Shields Kelly J, Beckman Matthew J, Bowlin Gary L, Wayne Jennifer S
Orthopedic Research Laboratory, Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia 23298-0694, USA.
Tissue Eng. 2004 Sep-Oct;10(9-10):1510-7. doi: 10.1089/ten.2004.10.1510.
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 crosslinked/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 microm. 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.
当前方法的不足使得需要一种合适的关节软骨修复和置换技术。静电纺丝通过制备纤维直径在天然细胞外基质范围内的支架,在软骨修复方面具有潜力。接种到这种支架上的软骨细胞可能更喜欢这种环境来进行分化和增殖,从而接近功能性软骨替代组织。通过静电纺丝技术制备了II型胶原蛋白支架。制备了单个支架样本,并对其进行未交联、交联或交联/接种评估。未交联支架的最小纤维直径和平均纤维直径分别为70纳米和496纳米,而交联支架的直径为140纳米和1.46微米。未交联支架的平均厚度为0.20±0.02毫米,交联支架的平均厚度为0.52±0.07毫米。未交联支架的单轴拉伸试验显示平均切线模量、极限拉伸强度和极限应变为172.5±36.1兆帕、3.3±0.3兆帕和0.026±0.005毫米/毫米。用软骨细胞培养的交联支架的扫描电子显微镜显示细胞能够渗透到支架表面和内部。静电纺丝II型胶原蛋白支架为软骨细胞生长提供了合适的环境,这可能为关节软骨修复的发展奠定基础。