TiO2-coated CoCrMo: Improving the osteogenic differentiation and adhesion of mesenchymal stem cells in vitro

被引:24
|
作者
Logan, Niall [1 ]
Sherif, Anas [1 ]
Cross, Alison J. [2 ]
Collins, Simon N. [3 ]
Traynor, Alison [3 ]
Bozec, Laurent [1 ]
Parkin, Ivan P. [2 ]
Brett, Peter [1 ]
机构
[1] UCL, Eastman Dent Inst, London WC1X 8LD, England
[2] UCL, Dept Chem, London WC1H 0AJ, England
[3] Corin Ltd, Cirencester GL7 1YJ, Glos, England
基金
英国工程与自然科学研究理事会;
关键词
osteogenesis; titanium oxide; cobalt alloy; AFM; mesenchymal stem cells; MECHANICAL-PROPERTIES; OSTEOBLAST ADHESION; SURFACE-TOPOGRAPHY; MATRIX COMPONENTS; TIO2; NANOTUBES; TITANIUM; CYTOSKELETAL; OSSEOINTEGRATION; COATINGS; SCIENCE;
D O I
10.1002/jbm.a.35264
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The current gold standard material for orthopedic applications is titanium (Ti), however, other materials such as cobalt-chromium-molybdenum (CoCrMo) are often preferred due to their wear resistance and mechanical strength. This study investigates if the bioactivity of CoCrMo can be enhanced by coating the surface with titanium oxide (TiO2) by atmospheric pressure chemical vapor deposition (CVD), thereby replicating the surface oxide layer found on Ti. CoCrMo, TiO2-coated CoCrMo (CCMT) and Ti substrates were used for this study. Cellular f-actin distribution was shown to be noticeably different between cells on CCMT and CoCrMo after 24 h in osteogenic culture, with cells on CCMT exhibiting greater spread with developed protrusions. Osteogenic differentiation was shown to be enhanced on CCMT compared to CoCrMo, with increased calcium ion content per cell (p<0.05), greater hydroxyapatite nodule formation (p<0.05) and reduced type I collagen deposition per cell (p<0.05). The expression of the focal adhesion protein vinculin was shown to be marginally greater on CCMT compared to CoCrMo, whereas AFM results indicated that CCMT required more force to remove a single cell from the substrate surface compared to CoCrMo (p<0.0001). These data suggest that CVD TiO2 coatings may have the potential to increase the biocompatibility of CoCrMo implantable devices. (c) 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 1208-1217, 2015.
引用
收藏
页码:1208 / 1217
页数:10
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