Multi-responsive hydrogel structures from patterned droplet networks

自愈水凝胶 化学 微尺度化学 纳米技术 制作 软物质 脂质双层 软质材料 微流控 材料科学 医学 生物化学 数学教育 数学 替代医学 有机化学 胶体 病理 物理化学
作者
Florence G. Downs,David J. Lunn,Michael J. Booth,Joshua B. Sauer,William J. Ramsay,R. George Klemperer,Craig J. Hawker,Hagan Bayley
出处
期刊:Nature Chemistry [Nature Portfolio]
卷期号:12 (4): 363-371 被引量:247
标识
DOI:10.1038/s41557-020-0444-1
摘要

Responsive hydrogels that undergo controlled shape changes in response to a range of stimuli are of interest for microscale soft robotic and biomedical devices. However, these applications require fabrication methods capable of preparing complex, heterogeneous materials. Here we report a new approach for making patterned, multi-material and multi-responsive hydrogels, on a micrometre to millimetre scale. Nanolitre aqueous pre-gel droplets were connected through lipid bilayers in predetermined architectures and photopolymerized to yield continuous hydrogel structures. By using this droplet network technology to pattern domains containing temperature-responsive or non-responsive hydrogels, structures that undergo reversible curling were produced. Through patterning of gold nanoparticle-containing domains into the hydrogels, light-activated shape change was achieved, while domains bearing magnetic particles allowed movement of the structures in a magnetic field. To highlight our technique, we generated a multi-responsive hydrogel that, at one temperature, could be moved through a constriction under a magnetic field and, at a second temperature, could grip and transport a cargo. Responsive hydrogels are of interest for a range of potential applications, including microscale soft robotic and biomedical devices. Now, a versatile fabrication approach has been developed to prepare patterned, multi-material and multi-responsive hydrogels. Pre-gel droplets are connected through lipid bilayers in predetermined architectures and photopolymerized to yield continuous hydrogel structures that respond to a variety of stimuli.
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