多粘菌素
粘菌素
鲍曼不动杆菌
抗菌剂
抗生素
多粘菌素B
微生物学
医学
生物
药理学
细菌
铜绿假单胞菌
遗传学
作者
Abdullah Tarık Aslan,Murat Akova,David L. Paterson
出处
期刊:Antibiotics
[MDPI AG]
日期:2022-11-27
卷期号:11 (12): 1711-1711
被引量:14
标识
DOI:10.3390/antibiotics11121711
摘要
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 Acinetobacter baumannii 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.
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