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伊曲康唑:一种新型三唑类抗真菌药物。

Itraconazole: a new triazole antifungal agent.

作者信息

Zuckerman J M, Tunkel A R

机构信息

Division of Infectious Diseases, Medical College of Pennsylvania, Philadelphia 19129.

出版信息

Infect Control Hosp Epidemiol. 1994 Jun;15(6):397-410. doi: 10.1086/646938.

Abstract

The azole antifungal agents represent a major advance in the management of superficial and systemic fungal infections. Itraconazole appears to have a broad spectrum of in vitro activity and is the first azole antifungal agent to have activity against Aspergillus species. Itraconazole acts primarily by impairing the synthesis of ergosterol, resulting in a defective fungal cell membrane with altered permeability and function. It is effective for a wide variety of mycotic infections and some fungal meningeal infections. Most adverse effects have been relatively minor and do not lead to discontinuation of therapy.

摘要

唑类抗真菌药物是浅表和全身性真菌感染治疗方面的一项重大进展。伊曲康唑似乎具有广泛的体外活性,是首个对曲霉菌属有活性的唑类抗真菌药物。伊曲康唑主要通过损害麦角固醇的合成起作用,导致真菌细胞膜有缺陷,通透性和功能改变。它对多种霉菌感染和一些真菌性脑膜炎感染有效。大多数不良反应相对较轻,不会导致治疗中断。

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