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药物纳米混悬剂释放系统 被引量:5

Drug delivering system of nanosuspension
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作者 黄胜炎
出处 《上海医药》 CAS 2005年第10期464-467,共4页 Shanghai Medical & Pharmaceutical Journal
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同被引文献108

  • 1艾萍,金义光,王林校.药物传送中的纳米混悬液[J].国外医学(药学分册),2005,32(1):61-63. 被引量:9
  • 2朱建芬,吴祥根.纳米混悬剂的制备方法及在药剂学中应用的研究进展[J].中国医药工业杂志,2006,37(3):196-200. 被引量:38
  • 3钱帅,张建军,高缘,周建平.纳米混悬剂研究进展[J].药学进展,2007,31(1):9-14. 被引量:16
  • 4熊若兰,陆伟根.纳米混悬剂研究进展[J].世界临床药物,2007,28(2):117-121. 被引量:14
  • 5Kesisoglou F, Panmai S, Wu Y. Nanosizing oral formulation development and biopharmaceutical evaluation. Adv Drug Deliv Rev, 2007, 59(7): 631.
  • 6Van Eerdenbrugh B, Froyen L, Martens JA, et al. Characterization of physico-chernical properties and pharmaceutical performance of sucrose co-freeze-dried solid nanoparticulate powders of the anti HIV agent loviride prepared by media milling. Int J Pharm, 2007, 338(1-2) : 198.
  • 7Vogt M, Kunath K, Dressman JB, Dissolution enhancement of fenofibrate by micronization, cogrinding and spray drying: comparison with commercial preparations. Eur J Pharm Biopharm, 2008, 68(2): 283.
  • 8Jung JY, Yoo SD, Lee SH, et al. Enhanced solubility and dissolution rate of itraconazole by a solid dispersion technique. Int J Pharm, 1999, 187(2): 209.
  • 9Al-Marzouqi HA, Elwy MH, Shehadi I, et al. Physicochemical properties of antifungal drug-cyclodextrin complexes prepared by supereritical carbon dioxide and by conventional techniques. J Pharm Biomed Anal, 2009, 49(2): 227.
  • 10Kassem MA, Abdel Rahman AA, Ghorab MM, et al. nanosuspension as an ophthalmic delivery system for certain glucocorticoid drugs. Int J Pharm, 2007, 340(1-2):126.

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