Evaluation of cellular affinity and compatibility to biodegradable polyesters and type-II collagen-modified scaffolds using immortalized rat chondrocytes

被引:36
作者
Hsu, SH
Tsai, CL [1 ]
Tang, CM
机构
[1] Natl Taiwan Univ, Dept Orthoped, Coll Med, Taipei 10764, Taiwan
[2] Natl Chung Hsing Univ, Dept Chem Engn, Taichung 40227, Taiwan
关键词
biodegradable polyester scaffolds; cartilage tissue engineering; chondrocyte seeding; tissue engineering;
D O I
10.1046/j.1525-1594.2002.06889.x
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Immortalized rat chondrocytes (IRCs) were employed to evaluate the cytocompatibility of different biodegradable polyester scaffolds for chondrocyte seeding and cartilage tissue engineering in vitro due to the limitation of using freshly harvested chondroctyes. Cells were seeded onto the films and the porous substrates as well as into the three-dimensional scaffolds made of the biodegradable polyesters including poly(L-lactide) (PLLA) and two poly(lactide-co-glycolide)s (PLGAs). The materials were characterized by water contact angle, electron spectroscopy for chemical analysis (ESCA), and microscopy. PLGA50/50, one of the PLGAs, had the largest cell numbers at 24 h and 96 h (close to the tissue culture polystyrene control), possibly due to its lower contact angle, higher oxygen/carbon (O/C) atomic ratio, and larger degradation rate. When the surface was further modified by cross-linked Type-II collagen, cell population was significantly enhanced (two- to fourfold). The adhesion and proliferation behavior of IRCs on different materials was parallel to that of rabbit chondrocytes, but was more reproducible in general. IRCs are thus suitable for evaluation of different polymer scaffolds. Despite the favorable cytocompatibility of PLGA50/50, blending with a small portion of PLLA is required for easy fabrication and collagen modification. Scaffolds made of blended materials by freeze-drying procedure with the surface modified by cross-linked Type-II collagen were demonstrated as the ideal templates for chondrocyte seeding in our study.
引用
收藏
页码:647 / 658
页数:12
相关论文
共 54 条
[41]  
Sittinger M, 1996, J BIOMED MATER RES, V33, P57, DOI 10.1002/(SICI)1097-4636(199622)33:2<57::AID-JBM1>3.0.CO
[42]  
2-K
[43]   Microfracture: Surgical technique and rehabilitation to treat chondral defects [J].
Steadman, JR ;
Rodkey, WG ;
Rodrigo, JJ .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2001, (391) :S362-S369
[44]   Review: tissue engineering for regeneration of articular cartilage [J].
Temenoff, JS ;
Mikos, AG .
BIOMATERIALS, 2000, 21 (05) :431-440
[45]  
Thomson RC, 1995, ADV POLYM SCI, V122, P245
[46]  
Toolan BC, 1996, J BIOMED MATER RES, V31, P273, DOI 10.1002/(SICI)1097-4636(199606)31:2<273::AID-JBM15>3.0.CO
[47]  
2-M
[48]  
Toolan BC, 1998, J BIOMED MATER RES, V41, P244, DOI 10.1002/(SICI)1097-4636(199808)41:2<244::AID-JBM9>3.0.CO
[49]  
2-I
[50]   Effect of different solvents and crosslinkers on cytocompatibility of Type II collagen scaffolds for chondrocyte seeding [J].
Tsai, CL ;
Hsu, SH ;
Cheng, WL .
ARTIFICIAL ORGANS, 2002, 26 (01) :18-26