Suppr超能文献

合成并表征一氧化氮释放氨苄西林作为一种潜在的抗细菌生物膜形成策略。

Synthesis and Characterization of Nitric Oxide-Releasing Ampicillin as a Potential Strategy for Combatting Bacterial Biofilm Formation.

机构信息

School of Chemical, Materials, and Biomedical Engineering, University of Georgia, Athens, Georgia 30602, United States.

Pharmaceutical and Biomedical Sciences Department, College of Pharmacy, University of Georgia, Athens, Georgia 30602, United States.

出版信息

ACS Appl Mater Interfaces. 2023 Mar 29;15(12):15185-15194. doi: 10.1021/acsami.3c00140. Epub 2023 Mar 16.

Abstract

Biofilm formation on biomaterial interfaces and the development of antibiotic-resistant bacteria have decreased the effectiveness of traditional antibiotic treatment of infections. In this project, ampicillin, a commonly used antibiotic, was conjugated with -nitroso--acetylpenicillamine (SNAP), an -nitrosothiol compound (RSNO) used for controlled nitric oxide (NO) release. This novel multifunctional molecule is the first of its kind to provide combined antibiotic and NO treatment of infectious pathogens. Characterization of the molecule included NMR, FTIR, and mass spectrometry. NO release behavior was also measured and compared to pure, unmodified SNAP. When evaluating the antimicrobial efficacy, the synthesized SNAPicillin molecule showed the lowest MIC value against Gram-negative and Gram-positive methicillin-resistant compared to ampicillin and SNAP alone. SNAPicillin also displayed enhanced biofilm dispersal and killing of both bacterial strains when treating a 48 h biofilm preformed on a polymer surface. The antibacterial results combined with the biocompatibility of the molecule show great promise for infection prevention and treatment of polymeric interfaces to reduce medical device-related infections.

摘要

生物材料界面上生物膜的形成和抗生素耐药菌的发展降低了传统抗生素治疗感染的效果。在这个项目中,氨苄西林是一种常用的抗生素,与 - 亚硝基 - 乙酰青霉胺 (SNAP) 偶联, - 亚硝基硫醇化合物 (RSNO) 用于控制一氧化氮 (NO) 的释放。这种新型多功能分子是第一个提供抗生素和 NO 联合治疗感染病原体的药物。该分子的特征包括 NMR、FTIR 和质谱。还测量了 NO 的释放行为,并与纯的、未修饰的 SNAP 进行了比较。在评估抗菌功效时,与单独的氨苄西林和 SNAP 相比,合成的 SNAPicillin 分子对革兰氏阴性菌和耐甲氧西林的革兰氏阳性菌的最低 MIC 值。当处理聚合物表面上形成的 48 小时生物膜时,SNAPicillin 还显示出增强的生物膜分散和两种细菌的杀伤作用。抗菌效果结合该分子的生物相容性,为预防感染和治疗聚合物界面提供了很大的希望,以减少与医疗器械相关的感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa15/10064314/8fab6defd92d/am3c00140_0002.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验