Development and evaluation of a novel decellularized vascular xenograft

被引:216
作者
Conklin, BS
Richter, ER
Kreutziger, KL
Zhong, DS
Chen, C
机构
[1] Emory Univ, Sch Med, Dept Surg, Atlanta, GA 30322 USA
[2] Georgia Inst Technol, Sch Mech Engn, Atlanta, GA 30332 USA
[3] Univ Rochester, Dept Biomed Engn, Rochester, NY 14627 USA
关键词
vascular graft; xenograft; decellularized; heparin; compliance;
D O I
10.1016/S1350-4533(02)00010-3
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Although autogenous saphenous vein remains the standard for coronary and infrapopliteal bypass, many patients do not have a suitable vein. Attempts at developing a small-caliber vascular graft have failed largely due to occlusion, neointimal hyperplasia, or aneurismal degradation. We have designed and characterized a novel small-caliber vascular xenograft that may overcome these failure modes. To reduce immune reactions, porcine common carotid arteries were decellularized by enzymatic and detergent treatments. Histology and electron microscopic examination showed complete removal of cellular components while the extracellular matrix structure remained intact. To reduce thrombogeneity, decellularized vascular grafts were covalently linked with heparin. The efficiency of heparin linkage was demonstrated with toluidine blue staining and the antithrombogeneity of the heparin-treated grafts was demonstrated with a clot time test. Mechanical testing of the graft was performed. Decellularized-heparin-treated grafts were similar in compliance to fresh vessels and burst testing showed grafts to withstand pressures exceeding 10 times physiologic blood pressure. There was no difference in suture retention strength between fresh vessels and decellularized-heparin-treated grafts. Decellularized, heparinized grafts were implanted in dogs as carotid artery bypass grafts and showed smooth muscle cells densely populating the wall, and endothelial cells lining the lumen by two months. This study provides a new strategy to develop a small-caliber vascular graft with excellent mechanical properties, antithrombogeneity, and tissue compatibility. (C) 2002 IPEM. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:173 / 183
页数:11
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