Dubini F, Bellotti M G, Riviera L
Institute of Medical Microbiology, University of Milan.
G Ital Chemioter. 1992 Jan-Dec;39(1-3):17-21.
The therapeutic activity of two new benzofuran-imidazoles, IM/B/4-62 and IM/B/4-66, formulated as 1% cream, has been evaluated against Candida albicans and Trichophyton mentagrophytes by inducing experimental vaginal candidosis in female rats and dermatophytosis in female guinea pigs. Results of the treatment were compared with those obtained by the same therapeutic regimen carried out with bifonazole. IM/B/4-66 proved to possess superior antimycotic activity to that of IM/B/4-62 and similar to that of bifonazole in both infections. Nmaley vaginal candidosis was cured in all the treated in animals at 6 days post-inoculation and skin lesions were healed in 9 of 10 animals at 15 days after infection, with negative cultures from all the infected sites.
两种新型苯并呋喃 - 咪唑类化合物IM/B/4 - 62和IM/B/4 - 66配制成1%乳膏,通过在雌性大鼠中诱导实验性阴道念珠菌病以及在雌性豚鼠中诱导皮肤癣菌病,评估了其对白色念珠菌和须癣毛癣菌的治疗活性。将治疗结果与用联苯苄唑进行相同治疗方案所获得的结果进行比较。结果表明,在两种感染中,IM/B/4 - 66的抗真菌活性优于IM/B/4 - 62,且与联苯苄唑相似。在接种后6天,所有接受治疗的动物的阴道念珠菌病均被治愈;感染后15天,10只动物中有9只的皮肤损伤愈合,所有感染部位的培养结果均为阴性。