自愈水凝胶
透明质酸
纳米技术
脚手架
组织工程
细胞外基质
材料科学
再生(生物学)
生物相容性材料
化学
计算机科学
高分子化学
生物医学工程
生物化学
解剖
医学
数据库
生物
细胞生物学
作者
Xian Xu,Amit K. Jha,Daniel A. Harrington,Mary C. Farach‐Carson,Xinqiao Jia
出处
期刊:Soft Matter
[Royal Society of Chemistry]
日期:2012-01-01
卷期号:8 (12): 3280-3280
被引量:580
摘要
Hyaluronic acid (HA) is one of nature's most versatile and fascinating macromolecules. Being an essential component of the natural extracellular matrix (ECM), HA plays an important role in a variety of biological processes. Inherently biocompatible, biodegradable and non-immunogenic, HA is an attractive starting material for the construction of hydrogels with desired morphology, stiffness and bioactivity. While the interconnected network extends to the macroscopic level in HA bulk gels, HA hydrogel particles (HGPs, microgels or nanogels) confine the network to microscopic dimensions. Taking advantage of various scaffold fabrication techniques, HA hydrogels with complex architecture, unique anisotropy, tunable viscoelasticity and desired biologic outcomes have been synthesized and characterized. Physical entrapment and covalent integration of hydrogel particles in a secondary HA network give rise to hybrid networks that are hierarchically structured and mechanically robust, capable of mediating cellular activities through the spatial and temporal presentation of biological cues. This review highlights recent efforts in converting a naturally occurring polysaccharide to drug releasing hydrogel particles, and finally, complex and instructive macroscopic networks. HA-based hydrogels are promising materials for tissue repair and regeneration.
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