Biostability of polyurethanes.

E Hennig, A John, F Zartnack, W Lemm, E S Bücherl, G Wick, K Gerlach
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Abstract

Aside from the medical requirements a material has to fulfill to qualify as biocompatible, for the bioengineer, who is involved in the design, construction and fabrication of prosthetic devices, the mechanical, physical and chemical properties of the material as well as its possible manufacturing procedures and, last but not least, its biostability are of the same importance. In the very aggressive biological environment, the material should behave inertly, showing no surface erosions, molecular chain disruptions, uptake of low molecular weight biological materials, local chemical imbalances, tendency to calcification or negative changes of mechanical properties. With regard to this aspect, different polyurethanes have been evaluated in-vitro and in-vivo as basic materials and already fabricated devices (blood pumps and heart valves). The comparison of the results stresses the necessity of further efforts to achieve a standardized test protocol for the prove of the biostability of polymers, containing appropriate, well-defined in-vitro and in-vivo test methods to establish the necessary data basa for the materials' clinical approval.

聚氨酯的生物稳定性。
除了医学要求外,材料必须满足生物相容性的要求,对于参与假肢装置的设计、建造和制造的生物工程师来说,材料的机械、物理和化学特性以及可能的制造程序,最后但并非最不重要的是,它的生物稳定性也同样重要。在极具侵略性的生物环境中,材料的行为应该是惰性的,没有表面侵蚀、分子链断裂、低分子量生物材料的吸收、局部化学失衡、钙化倾向或机械性能的负面变化。关于这方面,不同的聚氨酯已经在体外和体内作为基本材料和已经制造的设备(血泵和心脏瓣膜)进行了评估。结果的比较强调了进一步努力实现标准化测试方案的必要性,以证明聚合物的生物稳定性,包含适当的,定义明确的体外和体内测试方法,为材料的临床批准建立必要的数据基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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