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基于三嵌段共聚物的呼吸型 CO 、 O 、光响应囊泡用于调控药物释放速率

"Breathing" CO -, O -, and Light-Responsive Vesicles from a Triblock Copolymer for Rate-Tunable Controlled Release.

机构信息

Institute for Technical and Macromolecular Chemistry, University of Hamburg, Bundesstrasse 45, D-20146, Hamburg, Germany.

出版信息

Macromol Rapid Commun. 2018 Jan;39(1). doi: 10.1002/marc.201700313. Epub 2017 Aug 9.

Abstract

A well-defined amphiphilic triblock copolymer, poly[(ethylene glycol)methyl ether]-block-poly(N,N-dimethylamino ethyl methacrylate-co-2,2,2-trifluoroethyl methacrylate)-block-poly(4-(4-methoxy-phenylazo)phenoxy methacrylate) (PEG-b-P(DMAEMA-co-TFEMA)-b-PMEPPMA), is successfully synthesized by stepwise atom transfer radical polymerization. Owing to its amphiphilic nature, PEG-b-P(DMAEMA-co-TFEMA)-b-PMEPPMA can self-assemble into vesicles in aqueous solution and exhibits a reversible triple-responsive behavior toward CO , O , and light stimuli. More importantly, such vesicles can exhibit a controlled "breathing" behavior via external stimuli due to their suitable chemical structure and stimuli responsiveness. Consequently, these vesicles can be employed as nanocarriers for rate-tunable controlled release via adjustment of their membrane permeability by a single stimulus or various stimuli combinations.

摘要

一种具有明确两亲性的嵌段共聚物,聚[(乙二醇)甲醚]-嵌段-聚(N,N-二甲基氨基乙基甲基丙烯酸酯-co-2,2,2-三氟乙基甲基丙烯酸酯)-嵌段-聚(4-(4-甲氧基偶氮)苯氧基甲基丙烯酸酯)(PEG-b-P(DMAEMA-co-TFEMA)-b-PMEPPMA),通过逐步原子转移自由基聚合成功合成。由于其两亲性,PEG-b-P(DMAEMA-co-TFEMA)-b-PMEPPMA 可以在水溶液中自组装成囊泡,并对 CO、O 和光刺激表现出可逆的三重响应行为。更重要的是,由于其合适的化学结构和刺激响应性,这些囊泡可以通过外部刺激表现出可控的“呼吸”行为。因此,这些囊泡可以用作纳米载体,通过单一刺激或各种刺激组合来调整其膜通透性,实现可控的药物释放。

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