Ebselen and diphenyl diselenide against fungal pathogens: A systematic review

二苯基二硒醚 伊布塞伦 抗菌剂 曲霉 生物 杀菌剂 微生物学 最小抑制浓度 二硒醚 抗真菌 孢子丝菌 药理学 化学 孢子丝菌病 生物化学 免疫学 植物 抗氧化剂 过氧化氢酶 有机化学 谷胱甘肽过氧化物酶
作者
Jéssica Louise Benelli,Vanice Rodrigues Poester,Lívia Silveira Munhoz,Aryse Martins Melo,Mariana Rodrigues Trápaga,David A. Stevens,Melissa Orzechowski Xavier
出处
期刊:Medical Mycology [Oxford University Press]
卷期号:59 (5): 409-421 被引量:34
标识
DOI:10.1093/mmy/myaa115
摘要

Abstract Fungal infections are one of the most prevalent diseases in the world and there is a lack of new antifungal drug development for these diseases. We conducted a systematic review of the literature regarding the in vitro antifungal activity of the organoselenium compounds ebselen (Eb) and diphenyl diselenide [(PhSe)2]. A systematic review was carried out based on the search for articles with data concerning Minimal Inhibitory Concentration (MIC) values, indexed in international databases and published until August 2020. A total of 2337 articles were found, and, according to the inclusion and exclusion criteria used, 22 articles were included in the study. Inhibitory activity against 96% (200/208) and 95% (312/328) of the pathogenic fungi tested was described for Eb and [(PhSe)2], respectively. Including in these 536 fungal isolates tested, organoselenium activity was highlighted against Candida spp., Cryptococcus ssp., Trichosporon spp., Aspergillus spp., Fusarium spp., Pythium spp., and Sporothrix spp., with MIC values lower than 64 μg/mL. In conclusion, Eb and [(PhSe)2] have a broad spectrum of in vitro inhibitory antifungal activity. These data added with other pharmacological properties of these organoselenium compounds suggest that both compounds are potential future antifungal drugs. Whether MICs toward the upper end of the ranges described here are compatible with efficacious therapy, and whether they may achieve such end as a result of the favorable non-antimicrobial effects of selenium on the host, requires more in vivo testing.
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