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肠道贾第虫对药物的体外敏感性。

The sensitivity of Giardia intestinalis to drugs in vitro.

作者信息

Boreham P F, Phillips R E, Shepherd R W

出版信息

J Antimicrob Chemother. 1984 Nov;14(5):449-61. doi: 10.1093/jac/14.5.449.

Abstract

Techniques are described for the isolation, microculture and assessment of viability of Giardia intestinalis. The susceptibility of five recent Brisbane isolates and the Portland 1 stock to metronidazole, tinidazole, furazolidone and quinacrine has been determined. All stocks showed little variation in sensitivity to these drugs. The 3H-thymidine incorporation assay proved to be a much more sensitive method of assessing relative drug activity than either motility or dye exclusion methods. Tinidazole proved to be the most effective drug in vitro followed by furazolidone and metronidazole. Quinacrine was the least effective. The generation time of stocks in vitro varied from 12.5 to 44.2 h and the possible significance of this to failures in treatment is discussed.

摘要

本文描述了用于分离、微培养和评估肠贾第虫活力的技术。已测定了最近从布里斯班分离出的五株菌株以及波特兰1号菌株对甲硝唑、替硝唑、呋喃唑酮和喹吖因的敏感性。所有菌株对这些药物的敏感性几乎没有差异。与运动性或染料排除法相比,3H-胸腺嘧啶核苷掺入试验被证明是一种评估相对药物活性更为灵敏的方法。替硝唑被证明是体外最有效的药物,其次是呋喃唑酮和甲硝唑。喹吖因效果最差。体外培养菌株的代时从12.5小时到44.2小时不等,并讨论了这对治疗失败可能具有的意义。

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