Surface engineering of stainless steel materials by covalent collagen immobilization to improve implant biocompatibility

被引:107
作者
Müller, R
Abke, J
Schnell, E
Macionczyk, F
Gbureck, U
Mehrl, R
Ruszczak, Z
Kujat, R
Englert, C
Nerlich, M
Angele, P
机构
[1] Univ Regensburg, Inst Phys & Theoret Chem, D-93053 Regensburg, Germany
[2] Univ Wurzburg, Dept Funct Mat Med & Dent, D-97070 Wurzburg, Germany
[3] Innocoll Innovat Collagen Prod, D-93342 Saal An Der Donau, Germany
[4] Univ Hosp Regensburg, Dept Trauma Surg, D-93053 Regensburg, Germany
关键词
surface modification; steel; tantalum; collagen; coupling agents; cross-linking; mesenchymal stem cells;
D O I
10.1016/j.biomaterials.2005.05.013
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
It was shown recently that the deposition of thin films of tantalum and tantalum oxide enhanced the long-term biocompatibility of stainless steel biomaterials due to an increase in their corrosion resistance. In this study, we used this tantalum oxide coating as a basis for covalent immobilization of a collagen layer, which should result in a further improvement of implant tissue integration. Because of the high degradation rate of natural collagen in vivo, covalent immobilization as well as carbodiimide induced cross-linking of the protein was performed. It was found that the combination of the silane-coupling agent aminopropyl triethoxysilane and the linker molecule N,N'-disulphosuccinimidyl suberate was a very effective system for collagen immobilizing. Mechanical and enzymatic stability testing revealed a higher stability of covalent bound collagen layers compared to physically adsorbed collagen layers. The biological response induced by the surface modifications was evaluated by in vitro cell culture with human mesenchymal stem cells as well as by in vivo subcutaneous implantation into nude mice. The presence of collagen clearly improved the cytocompatibility of the stainless steel implants which, nevertheless, significantly depended on the cross-linking degree of the collagen layer. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6962 / 6972
页数:11
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