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硝羟喹啉对念珠菌属临床分离株的体外活性。

In vitro activity of nitroxoline against clinical isolates of Candida species.

作者信息

Hernández Molina J M, Llosá J, Ventosa A

机构信息

Servicio de Microbiología, Hospital Virgen de las Nieves, Granada, Spain.

出版信息

Mycoses. 1991 Jul-Aug;34(7-8):323-5. doi: 10.1111/j.1439-0507.1991.tb00669.x.

Abstract

The in vitro antifungal activity of the quinoline nitroxoline has been compared with those of amphotericin B, flucytosine, and two azoles, miconazole and ketoconazole, against clinical isolates of Candida spp. A total of 186 isolates of 10 species of Candida and two culture collection strains were tested by an agar-dilution technique. Nitroxoline was highly active against Candida spp. MICs for nitroxoline ranged between 0.25-2 micrograms ml-1 for 186 representative strains. With MIC90 as the measure of antifungal activity, nitroxoline appeared to be superior to the imidazoles studied. Data for individual species of Candida revealed that the activities of nitroxoline and amphotericin B were generally just as effective against C. albicans, whereas flucytosine was the most active agent against Candida spp.

摘要

已将喹啉硝咯的体外抗真菌活性与两性霉素B、氟胞嘧啶以及两种唑类药物(咪康唑和酮康唑)针对念珠菌属临床分离株的活性进行了比较。采用琼脂稀释技术对总共186株10种念珠菌的分离株和两种培养保藏菌株进行了测试。硝咯对念珠菌属具有高度活性。186株代表性菌株的硝咯最低抑菌浓度(MIC)范围在0.25至2微克/毫升之间。以MIC90作为抗真菌活性的衡量指标,硝咯似乎优于所研究的咪唑类药物。针对念珠菌各个物种的数据显示,硝咯和两性霉素B对白色念珠菌的活性通常同样有效,而氟胞嘧啶是针对念珠菌属最具活性的药物。

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