过氧亚硝酸盐
单线态氧
共聚物
光毒性
蒽醌
光化学
活性氧
光动力疗法
活性氮物种
化学
氧气
有机化学
聚合物
体外
生物化学
酶
超氧化物
作者
Soumya Paul,Shilpendu Ghosh,Tanmoy Maity,Priyanka Priyadarshini Behera,Arindam Mukherjee,Priyadarsi De
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2024-02-18
卷期号:13 (3): 288-295
被引量:4
标识
DOI:10.1021/acsmacrolett.3c00728
摘要
We report a facile stimuli-responsive strategy to generate reactive oxygen and nitrogen species (ROS and RNS) in the biological milieu from a photocleavable water-soluble block copolymer under visible light irradiation (427 nm, 2.25 mW/cm2). An anthraquinone-based water-soluble polymeric nitric oxide (NO) donor (BCPx-NO) is synthesized, which exhibits NO release in the range of 40–65 μM within 10 h of photoirradiation with a half-life of 30–103 min. Additionally, BCPx-NO produces peroxynitrite (ONOO–) and singlet oxygen (1O2) under photoirradiation. To understand the mechanism of NO release and photolysis of the functional group under blue light, we prepared a small-molecule anthraquinone-based N-nitrosamine (NOD). The cellular investigation of the effect of spatiotemporally controlled ONOO– and 1O2 generation from the NO donor polymeric nanoparticles in a triple negative breast adenocarcinoma (MDA-MB-231) under visible light irradiation (white light, 5.83 mW/cm2; total dose 31.5 J/cm2) showed an IC50 of 0.6 mg/mL. The stimuli-responsive strategy using a photolabile water-soluble block copolymer employed to generate ROS and RNS in a biological setting widens the horizon for their potential in cancer therapy.
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