自愈水凝胶
生物相容性
组织工程
材料科学
脚手架
生物医学工程
软骨
微晶纤维素
再生(生物学)
纤维素
化学
解剖
高分子化学
细胞生物学
生物化学
冶金
生物
医学
作者
Xinding Yu,Xi Li,Liang Kan,Peng Pan,Xi Wang,Wentao Liu,Jinsong Zhang
标识
DOI:10.1016/j.ijbiomac.2023.124113
摘要
Cartilage tissue regeneration is tremendously tough, it has become a major clinical challenge for the orthopedic medical community. Because of their bionic structure, high water content, biocompatibility, and biodegradability, hydrogels derived from natural polysaccharide are excellent candidates for cartilage tissue engineering. However, these materials often face problems such as poor mechanical strength and excessive swelling, which limit their clinical application. This study used a chemical-physical multi-step cross-linking strategy to create double-network (DN) microcrystalline cellulose (MCC) hydrogels. The hydrogels' intrinsic biomimetic macroporous shape and high water content made them ideal for chondrocyte adhesion and proliferation. The performance requirements for cartilage tissue engineering scaffolds are met by DN hydrogels, which have a sufficiently high compressive strength (4.53 MPa), superior compression recovery, and fatigue resistance, compared to single-network (SN) hydrogels. According to in vitro findings, DN hydrogels could boost cell adhesion and proliferation due to their safe and non-toxic nature. Hydrogels were demonstrated to be stable over the long-term performance, to degrade slowly, and to have strong histocompatibility by in vivo implantation. To construct cartilage tissue engineering scaffold and conduct three-dimensional cell culture, DN hydrogels have significant potential.
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