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下一代多粘菌素类抗生素:照亮黑暗之路的一线希望

Next-Generation Polymyxin Class of Antibiotics: A Ray of Hope Illuminating a Dark Road.

作者信息

Aslan Abdullah Tarık, Akova Murat, Paterson David L

机构信息

Department of Internal Medicine, Gölhisar State Hospital, Gölhisar, Burdur 15100, Turkey.

UQ Centre for Clinical Research, Faculty of Medicine, University of Queensland, Brisbane, QLD 4029, Australia.

出版信息

Antibiotics (Basel). 2022 Nov 27;11(12):1711. doi: 10.3390/antibiotics11121711.

Abstract

Although new-generation antimicrobials, in particular β-lactam/β-lactamase inhibitors, have largely replaced polymyxins in carbapenem-resistant Gram-negative bacterial infections, polymyxins are still needed for carbapanem-resistant infections and in settings where novel agents are not readily available. Despite their potent in vitro activity, the clinical utility of polymyxins is significantly limited by their pharmacokinetic properties and nephrotoxicity risk. There is significant interest, therefore, in developing next-generation polymyxins with activity against colistin-resistant strains and lower toxicity than existing polymyxins. In this review, we aim to present the antibacterial activity mechanisms, in vitro and in vivo efficacy data, and toxicity profiles of new-generation polymyxins, including SPR206, MRX-8, and QPX9003, as well as the general characteristics of old polymyxins. Considering the emergence of colistin-resistant strains particularly in endemic regions, the restoration of the antimicrobial activity of polymyxins via PBT2 is also described in this review.

摘要

尽管新一代抗菌药物,特别是β-内酰胺/β-内酰胺酶抑制剂,在耐碳青霉烯革兰氏阴性菌感染中已在很大程度上取代了多粘菌素,但在耐碳青霉烯感染以及新型药物难以获得的情况下,多粘菌素仍是必需的。尽管多粘菌素具有强大的体外活性,但其临床应用因药代动力学特性和肾毒性风险而受到显著限制。因此,开发对耐黏菌素菌株有活性且毒性低于现有多粘菌素的新一代多粘菌素具有重大意义。在本综述中,我们旨在介绍新一代多粘菌素(包括SPR206、MRX-8和QPX9003)的抗菌活性机制、体外和体内疗效数据以及毒性概况,以及旧多粘菌素的一般特征。鉴于耐黏菌素菌株尤其是在流行地区的出现,本综述还描述了通过PBT2恢复多粘菌素抗菌活性的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8be8/9774142/2efe0fb5e269/antibiotics-11-01711-g001.jpg

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