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开发一种基于头孢氨苄的释放一氧化氮的杂化化合物,以增强抗菌效果和破坏生物膜。

Development of a nitric oxide-releasing cephalexin-based hybrid compound for enhanced antimicrobial efficacy and biofilm disruption.

作者信息

Kumar Sumit, Parker Myddelton C, Wu Yi, Marx Anastasia, Handa Hitesh, Brisbois Elizabeth J

机构信息

School of Chemical, Materials, and Biomedical Engineering, College of Engineering, University of Georgia Athens GA 30602 USA

Pharmaceutical and Biomedical Science Department, College of Pharmacy, University of Georgia Athens GA 30602 USA.

出版信息

RSC Med Chem. 2025 Sep 3. doi: 10.1039/d5md00602c.

Abstract

Biofilm formation on medical devices and the rise of antibiotic resistance have undermined conventional antibiotics such as cephalexin (CEX), which is effective against Gram-positive infections but has limited activity against Gram-negative pathogens and biofilms. To overcome these limitations, we developed a hybrid nitric oxide (NO)-releasing conjugate (SNAP_CEX) by covalently attaching the NO donor -nitroso--acetylpenicillamine (SNAP) to CEX. SNAP_CEX exhibited a sustained NO release profile over 30 days, indicating enhanced stability compared to SNAP's rapid degradation, even though the Griess assay showed NO release from SNAP over 30 days. The hybrid maintained strong antibacterial activity against (; MIC = 7 μM 2.5 μM for CEX) and dramatically improved efficacy against (; MIC = 3 mM 16 mM for CEX). SNAP_CEX also significantly disrupted established biofilms, reducing biofilm biomass by ∼75% ( ∼33% by CEX) and viable cells by ∼99%, and achieving ∼67% biomass reduction and 77% killing in biofilms ( ∼25% and 18% by CEX). These effects demonstrate that SNAP_CEX combines NO's biofilm-disruptive action with antibiotic therapy to combat biofilm-associated resistant infections, while remaining cytocompatible at therapeutic concentrations.

摘要

医疗设备上生物膜的形成以及抗生素耐药性的增加削弱了诸如头孢氨苄(CEX)等传统抗生素的作用,CEX对革兰氏阳性感染有效,但对革兰氏阴性病原体和生物膜的活性有限。为了克服这些局限性,我们通过将一氧化氮(NO)供体——亚硝基乙酰青霉胺(SNAP)共价连接到CEX上,开发了一种释放NO的杂合共轭物(SNAP_CEX)。SNAP_CEX在30天内呈现出持续的NO释放曲线,这表明与SNAP的快速降解相比其稳定性增强,尽管格里斯试验显示SNAP在30天内都有NO释放。该杂合共轭物对金黄色葡萄球菌保持着较强的抗菌活性(CEX的MIC = 7 μM,而它的MIC = 2.5 μM),并且对大肠杆菌的疗效显著提高(CEX的MIC = 3 mM,而它的MIC = 16 mM)。SNAP_CEX还能显著破坏已形成的生物膜,使金黄色葡萄球菌生物膜的生物量减少约75%(CEX约为33%),活菌数量减少约99%,在大肠杆菌生物膜中生物量减少约67%,杀菌率达77%(CEX分别约为25%和18%)。这些结果表明,SNAP_CEX将NO的生物膜破坏作用与抗生素疗法相结合,以对抗与生物膜相关的耐药感染,同时在治疗浓度下保持细胞相容性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9cd/12435586/daa7d4f29f18/d5md00602c-s1.jpg

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