自愈水凝胶
甲基丙烯酸
乳状液
水溶液
化学工程
化学
膜
微流控
甲基丙烯酸酯
肿胀 的
高分子化学
水解
材料科学
纳米技术
共聚物
聚合物
有机化学
工程类
生物化学
作者
Jörg G. Werner,Saraf Nawar,Alexander A. Solovev,David A. Weitz
出处
期刊:Macromolecules
[American Chemical Society]
日期:2018-07-24
卷期号:51 (15): 5798-5805
被引量:51
标识
DOI:10.1021/acs.macromol.8b00843
摘要
Dynamic microcapsules are a highly sought-after class of encapsulant for advanced delivery applications with dynamically tunable release profiles, as actively manipulatable microreactors, or as selective microtraps for molecular separation and purification. Such dynamic microcapsules can only be realized with a nondestructive trigger-response mechanism that changes the permeability of the shell membrane reversibly, as found in hydrogels. However, the direct synthesis of a trigger-responsive hydrogel membrane around a water drop without the use of sacrificial templates remains elusive due to the incompatibility of the synthesis chemistry with aqueous emulsion processing. Here, we report on a facile approach to fabricate reversibly responsive hydrogel microcapsules utilizing reactive anhydride chemistry. Cross-linked and hydrophobic poly(methacrylic anhydride) microcapsules are obtained from microfluidic double emulsion drop templating that enables direct encapsulation of hydrophilic, water-suspended cargo within the aqueous core. Hydrolysis in aqueous environment yields microcapsules with a poly(acid) hydrogel shell that exhibit high mechanical and chemical stability for repeated cycling between its swollen and nonswollen states without rupture or fatigue. The permeability of the microcapsules is strongly dependent on the degree of swelling and hence can be actively and dynamically modified, enabling repeated capture, trap, and release of aqueous cargo over numerous cycles.
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