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几种微生物来源的免疫抑制药在眼角膜移植中的应用 被引量:1

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出处 《沈阳部队医药》 2008年第3期210-212,共3页
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  • 1吴顺芹,李三鸣,郎轶咏,刘华,刘洪卓.水包油型微乳形成因素的考察[J].沈阳药科大学学报,2005,22(2):96-99. 被引量:21
  • 2XUE Weiming,LIU Xiudong,YU Weiting,MA Xiaojun.Preparation of protein-loaded microspheres with size ≤ 10 μm by electrostatic droplet generation technology[J].Chinese Science Bulletin,2006,51(3):279-286. 被引量:3
  • 3袁悦,李英,李三鸣.注射用环孢素A亚微乳的制备[J].中国新药杂志,2006,15(12):982-985. 被引量:9
  • 4梁志波,李小飞,刘锟,吴红,赵晋波.局部应用环孢素A聚乳酸微球的性状及释药研究[J].中国药物与临床,2007,7(1):9-12. 被引量:6
  • 5Christians U.Transport proteins and intestinal metabolism; P-glycoproteinand cytochrome P4503A.. Therapeutic Drug Monitoring . 2009
  • 6Hirunpanich V,KatagiJ,Sethabouppha B,et al.Demonstration of docosahexaenoic acid as a bioavailability enhancer for CYP3A substrates:in vitro and in vivo evidence using cyclosporin in rats. Drug Metab.Dispos . 2008
  • 7Midtvedt K.Therapeutic drug monitoring of cyclosporine. Transplant,Proc . 2009
  • 8Hirunpanich V,Murakoso K,Sato H.Inhibitory effect of docosahexaenoic acid (DHA-EE) on the intestinal metabolism of midazolam;in vitro and in vivo studies in rats. Int.].Pharm . 2008
  • 9Hirunpanich V,Sato H.Docosahexaenoic acid (DHA-EE) inhibits saquinavirmetabolism in vitro and enhances its bioavailability in rats. Pharm- Pharmacol . 2010
  • 10Hiroshi ARAYA,Mikio TOMITA,Masahiro HAYASHI.The novel formulation design of serf-emulsifying drug delivery systems(SEDDS)type O/W microemul- sionⅢ:The permeation mechanism of a poorly water soluble drug entrapped O/W mieroemulsion in rat isolated intestinal membrane by the uasing chamber methad. Drug Metab Pharmacokinet . 2006

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