Biomaterials and Modifications in the Development of Small-Diameter Vascular Grafts

被引:91
作者
Hiob, Matti A. [1 ,2 ]
She, Shelley [1 ,2 ]
Muiznieks, Lisa D. [3 ]
Weiss, Anthony S. [1 ,2 ,4 ]
机构
[1] Univ Sydney, Sch Life & Environm Sci, Sydney, NSW 2006, Australia
[2] Univ Sydney, Charles Perkins Ctr, Sydney, NSW 2006, Australia
[3] Hosp Sick Children, Res Inst, Mol Struct & Funct Program, 555 Univ Ave, Toronto, ON M5G 1X8, Canada
[4] Univ Sydney, Bosch Inst, Sydney, NSW 2006, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
blood vessel; bypass; coronary artery; endothelialization; extracellular matrix; peripheral artery; ENGINEERED BLOOD-VESSELS; EXPANDED POLYTETRAFLUOROETHYLENE GRAFTS; PERCUTANEOUS CORONARY INTERVENTION; LONG-TERM PERFORMANCE; IN-VITRO EVALUATION; ENDOTHELIAL-CELLS; SAPHENOUS-VEIN; BYPASS GRAFTS; HEALING CHARACTERISTICS; MECHANICAL-PROPERTIES;
D O I
10.1021/acsbiomaterials.6b00220
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
There remains a significant clinical need for an alternative to autologous vein grafts in small-diameter applications such as coronary bypass, but no clinically viable, synthetic small-diameter vascular grafts have been developed. While ePTFE and Dacron have long been used for large diameter grafts, it is likely that in small-diameter, low flow conditions, alternative materials and techniques are required, which have shown promising experimental results through enhancing compliance, biocompatibility, and endothelialization of vascular grafts. It is likely that the integration of synthetic materials that possess optimized mechanical properties combined with techniques for improved biocompatibility, such as the use of pure extracellular matrix proteins, will be the impetus for the creation of a new generation of clinically viable, small diameter vascular substitutes.
引用
收藏
页码:712 / 723
页数:12
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