乙烯醇
乙二醇
生物相容性
材料科学
自愈水凝胶
聚乙烯醇
甘油
复合数
化学工程
PEG比率
极限抗拉强度
复合材料
增塑剂
聚合物
高分子化学
化学
有机化学
财务
经济
工程类
冶金
作者
Zishuo Ye,Hailin Lu,Guiquan Chai,Changlei Wu,Jian Chen,Leifeng Lv
摘要
Abstract Poly(vinyl alcohol) (PVA) hydrogels have shown potential applications in bionic articular cartilage due to their tissue‐like viscoelasticity, good biocompatibility and low friction. However, their lack of adequate mechanical properties is a key obstacle for PVA hydrogels to replace natural cartilage. In this study, poly(ethylene glycol) (PEG) and glycerol were introduced into PVA, and a PVA/PEG–glycerol composite hydrogel was synthesized using a mixing physical crosslinking method. The mechanical properties, hydrophilicity and tribological behavior of the PVA/PEG–glycerol hydrogel were investigated by changing the concentration of glycerol in PEG. The results showed that the tensile strength of the hydrogel reached 26.6 MPa at 270% elongation at break with 20 wt% of glycerol plasticizer, which satisfied the demand of natural cartilage. In addition, the excellent hydrophilicity of glycerol provides good lubricating properties for the composite gel under dry friction. Meanwhile, self‐healing and cellular immunity assays demonstrated that the composite gel could have good self‐healing ability and excellent biocompatibility even in the absence of external stimuli. This study provides a new candidate material for the design of articular cartilage, which has the potential to facilitate advances in artificial joint cartilage repair. © 2022 Society of Industrial Chemistry.
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