Bilayer hydrogel actuators with tight interfacial adhesion fully constructed from natural polysaccharides

被引:155
作者
Duan, Jiangjiang [1 ]
Liang, Xichao [1 ]
Zhu, Kunkun [1 ]
Guo, Jinhua [1 ]
Zhang, Lina [1 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
RESPONSIVE HYDROGELS; SHAPE; CHITOSAN; MICROSTRUCTURES; MICROLENSES; LENS; GEL;
D O I
10.1039/c6sm02089e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Smart hydrogel actuators with excellent biocompatibility and biodegradation are extremely desired for biomedical applications. Herein, we have constructed bio-hydrogel actuators inspired by the bilayer structures of plant organs from chitosan and cellulose/carboxymethylcellulose (CMC) solution in an alkali/urea aqueous system containing epichlorohydrin (ECH) as a crosslinker, and demonstrated tight adhesion between two layers through strong electrostatic attraction and chemical crosslinking. The bilayer hydrogels with excellent mechanical properties could carry out rapid, reversible, and repeated self-rolling deformation actuated by pH-triggered swelling/deswelling, and transformed into rings, tubules, and flower-, helix-, bamboo-, and wave-like shapes by effectively designing the geometric shape and size. The significant difference in the swelling behavior between the positively charged chitosan and the negatively charged cellulose/CMC layers generated enough force to actuate the performance of the hydrogels as soft grippers, smart encapsulators, and bioinspired lenses, showing potential applications in a wide range of fields including biomedicine, biomimetic machines, etc.
引用
收藏
页码:345 / 354
页数:10
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