Mechanical properties and cellular proliferation of electrospun collagen type II

被引:159
作者
Shields, KJ
Beckman, MJ
Bowlin, GL
Wayne, JS
机构
[1] Virginia Commonwealth Univ, Dept Biomed Engn, Orthoped Res Lab, Richmond, VA 23298 USA
[2] Virginia Commonwealth Univ, Dept Biochem, Orthoped Res Lab, Richmond, VA 23298 USA
[3] Virginia Commonwealth Univ, Dept Orthoped Surg, Orthoped Res Lab, Richmond, VA 23298 USA
[4] Virginia Commonwealth Univ, Dept Biomed Engn, Tissue & Cellular Engn Lab, Richmond, VA 23298 USA
来源
TISSUE ENGINEERING | 2004年 / 10卷 / 9-10期
关键词
D O I
10.1089/1076327042500373
中图分类号
Q813 [细胞工程];
学科分类号
摘要
A suitable technique for articular cartilage repair and replacement is necessitated by inadequacies of current methods. Electrospinning has potential in cartilage repair by producing scaffolds with fiber diameters in the range of native extracellular matrix. Chondrocytes seeded onto such scaffolds may prefer this environment for differentiation and proliferation, thus approaching functional cartilage replacement tissue. Scaffolds of collagen type II were created by an electrospinning technique. Individual scaffold specimens were prepared and evaluated as uncross-linked, cross-linked, or cross-linked/seeded. Uncross-linked scaffolds contained a minimum and average fiber diameter of 70 and 496 nm, respectively, whereas cross-linked scaffolds possessed diameters of 140 nm and 1.46 mum. The average thickness for uncross-linked scaffolds was 0.20+/-0.02 mm and 0.52+/-0.07 mm for cross-linked scaffolds. Uniaxial tensile tests of uncross-linked scaffolds revealed an average tangent modulus, ultimate tensile strength, and ultimate strain of 172.5+/-36.1 MPa, 3.3+/-0.3 MPa, and 0.026+/-0.005 mm/mm, respectively. Scanning electron microscopy of cross-linked scaffolds cultured with chondrocytes demonstrated the ability of the cells to infiltrate the scaffold surface and interior. Electrospun collagen type II scaffolds produce a suitable environment for chondrocyte growth, which potentially establishes the foundation for the development of articular cartilage repair.
引用
收藏
页码:1510 / 1517
页数:8
相关论文
共 51 条
[1]   VARIATIONS IN THE INTRINSIC MECHANICAL PROTERTIES OF HUMAN ARTICULAR-CARTILAGE WITH AGE, DEGENERATION, AND WATER-CONTENT [J].
ARMSTRONG, CG ;
MOW, VC .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1982, 64 (01) :88-94
[2]  
Baker TL, 1997, IN VITRO CELL DEV-AN, V33, P358
[3]  
BELL M, DYNAMICS STEADY TAYL
[4]  
BELL M, 1998, TAYLOR CONES ELECTRO
[5]   HOW DOES THE EXTRACELLULAR-MATRIX DIRECT GENE-EXPRESSION [J].
BISSELL, MJ ;
HALL, HG ;
PARRY, G .
JOURNAL OF THEORETICAL BIOLOGY, 1982, 99 (01) :31-68
[6]   Tailoring tissue engineering scaffolds using electrostatic processing techniques: A study of poly(glycolic acid) electrospinning [J].
Boland, ED ;
Wnek, GE ;
Simpson, DG ;
Pawlowski, KJ ;
Bowlin, GL .
JOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY, 2001, 38 (12) :1231-1243
[7]   Processing and microstructural characterization of porous biocompatible protein polymer thin films [J].
Buchko, CJ ;
Chen, LC ;
Shen, Y ;
Martin, DC .
POLYMER, 1999, 40 (26) :7397-7407
[8]   Articular cartilage .2. Degeneration and osteoarthrosis, repair, regeneration, and transplantation [J].
Buckwalter, JA ;
Mankin, HJ .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1997, 79A (04) :612-632
[9]  
Burg KJL, 2000, J BIOMED MATER RES, V52, P576, DOI 10.1002/1097-4636(20001205)52:3<576::AID-JBM18>3.0.CO
[10]  
2-C