Preparation and evaluation of thermo-reversible copolymer hydrogels containing chitosan and hyaluronic acid as injectable cell carriers

被引:104
作者
Chen, Jyh-Ping [1 ]
Cheng, Tai-Hong [1 ]
机构
[1] Chang Gung Univ, Dept Chem & Mat Engn, Tao Yuan 333, Taiwan
关键词
Hydrogel; Poly(N-isopropylacrylamide); Chitosan; ARTIFICIAL EXTRACELLULAR-MATRIX; CARTILAGE; POLY(N-ISOPROPYLACRYLAMIDE); CHONDROCYTES; PROLIFERATION; SCAFFOLDS; GELATIN; CHITIN;
D O I
10.1016/j.polymer.2008.10.045
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(N-isopropylacrylamide) end-capped with a carboxyl group (PNIPAM-COOH) was grafted to chitosan for synthesizing thermo-reversible chitosan-g-poly(N-isopropylacrylamide) (CPN), which was further grafted with hyaluronic acid (HA) to form hyaluronic acid-g-CPN (HA-CPN). PNIPAM-COOH, CPN and HA-CPN formed injectable free-flowing aqueous solutions and exhibited reversible sol-to-gel phase transition (above 5% polymer concentration) at 30 degrees C. Chemical properties and temperature-dependent physical properties of the polymer hydrogels, such as rheological behavior, phase transition kinetics, and water content were characterized in detail. The mechanical stiffness of hydrogels increased with the presence of chitosan in the copolymer, but decreased after conjugation with HA. Chitosan and HA grafting also endowed higher water content and resistance to volume contraction during phase change of the copolymer solution. In vitro cell culture experiments with chondrocytes and meniscus cells in HA-CPN hydrogel showed beneficial effects on the cell phenotypic morphology, proliferation, and differentiation. Progressive tissue formation was demonstrated by monotonic increases in extracellular matrix contents and mechanical properties. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:107 / 116
页数:10
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