化学
生物膜
聚乙二醇
PEG比率
纳米颗粒
共聚物
一氧化氮
聚合物
可生物降解聚合物
嫁接
脂肪酶
聚氧化乙烯
化学工程
聚乙烯
生物污染
生物物理学
环氧乙烷
生物降解
组合化学
分子
小分子
块(置换群论)
乙二醇
毒品携带者
高分子化学
控制释放
纳米技术
右旋糖酐
稳定器(航空)
细胞毒性
作者
Yuan Qu,Mary B. Chan‐Park
标识
DOI:10.1021/acsapm.5c02534
摘要
Nitric oxide (NO) has shown promising potential for biofilm dispersal, but small NONOate (diazeniumdiolate) molecules have rapid diffusion, short half-life, and uncontrolled release, which limit their therapeutic applications. Grafting NO donors onto a polymer backbone reduces uncontrolled release and toxicity. However, previous works generally have uncontrolled NO release in water and are not responsive to the bacterial microenvironment. Herein, biodegradable block copolymers of polyethylene glycol (PEG)-block-polycaprolactone (PCL) derivatives as scaffolds were employed. The PCL block was diazeniumdiolate (NONOate)-functionalized, and the PEG-to-PCL ratio was varied. Two series of lipase-responsive NO-releasing biodegradable nanoparticles were made from (a) anionic and (b) mixed-charge NONOate species. The mixed-charge series with PEG produces a stable core–shell morphology that does not release NO by itself but can be triggered to release NO only when lipase is present. The lead nanoparticle exhibits superior efficacy in dispersing biofilms of both Gram-negative and Gram-positive bacteria.
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