Graybill J R, Mitchell L, Levine H B
Antimicrob Agents Chemother. 1978 Feb;13(2):277-83. doi: 10.1128/AAC.13.2.277.
Miconazole was compared with amphotericin B in the treatment of murine cryptococcosis. Both subcutaneous and intraperitoneal administration of miconazole produced serum levels higher than the minimum inhibitory concentration for the challenge strain. However, maximal tolerable doses of miconazole gave no increase in survival. When combined with amphotericin B, miconazole demonstrated neither additive nor antagonistic effects on survival. Spleen and brain counts of cryptococci were not lowered by miconazole; also, miconazole did not alter the effect of amphotericin B on reducing tissue counts. In vitro studies confirmed that the strain of Cryptococcus neoformans was quite susceptible to both miconazole and amphotericin B. However, miconazole had a delayed onset of antifungal activity. This was apparent even at miconazole levels 20 times greater than the minimum inhibitory concentration. Also, the antifungal activity of miconazole was markedly inhibited by serum. Delayed antifungal activity and serum inhibition may limit the in vivo effectiveness of miconazole in murine cryptococcosis.
在小鼠隐球菌病治疗中,将咪康唑与两性霉素B进行了比较。皮下和腹腔注射咪康唑均可使血清水平高于攻击菌株的最低抑菌浓度。然而,咪康唑的最大耐受剂量并未提高生存率。当与两性霉素B联合使用时,咪康唑对生存率既无相加作用也无拮抗作用。咪康唑未降低脾脏和脑中隐球菌的数量;此外,咪康唑也未改变两性霉素B对减少组织中隐球菌数量的作用。体外研究证实,新型隐球菌菌株对咪康唑和两性霉素B均相当敏感。然而,咪康唑的抗真菌活性起效延迟。即使在咪康唑水平比最低抑菌浓度高20倍时,这一现象仍很明显。此外,咪康唑的抗真菌活性受到血清的显著抑制。抗真菌活性延迟和血清抑制可能会限制咪康唑在小鼠隐球菌病中的体内疗效。