Synthesis and characterization of novel thermoresponsive-co-biodegradable hydrogels composed of N-isopropylacrylamide, poly(L-lactic acid), and dextran

被引:16
作者
Xiao, H
Nayak, BR
Lowe, TL [1 ]
机构
[1] Penn State Univ, Dept Surg, Hershey, PA 17033 USA
[2] Penn State Univ, Dept Bioengn, Hershey, PA 17033 USA
[3] Penn State Univ, Dept Mat Sci & Engn, Hershey, PA 17033 USA
关键词
hydrogels; thermoresponsive; biodegradable; LCST; N-isopropylacrylamide; poly(L-lactic acid); dextran; dynamic swelling; drug delivery; tissue engineering;
D O I
10.1002/pola.20327
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of novel multifunctional hydrogels that combined the merits of both thermoresponsive and biodegradable polymeric materials were designed, synthesized, and characterized. The hydrogels were copolymeric networks composed of Nisopropylacrylamide (NIPAAM) as a thermoresponsive component, poly(L-lactic acid) (PLLA) as a hydrolytically degradable and hydrophobic component, and dextran as an enzymatically degradable and hydrophilic component. The chemical structures of the hydrogels were characterized by an attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR) technique. The hydrogels were thermoresponsive, showing a lower critical solution temperature (LCST) at approximately 32 degreesC, and their swelling properties strongly depended on temperature changes, the balance of the hydrophilic/hydrophobic components, and the degradation of the PLLA component. The degradation of the hydrogels caused by hydrolytic cleavage of ester bonds in the PLLA component was faster at 25 degreesC below the LCST than at 37 degreesC above the LCST, determined by the ATR-FTIR technique. Due to their multifunctional properties, the designed hydrogels show great potential for biomedical applications, including drug delivery and tissue engineering. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:5054 / 5066
页数:13
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