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新型咪唑衍生物噻康唑(UK-20,349)的抗真菌活性

Antifungal activity of tioconazole (UK-20,349), a new imidazole derivative.

作者信息

Jevons S, Gymer G E, Brammer K W, Cox D A, Leeming M R

出版信息

Antimicrob Agents Chemother. 1979 Apr;15(4):597-602. doi: 10.1128/AAC.15.4.597.

Abstract

Tioconazole (UK-20,349), a new antifungal imidazole derivative, was compared with miconazole for activity in vitro against Candida spp., Torulopsis glabrata, Cryptococcus neoformans, Aspergillus spp., and dermatophyte fungi (Trichophyton spp. and Microsporum spp.). Tioconazole was more active than miconazole against all the fungal species examined except Aspergillus, against which both agents showed similar activity. Both tioconazole and miconazole inhibited the growth of all fungi examined at concentrations well below their quoted minimum inhibitory concentrations. Their activity against fungi in vivo was investigated in mice infected systemically with Candida albicans. Both agents significantly reduced the numbers of viable Candida cells recoverable from the kidneys of infected animals, with tioconazole producing a generally more marked reduction. After administration of a single oral dose (25 mg/kg) to beagle dogs or white mice, higher and more sustained circulating levels of bioactive drug were detectable of tioconazole than of miconazole. These observations suggest that tioconazole may have potential in the treatment of both superficial and systemic mycoses in humans.

摘要

噻康唑(UK - 20,349)是一种新型抗真菌咪唑衍生物,将其与咪康唑在体外抗念珠菌属、光滑球拟酵母菌、新型隐球菌、曲霉属以及皮肤癣菌(毛癣菌属和小孢子菌属)的活性方面进行了比较。除曲霉外,噻康唑对所有检测的真菌种类的活性均高于咪康唑,而二者对曲霉的活性相似。噻康唑和咪康唑在远低于其公布的最低抑菌浓度的浓度下就能抑制所有检测真菌的生长。在全身性感染白色念珠菌的小鼠体内研究了它们对真菌的活性。两种药物均能显著减少感染动物肾脏中可恢复的活念珠菌细胞数量,噻康唑的减少作用通常更为显著。对比格犬或白色小鼠单次口服给药(25mg/kg)后,可检测到噻康唑的生物活性药物循环水平高于咪康唑,且维持时间更长。这些观察结果表明,噻康唑在治疗人类浅表和全身性真菌病方面可能具有潜力。

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