Fabrication of injectable high strength hydrogel based on 4-arm star PEG for cartilage tissue engineering

材料科学 组织工程 自愈水凝胶 软骨 PEG比率 生物医学工程 软骨细胞 细胞外基质 乙二醇 透明软骨 化学工程 解剖 化学 高分子化学 骨关节炎 关节软骨 病理 替代医学 经济 工程类 医学 生物化学 财务
作者
Jianqi Wang,Fengjie Zhang,Wing Pui Tsang,Chao Wan,Chi Wu
出处
期刊:Biomaterials [Elsevier]
卷期号:120: 11-21 被引量:175
标识
DOI:10.1016/j.biomaterials.2016.12.015
摘要

Hydrogels prepared from poly(ethylene glycol) (PEG) are widely applied in tissue engineering, especially those derived from a combination of functional multi-arm star PEG and linear crosslinker, with an expectation to form a structurally ideal network. However, the poor mechanical strength still renders their further applications. Here we examined the relationship between the dynamics of the pre-gel solution and the mechanical property of the resultant hydrogel in a system consisting of 4-arm star PEG functionalized with vinyl sulfone and short dithiol crosslinker. A method to prepare mechanically strong hydrogel for cartilage tissue engineering is proposed. It is found that when gelation takes place at the overlap concentration, at which a slow relaxation mode just appears in dynamic light scattering (DLS), the resultant hydrogel has a local maximum compressive strength ∼20 MPa, while still keeps ultralow mass concentration and Young's modulus. Chondrocyte-laden hydrogel constructed under this condition was transplanted into the subcutaneous pocket and an osteochondral defect model in SCID mice. The in vivo results show that chondrocytes can proliferate and maintain their phenotypes in the hydrogel, with the production of abundant extracellular matrix (ECM) components, formation of typical chondrocyte lacunae structure and increase in Young's modulus over 12 weeks, as indicated by histological, immunohistochemistry, gene expression analyses and mechanical test. Moreover, newly formed hyaline cartilage was observed to be integrated with the host articular cartilage tissue in the defects injected with chondrocytes/hydrogel constructs. The results suggest that this hydrogel is a promising candidate scaffold for cartilage tissue engineering.
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