摘要
目的:检测一种新型的血管内速溶支架的生物相容性。方法:分别对血管内速溶支架进行细胞毒性实验和皮下植入实验。细胞毒性实验:速溶支架粉末与L929细胞接触培养,倒置显微镜观察形态,采用MTT(四唑盐)比色法量化细胞毒性,并进行毒性分级。皮下植入实验:在12只新西兰白兔右侧背部皮下植入血管内速溶支架,左侧作为空白对照,分别于植于支架后3、7、14、28 d,肉眼和镜下观察植入点炎症反应情况。结果:血管内速溶支架细胞毒性为0级。皮下植入后无炎症反应,局部组织无刺激。结论:该课题组黏合吻合血管用血管内速溶支架材料满足ISO 10993要求,具有良好的生物相容性。
Objective To test the biocompatibility of a new intravascular quick-dissolving stent.Methods Cytotoxicity and implant experiment were done to the stent separately.Cytotoxicity test:L929 cells were cultured with the stent powder.The cellular morphology was observed by inverted microscopy.The proliferation was examined using MTT method and cytotoxicity grade was evaluated.Implant test:intravascular quick-dissolving stents were implanted in the right back of 12 New Zealand white rabbits,the left as a blank control.The inflammatory reaction was examined by gross and microscopic observation 3,7,14,28 d after the implantation.Results The cytotoxicity grade of the stent powder was 0.Implant test showed intravascular quick-dissolving stents had no stimulation to the local tissue.Conclusion The cytotoxicity test and implant test of the new intravascular quick-dissolving stent accord with the standard of ISO-10993,which shows good biocompatibility.
出处
《医疗卫生装备》
CAS
2012年第5期4-6,共3页
Chinese Medical Equipment Journal
基金
中美国际合作项目(2009DFA31340)
关键词
血管吻合
速溶支架
细胞毒性实验
皮下植入实验
vascular anastomosis
quick-dissolving stent
cytotoxicity test
implant test