自愈水凝胶
生物相容性
壳聚糖
材料科学
羧甲基纤维素
极限抗拉强度
复合材料
纤维素
聚丙烯酰胺
抗压强度
吸附
甲基纤维素
化学工程
纳米技术
高分子化学
化学
有机化学
钠
冶金
工程类
作者
Weijuan Huang,Yixiang Wang,Lynn M. McMullen,Mark T. McDermott,Hongbing Deng,Yumin Du,Lingyun Chen,Lina Zhang
标识
DOI:10.1016/j.carbpol.2019.114977
摘要
As medical practitioners' interest in hydrogels continues to grow, their new expectations in terms of mechanical properties, biocompatibility and durability are changed. Here, we demonstrated a new strategy to improve both mechanical properties and self-recovery of double network (DN) hydrogels by introducing a self-healing network, consisting of carboxymethyl chitosan (CMC) and dialdehyde cellulose nanocrystals (DACNC). Notably, the hydrogel could be repeatedly stretched to 4 times its initial length and has tensile strength of 244 kPa, and completely recovered its shape when compressed by 90% and had the compressive strength up to 8 MPa. In addition, the deformed hydrogel recovered 81.3% of its dissipated energy at room temperature without any external stimuli. The hydrogel also exhibited good biocompatibility. We have developed a new method to fabricate stretchable and tough hydrogels that could spontaneously self-repair following mechanical deformation. They are promising for controlled drug release and dye adsorption.
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