TW460301B - A sugar coating composition for controlled release of steroids and related compressed tablet - Google Patents
A sugar coating composition for controlled release of steroids and related compressed tablet Download PDFInfo
- Publication number
- TW460301B TW460301B TW085100468A TW85100468A TW460301B TW 460301 B TW460301 B TW 460301B TW 085100468 A TW085100468 A TW 085100468A TW 85100468 A TW85100468 A TW 85100468A TW 460301 B TW460301 B TW 460301B
- Authority
- TW
- Taiwan
- Prior art keywords
- sugar
- patent application
- item
- coated
- steroid
- Prior art date
Links
- 150000003431 steroids Chemical class 0.000 title claims abstract description 39
- 238000009495 sugar coating Methods 0.000 title claims abstract description 28
- 239000008199 coating composition Substances 0.000 title claims abstract description 6
- 239000007891 compressed tablet Substances 0.000 title claims description 10
- 238000013270 controlled release Methods 0.000 title claims 2
- 235000000346 sugar Nutrition 0.000 claims abstract description 50
- 229920000168 Microcrystalline cellulose Polymers 0.000 claims abstract description 5
- 235000019813 microcrystalline cellulose Nutrition 0.000 claims abstract description 5
- 239000008108 microcrystalline cellulose Substances 0.000 claims abstract description 5
- 229940016286 microcrystalline cellulose Drugs 0.000 claims abstract description 5
- 230000003054 hormonal effect Effects 0.000 claims abstract 3
- 239000003826 tablet Substances 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 22
- 229940088597 hormone Drugs 0.000 claims description 21
- 239000005556 hormone Substances 0.000 claims description 21
- -1 methyl norethisterone Chemical compound 0.000 claims description 20
- 239000001913 cellulose Substances 0.000 claims description 14
- 229920002678 cellulose Polymers 0.000 claims description 14
- 235000010980 cellulose Nutrition 0.000 claims description 14
- RJKFOVLPORLFTN-LEKSSAKUSA-N Progesterone Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)C)[C@@]1(C)CC2 RJKFOVLPORLFTN-LEKSSAKUSA-N 0.000 claims description 12
- 229940053934 norethindrone Drugs 0.000 claims description 9
- BFPYWIDHMRZLRN-UHFFFAOYSA-N 17alpha-ethynyl estradiol Natural products OC1=CC=C2C3CCC(C)(C(CC4)(O)C#C)C4C3CCC2=C1 BFPYWIDHMRZLRN-UHFFFAOYSA-N 0.000 claims description 8
- BFPYWIDHMRZLRN-SLHNCBLASA-N Ethinyl estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 BFPYWIDHMRZLRN-SLHNCBLASA-N 0.000 claims description 8
- 230000002079 cooperative effect Effects 0.000 claims description 8
- 229960002568 ethinylestradiol Drugs 0.000 claims description 8
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 claims description 7
- 229930182833 estradiol Natural products 0.000 claims description 7
- 229960005309 estradiol Drugs 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- 238000007906 compression Methods 0.000 claims description 5
- 230000006835 compression Effects 0.000 claims description 5
- 229940011871 estrogen Drugs 0.000 claims description 5
- 239000000262 estrogen Substances 0.000 claims description 5
- VIKNJXKGJWUCNN-XGXHKTLJSA-N norethisterone Chemical compound O=C1CC[C@@H]2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 VIKNJXKGJWUCNN-XGXHKTLJSA-N 0.000 claims description 5
- 229960003387 progesterone Drugs 0.000 claims description 5
- 239000000186 progesterone Substances 0.000 claims description 5
- PROQIPRRNZUXQM-UHFFFAOYSA-N (16alpha,17betaOH)-Estra-1,3,5(10)-triene-3,16,17-triol Natural products OC1=CC=C2C3CCC(C)(C(C(O)C4)O)C4C3CCC2=C1 PROQIPRRNZUXQM-UHFFFAOYSA-N 0.000 claims description 4
- DBPWSSGDRRHUNT-CEGNMAFCSA-N 17α-hydroxyprogesterone Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(=O)C)(O)[C@@]1(C)CC2 DBPWSSGDRRHUNT-CEGNMAFCSA-N 0.000 claims description 4
- 229960004976 desogestrel Drugs 0.000 claims description 4
- RPLCPCMSCLEKRS-BPIQYHPVSA-N desogestrel Chemical compound C1CC[C@@H]2[C@H]3C(=C)C[C@](CC)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 RPLCPCMSCLEKRS-BPIQYHPVSA-N 0.000 claims description 4
- PROQIPRRNZUXQM-ZXXIGWHRSA-N estriol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H]([C@H](O)C4)O)[C@@H]4[C@@H]3CCC2=C1 PROQIPRRNZUXQM-ZXXIGWHRSA-N 0.000 claims description 4
- 229960001348 estriol Drugs 0.000 claims description 4
- 229960002899 hydroxyprogesterone Drugs 0.000 claims description 4
- 229960001786 megestrol Drugs 0.000 claims description 4
- RQZAXGRLVPAYTJ-GQFGMJRRSA-N megestrol acetate Chemical compound C1=C(C)C2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(C)=O)(OC(=O)C)[C@@]1(C)CC2 RQZAXGRLVPAYTJ-GQFGMJRRSA-N 0.000 claims description 4
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 4
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 4
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- IMONTRJLAWHYGT-ZCPXKWAGSA-N Norethindrone Acetate Chemical compound C1CC2=CC(=O)CC[C@@H]2[C@@H]2[C@@H]1[C@@H]1CC[C@](C#C)(OC(=O)C)[C@@]1(C)CC2 IMONTRJLAWHYGT-ZCPXKWAGSA-N 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- AOXRBFRFYPMWLR-XGXHKTLJSA-N ethylestrenol Chemical compound C1CC2=CCCC[C@@H]2[C@@H]2[C@@H]1[C@@H]1CC[C@](CC)(O)[C@@]1(C)CC2 AOXRBFRFYPMWLR-XGXHKTLJSA-N 0.000 claims description 3
- 229960001460 ethylestrenol Drugs 0.000 claims description 3
- 229960001652 norethindrone acetate Drugs 0.000 claims description 3
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 claims 4
- SYRJYECRYDNOBM-QURGRASLSA-N 4-[(E)-5-(4-hydroxyphenyl)-3,6-dimethyloct-4-en-4-yl]phenol Chemical compound C(C)C(/C(=C(/C(C)CC)\C1=CC=C(O)C=C1)/C1=CC=C(O)C=C1)C SYRJYECRYDNOBM-QURGRASLSA-N 0.000 claims 3
- 229960002985 medroxyprogesterone acetate Drugs 0.000 claims 3
- PSGAAPLEWMOORI-PEINSRQWSA-N medroxyprogesterone acetate Chemical compound C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2CC[C@]2(C)[C@@](OC(C)=O)(C(C)=O)CC[C@H]21 PSGAAPLEWMOORI-PEINSRQWSA-N 0.000 claims 3
- ICMWWNHDUZJFDW-DHODBPELSA-N oxymetholone Chemical compound C([C@@H]1CC2)C(=O)\C(=C/O)C[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@](C)(O)[C@@]2(C)CC1 ICMWWNHDUZJFDW-DHODBPELSA-N 0.000 claims 3
- 229960005244 oxymetholone Drugs 0.000 claims 3
- ICMWWNHDUZJFDW-UHFFFAOYSA-N oxymetholone Natural products C1CC2CC(=O)C(=CO)CC2(C)C2C1C1CCC(C)(O)C1(C)CC2 ICMWWNHDUZJFDW-UHFFFAOYSA-N 0.000 claims 3
- 244000025254 Cannabis sativa Species 0.000 claims 2
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 claims 2
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 claims 2
- 244000061176 Nicotiana tabacum Species 0.000 claims 2
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims 2
- 235000009120 camo Nutrition 0.000 claims 2
- 235000005607 chanvre indien Nutrition 0.000 claims 2
- 239000011487 hemp Substances 0.000 claims 2
- 229960001252 methamphetamine Drugs 0.000 claims 2
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 claims 2
- 239000000583 progesterone congener Substances 0.000 claims 2
- 229940076279 serotonin Drugs 0.000 claims 2
- 150000008163 sugars Chemical class 0.000 claims 2
- 239000013589 supplement Substances 0.000 claims 2
- VTHUYJIXSMGYOQ-KOORYGTMSA-N 17-hydroxyprogesterone acetate Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(C)=O)(OC(=O)C)[C@@]1(C)CC2 VTHUYJIXSMGYOQ-KOORYGTMSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 230000001276 controlling effect Effects 0.000 claims 1
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 claims 1
- 239000000047 product Substances 0.000 claims 1
- 239000003814 drug Substances 0.000 description 13
- 239000010410 layer Substances 0.000 description 10
- 229940079593 drug Drugs 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 239000008298 dragée Substances 0.000 description 8
- 239000007940 sugar coated tablet Substances 0.000 description 8
- 238000004090 dissolution Methods 0.000 description 6
- 239000011782 vitamin Substances 0.000 description 6
- 229940088594 vitamin Drugs 0.000 description 6
- 239000013078 crystal Substances 0.000 description 5
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 4
- 229930006000 Sucrose Natural products 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 238000000338 in vitro Methods 0.000 description 4
- 239000000546 pharmaceutical excipient Substances 0.000 description 4
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 4
- 239000005720 sucrose Substances 0.000 description 4
- 229930003231 vitamin Natural products 0.000 description 4
- 235000013343 vitamin Nutrition 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000007937 lozenge Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 230000036470 plasma concentration Effects 0.000 description 2
- 230000035935 pregnancy Effects 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000000052 vinegar Substances 0.000 description 2
- 235000021419 vinegar Nutrition 0.000 description 2
- GCKMFJBGXUYNAG-UHFFFAOYSA-N 17alpha-methyltestosterone Natural products C1CC2=CC(=O)CCC2(C)C2C1C1CCC(C)(O)C1(C)CC2 GCKMFJBGXUYNAG-UHFFFAOYSA-N 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- 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 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- 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 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- GCKMFJBGXUYNAG-HLXURNFRSA-N Methyltestosterone Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@](C)(O)[C@@]1(C)CC2 GCKMFJBGXUYNAG-HLXURNFRSA-N 0.000 description 1
- 229920001410 Microfiber Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
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- 239000013543 active substance Substances 0.000 description 1
- 150000001345 alkine derivatives Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000002220 antihypertensive agent Substances 0.000 description 1
- 229940030600 antihypertensive agent Drugs 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000599 controlled substance Substances 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000007922 dissolution test Methods 0.000 description 1
- 239000002934 diuretic Substances 0.000 description 1
- 230000001882 diuretic effect Effects 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229960001566 methyltestosterone Drugs 0.000 description 1
- 239000003658 microfiber Substances 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 210000002381 plasma Anatomy 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- RJKFOVLPORLFTN-UHFFFAOYSA-N progesterone acetate Natural products C1CC2=CC(=O)CCC2(C)C2C1C1CCC(C(=O)C)C1(C)CC2 RJKFOVLPORLFTN-UHFFFAOYSA-N 0.000 description 1
- 235000011962 puddings Nutrition 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 235000015170 shellfish Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000185 sucrose group Chemical group 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 229940098465 tincture Drugs 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
- A61K31/566—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol having an oxo group in position 17, e.g. estrone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
- A61K31/567—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol substituted in position 17 alpha, e.g. mestranol, norethandrolone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
- A61K31/568—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol substituted in positions 10 and 13 by a chain having at least one carbon atom, e.g. androstanes, e.g. testosterone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
- A61K31/568—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol substituted in positions 10 and 13 by a chain having at least one carbon atom, e.g. androstanes, e.g. testosterone
- A61K31/569—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol substituted in positions 10 and 13 by a chain having at least one carbon atom, e.g. androstanes, e.g. testosterone substituted in position 17 alpha, e.g. ethisterone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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Description
d 6 〇3〇^ Λ7 R7 經濟部中央標準局員工消費合作社印製 五、發明説明( 1 ) ! 1 m 明 背 1 1 過 去 三 個 世 紀 間 致 力 於 確 d<L、 控 制 藥 物 S 藥 錠 釋 放 之 速 1 ! 度 之 方 法 0 賦 形 劑 被 混 入 錠 核 中 以 控 制 溶 作 用 » 並 因 -、· 請 1 先 而 控 制 藥 物 之 吸 牧 〇 錠 劑 與 球 狀 體 以 聚 合 物 塗 覆 提 供 藥 閲 讀 物 慢 速 擴 散 制 放 或 部 位 持 異 性 制 放 0 背 1 I 之 ! 含 多 種 藥 物 之 錠 劑 及 包 膠 之 球 狀 體 劑 型 亦 己 製 成 混 合 意 1 或 事 ! 物 或 呈 不 同 錠 層 或 球 狀 體 〇 提 供 藥 物 進 行 多 種 功 能 相 項 再 1 乘 效 果 〇 如 此 之 錠 劑 持 別 有 用 於 該 等 指 定 使 用 種 以 上 填 寫 本 1 r 具 有 不 同 但 相 容 活 性 之 藥 物 之 傳 統 治 療 上 0 例 如 V 利 尿 頁 i i 劑 常 與 抗 高 血 壓 劑 併 用 > 及 孕 前 劑 (P Γ 0 s e S t at 1 0 n a 1 1 1 a g e η t ) 與 雌 激 素 併 用 〇 i i 明 概 怵 ! 訂 根 據 本 發 明 * 提 供 含 二 或 多 種 藥 理 活 性 劑 之 壓 縮 糖 衣 I m 錠 0 壓 縮 錠 可 含 賦 形 劑 以 提 供 藥 劑 快 速 或 慢 速 之 釋 放 i 1 〇 糖 衣 含 治 療 量 之 激 素 類 固 醇 及 激 素 類 固 醇 制 放 量 之 徹 1 i 晶 m 雒 素 0 存 在 於 錠 核 之 藥 劑 可 包 括 任 —" 習 知 可 與 激 素 1 1 類 固 醇 併 用 之 劑 〇 糖 衣 錠 亦 可 以 色 層 作 最 後 層 之 塗 飾 级 i 並 如 一 般 糖 衣 錠 劑 被 磨 光 0 1 錠 核 之 内 容 物 與 糖 衣 全 敗 / 1V> 不 相 關 * 在 於 糖 衣 及 所 含 激 I 1 素 類 固 醇 在 壓 縮 錠 崩 散 及 藥 物 成 分 溶 解 前 業 己 溶 解 0 因 ! ! 此 * 錠 核 配 方 中 所 用 成 分 可 包 括 醫 藥 可 接 受 性 f 水 溶 性 1 1 及 / 或 非 溶 性 物 質 如 乳 糖 t 磷 酸 鈣 澱 粉 > m 酸 鈣 t 右 1 I 旋 耱 r 山 梨 醇 , 甘 露 醇 9 徹 晶 狀 m 維 素 > m 糖 * 聚 乙 烯 I i 吡 咯 酮 * 甲 基 m 維 素 « 羧 3 基 甲 基 m 維 素 > 海 m 酸 鹽 羥 i 1 1 1 1 1 本紙張尺度適用中國國家標隼(CNS ) Λ4规格UlOX 297公錄) B7 經濟部中央標準局員工消費合作社印製 五、發明説明( 2 ) 1 ! 基 丙 基 m 維 素 f 羥 基 丙 基 甲 基 m Μ 素 % 乙基 纖 雒 素 • 克 1 1 羅 氏 卡 美 羅 斯 銷 f C Γ 0 S C a r m e 11 os e so d i u m ) ♦ 澱粉羥基 1 1 醋 酸 鈉 * 硬 脂 酸 m , 硬 脂 酸 » 聚 乙 二 醇 ,月 桂 基 硫 酸 銷 r—v 請 f 先 t 發 煙 矽 石 » 滑 石 等 〇 閱 讀 含 激 素 類 固 醇 三 糖 衣 亦 含 類 固 醇 釋 放 速度 控 制 量 之 徹 背 面 i 1 之 1 晶 狀 m 雒 素 及· 於 特 定 情 形 下 含 聚 乙 烯 吡 咯酮 以 助 益 糖 衣 注 意 1 Ψ ! 之 應 用 〇 項 再 ! 鍵 核 藉 由 壓 縮 類 固 醇 相 同 藥 物 與 其 他 醫藥 可 接 受 性 賦 填 寫 L 本 形 劑 之 混 合 物 製 得 該 混 合 物 較 佳 成 顆 粒狀 0 鍵 核 可 具 頁 1 I 未 塑 化 或 塑 化 之 密 封 層 其 設 計 以 修 正 核内 所 含 藥 物 之 1 1 藥 物 釋 放 恃 性 或 使 其 免 受 濕 氣 及 / 或 氣 氣。 1 ! 明 詳 ! 訂 本 發 明 提 供 改 良 之 壓 縮 錠 > 其 中 除 了 習知 内 鍵 核 外 尚 I 包 括 耱 衣 9 該 核 含 有 一 種 或 多 種 與 外 耱 衣之 類 固 醇 醫 藥 1 i 相 同 之 藥 物 及 糖 衣 之 含 約 0 . 1至約2 0, 重量百分比之激素 1 i 類 固 醇 » 約 0 . 1至約3 重量百分比之徹晶狀纖維素約〇 至 1 1 约 5 重 量 百 分 比 之 聚 乙 烯 吡 咯 m 及 糖 (上述重量百分比 缠.. 偽 以 糖 衣 重 量 計 )0 以單位劑量計, 錠劑含約0 .0 5至約 i I 50 毫 克 t 較 佳 約 0 . 1至30毫克之激素類固醇於所填裝之 1 1 糖 衣 層 〇 若 需 要 赘 可 在 類 固 醇 填 装 糖 衣 層前 於 惰 性 填 充 1 I 糖 衣 層 塗 上 密 封 層 〇 含 惰 性 填 充 料 之 底 層糖 衣 可 由 含 約 1 1 7 . 5至約1 5百分比撤晶狀纖維素之蔗糖製成。 外糖衣可 1 1 含 著 色 劑 如 二 氧 化 鈦 或 打 錠 藥 常 用 之 主 要, 次 要 或 灰 色 1 I 色 彩 〇 若 需 要 , 著 色 劑 可 4 以 分 別 之 塗 層 塗敷 於 外 糖 層 0 1 i 1 ! 1 1 本紙張尺度適用中國國家標準(CNS ) Λ4規格(210Χ 297公货) 460301 A7 B7 五、發明説明(3 ) 最後將錠劑磨光。 (請先閱讀背而之注意事項再填寫本頁) 本説明書所提糖衣製備所用之糖為糖産物,如Μ糖, 衍生自甜菜或甘蔗源或澱粉,醣或多醣轉化源,其適用 於錠劑塗層上。目前較佳之糖為蔗糖。 已發現激素類固醇自糖衣之釋放可藉由限制撤晶狀纖 雒素之量至約0.1至約3重量百分比(以糖衣重量計)。 使用少量檝晶狀纖維素於糖衣中與此賦形劑用作壓縮助 劑或輔肋錠核崩散之用途不同。用於後者時,徹晶狀纖 雒素之濃度可升高至15至30重量百分比。 適用於混入本發明糖衣配方之激素類固醇實例包括6ct -甲—17 -羥孕_醋酸酯,乙基羥基二降孕甾烯炔國,甲 地妊娠素,二甲去氫孕酮,雌二醇,雌三醇,炔雌醇, 炔雌醇甲醚,雌甾_ .雙烯雌酚,己烷雌酚,二乙基己 稀雌酣,孕_ ,二氧脱氧孕錯铺快酮(desogestrel),防 炔諾酯,羥基孕_,炔諾酮,炔諾酮醋酸酯,甲基炔諾 酮,甲地羥孕_醋酸酯,甲基睾丸素,乙基雌烯醇,去 氫甲睾圈,三甲地羥孕酮(t r ί m e g e s t ο n e )等。 經濟部中央標準局員工消費合作社印製 為說明類固醇於徹晶狀纖維素之存在及不存在下之活 體外溶解速度,提出下列説明性實例而無限制: 奮例1 使用未穿孔或穿孔之塗佈盤將由下列固體組成之糖衣 塗至錠核上: 本紙張尺度適用中國國家標隼(CNS ) Λ4规格(210_xm公焓) Α7 Β7 Α、.發明説明(立) 蔗糖,N F 8 7 % 聚乙烯吡咯_ 3 % 6α -甲-17 -羥孕酮醋酸酯 10% 類固醇之溶解速度依USPXX, p.959(198Q)<711>,經 由六個重覆試驗中於37 °C下溶解於0.54%月桂基硫酸鈉 (於水中),使用裝置2於50 r pm下操作而測得(方法A), CV表示此等試驗以重量百分比表示之變異僳數。 時問(分簏) 類固釋的之百分hh ( C V % ) 5 93(5.2) 1 0 94(5.3) 30 95(5.3) 6 0 95(5.4) 12 0 95(5.4) 富例2 具如上述之相同糖衣,以相同方法所塗覆之錠劑於六 個試驗中使用U S P裝置1於1 0 0 r p m , 3 7 %下溶於0 . 1 3 % 月桂基硫酸鈉(於〇·1Ν HC1)中(方法B)。研究結果為: ij------裝------訂---—丨—線 (請先閱讀背面之注意事項再填寫本頁) 經濟部中央橾隼局貝X.消費合作fi印裝 間(分籀) 類固醇釋协:>再分屮(TV%) 5 83(6.0) 10 85(5.8) 3 0 85(6.2) 6 0 85(6.1) 12 0 85(6.2) 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公漦) 460301 A7 B7 五、發明説明(5 ) 奮例 具相同糖衣組成物,以相同方法所塗覆之額外錠劑使 用SOTAX Dissotest裝置於5.7毫升/分鐘流速下,37Ό 下於0.12%月桂基硫酸鈉(於〇·1Η HC1 HC1)中進行流過 (f low-through)溶解試驗(方法C)。三値分別回含之結果 如下: 顆因酲釋协夕再分hh (CV%) 30 60 90 120 2 10 300 90.9(2.9) 94.2(3.0) 95.3(2.9) 96.0(3.0) 97.4(3.0) 98.9(3.6) (请先閲讀背面之注意事項再填K本頁) 、1ίτ 由此等活體外研究清楚可見在此所用6α -甲-17 -羥孕 _醋酸酯作為典型之激素類固醇可由糖衣極快速地釋放 為作tb較用及說明本發明糖衣之不可預期之性質,將 由下列固體組成之糖衣塗敷至錠核上: 蔗糖,HF 86.5¾ 徹晶狀_維素 0.5% 聚乙烯吡咯_ 3·0% 6 ct -甲-17-羥孕_醋酸酯 10.0% 使用含徹晶狀纖維素之糖衣錠及依照方法自三掴 回合取得下列活性外溶解數據: 本紙張尺度適用中國國家標準(CNS ) Λ4規格(ίίοχ;^7公釐) 終IT- 經濟部中央標準局員工消費合作社印製 經濟部中央標準局員工消費合作社印製 460301 A 7 B7 五、發明説明(合) m·*^· 時間(分籀) 類因醇釋放夕百分f~h 5 19.5(49.5) 1 0 29.9(32.8) 3 0 50.0(23.0) 6 0 61.6(19.5) 1 2 0 74.2(19.2) 窖例5 使用依如上之相同方法製得之額外含徹晶狀纖維素糖 衣錠,依照方法B進行之,回合,取得下列數據: 時間(分鐘) 類因醇协百分屮 5 2.3(34.4) 10 8.2(27.0) 3 0 17.9(16.1) 6 0 26.5(13.6) 12 0 32.7(16.6) 窗例fi 使用含微晶狀纖維素於糖衣之錠劑並依照方法C進行 三回合,取得下列數據: 時間(分鐘) 額因醇 >釋协苒分吒(CV%) 30 2.8(34.4) 6 0 4.1(24.8) 90 5.1(22.3) 12 0 6.4(22.3) 2 10 11.0(19.4) 300 14,3(11.0) 本紙張尺度適用中國國家標準(CNS ) Λ4規格(210X 297公釐) I--:------裝------訂------線~ (請先閱讀背面之注意事項再填寫本頁) 460301 經濟部中央標準局員工消費合作社印製 Λ 7 Β7 五、發明説明(〜十_) - 由此等數據明顯可知糖衣中之少量徹晶狀纖維素(此 例中0.5重量百分比,以糖衣固體重量計)已顯箸延缓激 素類固醇之釋放速度。 製 備 糖 衣 錠 * 其中 該糖 衣含 有 0.0¾. 0 .5% 或2%徹 晶 狀 m 維 素 與 3 . 0%聚乙烯毗咯_, 10. 0 96 6 a -巾- 17 -翔 孕 酮 醋 酸 酯 及 m 糖併 用。 此等 錠 劑餵予 饑 餓狀 態下 之 四 隻 小 獵 犬 並 在 〇, 0.5 .1 , 1.5 f 2 , 3 , 5 , 8 , 12 , 16及 24小 時 測 定 類 固 醇之 血液 血漿 濃 度。繪 出 所得 結果 * 测 定 24小 時 時 段 所 計算 曲線 (AUC)下面積及達最大血漿濃 度 之 時 間 如 下 : 徹 晶 狀 AUC (0-24小時) t max C m a X 激維袤% 雜 克 X小 脖/辜# (小時) (雒克/ 牽升 ) 0 . 0 345 0 .6 37 . 8 0 . 5 294 1 .0 3 6. 9 2 . 0 294 1 .1 24 . 6 由 此 等 活 體 内 狗之 數據 *顯 狀 可知當 徹 晶狀 纖維 素 於 糖 衣 之 Μ m 度 白 〇. 0至含0 , 5 至2. 0%徹晶狀缴維素時, 激 素 類 固 醇 之 生 物 可利 用率 有顯 箸 之變化 0 因此 ,U 入 糖 衣 之 激 素 類 固 醇 之釋 放速 度可 Μ 由混入 少 量徹 晶狀 m 維 素 於 糖 衣 中 控 制 〇 奮例 i? 製 備 耱 衣 錠 其中 該糖 衣含 0 . 25¾ , 0 . 5% 或 0.8% 徹 晶 狀 m 雒 素 與 0 . 5%聚乙烯吡咯酮,5.0 >96 6α- 甲-1 7- 羥 本紙張尺度適用中国國家標準(CNS ) Λ·4規格(210\;m> {清先閱这責而之注--'-''^再-荇衣莨)
4.60301 五、發明説明如备)
解據 溶數 納驗 酸試 硫列 基下 US桂得 用月取 使%。分 劑54驗百 錠0.試酷 等與解酸 此0)溶酷 8 iLr ρΞ Ο 9 夕西 用(1體孕 併58活镩 耱P9行 蔗>,進 及01下里 i§<27°c 酸 ,3 醋XX於^I S3P 質 1 孕US介I 置 装 散 崩 % 狀素 25晶維 G徹纖 間鐘 時分 % % 8 ο 5 0 5 0 0 1 3 4 6 9 狀素9. 晶維 6 徹纖2 7 狀素 晶維 微纖 9 8 2 2 6 4 4 8 3 6 7 8 9 9 研體集下 率個收得 }丨}}用性時取 6 7 ο 3 ϋ λ , , . 和女 ΤΓ 。 (5(5(6(5可之12酯 2394物康及酸 9598QQ02生健 8 醋 1L lx -L_、 I > , l·· 1X 類個 6 酮 _ \JJ. \J/ \J- \ly~o 2 2 3 6 H > SJ (. * · _ Co Cv 5555 於十 -^u 3 1 9 3郭 予 7 9 9 9 0^施 3 I 9 9 9 ο _ - 丨 >· L. 1 劑計 ,甲狀 等設.5-晶 2^: 此換 6 微 互 2 獎 時 小 8 6 /(V ,―V 8 6 以 5’ 型1. 劑 - 1X 估5, 評0. 中於 究。 血 析 分 並 本 ·‘ 樣據 液數 血列 ——------絮— (請先閱讀背面之注意事項再填寫本頁) 袤 維 ft 經濟部中央標準局貝工消費合作社印製 % 土 值 %%均 5 8 . * 土 土 土 ± 土 差 誤 準 擦 本紙張尺度適用中國國家標準(CNS ) Λ4规格(210XM7公釐) 并 蠆 / 克 0 土 土 460301 Λ7 B7 經濟部中央榇準局員工消費合作社印製 五、發明説明( 9 ) 由 活 體 外 溶 解 及 活 體 内 人 類 生 物 可 利用 率 數據 可 清楚 1 1 得 知 激 素 類 固 醇 之 藥 物 釋 放 特 性 及 生 物可 利 用率 經 由撤 1 1 晶 狀 纖 維 素 於 糖 衣 中 之 濃 度 控 制 0 請 1 先 ί s_ 例 9 閲 讀 1 1 含 5 毫 克 二 甲 去 氫 孕 m (於具0 .496 徽晶 狀 纖維 素 之簾 背 1 I 之 1 糖 基 體 中 1與〇 .5 聚 乙 烯 毗 咯 酮 之 糖 衣 經塗 覆 至密 封 之糖 注 意 1 Ι 衣 錠 核 〇 此 劑 型 之 活 體 外 溶 解 態 樣 與 含5 毫 克二 甲 去氫 事 1 I 再 1 J 孕 酮之快速崩 散 壓 m 鍵 使 用 USP ΧΧ<711>( ρ .959 ( 1 9 80 )所 填 寫 1 述 之 溶 Λ77 m 試 驗 作 比 較 * 該 試 驗 使 用 裝 置2 於 50r . Ρ · m *下 .表 頁 、_^ 1 操 作 及 37 下 900毫升0 .54%月桂基硫酸納。 取得下列 I 1 數 據 1 | 釋 放 P 二 甲 夫 領i 孕 酮 平 均 丙 分 1 (C ) ! 訂 時間 習 知 快 速 含 二 甲 去 氫 孕 酮 1 (分鐘) «» 明 散 錠 於 耱 衣 之 糖 衣 錠 1 1 15 95 (2 .0) 6 ( 11 .2 ) 1 ! 30 95 (2 .9 ) 1 1 ί 6 . 9) 1 1 45 97 (1 .6 ) 1 5(6. 4) .良 60 97 (1 .9 ) 1 8 ( 6 . 6) ϊ 120 98 (1 .9 ) 25(6. 2) 1 i 激 素 混 入 含 0 . 4%徹晶狀纖維素之糖衣時, 降低二甲 1 i 去 氫 孕 m 之 溶 解 之 顯 著 效 用 可 明 顯 證 實。 1 1 本 發 明 之 較 佳 具 體 例 為 壓 縮 錠 » 其 中錠 核 含約 0 1至 1 i 約 5 0毫克或較佳专 勺C .3至 約 2 . 5毫克之單位劑量之雌激 1 1 素 化 合 物 或 其 混 合 物 與 標 準 賦 形 劑 壓縮 肋 劑及 填 充劑 1 1 -1 1 - 1 1 I 1 本紙乐尺度適用中國國家標单(CNS ) Λ4規格(21()Χ 297公货.) 460301 Λ7 B7五、發明説明(10 ) 經濟部中央標準局員工消费合作社印製 用 併 S e ο Γ 包 佳)ΐ 最eη 素 激 雌 合 拼 之 現 發 中 核 錠 於 e r p 為 知 已 含 ec® ί〇 素 US激 nj雌 CO合 L拼 然 天 之 及 克 毫 ο 5 約 至 11 約 含 一 號 敷 塗之Ξ亮 ^ ^ ^ 縮51曰取 壓 1 及 在約層 C, 佳色 物較 . a 甲 衣 糖 之 酯 酸 醋 酮 孕 羥 (請先閱讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) Λ4規格(210乂297公葰)
Claims (1)
- 4603〇t Λ 本 A8B8C8D8六、申請專利範圍 補充 ",| / 第851 00468號「制放類固醇之糖衣組成物及相關壓縮錠」 專利案 (89年10月修正) 六、申請專利範園: 1. 一種應用於壓縮藥錠之糖衣組成物,包含蔴糖,0.1 至0.3重量%之微晶狀纖維素,0.1至20重量%之激 素類固醇及水之溶液。 2. 如申請專利範圍第1項之糖衣組成物,更進一步包括 至多爲重量5¾的聚乙烯吡咯酮。 3. 如申請專利範圍第1項之糖衣組成物,其中該激素類 固醇爲6α -甲-17 -羥孕酮醋酸酯,乙基羥基二降孕甾 烯炔酮,甲地妊娠素,二甲去氫孕酮,雌二醇,雌三 醇,炔雌醇,炔雌醇甲醚,雌留酮,雙烯雌酚,己烷 雌酚,二乙基己烯雌酚,孕酮,二氫脫氧孕甾烯炔酮 (desogestrel) |肪炔諾酯,羥基孕酮,炔諾酮,炔 諾酮醋酸酯,甲基炔諾酮,甲地羥孕酮醋酸酯,甲基 翠九素,乙基雌烯醇,去氫甲睪酮,氧甲氫龍或三甲 (請先聞讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 合範 有50 掛專 含至 含請 錠 G 括申 該 1 包如 中有 其及 其含 , 核 ,衣 物錠 物糖 成之 成該 組S)組及 衣ell衣素 。糖og糖激 e 之 t 。之雌 on項es物項合。 s 1 d 成 1 拼醇 ge第te組第之固 rile圍ga衣圍克類 ri範JU糖範毫素 f 利on之利 ο 激 酮專(C項專 5 該 孕請素 1 請至之 煙申激第申 1 克 地如雌圍如 ο 毫 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 4.60301 | D8 六、申請專利範圍 C請先閱讀背面之注意事項再填寫本頁) 6. 如申請專利範圍第1項之糖衣組成物,其中該錠核含 有0.3至2.5毫克之拼合雌激素及該糖衣含有1,5至 30毫克之6α -甲-17-羥孕酮酸酸酯。 7. 如申請專利範圍第2項之糖衣組成物,其中該激素類 固醇爲6α -甲·17 -羥孕酮醋酸酯,乙基羥基二降孕甾 烯炔酮,甲地妊娠素,二甲去氫孕酮,雌二醇,雌三 醇,炔雌醇,炔雌醇甲醚,雌留酮,雙烯雌酚,己烷 雌酚,二乙基己烯雌酚,孕酮,二氫脫氧孕甾烯炔酮 (desogestrel),肪炔諾醋,羥基孕酮,炔諾酮,炔 諾酮酸酸酯,甲基炔諾酮,甲地羥孕酮醋酸酯,甲基 睪九素,乙基雌烯醇,去氫甲睪酮,氧甲氫龍或三甲 地羥孕酿(triroegestone) * 8. 如申請專利範圍第2項之糖衣組成物,其包括含拼合 雌激素之錠核及如申請專範圍第1項之糖衣組成物。 9. 如申請專利範圍第2項之糖衣組成物,其中該錠含有 0.1至5.0毫克之拼合雌激素及該糖衣含有1.0至50 毫克之該激素類固醇》 經濟部智慧財產局員工消費合作杜印製 10.如申請專利範圍第2項之糖衣組成物,其中該錠核含 有0.3至2.5毫克之拼合雎激素及該糖衣含有1.5至 30毫克之6α ·甲-17-羥孕酮醅酸酯《 本紙張尺度適用中國國家標準(CNS)A4規格(210 χ 297公釐)申請曰斯 π小U 案 號 1…Λ R 類 別 Ai\KV,i {以上各櫊由本.局460301 經濟部中央棹準局舅工消費合作社印衷 II 專利説明書88年9月修正> 發明 一、新型名稱 中文 制放類固醇之耱衣組成物及相關壓縮綻 英 文 A SUGAR COATING COMPOSITION FOR CONTROLLED RELEASE OF STEROIDS AND RELATED COMPRESSED TABLET 姓 名 瑞吉納徳約瑟巴康 Reginald Joseph Barcomb — 發明 一、創作 國 籍 美國 住、居所 美國紐約州129 5 9摩爾斯福克斯布雷克曼寇纳 斯路9號 姓 名 (名稱) 美國家庭産品股份有限公司 American Home Products Corporation 國 籍 美國 三、申請人 住、居所 (事務所) 美國紐澤西州07940-7160曼迪森5吉拉德農場 代表人 姓 名 依岡E ·貝格 Egon E * Berg 本紙張尺度適用中國國家標隼(CNS ) Α4規格(210 X 297公釐) 裝------.η------^ 四 鄉Ίή Β5 ί 中文發明摘要(發明U稱:制放類固-醇-之-糖衣-組成物及相關壓縮錠丨 應用於歷縮藥録之糖衣組成物,包糖,劑量之激素 類固酵及類固醇釋放速度控制量之徼晶狀纖維素。 英文發明摘要(發明之名稱:A SUGAR °°ΑΤΙΝί3 C0MP0SITI0N F0R C0NTR0LLED ) RELEASE OF STEROIDS AND RELATED COMPRESSED TABLET A sugar coating composition for application to a compressed medicinal tablet comprising a sugar, a dose of a hormonal steroid and a steroid release rate controlling amount of microcrystalline cellulose. ----------—裝----^---訂------ 線 (請先閱讀背面之注意事項再填寫本頁各櫊) 經濟部中央標準局員工消費合作社印裝 本紙張尺度適用中國國家標準(CNS ) A4規格(210 X 297公釐) 4603〇t Λ 本 A8B8C8D8六、申請專利範圍 補充 ",| / 第851 00468號「制放類固醇之糖衣組成物及相關壓縮錠」 專利案 (89年10月修正) 六、申請專利範園: 1. 一種應用於壓縮藥錠之糖衣組成物,包含蔴糖,0.1 至0.3重量%之微晶狀纖維素,0.1至20重量%之激 素類固醇及水之溶液。 2. 如申請專利範圍第1項之糖衣組成物,更進一步包括 至多爲重量5¾的聚乙烯吡咯酮。 3. 如申請專利範圍第1項之糖衣組成物,其中該激素類 固醇爲6α -甲-17 -羥孕酮醋酸酯,乙基羥基二降孕甾 烯炔酮,甲地妊娠素,二甲去氫孕酮,雌二醇,雌三 醇,炔雌醇,炔雌醇甲醚,雌留酮,雙烯雌酚,己烷 雌酚,二乙基己烯雌酚,孕酮,二氫脫氧孕甾烯炔酮 (desogestrel) |肪炔諾酯,羥基孕酮,炔諾酮,炔 諾酮醋酸酯,甲基炔諾酮,甲地羥孕酮醋酸酯,甲基 翠九素,乙基雌烯醇,去氫甲睪酮,氧甲氫龍或三甲 (請先聞讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 合範 有50 掛專 含至 含請 錠 G 括申 該 1 包如 中有 其及 其含 , 核 ,衣 物錠 物糖 成之 成該 組S)組及 衣ell衣素 。糖og糖激 e 之 t 。之雌 on項es物項合。 s 1 d 成 1 拼醇 ge第te組第之固 rile圍ga衣圍克類 ri範JU糖範毫素 f 利on之利 ο 激 酮專(C項專 5 該 孕請素 1 請至之 煙申激第申 1 克 地如雌圍如 ο 毫 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/373,667 US5547948A (en) | 1995-01-17 | 1995-01-17 | Controlled release of steroids from sugar coatings |
Publications (1)
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| TW460301B true TW460301B (en) | 2001-10-21 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW085100468A TW460301B (en) | 1995-01-17 | 1996-01-16 | A sugar coating composition for controlled release of steroids and related compressed tablet |
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Families Citing this family (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5759577A (en) * | 1995-01-17 | 1998-06-02 | American Home Products Corporation | Controlled release of steroids from sugar coatings |
| US5547948A (en) * | 1995-01-17 | 1996-08-20 | American Home Products Corporation | Controlled release of steroids from sugar coatings |
| BE1009856A5 (fr) * | 1995-07-14 | 1997-10-07 | Sandoz Sa | Composition pharmaceutique sous la forme d'une dispersion solide comprenant un macrolide et un vehicule. |
| WO1997004752A1 (en) * | 1995-07-26 | 1997-02-13 | Duramed Pharmaceuticals, Inc. | Pharmaceutical compositions of conjugated estrogens and methods for their use |
| US6479475B1 (en) * | 1996-07-26 | 2002-11-12 | Wyeth | Oral contraceptive |
| US6451778B1 (en) * | 1996-07-26 | 2002-09-17 | Wyeth | Oral contraceptive |
| CA2230748C (en) * | 1997-03-14 | 2010-08-03 | American Home Products Corporation | Rapamycin formulations for oral administration |
| DE19715594A1 (de) | 1997-04-15 | 1998-10-22 | Bayer Ag | Analgetika-Kombination |
| ATE283687T1 (de) * | 1997-06-13 | 2004-12-15 | Wyeth Corp | Rapamycin-formulierungen zur oralen verabreichung |
| US5985325A (en) * | 1997-06-13 | 1999-11-16 | American Home Products Corporation | Rapamycin formulations for oral administration |
| US5997905A (en) * | 1998-09-04 | 1999-12-07 | Mcneil-Ppc | Preparation of pharmaceutically active particles |
| US6432448B1 (en) | 1999-02-08 | 2002-08-13 | Fmc Corporation | Edible coating composition |
| US6723342B1 (en) | 1999-02-08 | 2004-04-20 | Fmc Corporation | Edible coating composition |
| US6500462B1 (en) | 1999-10-29 | 2002-12-31 | Fmc Corporation | Edible MCC/PGA coating composition |
| AT500063A1 (de) | 1999-11-23 | 2005-10-15 | Sandoz Ag | Beschichtete tablettenkerne |
| FR2801218B1 (fr) * | 1999-11-23 | 2001-12-28 | Hoechst Marion Roussel Inc | Compositions pharmaceutiques comprenant de la trimegestone, leurs procedes de preparation ainsi que le conditionnement primaire les renfermant |
| US7989436B2 (en) | 2003-07-23 | 2011-08-02 | Duramed Pharmaceuticals, Inc. | Estrogenic compounds and pharmaceutical formulations comprising the same |
| US6660726B2 (en) | 2000-03-10 | 2003-12-09 | Endeavor Pharmaceuticals | Estrogenic compounds, pharmaceutical compositions thereof, and methods of using same |
| US6855703B1 (en) | 2000-03-10 | 2005-02-15 | Endeavor Pharmaceuticals | Pharmaceutical compositions of conjugated estrogens and methods of analyzing mixtures containing estrogenic compounds |
| US7459445B2 (en) * | 2000-03-10 | 2008-12-02 | Duramed Pharmaceuticals, Inc. | Estrogenic compounds and topical pharmaceutical formulations of the same |
| US20010034340A1 (en) * | 2000-03-20 | 2001-10-25 | American Home Products Corporation | Hormone replacement therapy |
| US6932861B2 (en) | 2000-11-28 | 2005-08-23 | Fmc Corporation | Edible PGA coating composition |
| AU2002225763A1 (en) | 2000-11-28 | 2002-06-11 | Fmc Corporation | Edible pga(propylene glycol alginate) coating composition |
| US6630166B1 (en) * | 2001-02-12 | 2003-10-07 | Watson Pharmaceuticals, Inc. | Compositions for conjugated estrogens and associated methods |
| US7303763B2 (en) * | 2001-02-12 | 2007-12-04 | Watson Laboratories, Inc. | Compositions for conjugated estrogens and associated methods |
| AU2002338277B2 (en) * | 2001-03-16 | 2007-11-22 | Wyeth | Estrogen replacement therapy |
| NZ528373A (en) * | 2001-03-16 | 2005-07-29 | Wyeth Corp | Hormone replacement therapy |
| UA77200C2 (en) | 2001-08-07 | 2006-11-15 | Wyeth Corp | Antineoplastic combination of cci-779 and bkb-569 |
| TW200306196A (en) * | 2002-04-03 | 2003-11-16 | Wyeth Corp | Hormone replacement therapy |
| TW200306846A (en) * | 2002-04-03 | 2003-12-01 | Wyeth Corp | Hormone replacement therapy |
| TW200306851A (en) * | 2002-04-29 | 2003-12-01 | Wyeth Corp | Hormone replacement therapy |
| TW200400040A (en) * | 2002-05-17 | 2004-01-01 | Wyeth Corp | Hormone replacement therapy |
| RU2224517C1 (ru) * | 2002-10-09 | 2004-02-27 | Открытое акционерное общество "Ирбитский химико-фармацевтический завод" | Способ получения противомикробного лекарственного средства |
| US6992075B2 (en) * | 2003-04-04 | 2006-01-31 | Barr Laboratories, Inc. | C(14) estrogenic compounds |
| EP1622623A4 (en) * | 2003-04-11 | 2009-03-18 | Barr Lab Inc | METHOD FOR THE ADMINISTRATION OF ESTROGENIC AND TESTED |
| EP1673071A1 (en) * | 2003-09-29 | 2006-06-28 | Novo Nordisk Femcare AG | Improved stability of progestogen formulations |
| ES2623363T3 (es) * | 2004-06-07 | 2017-07-11 | Wyeth Llc | Revestimientos de azúcar y procedimientos para su obtención |
| JP2008513584A (ja) * | 2004-09-23 | 2008-05-01 | エフ エム シー コーポレーション | 被覆組成物 |
| WO2006084082A1 (en) * | 2005-02-03 | 2006-08-10 | Duramed Pharmaceuticals, Inc. | Compositions of unconjugated estrogens and methods for their use |
| AR054806A1 (es) * | 2005-06-29 | 2007-07-18 | Wyeth Corp | Formulaciones de estrogenos conjugados y bazedoxifeno |
| WO2008058074A2 (en) * | 2006-11-07 | 2008-05-15 | Wyeth | Sugar coatings and methods therefor |
| JP2010511062A (ja) * | 2006-11-29 | 2010-04-08 | ワイス エルエルシー | エストロゲン/sermおよびエストロゲン/プロゲスチン二層錠剤 |
| WO2012120365A1 (en) | 2011-03-07 | 2012-09-13 | Aurobindo Pharma Limited | Stable pharmaceutical composition comprising ethinyl estradiol |
| EP2709597A2 (en) * | 2011-05-13 | 2014-03-26 | Emotional Brain B.V. | Drug delivery system |
| CA2856520C (en) | 2011-11-23 | 2021-04-06 | Therapeuticsmd, Inc. | Natural combination hormone replacement formulations and therapies |
| US9301920B2 (en) | 2012-06-18 | 2016-04-05 | Therapeuticsmd, Inc. | Natural combination hormone replacement formulations and therapies |
| US10806740B2 (en) | 2012-06-18 | 2020-10-20 | Therapeuticsmd, Inc. | Natural combination hormone replacement formulations and therapies |
| US20150196640A1 (en) | 2012-06-18 | 2015-07-16 | Therapeuticsmd, Inc. | Progesterone formulations having a desirable pk profile |
| US10806697B2 (en) | 2012-12-21 | 2020-10-20 | Therapeuticsmd, Inc. | Vaginal inserted estradiol pharmaceutical compositions and methods |
| US20130338122A1 (en) | 2012-06-18 | 2013-12-19 | Therapeuticsmd, Inc. | Transdermal hormone replacement therapies |
| US10537581B2 (en) | 2012-12-21 | 2020-01-21 | Therapeuticsmd, Inc. | Vaginal inserted estradiol pharmaceutical compositions and methods |
| US10471072B2 (en) | 2012-12-21 | 2019-11-12 | Therapeuticsmd, Inc. | Vaginal inserted estradiol pharmaceutical compositions and methods |
| US11246875B2 (en) | 2012-12-21 | 2022-02-15 | Therapeuticsmd, Inc. | Vaginal inserted estradiol pharmaceutical compositions and methods |
| US10568891B2 (en) | 2012-12-21 | 2020-02-25 | Therapeuticsmd, Inc. | Vaginal inserted estradiol pharmaceutical compositions and methods |
| US9180091B2 (en) | 2012-12-21 | 2015-11-10 | Therapeuticsmd, Inc. | Soluble estradiol capsule for vaginal insertion |
| US11266661B2 (en) | 2012-12-21 | 2022-03-08 | Therapeuticsmd, Inc. | Vaginal inserted estradiol pharmaceutical compositions and methods |
| EP2970839B1 (en) * | 2013-03-15 | 2017-02-22 | Monosol, LLC | Water-soluble film for delayed release |
| US10808210B2 (en) | 2013-03-15 | 2020-10-20 | Monosol, Llc | Water-soluble film for delayed release |
| MX2016014281A (es) | 2014-05-22 | 2017-02-22 | Therapeuticsmd Inc | Formulaciones y terapias de reemplazo de combinación de hormonas naturales. |
| US10328087B2 (en) | 2015-07-23 | 2019-06-25 | Therapeuticsmd, Inc. | Formulations for solubilizing hormones |
| WO2017173044A1 (en) | 2016-04-01 | 2017-10-05 | Therapeuticsmd Inc. | Steroid hormone compositions in medium chain oils |
| MX2018011705A (es) | 2016-04-01 | 2019-06-10 | Therapeuticsmd Inc | Composicion farmaceutica de hormona esteroide. |
| US11633405B2 (en) | 2020-02-07 | 2023-04-25 | Therapeuticsmd, Inc. | Steroid hormone pharmaceutical formulations |
| CN116236453A (zh) * | 2023-02-08 | 2023-06-09 | 江苏和汇医药科技有限公司 | 一种延长药品释放的糖包衣及其制备方法 |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB844772A (en) * | 1956-04-19 | 1960-08-17 | Pfizer & Co C | Granular pharmaceutical compositions and process for preparing same |
| GB888631A (en) * | 1959-02-24 | 1962-01-31 | Upjohn Co | Improvements in or relating to oral therapeutic compositions comprising steroids |
| FR1396710A (fr) * | 1964-06-15 | 1965-04-23 | Diwag Chemische Fabriken G M B | Procédé pour la fabrication de charges ou supports perfectionnés et produits obtenus |
| US3980766A (en) * | 1973-08-13 | 1976-09-14 | West Laboratories, Inc. | Orally administered drug composition for therapy in the treatment of narcotic drug addiction |
| US4154820A (en) * | 1976-02-23 | 1979-05-15 | Akzona Incorporated | Compositions containing alkali metal sulfate salts of conjugated estrogens and antioxidants as stabilizers |
| US4248856A (en) * | 1979-07-10 | 1981-02-03 | American Home Products Corporation | Sustained release pharmaceutical compositions |
| US4309404A (en) * | 1979-08-09 | 1982-01-05 | American Home Products Corporation | Sustained release pharmaceutical compositions |
| US4309405A (en) * | 1979-08-09 | 1982-01-05 | American Home Products Corporation | Sustained release pharmaceutical compositions |
| US4327076A (en) * | 1980-11-17 | 1982-04-27 | Life Savers, Inc. | Compressed chewable antacid tablet and method for forming same |
| US4425339A (en) * | 1981-04-09 | 1984-01-10 | Syntex (U.S.A.) Inc. | Treatment of menopausal symptoms |
| US4415546A (en) * | 1981-05-12 | 1983-11-15 | Janakiraman Ramachandran | Biologically active analogs of ACTH and radioimmuno assay therefor |
| US4390531A (en) * | 1981-08-10 | 1983-06-28 | Syntex Pharmaceuticals International Ltd. | Method of contraception using peak progestogen dosage |
| US4415547A (en) * | 1982-06-14 | 1983-11-15 | Sterling Drug Inc. | Sustained-release pharmaceutical tablet and process for preparation thereof |
| JPS604120A (ja) * | 1983-06-22 | 1985-01-10 | Shionogi & Co Ltd | 作用持続型ピナシジル製剤 |
| US4826831A (en) * | 1983-08-05 | 1989-05-02 | Pre Jay Holdings Limited | Method of hormonal treatment for menopausal or post-menopausal disorders involving continuous administration of progestogens and estrogens |
| GB8403360D0 (en) * | 1984-02-08 | 1984-03-14 | Erba Farmitalia | Pharmaceutical compositions |
| US4716041A (en) * | 1984-02-10 | 1987-12-29 | A/S Alfred Benzon | Diffusion coated multiple-units dosage form |
| GB8414221D0 (en) * | 1984-06-04 | 1984-07-11 | Sterwin Ag | Unit dosage form |
| SE8404467D0 (sv) * | 1984-09-06 | 1984-09-06 | Ferrosan Ab | Controlled-release medical preparations |
| US4755386A (en) * | 1986-01-22 | 1988-07-05 | Schering Corporation | Buccal formulation |
| US5208225A (en) * | 1986-02-27 | 1993-05-04 | Warner-Lambert Company | Compositions containing fixed combinations |
| GB8705083D0 (en) * | 1987-03-04 | 1987-04-08 | Euro Celtique Sa | Spheroids |
| US4927816A (en) * | 1987-08-20 | 1990-05-22 | Ester George C | Formulae and methods for sublingual ingestion of natural progesterone |
| US5108995A (en) * | 1987-09-24 | 1992-04-28 | Jencap Research Ltd. | Hormone preparation and method |
| IT1227626B (it) * | 1988-11-28 | 1991-04-23 | Vectorpharma Int | Farmaci supportati aventi velocita' di dissoluzione aumentata e procedimento per la loro preparazione |
| US5073374A (en) * | 1988-11-30 | 1991-12-17 | Schering Corporation | Fast dissolving buccal tablet |
| DK469989D0 (da) * | 1989-09-22 | 1989-09-22 | Bukh Meditec | Farmaceutisk praeparat |
| JP2542122B2 (ja) * | 1990-04-18 | 1996-10-09 | 旭化成工業株式会社 | 球状核、球形顆粒およびその製造方法 |
| US5316772A (en) * | 1990-12-19 | 1994-05-31 | Solvay & Cie, S.A. (Societe Anonyme) | Bilayered oral pharmaceutical composition with pH dependent release |
| US5223268A (en) * | 1991-05-16 | 1993-06-29 | Sterling Drug, Inc. | Low solubility drug-coated bead compositions |
| JP3722294B2 (ja) * | 1993-02-23 | 2005-11-30 | ワーナー−ランバート・コンパニー | 実質的にアルコールを含有しない医薬組成物の製造方法 |
| ZA949929B (en) * | 1993-12-23 | 1995-08-23 | Akzo Nobel Nv | Sugar-coated pharmaceutical dosage unit. |
| US5547948A (en) * | 1995-01-17 | 1996-08-20 | American Home Products Corporation | Controlled release of steroids from sugar coatings |
-
1995
- 1995-01-17 US US08/373,667 patent/US5547948A/en not_active Expired - Lifetime
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1996
- 1996-01-10 AR ARP960100946A patent/AR002019A1/es unknown
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- 1996-01-11 SK SK49-96A patent/SK280484B6/sk not_active IP Right Cessation
- 1996-01-12 JP JP00368196A patent/JP3833292B2/ja not_active Expired - Lifetime
- 1996-01-15 DK DK96300284T patent/DK0722720T3/da active
- 1996-01-15 MY MYPI96000145A patent/MY115786A/en unknown
- 1996-01-15 ZA ZA96301A patent/ZA96301B/xx unknown
- 1996-01-15 IS IS4318A patent/IS1878B/is unknown
- 1996-01-15 AU AU40982/96A patent/AU705879B2/en not_active Expired
- 1996-01-15 AT AT96300284T patent/ATE185482T1/de active
- 1996-01-15 CO CO96001228A patent/CO4370096A1/es unknown
- 1996-01-15 NZ NZ280826A patent/NZ280826A/en not_active IP Right Cessation
- 1996-01-15 SI SI9630070T patent/SI0722720T1/xx unknown
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- 1996-01-15 EP EP96300284A patent/EP0722720B1/en not_active Expired - Lifetime
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- 1996-01-16 UA UA96010195A patent/UA37236C2/uk unknown
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- 1996-01-16 IL IL11677296A patent/IL116772A/xx not_active IP Right Cessation
- 1996-01-16 CN CN96104096A patent/CN1106839C/zh not_active Expired - Lifetime
- 1996-01-16 NO NO19960191A patent/NO315307B1/no not_active IP Right Cessation
- 1996-01-16 TR TR96/00038A patent/TR199600038A2/xx unknown
- 1996-01-16 KR KR1019960000693A patent/KR100338581B1/ko not_active Expired - Lifetime
- 1996-01-16 HU HU9600090A patent/HU223781B1/hu active IP Right Grant
- 1996-01-16 CZ CZ1996128A patent/CZ286102B6/cs not_active IP Right Cessation
- 1996-01-16 TW TW085100468A patent/TW460301B/zh not_active IP Right Cessation
- 1996-01-16 BR BRPI9600100-3A patent/BR9600100B1/pt active IP Right Grant
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1999
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