Sustainable mechanochemical growth of double-network hydrogels supported by vascular-like perfusion

自愈水凝胶 材料科学 血管网 灌注 化学工程 业务 生物医学工程 医学 内科学 高分子化学 解剖 工程类
作者
Gumi Wei,Yumeko Kudo,Takahiro Matsuda,Zhi Jian Wang,Qi Mu,Daniel R. King,Tasuku Nakajima,Jian Ping Gong
出处
期刊:Materials horizons [The Royal Society of Chemistry]
卷期号:10 (11): 4882-4891 被引量:13
标识
DOI:10.1039/d3mh01038d
摘要

Double-network (DN) gels are unique mechanochemical materials owing to their structures that can be dynamically remodelled during use. The mechanical energy applied to DN gels is efficiently transferred to the chemical bonds of the brittle network, generating mechanoradicals that initiate the polymerisation of pre-loaded monomers, thereby remodelling the materials. To attain continuous remodelling or growth in response to repetitive mechanical stimuli, a sustainable supply of chemical reagents to such dynamic materials is essential. In this study, inspired by the vascular perfusion transporting nutrients to cells, we constructed a circulatory system for a continuous supply of chemicals to channel-containing DN hydrogels (c-DN gels). The perfusion of monomer solutions through the channel and permeability of the c-DN gels not only replenishes the monomers consumed by the polymerisation but also replenishes the water loss caused by the surface evaporation of hydrogel, thereby freeing the mechanochemical process of DN gels from the constraints of the underwater environment. The facile chemical supply enabled us to modulate the mechanical enhancement of the c-DN gel and attain muscle-like strengthening under repeated mechanical training in deoxygenated air. We also studied the kinetics of polymer growth and strengthening and deciphered unique features of mechanochemical reaction in DN gels including the extremely long-living radicals and delayed mechanical strengthening.
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