自愈水凝胶
生物粘附
材料科学
软骨
壳聚糖
再生(生物学)
生物医学工程
极限抗拉强度
胶粘剂
组织工程
聚合物
化学工程
高分子化学
复合材料
解剖
图层(电子)
细胞生物学
工程类
生物
医学
作者
Sattwikesh Paul,Karsten Schrobback,Phong Anh Tran,Christoph Meinert,Jordan W. Davern,Angus Weekes,Travis Jacob Klein
标识
DOI:10.1002/adhm.202302078
摘要
Abstract Hydrogels provide a promising platform for cartilage repair and regeneration. Although hydrogels have shown some efficacy, they still have shortcomings including poor mechanical properties and suboptimal integration with surrounding cartilage. Herein, hydrogels that are injectable, cytocompatible, mechanically robust, and highly adhesive to cartilage are developed. This approach uses GelMA‐glycol chitosan (GelMA‐GC) that is crosslinkable with visible light and photoinitiators (lithium acylphosphinate and tris (2,2′‐bipyridyl) dichlororuthenium (II) hexahydrate ([RuII(bpy) 3 ] 2+ and sodium persulfate (Ru/SPS)). Ru/SPS‐cross‐linked hydrogels have higher compressive and tensile modulus, and most prominently higher adhesive strength with cartilage, which also depends on inclusion of GC. Tensile and push‐out tests of the Ru/SPS‐cross‐linked GelMA‐GC hydrogels demonstrate adhesive strength of ≈100 and 46 kPa, respectively. Hydrogel precursor solutions behave in a Newtonian manner and are injectable. After injection in focal bovine cartilage defects and in situ cross‐linking, this hydrogel system remains intact and integrated with cartilage following joint manipulation ex vivo. Cells remain viable (>85%) in the hydrogel system and further show tissue regeneration potential after three weeks of in vitro culture. These preliminary results provide further motivation for future research on bioadhesive hydrogels for cartilage repair and regeneration.
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