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地氯雷他定对多重耐药的抗菌和抗生物膜活性。

Antimicrobial and antibiofilm activities of desloratadine against multidrug-resistant .

机构信息

Universidade Federal da Grande Dourados (UFGD), Laboratório de Pesquisa em Ciências da Saúde, Dourados, Mato Grosso do Sul, 79804-970, Brazil.

Grupo de Pesquisa Nano & Photon, Instituto de Física, Universidade Federal do Mato Grosso do Sul, Campo Grande, Mato Grosso do Sul, 79070-900, Brazil.

出版信息

Future Microbiol. 2023 Jan;18:15-25. doi: 10.2217/fmb-2022-0085. Epub 2022 Nov 10.

Abstract

The antimicrobial and antibiofilm activities of the antihistamine desloratadine against multidrug-resistant (MDR) were evaluated. Desloratadine inhibited 90% bacterial growth at a concentration of 64 μg/ml. The combination of desloratadine with meropenem reduced the MIC by twofold in the planktonic state and increased the antibiofilm activity by eightfold. Survival curves showed that combinations of these drugs were successful in eradicating all bacterial cells within 16 h. Scanning electron microscopy also confirmed a synergistic effect in imparting a harmful effect on the cellular structure of MDR . An model showed significant protection of up to 83% of infected with MDR . Our results indicate that repositioning of desloratadine may be a safe and low-cost alternative as an antimicrobial and antibiofilm agent for the treatment of MDR infections.

摘要

我们评估了抗组胺药地氯雷他定对多药耐药菌(MDR)的抗菌和抗生物膜活性。地氯雷他定在 64μg/ml 的浓度下抑制 90%的细菌生长。地氯雷他定与美罗培南联合使用可使浮游状态下的 MIC 降低两倍,并使抗生物膜活性增加八倍。生存曲线表明,这些药物的组合可成功地在 16 小时内消灭所有细菌细胞。扫描电子显微镜也证实了联合用药对多药耐药菌细胞结构的协同作用。动物感染模型显示,高达 83%的感染多药耐药菌的动物得到了显著保护。我们的研究结果表明,重新定位地氯雷他定可能是一种安全且低成本的替代方案,可作为治疗多药耐药菌感染的抗菌和抗生物膜药物。

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