Monk J P, Brogden R N
Adis International Limited, Auckland, New Zealand.
Drugs. 1991 Oct;42(4):659-72. doi: 10.2165/00003495-199142040-00008.
Naftifine is an allylamine derivative for topical administration with a mechanism of action distinct from that of other classes of antifungal agents. It inhibits squalene epoxidase and may have certain anti-inflammatory properties, but its precise mechanism of action is as yet unclear. In vitro, naftifine has potent fungistatic and fungicidal activity against dermatophytes. This correlates well with its clinical and mycological activity in patients with dermatophytoses. There is improvement in clinical symptoms and overall therapeutic success after a 2- to 5-week course of therapy in a high percentage of patients (usually over 80%) with tinea cruris or corporis, and in a slightly smaller percentage of those with tinea pedis. Naftifine is moderately active in vitro against moulds, but is generally less active against yeasts, including Candida albicans. However, it has proved reasonably effective in the treatment of patients with cutaneous candidiasis, although further studies are necessary to establish its place in therapy for this indication. In view of its good local tolerability, absence of systemic adverse effects, novel mechanism of action and effectiveness with once-daily application, naftifine offers a useful addition to available pharmaceutical options in patients with dermatomycoses.
萘替芬是一种用于局部给药的烯丙胺衍生物,其作用机制与其他类抗真菌药物不同。它抑制角鲨烯环氧酶,可能具有一定的抗炎特性,但其确切作用机制尚不清楚。在体外,萘替芬对皮肤癣菌具有强大的抑菌和杀菌活性。这与其在皮肤癣菌病患者中的临床和真菌学活性密切相关。在股癣或体癣患者中,经过2至5周的治疗疗程后,高比例(通常超过80%)的患者临床症状得到改善且总体治疗成功,足癣患者的比例略低。萘替芬在体外对霉菌有中等活性,但对包括白色念珠菌在内的酵母菌通常活性较低。然而,尽管有必要进行进一步研究以确定其在该适应症治疗中的地位,但它已被证明在治疗皮肤念珠菌病患者方面相当有效。鉴于其良好的局部耐受性、无全身不良反应、新颖的作用机制以及每日一次应用的有效性,萘替芬为皮肤真菌病患者现有的药物选择增添了一种有用的药物。