自愈水凝胶
明胶
乙二醇
组织工程
聚合物
材料科学
生物相容性材料
细胞包封
聚乙二醇
高分子化学
化学工程
化学
纳米技术
有机化学
生物医学工程
工程类
医学
作者
Chun‐Wei Chang,Yi‐Cheun Yeh
标识
DOI:10.1002/mabi.202100248
摘要
Abstract Synthetic polymers have been widely employed to prepare hydrogels for biomedical applications, such as cell culture, drug delivery, and tissue engineering. However, the activity of cells cultured in the synthetic polymer‐based hydrogels faces the challenges of limited cell proliferation and spreading compared to cells cultured in natural polymer‐based hydrogels. To address this concern, a hybrid hydrogel strategy is demonstrated by incorporating thiolated gelatin (GS) into the norbornene‐functionalized poly (glycerol sebacate) ‐co‐ polyethylene glycol (Nor_PGS‐ co ‐PEG, NPP) network to prepare highly biocompatible NPP/GS_UV hydrogels after the thiol‐ene photo‐crosslinking reaction. The GS introduces several desirable features (i.e., enhanced water content, enlarged pore size, increased mechanical property, and more cell adhesion sites) to the NPP/GS_UV hydrogels, facilitating the cell proliferation and spreading inside the network. Thus, the highly biocompatible NPP/GS_UV hydrogels are promising materials for cell encapsulation and tissue engineering applications. Taken together, the hybrid hydrogel strategy is demonstrated as a powerful approach to fabricate hydrogels with a highly friendly environment for cell culture, expanding the biomedical applications of hydrogels.
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