制霉菌素、米卡芬净联合氯己定对白色念珠菌的体外相互作用。

Q3 Medicine
Maede Salehi, Ali Malekzadeh Shafaroudi, Maryam Daryani, Alireza Khalilian, Fatemeh Ahangarkani, Tahere Molania
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引用次数: 0

摘要

背景与目的:口腔念珠菌病已成为世界范围内医院日益严重的问题,念珠菌种类抗真菌耐药性的发展是一个严重的问题。本研究旨在评价制霉菌素和米卡芬净联合氯己定对氟康唑耐药和氟康唑敏感的白色念珠菌(C. albicans)的体外疗效。材料与方法:本实验实验室研究从伊朗萨里Mazandaran医科大学侵袭真菌研究中心的参比培养标本中获得20株氟康唑耐药(n=10)和氟康唑敏感(n=10)白色念珠菌。根据美国临床与实验室标准协会的指南,采用微量稀释棋盘法对制霉菌素和米卡芬净与氯己定进行体外联合试验。结果:米卡芬金对白色念珠菌敏感菌和耐药菌的抑菌活性最高,几何平均值分别为(GM) =0.008µg/ml和GM=0.008µg/ml,制霉菌素对白色念珠菌耐药菌和敏感菌的抑菌活性分别为0.06µg/ml和0.042µg/ml,氯己定对白色念珠菌耐药菌和敏感菌的抑菌活性分别为0.25µg/ml和0.165µg/ml。米卡芬净和制霉菌素与氯己定的相互作用显示出对大多数白色念珠菌的协同作用。此外,米卡芬净、制霉菌素和氯己定对白色念珠菌没有拮抗作用。结论:米卡芬净与氯己定协同作用对耐唑白色念珠菌具有拮抗作用,为克服抗真菌药物耐药性提供了新的途径。然而,需要进一步的体内评价研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro interactions of nystatin and micafungin combined with chlorhexidine against Candida albicans isolates.

Background and purpose: Oral candidiasis has become a growing problem in hospitals worldwide, and the development of antifungal drug resistance in Candida species constitutes a serious concern. This study aimed to evaluate the in vitro efficacy of nystatin, and micafungin with chlorhexidine against fluconazole-resistant and fluconazole-sensitive Candida albicans (C. albicans) isolates.

Materials and methods: In this experimental-laboratory study, a total of 20 fluconazole-resistant (n=10) and fluconazole-susceptible (n=10) C. albicans strains were obtained from the reference culture collection of the Invasive Fungi Research Center in Mazandaran University of Medical Sciences, Sari, Iran. In vitro combination of nystatin and micafungin with chlorhexidine was performed using a microdilution checkerboard method based on the Clinical and Laboratory Standards Institute guideline.

Results: Micafungin had the highest antifungal activity against C. albicans susceptible and resistant strains, with a Geometric mean of (GM) =0.008µg/ml and GM=0.008µg/ml, followed by nystatin with GM=0.06µg/ml and GM=0.042µg/ml and chlorhexidine with GM=0.25µg/ml and GM=0.165µg/ml against C. albicans resistant and sensitive strains, respectively. The interaction of micafungin and nystatin with chlorhexidine showed a synergistic interaction against most C. albicans strains. In addition, no antagonistic interaction was observed between micafungin, nystatin, and chlorhexidine against C. albicans strains.

Conclusion: The synergistic interaction of micafungin with chlorhexidine against azole-resistant C. albicans suggests an alternative approach to overcome antifungal drug resistance. However, further studies are needed for in vivo evaluation.

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来源期刊
Current Medical Mycology
Current Medical Mycology Medicine-Infectious Diseases
CiteScore
2.10
自引率
0.00%
发文量
16
审稿时长
4 weeks
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