RU2004124065A - Фармацевтическая таблетка - Google Patents
Фармацевтическая таблетка Download PDFInfo
- Publication number
- RU2004124065A RU2004124065A RU2004124065/15A RU2004124065A RU2004124065A RU 2004124065 A RU2004124065 A RU 2004124065A RU 2004124065/15 A RU2004124065/15 A RU 2004124065/15A RU 2004124065 A RU2004124065 A RU 2004124065A RU 2004124065 A RU2004124065 A RU 2004124065A
- Authority
- RU
- Russia
- Prior art keywords
- agents
- tablet according
- drugs
- pyrene pyrene
- acid
- Prior art date
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- 229940079593 drug Drugs 0.000 claims abstract 27
- 239000003814 drug Substances 0.000 claims abstract 27
- 229920002148 Gellan gum Polymers 0.000 claims abstract 4
- 239000000216 gellan gum Substances 0.000 claims abstract 4
- 235000010492 gellan gum Nutrition 0.000 claims abstract 4
- 239000011159 matrix material Substances 0.000 claims abstract 2
- 239000002245 particle Substances 0.000 claims abstract 2
- 239000007787 solid Substances 0.000 claims abstract 2
- -1 adaptrolol Chemical compound 0.000 claims 35
- 239000003795 chemical substances by application Substances 0.000 claims 17
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 claims 6
- 239000002253 acid Substances 0.000 claims 6
- OROGSEYTTFOCAN-DNJOTXNNSA-N codeine Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC OROGSEYTTFOCAN-DNJOTXNNSA-N 0.000 claims 6
- 229910052760 oxygen Inorganic materials 0.000 claims 5
- 239000000730 antalgic agent Substances 0.000 claims 4
- 230000001754 anti-pyretic effect Effects 0.000 claims 4
- 239000002221 antipyretic Substances 0.000 claims 4
- 229940125716 antipyretic agent Drugs 0.000 claims 4
- OROGSEYTTFOCAN-UHFFFAOYSA-N hydrocodone Natural products C1C(N(CCC234)C)C2C=CC(O)C3OC2=C4C1=CC=C2OC OROGSEYTTFOCAN-UHFFFAOYSA-N 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 230000000202 analgesic effect Effects 0.000 claims 3
- 229940121363 anti-inflammatory agent Drugs 0.000 claims 3
- 239000002260 anti-inflammatory agent Substances 0.000 claims 3
- 229940125684 antimigraine agent Drugs 0.000 claims 3
- 239000002282 antimigraine agent Substances 0.000 claims 3
- 239000002246 antineoplastic agent Substances 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 229960004126 codeine Drugs 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 239000003112 inhibitor Substances 0.000 claims 3
- IXHBTMCLRNMKHZ-LBPRGKRZSA-N levobunolol Chemical compound O=C1CCCC2=C1C=CC=C2OC[C@@H](O)CNC(C)(C)C IXHBTMCLRNMKHZ-LBPRGKRZSA-N 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 229960005489 paracetamol Drugs 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 230000000391 smoking effect Effects 0.000 claims 3
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 claims 2
- LVYLCBNXHHHPSB-UHFFFAOYSA-N 2-hydroxyethyl salicylate Chemical compound OCCOC(=O)C1=CC=CC=C1O LVYLCBNXHHHPSB-UHFFFAOYSA-N 0.000 claims 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 2
- 201000004384 Alopecia Diseases 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- FWKQNCXZGNBPFD-UHFFFAOYSA-N Guaiazulene Chemical compound CC(C)C1=CC=C(C)C2=CC=C(C)C2=C1 FWKQNCXZGNBPFD-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 claims 2
- DEXMFYZAHXMZNM-UHFFFAOYSA-N Narceine Chemical compound OC(=O)C1=C(OC)C(OC)=CC=C1C(=O)CC1=C(CCN(C)C)C=C(OCO2)C2=C1OC DEXMFYZAHXMZNM-UHFFFAOYSA-N 0.000 claims 2
- MITFXPHMIHQXPI-UHFFFAOYSA-N Oraflex Chemical compound N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 claims 2
- 102100038280 Prostaglandin G/H synthase 2 Human genes 0.000 claims 2
- 108050003267 Prostaglandin G/H synthase 2 Proteins 0.000 claims 2
- 150000007513 acids Chemical class 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 239000002160 alpha blocker Substances 0.000 claims 2
- 239000003242 anti bacterial agent Substances 0.000 claims 2
- 229940124350 antibacterial drug Drugs 0.000 claims 2
- 239000003146 anticoagulant agent Substances 0.000 claims 2
- 239000002220 antihypertensive agent Substances 0.000 claims 2
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzydamine Chemical compound C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 claims 2
- 239000002876 beta blocker Substances 0.000 claims 2
- 229950004443 bunolol Drugs 0.000 claims 2
- 229960000590 celecoxib Drugs 0.000 claims 2
- RZEKVGVHFLEQIL-UHFFFAOYSA-N celecoxib Chemical compound C1=CC(C)=CC=C1C1=CC(C(F)(F)F)=NN1C1=CC=C(S(N)(=O)=O)C=C1 RZEKVGVHFLEQIL-UHFFFAOYSA-N 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 239000003136 dopamine receptor stimulating agent Substances 0.000 claims 2
- 229960004945 etoricoxib Drugs 0.000 claims 2
- MNJVRJDLRVPLFE-UHFFFAOYSA-N etoricoxib Chemical compound C1=NC(C)=CC=C1C1=NC=C(Cl)C=C1C1=CC=C(S(C)(=O)=O)C=C1 MNJVRJDLRVPLFE-UHFFFAOYSA-N 0.000 claims 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 claims 2
- 239000003172 expectorant agent Substances 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 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 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 230000004410 intraocular pressure Effects 0.000 claims 2
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 claims 2
- 230000003533 narcotic effect Effects 0.000 claims 2
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 claims 2
- 108090000765 processed proteins & peptides Proteins 0.000 claims 2
- 102000004196 processed proteins & peptides Human genes 0.000 claims 2
- AQHHHDLHHXJYJD-UHFFFAOYSA-N propranolol Chemical compound C1=CC=C2C(OCC(O)CNC(C)C)=CC=CC2=C1 AQHHHDLHHXJYJD-UHFFFAOYSA-N 0.000 claims 2
- 229960000371 rofecoxib Drugs 0.000 claims 2
- RZJQGNCSTQAWON-UHFFFAOYSA-N rofecoxib Chemical compound C1=CC(S(=O)(=O)C)=CC=C1C1=C(C=2C=CC=CC=2)C(=O)OC1 RZJQGNCSTQAWON-UHFFFAOYSA-N 0.000 claims 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims 2
- WVYADZUPLLSGPU-UHFFFAOYSA-N salsalate Chemical compound OC(=O)C1=CC=CC=C1OC(=O)C1=CC=CC=C1O WVYADZUPLLSGPU-UHFFFAOYSA-N 0.000 claims 2
- 229940125723 sedative agent Drugs 0.000 claims 2
- 239000000932 sedative agent Substances 0.000 claims 2
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 claims 2
- 239000000952 serotonin receptor agonist Substances 0.000 claims 2
- 230000003637 steroidlike Effects 0.000 claims 2
- 229960002004 valdecoxib Drugs 0.000 claims 2
- LNPDTQAFDNKSHK-UHFFFAOYSA-N valdecoxib Chemical compound CC=1ON=C(C=2C=CC=CC=2)C=1C1=CC=C(S(N)(=O)=O)C=C1 LNPDTQAFDNKSHK-UHFFFAOYSA-N 0.000 claims 2
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 claims 1
- UVITTYOJFDLOGI-UHFFFAOYSA-N (1,2,5-trimethyl-4-phenylpiperidin-4-yl) propanoate Chemical compound C=1C=CC=CC=1C1(OC(=O)CC)CC(C)N(C)CC1C UVITTYOJFDLOGI-UHFFFAOYSA-N 0.000 claims 1
- SSEBTPPFLLCUMN-CYBMUJFWSA-N (1r)-2-(tert-butylamino)-1-(7-ethyl-1-benzofuran-2-yl)ethanol Chemical compound CCC1=CC=CC2=C1OC([C@H](O)CNC(C)(C)C)=C2 SSEBTPPFLLCUMN-CYBMUJFWSA-N 0.000 claims 1
- RJMIEHBSYVWVIN-LLVKDONJSA-N (2r)-2-[4-(3-oxo-1h-isoindol-2-yl)phenyl]propanoic acid Chemical compound C1=CC([C@H](C(O)=O)C)=CC=C1N1C(=O)C2=CC=CC=C2C1 RJMIEHBSYVWVIN-LLVKDONJSA-N 0.000 claims 1
- ZFKBWSREWJOSSJ-VIFPVBQESA-N (2s)-6,8-dichloro-2-(trifluoromethyl)-2h-chromene-3-carboxylic acid Chemical compound ClC1=CC(Cl)=C2O[C@H](C(F)(F)F)C(C(=O)O)=CC2=C1 ZFKBWSREWJOSSJ-VIFPVBQESA-N 0.000 claims 1
- LGFMXOTUSSVQJV-NEYUFSEYSA-N (4r,4ar,7s,7ar,12bs)-9-methoxy-3-methyl-2,4,4a,7,7a,13-hexahydro-1h-4,12-methanobenzofuro[3,2-e]isoquinoline-7-ol;(4r,4ar,7s,7ar,12bs)-3-methyl-2,4,4a,7,7a,13-hexahydro-1h-4,12-methanobenzofuro[3,2-e]isoquinoline-7,9-diol;1-[(3,4-dimethoxyphenyl)methyl]-6 Chemical compound Cl.Cl.Cl.O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O.C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC.C1=C(OC)C(OC)=CC=C1CC1=NC=CC2=CC(OC)=C(OC)C=C12 LGFMXOTUSSVQJV-NEYUFSEYSA-N 0.000 claims 1
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims 1
- METKIMKYRPQLGS-GFCCVEGCSA-N (R)-atenolol Chemical compound CC(C)NC[C@@H](O)COC1=CC=C(CC(N)=O)C=C1 METKIMKYRPQLGS-GFCCVEGCSA-N 0.000 claims 1
- TVYLLZQTGLZFBW-ZBFHGGJFSA-N (R,R)-tramadol Chemical compound COC1=CC=CC([C@]2(O)[C@H](CCCC2)CN(C)C)=C1 TVYLLZQTGLZFBW-ZBFHGGJFSA-N 0.000 claims 1
- TWBNMYSKRDRHAT-RCWTXCDDSA-N (S)-timolol hemihydrate Chemical compound O.CC(C)(C)NC[C@H](O)COC1=NSN=C1N1CCOCC1.CC(C)(C)NC[C@H](O)COC1=NSN=C1N1CCOCC1 TWBNMYSKRDRHAT-RCWTXCDDSA-N 0.000 claims 1
- ZZMSHBOVYPIYOB-UHFFFAOYSA-N 1,4-diphenylpyrazolidine-3,5-dione Chemical compound O=C1NN(C=2C=CC=CC=2)C(=O)C1C1=CC=CC=C1 ZZMSHBOVYPIYOB-UHFFFAOYSA-N 0.000 claims 1
- XOZLRRYPUKAKMU-UHFFFAOYSA-N 1,5-dimethyl-2-phenyl-4-(propan-2-ylamino)-3-pyrazolone Chemical compound O=C1C(NC(C)C)=C(C)N(C)N1C1=CC=CC=C1 XOZLRRYPUKAKMU-UHFFFAOYSA-N 0.000 claims 1
- ULFYMTMZNITFSB-UHFFFAOYSA-N 2-(3,5-difluorophenyl)-3-(4-methylsulfonylphenyl)cyclopent-2-en-1-one Chemical compound C1=CC(S(=O)(=O)C)=CC=C1C1=C(C=2C=C(F)C=C(F)C=2)C(=O)CC1 ULFYMTMZNITFSB-UHFFFAOYSA-N 0.000 claims 1
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims 1
- XLVXAUNDHWERBM-IVGWJTKZSA-N 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]-n-[(2r,3r,4s,5r)-3,4,5,6-tetrahydroxy-1-oxohexan-2-yl]acetamide Chemical compound CC1=C(CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)[C@H](O)CO)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 XLVXAUNDHWERBM-IVGWJTKZSA-N 0.000 claims 1
- BOFYHBVFGWJLIZ-UHFFFAOYSA-N 2-[2-(diethylamino)ethoxy]-n-phenylbenzamide Chemical compound CCN(CC)CCOC1=CC=CC=C1C(=O)NC1=CC=CC=C1 BOFYHBVFGWJLIZ-UHFFFAOYSA-N 0.000 claims 1
- XILVEPYQJIOVNB-UHFFFAOYSA-N 2-[3-(trifluoromethyl)anilino]benzoic acid 2-(2-hydroxyethoxy)ethyl ester Chemical compound OCCOCCOC(=O)C1=CC=CC=C1NC1=CC=CC(C(F)(F)F)=C1 XILVEPYQJIOVNB-UHFFFAOYSA-N 0.000 claims 1
- JIEKMACRVQTPRC-UHFFFAOYSA-N 2-[4-(4-chlorophenyl)-2-phenyl-5-thiazolyl]acetic acid Chemical compound OC(=O)CC=1SC(C=2C=CC=CC=2)=NC=1C1=CC=C(Cl)C=C1 JIEKMACRVQTPRC-UHFFFAOYSA-N 0.000 claims 1
- IQPPOXSMSDPZKU-JQIJEIRASA-N 2-[4-[(3e)-3-hydroxyiminocyclohexyl]phenyl]propanoic acid Chemical compound C1=CC(C(C(O)=O)C)=CC=C1C1CC(=N/O)/CCC1 IQPPOXSMSDPZKU-JQIJEIRASA-N 0.000 claims 1
- BURBNIPKSRJAIQ-UHFFFAOYSA-N 2-azaniumyl-3-[3-(trifluoromethyl)phenyl]propanoate Chemical compound OC(=O)C(N)CC1=CC=CC(C(F)(F)F)=C1 BURBNIPKSRJAIQ-UHFFFAOYSA-N 0.000 claims 1
- JUIKUQOUMZUFQT-UHFFFAOYSA-N 2-bromoacetamide Chemical compound NC(=O)CBr JUIKUQOUMZUFQT-UHFFFAOYSA-N 0.000 claims 1
- MECVOSKQBMPUFG-UHFFFAOYSA-N 2-carboxyphenolate;morpholin-4-ium Chemical compound C1COCCN1.OC(=O)C1=CC=CC=C1O MECVOSKQBMPUFG-UHFFFAOYSA-N 0.000 claims 1
- 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims 1
- SGUAFYQXFOLMHL-UHFFFAOYSA-N 2-hydroxy-5-{1-hydroxy-2-[(4-phenylbutan-2-yl)amino]ethyl}benzamide Chemical compound C=1C=C(O)C(C(N)=O)=CC=1C(O)CNC(C)CCC1=CC=CC=C1 SGUAFYQXFOLMHL-UHFFFAOYSA-N 0.000 claims 1
- UJABSZITRMATFL-UHFFFAOYSA-N 2-methyl-5-phenylfuran-3-carbonyl chloride Chemical compound ClC(=O)C1=C(C)OC(C=2C=CC=CC=2)=C1 UJABSZITRMATFL-UHFFFAOYSA-N 0.000 claims 1
- YMKHHGTWRZZWEY-UHFFFAOYSA-N 2-phenylquinoline-5-carboxylic acid Chemical compound C=1C=C2C(C(=O)O)=CC=CC2=NC=1C1=CC=CC=C1 YMKHHGTWRZZWEY-UHFFFAOYSA-N 0.000 claims 1
- IYNWSQDZXMGGGI-NUEKZKHPSA-N 3-hydroxymorphinan Chemical compound C1CCC[C@H]2[C@H]3CC4=CC=C(O)C=C4[C@]21CCN3 IYNWSQDZXMGGGI-NUEKZKHPSA-N 0.000 claims 1
- KNKRHSVKIORZQB-UHFFFAOYSA-N 4-bromo-2-(hydroxymethyl)phenol Chemical compound OCC1=CC(Br)=CC=C1O KNKRHSVKIORZQB-UHFFFAOYSA-N 0.000 claims 1
- IMKNHLPRDSWAHW-UHFFFAOYSA-N 4-butyl-1,2-diphenylpyrazolidine-3,5-dione;4,5-dihydro-1,3-thiazol-2-amine Chemical compound NC1=NCCS1.O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 IMKNHLPRDSWAHW-UHFFFAOYSA-N 0.000 claims 1
- UZFMOKQJFYMBGY-UHFFFAOYSA-N 4-hydroxy-TEMPO Chemical compound CC1(C)CC(O)CC(C)(C)N1[O] UZFMOKQJFYMBGY-UHFFFAOYSA-N 0.000 claims 1
- ORLGLBZRQYOWNA-UHFFFAOYSA-N 4-methylpyridin-2-amine Chemical compound CC1=CC=NC(N)=C1 ORLGLBZRQYOWNA-UHFFFAOYSA-N 0.000 claims 1
- DVEQCIBLXRSYPH-UHFFFAOYSA-N 5-butyl-1-cyclohexylbarbituric acid Chemical compound O=C1C(CCCC)C(=O)NC(=O)N1C1CCCCC1 DVEQCIBLXRSYPH-UHFFFAOYSA-N 0.000 claims 1
- BSYNRYMUTXBXSQ-FOQJRBATSA-N 59096-14-9 Chemical compound CC(=O)OC1=CC=CC=C1[14C](O)=O BSYNRYMUTXBXSQ-FOQJRBATSA-N 0.000 claims 1
- USSIQXCVUWKGNF-UHFFFAOYSA-N 6-(dimethylamino)-4,4-diphenylheptan-3-one Chemical compound C=1C=CC=CC=1C(CC(C)N(C)C)(C(=O)CC)C1=CC=CC=C1 USSIQXCVUWKGNF-UHFFFAOYSA-N 0.000 claims 1
- MYYIMZRZXIQBGI-HVIRSNARSA-N 6alpha-Fluoroprednisolone Chemical compound O=C1C=C[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3C[C@H](F)C2=C1 MYYIMZRZXIQBGI-HVIRSNARSA-N 0.000 claims 1
- 239000005541 ACE inhibitor Substances 0.000 claims 1
- WKEMJKQOLOHJLZ-UHFFFAOYSA-N Almogran Chemical compound C1=C2C(CCN(C)C)=CNC2=CC=C1CS(=O)(=O)N1CCCC1 WKEMJKQOLOHJLZ-UHFFFAOYSA-N 0.000 claims 1
- XYLJNLCSTIOKRM-UHFFFAOYSA-N Alphagan Chemical compound C1=CC2=NC=CN=C2C(Br)=C1NC1=NCCN1 XYLJNLCSTIOKRM-UHFFFAOYSA-N 0.000 claims 1
- RLFWWDJHLFCNIJ-UHFFFAOYSA-N Aminoantipyrine Natural products CN1C(C)=C(N)C(=O)N1C1=CC=CC=C1 RLFWWDJHLFCNIJ-UHFFFAOYSA-N 0.000 claims 1
- RMMXTBMQSGEXHJ-UHFFFAOYSA-N Aminophenazone Chemical compound O=C1C(N(C)C)=C(C)N(C)N1C1=CC=CC=C1 RMMXTBMQSGEXHJ-UHFFFAOYSA-N 0.000 claims 1
- MNIPYSSQXLZQLJ-UHFFFAOYSA-N Biofenac Chemical compound OC(=O)COC(=O)CC1=CC=CC=C1NC1=C(Cl)C=CC=C1Cl MNIPYSSQXLZQLJ-UHFFFAOYSA-N 0.000 claims 1
- LIAWQASKBFCRNR-UHFFFAOYSA-N Bucetin Chemical compound CCOC1=CC=C(NC(=O)CC(C)O)C=C1 LIAWQASKBFCRNR-UHFFFAOYSA-N 0.000 claims 1
- VOVIALXJUBGFJZ-KWVAZRHASA-N Budesonide Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@@H]2[C@@H]1[C@@H]1C[C@H]3OC(CCC)O[C@@]3(C(=O)CO)[C@@]1(C)C[C@@H]2O VOVIALXJUBGFJZ-KWVAZRHASA-N 0.000 claims 1
- 229940127291 Calcium channel antagonist Drugs 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 claims 1
- UDKCHVLMFQVBAA-UHFFFAOYSA-M Choline salicylate Chemical compound C[N+](C)(C)CCO.OC1=CC=CC=C1C([O-])=O UDKCHVLMFQVBAA-UHFFFAOYSA-M 0.000 claims 1
- 206010008874 Chronic Fatigue Syndrome Diseases 0.000 claims 1
- 101150065749 Churc1 gene Proteins 0.000 claims 1
- OIRAEJWYWSAQNG-UHFFFAOYSA-N Clidanac Chemical compound ClC=1C=C2C(C(=O)O)CCC2=CC=1C1CCCCC1 OIRAEJWYWSAQNG-UHFFFAOYSA-N 0.000 claims 1
- RGJOEKWQDUBAIZ-IBOSZNHHSA-N CoASH Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCS)O[C@H]1N1C2=NC=NC(N)=C2N=C1 RGJOEKWQDUBAIZ-IBOSZNHHSA-N 0.000 claims 1
- 201000003883 Cystic fibrosis Diseases 0.000 claims 1
- IJVCSMSMFSCRME-KBQPJGBKSA-N Dihydromorphine Chemical compound O([C@H]1[C@H](CC[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O IJVCSMSMFSCRME-KBQPJGBKSA-N 0.000 claims 1
- 229940121891 Dopamine receptor antagonist Drugs 0.000 claims 1
- URJQOOISAKEBKW-UHFFFAOYSA-N Emorfazone Chemical compound C1=NN(C)C(=O)C(OCC)=C1N1CCOCC1 URJQOOISAKEBKW-UHFFFAOYSA-N 0.000 claims 1
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Claims (30)
1. Фармацевтическая таблетка, включающая сердцевину и связанную с ней оболочку, в которой (а) сердцевина содержит твердые частицы водорастворимого красителя, рассредоточенного в матриксе, и (б) оболочка содержит геллановую камедь.
2. Таблетка по п.1, имеющая пятнистую поверхность.
3. Таблетка по п.1, в которой сердцевина содержит препарат в терапевтически и/или профилактически эффективном количестве.
4. Таблетка по п.3, в которой препарат выбирают из группы, состоящей из ингибиторов ангиотензин-превращающего фермента; α-адренергических агонистов; β-адренергических агонистов; α-адренергических блокаторов; β-адренергических блокаторов (бета блокаторов); ингибиторов алкоголя; ингибиторов альдозоредуктазы; антагонистов альдостерона; аминокислот; анаболиков; анальгетиков (как наркотических, так и ненаркотических); анестетиков; анорексиков; антацидов; антигельминтных препаратов; агентов против угревой сыпи; противоаллергических препаратов; антиандрогенов; антиангинальных агентов; седативных агентов; антиаритмиков; противоастматических препаратов; антибактериальных агентов и антибиотиков; препаратов против алопеции и облысения, противоамебных средств; антител; антихолинергических препаратов; антикоагулянтов и разжижителей крови; антиколитических препаратов; противосудорожных средств; антициститических препаратов; антидепрессантов; антидиабетических агентов; антидиарейных средств; антидиуретиков; антидотов; противорвотных средств; антиэстрогенов; антифлятулентов; противогрибковых агентов; антигенов; антиглаукомальных агентов; антигистаминных средств; антигиперактивных средств; антигиперлипопротеинемических средств; антигипертензивных средств; антигипертиреоидных агентов; антигипотензивных средств; антигипотиреоидиных средств; противоинфекционных средств; противовоспалительных (как стероидных, так и нестероидных) средств; антималярийных агентов; агентов против мигрени; антинеопластиков; средств против ожирения; антипаркинсонических агентов и антидискинетиков; антипневмонических агентов; антипротозойных агентов; противозудных средств; антипсориатиков; нейролептиков; антипиретиков; антиревматических средств; антисекреторных агентов; антишоковых медикаментов; антиспазмодиков; антитромботических средств; противораковых агентов; противокашлевых средств; противоязвенных средств; противовирусных агентов; анксиолитиков; бактерицидных средств; уплотнителей костей; бронходилататоров; блокаторов кальциевых каналов; ингибиторов карбоангидразы; кардиотоников и кардиостимуляторов; хемотерапевтических средств; желчегонных средств; холинергических средств; средств для лечения синдрома хронической усталости; стимуляторов ЦНС; коагулянтов; контрацептивов; средств для лечения кистозного фиброза; противоотечных средств; диуретиков; агонистов рецептора допамина; антагонистов рецептора допамина; энзимов; эстрогенов; отхаркивающих средств; средств для лечения желудочной гиперактивности; глюкокортикоидов; гемостатиков; ингибиторов редуктазы коэнзима А человеческого менопаузального гонадотропина; гормонов; снотворных средств; иммуномодуляторов; иммунодепрессантов; слабительных; средств для лечения заболеваний ротовой полости и периодонтальных заболеваний; миотиков; ингибиторов моноаминоксидазы; муколитических средств; средств для лечения рассеянного склероза; мышечных релаксантов; мидриатиков; наркотических антагонистов; антагонистов рецептора NMDA; олигонуклеотидов; офтальмологических препаратов; родоускоряющих средств; пептидов, полипептидов и белков; полисахаридов; прогестрогенов; простагландинов; ингибиторов протеазы; стимуляторов дыхания; седативных средств; ингибиторов накопления серотонина; половых гормонов, включая эндрогены; препаратов, используемых для борьбы с курением; релаксантов гладкой мускулатуры; стимуляторов гладкой мускулатуры; тромболитиков; транквилизаторов; подкислителей мочи; медикаментов для лечения недержания мочи; вазодилататоров; вазопротектантов; и их сочетаний.
5. Таблетка по п.3, в которой препарат является препаратом, используемым для борьбы с курением.
6. Таблетка по п.5, в которой препарат, используемый для борьбы с курением, выбирают из бупропиона, ибогаина, никотина и его метаболитов.
7. Таблетка по п.3, в которой препарат является антибактериальныи препаратом.
8. Таблетка по п.7, в которой антибактериальный препарат является оксазолидиноном.
9. Таблетка по п.8, в которой оксазолидинон выбирают из эперезолида, линезолида, N-[(5S)-3-[3-фтор-4-[4-(2-фторэтил)-3-оксо-1-пиперазинил]фенил-2-оксо-5-оксазолидинил]метил]ацетамида, (S)-N-[[3-[5-(3-пиридил)тиофен-2-ил]-2-оксо-5-оксазолидинил]метил]ацетамида и (S)-N-[[3-[5-(4-пиридил)пирид-2-ил]-2-оксо-5-оксазолидинил]метил]ацетамидгидрохлорида.
10. Таблетка по п.3, в которой препарат является агентом против мигрени.
11. Таблетка по п.10, в которой агент против мигрени является агонистом 5-НТ-рецептора.
12. Таблетка по п.11, в которой агонист 5-НТ-рецептора выбирают из группы, состоящей из алмотриптана, элетриптана, фроватриптана, наратриптана, ризатриптана, суматриптана или золмитриптана.
13. Таблетка по п.3, в которой препарат используется для лечения или профилактики офтальмологических расстройств.
14. Таблетка по п.13, в которой препарат является понижающим внутриглаукомальное или внутриглазное давление агентом.
15. Таблетка по п.14, в которой понижающий внутриглаукомальное или внутриглазное давление агент выбирают из группы, состоящей из адренолона, апраклонидина, бримонидина, дипивефрина, ацебутолола, адапролола, алпренолола, атенолола, бетаксолола, буфетолола, буфуралола, бунитролола, бунолола, бупранолола, картеолола, карведилола, цетамолола, декспропанолола, лабеталола, левобунолола, метипранолола, метопролола, надолола, нифеналола, оксипренолола, пенбутолола, пиндолола, практолола, пронеталола, пропранолола, соталола, тимолола, толамолола, толипролола, ванинолола, ацетазоламида, дорзоламида, биматопроста, латанопроста, травопроста, унопростонизопропила и их сочетаний.
16. Таблетка по п.3, в которой препарат является анальгетиком, антипиретиком или противовоспалительным агентом.
17. Таблетка по п.16, в которой анальгетик, антипиретик или противовоспалительный агент выбирают из группы, состоящей из ацеклофенака, ацеметацина, е-ацетамидокапроновой кислоты, ацетаминофена, ацетаминосалола, ацетанилида, ацетилсалициловой кислоты, S-аденозилметионина, алклофенака, алклометазона, алфентанила, алгестона, аллилпродина, алминопрофена, алоксиприна, альфапродина, бис(ацетилсалицилата) алюминия, амцинонида, амфенака, аминохлортеноксазина, 3-амино-4-гидроксимасляной кислоты, 2-амино-4-пиколина, аминопропилона, аминопирина, амиксетрина, аммонийсалицилата, ампироксикама, амтолметингуацила, анилеридина, антипирина, антрафенина, апазона, беклометазона, бендазака, бенорилата, беноксапрофена, бензпиперилона, бензидамина, бензилморфина, бермопрофена, бетаметазона, безитрамида, α-бисаболола, бромфенака, р-бромоацетанилида, ацетата 5-бромосалициловой кислоты, бромосалигенина, буцетина, буклоксовой кислоты, буколома, будезонида, буфексамака, бумадизона, бупренорфина, бутацетина, бутибуфена, бутофанола, карбамазепина, карбифена, карпрофена, карсалама, целекоксиба, хлорбутанола, хлорпреднизона, хлортеноксазина, холинсалицилата, цинхофена, цинметацина, цирамадола, клиданака, клобетазола, клокортолона, клометацина, клонитазена, клониксина, клопирака, клопреднола, гвоздики, кодеина, кодеинметилбромида, кодеинфосфата, кодеинсульфата, кортизона, кортивазола, кропропамида, кротетамида, дефлазакорта, дезоморфина, дезонида, дезоксиметазона, дексаметазона, дексоксадрола, декстроморамида, дезоцина, диампромида, диклофенака, дифенамизола, дифенпирамида, дифлоразона, дифлукортолона, дифлунизала, дифлупредната, дигидрокодеина, дигидрокодеиноненолацетата, дигидроморфина, дигидроксиалюминий ацетилсалицилата, дименоксадола, димефептанола, диметилтиамбутена, диоксафетилбутирата, дипипанона, дипроцетила, дипирона, дитазола, дроксикама, эморфазона, энфенамовой кислоты, эноксолона, эпиризола, эптазоцина, этерсалата, этензамида, этогептазина, этоксазена, этилметилтиамбутена, этилморфина, этодолака, этофенамата, этонитазена, эторикоксиба, эугенола, фелбинака, фенбуфена, фенклозовой кислоты, фендозала, фенопрофена, фентанила, фентиазака, фепрадинола, фепразона, флоктафенина, флуазакорта, флуклоронида, флуфенамовой кислоты, флуметазона, флунизолида, флуниксина, флуноксапрофена, флуоцинолонацетонида, флуоцинонида, флуокортинбутила, флуокортолона, флуорезона, флуорометолона, флуперолона, флупиртина, флупреднидена, флупреднизолона, флупроквазона, флурандренолида, флурбипрофена, формокортала, фосфозала, гентизиновой кислоты, глафенина, глукаметацина, гликольсалицилата, гвайазулена, гальцинонида, галометазона, галопреднона, гидрокодона, гидрокортамата, гидрокортизона, гидроморфона, гидроксипетидина, ибуфенака, ибупрофена, ибупроксама, имидазолсалицилата, индометацина, индопрофена, изофезолака, изоладола, изометадона, изониксина, изоксепака, изоксикама, кетобемидона, кетопрофена, кеторолака, п-лактофенетида, лефетамина, леворфанола, лофентанила, лоназолака, лорноксикама, локсопрофена, лизинацетилсалицилата, мазипредона, меклофенамовой кислоты, медризона, мефенамовой кислоты, меперидина, мепреднизона, мептазинола, мезаламина, метазоцина, метадона, метотримепразина, метилпреднизолона, метиазиновой кислоты, метофолина, метопона, мофебутазона, мофезолака, моразона, морфина, морфингидрохлорида, морфинсульфата, морфолинсалицилата, мирофина, набуметона, налбуфина, 1-нафтилсалицилата, напроксена, нарцеина, нефопама, никоморфина, нифеназона, нифлумовой кислоты, нимесулида, 5’-нитро-2’-пропоксиацетанилида, норлеворфанола, норметадона, норморфина, норпипанона, олсалазина, опия, оксацепрола, оксаметацина, оксапрозина, оксикодона, оксиморфона, оксифенбутазона, папаверетума, параметазона, паранилина, парекоксиба, парсалмида, пентазоцина, перизоксаля, фенацетина, фенадоксона, феназоцина, феназопиридингидрохлорида, феноколла, феноперидина, фенопиразона, фенилацетилсалицилата, фенилбутазона, фенилсалицилата, фенирамидола, пикетопрофена, пиминодина, пипебузона, пиперилона, пипрофена, пиразолака, пиритрамида, пироксикама, пранопрофена, предникарбата, преднизолона, преднизона, преднивала, преднилидена, проглуметацина, прогептазина, промедола, пропацетамола, пропирама, пропоксифена, пропифеназона, проквазона, протизиновой кислоты, проксазола, рамифеназона, ремифентанила, римазолийметилсульфата, рофекоксиба, салацетамида, салицина, салициламида, салициламид-о-уксусной кислоты, салициловой кислоты, салицилсерной кислоты, салсалата, салверина, симетрида, суфентанила, сульфасалазина, сулиндака, супероксиддисмутазы, супрофена, суксибузона, талнифлумата, тенидапа, теноксикама, терофенамата, тетрандрина, тиазолинобутазона, тиапрофеновой кислоты, тиарамида, тилидина, тиноридина, тиксокортола, толфенамовой кислоты, толметина, трамадола, триамцинолона, тропезина, вальдекоксиба, виминола, ксенбуцина, ксимопрофена, зальтопрофена и зомепирака.
18. Таблетка по п.16, в которой анальгетик, антипиретик или противовоспалительный агент являются избирательным СОХ-2 ингибиторным препаратом.
19. Таблетка по п.18, в которой избирательный СОХ-2 ингибиторный препарат является соединением, имеющим формулу
где R15 обозначает метил, аминогруппу или имидогруппу, R16 обозначает водород или С1-4-алкил или -алкоксигруппа, Х обозначает N или CR17, где R17 обозначает водород или галоген, Y и Z независимо обозначают атомы углерода или азота, определяющие соседние атомы пяти- и шестичленного цикла, который незамещен или замещен в одном или более положений оксо-, галоидной, метиловой или галогенметиловой группами.
20. Таблетка по п.18, в которой избирательный СОХ-2 ингибитор выбирают из группы, состоящей из целекоксиба, деракоксиба, вальдекоксиба, парекоксиба, рофекоксиба, эторикоксиба, 2-(3,5-дифторфенил)-3-[4-(метилсульфонил)фенил]-2-циклопентен-1-она, (S)-6,8-дихлор-2-(трифторметил)-2Н-1-бензопиран-3-карбоновой кислоты, 2-(3,4,-дифторфенил)-4-(3-гидрокси-3-метил-1-бутокси)-5-[4-(метилсульфонил)фенил]-3-(2Н)-пиридазинона и их солей.
21. Таблетка по п.3, в которой препарат является агентом, используемым лечения и/или профилактики половых дисфункций.
22. Таблетка по п.21, в которой агент выбирают из группы, состоящей из ингибиторов ФДЭ5, активаторов циклоАМФ, α-адренергических антагонистов и допаминэргических агонистов.
23. Таблетка по п.21, в которой агент является соединением формулы
или его фармацевтически приемлемой солью,
где R1, R2 и R3, одинаковые или разные, обозначают Н, С1-6-алкил (возможно фенилзамещенный), С3-5-алкенил или -алкинил или C3-10-циклоалкил, или где R3 такой, как указано выше, а R1 и R2 циклизованы со связанным с ним атомом N, в форме пирролидиниловой, пиперидиниловой, морфолиниловой, 4-метилпиперазинила или имидазолиловой групп;
Х обозначает Н, F, Cl, Br, I, OH, C1-6-алкил или -алкоксигруппа, CN, карбоксамид, карбоксил или (С1-6алкил)карбонил;
А обозначает CH, CH2, CHF, CHCl, CHBr, CHI, CHCH3, C=O, C=S, CSCH3, C=NH, CNH2, CNHCH3, CNHCOOCH3, CNHCN, SO2 или N;
В обозначает CH, CH2, CHF, CHCl, CHBr, CHI, C=O, N, NH или NCH3, и n равно 0 или 1; и
D обозначает CH, CH2, CHF, CHCl, CHBr, CHI, C=O, О, N, NH или NCH3.
25. Таблетка по п.1, которая пригодна для перорального введения.
26. Таблетка по п.1, которая пригодна для интраперорального введения.
27. Таблетка по п.1, в которой оболочка присутствует в количестве, представляющем прирост веса от около 0,1 до около 5%.
28. Таблетка по п.1, в которой геллановая камедь составляет приблизительно от 25 до 100% веса оболочки.
29. Таблетка по п.1, в которой геллановая камедь составляет приблизительно от 50 до 100% веса оболочки.
30. Таблетка по п.1, в которой оболочка дополнительно содержит по меньшей мере один дополнительный наполнитель, выбранный из группы, состоящей из буферных агентов, пластификаторов, диспергирующих и эмульгирующих агентов.
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US35570502P | 2002-02-07 | 2002-02-07 | |
US60/355,705 | 2002-02-07 |
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RU2273473C2 RU2273473C2 (ru) | 2006-04-10 |
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EP (1) | EP1480624B1 (ru) |
JP (1) | JP4174426B2 (ru) |
KR (1) | KR100661684B1 (ru) |
CN (1) | CN1267087C (ru) |
AT (1) | ATE346591T1 (ru) |
AU (1) | AU2003210930B2 (ru) |
BR (1) | BR0307593A (ru) |
CA (1) | CA2474921A1 (ru) |
CO (1) | CO5611097A2 (ru) |
DE (1) | DE60310039T2 (ru) |
DK (1) | DK1480624T3 (ru) |
ES (1) | ES2274248T3 (ru) |
HK (1) | HK1074581A1 (ru) |
MX (1) | MXPA04006799A (ru) |
NO (1) | NO20043716L (ru) |
NZ (1) | NZ533957A (ru) |
PL (1) | PL372250A1 (ru) |
RU (1) | RU2273473C2 (ru) |
WO (1) | WO2003066030A2 (ru) |
ZA (1) | ZA200405556B (ru) |
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US20050186294A1 (en) * | 1999-07-01 | 2005-08-25 | Thompson James M. | Method of using a compound of menthol and L-arginine as a preparation for the topical delivery of vardenafil for the treatment of female sexual dysfunction |
CN100346832C (zh) * | 2002-02-07 | 2007-11-07 | 法玛西雅公司 | 经粘膜递送的药物剂型 |
MXPA05004297A (es) * | 2002-10-25 | 2005-08-03 | Pharmacia & Upjohn Co Llc | Uso de compuestos heterociclicos tipo amina como agentes neuroprotectores. |
US20040202717A1 (en) | 2003-04-08 | 2004-10-14 | Mehta Atul M. | Abuse-resistant oral dosage forms and method of use thereof |
CA2539051C (en) * | 2003-09-19 | 2014-08-12 | Penwest Pharmaceuticals Co. | Delayed release dosage forms |
US20050101608A1 (en) * | 2003-09-24 | 2005-05-12 | Santel Donald J. | Iloprost in combination therapies for the treatment of pulmonary arterial hypertension |
WO2005123407A2 (en) | 2004-06-14 | 2005-12-29 | Ackley Machine Corporation | Methods and systems for inspection and/or identification of pellet-shaped articles |
US8524294B2 (en) | 2006-03-03 | 2013-09-03 | Symrise Ag | Pressed agglomerates suitable for consumption having retarded aroma release |
GB2437054B (en) * | 2006-04-11 | 2010-09-22 | Michael Hilary Burke | A process for the preparation of an orally administered unit dose tablet |
WO2008096918A1 (en) * | 2007-02-09 | 2008-08-14 | Kolon Industries, Inc | Reactive antibioties and a method of preparing the same and antibacterial fiber treated thereby |
WO2008120249A1 (en) * | 2007-03-30 | 2008-10-09 | Sifi S.P.A. | Pharmaceutical formulations based on apolar and polar lipids for ophthalmic use |
US20080300322A1 (en) * | 2007-06-01 | 2008-12-04 | Atlantic Pharmaceuticals, Inc. | Delivery vehicles containing rosin resins |
US20090036414A1 (en) * | 2007-08-02 | 2009-02-05 | Mutual Pharmaceutical Company, Inc. | Mesalamine Formulations |
EP2254558B1 (en) * | 2008-02-05 | 2019-03-13 | Alpex Pharma SA | Orally disintegrating tablets with speckled appearance |
KR101018894B1 (ko) * | 2008-08-27 | 2011-03-04 | 근화제약주식회사 | 체내 흡수가 증진된 탈니플루메이트 함유 서방정 |
CN101757623B (zh) * | 2008-10-09 | 2013-12-04 | 北京德众万全药物技术开发有限公司 | 一种5-ht受体激动剂固体药物组合物 |
US11464781B2 (en) | 2009-02-25 | 2022-10-11 | Intra-Cellular Therapies, Inc. | PDE1 inhibitors for ophthalmic disorders |
CN101822649B (zh) * | 2010-05-27 | 2011-12-07 | 中国药科大学 | 一种带花彩的片剂的制备方法 |
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US20150118300A1 (en) * | 2013-10-31 | 2015-04-30 | Cima Labs Inc. | Immediate Release Abuse-Deterrent Granulated Dosage Forms |
US9492444B2 (en) | 2013-12-17 | 2016-11-15 | Pharmaceutical Manufacturing Research Services, Inc. | Extruded extended release abuse deterrent pill |
US10172797B2 (en) | 2013-12-17 | 2019-01-08 | Pharmaceutical Manufacturing Research Services, Inc. | Extruded extended release abuse deterrent pill |
US9561233B2 (en) | 2014-03-13 | 2017-02-07 | Demerx, Inc. | Use of ibogaine for the treatment of pain |
US9707184B2 (en) | 2014-07-17 | 2017-07-18 | Pharmaceutical Manufacturing Research Services, Inc. | Immediate release abuse deterrent liquid fill dosage form |
US9592239B2 (en) | 2014-09-12 | 2017-03-14 | Demerx, Inc. | Methods and compositions for ibogaine treatment of impulse control disorder, anxiety-related disorders, violence and/or anger, or regulating food intake |
CA2964628A1 (en) | 2014-10-20 | 2016-04-28 | Pharmaceutical Manufacturing Research Services, Inc. | Extended release abuse deterrent liquid fill dosage form |
WO2016126272A1 (en) * | 2015-02-04 | 2016-08-11 | Robert Rand | Rapid method of reducing motor and non-motor symptoms of parkinson's disease |
US11021437B2 (en) | 2016-11-13 | 2021-06-01 | Iono Pharma, Llc | Pharmaceutical formulation for sublingual or buccal delivery of epinephrine or a pro-drug thereof |
CN109419780B (zh) * | 2017-09-04 | 2021-05-11 | 张家港市中医医院 | 一种盐酸索他洛尔片剂及其制备方法 |
GB2571696B (en) | 2017-10-09 | 2020-05-27 | Compass Pathways Ltd | Large scale method for the preparation of Psilocybin and formulations of Psilocybin so produced |
CN111072767B (zh) * | 2018-10-22 | 2021-09-14 | 中国水产科学研究院 | 一种丁香酚完全抗原的合成方法 |
US11213484B2 (en) * | 2019-03-01 | 2022-01-04 | Insignis Therapeutics, Inc. | Dipivefrin orally disintegrating tablet formulations |
CN114206349A (zh) | 2019-04-17 | 2022-03-18 | 指南针探路者有限公司 | 治疗神经认知障碍、慢性疼痛及减轻炎症的方法 |
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US4034035A (en) * | 1975-07-14 | 1977-07-05 | Merck & Co., Inc. | Method of preparing multi-toned tablets |
US5273975A (en) * | 1989-06-09 | 1993-12-28 | The Upjohn Company | Heterocyclic amines having central nervous system activity |
US5411746A (en) * | 1993-02-24 | 1995-05-02 | Warner-Jenkinson Company, Inc. | Dye compositions and methods for film coating tablets and the like |
US6113945A (en) * | 1996-02-26 | 2000-09-05 | L. Perrigo Company | Multi-colored medicament |
EP1032425A1 (en) * | 1997-10-31 | 2000-09-06 | Monsanto Company | Gellan gum tablet coating |
AU5251999A (en) * | 1998-08-04 | 2000-02-28 | Wisconsin Alumni Research Foundation | Method of reducing retinal ganglion cell degeneration |
US6485747B1 (en) * | 1998-10-30 | 2002-11-26 | Monsanto Company | Coated active tablet(s) |
US6552024B1 (en) * | 1999-01-21 | 2003-04-22 | Lavipharm Laboratories Inc. | Compositions and methods for mucosal delivery |
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2003
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- 2003-02-06 DE DE60310039T patent/DE60310039T2/de not_active Expired - Fee Related
- 2003-02-06 NZ NZ533957A patent/NZ533957A/en unknown
- 2003-02-06 JP JP2003565454A patent/JP4174426B2/ja not_active Expired - Fee Related
- 2003-02-06 CA CA002474921A patent/CA2474921A1/en not_active Abandoned
- 2003-02-06 US US10/359,939 patent/US20030180357A1/en not_active Abandoned
- 2003-02-06 DK DK03737712T patent/DK1480624T3/da active
- 2003-02-06 EP EP03737712A patent/EP1480624B1/en not_active Expired - Lifetime
- 2003-02-06 MX MXPA04006799A patent/MXPA04006799A/es unknown
- 2003-02-06 PL PL03372250A patent/PL372250A1/xx unknown
- 2003-02-06 WO PCT/US2003/003837 patent/WO2003066030A2/en active IP Right Grant
- 2003-02-06 BR BR0307593-1A patent/BR0307593A/pt not_active IP Right Cessation
- 2003-02-06 ES ES03737712T patent/ES2274248T3/es not_active Expired - Lifetime
- 2003-02-06 AT AT03737712T patent/ATE346591T1/de not_active IP Right Cessation
- 2003-02-06 RU RU2004124065/15A patent/RU2273473C2/ru not_active IP Right Cessation
- 2003-02-06 CN CNB038035804A patent/CN1267087C/zh not_active Expired - Fee Related
- 2003-02-06 KR KR1020047012111A patent/KR100661684B1/ko not_active IP Right Cessation
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- 2004-08-09 CO CO04077266A patent/CO5611097A2/es not_active Application Discontinuation
- 2004-09-06 NO NO20043716A patent/NO20043716L/no not_active Application Discontinuation
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Also Published As
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PL372250A1 (en) | 2005-07-11 |
CN1267087C (zh) | 2006-08-02 |
ZA200405556B (en) | 2005-08-10 |
NZ533957A (en) | 2006-02-24 |
KR20050002821A (ko) | 2005-01-10 |
WO2003066030A2 (en) | 2003-08-14 |
ATE346591T1 (de) | 2006-12-15 |
JP4174426B2 (ja) | 2008-10-29 |
RU2273473C2 (ru) | 2006-04-10 |
ES2274248T3 (es) | 2007-05-16 |
CO5611097A2 (es) | 2006-02-28 |
HK1074581A1 (en) | 2005-11-18 |
JP2005517693A (ja) | 2005-06-16 |
DK1480624T3 (da) | 2007-03-12 |
AU2003210930A1 (en) | 2003-09-02 |
AU2003210930B2 (en) | 2007-01-04 |
DE60310039D1 (de) | 2007-01-11 |
EP1480624B1 (en) | 2006-11-29 |
DE60310039T2 (de) | 2007-04-05 |
CN1630512A (zh) | 2005-06-22 |
KR100661684B1 (ko) | 2006-12-26 |
EP1480624A2 (en) | 2004-12-01 |
MXPA04006799A (es) | 2004-12-06 |
NO20043716L (no) | 2004-09-06 |
CA2474921A1 (en) | 2003-08-14 |
US20030180357A1 (en) | 2003-09-25 |
WO2003066030A3 (en) | 2003-10-16 |
BR0307593A (pt) | 2005-02-01 |
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