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与酮康唑相比,环吡酮胺单独及与吡硫翁锌联合使用对球形马拉色菌和限制马拉色菌参考菌株的体外抗真菌疗效。

In vitro antifungal efficacy of ciclopirox olamine alone and associated with zinc pyrithione compared to ketoconazole against Malassezia globosa and Malassezia restricta reference strains.

作者信息

Roques Christine, Brousse Sabine, Panizzutti Cédric

机构信息

Faculty of Pharmaceutical Sciences, FONDEREPHAR, Toulouse, France.

出版信息

Mycopathologia. 2006 Dec;162(6):395-400. doi: 10.1007/s11046-006-0075-0.

Abstract

The aim of this study was to determine the in vitro fungicidal and growth inhibitory activity of ciclopirox olamine alone (1% and 1.5%) or in association with 1% zinc pyrithione compared to 2% ketoconazole, against Malassezia species particularly involved in the pathogenesis of seborrheic dermatitis. Experiments were performed on Malassezia globosa IP 2387.96 and M. restricta IP 2392.96 strains. Growth inhibitory activity of the active compounds in solution was evaluated by measuring minimal inhibitory concentrations using a broth micro-method and their fungicidal activity by a filtration method after contact times between solutions and yeasts ranging from 3-5 to 30 min. Concerning the determination of minimal inhibitory concentration of ciclopirox olamine/zinc pyrithione, it revealed the marked synergistic inhibitory effect of the association, leading to a higher efficacy compared to ketoconazole. As to the fungicidal activity of ciclopirox olamine, it significantly increased with the contact time. After 15-30 min of contact between 1.5% ciclopirox olamine and Malassezia strains, a 2-log reduction of Malassezia counts was observed. The 1.5% ciclopirox olamine/1% zinc pyrithione association was characterized by a steady fungicidal efficacy whereas the 2% ketoconazole solution did not express any fungicidal effect. In conclusion, this study demonstrates the in vitro inhibitory and fungicidal efficacy of the ciclopirox olamine/zinc pyrithione association against Malassezia species and underscores its potential interest in the treatment of seborrheic dermatitis.

摘要

本研究的目的是确定单独使用环吡酮胺(1%和1.5%)或与1%的吡啶硫酮锌联合使用时,与2%酮康唑相比,对特别参与脂溢性皮炎发病机制的马拉色菌属的体外杀菌和生长抑制活性。实验在球形马拉色菌IP 2387.96和限制马拉色菌IP 2392.96菌株上进行。通过肉汤微量法测量最低抑菌浓度来评估溶液中活性化合物的生长抑制活性,并在溶液与酵母接触3 - 5至30分钟后通过过滤法评估其杀菌活性。关于环吡酮胺/吡啶硫酮锌最低抑菌浓度的测定,结果显示联合使用具有显著的协同抑制作用,与酮康唑相比疗效更高。至于环吡酮胺的杀菌活性,它随接触时间显著增加。在1.5%环吡酮胺与马拉色菌菌株接触15 - 30分钟后,观察到马拉色菌数量减少了2个对数级。1.5%环吡酮胺/1%吡啶硫酮锌联合使用具有稳定的杀菌效果,而2%酮康唑溶液未表现出任何杀菌作用。总之,本研究证明了环吡酮胺/吡啶硫酮锌联合使用对马拉色菌属的体外抑制和杀菌效果,并强调了其在脂溢性皮炎治疗中的潜在价值。

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