化学
两亲性
抗菌活性
共聚物
电子顺磁共振
一氧化氮
胶束
水溶液
核化学
控制释放
高分子化学
光化学
组合化学
有机化学
细菌
纳米技术
聚合物
材料科学
物理
生物
遗传学
核磁共振
作者
Soumya Paul,Priya Ashrit,Manish Kumar,Sourav Mete,Shilpendu Ghosh,Praveen Kumar Vemula,Arindam Mukherjee,Priyadarsi De
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2023-12-04
卷期号:25 (1): 77-88
被引量:14
标识
DOI:10.1021/acs.biomac.3c00822
摘要
N-Nitrosamines are well established motifs to release nitric oxide (NO) under photoirradiation. Herein, a series of amphiphilic N-nitrosamine-based block copolymers (BCPx-NO) are developed to attain controlled NO release under photoirradiation (365 nm, 3.71 mW/cm2). The water-soluble BCPx-NO forms micellar architecture in aqueous medium and exhibits a sustained NO release of 92-160 μM within 11.5 h, which is 36.8-64.0% of the calculated value. To understand the NO release mechanism, a small molecular NO donor (NOD) resembling the NO releasing functional motif of BCPx-NO is synthesized, which displays a burst NO release in DMSO within 2.5 h. The radical nature of the released NO is confirmed by electron paramagnetic resonance (EPR) spectroscopy. The gradual NO release from micellar BCPx-NO enhances antibacterial activity over NOD and exhibits a superior bactericidal effect on Gram-positive Staphylococcus aureus. In relation to biomedical applications, this work offers a comprehensive insight into tuning light-triggered NO release to improve antibacterial activity.
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