TWI344850B - - Google Patents
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- TWI344850B TWI344850B TW092130104A TW92130104A TWI344850B TW I344850 B TWI344850 B TW I344850B TW 092130104 A TW092130104 A TW 092130104A TW 92130104 A TW92130104 A TW 92130104A TW I344850 B TWI344850 B TW I344850B
- Authority
- TW
- Taiwan
- Prior art keywords
- parts
- acid
- adhesive composition
- polyol
- water
- Prior art date
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- 239000000203 mixture Substances 0.000 claims description 86
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 79
- -1 aluminum compound Chemical class 0.000 claims description 73
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 57
- 239000000853 adhesive Substances 0.000 claims description 50
- 230000001070 adhesive effect Effects 0.000 claims description 50
- 235000011187 glycerol Nutrition 0.000 claims description 37
- 229920005862 polyol Polymers 0.000 claims description 35
- 150000003077 polyols Chemical class 0.000 claims description 35
- 229920000642 polymer Polymers 0.000 claims description 31
- 229920001577 copolymer Polymers 0.000 claims description 29
- 150000001875 compounds Chemical class 0.000 claims description 24
- 229920000058 polyacrylate Polymers 0.000 claims description 22
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 19
- 229910052749 magnesium Inorganic materials 0.000 claims description 19
- 239000011777 magnesium Substances 0.000 claims description 19
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 18
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 18
- 229910052782 aluminium Inorganic materials 0.000 claims description 18
- YKPUWZUDDOIDPM-SOFGYWHQSA-N capsaicin Chemical compound COC1=CC(CNC(=O)CCCC\C=C\C(C)C)=CC=C1O YKPUWZUDDOIDPM-SOFGYWHQSA-N 0.000 claims description 18
- 239000000243 solution Substances 0.000 claims description 16
- 229940047670 sodium acrylate Drugs 0.000 claims description 12
- 235000017663 capsaicin Nutrition 0.000 claims description 9
- 229960002504 capsaicin Drugs 0.000 claims description 9
- 239000004615 ingredient Substances 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 6
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 4
- 229920000573 polyethylene Polymers 0.000 claims description 4
- 229960001193 diclofenac sodium Drugs 0.000 claims description 3
- JGMJQSFLQWGYMQ-UHFFFAOYSA-M sodium;2,6-dichloro-n-phenylaniline;acetate Chemical compound [Na+].CC([O-])=O.ClC1=CC=CC(Cl)=C1NC1=CC=CC=C1 JGMJQSFLQWGYMQ-UHFFFAOYSA-M 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- XURMLLREPYIRPJ-UHFFFAOYSA-N N'-ethenylethanimidamide Chemical compound C(=C)NC(C)=N XURMLLREPYIRPJ-UHFFFAOYSA-N 0.000 claims 1
- 238000001514 detection method Methods 0.000 claims 1
- 150000003606 tin compounds Chemical class 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 33
- 229920002125 Sokalan® Polymers 0.000 description 30
- 239000003814 drug Substances 0.000 description 26
- 239000000126 substance Substances 0.000 description 25
- 229940079593 drug Drugs 0.000 description 24
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 19
- 239000003795 chemical substances by application Substances 0.000 description 19
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 18
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 18
- 239000002253 acid Substances 0.000 description 18
- 229940024545 aluminum hydroxide Drugs 0.000 description 18
- 229940091250 magnesium supplement Drugs 0.000 description 18
- 239000000084 colloidal system Substances 0.000 description 16
- 239000008279 sol Substances 0.000 description 16
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 14
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 13
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 11
- 239000004584 polyacrylic acid Substances 0.000 description 11
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 11
- 239000003921 oil Substances 0.000 description 10
- 235000019198 oils Nutrition 0.000 description 10
- 229910052708 sodium Inorganic materials 0.000 description 10
- 239000011734 sodium Substances 0.000 description 10
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 9
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 9
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 239000000194 fatty acid Substances 0.000 description 9
- 229930195729 fatty acid Natural products 0.000 description 9
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 8
- 238000009472 formulation Methods 0.000 description 8
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 8
- 239000008213 purified water Substances 0.000 description 8
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 7
- 238000004132 cross linking Methods 0.000 description 7
- 229920001971 elastomer Polymers 0.000 description 7
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 7
- 239000005060 rubber Substances 0.000 description 7
- 229960004889 salicylic acid Drugs 0.000 description 7
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 description 6
- NCKMMSIFQUPKCK-UHFFFAOYSA-N 2-benzyl-4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1CC1=CC=CC=C1 NCKMMSIFQUPKCK-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 description 6
- 150000002576 ketones Chemical class 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- OTIXUSNHAKOJBX-UHFFFAOYSA-N 1-(aziridin-1-yl)ethanone Chemical compound CC(=O)N1CC1 OTIXUSNHAKOJBX-UHFFFAOYSA-N 0.000 description 5
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 5
- 239000004166 Lanolin Substances 0.000 description 5
- 208000002193 Pain Diseases 0.000 description 5
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 5
- 239000012790 adhesive layer Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 229940039717 lanolin Drugs 0.000 description 5
- 235000019388 lanolin Nutrition 0.000 description 5
- 230000014759 maintenance of location Effects 0.000 description 5
- 229940041616 menthol Drugs 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 235000002906 tartaric acid Nutrition 0.000 description 5
- 239000011975 tartaric acid Substances 0.000 description 5
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 4
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 4
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 235000002566 Capsicum Nutrition 0.000 description 4
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 4
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 4
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 239000004202 carbamide Substances 0.000 description 4
- 239000002738 chelating agent Substances 0.000 description 4
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 4
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 4
- 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 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- MMXKVMNBHPAILY-UHFFFAOYSA-N ethyl laurate Chemical compound CCCCCCCCCCCC(=O)OCC MMXKVMNBHPAILY-UHFFFAOYSA-N 0.000 description 4
- IVLVTNPOHDFFCJ-UHFFFAOYSA-N fentanyl citrate Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O.C=1C=CC=CC=1N(C(=O)CC)C(CC1)CCN1CCC1=CC=CC=C1 IVLVTNPOHDFFCJ-UHFFFAOYSA-N 0.000 description 4
- 239000000796 flavoring agent Substances 0.000 description 4
- 235000019634 flavors Nutrition 0.000 description 4
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 229910001701 hydrotalcite Inorganic materials 0.000 description 4
- 229960001545 hydrotalcite Drugs 0.000 description 4
- 239000004310 lactic acid Substances 0.000 description 4
- 235000014655 lactic acid Nutrition 0.000 description 4
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 4
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 4
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
- 239000000123 paper Substances 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 239000000600 sorbitol Substances 0.000 description 4
- 150000005846 sugar alcohols Polymers 0.000 description 4
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 3
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- 235000019489 Almond oil Nutrition 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 3
- 240000008574 Capsicum frutescens Species 0.000 description 3
- 241000723346 Cinnamomum camphora Species 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 229930182558 Sterol Natural products 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 229940048053 acrylate Drugs 0.000 description 3
- 239000008168 almond oil Substances 0.000 description 3
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 150000003863 ammonium salts Chemical class 0.000 description 3
- 239000000739 antihistaminic agent Substances 0.000 description 3
- 210000004556 brain Anatomy 0.000 description 3
- 229930008380 camphor Natural products 0.000 description 3
- 229960000846 camphor Drugs 0.000 description 3
- 239000001390 capsicum minimum Substances 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 3
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229960002428 fentanyl Drugs 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 230000001965 increasing effect Effects 0.000 description 3
- 229960000905 indomethacin Drugs 0.000 description 3
- 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 3
- 238000000465 moulding Methods 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- KSCKTBJJRVPGKM-UHFFFAOYSA-N octan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-] KSCKTBJJRVPGKM-UHFFFAOYSA-N 0.000 description 3
- 229940056211 paraffin Drugs 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 3
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 235000003702 sterols Nutrition 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
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Classifications
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- 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
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
-
- 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
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
- A61K9/7023—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
- A61K9/703—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms characterised by shape or structure; Details concerning release liner or backing; Refillable patches; User-activated patches
- A61K9/7038—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer
- A61K9/7046—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds
- A61K9/7053—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds obtained by reactions only involving carbon to carbon unsaturated bonds, e.g. polyvinyl, polyisobutylene, polystyrene
- A61K9/7061—Polyacrylates
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Description
(2) (2)1344850 膠、角叉萊膠、達蘭膠(Durr an gUm)、藻酸鈉、甘露聚 糖、明膠等天然水溶性高分子,聚丙烯酸或聚甲基丙烯酸 鹽、聚乙烯醇、聚丙烯醯胺等合成高分子,於上述高分子 中配合多元醇等保濕劑等而構成。由於此等黏著劑基材爲 親水性對皮膚刺激性少而適於長期使用,惟缺乏黏著性, 且從皮膚吸收之藥物基本上以親油性者均多。因此,藥物 難以溶解於含多量水之該製劑中,結果吸收性差。此外對 容易水解之藥物等亦難以確保其經時安定性。 爲迴避上述問題,例如,日本特開平4 - 1 7 8 3 2 3號公 報(專利文獻1)揭示將聚丙烯酸溶解於多元醇中,並以 矽酸鋁酸鎂使其交聯者。 然而聚丙烯酸具有親水性雖可預期其刺激性少,但因 實質上不含水而幾乎不會進行鋁與羧基之交聯反應,而產 生發黏現象或對皮膚發生所謂「漿糊發硬」現象而使用感 顯著劣化。此外,聚丙烯酸雖溶解於甘油,但其增黏性低 而難以提高黏著力。 又’日本特開平6 -1 2 8 1 5 1號公報(專利文獻2 )揭 示由特定通式所示之聚丙烯酸及/或同特定通式所示之聚 甲基丙烯酸之1價鹽與聚丙烯酸及/或聚甲基丙烯酸、規 定量之鋁鹽及醇所構成之貼劑基材。然而此處所示聚合物 之醇親合性低’隨者醇濃度提高聚合物會凝集進而析出而 不能表現黏性,結果不能表現黏著力。 [專利文獻1]日本特開平4- 1 7 8 3 23號公報 [專利文獻2]日本特開平6-12815 1號公報 (3)1344850 [非專利文獻1]日本接著學會誌,27 >526 ( 1991)。 【發明內容】 發明欲解決的問題 本發明爲解決上述以往技術之問題而提供藥物經皮吸 收性高之貼劑用黏著劑,該黏著劑對被黏著體之黏著性良 好’不僅對皮膚之刺激性小且不會產生離漿液,且爲單純 組成而容易調製者。 有鑑於上述情況,本發明人經深入重覆檢討之結果, 發現藉由以特定之(甲基)丙烯酸系聚合物或該等之共聚 物及多元醇爲主成分’可使貼劑用黏著劑中之水含量實質 上小於3 0質量% ’而使用此種成分之貼劑用黏著劑具有 優越之經皮吸收性。 亦即’本發明係有關以下之貼劑用黏著劑組成物及其 製造方法。 1 ·貼劑用黏著劑組成物,其特徵爲含有:由重覆單元 爲通式(1 )及(2 ): R1
-CHg—C-
COOM R2 ΌΗ2—C-
COOH (5) (5)1344850 7 ·上述1項記載之貼劑用黏著劑組成物,其中,鋁化 合物之含量爲組成物全量之0.01至20質量%者。 8 .上述1項記載之貼劑用黏著劑組成物,係另含與多 元醇之親合力高之高分子化合物(E )者。 9.上述8項記載之貼劑用黏著劑組成物,其中,與多 元醇之親合力高之高分子化合物(E)係選自羧乙烯聚合 物及N-乙烯乙醯胺-丙烯酸鈉共聚物之至少一種者。 1 0 _上述8或9項記載之貼劑用黏著劑組成物,其中 ’與多元醇之親合力高之高分子化合物之含量爲組成物全 量之0.01至20質量%者。 1 1.上述1至1 〇項記載之貼劑用黏著劑組成物,係含 有雙氯滅痛鈉(diclofenac sodium)作爲藥效成分。 1 2 ·上述1至1 0項記載之貼劑用黏著劑組成物,係含 有辣椒素(capsaicin)作爲藥效成分。 13. 一種貼劑用黏著劑組成物之製造方法,係於含有 由重覆單元通式(1)及式(2): --CH2—C---⑴ I Λ L COOM 」 R2 --ch2—c— --( 2 ) COOH . (式中之符號如同前述1之意義)爲(1) / (2) =100/0 -9- (6) (6)1344850 至9 0/10(莫耳比)之(甲基)丙烯酸系聚合物(a)、 水(B )、多元醇(C )、鋁化合物(D )爲必須成分,及 視需要含有與多元醇親合力高之高分子化合物(E),而 水(B )之含量爲5至30質量%之貼劑用黏著劑組成物之 製造方法,其特徵爲將(甲基)丙烯酸系聚合物(A)與 多元醇(C )之水(B )溶液混合使其等總質量中水分濃 度達50%以上’然後添加餘留成分(餘留之多元醇(c ) '銘化合物(D )及視需要之高分子化合物(e ))並加 以混合’調整水分濃度使達5至3 0 %範圍。 【實施方式】 下文詳細說明本發明。 本發明人等觀察聚丙烯酸、聚丙烯酸部分中和物(丙 烯酸-丙烯酸鹽共聚物)及聚丙烯酸鹽對高濃度多元醇水 溶液之溶解性。聚丙烯酸爲溶解於高濃度多元醇水溶液之 聚合物’惟該聚合物凝集性高因而溶液略呈白濁。另檢討 有關聚丙烯酸部分中和物隨者丙烯酸與丙烯酸鹽之共聚比 例而變化之溶解性,果然與醇類親合力高之丙烯酸含量增 高時係呈現高溶解性。但令人訝異的是丙烯酸含量爲1〇 莫耳%以下時反而對高濃度多元醇水溶液呈現良好的溶解 性’於焉完成本發明。含多量丙烯酸鹽者呈現高溶解性之 理由雖仍不明,咸認係因有水存在而鹽解離,亦即,由於 多量存在之羧酸根而增高與多元醇之親和性。另一方面咸 認因丙烯酸或甲基丙烯酸(下文將「丙烯酸或甲基丙烯酸 -10 - (7) (7)1344850 」簡稱爲「(甲基)丙稀酸」)含量增加時,聚合物分子 鏈之中游離羧基增加’聚合物凝集(捲縮)而抑制鹽之解 離,使羧酸根之量減少之故。 又’(甲基)丙稀酸系聚合物基材爲水溶性因而可提 升黏著層之親水性’由於可吸收皮膚表面分泌之水分,除 了可維持貼劑之皮膚密貼性亦可獲得充分滿足之藥理效果 ’此外與外界之水蒸氣間成爲平衡狀態而可防止皮膚起皺 或產生斑疹。 本發明之貼劑用黏著劑具有優越之性質而可應用於以 下各種用途。 (I) 醫藥品:經皮吸收用製劑、經黏膜吸收用製劑 等貼劑等, (II) 醫療用具:發熱時之患部冷卻劑、創傷治癒劑、 治療用墼、手術用吸液劑、烫傷治癒劑等, (ΠΙ)化妝品、醫藥外用品:貼敷劑、曬斑用劑、面 膜、青春痘用劑等。 本發明之貼劑用黏著劑組成物係以(甲基)丙烯酸系 聚合物(成分A)與水(成分B)、多元醇(成分C)及 鋁化合物(成分D)爲必須成分所構成,而水之含量爲實 質上甚低之5至30質量%者。 本發明所用之(甲基)丙烯酸系聚合物(成分A), 對成分A至成分C之全量以使用〇.5至30質量% (下文 簡稱爲%)之範圍較佳,2至2 0質量%之範圍更佳。小於 0.5 %時,自膠體生成離漿液而成爲不均勻黏著層’若超過 -11 - (8) 1344850 3 〇%則成形時溶膠黏度升高,使得成形或與其他成分之混 合變得困難。 構成上述成分(A)之重覆單元爲通式(1)及(2) 且(1) / (2) =100/0至90/10(莫耳比)之(甲基)丙烯 酸系聚合物: R1
I CH2—C1-
COOM R2
I CH〇—C*- i
COOH (式中,R1及R2各自分別示氫原子或甲基,M示NH4 +或 鹼金屬),可具體例舉如: (1)丙烯酸或甲基丙烯酸之鈉鹽、鉀鹽等鹼金屬鹽 、銨鹽等之單聚物、(2)丙烯酸或甲基丙烯酸之鈉鹽、 鉀鹽等鹼金屬鹽、銨鹽等與丙烯酸之共聚物、 (3)丙烯酸或甲基丙烯酸之鈉鹽、鉀鹽等鹼金屬鹽 、銨鹽等與甲基丙烯酸之共聚物等。 又,上述(甲基)丙烯酸系聚合物(A)之0_2質量 %水溶液之黏度以 400mPa · s以上爲佳。黏度低於 40 0 mPa · s則膠體生成離漿液而成爲不均勻黏著層。 又’本發明之貼劑用黏著劑組成物中,上述(A )成 分之(甲基)丙烯酸系聚合物之外,亦可在不超過上述( -12- (9) (9)1344850 A)成分之添加量之範圍,且對組成物之全部質量不超過 5 %之範圍下,添加超過上述(〗)/ (2)之莫耳比範圍( 亦即’(甲基)丙烯酸之莫耳比超過1〇莫耳。/。)之(甲 基)丙烯酸系聚合物。 水係爲了提高(甲基)丙烯酸系聚合物之溶解性及增 加增黏性而添加,其添加量爲5至30%。小於5%時,由 於(甲基)丙烯酸系聚合物對多元醇之溶解性變差,而增 黏效果減少’該聚合物會殘留於剝離紙上或使用之皮膚上 而產生所謂「糊殘留」現象,或自支持體取下貼劑用黏著 劑時會產生所謂「撕扯」現象等。而若多於3 0%則組成物 中之藥物溶解性變差,藥物之擴散速度降低,結果導致皮 膚之吸收性降低。 多元醇(C )係爲了提高貼劑用黏著劑中藥物之溶解 性及活性量,以及提升對皮膚之轉移性之目的而配合者。 多元醇可例舉如乙二醇、丙二醇' 1,3 -丁二醇、二乙二 醇、三乙二醇、1,4-丁二醇(二元醇),甘油、三羥基 異丁烷(三元醇),赤蘚醇、季戊四醇(四元醇),木糖 醇、核糖醇(五元醇),阿洛糖醇、山梨糖醇、山梨糖醇 液、甘露糖醇(六元醇),聚甘油、二丙二醇等,但不限 於此等。此等之中就安全性及對(甲基)丙烯酸系聚合物 之親合性而言以甘油爲佳。多元醇可單獨使用亦可使用2 種以上。 多元醇之添加量對組成物全體而言宜爲至94.5% 之範圍,以70至90%之範圍更佳。添加量小於40%時因 -13- (10) (10)1344850 藥物於基劑中之溶解性不足,結果導致皮膚之吸收性降低 〇 若超過94.5 %則難以表現因(甲基)丙烯酸系聚合物 引起之增黏效果,而黏著層難以獲得充分之保型性。 又,視需要亦可添加多元醇以外之溶劑。此等溶劑可 例舉如甲醇、乙醇 '丙醇、苯甲醇、苯乙醇' 異丙醇、異 丁醇、己醇、2 -乙基己醇、環己醇、辛醇、丁醇、戊醇等 一元醇、丙酮、甲基乙基酮等酮類,溶纖素、二噁烷、二 甲基甲醯胺、N -甲基吡咯烷酮、二甲基亞硕等與水混合之 有機溶劑,以及乙酸乙醋、克羅米通(crotamiton)等不 與水混合之有機溶劑。 本發明之貼劑用黏著劑中爲了提高膠體之保型性,且 爲防止「糊殘留」現象亦可添加鋁化合物(D )作爲交聯 劑。 此等鋁化合物(D )對組成物之全量宜添加0.0 1至 20%之範圍,以0.1至10%之範圍更佳。添加量小於〇.〇1 時,交聯不夠充分基劑中產生拉絲現象。若超過20%則膠 體過硬,組成物之黏著性變差。又,藉由改變鋁化合物之 量即可自由控制黏著性。 鋁化合物可例舉如氯化鋁、鉀明礬、銨明礬、硝酸鋁 、硫酸鋁、EDTA-鋁、氫氧化鋁、碳酸氫鈉共沉物(例如 ,協和化學工業(股)製「庫穆來得」等)、合成矽酸鋁 、硬脂酸鋁、阿蘭酸鋁(aluminium alantonate )、合成水 滑石(例如,協和化學工業(股)製「阿卡嗎庫」「阿卡 -14- (11) (11)1344850 麥札」「寇蛙德」等)、氫氧化鋁•鎂(例如’協和化學 工業(股)製「薩納璐銘」等)、氫氧化鋁(例如,協和 化學工業(股)製「乾燥氫氧化鋁膠s_100」等)、乙酸 銘、胺基乙酸二羥基鋁(例如,協和化學工業(股)製「 革利熙那魯」等)、高嶺土、矽酸鋁酸鎂(例如,富士化 學工業(股)製「諾依夕靈」等)、矽酸鋁酸鎂等。此等 銘化合物爲水溶性物或難溶於水者均無妨。又此等鋁化合 物可使用1種或2種以上。此等鋁化合物中藉由倂用水溶 性物與氫氧化鋁•鎂’藉前者進行初期交聯,藉後者進行 後期交聯’而可於短時間內獲得保型性優越之黏著層。 亦可添加鋁化合物以外之交聯劑。此等可例舉如鈣、 錫、鐵、鎂、錳、鋅、鋇等之無機酸鹽(例如,氯化鈣、 氯化鎂、鐵明礬、硫酸鐵、硫酸嫫、EDTA-鈣、EDTA-鎂 '氯化亞鐵 '碳酸鈣、磷酸鈣、磷酸氫鈣、碳酸鎂、碳酸 鋇、矽酸鎂、硬脂酸鎂、檸檬酸鎂)、氫氧化物(例如, 氫氧化鈣、氫氧化鋇、氫氧化鎂(例如,協和化學工業( 股)製「戚斯瑪(Kisma )」等)、氫氧化鐵、氫氧化亞 錫等)、氧化物(例如,氧化鎂(例如,協和化學工業( 股)製「戚佑瓦瑪固(Keowamagu)」「瑪固沙辣特( Magusalat)」等)、甲醛、乙二醇二縮水甘油醚、甘油 二縮水甘油醚、聚乙二醇二縮水甘油醚、丙二醇二縮水甘 油醚、聚丙二醇二縮水甘油醚等環氧化合物等。此等交聯 劑可使用1種或2種以上。 此外’交聯反應之速度調整劑可使用酒石酸、檸檬酸 -15- (12) (12)1344850 '乳酸、乙二醇酸、蘋果酸、水楊酸、富馬酸、甲磺酸、 馬來酸 '乙酸' EDTA-2鈉、尿素 '三乙胺、氨等對金屬 離子之螯合劑或持有配位能之有機酸、有機酸鹽、有機鹼 等以及鹽酸 '磷酸、硫酸、硝酸、氫溴酸等無機酸等。 本發明之貼劑用黏著劑中爲提升多元醇之保持性,可 添加對多元醇親合性高之高分子。此等高分子可例舉如聚 乙烯吡咯烷酮、交聯型聚丙烯酸之羧乙烯聚合物、乙烯吡 咯烷酮-丙烯酸乙酯共聚物、N-乙烯乙醯胺-丙烯酸鈉共聚 物類之乙烯乙醯胺系共聚物、N -乙烯乙醯胺單聚物 '聚乙 烯磺酸、N·乙烯乙醯胺交聯物、聚衣康酸、羥丙基纖維素 、羥丙基甲基纖維素等。此等中以添加使(甲基)丙烯酸 鹽之聚合物交聯之交聯劑而交聯者爲特佳。具體言之,以 羧乙烯聚合物、N -乙烯乙醯胺-丙烯酸鈉共聚物、聚乙烯 磺酸等爲佳,惟就保持性能方面而言以羧乙烯聚合物與 N -乙烯乙醯胺-丙烯酸鈉共聚物爲最佳。又,…乙烯乙醯 胺-丙烯酸鈉共聚物中N -乙烯乙醯胺與丙烯酸鈉之質量比 以99.9至6.0:0.1至40之範圍爲佳。 此等高分子對組成物全量以添加0.1至2 0 %之範圍較 佳’ 1至1 〇 %之範圍更佳。添加量小於〇 .丨%時,多元醇之 保持力不足,若超過20 %則黏著層變硬,與皮膚之密貼感 惡化而使得藥物之吸收性變差。 可使用本發明之膠體投與之藥劑眾多。以下列舉具體 例,但並非限定於此等者。 (a)皮質類固醇:氫化可體松(hydrocortisone)、 -16- (13) (13)1344850 強的松龍 (prednisolone )、丙酸倍氯美松 ( beclomethasone propionate )、特戊酸氟米松( flumethasone pivalate )、丙酮特安皮質醇( triamcinolone acetonide)、氟新晉I ( fluocinolone)、丙 酮化氟新龍(fluocinolone acetonide)、乙酸丙酮化氟新 龍(fluocinolone acetonide acetate)、丙酸氯氟美松( clobetasol propionate )等; (b)消炎鎭痛劑:水楊酸、水楊酸二醇、水楊酸甲酯 、1-薄荷醇、樟烷、舒林酸(sulindac )、甲苯醯吡酸鈉 (tolmetin sodium )、甲氧萘丙酸(naproxen)、聯苯丁 酮酸(fenbufen )、炎痛喜康(piroxicam )、特安皮質醇 (triamcinolone )、乙酸氫化可體松(hydrocortisone acetate )、消炎痛(indomethacin)、酮基苯丙酸( ketoprofen)、乙醯胺基酣(acetoaminophen)、美非那 酸(mefenamic acid.)、氟芬那酸(F1 u f e n a m i c a c i d )、 伊布菲納喀(ibufenak ) '氯索洛芬(i〇xoprofen)、泰普菲 酸(Tiaprofenic acid)、普拉洛芬(pranoprofen)、芬普拉 洛芬.(Fenprofen)、二克氯吩(diclofenac)、二克氯吩 鈉(diclofenac sodium)、耳克氯吩(alclofenac)、氯諾 曰康(Lornoxicam)、氧基苯 丁哩嗣(oxyphenylbutazone )、異丁苯丙酸(ibuprofen )、非恩皮訥庫(fenpinaku )、同訥庫(ketonaku ) '貝摩樸羅吩(be 1 moprofeη )、 那撲滅痛(napumeton )、氟雙樸羅吩(flubiprofen )、 氟歐西德(fluosinonid )、丙酸氯貝它隆(cl〇betazon -17- (14) (14)1344850 propionic acid) 、COX-2 抑制劑(尼滅斯德(nimeslid) 、滅羅昔康(meroxicam)、二乙基四氫M喃并卩引U朵乙酸 (etodolac )、歇雷克布(serekoxib)、羅非克布( rofekoxib )等)等; (C )抗真菌劑:克黴唑(Clotrimazole )、托萘酯( Tolnaftate) 硝酸益康哩(econazole nitrate)、硝酸 歐莫康卩坐(omoconazole nitrate )、硝酸硫康哩 ( thioconazole nitrate )、硝酸酮康哩(omoconazole nitrate)、硝酸密康哩(miconazole nitrate)、硝酸異康 哩(isoconazole nitrate)、匹馬符素(Pimafucin)、硝 酸擴康哩(sulconazole nitrate)、發癬退(tolnaftate) 、硝啦咯菌素(Pyrrolnitrin) 、Η--稀酸(Undecylenic acid ) 、癬可寧(Siccanin)、制霉菌素(Nystatin) ' 去顯退(nornaftate)、衣刹米德(exalamid)、硕苯基 -f--稀酸酯(phenyl undecylenate iodide)、二甲基噻蒽 (Thianthol)、環卩比酮胺(Ciclopiroxolamine)、鹵普羅 景(haloprozin)、曲古黴素(Trichomycin)、擬青黴素 (Variotin ) '戊黴素(pentamycin )、兩性黴素 B( amphotericin B )等; (d )抗組織胺劑:鹽酸四環黴素(Tetracycline hydrochloride )、鹽酸苯海拉明(diphenhydramine hydrochloride)、氯苯那敏(Chlorpheniramine)、二苯 基咪唑、氯黴素(chloramphenicol)等抗生物質,二苯胺 明(diphenhydramine)、馬來酸氯苯那敏(maleic acid -18- (16) (16)1344850 咲喃(Nitrofurazone) '制霉菌素(Nystatin)、乙酿氨 磺醯、克黴唑(Clotrimazole)等; (1 )維他命劑:維他命 A、維他命 D2 ( Ergocalciferol)、維他命 D3 ( Cholecalciferol)、持續性 維他命B1 ( octothiamne B1)、核黃素丁酸酯等; (m)抗癲癲間劑:硝基安定(nitrazepam)、安甲丙 二醋(meprobamate)、氯硝西泮(clonazepam)等; (η )冠血管擴充劑:硝化甘油、硝基二醇、二硝酸異 山梨醇酯、四硝酸赤蘚醇酯、四硝酸季戊四醇酯、硝酸丙 炔醇酯等; (〇 )抗組織胺劑:鹽酸苯海拉明、氯苯那敏、二苯基 咪唑等、 (Ρ)鎭咳劑:右美沙芬(Dextromethorphan)、叔丁 喘寧(terbutaline)、麻黄素(Ephedrin)、鹽酸麻黃鹼 » (q) 性核爾蒙:黃體酮、雌二醇等; (r) 抗憂馨劑:多慮平(doxepin)等; (s) 狹心症治療劑:二乙酿胺(diethylamid)、棒腦 等治汗劑、硝酸異山梨酯等; (t ) 麻藥性鎭痛劑:鹽酸嗎啡 (Morphine hydrochloride )、鹽酸乙基嗎啡(Ethylmorphine hydrochloride)、硫酸嗎啡(morphine sulfate) ' 鹽酸古 柯鹼(Cocaine hydrochloride)、鹽酸哌替啶(Pethidine hydrochloride)、磷酸可待因(codeine phosphate)、磷 -20- (17) (17)1344850 酸二氣可待因(dihydrocodeine phosphate )、檸檬酸芬太 尼(Fentanyl Citrate )、杜石芬太尼(Fentanyl sphene ) 、鹽酸佩西汀(meperidine hydrochloride )等; (u)生藥:黃檗、櫻皮、遠志、我術、母菊 '瓜蔞子 、甘草、桔梗、杏仁、牛黃、五味子、皂莢、柴胡、細辛 、車前子、生麻、美遠志、蒼朮、桑白皮、丁香、陳皮、 土根、南天實、貝母 '麥門冬 '半夏、白朮、莨菪、防風 、麻黃、辣椒精油等; (V)其他:5 -氟尿嘧啶、二氫麥角胺、吩坦尼( fentanyl)、去氨加壓素(DESMOPRESSIN)、毛地黃( Digoxin)、胃復安(metoclopramide)、東珮利得( donpelid)、東萇菩鹼(Scopolamine)、氫漠酸東苠菩驗 等以及動物用醫藥品、睡眠藥、循環器系治療藥、腦代謝 賦活藥、殺菌劑、酵素製劑、酵素抑制劑、活體醫藥(多 肽)' 角化症治療藥、麻藥、抗惡性腫瘤劑、全身麻醉劑 、抗不安劑 '氣喘•鼻過敏劑、抗柏金森劑、化學療法劑 、驅蟲劑、抗原蟲劑、止血劑、強心劑、興奮劑·提神劑 、習慣性中毒用劑、漢方劑、放射性醫藥品、泌尿生殖器 及肛門用劑、血糖降下劑、抗潰瘍劑、頭髮用劑、金屬離 子閉鎖劑 '發汗防止劑、鎭靜劑、抗凝血劑、抗風濕劑、 抗痛風劑及抗凝固藥等。 上述藥物視需要亦可2種以上倂用。藥物之配合比例 對上述貼劑用黏著劑之全質量以調整至0 · 0 1至3 0質量% 爲宜,2至20質量%爲佳。 -21 - (18) (18)1344850 上述藥物中’已知例如辣椒精油中所含之辣椒素與多 量水共存時,對皮膚之刺激性增高。依據本發明,可減少 貼劑用黏著劑之水含量’而製作對皮膚刺激性小之含辣椒 素之溫熱型貼劑。 此外’近年來已知辣椒之辛辣成分辣椒素之受體VR1 係替代辣椒素’即使於43 °C以上之熱或酸度上升下亦會 將熱度或疼痛刺激傳送到腦部(沼崎滿子等:r醫學之進 展」第13卷,1071-1075 (2002))。利用該知識正進行 發展以辣椒素作爲鎭痛劑之硏究。亦即,藉由使用本發明 之黏著劑組成物可獲得刺激性小之含辣椒素之溫熱型貼劑 (鎭痛劑)。此種貼劑特別適用於帶狀疱疹後神經痛。該 帶狀疱疹後神經痛係沿著神經發生,疼痛係呈帶狀存在。 因而’貼劑係考慮以下之型態。例如,做成寬丨至1 0cm 之圓筒狀’依疼痛發生部位切取適當長度貼付之。小型者 亦可爲將直徑1至10公分之圓形或毎片1至l〇cm之正 方形' 小長方形貼劑貼付於發生疼痛之部位者。 於本發明之貼劑用黏著劑中,藥劑可於溶液階段(或 膠體懸濁階段)或爲達交聯反應之熟成階段後添加。較佳 方法係視該藥劑之物性、投與部位及所欲釋出之速度等而 加以選擇。 又’亦可添加促進該等藥劑吸收之補助劑。此種補助 劑可配合一種以上例舉如乙醇、異丙醇、正丁醇、1,3_ 丁二醇、丙二醇、聚乙二醇#4〇〇、甘油、克羅米通、苯甲 醇 '本基乙醇、碳酸丙嫌酯、己基十二院醇、丙醇、水楊 -22- (19) (19)1344850 酸、脲基海因(allantoin )、二甲基亞硕 '二甲基乙醯胺 、二甲基甲醯胺、二異丙基己二酸酯、二乙基癸二酸酯、 乙基月桂酸酯、羊毛脂、耶逸戎(yeizon) 、1-香葉基氮 雜環丁烷-2-酮(GACH)、脂肪酸二烷醇醯胺、水楊酸、 水楊酸衍生物、尿素、離子等角質軟化劑,吡咯烷酮碳酸 等保濕劑、丙二醇單油酸酯' 聚氧乙烯山梨糖醇酐單硬脂 酸酯、山梨糖醇酐單硬脂酸酯、甘油單硬脂酸酯等界面活 性劑,肉宣蔻酸異丙酯、癸二酸二乙酯等酯類、油醇、硬 脂醇、月桂醇等高級醇類’硬脂酸、己酸、壬酸、癸酸、 十二烷酸、十四烷酸、十六烷酸、十八烷酸、油酸、亞油 酸等脂肪酸,薄荷醇、薄荷酮、檸檬烯、蒎烯、六氫吡咯 烷酮、松油烯、萜品烯、雙縮松油醇、香芹醇等萜品烯系 化合物及界面活性劑,脲基海因、二甲基亞砚、二甲基乙 醯胺' 二甲基甲醯胺、二異丙基己二酸酯、二乙基癸二酸 酯、乙基月桂酸酯、羊毛脂' 耶逸戎等助劑,又,視需要 亦可配合一種以上之薄荷醇、樟腦等淸涼劑,杏仁油、橄 欖油、山茶油、杏仁油、薄荷油、芝麻油、大豆油、貂油 、棉子油、玉米油、葵花油、椰子油、由加利油、蓖麻油 、流動石蠟、凡士林、角鯊烯' 角鯊烷、羊毛脂等油成分 ’羧乙烯聚合物等膠化劑,二異丙醇胺等中合劑等。考慮 皮膚之刺激性等’此等物質之配合量對藥劑丨〇 〇質量份以 0.1至5質量份爲宜。 本發明中所用之組成物中’爲更能表現其特性或以提 升加工•成形性及品質及提升膠體中藥劑分散性與安定性 -23- (21) (21)1344850 乙酯共聚物、乙烯吡咯烷酮-苯乙烯共聚物,乙烯吡咯烷 酮·乙酸乙烯酯共聚物、乙酸乙烯酯-(甲基)丙烯酸共聚 物、聚乙酸乙烯酯-丁烯酸共聚物、N -乙烯乙醯胺-丙烯酸 鈉共聚物等N_乙烯乙醯胺系共聚物,聚乙烯磺酸、N -乙 烯乙醯胺交聯物、聚衣康酸、聚羥乙基丙烯酸酯、聚丙烯 醯胺、苯乙烯-馬來酸酐共聚物、丙烯醯胺、苯乙烯-馬來 酸酐共聚物、丙烯醯胺、苯乙烯-馬來酸酐共聚物、丙烯 醯胺-丙稀酸共聚物合成高分子等。 (5 )黏著性賦予物質 砂酮橡膠、聚異蒲勒醇(isopulegol)、苯乙稀-嵌段 共聚物橡膠、丙烯酸橡膠、天然橡膠等各種黏著性物質等 〇 (6)止癢劑:樟腦、百里香酚、薄荷醇、聚氧乙烯月 桂醚、抗組織胺劑、胺基苯甲酸乙酯等。 (7 )角質軟化剥離劑:硫、噻唑酮、硫化硒、水楊酸 、間苯二酚等。 (8 )誤食防止物:辣椒粉、辣椒精油等。 (9) 粉體原料:蒙托石、矽酸酐、石膏、碳黑、矽藻 土、氧化鐵紅、碳酸耗 '水滑石 '滑石 '玻璃、高嶺土' 膨潤土、金屬皂、氣溶膠、雲母鈦、氯氧化銻、魚鱗箔等 ,鋅白、二氧化鈦等。 (10) 油性原料:杏仁油、橄欖油、硬化油、山茶子 油、蓖麻油、木蠟油、椰子油、蜜蠟、鯨蠟、羊毛脂、巴 西棕櫚蠟 '小燭樹蠟、流動石蠟、凡士林' 微晶纖維素蠟 -25- (22) (22)1344850 '純地蠟、角鯊烯、月桂酸、肉宣蔻酸、棕櫚酸、硬脂酸 、異硬脂酸、油酸、月桂醇、鯨蠟醇、硬脂醇、油醇、辛 基十二烷醇、膽固醇、己基癸醇、外脫固醇(wit 〇 sterol )、乳酸鯨蠟酯、肉萱蔻酸異丙酯、月桂酸己酯、肉宣蔻 酸肉宣蔻酯' 棕櫚酸異丙酯、肉登蔻酸辛基十二烷醇、硬 脂酸丁酯、可可油、荷荷芭油 '葡萄子油、鱷梨油、貂油 、蛋黃油、純地蠟、石蠟、二十二烷酸、己二酸異丙酯' 肉宣蔻酸辛基十二院酯、油酸辛基十二院酯、膽固醇油酸 酯等。 (1 1 )界面活性劑:月桂基硫酸酯鹽、聚氧乙烯烷基 醚硫酸鹽、烷基苯磺酸鹽、聚氧乙烯烷基醚磷酸、聚氧乙 烯烷基苯基醚磷酸、N-醯基胺基酸鹽、硬脂酸鈉、棕櫚酸 鉀、鯨鱲基硫酸鈉、月桂基硫酸鈉、棕櫚酸三乙醇胺、聚 氧乙烯月桂基磷酸鈉、醯基麩胺酸鈉、硫活菌素等陰離子 界面活性劑,氯化苄烷錶、氯化苄乙氧銨、氯化硬脂醯三 甲銨、氯化二硬脂醯二甲銨、氯化硬脂醯二甲基苄銨等陽 離子界面活性劑,鹽酸烷二胺乙基甘胺酸、2-烷基-N-羧 甲基-N-羥乙基咪唑鑰甜菜鹼、月桂基二甲胺基乙酸甜菜 鹼、卵磷酯等兩性界面活性劑,聚醇脂肪酸酯、單硬脂酸 甘油、親油型單油酸甘油、單硬脂酸乙二醇、單硬脂酸丙 二醇、山梨糖醇酐脂肪酸酯、聚氧乙烯山梨糖醇酐脂肪酸 酯、聚氧乙烯脂肪酸酯、聚氧乙烯烷基酚醚、聚氧乙烯山 梨糖醇脂肪酸酯、N-醯基胺基酸酯、蔗糖脂肪酸酯、脂肪 酸烷醇醯胺 '聚氧乙烯化固醇、聚氧乙烯化羊毛脂、聚氧 -26. (23) (23)1344850 乙烯硬化蓖麻油等非離子性界面活性劑等。 (1 2 )著色劑:氧化鐵黃、氧化鐵紅、氧化鐵黑、群 青、碳黑、氫氧化鉻、焦油色素、色澱、紅色2號、紅色 3號、紅色102號、紅色201號、黃色4號、黃色5號、 青色〗號 '青色2號等。 (13)香料:芥子油、橘子油、胡椒油、茉莉花油、 杉油、昌浦油、萜品嫌油、橙花油、玫瑰油、由加利油、 酸橙油、檸檬油、日本薄荷油、迷迭香油等植物性香料, 靡香、香猫香、海狸香、龍涎香等動物性香料,溴苯乙烯 、蔽稀、檸檬烯等烴系香料,苄醇薄荷醇等醇系香料, 乙酸乙酯 '水楊酸甲酯等紙類系香料 '苯甲醛、水楊醛等 醛類系香料,樟腦、麝香酮、酮麝香、〗_薄荷酮等酮類系 香料,萸樟素等醚類系香料 '內酯類系香料苯基乙酸等 酸系香料、Π引哚等氮化合物系香料等。 (Μ )紫外線遮斷劑:ASL_24,cyasorb UV-9, Uvinul Μ·4〇等二苯甲酮系’薩羅(Sai〇i)等苯甲酸系, TlnUVln P 等唑系,Uvinul N-35 等腈系、Anc〇ur UA 等尿 素系,Ne〇 Heiiopan Give tan F,2羥基_4甲氧基二苯甲 酮系辛基—甲基對胺基苯甲酸酯,乙基己基對甲氧基薩 那美酸(ethylhexylparamethosainamate)等對胺基酸系、 水楊酸系、苯并呋喃系、香豆素、唑系等。 (1 5 )防腐殺囷劑:苯甲酸、水楊酸、脫氫乙酸 '山 木酸硼酸寺酸類及其鹽類,酚、氯甲酚、氯二甲酚、異 丙基甲基酚 '間苯二酚、鄰苯基酚、對氧基苯甲酸酯、苯 -27- (24) (24)1344850 氧基乙醇、百里酚、日松醇、日松酮、噻唑索隆( thioxolon)等酚類,雙三氯酚,2,4,4'-三氯-21·羥基二 苯基醚等鹵化雙酚類,三氯甲腈、三氟甲基二氯碳醯替苯 胺、十一稀酸單乙醇醯胺 (udecenic acid monoethanolamide)等醯胺化合物類,氯化卡垸銨、溴化 烷基異喹琳鑰、氯化苄乙氧銨、氯化鯨臘基吡啶鑰等四級 銨化合物類,月桂基二(胺乙基)甘胺酸等兩性界面活性 劑,2-吡啶硫醇-1 -氧化物鋅鹽、葡萄糖酸、洗必太( chlorhexidine)、硫嵐(Chilham) 、N -三氯甲基硫-4 -環 己烯-1,2·二羧醯亞胺、氯丁醇等。 (16) 抗氧化劑:降二氫愈瘡木酸、愈瘡木脂、没食 子酸丙酯、丁基羥基回香醚、二丁基羥基甲苯(BHT )、 生育酚(維他命E) 、2,2·-亞甲基雙(4 -甲基-6-第三丁 基)酚等。 (17) 螯合劑:衣地酸鹽、焦磷酸鹽、六偏磷酸鹽、 檸檬酸、酒石酸、葡萄糖酸等。 (1 8 )紫外線散射劑:氧化鈦、高嶺土、滑石等。 (19) pH調整劑:可使用氫氧化鈉、氫氧化鉀、氫氧 化鈣、氫氧化鎂、氨、氨水、三乙醇胺、二甲胺、二乙胺 、三甲胺、三乙胺、三異丙醇胺、磷酸三鈉、磷酸氫二鈉 、隣酸氫二鉀 '單乙醇胺、二乙醇胺、二異丙醇胺、聚乙 醇胺等鹼金屬氫氧化物、鹼土金屬氫氧化物、一級、二級 或三級烷胺’或一級、二級或三級烷醇胺等之鹼及檸檬酸 、酒石酸、乳酸'乙二醇酸、鹽酸、硝酸、蘋果酸、磷酸 -28- (25) (25)1344850 等酸,以及呈現酸性或鹼性之高分子’例如藻酸' 聚麩胺 酸、聚天門冬胺酸、澱粉-丙烯酸接枝聚合物、聚丙烯酸 、乙烯乙酸酯-丁烯酸共聚物、乙烯乙酸酯-(甲基)丙烯 酸共聚物、乙酸乙烯酯-丁烯酸共聚物、聚乙烯磺酸、聚 衣康酸、苯乙烯-馬來酸酐共聚物、丙烯醯胺-丙烯酸共聚 物等。 此等之外,亦可添加安定劑、塡充劑、保存劑、可塑 劑、軟化劑、劣化防止劑等。此等添加劑可在不影響貼劑 用黏著劑之特性範圍內任意添加。 本發明中貼劑用黏著劑係直接將各種原料混合後,以 溶膠狀態注入適當模型中,於模型內交聯成形,使用適當 之成形機、打錠機等將交聯後之膠體直接調製爲各種成形 物。原料之混合可適當選擇使用捏合機、混練擠壓機、捏 練混合器、阿紀均質機(azihomomixer )、周轉式混合機 、雙周轉式混合機等而進行。 此時,係將上述(甲基)丙烯酸系聚合物(A)與多 元醇(C )之水(B )溶液,以使此等總質量中水分濃度 成爲50%以上加以混合’然後添加餘留成份(餘留之多元 醇(C )、鋁化合物(D )及視需要之高分子化合物(e ) )並混合’將水分濃度調整爲5至3 0 %,使(甲基)丙烯 酸系聚合物容易溶解’而以更短時間即可製造本發明之貼 劑用黏著劑。 例如’將5 g聚丙烯酸鈉充分分散於4 5 g甘油中,將 該分散液緩緩加至5 0 g水中練合。操作時之水分濃度爲 -29- (26) (26)1344850 5 0%聚合物於短時間溶解,而易成爲均勻系。於確認聚合 物均勻溶解後,一邊添加餘留之1 00g甘油一邊練合使最 終組成物中之水濃度爲2 5 %。該方法之特徵爲一旦將聚合 物溶解後,於後續添加多元醇時聚合物亦不會析出,而維 持溶解狀態。 於將貼劑用黏著劑片狀化時,可於紙、木材、金屬、 玻璃纖維、布(絨布、織布、不織布等)、合成樹脂(聚 脲烷 '乙烯-乙酸乙烯酯共聚物 '聚氯化乙烯 '聚酯)( 例如,聚苯二甲酸乙二醇酯)、聚烯烴(例如,聚乙烯、 聚丙烯等)、聚醯胺(例如尼龍6、尼龍66等)、聚偏 氯乙烯、聚四氟乙烯等,鋁等金屬箔、橡膠或纖維素衍生 物及此等與塑膠薄膜之基層薄膜等之成形品、薄片(箔) 或膠帶等支持體之1面或2面上適量塗布貼劑用黏著劑即 可。爲使所得片狀貼劑用黏著劑之保存容易,於塗布貼劑 用黏著劑之面上’可黏貼以矽或其他適當方法處理之剝離 片,或者於未塗布貼劑用黏著劑之面上以砂或其他適當方 法處理作爲剝離面,使未塗布膠體之面重疊或捲繞重疊放 置。又,可使用聚乙稀薄膜、聚丙稀薄膜、剝離紙、玻璃 紙、聚氯乙烯、聚酯等。 [實施例] 下文例舉實施例說明本發明之有用性,但本發明並非 侷限於此者。又,”份"係指"質量份"。 -30- (27) (27)1344850 實施例1 : [配合成分與比例] 聚丙烯酸鈉(黏度* 560mPa · s ) 2份 甘油 75.9 份 硫酸鋁 1份 氫氧化鋁•鎂 0.5份 水 18.975 份 氫氧化鈉 0.625 份 羧乙烯聚合物 1份 *黏度係以B型黏度計(20〇c ’旋轉頭編號2,3〇rpm ,30分鐘)測定〇·2質量%水溶液所得之値(以下同)。 [配方] 於水(12.5份)及硫酸銘(1份)之混合液中,添加 聚丙烯酸鈉(「畢斯滅特(Biscomate) F480SS」:昭和電 工(目又)製)(2份)與甘油(1〇份)之分散液並加以混 合。聚合物溶解開始增黏時添加甘油(65.9份)與羧乙烯 聚合物(「AQUPEC HV-504E」:住友精化(股)製)(1 份)及氫氧化鋁•鎂(「薩納璐銘(Sanalumin )」:協和 化學工業(股)製)(0 · 5份)之混合液,最後緩緩加入 氫氧化鈉(0.625份)及水(6.475份)之溶液,練合至 均勻。 使所得溶膠成形並密封後於約2 0 °C下熟成3日後, 自容器取出之膠體以手指接觸有伸展性及強反彈力。 -31 - (28) (28)1344850 實施例2 : [配合成分與比例] 丙烯酸/丙烯酸鈉 (10/90 (莫耳比) 共聚物(黏度401mPa · s ) 5 · 5 份 甘油 75.86 份 辣椒素 〇·5份 硫酸鋁 1.6份 精製水 1 4.5 4 份 N-乙烯乙醯胺/丙烯酸鈉 (9 0 /1 0 (質量比) )共聚物 2份 [配方] 於硫酸鋁(1 . 6份)及精製水(1 4.54份)之混合液 中,緩緩添加丙烯酸/丙烯酸鈉共聚物(5.5份)、甘油( 12.94份)、辣椒素(0.5份)及N-乙烯乙醯胺·丙烯酸 鈉共聚物(2份)之混合液,均勻混合後緩緩將甘油( 62.92份)加至其中,練合至均勻。 使所得溶膠成形並密封後於約20°C下熟成3日後, 自容器取出之膠體以手指接觸時有伸展性及強反彈力》 實施例3 : [配合成分與比例] 聚丙烯酸鈉(黏度675mPa.s) 4份 甘油 57.9份 -32- (29) 1344850
丙二醇 硫酸鋁 1份 精製水 1 8.6 份 羧乙烯聚合物 2份 二克氯吩鈉 1份 氫氧化鋁•鎂 〇.5份 [配方] 於硫酸鋁(1份)及精製水(1 8 · 6份)之混合液中添 加聚丙烯酸鈉(4份)、甘油(13.6份)並練合至均勻。 再緩緩添加甘油(44 · 3份)、丙二醇(1 5份)、羧乙烯 聚合物(「碳普爾(Carbopoll) 934」:NOVEON公司製) (2份)及氫氧化鋁•鎂(「薩納璐銘」··協和化學工業( 股)製)(0.5份)之混合液,最後再添加二克氯吩鈉(1 份)並練合之。 使所得溶膠成形並密封後於約20°C下熟成3日後, 自容器取出之膠體以手指接觸時有伸展性及強反彈力。 另一方面,將所得溶膠以刀型塗布器以〇.5mm厚度 塗敷於氯乙烯支持體上,於約20°C下熟成3日後,測定 經皮吸收性。 實施例4 : [配合成分與比例] 聚丙烯酸鉀(黏度525mPa,s) 4份 -33- (30) (30)1344850 丙烯酸/丙烯酸鈉 (65/35(莫耳比)共聚物 0.5份 酒石酸 1份 合成水滑石 1份 硫酸鉀鋁 1份 氧化銘 1 8份 甘油 6 1 . 5份 N -乙烯乙醯胺交聯物 2份 精製水 5份 克羅米通 5份 消炎痛 1份 [配方] 於精製水(5份)及甘油(0.5份)之混合液中,一 次添加聚丙烯酸鉀(4份)及丙烯酸/丙烯酸鈉共聚物( 0.5份)之混合物並充分練合。繼之,緩緩添加酒石酸 份)、合成水滑石(「阿咖馬克(Alukamak)」:協和化 學工業(股)製)(1份)、硫酸鉀鋁(1份)'氧化鋁 (1 8份)、N-乙烯乙醯胺交聯物(2份)及甘油(61份 )之混合液並再度練合之。確認已成爲均勻狀態後,再緩 緩添加克羅米通(5份)及消炎痛(1份)之溶液並練合 至均勻。 使所得溶膠成形並密封後於約20 °C下熟成3日後, 自容器取出之膠體以手指接觸時有伸展性及強反彈力。 -34 - (31) 1344850 實施例5 : [配合成分與比例] 丙烯酸鈉/甲基丙烯酸鉀 (50/50(莫耳比)共聚物(黏度513mPa· s) 30份 乳酸 〇 · 〇 1份 氫氧化鋁 〇. 〇 1份 山梨糖醇聚縮水甘油醚 0.1份
甘油 1 9 · 8 8份 1,3-丁二醇 10 份 丙二醇 1 〇份 精製水 3 0份 [配方]
於精製水(30份)中一次添加丙烯酸鈉/甲基丙烯酸 鉀共聚物(30份)及甘油(19.88份)之混合液並充分練 合至均勻。繼之,緩緩添加乳酸(〇.〇1份)、山梨糖醇聚 縮水甘油醚(「第納醇(Denacol ) EX-614B」:長賴( Nagase )化成工業(股)製)(0.1份)、乾燥氫氧化鋁 膠(協和化學工業(股)製)(〇.〇1份)、1,3-丁二醇 (10份)及丙二醇(1〇份)之混合液並練合之。 使所得溶膠成形並密封後於約20°C下熟成3曰後’ 自容器取出之膠體以手指接觸時有伸展性及強反弹力° 實施例6 : -35- (32) 1344850 [配合成分與比例] 聚丙烯酸鈉(黏度560mPa.s) 2份 甘油 75·5份 硫酸鋁 0.5份 氫氧化鋁•鎂 〇 · 1 5份 乾燥氫氧化鋁膠 〇 · 2 0份 水 20.025份
氫氧化鈉 〇 . 6 2 5份 羧乙烯聚合物 1份 [配方]
於水(1 2.02 5份)及硫酸鋁(〇.5份)之混合液中添 加聚丙烯酸鈉(「畢斯滅特F480SS」:昭和電工(股)製 )(2份)與甘油(1 0份)之分散液並加以混合°聚合物 溶解開始增黏時添加甘油(65.5份)與羧乙烯聚合物(「 AQUPEC HV-504E」:住友精化(股)製)(1份)及乾燥 氫氧化鋁膠(協和化學工業(股)製,低含水型)(0.20 份)及氫氧化鋁•鎂(「薩納璐銘」:協和化學工業(股 )製)(〇 · 1 5份)之混合液,最後緩緩加入氫氧化鈉( 0.625份)及水(8.00份)之溶液,練合至均勻》 使所得溶膠成形並密封後於約20°C下熟成3日後, 自容器取出之膠體以手指接觸時有伸展性及強反彈力。 實施例7 -36- (33) (33)1344850 [配合成分與比例] 聚丙烯酸鈉(黏度560mPa,s) 2份 甘油 6 8.6份 肉蔻蔻酸異丙酯 7份 硫酸鋁 0.2 5份 氫氧化鋁•鎂 0.25份 水 20.1 53份 氫氧化鈉 0 · 5 4 7份 聚氧乙烯山梨糖醇酐單油酸酯 0_20份 羧乙烯聚合物 1份 [配方] 於水(12.153份)、聚氧乙烯山梨糖醇酐單油酸酯( 「土溫(Tween ) 80」:和光純藥(股)製)(0.20份)及 硫酸鋁(〇. 2 5份)之混合液中,添加聚丙烯酸鈉(「畢斯 滅特F480SS」:昭和電工(股)製)(2份)與甘油(10 份)之分散液並加以混合。聚合物溶解開始增黏時添加甘 油(58.6份)與肉宣蔻酸異丙酯(7份)、羧乙烯聚合物 (「AQUPEC HV-5 04E」:住友精化(股)製)(1份)及 氫氧化鋁•鎂(「薩納璐銘」:協和化學工業(股)製) (〇 · 2 5份)之混合液,最後緩緩加入氫氧化鈉(〇 . 5 4 7份 )及水(8 · 0 0份)之溶液,練合至均勻。 使所得溶膠成形並密封後於5 0 °C下熟成1日後,自 容器取出之膠體以手指接觸時有伸展性及強反彈力。 -37- (34) (34)1344850 比較例1 : [配合成分與比例] 丙烯酸/丙烯酸鈉=3 0/70 (莫耳比)共聚物 (黏度 531mPa«s) 4 份 甘油 7 4份 硫酸鋁 1份 氫氧化鋁•鎂 1份 水 1 6.7 5份 氫氧化鈉 1.25份 羧乙烯聚合物 2份 [配方] 於水(1 〇份)及硫酸鋁(1份)之混合液中添加丙烯 酸/丙烯酸鈉共聚物(「畢斯滅特NP_600」:昭和電工(股 )製)(4份)與甘油(1 0份)之分散液並加以混合。聚 合物溶解開始增黏時緩緩添加甘油(64份)與羧乙烯聚 合物(「AQUPEC HV-5 04E」:住友精化(股)製)(2份 )及氫氧化鋁•鎂(「薩納璐銘」:協和化學工業(股) 製)(1份)之混合液,最後緩緩加入氫氧化鈉(1 .25份 )及水(6.75份)之溶液,練合至均勻。 使所得溶膠成形並密封後於約20°C下熟成3日後, 自容器取出之膠體以手指接觸完全無反彈力,甘油開始滲 入而溶膠沾黏手指。 -38- (35) (35)1344850 比較例2 : [配合成分與比例] 聚丙烯酸 4份 甘油 7 4份 硫酸銘 1份 氣氧化銘•鎂 1份 水 16.75份 氫氧化鈉 1 . 2 5份 羧乙烯聚合物 2份 [配方] 於水(1 〇份)及硫酸鋁(1份)之混合液中添加聚丙 烯酸(Mw = 400萬:阿魯得戚(Aludelich) ) (4份)與甘 油(1 〇份)之分散液並加以混合。聚合物溶解開始增黏 時緩緩添加甘油(64份)與羧乙烯聚合物(「AQUPEC HV-504E」:住友精化(股)製)(2份)及氫氧化鋁•鎂 (「薩納璐銘」:協和化學工業(股)製)(1份)之混合 液,最後緩緩加入氫氧化鈉(1 · 2 5份)及水(6 · 7 5份) 之溶液,練合至均句。 使所得溶膠成形並密封後於約2(TC下熟成3日後, 自容器取出之膠體以手指接觸完全無反彈力,而溶膠沾黏 手指。 比較例3: -39- (36) (36)1344850 [配合成分與比例] 聚丙烯酸鈉(黏度560mPa.s) 4份 甘油 3 〇份 硫酸鋁 1份 精製水 6 1 · 5份 羧乙烯聚合物 2份 二克氯吩鈉 1份 氫氧化鋁•鎂 0 _ 5份 [配方] 於硫酸鋁(1份)及精製水(61 .5份)之混合液中添 加聚丙烯酸鈉(4份)、甘油(1 3 · 6份)並練合至均勻。 再緩緩添加甘油(16.4份)、羧乙烯聚合物(「碳普爾 934」:NOVEON公司製)(2份)及氫氧化鋁•鎂(「薩 納璐銘」:協和化學工業(股)製)(〇 · 5份)之混合液’ 最後再添加二克氯吩鈉(1份)並練合之。 使所得溶膠成形並密封後於約20°C下熟成3日後, 自容器取出之膠體以手指接觸時有伸展性及強反彈力。 另一方面,將所得溶膠以刀型塗布器以〇.5mm厚度 塗敷於氯乙烯支持體上,於約2(TC下熟成3日後,測定 經皮吸收性。 試驗例:二克氯吩鈉貼劑之經皮吸收性 將180g至220g之溫斯特(Wister )系老鼠之背部中 -40- (37) 1344850 間部位剃毛,以50mg/kg之投與量貼敷實施例3及比較例 3之貼劑,以高效液體層析(Η P L C )測定經時之血中濃 度’觀察血漿中濃度之變化,結果示於表1。 表1 二克氯吩鈉貼劑之經皮吸收性 時間(h ) 2 4 6 8 實施例3:濃度(# g/ml血漿) 0.28 0.44 0.63 0.85 比較例3:濃度(β g/ml血漿) 0.06 0.08 0.11 0.14
[發明之效果]
本發明之貼劑用黏著劑係將(甲基)丙烯酸系聚合物 及經皮吸收性藥物分散或溶解於高濃度多元醇水溶液中所 成者’而於黏著層之骨架間可含大量多元醇,且該等不會 離漿而可形成安定之基材。 使用本發明之貼劑用黏著劑之貼劑爲釋出特性、黏著 性均優越且安全性高者。 -41 -
Claims (1)
1344850 _ 公告本 第092130104號專利申請案中文申請專利範圍修正本 民國100年4月11日修正 拾、申請專利範圍 1. 一種貼劑用黏著劑組成物,其特徵爲含有:重覆單 位爲通式(1)及(2): R1 CH2—C--(1 ) _ COOM _ R2 CH2—C---( 2 ) - COOH _ (式中’ R1及R2各自分別示氫原子或甲基,Μ示NH4 +或 驗金屬),且/ (2) =100/0〜90/10(莫耳比)之(甲 基)丙烯酸系聚合物(A)、水(B)、多元醇(C)及鋁 化合物(D),而水(B)之含量爲5〜18.975質量%者。 2 ‘如申請專利範圍第1項之貼劑用黏著劑組成物,其 中重覆單位爲通式(1)及式(2)之(甲基)丙烯酸系聚 合物(A ): 1344850 CHz—C- COOM R2 (2) I CH2—c- I COOH (式中各符號之意義同申請專利範圍第1項)之0.2質量 %水溶液之黏度爲400mPa· s以上。
其 3 ·如申請專利範圍第1項之貼劑用黏著劑組成物 中多元醇爲含3元以上之醇。 4.如申請專利範圍第3項之貼劑用黏著劑組成物,其 中多元醇爲甘油者。 5 ·如申請專利範圍第1項之貼劑用黏著劑組成物,其 中多元醇之含量爲組成物全量之40〜94.5質量%。
6.如申請專利範圍第1項之貼劑用黏著劑組成物,其 中錫化合物係倂用水溶性鋁化合物與氫氧化鋁•鎂。 7·如申請專利範圍第1項之貼劑用黏著劑組成物,其 中fg化;合物之含量爲組成物全量之〇.〇1〜2〇質量。/。。 8 ·如申請專利範圍第1項之貼劑用黏著劑組成物,其 進而含有與多元醇之親合力高之高分子化合物(E)。 9.如申請專利範圍第8項之貼劑用黏著劑組成物,其 中與多元醇親合力高之高分子化合物(E)係至少一種選 自殘基乙稀聚合物及N-乙烯基乙醯胺-丙烯酸鈉共聚物者 1 〇·如申請專利範圍第9項之貼劑用黏著劑組成物 -2- 1344850 其中與多元醇親合力高之高分子化合物之含量爲組成物全 量之0·0 1〜20質量%者》 11. 如申請專利範圍第1至1 0項中任一項之貼劑用黏 著劑組成物’其係含有雙氯滅痛鈉作爲藥效成分。 12. 如申請專利範圍第1至1 〇項中任一項之貼劑用黏 著劑組成物’其係含有辣椒素作爲藥效成分。 1 3 · —種貼劑用黏著劑組成物之製造方法,其係含有 重覆單位爲通式(1)及式(2): R1 --CH2—C--(1〉 I _ COOM _ R2 I ' --CH2—C--( 2 ) COOH (式中之符號同申請專利範圍第1項)且(1 ) / ( 2 ) =10 0/0〜90/10 (莫耳比)之(甲基)丙烯酸系聚合物(a ) '水(B )、多元醇(C )、鋁化合物(D )爲必須成分 ’及視需要含有與多元醇與親合力高之高分子化合物(E )’而水(B)之含量爲5至18·975質量%之貼劑用黏著 劑組成物之製造方法’其特徵爲將(甲基)丙烯酸系聚合 物(A )與多元醇(c )之水(β )溶液混合使該等總質量 中水分濃度爲5 0 %以上,然後添加所餘成分(所餘之多元 醇(C )、鋁化合物(D )及視需要之高分子化合物(E ) )並加以混合,而調整水分濃度爲5〜1 8 975質量%者。
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| PL1786481T3 (pl) * | 2004-09-06 | 2010-04-30 | Vollert Kai | Kompres do kombinowanej aplikacji naturalnych substancji leczniczych i promieni elektromagnetycznych |
| WO2006112533A1 (en) * | 2005-04-18 | 2006-10-26 | Showa Denko K.K. | Water-containing gel form and production method thereof |
| ES2657403T3 (es) | 2007-08-06 | 2018-03-05 | Otsuka Pharmaceutical Co., Ltd. | Composición de gel para aplicación externa que contiene un compuesto de adenina |
| WO2009142993A1 (en) * | 2008-05-21 | 2009-11-26 | The Regents Of The University Of California | Topical application of analgesic for pain relief |
| ITMI20081552A1 (it) | 2008-08-29 | 2010-02-28 | Biofarmitalia Spa | Composizione migliorata per la trasmissione topica di principi attivi nel corpo umano od animale |
| WO2011129269A1 (ja) * | 2010-04-13 | 2011-10-20 | 東亞合成株式会社 | 医療用粘着剤組成物、医療用貼付剤及び該組成物の製造方法 |
| US20110301260A1 (en) * | 2010-06-07 | 2011-12-08 | Elmer's Products, Inc. | High-strength glue stick formulation |
| CA2826003C (en) * | 2011-02-02 | 2019-01-08 | Yasuaki Okada | Blonanserin-containing patch preparation |
| FI20115692L (fi) | 2011-06-30 | 2012-12-31 | Silverphase Oy | Polymeerinen antimikrobinen lisäaine |
| KR101367105B1 (ko) | 2011-10-04 | 2014-02-26 | 주식회사 제닉 | 마스크 기재용 하이드로겔 조성물 및 이를 이용한 하이드로겔의 제조방법 |
| KR101320297B1 (ko) * | 2011-10-26 | 2013-10-22 | 주식회사 제닉 | 쌀가루를 포함하는 경피 흡수용 점착 조성물 및 이의 제조방법 |
| JP2013211345A (ja) * | 2012-03-30 | 2013-10-10 | Nihon Gore Kk | 電気二重層キャパシタ用の分極性電極 |
| HK1243330A1 (zh) * | 2014-12-22 | 2018-07-13 | 久光制药株式会社 | 泥罨剂 |
| KR101883203B1 (ko) * | 2017-09-13 | 2018-07-31 | 주식회사 설매 | 스티커형 마스크팩 시트의 제조방법 및 이러한 방법으로 제조된 스티커형 마스크팩 시트 |
| US12403214B2 (en) * | 2018-05-21 | 2025-09-02 | Milliken & Company | Wound care device having fluid transfer and adhesive properties |
| US12478708B2 (en) * | 2018-05-21 | 2025-11-25 | Milliken & Company | Wound care device having fluid transfer and adhesive properties |
| CN112405734B (zh) * | 2020-11-10 | 2022-05-10 | 漳州市德根工贸有限公司 | 一种胶合板生产工艺及其设备 |
| CN113616721A (zh) * | 2021-09-02 | 2021-11-09 | 四川天福精细化工有限公司 | 一种治疗口腔溃疡的药物组合物及其制备方法和应用 |
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| US4386120A (en) * | 1980-01-07 | 1983-05-31 | Nippon Kayaku Kabushiki Kaisha | Process for producing polyacrylic acid salt granules easily soluble in water |
| US4313958A (en) * | 1980-10-24 | 1982-02-02 | The Procter & Gamble Company | Method of producing analgesia |
| JP3526887B2 (ja) * | 1993-04-23 | 2004-05-17 | 帝國製薬株式会社 | 消炎鎮痛外用貼付剤 |
| US5795916A (en) * | 1994-08-09 | 1998-08-18 | Tsumura & Co. | Composition of external preparation |
| CN1210463A (zh) * | 1996-02-07 | 1999-03-10 | 株式会社津村 | 透明双氯芬酸钠的水溶液以及它的药物组合物 |
| JPH10265374A (ja) * | 1997-03-24 | 1998-10-06 | Saitama Daiichi Seiyaku Kk | 外用剤組成物及びその製造方法 |
| IT1312088B1 (it) * | 1999-04-21 | 2002-04-04 | Altergon Sa | Cerotto per uso topico contenente eparina e diclofenac. |
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| US20060079640A1 (en) | 2006-04-13 |
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| CN1738609A (zh) | 2006-02-22 |
| AU2003276707A8 (en) | 2004-05-25 |
| WO2004039358A1 (en) | 2004-05-13 |
| WO2004039358A8 (en) | 2005-05-12 |
| EP1558225A1 (en) | 2005-08-03 |
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