Sugar A M, Picard M
Evans Memorial Department of Clinical Research, Boston University Medical Center Hospital, MA 02118, USA.
Antimicrob Agents Chemother. 1995 Apr;39(4):996-7. doi: 10.1128/AAC.39.4.996.
The in vitro and in vivo activities of a new broad-spectrum triazole derivative, SCH 51048, against Blastomyces dermatitidis were evaluated. As determined by using the new National Committee for Clinical Laboratory Standards proposed standard for susceptibility testing of yeasts, SCH 51048 was the most active of the four agents tested in vitro against 13 strains of B. dermatitidis. In a well-described murine model of acute pulmonary blastomycosis, SCH 51048 was comparable to amphotericin B and at least 30 times more active than itraconazole. On the basis of these experiments, clinical evaluation of SCH 51048 for the use in treatment of human blastomycosis should proceed.
对一种新型广谱三唑衍生物SCH 51048抗皮炎芽生菌的体外和体内活性进行了评估。按照新的美国国家临床实验室标准委员会提出的酵母药敏试验标准测定,SCH 51048是体外测试的四种药物中对13株皮炎芽生菌活性最强的。在一个详细描述的急性肺芽生菌病小鼠模型中,SCH 51048与两性霉素B相当,活性至少是伊曲康唑的30倍。基于这些实验,应开展SCH 51048用于治疗人类芽生菌病的临床评估。