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纳米氟康唑和传统氟康唑对临床重要皮肤癣菌的体外活性

In-Vitro Activity of Nano Fluconazole and Conventional Fluconazole against Clinically Important Dermatophytes.

作者信息

Musavi Bafrui Najmossadat, Hashemi Hazaveh Seyed Jamal, Bayat Mansour

机构信息

Department of Microbiology, Faculty of Veterinary Specialized Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.

Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Public Health. 2020 Oct;49(10):1970-1976. doi: 10.18502/ijph.v49i10.4701.

Abstract

BACKGROUND

Dermatophytosis is one of the most common fungal infections in humans. Antifungals such as fluconazole are effectively used for treating dermatophytosis; however, drug resistance was observed in many cases. Therefore, a newer treatment strategy is essential.

METHODS

This study (Conducted in the Laboratory of the School of Public Health, Tehran University of Medical Sciences, Tehran, Iran in 2018) evaluated the antifungal susceptibility of nano fluconazole compared to conventional fluconazole on dermatophyte isolates using CLSI M38-A2guidelines. Dermatophyte species isolated from clinical cases of dermatophytosis were identified using PCR sequencing techniques. Zeta potential and size of the nano particles containing fluconazole were measured; scanning electron microscope (SEM) was used to determine nano particle structure.

RESULTS

The size of liposomal fluconazole obtained was 88.9 ± 12.14 nm with -20.12 ± 3.8 mV for zeta potential. The encapsulation rate for fluconazole was 75.1± 4.2%. MIC for the three tested species was 32, 16, and 8 g/ml for , , and isolates, respectively. The corresponding values for nano fluconazole were 8 g/ml for the three tested species.

CONCLUSION

MIC value for nano-fluconazole was lower than conventional fluconazole in all dermatophytes species tested; therefore, nano-fluconazole could inhibit the growth of dermatophytes better than fluconazole at a lower concentration of the drug.

摘要

背景

皮肤癣菌病是人类最常见的真菌感染之一。氟康唑等抗真菌药物可有效用于治疗皮肤癣菌病;然而,在许多病例中观察到了耐药性。因此,一种更新的治疗策略至关重要。

方法

本研究(于2018年在伊朗德黑兰医科大学公共卫生学院实验室进行)根据CLSI M38 - A2指南,评估了纳米氟康唑与传统氟康唑相比对皮肤癣菌分离株的抗真菌敏感性。使用PCR测序技术鉴定从皮肤癣菌病临床病例中分离出的皮肤癣菌种类。测量了含氟康唑纳米颗粒的zeta电位和大小;使用扫描电子显微镜(SEM)确定纳米颗粒结构。

结果

获得的脂质体氟康唑大小为88.9±12.14 nm,zeta电位为 - 20.12±3.8 mV。氟康唑的包封率为75.1±4.2%。对于受试的三种菌种, 、 和 分离株的最低抑菌浓度(MIC)分别为32、16和8 μg/ml。纳米氟康唑对三种受试菌种的相应值均为8 μg/ml。

结论

在所有受试的皮肤癣菌种类中,纳米氟康唑的MIC值均低于传统氟康唑;因此,在较低药物浓度下,纳米氟康唑比氟康唑能更好地抑制皮肤癣菌的生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9ee/7719649/52483c3c3e62/IJPH-49-1970-g001.jpg

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