期刊文献+

生物可降解材料聚乳酸在血管支架制备中的应用 被引量:5

Application of biodegradable poly L-lactic acid in the preparation of vascular stents
在线阅读 下载PDF
导出
摘要 第二代药物洗脱支架作为异物,对血管壁有长期炎症反应,这是导致支架术后远期血栓形成和支架内再狭窄的重要诱因。而生物可降解支架能克服这一缺陷。目前,生物可降解支架材料选择分为高分子聚合物材料和合金材料。在可降解高分子材料中,聚乳酸和其改性共聚物备受关注。聚乳酸是一种具有良好生物相容性和可降解性能的高分子材料,在血管支架的制备中具有广泛运用。聚乳酸既是一种很优秀的支架药物涂层的载体,也可以被开发作为支架骨架结构。 The second-generation drug-eluting stents, as foreign bodies, have long-term inflammatory response to the vessel wall, which is an important cause of long-term thrombosis and in-stent restenosis after stenting. Biodegradable stents can overcome this drawback. At present, the biodegradable scaffold material is divided into polymer materials and alloy materials. Among biodegradable polymers, polylactic acid and its modified copolymers attract much attention. Polylactic acid is a kind of polymer material with good biocompatibility and biodegradability. It is widely used in the preparation of vascular stents. Polylactic acid is both a good carrier for stent drug coatings and can also be developed as a scaffold framework.
作者 朱月琳 汤文浩 胡双龙 赵杰 周敏 李晓强 ZhuYuelin1, Tang Wenhao1, Zhou Min2 ,Hu Shuanglong2, Zhao Jie2(1 School of Medicine, Southeast University, Nanjing 210009, China; 2 Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing 210008, Chin)
出处 《血管与腔内血管外科杂志》 2017年第5期968-971,976,共5页 Journal of Vascular and Endovascular Surgery
关键词 生物可降解 聚乳酸 血管支架 biodegradable polylactic acid vascular stent.
  • 相关文献

参考文献3

二级参考文献38

  • 1陈丹,吕安林,苑媛,李丹.药物涂层支架研究进展[J].心脏杂志,2006,18(5):591-594. 被引量:9
  • 2涂兵,贺红,杨发林,刘贤锡,苏继新.阿司匹林对血管平滑肌细胞增殖及增殖细胞核抗原表达的影响[J].中国动脉硬化杂志,2007,15(5):358-360. 被引量:3
  • 3DEGERTEKIN M, SERRUYS P W, FOLEY D P, et al. Persistent inhibition of neointimal hyperplasia after sirolimus- eluting stent implantation: long-term (up to 2 years) clinical, angiographic, and intravascular ultrasound follow-up [J]. Circulation, 2002, 106(13): 1610-1613.
  • 4BABAPULLE M N, JOSEPH L, BELISLE P, et al. A hierarchical Bayesian meta-analysis of randomised clinical trials of drug-eluting stents[J]. Lancet, 2004, 364(9434): 583-591.
  • 5SILBER S, ALBERTSSON P, AVILES F F, et al. Guidelines for percutaneous coronary interventions. The Task Force for Percutaneous Coronary Interventions of the European Society of Cardiology[J]. Eur Heart J, 2005, 26(8): 804-847.
  • 6REIMERS B, MOUSSA I, AKIYAMA T, et al. Long-term clinical follow-up after successful repeat percutaneous intervention for stent restenosis[J]. J Am Coll Cardiol, 1997, 30(1): 186-192.
  • 7SCHOFER J, SCHLUTER M, GERSHLICK A H, et al. Sirolimus eluting stents for treatment of patients with long atherosclerotic lesions in small coronary arteries: double-blind, randomised controlled trial (E-SIRIUS)[J]. Lancet, 2003, 362(9390): 1093-1099.
  • 8SCHAMPAERT E, COHEN E A, SCHLUTER M, et al. The Canadian study of the sirolimus-eluting stent in the treatment of patients with long de novo lesions in small native coronary arteries (C-SIRIUS)[J]. J Am Coll Cardiol, 2004, 43(6) : 1110-1115.
  • 9LIM S Y, JEONG M H, HONG S J, et al. Inflammation and delayed endothelization with overlapping drug-eluting stents in a porcine model of in-stent restenosis[J]. Cire J, 2008, 72 (3) : 463-468.
  • 10JONER M, FINN A V, FARB A, et al. Pathology of drugeluting stents in humans: delayed healing and late thrombotic risk[J]. J Am Coll Cardiol, 2006, 48(1): 193-202.

共引文献2

同被引文献33

引证文献5

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部