JP2020019767A - 眼科組成物 - Google Patents
眼科組成物 Download PDFInfo
- Publication number
- JP2020019767A JP2020019767A JP2019133038A JP2019133038A JP2020019767A JP 2020019767 A JP2020019767 A JP 2020019767A JP 2019133038 A JP2019133038 A JP 2019133038A JP 2019133038 A JP2019133038 A JP 2019133038A JP 2020019767 A JP2020019767 A JP 2020019767A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- salt
- salts
- group
- pranoprofen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 245
- 150000003839 salts Chemical class 0.000 claims abstract description 196
- TVQZAMVBTVNYLA-UHFFFAOYSA-N Pranoprofen Chemical compound C1=CC=C2CC3=CC(C(C(O)=O)C)=CC=C3OC2=N1 TVQZAMVBTVNYLA-UHFFFAOYSA-N 0.000 claims abstract description 80
- 229960003101 pranoprofen Drugs 0.000 claims abstract description 80
- WHWZLSFABNNENI-UHFFFAOYSA-N epinastine Chemical compound C1C2=CC=CC=C2C2CN=C(N)N2C2=CC=CC=C21 WHWZLSFABNNENI-UHFFFAOYSA-N 0.000 claims abstract description 68
- 229960003449 epinastine Drugs 0.000 claims abstract description 51
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- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- 210000004083 nasolacrimal duct Anatomy 0.000 description 1
- OSZNNLWOYWAHSS-UHFFFAOYSA-M neostigmine methyl sulfate Chemical compound COS([O-])(=O)=O.CN(C)C(=O)OC1=CC=CC([N+](C)(C)C)=C1 OSZNNLWOYWAHSS-UHFFFAOYSA-M 0.000 description 1
- 229960002253 neostigmine methylsulfate Drugs 0.000 description 1
- VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 description 1
- GSGDTSDELPUTKU-UHFFFAOYSA-N nonoxybenzene Chemical compound CCCCCCCCCOC1=CC=CC=C1 GSGDTSDELPUTKU-UHFFFAOYSA-N 0.000 description 1
- 239000000820 nonprescription drug Substances 0.000 description 1
- 229960001180 norfloxacin Drugs 0.000 description 1
- OGJPXUAPXNRGGI-UHFFFAOYSA-N norfloxacin Chemical compound C1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC(F)=C1N1CCNCC1 OGJPXUAPXNRGGI-UHFFFAOYSA-N 0.000 description 1
- 239000000574 octyl gallate Substances 0.000 description 1
- 235000010387 octyl gallate Nutrition 0.000 description 1
- NRPKURNSADTHLJ-UHFFFAOYSA-N octyl gallate Chemical compound CCCCCCCCOC(=O)C1=CC(O)=C(O)C(O)=C1 NRPKURNSADTHLJ-UHFFFAOYSA-N 0.000 description 1
- 229960001699 ofloxacin Drugs 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 229940125702 ophthalmic agent Drugs 0.000 description 1
- 229940069265 ophthalmic ointment Drugs 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- BAINIUMDFURPJM-UHFFFAOYSA-N oxatomide Chemical compound O=C1NC2=CC=CC=C2N1CCCN(CC1)CCN1C(C=1C=CC=CC=1)C1=CC=CC=C1 BAINIUMDFURPJM-UHFFFAOYSA-N 0.000 description 1
- 229960002698 oxatomide Drugs 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 229960001528 oxymetazoline Drugs 0.000 description 1
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- 150000002942 palmitic acid derivatives Chemical class 0.000 description 1
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- HIANJWSAHKJQTH-UHFFFAOYSA-N pemirolast Chemical compound CC1=CC=CN(C2=O)C1=NC=C2C=1N=NNN=1 HIANJWSAHKJQTH-UHFFFAOYSA-N 0.000 description 1
- 229960004439 pemirolast Drugs 0.000 description 1
- 230000010412 perfusion Effects 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229960003733 phenylephrine hydrochloride Drugs 0.000 description 1
- OCYSGIYOVXAGKQ-FVGYRXGTSA-N phenylephrine hydrochloride Chemical compound [H+].[Cl-].CNC[C@H](O)C1=CC=CC(O)=C1 OCYSGIYOVXAGKQ-FVGYRXGTSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229940093448 poloxamer 124 Drugs 0.000 description 1
- 229920001993 poloxamer 188 Polymers 0.000 description 1
- 229940044519 poloxamer 188 Drugs 0.000 description 1
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 239000011116 polymethylpentene Substances 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010483 polyoxyethylene sorbitan monopalmitate Nutrition 0.000 description 1
- 239000000249 polyoxyethylene sorbitan monopalmitate Substances 0.000 description 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
- 235000010988 polyoxyethylene sorbitan tristearate Nutrition 0.000 description 1
- 239000001816 polyoxyethylene sorbitan tristearate Substances 0.000 description 1
- 229940099429 polyoxyl 40 stearate Drugs 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229940068977 polysorbate 20 Drugs 0.000 description 1
- 229940101027 polysorbate 40 Drugs 0.000 description 1
- 229940113124 polysorbate 60 Drugs 0.000 description 1
- 229940099511 polysorbate 65 Drugs 0.000 description 1
- 229940068965 polysorbates Drugs 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920002215 polytrimethylene terephthalate Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- VUOLWBPDWWANLX-FJXQXJEOSA-M potassium 3-[[(2R)-2,4-dihydroxy-3,3-dimethylbutanoyl]amino]propanoate Chemical compound [K+].OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O VUOLWBPDWWANLX-FJXQXJEOSA-M 0.000 description 1
- 229960004109 potassium acetate Drugs 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- 229960002635 potassium citrate Drugs 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 235000011082 potassium citrates Nutrition 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 1
- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- JVUYWILPYBCNNG-UHFFFAOYSA-N potassium;oxido(oxo)borane Chemical compound [K+].[O-]B=O JVUYWILPYBCNNG-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 229960001309 procaine hydrochloride Drugs 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920005653 propylene-ethylene copolymer Polymers 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 229960003581 pyridoxal Drugs 0.000 description 1
- 235000008164 pyridoxal Nutrition 0.000 description 1
- 239000011674 pyridoxal Substances 0.000 description 1
- 235000007682 pyridoxal 5'-phosphate Nutrition 0.000 description 1
- 239000011589 pyridoxal 5'-phosphate Substances 0.000 description 1
- 229960001327 pyridoxal phosphate Drugs 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229960000342 retinol acetate Drugs 0.000 description 1
- QGNJRVVDBSJHIZ-QHLGVNSISA-N retinyl acetate Chemical compound CC(=O)OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C QGNJRVVDBSJHIZ-QHLGVNSISA-N 0.000 description 1
- 235000019173 retinyl acetate Nutrition 0.000 description 1
- 239000011770 retinyl acetate Substances 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
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- 229960001516 silver nitrate Drugs 0.000 description 1
- 229960004249 sodium acetate Drugs 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 235000011083 sodium citrates Nutrition 0.000 description 1
- 235000019259 sodium dehydroacetate Nutrition 0.000 description 1
- 229940079839 sodium dehydroacetate Drugs 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 229940073490 sodium glutamate Drugs 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- DSOWAKKSGYUMTF-GZOLSCHFSA-M sodium;(1e)-1-(6-methyl-2,4-dioxopyran-3-ylidene)ethanolate Chemical compound [Na+].C\C([O-])=C1/C(=O)OC(C)=CC1=O DSOWAKKSGYUMTF-GZOLSCHFSA-M 0.000 description 1
- WTWSHHITWMVLBX-DKWTVANSSA-M sodium;(2s)-2-aminobutanedioate;hydron Chemical compound [Na+].[O-]C(=O)[C@@H](N)CC(O)=O WTWSHHITWMVLBX-DKWTVANSSA-M 0.000 description 1
- GEYJUFBPCGDENK-UHFFFAOYSA-M sodium;3,8-dimethyl-5-propan-2-ylazulene-1-sulfonate Chemical compound [Na+].CC(C)C1=CC=C(C)C2=C(S([O-])(=O)=O)C=C(C)C2=C1 GEYJUFBPCGDENK-UHFFFAOYSA-M 0.000 description 1
- 235000011071 sorbitan monopalmitate Nutrition 0.000 description 1
- 239000001570 sorbitan monopalmitate Substances 0.000 description 1
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- 239000008107 starch Substances 0.000 description 1
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- 230000000638 stimulation Effects 0.000 description 1
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- 150000008163 sugars Chemical class 0.000 description 1
- 229960005404 sulfamethoxazole Drugs 0.000 description 1
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- 229960001975 sulfisomidine Drugs 0.000 description 1
- FEPTXVIRMZIGFY-UHFFFAOYSA-N sulfisoxazole diolamine Chemical compound OCCNCCO.CC1=NOC(NS(=O)(=O)C=2C=CC(N)=CC=2)=C1C FEPTXVIRMZIGFY-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- JLKIGFTWXXRPMT-UHFFFAOYSA-N sulphamethoxazole Chemical compound O1C(C)=CC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 JLKIGFTWXXRPMT-UHFFFAOYSA-N 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 229950011558 tazanolast Drugs 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- BJORNXNYWNIWEY-UHFFFAOYSA-N tetrahydrozoline hydrochloride Chemical compound Cl.N1CCN=C1C1C2=CC=CC=C2CCC1 BJORNXNYWNIWEY-UHFFFAOYSA-N 0.000 description 1
- 229940021790 tetrahydrozoline hydrochloride Drugs 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 125000002640 tocopherol group Chemical class 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- 229950009883 tocopheryl nicotinate Drugs 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- GYDJEQRTZSCIOI-LJGSYFOKSA-N tranexamic acid Chemical compound NC[C@H]1CC[C@H](C(O)=O)CC1 GYDJEQRTZSCIOI-LJGSYFOKSA-N 0.000 description 1
- 229960000401 tranexamic acid Drugs 0.000 description 1
- KBPHJBAIARWVSC-XQIHNALSSA-N trans-lutein Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2C(=CC(O)CC2(C)C)C KBPHJBAIARWVSC-XQIHNALSSA-N 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
- WYXIGTJNYDDFFH-UHFFFAOYSA-Q triazanium;borate Chemical compound [NH4+].[NH4+].[NH4+].[O-]B([O-])[O-] WYXIGTJNYDDFFH-UHFFFAOYSA-Q 0.000 description 1
- 235000013337 tricalcium citrate Nutrition 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
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- FJHBOVDFOQMZRV-XQIHNALSSA-N xanthophyll Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2C=C(C)C(O)CC2(C)C FJHBOVDFOQMZRV-XQIHNALSSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
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- 229940050168 zinc lactate Drugs 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
Abstract
Description
[1]
(A)プラノプロフェン及びその塩からなる群より選択される1種以上、並びに
(B)エピナスチン及びその塩からなる群より選択される1種以上を含有する、眼科組成物。
[2]
(A)成分を0.005〜0.5w/v%含有する[1]記載の組成物。
[3]
(B)成分を0.005〜0.5w/v%含有する[1]又は[2]記載の組成物。
[4]
(B)成分の割合が、(A)成分1質量部に対して0.01〜100質量部である[1]〜[3]のいずれかに記載の組成物。
[5]
pHが4〜9である[1]〜[4]のいずれかに記載の組成物。
[6]
容器に収容されている組成物であって、容器のうち、組成物と接触する部分の材質の少なくとも一部が、ガラス及び/又はプラスチックである、[1]〜[5]のいずれかに記載の組成物。
[7]
(A)成分の割合が0.01〜0.15w/v%であり、
(B)成分の割合が0.01〜0.15w/v%であり、
(B)成分の割合が、(A)成分1質量部に対して0.2〜5質量部であり、
pHが5〜8であり、
容器に収容されており、容器のうち、組成物と接触する部分の材質の少なくとも一部がプラスチックである、
[1]〜[6]のいずれかに記載の組成物。
[8]
容器に収容されている組成物であって、容器のうち、組成物と接触する部分の材質の少なくとも一部が、ポリエチレンテレフタレートである、[1]〜[7]のいずれかに記載の組成物。
[9]
(A)プラノプロフェン及びその塩からなる群より選択される1種以上と、(B)エピナスチン及びその塩からなる群より選択される1種以上とを組み合わせることにより、眼科組成物における泡立ちを抑制する方法。
[10]
(A)プラノプロフェン及びその塩からなる群より選択される1種以上と、(B)エピナスチン及びその塩からなる群より選択される1種以上とを組み合わせることにより、眼科組成物における消泡速度を向上する方法。
[11]
(A)プラノプロフェン及びその塩からなる群より選択される1種以上と、(B)エピナスチン及びその塩からなる群より選択される1種以上とを組み合わせることにより、眼科組成物における光安定性を向上する方法。
[12]
(A)プラノプロフェン及びその塩からなる群より選択される1種以上を含む眼科組成物において、泡立ちを抑制し、消泡速度を向上し、かつ光安定性を向上する方法であって、(B)エピナスチン及びその塩からなる群より選択される1種以上を眼科組成物に含有させる方法。
[13]
眼科組成物が、容器に収容されており、容器のうち、組成物と接触する部分の材質の少なくとも一部が、ガラス及び/又はプラスチックである、[9]〜[12]のいずれかに記載の方法。
[14]
眼科組成物が、容器に収容されており、容器のうち、組成物と接触する部分の材質の少なくとも一部が、ポリエチレンテレフタレートである、[9]〜[13]のいずれかに記載の方法。
本発明の眼科組成物は、(A)プラノプロフェン及び/又はその塩、並びに(B)エピナスチン及び/又はその塩を少なくとも含有する。
プラノプロフェンの塩としては、薬学的又は生理学的に許容される塩であればよく、酸との塩(例えば、無機酸との塩、有機酸との塩等の後述の(B)成分の項で例示の塩)の他、塩基との塩{例えば、有機塩基との塩(例えば、メチルアミン、トリエチルアミン、トリエタノールアミン、モルホリン、ピペラジン、ピロリジン、トリピリジン、ピコリン等の有機アミンとの塩)、無機塩基との塩[例えば、アンモニウム塩;アルカリ金属(ナトリウム、カリウム等)、アルカリ土類金属(カルシウム、マグネシウム等)、アルミニウム等の金属との塩]など}などが挙げられ、例えば、硫酸塩、乳酸塩、塩酸塩、塩化物塩、ナトリウム塩、カリウム塩などが挙げられる。
好ましいプラノプロフェン及び/又はその塩は、プラノプロフェン及びその金属塩であり、特にプラノプロフェンが好ましい。
本発明の組成物は、プラノプロフェン及び/又はその塩に加えて、エピナスチン及び/又はその塩を含有する。本発明の組成物によれば、このように複数の有効成分を含んでいても、それぞれの機能(薬効)を効率良く発揮しうる。
本発明の組成物は、さらに他の成分を含有していてもよく、含有しなくてもよい。本発明では、他の成分を含有させても、本発明の効果を担保できる場合が多い。また、他の成分を含有することで、さらに本発明の効果をより有効に実現できる場合もある。
本発明の組成物は、アミノ酸類を含んでいてもよい。
アミノ酸としては、例えば、アミノ酸又はその塩、及びアミノ酸類似体を包含し、分子内にアミノ基とカルボキシル基又はスルホン基を有する化合物又はその誘導体などが含まれる。
このようなコンドロイチン硫酸は、どのような構造を有するものであってもよい。例えば、コンドロイチン4硫酸(コンドロイチン硫酸A)、コンドロイチン6硫酸(コンドロイチン硫酸C)、N−アセチルグルコサミンの4位及び6位が硫酸化されたコンドロイチン硫酸Eなどが挙げられる。また、コンドロイチン硫酸は、動物から抽出されたものであってもよい。
本発明の組成物は、清涼化剤を含んでいてもよい。
(A)成分及び(B)成分(さらには他の成分)を組み合わせることで、使用感が低下する又は損なわれる場合があるが、清涼化剤によりこのような使用感を向上又は改善しうる。例えば、溶解性等の観点で組成物のpHを高めることが有利な場合がある一方で、組成物のpHが高いほど、不快感が強くなり、使用感が損なわれることがあるが、清涼化剤の使用により、このような不快感を和らげ、使用感を効率良く向上しうる。
本発明の組成物は、脂溶性抗酸化剤を含んでいてもよい。
本発明の組成物は、抗アレルギー剤を含んでいてもよい。
本発明の組成物は、抗ヒスタミン剤を含んでいてもよい。
抗ヒスタミン剤(エピナスチン及びその塩以外の抗ヒスタミン剤)としては、抗ヒスタミン作用を有する物質であれば、特に制限されず、例えば、クロルフェニラミン、ジフェンヒドラミン、ケトチフェン、オロパタジン、レボカバスチン、イプロヘプチン及びそれらの塩が挙げられる。
本発明の組成物は、プラノプロフェン及びその塩以外の抗炎症剤を含んでいてもよい。
抗炎症剤(以下、プラノプロフェン及びその塩以外の抗炎症剤を指す)としては、抗炎症作用を有する物質であれば、特に制限されず、例えば、インドメタシン、アラントイン、ベルベリン、アズレンスルホン酸、ジクロフェナク、ブロムフェナク、グリチルリチン酸、亜鉛、銀、トラネキサム酸、リゾチーム及びそれらの塩などが挙げられる。
本発明の組成物は、界面活性剤を含んでいてもよい。界面活性剤としては、例えば、非イオン界面活性剤などが挙げられる。
本発明の組成物は、防腐剤を含んでいてもよい。
防腐剤としては、例えば、塩化ポリドロニウム、アルキルポリアミノエチルグリシン類(例えば、塩酸アルキルジアミノエチルグリシンなど)、安息香酸ナトリウム、エタノール、第四級アンモニウム塩(例えば、塩化ベンザルコニウム、塩化ベンゼトニウムなど)、グルコン酸クロルヘキシジン、アレキシジン、クロロブタノール、ソルビン酸、ソルビン酸カリウム、デヒドロ酢酸ナトリウム、パラオキシ安息香酸エステル(例えば、パラオキシ安息香酸メチル、パラオキシ安息香酸エチル、パラオキシ安息香酸プロピル、パラオキシ安息香酸ブチルなど)、硫酸オキシキノリン、フェネチルアルコール、ベンジルアルコール、ビグアニド化合物(例えば、塩酸ポリヘキサニドなど)、及びグローキル(ローディア社製)などが挙げられる。
本発明の組成物は、緩衝剤を含んでいてもよい。
緩衝剤としては、例えば、ホウ酸緩衝剤、リン酸緩衝剤、炭酸緩衝剤、クエン酸緩衝剤、酢酸緩衝剤等が挙げられる。
pH調節剤としては、例えば、塩酸、硫酸、ポリリン酸、有機酸(プロピオン酸、シュウ酸、グルコン酸、フマル酸、乳酸、酒石酸、リンゴ酸、コハク酸など)、水酸化ナトリウム、水酸化カリウム、水酸化カルシウム、水酸化マグネシウム、トリエタノールアミン、モノエタノールアミン、ジイソプロパノールアミンなどが挙げられる。
pH調整剤は、単独で又は2種以上組み合わせて使用してもよい。
等張化剤としては、例えば、塩化ナトリウム、塩化カリウム、塩化カルシウム、塩化マグネシウム、酢酸カリウム、酢酸ナトリウム、硫酸マグネシウム、グリセリン、及びプロピレングリコールなどが挙げられる。
等張化剤は、単独で又は2種以上組み合わせて使用してもよい。
本発明の眼科組成物は、増粘剤ないしは粘稠化剤を含むことができる。
増粘剤又は粘稠化剤は、単独で又は2種以上組み合わせて使用してもよい。
安定化剤としては、例えば、ヒドロキシアルキルアミン類(又はアミノアルカノール類又はアルカノールアミン類、例えば、モノエタノールアミン、ジエタノールアミン、トリエタノールアミン、トロメタモールなど)、ナトリウムホルムアルデヒドスルホキシレート(ロンガリット)、モノステアリン酸アルミニウム、及びモノステアリン酸グリセリンなどが挙げられる。
安定化剤は、単独で又は2種以上組み合わせて使用してもよい。
油分としては、スクワラン、精製ラノリンのような動物油、流動パラフィン、白色ワセリンのような鉱物油、ヒマシ油、ゴマ油のような植物油などが挙げられる。
糖類としては、単糖類、オリゴ糖(二糖類など)などが挙げられ、具体的には、グルコース、マルトース、トレハロース、スクロース、シクロデキストリン、キシリトール、ソルビトール、マンニトールなどが挙げられる。
多価アルコールとしては、ポリエチレングリコール、グリセリン、プロピレングリコール、キシリトール、ジエチレングリコール、マンニトール、ソルビトール、ポリビニルアルコール等が挙げられる。
無機塩類としては、例えば、塩化カリウム、塩化ナトリウム、塩化カルシウム、塩化マグネシウム、炭酸水素ナトリウム、炭酸ナトリウム(乾燥炭酸ナトリウムを含む)、炭酸水素カリウム、炭酸カリウム、硫酸マグネシウム、リン酸水素ナトリウム、リン酸水素カリウム、リン酸二水素ナトリウム、リン酸二水素カリウム、リン酸水素二ナトリウム、リン酸水素二カリウム、亜硫酸水素ナトリウム、亜硫酸ナトリウム、酢酸カリウム、酢酸ナトリウム、チオ硫酸ナトリウムなどが挙げられる。
中でも、塩化カリウム、塩化ナトリウム、塩化カルシウム、炭酸水素ナトリウム、炭酸ナトリウム(乾燥炭酸ナトリウムを含む)、硫酸マグネシウム、リン酸水素ナトリウム、リン酸二水素ナトリウム、リン酸二水素カリウムが好ましく、塩化カリウム、塩化ナトリウム、塩化カルシウム、リン酸水素ナトリウム、リン酸二水素ナトリウムがより好ましく、塩化カリウム、塩化ナトリウムがさらに好ましい。
水溶性の抗酸化剤としては、例えば、アスコルビン酸、アスコルビン酸誘導体(アスコルビン酸−2−硫酸2ナトリウム、アスコルビン酸ナトリウム、アスコルビン酸−2−リン酸マグネシウム、アスコルビン酸−2−リン酸ナトリウムなど)、亜硫酸水素ナトリウム、亜硫酸ナトリウム、ピロ亜硫酸ナトリウム、チオ硫酸ナトリウム、エデト酸又はその塩(エデト酸二ナトリウム、エデト酸四ナトリウムなど)などが挙げられる。
充血除去剤としては、例えば、α−アドレナリン作動薬、具体的にはオキシメタゾリン、テトラヒドロゾリン、ナファゾリン、又はそれらの塩酸塩、硝酸塩などの塩等のイミダゾリン系充血除去剤、エピネフリン、塩酸エピネフリン、塩酸エフェドリン、塩酸フェニレフリン、塩酸メチルエフェドリン、酒石酸水素エピネフリンなどが挙げられる。これらはd体、l体又はdl体のいずれでもよい。
眼筋調節剤としては、例えば、アセチルコリンと類似した活性中心を有するコリンエステラーゼ阻害剤、具体的にはメチル硫酸ネオスチグミン、トロピカミド、ヘレニエン、及び硫酸アトロピンなどが挙げられる。
ビタミン類としては、例えば、フラビンアデニンジヌクレオチド又はその塩(例えば、フラビンアデニンジヌクレオチドナトリウム)、コバラミン又はその塩(例えば、シアノコバラミン、メチルコバラミン)、レチノール、その塩又はその誘導体(例えば、酢酸レチノール、パルミチン酸レチノール)、ピリドキシン又はその塩(例えば、塩酸ピリドキシン)、パンテノール、パントテン酸又はその塩(例えば、パントテン酸ナトリウム、パントテン酸カリウム、パントテン酸カルシウム、パントテン酸マグネシウム)、トコフェロール、その塩又はその誘導体(例えば、酢酸トコフェロール、コハク酸トコフェロール、ニコチン酸トコフェロール)、ピリドキサール又はその塩(例えば、リン酸ピリドキサール)、アスコルビン酸又はその塩(例えばアスコルビン酸ナトリウム、アスコルビン酸カルシウム)などが挙げられる。
なお、本発明の組成物は、ピリドキシン及びその塩を含んでいなくてもよい。
抗菌剤又は殺菌剤としては、例えば、スルファメトキサゾール、スルフイソキサゾール、スルファメトキサゾールナトリウム、スルフイソキサゾールジエタノールアミン、スルフイソキサゾールモノエタノールアミン、スルフイソメゾールナトリウム、スルフイソミジンナトリウムのようなサルファ剤、アルキルポリアミノエチルグリシン、クロラムフェニコール、オフロキサシン、ノルフロキサシン、レボフロキサシン、及び塩酸ロメフロキサシンなどが挙げられる。
局所麻酔薬成分としては、例えば、塩酸プロカイン、塩酸リドカインなどが挙げられる。
本発明の組成物は、基剤又は担体を含んでいてもよい。
このような基剤又は担体を含む組成物は、例えば、上記各成分を、薬学的に許容される基剤又は担体と混合することにより、例えば、第17改正日本薬局方解説書に記載の慣用の方法で調製できる。なお、組成物の調製にあたり、適宜加温してもよい。
なお、このような組成物(特に、水性組成物)において、各成分は、通常、溶解していてもよい。
本発明の組成物の性状は、特に限定されず、例えば、液体状、流動状、ゲル状、又は半固形状などの何れの性状であってもよい。また、用時調製により、液体状、流動状、ゲル状、又は半固形状になったものも含まれる。半固形状は、例えば、軟膏剤のように、力を加えることにより変形させ得る塑性を有する性状をいう。好ましい組成物の性状は、液体状(液剤)である。
本発明の組成物のpHは、3以上(例えば、4以上)が好ましく、5以上(例えば、5.5以上)がより好ましく、6以上がさらに好ましい。また、10以下が好ましく、9以下がより好ましく、8.5以下がさらにより好ましい。
本発明では、上記のようなpHにおいても、泡立ち抑制効果などを効率よく実現しうる。
本発明の組成物の浸透圧比は、例えば、0.4以上が好ましく、0.5以上がより好ましく、0.6以上がさらにより好ましい。また、5以下が好ましく、3以下がより好ましく、2以下がさらにより好ましい。
本発明の組成物の剤型(剤形、形状、構造)は特に限定されず、例えば、点眼剤(点眼液又は点眼薬ともいう。また、点眼剤にはコンタクトレンズ装用中に点眼可能な点眼剤を含む)、洗眼剤、眼軟膏(水溶性眼軟膏、油溶性眼軟膏)、コンタクトレンズ装着液、眼内注射剤(例えば、硝子体内注射剤)、コンタクトレンズ用液(洗浄液、保存液、消毒液、マルチパーパスソリューション、パッケージソリューション)、移植用の角膜等の摘出眼組織の保存剤、手術時潅流液などが挙げられる。点眼剤、洗眼剤、眼軟膏には、コンタクトレンズ装着時に使用するものも含まれる。
本発明の組成物は、容器に収容(充填、注入、封入)されていてもよい。
容器は、組成物(製剤)と接触する部分(面)を有する包装体であればよく、例えば、組成物(例えば、液状の組成物)を収容する容器本体部分、容器の抽出口を含む部分(ノズル、中栓)、吸い上げチューブ、キャップなどで構成されていてもよい。
本発明の組成物の対象疾患(用途)は、眼科用である限り、特に限定されるものではないが、例えば、アレルギー症状、目の痒み、目の痛み、眼の炎症、眼瞼炎、目のかすみ、充血、異物感(コロコロする感じ等)、角膜ダメージ、角膜損傷、涙目(流涙症)、眼瞼結膜の濾胞、眼脂(目やに)などの緩和、改善、抑制、又は治療や、角膜バリア機能の亢進、正常化、角膜保護などに有用である。
本発明の組成物の使用方法(使用態様)は、その性状などに応じて適宜選択できる。
本実施形態に係る眼科組成物は、眼科組成物における、泡立ち(起泡)を抑制(又は防止)しうる(又は消泡性を向上又は改善しうる)。
本実施形態に係る眼科組成物は、眼科組成物における、消泡速度を向上(又は改善)しうる。
本実施形態に係る眼科組成物は、眼科組成物における、消泡状態(又は低減された泡立ち)を維持しうる。
本実施形態に係る眼科組成物は、眼科組成物における、光安定性を向上(又は改善)しうる。
本実施形態に係る眼科組成物は、眼科組成物における、着色(黄変など)を抑制(又は防止)しうる。なお、着色は、光(光曝露)による(伴う)ものであってもよい。
下記表に示す組成の水性眼科組成物(点眼剤)を調製し、次のようにして、泡立ちを評価した。
下記表のように、プラノプロフェン及び/又はエピナスチン塩酸塩の割合を変更したこと以外は、試験例1と同様にして、水性眼科組成物(点眼剤)を調製し、泡立ちを評価した。
試験例1において、容器をガラス製容器からポリエチレンテレフタレート(PET)製容器(容量50mL、遠沈管、Corning社製 No.430304)に変更し、試験例1と同様にして、下記表に示す水性眼科組成物(点眼剤)を調製し、泡立ちを評価した。
試験例3において、下記表に示す、水性眼科組成物(点眼剤)を調製・使用したこと以外は、試験例1と同様にして、泡立ちを評価した。
上記試験例1〜3では、プラノプロフェンをエピナスチン塩酸塩と組み合わせることなく使用した場合の泡立ちを、振とう終了直後において確認したが、このような泡立ちが、振とう後にどのように変化するか確認すべく試験を行った。
試験例4において、下記表に示す、水性眼科組成物(点眼剤)を調製・使用したこと以外は、試験例4と同様にして試験を行った。なお、容器にはPET容器を使用した。
下記表に示す組成の眼科用組成物(点眼剤)を調製し、光安定性(着色)を評価した。
すなわち、下記表に示す各眼科用組成物を13mL容量のポリエチレンテレフタレート(PET)製容器に5mLずつ充填し、光試験器(NAGANO製 LT120A WCD,11114、白色ランプ)にて、照射した。なお、照射条件は、4000Lx、442kLx・hとした。
上記のように、プラノプロフェンとエピナスチン塩酸塩とを併用した試験例の組成物(処方)につき、さらに性状等を調べた。
以下の表に記載の処方に従い、眼科組成物を調製した。なお、下記の表において、各成分の単位は(w/v%、g/100mL)である。
Claims (14)
- (A)プラノプロフェン及びその塩からなる群より選択される1種以上、並びに
(B)エピナスチン及びその塩からなる群より選択される1種以上を含有する、眼科組成物。 - (A)成分を0.005〜0.5w/v%含有する請求項1記載の組成物。
- (B)成分を0.005〜0.5w/v%含有する請求項1又は2記載の組成物。
- (B)成分の割合が、(A)成分1質量部に対して0.01〜100質量部である請求項1〜3のいずれかに記載の組成物。
- pHが4〜9である請求項1〜4のいずれかに記載の組成物。
- 容器に収容されている組成物であって、容器のうち、組成物と接触する部分の材質の少なくとも一部が、ガラス及び/又はプラスチックである、請求項1〜5のいずれかに記載の組成物。
- (A)成分の割合が0.01〜0.15w/v%であり、
(B)成分の割合が0.01〜0.15w/v%であり、
(B)成分の割合が、(A)成分1質量部に対して0.2〜5質量部であり、
pHが5〜8であり、
容器に収容されており、容器のうち、組成物と接触する部分の材質の少なくとも一部がプラスチックである、
請求項1〜6のいずれかに記載の組成物。 - 容器に収容されている組成物であって、容器のうち、組成物と接触する部分の材質の少なくとも一部が、ポリエチレンテレフタレートである、請求項1〜7のいずれかに記載の組成物。
- (A)プラノプロフェン及びその塩からなる群より選択される1種以上と、(B)エピナスチン及びその塩からなる群より選択される1種以上とを組み合わせることにより、眼科組成物における泡立ちを抑制する方法。
- (A)プラノプロフェン及びその塩からなる群より選択される1種以上と、(B)エピナスチン及びその塩からなる群より選択される1種以上とを組み合わせることにより、眼科組成物における消泡速度を向上する方法。
- (A)プラノプロフェン及びその塩からなる群より選択される1種以上と、(B)エピナスチン及びその塩からなる群より選択される1種以上とを組み合わせることにより、眼科組成物における光安定性を向上する方法。
- (A)プラノプロフェン及びその塩からなる群より選択される1種以上を含む眼科組成物において、泡立ちを抑制し、消泡速度を向上し、かつ光安定性を向上する方法であって、(B)エピナスチン及びその塩からなる群より選択される1種以上を眼科組成物に含有させる方法。
- 眼科組成物が、容器に収容されており、容器のうち、組成物と接触する部分の材質の少なくとも一部が、ガラス及び/又はプラスチックである、請求項9〜12のいずれかに記載の方法。
- 眼科組成物が、容器に収容されており、容器のうち、組成物と接触する部分の材質の少なくとも一部が、ポリエチレンテレフタレートである、請求項9〜13のいずれかに記載の方法。
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JP2020070301A (ja) * | 2018-10-31 | 2020-05-07 | 参天製薬株式会社 | ソフトコンタクトレンズの変質を抑制する眼科用組成物 |
JP2021169431A (ja) * | 2020-04-16 | 2021-10-28 | 参天製薬株式会社 | エピナスチン又はその塩を含有する水性組成物 |
JP2022062596A (ja) * | 2020-10-08 | 2022-04-20 | 参天製薬株式会社 | エピナスチン又はその塩を含有する花粉破裂抑制剤 |
WO2022138826A1 (ja) * | 2020-12-24 | 2022-06-30 | 参天製薬株式会社 | エピナスチン又はその塩を含有する塗布投与用医薬組成物 |
JP2022125347A (ja) * | 2020-04-16 | 2022-08-26 | 参天製薬株式会社 | エピナスチン又はその塩を含有する水性組成物 |
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