School of Chemistry and Physics, Faculty of Science, Queensland University of Technology, Brisbane, Queensland, 4001, Australia.
Centre for Materials Science, Queensland University of Technology, Brisbane, Queensland, 4001, Australia.
Chem Asian J. 2022 Jun 1;17(11):e202200201. doi: 10.1002/asia.202200201. Epub 2022 Apr 13.
Biofilms are part of the natural lifecycle of bacteria and are known to cause chronic infections that are difficult to treat. Most antibiotics are developed and tested against bacteria in the planktonic state and are ineffective against bacterial biofilms. The oxazolidinones, including the last resort drug linezolid, are one of the main classes of synthetic antibiotics progressed to clinical use in the last 50 years. They have a unique mechanism of action and only develop low levels of resistance in the clinical setting. With the aim of providing insight into strategies to design more potent antibiotic compounds with activity against bacterial biofilms, we review the biofilm activity of clinically approved oxazolidinones and report on structural modifications to oxazolidinones and their delivery systems which lead to enhanced anti-biofilm activity.
生物膜是细菌自然生命周期的一部分,已知会导致难以治疗的慢性感染。大多数抗生素是针对浮游状态的细菌开发和测试的,对细菌生物膜无效。恶唑烷酮类,包括最后的药物利奈唑胺,是过去 50 年来进展到临床使用的主要合成抗生素之一。它们具有独特的作用机制,在临床环境中仅产生低水平的耐药性。为了提供对抗细菌生物膜的更有效抗生素化合物设计策略的深入了解,我们综述了临床批准的恶唑烷酮类的生物膜活性,并报告了导致增强抗生物膜活性的恶唑烷酮类及其传递系统的结构修饰。