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基于恶唑啉的抗菌聚合物对金黄色葡萄球菌作用机制:体内抗菌活性评价。

Mechanism of Action of Oxazoline-Based Antimicrobial Polymers Against Staphylococcus aureus: In Vivo Antimicrobial Activity Evaluation.

机构信息

Department of Chemistry, University of Warwick, Coventry, CV4 7AL, UK.

Warwick Medical School, University of Warwick, Coventry, CV4 7AL, UK.

出版信息

Adv Healthc Mater. 2023 Nov;12(29):e2301961. doi: 10.1002/adhm.202301961. Epub 2023 Sep 6.

Abstract

Antimicrobial-resistant pathogens have reached alarming levels, becoming one of the most pressing global health issues. Hence, new treatments are necessary for the fight against antimicrobial resistance. Synthetic nanoengineered antimicrobial polymers (SNAPs) have emerged as a promising alternative to antimicrobial peptides, overcoming some of their limitations while keeping their key features. Herein, a library of amphiphilic oxazoline-based SNAPs using cationic ring-opening polymerization (CROP) is designed. Amphipathic compounds with 70% cationic content exhibit the highest activity against clinically relevant Staphylococcus aureus isolates, maintaining good biocompatibility in vitro and in vivo. The mechanism of action of the lead compounds against S. aureus is assessed using various microscopy techniques, indicating cell membrane disruption, while the cell wall remains unaffected. Furthermore, a potential interaction of the compounds with bacterial DNA is shown, with possible implications on bacterial division. Finally, one of the compounds exhibits high efficacy in vivo in an insect infection model.

摘要

抗微生物药物耐药病原体已经达到令人震惊的水平,成为最紧迫的全球卫生问题之一。因此,需要新的治疗方法来对抗抗微生物药物耐药性。合成纳米工程抗菌聚合物 (SNAPs) 作为抗菌肽的一种有前途的替代品出现,克服了它们的一些局限性,同时保留了它们的关键特征。在此,设计了使用阳离子开环聚合 (CROP) 的亲脂性恶唑啉基 SNAP 文库。具有 70%阳离子含量的两亲性化合物对临床相关金黄色葡萄球菌分离株表现出最高的活性,同时保持体外和体内良好的生物相容性。使用各种显微镜技术评估了先导化合物对金黄色葡萄球菌的作用机制,表明细胞膜破裂,而细胞壁不受影响。此外,还表明化合物与细菌 DNA 之间存在潜在的相互作用,这可能对细菌分裂产生影响。最后,其中一种化合物在昆虫感染模型中表现出很高的体内疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf63/11468764/484d8623741d/ADHM-12-2301961-g003.jpg

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