Palou de Fernandez E, Patino M M, Graybill J R, Tarbit M H
J Antimicrob Chemother. 1986 Aug;18(2):261-70. doi: 10.1093/jac/18.2.261.
Fluconazole is a recently developed triazole with activity in vitro against Cryptococcus neoformans, water solubility, and excellent oral absorption. We compared fluconazole in murine cryptococcosis with ketoconazole and amphotericin B. Fluconazole was highly effective in suppressing cryptococcosis in mice challenged by the intravenous and intranasal routes, and was comparable with the other two drugs in its protective capacity. However, fluconazole was superior to ketoconazole and comparable with amphotericin B after intracerebral challenge. Fluconazole may warrant clinical evaluation in cryptococcosis.
氟康唑是一种最近开发的三唑类药物,在体外对新型隐球菌具有活性,具有水溶性且口服吸收良好。我们将氟康唑与酮康唑和两性霉素B在小鼠隐球菌病模型中进行了比较。氟康唑在抑制经静脉和鼻内途径感染的小鼠隐球菌病方面非常有效,并且在保护能力上与其他两种药物相当。然而,在脑内感染后,氟康唑优于酮康唑,与两性霉素B相当。氟康唑可能值得在隐球菌病中进行临床评估。