CN1823729A - 丁苯酞静脉乳剂及其应用 - Google Patents
丁苯酞静脉乳剂及其应用 Download PDFInfo
- Publication number
- CN1823729A CN1823729A CNA2005101023552A CN200510102355A CN1823729A CN 1823729 A CN1823729 A CN 1823729A CN A2005101023552 A CNA2005101023552 A CN A2005101023552A CN 200510102355 A CN200510102355 A CN 200510102355A CN 1823729 A CN1823729 A CN 1823729A
- Authority
- CN
- China
- Prior art keywords
- oil
- butyl benzene
- water
- butyphthalide
- emulsion
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000839 emulsion Substances 0.000 title claims abstract description 29
- OCKPCBLVNKHBMX-UHFFFAOYSA-N butylbenzene Chemical compound CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 title claims description 32
- 210000003462 vein Anatomy 0.000 title claims description 16
- 239000003921 oil Substances 0.000 claims abstract description 38
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 35
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 14
- 239000008215 water for injection Substances 0.000 claims abstract description 10
- 238000010253 intravenous injection Methods 0.000 claims abstract description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 39
- 235000019198 oils Nutrition 0.000 claims description 37
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 claims description 17
- -1 fatty acid ester Chemical class 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 17
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims description 16
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 claims description 16
- 229940083466 soybean lecithin Drugs 0.000 claims description 16
- HJXMNVQARNZTEE-UHFFFAOYSA-N Butylphthalide Chemical compound C1=CC=C2C(CCCC)OC(=O)C2=C1 HJXMNVQARNZTEE-UHFFFAOYSA-N 0.000 claims description 12
- 229920001993 poloxamer 188 Polymers 0.000 claims description 11
- 229940044519 poloxamer 188 Drugs 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 9
- 229930003427 Vitamin E Natural products 0.000 claims description 8
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 claims description 8
- 239000003549 soybean oil Substances 0.000 claims description 8
- 235000012424 soybean oil Nutrition 0.000 claims description 8
- 239000003381 stabilizer Substances 0.000 claims description 8
- 235000019165 vitamin E Nutrition 0.000 claims description 8
- 229940046009 vitamin E Drugs 0.000 claims description 8
- 239000011709 vitamin E Substances 0.000 claims description 8
- 239000002671 adjuvant Substances 0.000 claims description 7
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims description 6
- ZEMPKEQAKRGZGQ-AAKVHIHISA-N 2,3-bis[[(z)-12-hydroxyoctadec-9-enoyl]oxy]propyl (z)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCCC(O)C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CC(O)CCCCCC)COC(=O)CCCCCCC\C=C/CC(O)CCCCCC ZEMPKEQAKRGZGQ-AAKVHIHISA-N 0.000 claims description 6
- 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 claims description 6
- 102000002322 Egg Proteins Human genes 0.000 claims description 6
- 108010000912 Egg Proteins Proteins 0.000 claims description 6
- 241000287828 Gallus gallus Species 0.000 claims description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 6
- LDVVMCZRFWMZSG-UHFFFAOYSA-N captan Chemical compound C1C=CCC2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C21 LDVVMCZRFWMZSG-UHFFFAOYSA-N 0.000 claims description 6
- KXGVEGMKQFWNSR-UHFFFAOYSA-N deoxycholic acid Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(O)=O)C)C1(C)C(O)C2 KXGVEGMKQFWNSR-UHFFFAOYSA-N 0.000 claims description 6
- 239000003814 drug Substances 0.000 claims description 6
- 239000004615 ingredient Substances 0.000 claims description 6
- 235000010445 lecithin Nutrition 0.000 claims description 6
- 239000000787 lecithin Substances 0.000 claims description 6
- 229940067606 lecithin Drugs 0.000 claims description 6
- 230000003204 osmotic effect Effects 0.000 claims description 6
- 210000004681 ovum Anatomy 0.000 claims description 6
- 210000000582 semen Anatomy 0.000 claims description 6
- 239000000600 sorbitol Substances 0.000 claims description 6
- 235000010356 sorbitol Nutrition 0.000 claims description 6
- 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 claims description 5
- 229930195725 Mannitol Natural products 0.000 claims description 5
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims description 5
- 239000000594 mannitol Substances 0.000 claims description 5
- 235000010355 mannitol Nutrition 0.000 claims description 5
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims description 5
- 229920000053 polysorbate 80 Polymers 0.000 claims description 5
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 5
- 239000008158 vegetable oil Substances 0.000 claims description 5
- 239000000811 xylitol Substances 0.000 claims description 5
- 235000010447 xylitol Nutrition 0.000 claims description 5
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims description 5
- 229960002675 xylitol Drugs 0.000 claims description 5
- BHQCQFFYRZLCQQ-UHFFFAOYSA-N (3alpha,5alpha,7alpha,12alpha)-3,7,12-trihydroxy-cholan-24-oic acid Natural products OC1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(O)=O)C)C1(C)C(O)C2 BHQCQFFYRZLCQQ-UHFFFAOYSA-N 0.000 claims description 4
- WECGLUPZRHILCT-GSNKCQISSA-N 1-linoleoyl-sn-glycerol Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OC[C@@H](O)CO WECGLUPZRHILCT-GSNKCQISSA-N 0.000 claims description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 4
- 239000004380 Cholic acid Substances 0.000 claims description 4
- 229920001213 Polysorbate 20 Polymers 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims description 4
- 235000019416 cholic acid Nutrition 0.000 claims description 4
- BHQCQFFYRZLCQQ-OELDTZBJSA-N cholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 BHQCQFFYRZLCQQ-OELDTZBJSA-N 0.000 claims description 4
- 229960002471 cholic acid Drugs 0.000 claims description 4
- 150000002646 long chain fatty acid esters Chemical class 0.000 claims description 4
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 4
- 239000004006 olive oil Substances 0.000 claims description 4
- 235000008390 olive oil Nutrition 0.000 claims description 4
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 claims description 4
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 claims description 4
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 claims 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 claims description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 3
- 239000002202 Polyethylene glycol Substances 0.000 claims description 3
- NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 claims description 3
- NWGKJDSIEKMTRX-BFWOXRRGSA-N [(2r)-2-[(3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)C1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-BFWOXRRGSA-N 0.000 claims description 3
- LWZFANDGMFTDAV-WYDSMHRWSA-N [2-[(2r,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(O)[C@H]1OC[C@H](O)[C@H]1O LWZFANDGMFTDAV-WYDSMHRWSA-N 0.000 claims description 3
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 3
- 229950005197 butylphthalide Drugs 0.000 claims description 3
- 239000008103 glucose Substances 0.000 claims description 3
- 125000005456 glyceride group Chemical group 0.000 claims description 3
- 229940074046 glyceryl laurate Drugs 0.000 claims description 3
- 229920001992 poloxamer 407 Polymers 0.000 claims description 3
- 229940044476 poloxamer 407 Drugs 0.000 claims description 3
- 229920001223 polyethylene glycol Polymers 0.000 claims description 3
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 claims description 3
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 claims description 3
- GHBFNMLVSPCDGN-UHFFFAOYSA-N rac-1-monooctanoylglycerol Chemical compound CCCCCCCC(=O)OCC(O)CO GHBFNMLVSPCDGN-UHFFFAOYSA-N 0.000 claims description 3
- 239000011780 sodium chloride Substances 0.000 claims description 3
- 235000011067 sorbitan monolaureate Nutrition 0.000 claims description 3
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 claims description 2
- JVKUCNQGESRUCL-UHFFFAOYSA-N 2-Hydroxyethyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OCCO JVKUCNQGESRUCL-UHFFFAOYSA-N 0.000 claims description 2
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 claims description 2
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims description 2
- LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 claims description 2
- 244000046052 Phaseolus vulgaris Species 0.000 claims description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 claims description 2
- 235000019485 Safflower oil Nutrition 0.000 claims description 2
- 229920001304 Solutol HS 15 Polymers 0.000 claims description 2
- 244000299461 Theobroma cacao Species 0.000 claims description 2
- 235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 claims description 2
- 235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 claims description 2
- AOBORMOPSGHCAX-UHFFFAOYSA-N Tocophersolan Chemical compound OCCOC(=O)CCC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C AOBORMOPSGHCAX-UHFFFAOYSA-N 0.000 claims description 2
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 claims description 2
- 229930003268 Vitamin C Natural products 0.000 claims description 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 claims description 2
- 235000001046 cacaotero Nutrition 0.000 claims description 2
- 229940107161 cholesterol Drugs 0.000 claims description 2
- 235000012000 cholesterol Nutrition 0.000 claims description 2
- 229960003964 deoxycholic acid Drugs 0.000 claims description 2
- KXGVEGMKQFWNSR-LLQZFEROSA-N deoxycholic acid Chemical compound C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 KXGVEGMKQFWNSR-LLQZFEROSA-N 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- FMMOOAYVCKXGMF-MURFETPASA-N ethyl linoleate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC FMMOOAYVCKXGMF-MURFETPASA-N 0.000 claims description 2
- 229940031016 ethyl linoleate Drugs 0.000 claims description 2
- LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 claims description 2
- 229940093471 ethyl oleate Drugs 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 235000001727 glucose Nutrition 0.000 claims description 2
- 238000005984 hydrogenation reaction Methods 0.000 claims description 2
- 230000007062 hydrolysis Effects 0.000 claims description 2
- 238000006460 hydrolysis reaction Methods 0.000 claims description 2
- 239000002563 ionic surfactant Substances 0.000 claims description 2
- FMMOOAYVCKXGMF-UHFFFAOYSA-N linoleic acid ethyl ester Natural products CCCCCC=CCC=CCCCCCCCC(=O)OCC FMMOOAYVCKXGMF-UHFFFAOYSA-N 0.000 claims description 2
- 150000002711 medium chain fatty acid esters Chemical class 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims description 2
- 238000012986 modification Methods 0.000 claims description 2
- 235000005713 safflower oil Nutrition 0.000 claims description 2
- 239000003813 safflower oil Substances 0.000 claims description 2
- 229960005480 sodium caprylate Drugs 0.000 claims description 2
- 235000002639 sodium chloride Nutrition 0.000 claims description 2
- BYKRNSHANADUFY-UHFFFAOYSA-M sodium octanoate Chemical compound [Na+].CCCCCCCC([O-])=O BYKRNSHANADUFY-UHFFFAOYSA-M 0.000 claims description 2
- 159000000000 sodium salts Chemical class 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 235000019155 vitamin A Nutrition 0.000 claims description 2
- 239000011719 vitamin A Substances 0.000 claims description 2
- 235000019154 vitamin C Nutrition 0.000 claims description 2
- 239000011718 vitamin C Substances 0.000 claims description 2
- 229940045997 vitamin a Drugs 0.000 claims description 2
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 abstract 2
- 239000007951 isotonicity adjuster Substances 0.000 abstract 1
- 230000010412 perfusion Effects 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- 238000005303 weighing Methods 0.000 description 16
- 238000005516 engineering process Methods 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 239000006185 dispersion Substances 0.000 description 8
- 230000001804 emulsifying effect Effects 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 5
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 5
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 5
- 201000006474 Brain Ischemia Diseases 0.000 description 5
- 239000005642 Oleic acid Substances 0.000 description 5
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 5
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 5
- 206010008118 cerebral infarction Diseases 0.000 description 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 3
- 206010008120 Cerebral ischaemia Diseases 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 206010018910 Haemolysis Diseases 0.000 description 2
- 239000003146 anticoagulant agent Substances 0.000 description 2
- 208000026106 cerebrovascular disease Diseases 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 210000003022 colostrum Anatomy 0.000 description 2
- 235000021277 colostrum Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 230000008588 hemolysis Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000003908 quality control method Methods 0.000 description 2
- 239000007901 soft capsule Substances 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 230000008685 targeting Effects 0.000 description 2
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 2
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- 206010061216 Infarction Diseases 0.000 description 1
- 229920002685 Polyoxyl 35CastorOil Polymers 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000000702 anti-platelet effect Effects 0.000 description 1
- 230000002785 anti-thrombosis Effects 0.000 description 1
- 239000001387 apium graveolens Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000003727 cerebral blood flow Effects 0.000 description 1
- 230000002490 cerebral effect Effects 0.000 description 1
- 238000005138 cryopreservation Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000037149 energy metabolism Effects 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000010579 first pass effect Methods 0.000 description 1
- RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 description 1
- 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 1
- 239000007902 hard capsule Substances 0.000 description 1
- 230000007574 infarction Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 230000000302 ischemic effect Effects 0.000 description 1
- 230000004089 microcirculation Effects 0.000 description 1
- 230000004898 mitochondrial function Effects 0.000 description 1
- QUANRIQJNFHVEU-UHFFFAOYSA-N oxirane;propane-1,2,3-triol Chemical compound C1CO1.OCC(O)CO QUANRIQJNFHVEU-UHFFFAOYSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 239000008389 polyethoxylated castor oil Substances 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 210000001202 rhombencephalon Anatomy 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- 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
- A61K9/10—Dispersions; Emulsions
- A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
-
- 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
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Dispersion Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dermatology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Hospice & Palliative Care (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Hematology (AREA)
- Inorganic Chemistry (AREA)
- Urology & Nephrology (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
Claims (10)
Priority Applications (15)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005101023552A CN100367951C (zh) | 2005-12-16 | 2005-12-16 | 丁苯酞静脉乳剂及其应用 |
EP06828348.0A EP1970050B1 (en) | 2005-12-16 | 2006-12-15 | Butylphthalide intravenous emulsion and application thereof |
US12/086,665 US20090281177A1 (en) | 2005-12-16 | 2006-12-15 | Butylphthalide Intravenous Emulsion and Application Thereof |
KR1020087016969A KR101061268B1 (ko) | 2005-12-16 | 2006-12-15 | 뷰틸프탈라이드 정맥주사용 유탁액 및 이의 용도 |
UAA200808969A UA89315C2 (en) | 2005-12-16 | 2006-12-15 | Butylbenzene phthalein intravenous emulsion |
BRPI0619915-1A BRPI0619915B1 (pt) | 2005-12-16 | 2006-12-15 | Emulsão intravenosa de butilftalida e aplicação da mesma |
AU2006324219A AU2006324219B2 (en) | 2005-12-16 | 2006-12-15 | Butylphthalide intravenous emulsion and application thereof |
PCT/CN2006/003434 WO2007068212A1 (fr) | 2005-12-16 | 2006-12-15 | Emulsion intraveineuse de butylbenzene phtaleine et son application |
CA2633170A CA2633170C (en) | 2005-12-16 | 2006-12-15 | Butylphthalide intravenous emulsion and application thereof |
JP2008544744A JP5571311B2 (ja) | 2005-12-16 | 2006-12-15 | ブチルフタリド静脈内エマルジョン及びその適用 |
EA200870060A EA014518B1 (ru) | 2005-12-16 | 2006-12-15 | Эмульсия бутилфталида для внутривенного введения и ее применение |
IL192169A IL192169A (en) | 2005-12-16 | 2008-06-15 | Intravenous butylphthalide emulsion and its use |
CU20080114A CU23814A3 (es) | 2005-12-16 | 2008-06-17 | Emulsión intravenosa de butilftalida y aplicación de la misma |
US13/112,180 US10463614B2 (en) | 2005-12-16 | 2011-05-20 | Butylphthalide intravenous emulsion and application thereof |
JP2012156784A JP2012193206A (ja) | 2005-12-16 | 2012-07-12 | ブチルフタリド静脈内エマルジョン及びその適用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005101023552A CN100367951C (zh) | 2005-12-16 | 2005-12-16 | 丁苯酞静脉乳剂及其应用 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1823729A true CN1823729A (zh) | 2006-08-30 |
CN100367951C CN100367951C (zh) | 2008-02-13 |
Family
ID=36934680
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2005101023552A Active CN100367951C (zh) | 2005-12-16 | 2005-12-16 | 丁苯酞静脉乳剂及其应用 |
Country Status (13)
Country | Link |
---|---|
US (2) | US20090281177A1 (zh) |
EP (1) | EP1970050B1 (zh) |
JP (2) | JP5571311B2 (zh) |
KR (1) | KR101061268B1 (zh) |
CN (1) | CN100367951C (zh) |
AU (1) | AU2006324219B2 (zh) |
BR (1) | BRPI0619915B1 (zh) |
CA (1) | CA2633170C (zh) |
CU (1) | CU23814A3 (zh) |
EA (1) | EA014518B1 (zh) |
IL (1) | IL192169A (zh) |
UA (1) | UA89315C2 (zh) |
WO (1) | WO2007068212A1 (zh) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102178643A (zh) * | 2011-04-29 | 2011-09-14 | 石药集团恩必普药业有限公司 | 一种丁苯酞或其衍生物的微乳透皮凝胶剂及其制备方法 |
CN102716121A (zh) * | 2012-06-06 | 2012-10-10 | 石药集团中奇制药技术(石家庄)有限公司 | 一种丁苯酞药物活性组合物及其制备方法 |
CN103505409A (zh) * | 2012-06-27 | 2014-01-15 | 石药集团中奇制药技术(石家庄)有限公司 | 一种丁苯酞注射液及其制备方法 |
CN103505414A (zh) * | 2012-06-28 | 2014-01-15 | 石药集团恩必普药业有限公司 | 丁苯酞滴鼻剂及其制备方法 |
CN105796486A (zh) * | 2016-03-17 | 2016-07-27 | 南京天翔医药科技有限公司 | 丁苯酞脂肪乳注射剂及其制备工艺 |
CN110101658A (zh) * | 2018-02-01 | 2019-08-09 | 北京睿悦生物医药科技有限公司 | 丁苯酞脂微球注射液及其制备方法 |
CN111407725A (zh) * | 2020-04-13 | 2020-07-14 | 中山大学 | 一种拉莫三嗪乳剂及其制备方法 |
CN114010595A (zh) * | 2021-10-14 | 2022-02-08 | 山东诚创蓝海医药科技有限公司 | 一种丁苯酞乳剂及其制备方法 |
CN114073694A (zh) * | 2020-08-14 | 2022-02-22 | 北京科莱博医药开发有限责任公司 | 丁苯酞制剂及其制备方法 |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX336071B (es) | 2009-08-14 | 2016-01-06 | Opko Health Inc | Formulaciones intravenosas de antagonistas de neurocinina 1. |
WO2014124132A1 (en) * | 2013-02-06 | 2014-08-14 | Jingjun Huang | Stable pharmaceutical composition of clopidogrel free base for oral and parenteral delivery |
TWI547280B (zh) * | 2014-04-24 | 2016-09-01 | 長弘生物科技股份有限公司 | 穩定醫藥組合物 |
CN105030760B (zh) | 2014-04-24 | 2018-10-02 | 长弘生物科技股份有限公司 | 稳定医药组合物 |
MX2018002462A (es) * | 2015-08-28 | 2018-06-19 | Caliway Biopharmaceuticals Co Ltd | Una composicion farmaceutica para reducir la grasa localizada y sus usos. |
CN110548004B (zh) * | 2018-05-30 | 2023-05-16 | 成都施贝康生物医药科技有限公司 | 一种稳定的丁苯酞大容量注射液及其制备方法 |
CN115177614A (zh) * | 2021-04-01 | 2022-10-14 | 长春藤生物科技股份有限公司 | 正丁基苯酞的应用 |
CN114886848B (zh) * | 2022-05-20 | 2024-03-08 | 山东泰合医药科技有限公司 | 一种纳米胶束组合物制备方法及制备的纳米胶束组合物 |
Family Cites Families (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0647533B2 (ja) * | 1984-08-10 | 1994-06-22 | 裕 水島 | 4−ビフエニリル酢酸系化合物含有脂肪乳剤 |
US4950567A (en) | 1988-01-15 | 1990-08-21 | E. I. Du Pont De Nemours And Company | Holographic optical combiners for head-up displays |
JPH01226807A (ja) * | 1988-03-04 | 1989-09-11 | Tsumura & Co | 脂肪乳剤およびその製造方法 |
US5364632A (en) * | 1989-04-05 | 1994-11-15 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Medicinal emulsions |
DE4015108A1 (de) * | 1990-05-11 | 1991-11-14 | Leopold Pharma Gmbh | Stabile emulsion zur applikation pharmakologisch aktiver wirkstoffe |
CN1029293C (zh) * | 1993-01-01 | 1995-07-12 | 浙江省中医院 | 薏苡仁中性油脂乳剂 |
CN1048158C (zh) * | 1993-09-09 | 2000-01-12 | 中国医学科学院药物研究所 | 芹菜甲素在制备预防和治疗哺乳动物或人类脑缺血引起的疾病的药中的应用 |
JP2000128786A (ja) * | 1998-10-28 | 2000-05-09 | Kobayashi Seiyaku Kogyo Kk | ミコナゾール含有水性注射剤およびその製造方法 |
CN1086942C (zh) | 1998-12-18 | 2002-07-03 | 中国医学科学院药物研究所 | 丁基苯酞在制备抗血栓形成及抗血小板聚集药物中的应用 |
JP2003277281A (ja) * | 2002-03-20 | 2003-10-02 | Kumamoto Technology & Industry Foundation | 静脈炎の予防及び治療のための医薬 |
CN1375288A (zh) * | 2002-05-13 | 2002-10-23 | 周桂荣 | 一种治疗脑血管疾病的药物组合物 |
AU2002327307B8 (en) | 2002-08-21 | 2009-02-26 | Shijiazhuang Pharma Group Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. | Clathrates of butylphtualide with cyclodextrin or its derivatives, a process for their preparations and the use there of |
CN1565441B (zh) | 2003-06-20 | 2010-05-26 | 中国医学科学院药物研究所 | 左旋正丁基苯酞在制备预防或治疗痴呆的药物中的用途 |
US7115230B2 (en) * | 2003-06-26 | 2006-10-03 | Intel Corporation | Hydrodynamic focusing devices |
US20050049209A1 (en) * | 2003-08-06 | 2005-03-03 | Chen Andrew Xian | Pharmaceutical compositions for delivering macrolides |
CN1254245C (zh) * | 2003-08-26 | 2006-05-03 | 曹永强 | 羟喜树碱乳剂及其制备方法 |
CN1605336A (zh) | 2003-10-10 | 2005-04-13 | 中国医学科学院药物研究所 | 左旋丁基苯酞在制备预防和治疗脑梗塞的药物中的应用 |
CN1647796A (zh) | 2004-01-20 | 2005-08-03 | 中奇制药技术(石家庄)有限公司 | 左旋丁苯酞在制备预防和治疗脑缺血疾病药物中的应用 |
EP1757286B1 (en) * | 2004-06-18 | 2017-09-06 | CSPC Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. | The application of l-n-butylphthalide in preventing and treating alzheimer's disease |
CN100361656C (zh) * | 2004-08-27 | 2008-01-16 | 石药集团中奇制药技术(石家庄)有限公司 | 丁苯酞自乳化释药体系及其制备方法和应用 |
CN1290491C (zh) | 2004-09-20 | 2006-12-20 | 周桂荣 | 一种治疗急性缺血性脑卒中的药剂及其制备方法 |
-
2005
- 2005-12-16 CN CNB2005101023552A patent/CN100367951C/zh active Active
-
2006
- 2006-12-15 WO PCT/CN2006/003434 patent/WO2007068212A1/zh active Application Filing
- 2006-12-15 CA CA2633170A patent/CA2633170C/en not_active Expired - Fee Related
- 2006-12-15 UA UAA200808969A patent/UA89315C2/ru unknown
- 2006-12-15 BR BRPI0619915-1A patent/BRPI0619915B1/pt active IP Right Grant
- 2006-12-15 US US12/086,665 patent/US20090281177A1/en not_active Abandoned
- 2006-12-15 EP EP06828348.0A patent/EP1970050B1/en active Active
- 2006-12-15 EA EA200870060A patent/EA014518B1/ru not_active IP Right Cessation
- 2006-12-15 KR KR1020087016969A patent/KR101061268B1/ko active IP Right Grant
- 2006-12-15 JP JP2008544744A patent/JP5571311B2/ja active Active
- 2006-12-15 AU AU2006324219A patent/AU2006324219B2/en not_active Ceased
-
2008
- 2008-06-15 IL IL192169A patent/IL192169A/en not_active IP Right Cessation
- 2008-06-17 CU CU20080114A patent/CU23814A3/es not_active IP Right Cessation
-
2011
- 2011-05-20 US US13/112,180 patent/US10463614B2/en active Active
-
2012
- 2012-07-12 JP JP2012156784A patent/JP2012193206A/ja active Pending
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102178643A (zh) * | 2011-04-29 | 2011-09-14 | 石药集团恩必普药业有限公司 | 一种丁苯酞或其衍生物的微乳透皮凝胶剂及其制备方法 |
CN102178643B (zh) * | 2011-04-29 | 2014-05-14 | 石药集团恩必普药业有限公司 | 一种丁苯酞或其衍生物的微乳透皮凝胶剂及其制备方法 |
CN102716121A (zh) * | 2012-06-06 | 2012-10-10 | 石药集团中奇制药技术(石家庄)有限公司 | 一种丁苯酞药物活性组合物及其制备方法 |
CN102716121B (zh) * | 2012-06-06 | 2017-10-24 | 石药集团中奇制药技术(石家庄)有限公司 | 一种丁苯酞药物活性组合物及其制备方法 |
CN103505409A (zh) * | 2012-06-27 | 2014-01-15 | 石药集团中奇制药技术(石家庄)有限公司 | 一种丁苯酞注射液及其制备方法 |
CN107970208A (zh) * | 2012-06-27 | 2018-05-01 | 石药集团中奇制药技术(石家庄)有限公司 | 一种丁苯酞注射液及其制备方法 |
CN103505414B (zh) * | 2012-06-28 | 2017-08-08 | 石药集团恩必普药业有限公司 | 丁苯酞滴鼻剂及其制备方法 |
CN103505414A (zh) * | 2012-06-28 | 2014-01-15 | 石药集团恩必普药业有限公司 | 丁苯酞滴鼻剂及其制备方法 |
CN105796486A (zh) * | 2016-03-17 | 2016-07-27 | 南京天翔医药科技有限公司 | 丁苯酞脂肪乳注射剂及其制备工艺 |
CN110101658A (zh) * | 2018-02-01 | 2019-08-09 | 北京睿悦生物医药科技有限公司 | 丁苯酞脂微球注射液及其制备方法 |
CN111407725A (zh) * | 2020-04-13 | 2020-07-14 | 中山大学 | 一种拉莫三嗪乳剂及其制备方法 |
CN114073694A (zh) * | 2020-08-14 | 2022-02-22 | 北京科莱博医药开发有限责任公司 | 丁苯酞制剂及其制备方法 |
CN114073694B (zh) * | 2020-08-14 | 2024-03-12 | 北京科莱博医药开发有限责任公司 | 丁苯酞制剂及其制备方法 |
CN114010595A (zh) * | 2021-10-14 | 2022-02-08 | 山东诚创蓝海医药科技有限公司 | 一种丁苯酞乳剂及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
CU23814A3 (es) | 2012-06-21 |
EP1970050A4 (en) | 2009-12-09 |
EA014518B1 (ru) | 2010-12-30 |
CA2633170C (en) | 2011-05-24 |
IL192169A0 (en) | 2008-12-29 |
US20110288167A1 (en) | 2011-11-24 |
UA89315C2 (en) | 2010-01-11 |
BRPI0619915A2 (pt) | 2011-10-25 |
BRPI0619915B1 (pt) | 2021-06-01 |
CN100367951C (zh) | 2008-02-13 |
WO2007068212A1 (fr) | 2007-06-21 |
IL192169A (en) | 2016-02-29 |
CA2633170A1 (en) | 2007-06-21 |
KR101061268B1 (ko) | 2011-08-31 |
EA200870060A1 (ru) | 2009-02-27 |
AU2006324219A1 (en) | 2007-06-21 |
KR20080091141A (ko) | 2008-10-09 |
US10463614B2 (en) | 2019-11-05 |
JP5571311B2 (ja) | 2014-08-13 |
CU20080114A7 (es) | 2010-08-30 |
JP2012193206A (ja) | 2012-10-11 |
US20090281177A1 (en) | 2009-11-12 |
EP1970050B1 (en) | 2016-05-11 |
JP2009519253A (ja) | 2009-05-14 |
EP1970050A1 (en) | 2008-09-17 |
AU2006324219B2 (en) | 2010-03-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1823729A (zh) | 丁苯酞静脉乳剂及其应用 | |
CN1309414C (zh) | 用于给予环孢菌素的亲水二元体系 | |
CN1384734A (zh) | 生物活性物质的表面改性微粒组合物 | |
CN101032467A (zh) | 一种静脉注射用高稳定长循环脂肪乳载药制剂 | |
CN1496253A (zh) | 新组合物 | |
RU2011148140A (ru) | Самомикроэмульгирующаяся оральная фармацевтическая композиция, содержащая гидрофильное лекарственное средство, и способ ее приготовления | |
CN1353613A (zh) | 药物组合物 | |
CN1273526A (zh) | 微分散给药系统 | |
CN1256939C (zh) | 含有辅酶q10的微乳剂预浓缩物和微乳剂 | |
CA3169511A1 (en) | Nanostructure lipid carrier delivery system, composition, and methods | |
KR20140016926A (ko) | 활성제로서 페닐아미노피리미딘 유도체를 포함하는 제제 | |
TWI599368B (zh) | 包含含有阿拉泊韋(alisporivir)的醫藥組合物之口服膠囊 | |
KR101735861B1 (ko) | 비경구적으로 투여되는 dha 에스테르를 포함하는 약학적 조성물 | |
CN1559407A (zh) | 二氢吡啶类钙离子拮抗剂的自微乳化软胶囊及其制备方法 | |
CN1893932A (zh) | 包括肾素抑制剂的微乳预浓缩物 | |
Kazi | Lipid‐based nano‐delivery for oral administration of poorly water soluble drugs (PWSDs): design, optimization and in-vitro assessment | |
CN1561970A (zh) | 脂溶性维生素冻干乳剂及其制备方法 | |
AU2015354848B2 (en) | Formulation for effective tocotrienol delivery | |
CN1717219A (zh) | 用于联苯二甲双酯口服给药的微乳组合物 | |
CN1698621A (zh) | 非那雄胺高浓度溶液及用途 | |
CN1823735A (zh) | 一种含有难溶性药物的自组装前体脂质体及其制备方法 | |
CN1161150C (zh) | 药物组合物 | |
CN1593449A (zh) | 灯盏花素自乳化软胶囊及其制备方法 | |
CN1596889A (zh) | 维生素e乳剂及其冻干乳剂的组方及制备方法 | |
CN1660257A (zh) | 柿叶提取物软胶囊及自乳化释药系统 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
ASS | Succession or assignment of patent right |
Owner name: ENBIPU PHARMACEUTICAL CO. Free format text: FORMER OWNER: ZHONGSHAN UNIV. Effective date: 20061229 |
|
C41 | Transfer of patent application or patent right or utility model | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20061229 Address after: 052160 No. 88, Yangzi Road, Shijiazhuang economic and Technological Development Zone, Hebei Applicant after: Enbipu Pharmacy Co., Ltd., Shiyao Group. Address before: 510089 No. two, No. 74, Zhongshan Road, Guangdong, Guangzhou Applicant before: Sun Yat-sen University |
|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant |