EP2097077A1 - Compositions comprenant du peroxyde de benzoyle, au moins un derive de l'acide naphtoïque et au moins un compose de type polymeres de polyurethane ou des derives de celui-ci, et leurs utilisations - Google Patents
Compositions comprenant du peroxyde de benzoyle, au moins un derive de l'acide naphtoïque et au moins un compose de type polymeres de polyurethane ou des derives de celui-ci, et leurs utilisationsInfo
- Publication number
- EP2097077A1 EP2097077A1 EP07858750A EP07858750A EP2097077A1 EP 2097077 A1 EP2097077 A1 EP 2097077A1 EP 07858750 A EP07858750 A EP 07858750A EP 07858750 A EP07858750 A EP 07858750A EP 2097077 A1 EP2097077 A1 EP 2097077A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition according
- naphthoic acid
- composition
- benzoyl peroxide
- acne
- 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- Withdrawn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
- 239000000203 mixture Substances 0.000 title claims abstract description 154
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 title claims abstract description 88
- 239000004814 polyurethane Substances 0.000 title claims abstract description 38
- 229920002635 polyurethane Polymers 0.000 title claims abstract description 38
- 150000001875 compounds Chemical class 0.000 title claims abstract description 31
- 239000002253 acid Substances 0.000 title claims description 6
- 239000004342 Benzoyl peroxide Substances 0.000 claims abstract description 86
- 235000019400 benzoyl peroxide Nutrition 0.000 claims abstract description 86
- 150000005209 naphthoic acids Chemical class 0.000 claims abstract description 38
- 239000002537 cosmetic Substances 0.000 claims abstract description 9
- 239000012071 phase Substances 0.000 claims description 53
- 206010000496 acne Diseases 0.000 claims description 51
- 208000002874 Acne Vulgaris Diseases 0.000 claims description 49
- LZCDAPDGXCYOEH-UHFFFAOYSA-N adapalene Chemical compound C1=C(C(O)=O)C=CC2=CC(C3=CC=C(C(=C3)C34CC5CC(CC(C5)C3)C4)OC)=CC=C21 LZCDAPDGXCYOEH-UHFFFAOYSA-N 0.000 claims description 45
- 229920000642 polymer Polymers 0.000 claims description 41
- 239000000499 gel Substances 0.000 claims description 36
- 239000006071 cream Substances 0.000 claims description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 31
- 239000003349 gelling agent Substances 0.000 claims description 27
- 239000000839 emulsion Substances 0.000 claims description 25
- 239000003995 emulsifying agent Substances 0.000 claims description 22
- 238000003756 stirring Methods 0.000 claims description 22
- 238000002360 preparation method Methods 0.000 claims description 21
- 239000000080 wetting agent Substances 0.000 claims description 20
- 239000003755 preservative agent Substances 0.000 claims description 19
- 239000000126 substance Substances 0.000 claims description 18
- 239000002738 chelating agent Substances 0.000 claims description 17
- 239000006185 dispersion Substances 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 16
- 239000003974 emollient agent Substances 0.000 claims description 15
- 239000008346 aqueous phase Substances 0.000 claims description 14
- 239000003921 oil Substances 0.000 claims description 14
- 239000000375 suspending agent Substances 0.000 claims description 14
- 239000004480 active ingredient Substances 0.000 claims description 11
- 239000003381 stabilizer Substances 0.000 claims description 11
- 238000011282 treatment Methods 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 239000006210 lotion Substances 0.000 claims description 9
- 239000003814 drug Substances 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 8
- 229920002401 polyacrylamide Polymers 0.000 claims description 8
- 239000004094 surface-active agent Substances 0.000 claims description 8
- GNFTZDOKVXKIBK-UHFFFAOYSA-N 3-(2-methoxyethoxy)benzohydrazide Chemical compound COCCOC1=CC=CC(C(=O)NN)=C1 GNFTZDOKVXKIBK-UHFFFAOYSA-N 0.000 claims description 7
- 239000007787 solid Substances 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 6
- 208000035475 disorder Diseases 0.000 claims description 6
- 239000008194 pharmaceutical composition Substances 0.000 claims description 6
- 208000020154 Acnes Diseases 0.000 claims description 5
- 239000000654 additive Substances 0.000 claims description 5
- 230000004663 cell proliferation Effects 0.000 claims description 5
- 230000004069 differentiation Effects 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 208000029443 keratinization disease Diseases 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- 208000002260 Keloid Diseases 0.000 claims description 4
- 206010023330 Keloid scar Diseases 0.000 claims description 4
- 239000012072 active phase Substances 0.000 claims description 4
- 238000013019 agitation Methods 0.000 claims description 4
- 210000001117 keloid Anatomy 0.000 claims description 4
- 230000001338 necrotic effect Effects 0.000 claims description 4
- 230000003472 neutralizing effect Effects 0.000 claims description 4
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 4
- 230000000306 recurrent effect Effects 0.000 claims description 4
- 201000004700 rosacea Diseases 0.000 claims description 4
- 206010039792 Seborrhoea Diseases 0.000 claims description 3
- 230000002265 prevention Effects 0.000 claims description 3
- 239000000725 suspension Substances 0.000 claims description 3
- TVIKMHRYESWHCR-UHFFFAOYSA-N 6-[3-(1-adamantyl)-4-decoxyphenyl]naphthalene-2-carboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C3=CC=C(C(=C3)C34CC5CC(CC(C5)C3)C4)OCCCCCCCCCC)=CC=C21 TVIKMHRYESWHCR-UHFFFAOYSA-N 0.000 claims description 2
- BCLMUIMQCLRLNV-UHFFFAOYSA-N 6-[3-(1-adamantyl)-4-hexoxyphenyl]naphthalene-2-carboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C3=CC=C(C(=C3)C34CC5CC(CC(C5)C3)C4)OCCCCCC)=CC=C21 BCLMUIMQCLRLNV-UHFFFAOYSA-N 0.000 claims description 2
- LDGIHZJOIQSHPB-UHFFFAOYSA-N CD437 Chemical compound C1C(C2)CC(C3)CC2CC13C1=CC(C2=CC3=CC=C(C=C3C=C2)C(=O)O)=CC=C1O LDGIHZJOIQSHPB-UHFFFAOYSA-N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- 239000004530 micro-emulsion Substances 0.000 claims description 2
- 239000003094 microcapsule Substances 0.000 claims description 2
- 239000011859 microparticle Substances 0.000 claims description 2
- 235000013336 milk Nutrition 0.000 claims description 2
- 239000008267 milk Substances 0.000 claims description 2
- 210000004080 milk Anatomy 0.000 claims description 2
- 230000037312 oily skin Effects 0.000 claims description 2
- 239000002674 ointment Substances 0.000 claims description 2
- 238000009736 wetting Methods 0.000 claims description 2
- 230000000087 stabilizing effect Effects 0.000 claims 1
- 230000000699 topical effect Effects 0.000 abstract description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 39
- 229960002916 adapalene Drugs 0.000 description 37
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 20
- 238000009472 formulation Methods 0.000 description 20
- 239000004698 Polyethylene Substances 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 229920001983 poloxamer Polymers 0.000 description 15
- -1 alkyl radical Chemical class 0.000 description 13
- 239000002736 nonionic surfactant Substances 0.000 description 13
- 239000008213 purified water Substances 0.000 description 13
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 12
- 235000019198 oils Nutrition 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 229960001484 edetic acid Drugs 0.000 description 11
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 10
- 235000011187 glycerol Nutrition 0.000 description 10
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 8
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 8
- 239000000470 constituent Substances 0.000 description 7
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 7
- 229920002125 Sokalan® Polymers 0.000 description 6
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 150000004492 retinoid derivatives Chemical class 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 6
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 5
- NWGKJDSIEKMTRX-BFWOXRRGSA-N [(2r)-2-[(3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)C1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-BFWOXRRGSA-N 0.000 description 5
- SHGAZHPCJJPHSC-YCNIQYBTSA-N all-trans-retinoic acid Chemical compound OC(=O)\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C SHGAZHPCJJPHSC-YCNIQYBTSA-N 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 5
- 238000006731 degradation reaction Methods 0.000 description 5
- 230000001804 emulsifying effect Effects 0.000 description 5
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 5
- 229920000053 polysorbate 80 Polymers 0.000 description 5
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- 229940086555 cyclomethicone Drugs 0.000 description 4
- 238000004945 emulsification Methods 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 4
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 4
- 229960002216 methylparaben Drugs 0.000 description 4
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 4
- 229960005323 phenoxyethanol Drugs 0.000 description 4
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 4
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 4
- 229960003415 propylparaben Drugs 0.000 description 4
- 229960001727 tretinoin Drugs 0.000 description 4
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 3
- 239000005711 Benzoic acid Substances 0.000 description 3
- 208000032544 Cicatrix Diseases 0.000 description 3
- ZDQWESQEGGJUCH-UHFFFAOYSA-N Diisopropyl adipate Chemical compound CC(C)OC(=O)CCCCC(=O)OC(C)C ZDQWESQEGGJUCH-UHFFFAOYSA-N 0.000 description 3
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 235000010233 benzoic acid Nutrition 0.000 description 3
- 238000012512 characterization method Methods 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 229940049657 cyclomethicone 5 Drugs 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 3
- 238000000265 homogenisation Methods 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 230000007794 irritation Effects 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 230000002335 preservative effect Effects 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 238000000518 rheometry Methods 0.000 description 3
- 231100000241 scar Toxicity 0.000 description 3
- 230000037387 scars Effects 0.000 description 3
- 229920002545 silicone oil Polymers 0.000 description 3
- 229940074404 sodium succinate Drugs 0.000 description 3
- ZDQYSKICYIVCPN-UHFFFAOYSA-L sodium succinate (anhydrous) Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O ZDQYSKICYIVCPN-UHFFFAOYSA-L 0.000 description 3
- 239000008362 succinate buffer Substances 0.000 description 3
- 239000001384 succinic acid Substances 0.000 description 3
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 2
- BANXPJUEBPWEOT-UHFFFAOYSA-N 2-methyl-Pentadecane Chemical compound CCCCCCCCCCCCCC(C)C BANXPJUEBPWEOT-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- CFKMVGJGLGKFKI-UHFFFAOYSA-N 4-chloro-m-cresol Chemical compound CC1=CC(O)=CC=C1Cl CFKMVGJGLGKFKI-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- SHGAZHPCJJPHSC-NUEINMDLSA-N Isotretinoin Chemical compound OC(=O)C=C(C)/C=C/C=C(C)C=CC1=C(C)CCCC1(C)C SHGAZHPCJJPHSC-NUEINMDLSA-N 0.000 description 2
- 229920003102 Methocel™ E4M Polymers 0.000 description 2
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 206010037888 Rash pustular Diseases 0.000 description 2
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- YTAHJIFKAKIKAV-XNMGPUDCSA-N [(1R)-3-morpholin-4-yl-1-phenylpropyl] N-[(3S)-2-oxo-5-phenyl-1,3-dihydro-1,4-benzodiazepin-3-yl]carbamate Chemical compound O=C1[C@H](N=C(C2=C(N1)C=CC=C2)C1=CC=CC=C1)NC(O[C@H](CCN1CCOCC1)C1=CC=CC=C1)=O YTAHJIFKAKIKAV-XNMGPUDCSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
- POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 description 2
- 229960000686 benzalkonium chloride Drugs 0.000 description 2
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 230000001143 conditioned effect Effects 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 125000002704 decyl 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])* 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- PZZHMLOHNYWKIK-UHFFFAOYSA-N eddha Chemical compound C=1C=CC=C(O)C=1C(C(=O)O)NCCNC(C(O)=O)C1=CC=CC=C1O PZZHMLOHNYWKIK-UHFFFAOYSA-N 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 239000007970 homogeneous dispersion Substances 0.000 description 2
- 229920001477 hydrophilic polymer Polymers 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 229920003111 hydroxyethyl cellulose HHX Polymers 0.000 description 2
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 2
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 2
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 2
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 2
- YCKRDADEZVWYPB-UHFFFAOYSA-N isocyanatocyclohexane Chemical compound O=C=N[C]1CCCCC1 YCKRDADEZVWYPB-UHFFFAOYSA-N 0.000 description 2
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 2
- 229960005280 isotretinoin Drugs 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 230000007170 pathology Effects 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 208000029561 pustule Diseases 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- 239000000230 xanthan gum Substances 0.000 description 2
- 229920001285 xanthan gum Polymers 0.000 description 2
- 235000010493 xanthan gum Nutrition 0.000 description 2
- 229940082509 xanthan gum Drugs 0.000 description 2
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 1
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 description 1
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- CRBBOOXGHMTWOC-NPDDRXJXSA-N 1,4-Anhydro-6-O-dodecanoyl-2,3-bis-O-(2-hydroxyethyl)-D-glucitol Chemical compound CCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](OCCO)[C@H]1OCCO CRBBOOXGHMTWOC-NPDDRXJXSA-N 0.000 description 1
- UXBIXOXDACBTDG-UHFFFAOYSA-N 1-adamantyl radical Chemical compound C1C(C2)CC3C[C]1CC2C3 UXBIXOXDACBTDG-UHFFFAOYSA-N 0.000 description 1
- LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 description 1
- HBXWUCXDUUJDRB-UHFFFAOYSA-N 1-octadecoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCCCC HBXWUCXDUUJDRB-UHFFFAOYSA-N 0.000 description 1
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/06—Ointments; Bases therefor; Other semi-solid forms, e.g. creams, sticks, gels
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/08—Antiseborrheics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/10—Anti-acne agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/004—Aftersun 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
- A61Q19/008—Preparations for oily skin
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/008—Preparations for oily hair
Definitions
- benzoyl peroxide is related to its decomposition when it is brought into contact with the skin. Indeed, it is the oxidizing properties of the free radicals produced during this decomposition that lead to the desired effect. Also, in order to maintain benzoyl peroxide optimal efficiency, it is important to prevent its decomposition before use, ie during storage.
- a stability study of two retinoids was performed by combining two commercial products, one containing retinoid (tretinoin or adapalene) and the second containing benzoyl peroxide (B. Martin et al., Br.J.Dermatol. (1998) 139, (suppl.52), 8-11).
- the presence of the benzoyl peroxide formulation causes a very rapid degradation of the oxidation-sensitive retinoids: it is measured that 50% of the tretinine degrades in 2 hours, and 95% in 24 hours. In the composition in which the retinoid is adapalene, no degradation of adapalene has been measured for 24 hours.
- active in dispersed form is meant an active ingredient in the form of solid particles, suspended in a given vehicle. Such particles in particular have a size greater than 10 microns.
- linear or branched alkyl radical having from 1 to 4 carbon atoms is preferably meant methyl, ethyl, propyl or butyl radicals.
- polyurethane polymers that can be used in the compositions according to the invention, mention may be made of the polyurethane polymers of general formula:
- low-HLB nonionic surfactants examples are:
- esters such as cetearyl isononanoate such as the product sold under the name Cetiol SNPH® by Cognis France, diisopropyl adipate, and the product sold under the name Ceraphyl 230® by the company.
- ISF isopropyl palmitate, such as the product sold under the name Crodamol IPP® by Croda
- caprylic capric triglyceride such as Miglyol 812® sold by HuIs / Lambert Rivière.
- purified water is introduced with stirring, the active ingredient (adapalene), the wetting agents (Synperonic type PE / L62, Synperonic PE / L44, propylene glycol). It is stirred until perfect dispersion.
- Step g Introduction of the single active phase obtained in e) in the aqueous phase obtained in c) for the cream gels and gels or in the phase obtained in f) for the emulsions.
- Simulgel 600PHA is introduced with stirring into the phase obtained in g). Maintain agitation until perfect homogeneity.
- Step c (optional): Preparation of the fatty phase:
- the present invention also relates to the composition as described above as a medicament.
- the invention relates to the use of a composition as described above for the preparation of a pharmaceutical composition for preventing or treating acne vulgaris.
- Stabi lity Data > Physical Stabi lity:
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Dermatology (AREA)
- Birds (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Emergency Medicine (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Inorganic Chemistry (AREA)
- Cosmetics (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0655138A FR2909000B1 (fr) | 2006-11-28 | 2006-11-28 | Compositions comprenant du peroxyde de benzoyle, au moins un derive de l'acide naphtoique et au moins un compose de type polymeres de polyurethane ou des derives de celui-ci, et leurs utilisations. |
| PCT/FR2007/052412 WO2008065306A1 (fr) | 2006-11-28 | 2007-11-28 | Compositions comprenant du peroxyde de benzoyle, au moins un derive de l'acide naphtoïque et au moins un compose de type polymeres de polyurethane ou des derives de celui-ci, et leurs utilisations |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2097077A1 true EP2097077A1 (fr) | 2009-09-09 |
Family
ID=37876974
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP07858750A Withdrawn EP2097077A1 (fr) | 2006-11-28 | 2007-11-28 | Compositions comprenant du peroxyde de benzoyle, au moins un derive de l'acide naphtoïque et au moins un compose de type polymeres de polyurethane ou des derives de celui-ci, et leurs utilisations |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8568704B2 (ru) |
| EP (1) | EP2097077A1 (ru) |
| JP (2) | JP2010520853A (ru) |
| KR (1) | KR20090085077A (ru) |
| CN (1) | CN101605537A (ru) |
| AU (1) | AU2007327358B2 (ru) |
| BR (1) | BRPI0717699A2 (ru) |
| CA (1) | CA2670599A1 (ru) |
| FR (1) | FR2909000B1 (ru) |
| MX (1) | MX2009005308A (ru) |
| RU (1) | RU2459612C2 (ru) |
| WO (1) | WO2008065306A1 (ru) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7820186B2 (en) | 2001-12-21 | 2010-10-26 | Galderma Research & Development | Gel composition for once-daily treatment of common acne comprising a combination of benzoyl peroxide and adapalene and/or adapalene salt |
| WO2007015243A2 (en) | 2005-08-02 | 2007-02-08 | Sol-Gel Technologies Ltd. | Metal oxide coating of water insoluble ingredients |
| FR2903604B1 (fr) * | 2006-07-13 | 2008-09-05 | Galderma Res & Dev S N C Snc | Composition comprenant un retinoide et du peroxyde de benzoyle |
| FR2910321B1 (fr) | 2006-12-21 | 2009-07-10 | Galderma Res & Dev S N C Snc | Gel creme comprenant au moins un retinoide et du peroxyde de benzole |
| FR2910320B1 (fr) | 2006-12-21 | 2009-02-13 | Galderma Res & Dev S N C Snc | Emulsion comprenant au moins un retinoide et du peroxyde de benzole |
| BRPI0808160A2 (pt) * | 2007-02-01 | 2014-09-23 | Sol Gel Technologies Ltd | Processo para revestir um material particulado sólido, insolúvel em água, com um óxido de metal, material particulado revestido, partículas, métodos para tratar uma condição de superfície em um indivíduo, e para prevenir, reduzir, ou eliminar pragas em um local, e, uso de material particulado revestido |
| EP2224908B1 (fr) * | 2007-11-30 | 2017-11-01 | Galderma Research & Development | Compositions comprenant au moins un derive de l'acide naphtoïque, du peroxyde de benzoyle et au moins un agent filmogene. |
| FR2980691B1 (fr) | 2011-09-30 | 2014-03-14 | Galderma Sa | Composition de lavage |
| BR112014020545A2 (pt) | 2012-02-21 | 2019-09-24 | Ranbaxy Laboratories Ltd | composição aquosa tópica estável, processo para o preparo da composição aquosa tópica estável e método para o tratamento de acne |
| JP5851921B2 (ja) * | 2012-04-18 | 2016-02-03 | 株式会社ブリヂストン | 空気入りタイヤ |
| US10610594B2 (en) * | 2012-11-13 | 2020-04-07 | Galderma S.A. | BPO wash gel composition |
| CN105007888B (zh) * | 2012-11-13 | 2018-08-07 | 盖尔德玛公司 | Bpo洗液乳状组合物 |
| CN108159425A (zh) * | 2012-11-27 | 2018-06-15 | 索尔-格尔科技有限公司 | 用于治疗红斑痤疮的组合物 |
| US9687465B2 (en) | 2012-11-27 | 2017-06-27 | Sol-Gel Technologies Ltd. | Compositions for the treatment of rosacea |
| JP2015196663A (ja) * | 2014-04-01 | 2015-11-09 | ロレアル | ナノ又はマイクロエマルションの形態の組成物 |
| MA40179B1 (fr) * | 2014-07-25 | 2020-10-28 | Galderma Res & Dev | Combinaison d'adapalène et de peroxyde de benzoyle pour le traitement de l'acné sévère |
| SG11201703027RA (en) * | 2014-10-15 | 2017-05-30 | Amorepacific Corp | Composition containing material for regulating expression of abh antigens |
| JP6811213B2 (ja) * | 2018-07-03 | 2021-01-13 | ソル − ゲル テクノロジーズ リミテッド | 酒さの治療のための組成物 |
| CA3130362A1 (en) | 2019-02-19 | 2020-08-27 | Sol-Gel Technologies Ltd. | Method for providing early onset of action in the treatment of rosacea |
| US20230390196A1 (en) | 2020-12-04 | 2023-12-07 | Maruho Co., Ltd. | Emulsion composition for external use |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3535422A (en) * | 1968-03-11 | 1970-10-20 | Stiefel Laboratories | Stable benzoyl peroxide composition |
| NZ194326A (en) * | 1979-07-25 | 1982-05-31 | Dermik Lab Inc | Stable aqueous benzoyl peroxide compositions and therapeutic compositions |
| US4387107A (en) | 1979-07-25 | 1983-06-07 | Dermik Laboratories, Inc. | Stable benzoyl peroxide composition |
| DE3852437T2 (de) * | 1987-07-16 | 1995-05-04 | Univ California | Mittel zur Steigerung der Hautpenetration von pharmakologisch aktiven Verbindungen. |
| FR2733684B1 (fr) * | 1995-05-03 | 1997-05-30 | Cird Galderma | Utilisation de retinoides dans une composition cosmetique ou pour la fabrication d'une composition pharmaceutique |
| US6358541B1 (en) * | 2000-05-03 | 2002-03-19 | David S. Goodman | Topical preparation for the treatment of hair loss |
| US20030147977A1 (en) * | 2000-05-03 | 2003-08-07 | Goodman David S. | Topical preparation for treating acne and hirsutism |
| US7820186B2 (en) * | 2001-12-21 | 2010-10-26 | Galderma Research & Development | Gel composition for once-daily treatment of common acne comprising a combination of benzoyl peroxide and adapalene and/or adapalene salt |
| FR2833841B1 (fr) * | 2001-12-21 | 2005-07-22 | Galderma Res & Dev | Gel comprenant au moins un retinoide et du peroxyde de benzoyle |
| CA2478237C (en) * | 2002-03-12 | 2009-05-12 | Michael Graeber | Use of adapalene for the treatment of dermatological disorders |
| FR2890861B1 (fr) * | 2005-09-16 | 2010-05-28 | Galderma Res & Dev | Compositions comprenant au moins un derive de l'acide naphtoique et au moins un compose de type polymeres de polyurethanes ou des derives de celui-ci, leurs procede de preparation, et leur utilisation |
-
2006
- 2006-11-28 FR FR0655138A patent/FR2909000B1/fr not_active Expired - Fee Related
-
2007
- 2007-11-28 RU RU2009124488/15A patent/RU2459612C2/ru not_active IP Right Cessation
- 2007-11-28 KR KR1020097010876A patent/KR20090085077A/ko not_active Application Discontinuation
- 2007-11-28 JP JP2009538755A patent/JP2010520853A/ja active Pending
- 2007-11-28 CN CNA200780043751XA patent/CN101605537A/zh active Pending
- 2007-11-28 CA CA002670599A patent/CA2670599A1/fr not_active Abandoned
- 2007-11-28 BR BRPI0717699-6A2A patent/BRPI0717699A2/pt not_active IP Right Cessation
- 2007-11-28 EP EP07858750A patent/EP2097077A1/fr not_active Withdrawn
- 2007-11-28 AU AU2007327358A patent/AU2007327358B2/en not_active Ceased
- 2007-11-28 WO PCT/FR2007/052412 patent/WO2008065306A1/fr active Application Filing
- 2007-11-28 MX MX2009005308A patent/MX2009005308A/es active IP Right Grant
-
2009
- 2009-05-28 US US12/453,968 patent/US8568704B2/en not_active Expired - Fee Related
-
2013
- 2013-08-29 JP JP2013177691A patent/JP2013241469A/ja active Pending
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2008065306A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20090085077A (ko) | 2009-08-06 |
| RU2009124488A (ru) | 2011-01-10 |
| US20100143285A1 (en) | 2010-06-10 |
| AU2007327358B2 (en) | 2013-05-02 |
| WO2008065306A1 (fr) | 2008-06-05 |
| JP2010520853A (ja) | 2010-06-17 |
| FR2909000B1 (fr) | 2009-02-06 |
| FR2909000A1 (fr) | 2008-05-30 |
| CA2670599A1 (fr) | 2008-06-05 |
| MX2009005308A (es) | 2009-05-28 |
| US8568704B2 (en) | 2013-10-29 |
| BRPI0717699A2 (pt) | 2014-12-30 |
| AU2007327358A1 (en) | 2008-06-05 |
| CN101605537A (zh) | 2009-12-16 |
| JP2013241469A (ja) | 2013-12-05 |
| RU2459612C2 (ru) | 2012-08-27 |
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