In vitro analyses of diamond-like carbon coated stents: Reduction of metal ion release, platelet activation, and thrombogenicity

被引:216
作者
Gutensohn, K
Beythien, C
Bau, J
Fenner, T
Grewe, P
Koester, R
Padmanaban, K
Kuehnl, P
机构
[1] Univ Hamburg, Univ Hosp Eppendorf, Dept Transfus Med & Transplantat Immunol, D-20246 Hamburg, Germany
[2] Univ Hosp Eppendorf, Dept Cardiol, D-20246 Hamburg, Germany
[3] Univ Hosp Bochum, Dept Cardiol, Bochum, Germany
[4] Fenner Labs, Hamburg, Germany
关键词
intracoronary stents; biocompatability; DLC;
D O I
10.1016/S0049-3848(00)00295-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Coronary artery stents can induce platelet activation by shear forces, contact to the biomaterial, and release of metal ions. This activation is one important trigger for thrombosis. Coating of stents is a possible approach to prevent this side effect. The purpose of this study was to evaluate in vitro the biocompatibility of stents coated with diamondlike carbon (DLC). Semiquantitative energy-dispersive X-ray microanalyses showed a complete coverage of the DLC stents. Flow cytometric analyses revealed a significantly higher increase of mean channel fluorescence intensity for the activation-dependent antigens CD62p and CD63 in non-coated compared to DLC-coated stents (p<0.05). Atomic adsorption spectrophotometry analyses revealed a significant release of nickel and chromium metal ions by non-coated stents over a storage period of 96 hours in human plasma (p<0.05). In contrast, only minimal concentrations of released ions could be detected in the case of DLC-coated stents. Similar observations were made with inductively coupled plasma mass spectrometry analyses. Here, high concentrations of molybdenum and manganese ions were released from non-coated stents (p<0.05), while release of these ions from DLC-coated stents was virtually undetectable (p=0.1 for molybdenum and p=0.4 for manganese). Coating of intracoronary stents with diamond-like carbon significantly improves biocompatibility. This biocompatible coating may therefore contribute to a reduction in thrombogenicity. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:577 / 585
页数:9
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