自愈水凝胶
果胶
韧性
极限抗拉强度
化学工程
材料科学
聚合物
高分子化学
丙烯酰胺
甲基丙烯酸酯
延伸率
化学
复合材料
聚合
单体
生物化学
工程类
作者
Xiaojun Wu,Hong Sun,Zhihui Qin,Pengcheng Che,Yi Xue,Qingyu Yu,Haitao Zhang,Xia Sun,Fanglian Yao,Junjie Li
标识
DOI:10.1016/j.ijbiomac.2020.01.297
摘要
Hydrogels derived from natural polymers have been extensively investigated in the biomedical field, while inherent brittleness and poor stability limit their applications. In this study, a tough pectin-Fe3+/poly (acrylamide-co-stearyl methacrylate) (P(AAm-co-SMA)) double physical crosslinking (DPC) network hydrogel is prepared using a three-step method. The first HPAAm network is formed via hydrophobic associations among the PSMA segment in P(AAm-co-SMA), and trivalent ions (Fe3+) crosslinked pectin network as the second network. Due to the reversibility of dual physical cross-linking structures, the pectin-Fe3+/HPAAm hydrogel exhibit excellent toughness (1.04–11.20 MJ m−3). In addition, the pectin-Fe3+/HPAAm DPC hydrogels have tunable mechanical properties (tensile strength: 0.97–1.61 MPa, elongation: 133–1346%, elastic modulus: 0.30–2.20 MPa) via adjusting the ratio of pectin network and HPAAm network. To explore their potential application in tissue engineering, ATDC5 chondrocytes were seeded on the prepared DPC hydrogels. Results suggest that the pectin-Fe3+/HPAAm DPC hydrogels can support the adhesion and proliferation of ATDC5, moreover, the ATDC5 cells can penetrate into the hydrogel. It is concluded that the prepared hydrogels exhibit potential application in the load-bearing tissue repair field.
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