Ionic Polymerization-Based Synthesis of Bioinspired Adhesive Hydrogel Microparticles with Tunable Morphologies from Microfluidics

材料科学 纳米技术 药物输送 微流控 自愈水凝胶 杰纳斯 杰纳斯粒子 胶粘剂 聚合 粒子(生态学) 分散性 微载波 粘附 化学工程 复合材料 聚合物 高分子化学 地质学 工程类 海洋学 生物 细胞培养 图层(电子) 遗传学
作者
Yingzhe Liu,Sida Ling,Zhuo Chen,Jianhong Xu
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:16 (28): 37028-37040 被引量:9
标识
DOI:10.1021/acsami.4c06578
摘要

Shape-anisotropic hydrogel microparticles have attracted considerable attention for drug-delivery applications. Particularly, nonspherical hydrogel microcarriers with enhanced adhesive and circulatory abilities have demonstrated value in gastrointestinal drug administration. Herein, inspired by the structures of natural suckers, we demonstrate an ionic polymerization-based production of calcium (Ca)-alginate microparticles with tunable shapes from Janus emulsion for the first time. Monodispersed Janus droplets composed of sodium alginate and nongelable segments were generated using a coflow droplet generator. The interfacial curvatures, sizes, and production frequencies of Janus droplets can be flexibly controlled by varying the flow conditions and surfactant concentrations in the multiphase system. Janus droplets were ionically solidified on a chip, and hydrogel beads of different shapes were obtained. The in vitro and in vivo adhesion abilities of the hydrogel beads to the mouse colon were investigated. The anisotropic beads showed prominent adhesive properties compared with the spherical particles owing to their sticky hydrogel components and unique shapes. Finally, a novel computational fluid dynamics and discrete element method (CFD-DEM) coupling simulation was used to evaluate particle migration and contact forces theoretically. This review presents a simple strategy to synthesize Ca-alginate particles with tunable structures that could be ideal materials for constructing gastrointestinal drug delivery systems.
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