Bioactive immobilization of r-hirudin on CVD-coated metallic implant devices

被引:114
作者
Lahann, J [1 ]
Klee, D [1 ]
Pluester, W [1 ]
Hoecker, H [1 ]
机构
[1] Rhein Westfal TH Aachen, Dept Macromol & Text Chem, D-52062 Aachen, Germany
关键词
stent; restenosis; hirudin; biomimetics; chemical vapor deposition; immobilization;
D O I
10.1016/S0142-9612(00)00244-1
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The poor biocompatibility of metallic coronary stents which leads to un-satisfying restenosis rates is mainly caused by contact activation of blood cells, smooth muscle cells and endothelial cells. Mimicking a metal surface with a biocompatible coating that actively suppresses mechanisms leading to restenosis may overcome today's limitations regarding the complications of metal stents. Nitinol coronary stents were coated by CVD polymerization of functionalized [2.2]paracyclophanes. The monomers 4-amino [2.2]paracyclophane, 4-hydroxy methyl [2.2]paracyclophane and [2.2]paracyclophane-4,5,12,13-tetracarboxylic acid dianhydride were previously synthesized. A suitable installation for the CVD polymerization procedure was designed and used for the polymerization procedures. Physical and chemical properties of the polymers were shown to fulfill the requirements regarding the application as a stent coating material. The functional groups of the polymer coatings were used for the immobilization of the thrombin inhibitor r-hirudin. In vitro results indicate that the bioactively coated stents are less thrombogenic than virgin metallic stents. Surface-bound r-hirudin decreases platelet adhesion drastically due to interactions between platelets and r-hirudin. (C) 2001 Published by Elsevier Science Ltd.
引用
收藏
页码:817 / 826
页数:10
相关论文
共 29 条
[2]   THE FUNCTIONAL DOMAIN OF HIRUDIN, A THROMBIN-SPECIFIC INHIBITOR [J].
CHANG, JY .
FEBS LETTERS, 1983, 164 (02) :307-313
[3]  
DEPALMA VA, 1972, J BIOMED MATER RES S, V3, P37
[4]   BIOCOMPATIBILITY OF POLYMER-COATED OVERSIZED METALLIC STENTS IMPLANTED IN NORMAL PORCINE CORONARY-ARTERIES [J].
DESCHEERDER, IK ;
WILCZEK, KL ;
VERBEKEN, EV ;
VANDORPE, J ;
LAN, PN ;
SCHACHT, E ;
DEGEEST, H ;
PIESSENS, J .
ATHEROSCLEROSIS, 1995, 114 (01) :105-114
[5]   THE COMPLETE AMINO-ACID-SEQUENCE OF HIRUDIN, A THROMBIN SPECIFIC INHIBITOR - APPLICATION OF COLOR CARBOXYMETHYLATION [J].
DODT, J ;
MULLER, HP ;
SEEMULLER, U ;
CHANG, JY .
FEBS LETTERS, 1984, 165 (02) :180-184
[6]  
DODT J, 1995, ANGEW CHEM, V107, P867
[7]  
FAIRBROTHER F, 1924, J CHEM SOC, P2319
[8]  
FENTON JW, 1992, SEMIN THROMBOSIS HAE, V18, P193
[9]   A RANDOMIZED COMPARISON OF CORONARY-STENT PLACEMENT AND BALLOON ANGIOPLASTY IN THE TREATMENT OF CORONARY-ARTERY DISEASE [J].
FISCHMAN, DL ;
LEON, MB ;
BAIM, DS ;
SCHATZ, RA ;
SAVAGE, MP ;
PENN, I ;
DETRE, K ;
VELTRI, L ;
RICCI, D ;
NOBUYOSHI, M ;
CLEMAN, M ;
HEUSER, R ;
ALMOND, D ;
TEIRSTEIN, PS ;
FISH, RD ;
COLOMBO, A ;
BRINKER, J ;
MOSES, J ;
SHAKNOVICH, A ;
HIRSHFELD, J ;
BAILEY, S ;
ELLIS, S ;
RAKE, R ;
GOLDBERG, S .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (08) :496-501
[10]  
Kim SW, 1996, BLOOD PURIFICAT, V14, P357