Rational development of GAG-augmented chitosan membranes by fractional factorial design methodology

被引:28
作者
Chen, YL
Chen, HC
Lee, HP
Chan, HY
Hu, YC [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Chem Engn, Hsinchu 300, Taiwan
[2] Food Ind Res & Dev Inst, Hsinchu 300, Taiwan
关键词
chondrocyte; chitosan; chondroitin sulfate; fractional factorial design; glycosaminoglycan; heparin;
D O I
10.1016/j.biomaterials.2005.10.029
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
To develop a novel biomaterial for chondrocyte culture, 8 glycosaminoglycan (GAG)/chitosan membranes (groups N1 N8) were prepared, with the aid of a 2-level 2(4-1) fractional factorial design, by co-immobilizing chondroitin-4-sulfate (CSA), chondroitin-6-sulfate (CSC), dermatan sulfate (DS), and heparin to chitosan membranes. The fractional factorial design allowed its to partly interpret the effects of individual GAGS and two-way interactions between GAGS. Within the level range of -1 and +1, low CSA level (2.6 mg) is favorable for collagen synthesis but not for cell proliferation. High CSC level (1.3 mg) is favorable for GAG production but not for cell proliferation. Conversely. high heparin (0.33 mg) and DS (0.13 mg) levels are desired for cell proliferation but not for the production of collagen and GAG. Moreover. the two-way interactions between GAGS influence the cell behavior. Among the 8 GAG/chitosan membranes, N1 and N4 (containing low CSA and heparin levels) lead to the maintenance of proper chondrocyte phenotype, as judged by the chondrocyte-like morphology, modest cell expansion, higher GAG and collagen production and proper cartilage marker gene expression. In conclusion, this approach provides a means of rationally predicting and evaluating the proper formulation of GAG/chitosan membranes and may facilitate the rational design of other tissue engineering scaffolds. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2222 / 2232
页数:11
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