QI Bo, LIU Qingfang. Evaluation of biocompatibility of a coronary artery stents sterilized by use of irradiation[J]. Journal of Radiation Research and Radiation Processing, 2007,25(5):283-288.
QI Bo, LIU Qingfang. Evaluation of biocompatibility of a coronary artery stents sterilized by use of irradiation[J]. Journal of Radiation Research and Radiation Processing, 2007,25(5):283-288.DOI:
评价聚酯聚乙烯复合膜/聚乙烯(冠状动脉支架系统)经辐射灭菌后的生物相容性,展望并促进辐射灭菌在高分子生物材料灭菌应用的可行性。按照国际标准化组织(International organization for standardization,ISO)111737 标准进行聚酯聚乙烯复合膜/聚乙烯(冠状动脉支架系统)初始污染菌检测,并依据ISO11137标准方法完成了辐照灭菌的剂量设定。设定初始污染菌数为332.49cfu/件,验证剂量为9.53kGy(SAL10,-2,),最低灭菌剂量为23.1kGy(SAL10,-6,),对经最低灭菌剂量辐照灭菌合格后的产品进行,包括人血细胞染色体遗传毒性试验、细胞毒性试验、致敏试验、皮内刺激试验、血液相容性试验等生物相容性评价。辐照灭菌后的聚酯聚乙烯复合膜/聚乙烯(冠状动脉支架系统)材料无细胞毒性、无遗传毒性(不会引起染色体畸变),不会致敏和引致皮内刺激,血液相容性良好,产品的包装材料材质和性能未改变。经设定剂量辐照灭菌后的聚酯聚乙烯复合膜/聚乙烯(冠状动脉支架系统)生物相容性好,辐照灭菌作为医用高分子生物材料灭菌方法值得推广应用。
Abstract
Based on ISO11137 and ISO10993, bio-burden of the coronary artery stents and the sterilizing dose were determined. Results indicted that when the average bio-burden was 332.49cfu per device, verification dose was 9.5292kGy (SAL10,-2,) the minimum sterilizing dose was determined to be 23.1kGy (SAL10,-6,). The irradiated samples were inspected their biocompatibility by the cytotoxicity test, sensitization test, local reactions of muscle embedding test, chromosome aberration test of human blood cell in vitro, haemolysis test. It was showed that the coronary artery stents sterilized by irradiation have no cytoxicity, no sensitivity, no mutagencity in chromosome aberration test and no haemolysis. Furthermore, the package kept sterile and no leakage was found. The good biocompatibility of coronary artery stents sterilized by irradiation can be used for further clinic application.