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新型及已上市三唑类药物对机会性丝状真菌和双相真菌的体外活性

In vitro activities of new and established triazoles against opportunistic filamentous and dimorphic fungi.

作者信息

González Gloria M, Fothergill Annette W, Sutton Deanna A, Rinaldi Michael G, Loebenberg David

机构信息

Departamento de Microbiología, Facultad de Medicina, Universidad Autónoma de Nuevo Léon, Monterrey, Nuevo Léon, México.

出版信息

Med Mycol. 2005 May;43(3):281-4. doi: 10.1080/13693780500088416.

Abstract

The in vitro activities of three new triazoles were determined and compared to those of itraconazole and fluconazole against 306 clinical isolates of Blastomyces dermatitidis, Cladophialophora carrionii, Coccidioides immitis, Fonsecaea pedrosoi, Fusarium spp., Histoplasma capsulatum, Paecilomyces lilacinus, Pseudallescheria boydii and Sporothrix schenckii. Minimum inhibitory concentrations (MIC) were determined by a broth macrodilution method of the National Committee for Clinical Laboratory Standards M38-A procedure. Itraconazole (geometric mean MIC, 0.16-0.65 microg/ml), voriconazole (geometric mean MIC, 0.18-1.44 microg/ml), ravuconazole (geometric mean MIC, 0.18-1.09 microg/ml), and posaconazole (geometric mean MIC, 0.18-1.38 microg/ml), had relatively uniform values showing potent in vitro inhibitory activity against B. dermatitidis, C. carrionii, C. immitis, F. pedrosoi, H. capsulatum, and S. schenckii. The in vitro activity was variable with strains of P. boydii, P. lilacinus and Fusarium spp.

摘要

测定了三种新型三唑类药物的体外活性,并将其与伊曲康唑和氟康唑对306株皮炎芽生菌、卡氏枝孢霉、粗球孢子菌、裴氏着色真菌、镰刀菌属、荚膜组织胞浆菌、淡紫拟青霉、波氏假阿利什霉和申克孢子丝菌临床分离株的活性进行比较。最低抑菌浓度(MIC)采用美国国家临床实验室标准委员会M38-A程序的肉汤稀释法测定。伊曲康唑(几何平均MIC,0.16 - 0.65微克/毫升)、伏立康唑(几何平均MIC,0.18 - 1.44微克/毫升)、雷夫康唑(几何平均MIC,0.18 - 1.09微克/毫升)和泊沙康唑(几何平均MIC,0.18 - 1.38微克/毫升)具有相对一致的值,显示出对皮炎芽生菌、卡氏枝孢霉、粗球孢子菌、裴氏着色真菌、荚膜组织胞浆菌和申克孢子丝菌有较强的体外抑制活性。对波氏假阿利什霉、淡紫拟青霉和镰刀菌属菌株的体外活性存在差异。

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