氟康唑
白色念珠菌
双氢青蒿素
药理学
微生物学
抗药性
药品
医学
生物
恶性疟原虫
抗真菌
免疫学
青蒿素
疟疾
作者
Hui Li,Hai‐Sheng Chen,Wenna Shi,Jing Shi,Jupeng Yuan,Cunxian Duan,Qing Fan,Yuguo Liu
出处
期刊:Future Microbiology
[Future Medicine]
日期:2021-05-01
卷期号:16 (7): 461-469
被引量:4
标识
DOI:10.2217/fmb-2020-0148
摘要
Aim: To investigate the effects of dihydroartemisinin combined with fluconazole against C. albicans in vitro and to explore the underlying mechanisms. Materials & methods: Checkerboard microdilution assay and time–kill curve method were employed to evaluate the static and dynamic antifungal effects against C. albicans. Reactive oxygen species (ROS) was measured by a fluorescent probe. Results: Combination of dihydroartemisinin and fluconazole exerted potent synergy against planktonic cells and biofilms of fluconazole-resistant C. albicans, with the fractional inhibitory concentration index values less than 0.07. A potent fungistatic activity of this drug combination could still be observed after 18 h. The accumulation of ROS induced by the drug combination might contribute to the synergy. Conclusion: Dihydroartemisinin reversed the resistance of C. albicans to fluconazole.
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