Poly(vinyl alcohol) hydrogel as a biocompatible viscoelastic mimetic for articular cartilage

被引:64
作者
Grant, Colin
Twigg, Pete [1 ]
Egan, Alex
Moody, Alexandra
Smith, Annie
Eagland, Donald
Crowther, Nicholas
Britland, Steve
机构
[1] Univ Bradford, Med Engn Grp, Sch Engn Design & Technol, Bradford BD7 1DP, W Yorkshire, England
[2] Univ Bradford, Sch Pharm, Bradford BD7 1DP, W Yorkshire, England
[3] AGT Sci, Unit 25, Bradford BD7 1HR, W Yorkshire, England
关键词
D O I
10.1021/bp060181u
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
The prevalence of suboptimal outcome for surgical interventions in the treatment of full-thickness articular cartilage damage suggests that there is scope for a materials-based strategy to deliver a more durable repair. Given that the superficial layer of articular cartilage creates and sustains the tribological function of synovial joints, it is logical that candidate materials should have surface viscoelastic properties that mimic native articular cartilage. The present paper describes force spectroscopy analysis by nano-indentation to measure the elastic modulus of the surface of a novel poly(vinyl alcohol) hydrogel with therapeutic potential as a joint implant. More than 1 order of magnitude decrease in the elastic modulus was detected after adsorption of a hyaluronic acid layer onto the hydrogel, bringing it very close to previously reported values for articular cartilage. Covalent derivatization of the hydrogel surface with fibronectin facilitated the adhesion and growth of cultured rat tibial condyle chondrocytes as evidenced morphologically and by the observance of metachromatic staining with toluidine blue dye. The present results indicate that hydrogel materials with potential therapeutic benefit for injured and diseased joints can be engineered with surfaces with biomechanical properties similar to those of native tissue and are accepted as such by their constituent cell type.
引用
收藏
页码:1400 / 1406
页数:7
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