Pasqualotto Alessandro C, Thiele Karoline O, Goldani Luciano Z
Hospital Dom Vicente Scherer, Santa Casa-Complexo Hospitalar, Serviço de Controle de Infecção Hospitalar, Avenida Independência 155, 90035-075, Porto Alegre, Brazil.
Curr Opin Investig Drugs. 2010 Feb;11(2):165-74.
Azoles are important compounds for the treatment of fungal infections. This review focuses on three azoles: isavuconazole, ravuconazole and albaconazole (Stiefel). These drugs exhibit a broad spectrum of activity in vitro, including activity against several fungal isolates that are resistant to other azoles. However, poor or limited activity of these compounds has been demonstrated against species of Fusarium and Scedosporium, as well as against Zygomycetes. As isavuconazole and ravuconazole have been developed both as intravenous and oral formulations, these compounds are suitable candidates for the treatment of various invasive fungal diseases. Most clinical trials with albaconazole have targeted mucocutaneous fungal infections. Although all of these agents appear to be well tolerated, cross-resistance is a concern in the azole family of compounds.
唑类是治疗真菌感染的重要化合物。本综述聚焦于三种唑类药物:艾沙康唑、雷夫康唑和阿巴康唑(施维雅公司)。这些药物在体外表现出广泛的活性,包括对几种对其他唑类耐药的真菌分离株的活性。然而,已证明这些化合物对镰刀菌属和赛多孢子菌属以及接合菌纲的活性较差或有限。由于艾沙康唑和雷夫康唑已开发出静脉和口服制剂,这些化合物是治疗各种侵袭性真菌病的合适候选药物。大多数关于阿巴康唑的临床试验针对的是皮肤黏膜真菌感染。尽管所有这些药物似乎耐受性良好,但唑类化合物家族中交叉耐药性仍是一个问题。