Martin-Mazuelos E, Aller A I, Morilla D, Montero O
Department of Microbiology, Valme University Hospital, Seville, Spain.
Chemotherapy. 1996 Mar-Apr;42(2):112-7. doi: 10.1159/000239430.
Sertaconazole is a new azolic derivative containing a benzo(b)-thiophene group, for topical use. It showed in vitro fungistatic and fungicidal activity against yeasts, dermatophytes, opportunistic filamentous fungi and Gram-positive bacteria. In this study, we have evaluated the activity of sertaconazole in vitro against 215 strains of Candida spp. Fluconazole and ketoconazole were used throughout as reference compounds. The minimum inhibitory concentration (MIC) was determined in Casitone medium and the breakpoint was obtained spectrophotometrically and visually. Visual reading of MICs correlated with the spectrophotometric determination, the values of MIC50 and MIC90 showed no difference (+/- 1 dilution) in any of the species tested (range 0.1-16 mg/l). These results show that sertaconazole is an excellent antifungal agent and fungicide in vitro against various species of Candida.
舍他康唑是一种含苯并(b)-噻吩基团的新型唑类衍生物,用于局部用药。它在体外对酵母、皮肤癣菌、机会性丝状真菌和革兰氏阳性菌显示出抑菌和杀菌活性。在本研究中,我们评估了舍他康唑在体外对215株念珠菌属菌株的活性。始终使用氟康唑和酮康唑作为参考化合物。在酪蛋白胨培养基中测定最小抑菌浓度(MIC),并通过分光光度法和肉眼观察获得断点。MIC的肉眼读数与分光光度法测定相关,在任何测试菌种中,MIC50和MIC90的值均无差异(±1个稀释度)(范围为0.1-16mg/l)。这些结果表明,舍他康唑在体外是一种针对各种念珠菌的优秀抗真菌剂和杀菌剂。