
- said surface treatment involves a grafting of molecules 5 to the respective surface of said particles 2, as illustrated in FIG. 2.
- said grafted molecules 5 comprise at least silicone chains, carbon chains, natural polymers or synthetic, organic molecules, or oxides of titanium or silicon.
- said compound 1 comprises in particular said waxy matrix 3 and said treated particles 2, which are provided with and / or comprise said grafted molecules 5.
- Said treated particles 2 are preferably dispersed regularly within the waxy matrix. 3, at least in part thanks to said grafted molecules 5, the presence of which thus preferentially reinforces the lipophilic and / or hydrophobic character of the particles 2 and / or advantageously decreases their capacity for absorbing the waxy matrix 3.
- said functional agent and said waxy matrix 3 together form at least 95%, preferably at least 97%, more preferably at least 99%, by weight, more preferably still all, of said compound 1.
- compound 1 does not comprise a surfactant, that is to say that it does not in particular comprise any substance whose primary function is to lower the surface tension, or else that compound 1 comprises a such substance but in a non-useful quantity, negligible by weight relative to the waxy matrix 3 and / or to the functional agent.
- the invention also relates as such, according to a second aspect partly illustrated by an exemplary embodiment in FIG. 3, a process for the manufacture of a compound 1, which is preferably compound 1 as described above (and below).
- the process of the invention makes it possible to manufacture a compound 1 comprising at least 50% by weight of a functional agent, preferably as mentioned above, said compound 1 optionally comprising (strictly) more than 50%, of preferably (strictly) more than 60%, more preferably at least 70%, by weight, more preferably still at least 80%, by weight or even at least 85%, by weight of said functional agent.
- the above description relating to compound 1 therefore also applies advantageously to the manufacturing process according to the invention (and conversely, the following description relating to the manufacturing process therefore also applies to compound 1 according to the invention).
- the manufacturing process comprises at least one step of heating ⁇ a waxy matrix 3 comprising at least one organosilicon (or organosilicon) material in order to obtain a fluid matrix 3.
- Said organosilicon material forms the major part in weight, preferably all, of said waxy matrix 3.
- the organosilicon material forms at least 50% by weight, advantageously at least 75% by weight, preferably at least 90% by weight, even more preferably substantially 100% by weight of said waxy matrix 3.
- Said waxy matrix 3 is preferably that already mentioned above, while said organosilicon material is also preferably as mentioned above, and is in particular polymethylsilsesquioxane.
- said waxy matrix 3 is heated, for example using at least one resistance or by convection, until it is fluidized, that is to say molten or sufficiently softened to no longer have the consistency of a solid, thus forming a fluid waxy matrix 3.
- said waxy matrix 3 is advantageously heated to a temperature equal to or greater than its melting point and / or softening.
- said waxy matrix 3 is for example heated to a temperature between 30 and 150 ° C inclusive, more preferably between 45 and 130 ° C inclusive, in order to be fluidized, or even at a temperature between 55 and 95 ° C inclusive or between 55 and 150 ° C inclusive.
- said cold waxy matrix 3 is thus substantially solid, while when hot, above a certain temperature, it is substantially fluid.
- the expression “fluid matrix” therefore designates the waxy matrix 3 heated until fluidization.
- the method further comprises a step of dispersing D said functional agent, formed of solid particles 2, within said fluid matrix 3.
- Said step of dispersing D advantageously comprises at least one step M of mixing said particles. 2 treated and said waxy matrix 3, the latter possibly being cold, in solid form, or hot, in fluidized form.
- Said solid particles 2 are preferably as mentioned above.
- the method also comprises a treatment step T (not shown) of said solid particles 2 during which the latter undergo a surface treatment resulting in a decrease in the absorption capacity of the fluid matrix 3 by the solid particles 2 treated, compared to solid particles of the same untreated nature, said treated solid particles 2 forming said functional agent.
- said treatment step T advantageously involves, as explained above, a grafting of molecules 5 to the respective surface of said particles 2 and / or an increase in the lipophilic and / or hydrophobic character of the solid particles 2 treated, compared with solid particles of the same nature untreated.
- said compound 1 is solid at room temperature and intended to be dispersed by fluidization and / or solubilization within a cosmetic and / or dermatological composition in order to integrate said functional agent therein, advantageously as described above.
- the method further comprises a step B of grinding said solid particles 2 aimed at reducing their average size.
- said solid particles 2 at the end of said grinding step B, said solid particles 2 have an average size substantially between 10 nm and 500 ⁇ m, preferably between 100 nm and 100 ⁇ m.
- said dispersion phase D comprises at least part of said grinding step B, so that during at least part of the latter, said fluid matrix 3 is mixed with said particles 2.
- the method further comprises a step of extruding said compound 1 so that the latter is in the form of granules, for example pellets or rods 4.
- the extrusion step E is carried out hot, said compound 1 exhibiting during this step a temperature of between 60 and 80 ° C.
- the process also comprises, after the dispersion step D, a cooling step F during which said compound 1 cools to room temperature so as to form a solid.
- the method successively involves: said mixing step M, during which the solid particles 2 treated and the waxy matrix 3 are mixed cold, the matrix 3 being solid, cold (room temperature), in the form of solid pellets, while the particles 2 are in coarse form, with too large a particle size and therefore unacceptable, then said heating step C, during which the waxy matrix 3 is heated and therefore fluidized, at the same time as the particles 2, which remain solid, then said grinding step B, during which the particles 2 are ground to an acceptable particle size, while being / remaining intimately mixed with the fluid matrix 3 which itself also undergoes, in a way, grinding, then a homogenization step H, during which the mixture formed by the crushed particles 2 and the matrix fl uide 3 is homogenized by any suitable means (agitation, blowing, shearing, etc.), then said extrusion step E, during which the hot mixture is compressed in order to pass through a die 6 to obtain a long product in the shape of a cylinder,
- the method advantageously involves the use of a heating twin-screw extruder 7, within which the steps described above are carried out.
- the invention also relates as such, according to a third aspect, to a method of manufacturing a cosmetic and / or dermatological composition, comprising a redispersion step R during which a compound 1, as described above is added to then mixed with one or more components acceptable in cosmetics and / or dermatology.
- a redispersion step R during which a compound 1, as described above is added to then mixed with one or more components acceptable in cosmetics and / or dermatology.
- said step of redispersion R further comprises a step of dissolving said compound 1 by one or more of said components which are acceptable in cosmetics and / or dermatology.
- said solubilization step comprises at least the solubilization (that is to say in particular the dispersion) of compound 1 within a fatty phase (in particular oil) or of a portion of said fatty phase of said cosmetic and / or dermatological composition.
- said redispersion step R further comprises a fluidization step, in which said added compound 1 is heated at least until fluidization, for example at a temperature above 50 ° C, which can be between 55 and 85 ° C.
- Said redispersion step R can also comprising said solubilization step and said fluidization step, for example one after the other or according to another example concomitantly.
- one or more of said components which are acceptable in cosmetics and / or in dermatology are substantially fluid at room temperature, facilitating the preparation. redispersion of said compound 1, whether via its solubilization and / or via its fluidization.
- the waxy matrix 3 of compound 1 of the invention is mainly or even totally formed (by weight) of said organosilicon material makes it possible in particular to obtain excellent dispersibility of compound 1 within a cosmetic and / or dermatological composition. , and more precisely within a fatty phase (oil) of such a composition.
- the waxy matrix 3 of compound 1, the invention allows in particular the solid particles 2 of compound 1 to be (re) dispersed effectively, without particular difficulty, or even without heating, that is to say at room temperature, with other components to form a cosmetic and / or dermatological composition, and in particular to color it when said solid particles 2 are pigments.
- Said solubilization step is thus, according to a particular embodiment, carried out (in particular within said fatty phase) at a temperature below 30 ° C, preferably below 25 ° C (and optionally above 15 ° C) , for example about 20 ° C (+/- 2 ° C).
- said redispersion step R therefore advantageously does not include heating of compound 1, and preferably no heating either of the cosmetic and / or dermatological composition, and in particular of the fatty phase ( oil) of the latter.
- Said solubilization step can therefore advantageously be carried out “cold”, that is to say at room temperature (in practice generally between 18 and 25 ° C approximately), thus saving energy and avoiding potential degradation due to the heat of one or more of the components of the cosmetic and / or dermatological composition, and in particular of the fatty phase of the latter.
- Said redispersion step R then does not include the step of fluidization by heating of compound 1, thanks to the properties of the organosilicon material chosen to form the waxy matrix 3, in particular polymethylsiisesquioxane.
- the organosilicon material of the waxy matrices 3 of the examples of compounds C1 to C3 is in particular polymethylsiisesquioxane.
- Compounds C1 to C6 were produced according to Table 1, and therefore each result from a mixture of respective solid particles (here pigments) and respective waxy matrix.
- the examples of compounds C1 to C6 are all in the form of solid granules at room temperature (approximately 20 to 25 ° C.).
- the solid particles 2 of the compounds C1 to C6 are in these non-limiting examples treated pigments, that is to say which solid particles 2 (of pigment type) having undergone a surface treatment resulting in a decrease in the absorption capacity of waxy matrix.
- the respective trade names (at the filing date of the present patent application) of these treated pigments are given in Table 1. These treated pigments are marketed under their respective trade names in particular by the company Miyoshi.
- the surface treatment of the pigments (which are solid particles) of the examples of compounds C1 to C6 can for example be carried out here with a treatment based on amino acids, preferably in accordance with the teaching of US Pat. No. 4,606,914, amino acids in particular in the form of metal salts of N-acylamino acid.
- said surface treatment consists for example in coating solid particles (and in particular pigments) raw, that is to say untreated, with, by weight of raw solid particles, 0.5 to 10% of one or more metal salts of N-acylamino acid (s).
- the N-acylamino acid is for example an N-acyl-L-glutamic acid, while the metal is for example aluminum, magnesium, calcium, zinc or even titanium.
- the metal salt of N-acylamino acid is for example made using sodium myristoyl glutamate and aluminum hydroxide.
- Such a surface treatment can in particular be used for the examples presented here, by way of illustration and without limitation, as well as in the rest of the description above and below.
- Said surface treatment, in particular said treatment with the aid of metal salts of N-acylamino acid preferably increases the hydrophobic character and the dispersibility in oil of the solid particles 2 treated relative to the raw solid particles (untreated ).
- the dispersibility of the examples of compounds C1 to C3 in accordance with the invention was then compared with that of the examples of compounds C4 to C6 not in accordance with the invention, by dispersing each of the examples of compounds C1 to C6 within a body respective liquid fat, always of the same nature and in the same proportions, the liquid fatty substance being chosen from the following components: linear silicone oil of dimethicone type, cyclic silicone oil of cyclopentasiloxane type, and branched silicone oil of methyl trimethicone type.
- the ratio (by weight) of the example compound (C1 to C6) and the fat is 1: 9.
- the dispersion (solubilization in this case) of the examples of compounds C1 to C6 was carried out with homogenization at 6000 rpm, for 5 to 15 min, at room temperature (between 20 and 25 ° C. approximately).
- each example of compound C1 to C6 within their respective liquid fatty substances makes it possible to obtain respective mixtures M1 to M6 (Mx therefore corresponds to the solubilization of the example of compound Cx in a respective liquid fatty substance, with x between 1 and 6).
- Mx therefore corresponds to the solubilization of the example of compound Cx in a respective liquid fatty substance, with x between 1 and 6.
- the dispersibility of the examples of compounds C1 to C3 (with matrix of organosilicon material) and of the examples of compounds C4 to C6 (with matrix of non-organosilicon material) was compared by observing the mixtures C1 to C6:
- the dispersibility of the examples of solid compounds 1 C1 to C3 comprising the waxy matrix 3 containing organosilicon material is complete (excellent solubilization) regardless of the type of pigments (solid particles 2) used, while the examples of solid C4 to C6 compounds with a non-organosilicon waxy matrix only dissolve incompletely (at room temperature here), their pigments forming unwanted lumps and agglomerates.
- the invention thus makes it possible to obtain a compound 1 comprising a high content of functional agent and facilitating the transport, storage and handling of the latter.
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Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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FR1904461A FR3095341B1 (en) | 2019-04-26 | 2019-04-26 | COMPOUND CONSISTING OF A FUNCTIONAL AGENT AND A WAX DIE INCLUDING AN ORGANOSILICIAL MATERIAL, AND RELATED MANUFACTURING PROCESS |
PCT/FR2020/050693 WO2020217024A1 (en) | 2019-04-26 | 2020-04-23 | Compound comprising a functional agent and a waxy matrix including an organosilicon material, and associated manufacturing method |
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EP3958986A1 true EP3958986A1 (en) | 2022-03-02 |
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EP20754313.3A Withdrawn EP3958986A1 (en) | 2019-04-26 | 2020-04-23 | Compound comprising a functional agent and a waxy matrix including an organosilicon material, and associated manufacturing method |
Country Status (6)
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US (1) | US20220183957A1 (en) |
EP (1) | EP3958986A1 (en) |
JP (1) | JP2022531145A (en) |
CN (1) | CN114040748A (en) |
FR (1) | FR3095341B1 (en) |
WO (1) | WO2020217024A1 (en) |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
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BE596623A (en) * | 1959-10-29 | |||
DE2652628C2 (en) * | 1976-11-19 | 1984-08-23 | Hoechst Ag, 6230 Frankfurt | Pigment preparations based on polypropylene wax |
NL193146C (en) * | 1980-01-24 | 1998-12-04 | Holland Colours Apeldoorn Bv | A method of preparing a particulate dye composition. |
JPS5872512A (en) | 1981-10-26 | 1983-04-30 | Miyoshi Kasei:Kk | Make-up cosmetic |
DE3151753A1 (en) * | 1981-12-29 | 1983-07-07 | Basf Ag, 6700 Ludwigshafen | HIGHLY CONCENTRATED, NON-DUSTING, SOLID AND EASILY DISTRIBUTABLE PIGMENT PREPARATION AND THEIR USE |
JPH0693201A (en) * | 1992-09-09 | 1994-04-05 | Tokyo Ink Kk | Color masterbatch and processed pigment |
US6024969A (en) * | 1996-07-29 | 2000-02-15 | Societe L'oreal S.A. | Cosmetic/dermatological compositions formulated as supple doughs |
US6316547B1 (en) * | 1997-09-11 | 2001-11-13 | The Procter & Gamble Company | Masterbatch composition |
DE19855058A1 (en) * | 1998-11-28 | 2000-06-15 | Goldschmidt Ag Th | Micronized polyolefins for the production of pigment concentrates |
JP4602506B2 (en) | 1999-07-08 | 2010-12-22 | 三好化成株式会社 | Novel coated powder having super-dispersibility and cosmetics containing the same |
PL2173793T3 (en) * | 2007-07-10 | 2013-09-30 | Lionel Nicholas Mantzivis | Masterbatch preparation process |
WO2012087905A2 (en) * | 2010-12-21 | 2012-06-28 | Lubrizol Advanced Materials, Inc. | Thermoplastic composition |
FR2990853B1 (en) * | 2012-05-22 | 2014-06-13 | Rhodia Poliamida E Especialidades Ltda | COSMETIC COMPOSITION CONTAINING PARTICLE DISPERSION BASED ON POLYMER AND MINERAL CHARGES |
CN104059273A (en) * | 2014-06-16 | 2014-09-24 | 蓝星(成都)新材料有限公司 | Special polyethylene coloring masterbatch for white thin film and preparation method of masterbatch |
WO2018213855A1 (en) * | 2017-05-15 | 2018-11-22 | Lionel Mantzivis | A process for preparing a masterbatch and a masterbatch |
-
2019
- 2019-04-26 FR FR1904461A patent/FR3095341B1/en active Active
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2020
- 2020-04-23 WO PCT/FR2020/050693 patent/WO2020217024A1/en unknown
- 2020-04-23 JP JP2021563208A patent/JP2022531145A/en active Pending
- 2020-04-23 CN CN202080045803.2A patent/CN114040748A/en active Pending
- 2020-04-23 EP EP20754313.3A patent/EP3958986A1/en not_active Withdrawn
- 2020-04-23 US US17/606,417 patent/US20220183957A1/en active Pending
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WO2020217024A1 (en) | 2020-10-29 |
US20220183957A1 (en) | 2022-06-16 |
FR3095341B1 (en) | 2021-05-14 |
JP2022531145A (en) | 2022-07-06 |
FR3095341A1 (en) | 2020-10-30 |
CN114040748A (en) | 2022-02-11 |
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