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伏立康唑抗致病真菌的研究进展 被引量:3

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摘要 伏立康唑是第二代合成的氟康唑衍生物 ,该文对其抗真菌机理进行了介绍 ,并就其与其他抗真菌剂对念珠菌属及念珠菌属以外的其他真菌的体外活性试验的比较结果 ,以及临床应用和与其他抗真菌剂的协同作用作一综述 ,为临床治疗真菌病推荐了一种新的有效药物。
作者 王英 顾军
出处 《国外医学(皮肤性病学分册)》 2002年第4期205-208,共4页 Foreign Medical Sciences(Section of Dermatology and Venereology)
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参考文献21

  • 1Sanati H, Belanger P, Fratti R, et al. A new triazole, voriconazole ( UK109,496), blocks sterol biosynthesis in Candida albicans and Candida krusei. Antimicrob Agents Chemother, 1997,41 ( 11 ): 2492-2496.
  • 2Sabo JA,Abdel-Rahman SM.Voriconazole: a new triazole antifungal. Ann Pharmacother, 2000,34(9): 1032-1043.
  • 3Hoban DJ, Zhanel GG, Karlowsky JA. In vitro susceptibilities of Candida and Cryptococcus neoformans isolates from blood cultures of neutropenic patients. Antimicrob Agents Chemother, 1999,43 (6): 1463-1464.
  • 4Vora S, Purimetla N, Brummer E, et al. Activity of voriconazole, a new triazole, combined with neutrophils or monocytes against Candida albicans: effect of granulocyte colony-stimulating factor and granulocytemacrophage colony-stimulating factor. Antimicrob Agents Chemother,1998,42(4) :907-910.
  • 5Belanger P, Nast CC, Fratti R, et al. Voriconazole (UK-109,496) inhibits the growth and alters the morphology of fluconazole-susceptible andresistant Candida species. Antimicrob Agents Chemother, 1997, 41 ( 8 ):1840-1842.
  • 6Fratti RA, Belanger PH, Sanati H, et al. The effect of the new triazole,voriconazole ( UK- 109,496), on the interactions of Candida albicans and Candida krusei with endothelial cells. J Chemother, 1998,10( 1 ): 7-16.
  • 7Clancy CJ, Nguyen MH. In vitro efficacy and fungicidal activity of voriconazole against Aspergillus and Fusarium species. Eur J Clin Microbiol Infect Dis, 1998,17(8) :573-575.
  • 8Vora S, Chauhan S, Brummer E, et al. Activity of voriconazole combined with neutrophils or monocytes against Aspergillus fumigatus: effects of granulocyte colony-stimulating factor and granulocyte-macrophage colonystimulating factor. Antimicrob Agents Chemother, 1998, 42 ( 9 ): 2299-2303.
  • 9Sutton DA, Sanche SE, Revankar SG, et al. In vitro amphotericin B resistance in clinical isolates of Aspergillus terreus, with a head-to-head comparison to voriconazole. J Clin Microbiol, 1999,37(7):2343-2345.
  • 10Nguyen MH, Yu CY. In vitro comparative efficacy of voriconazole and itraconazole against fluconazole-susceptible and -resistant Cryptococcus neoformans isolates. Antimicrob Agents Chemother, 1998,42(2) :471-472.

同被引文献22

  • 1中华人民共和国药典委员会.中国药典 二部[M].北京:化学工业出版社,2000.附录89.
  • 2刑来君 李明春.普通真菌学[M].北京:高等教育出版社,2001.21.
  • 3.[P].USP25.2442..
  • 4中华人民共和国药典委员会.中国药典.二部[M].北京:化学工业出版社,2000.附录89.
  • 5王思袭.SIPI4678和伏立康唑的合成[D].2006-06.
  • 6张文祥.制备伏立康唑的方法[P].CN1473825,2004-02-11.
  • 7黄维宣,崔东冬,郭金华.一种制备伏立康唑的新方法[P].CN1814597.2006-08-09.
  • 8周华明,周英.伏立康唑及其药用盐、中间体的一种新定向合成制备方法[P].CN1919846,2007-02-28.
  • 9王玉成,辜顺林.伏立康唑衍生物及其制备方法[P].100999618.2007-07-18.
  • 10Ray SJ, Riehardon k, Triazole antifungal agents [P]. EP 0440372, 1991-08-07 (CA1991, 115:256 -213).

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