Boreham P F, Phillips R E, Shepherd R W
J Antimicrob Chemother. 1985 Nov;16(5):589-95. doi: 10.1093/jac/16.5.589.
The activities of 11 5-nitroimidazole compounds have been compared against Giardia intestinalis in vitro using a 3H-thymidine incorporation assay. All the compounds were at least equipotent to, or more active than metronidazole with the exception of panidazole. Satranidazole, ronidazole and S75 0400 A were all about five times more active than metronidazole and warrant further study as potential chemotherapeutic agents for man. No major differences in the response to these compounds was found between two stocks of Giard. intestinalis with the exception of flunidazole. Several other antiprotozoal drugs showed activity against Giard. intestinalis. Berberine sulphate, paromomycin sulphate, erythromycin estolate and sulphasalazine, all of which have been used to treat human patients, showed no activity in vitro.
使用³H-胸腺嘧啶核苷掺入试验,在体外比较了11种5-硝基咪唑化合物对肠道贾第鞭毛虫的活性。除帕硝唑外,所有化合物的活性至少与甲硝唑相当或比甲硝唑更强。塞曲硝唑、罗硝唑和S75 0400 A的活性均比甲硝唑高约五倍,值得作为人类潜在化疗药物作进一步研究。除氟硝唑外,在两株肠道贾第鞭毛虫对这些化合物的反应中未发现重大差异。其他几种抗原虫药物对肠道贾第鞭毛虫有活性。硫酸小檗碱、硫酸巴龙霉素、无味红霉素和柳氮磺胺吡啶均已用于治疗人类患者,但在体外均无活性。