两亲性
聚合物囊泡
乙二醇
化学
共聚物
组合化学
单线态氧
药物输送
过氧化氢
高分子化学
有机化学
聚合物
氧气
作者
Yangwei Deng,Hui Chen,Xinfeng Tao,Fangyi Cao,Sylvain Trépout,Jun Ling,Min‐Hui Li
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2019-07-30
卷期号:20 (9): 3435-3444
被引量:50
标识
DOI:10.1021/acs.biomac.9b00713
摘要
Stimuli-responsive polymersomes formed by amphiphilic block copolymers have attracted substantial attention as smart and robust containers for drug delivery and nano/microreactors. Biosourced amphiphilic diblock copolypeptoids were developed that can self-assemble into oxidation-responsive unilamellar vesicles. These vesicles can burst under the action of reactive oxygen species which can be the hydrogen peroxide or the singlet oxygen produced by light-activation of a photosensitizer with spatiotemporal control. Polysarcosine (PSar, also called poly(N-methyl glycine)) was selected as the hydrophilic block because of its resistance to protein adsorption and low toxicity, similar to poly(ethylene glycol) (PEG). We designed and synthesized poly(N-3-(methylthio)propyl glycine) as the hydrophobic block. Its polyglycine backbone is the same as that of PSar, and especially, its hydrophobic N-substituents, thioether side chains, can be oxidized to hydrophilic sulfoxides. These oxidation-responsive polymersomes entirely based on N-substituted poly(amino acid)s were biocompatible as confirmed by cell viability tests and may find applications in drug delivery, biosensing, biodetection, and nano/microreactors.
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