Surface grafting of blood compatible zwitterionic poly(ethylene glycol) on diamond-like carbon-coated stent

被引:0
作者
Bong Soo Lee
Hong-Sub Shin
Kwideok Park
Dong Keun Han
机构
[1] Korea Institute of Science and Technology,Biomaterials Center
来源
Journal of Materials Science: Materials in Medicine | 2011年 / 22卷
关键词
Human Serum Albumin; Atom Transfer Radical Polymerization; Atom Transfer Radical Polymerization; TiNi; Fresh Freeze Plasma;
D O I
暂无
中图分类号
学科分类号
摘要
Blood compatibility is the most important aspect for blood-contacting medical devices including cardiovascular stents. In this study, the surface of nickel–titanium (TiNi) stent was coated with diamond-like carbon (DLC) and then subsequently grafted by using zwitterion (N+ and SO3−)-linked poly(ethylene glycol) (PEG). We hypothesize that this coupling of zwitterion and PEG may significantly improve blood compatibility of DLC-coated TiNi stent. The surface modified TiNi stents, including PEG-grafted stent (DLC-PEG) and zwitterionic PEG-grafted one (DLC-PEG-N-S) were the main focus on the tests of surface characteristics and blood compatibility. The zwitterionic PEG derivatives were obtained from a series of chemical reactions at room temperature. The results exhibited that as compared to the DLC-PEG, the hydrophilicity was much better with DLC-PEG-N-S and significantly increased atomic percentage of oxygen and nitrogen proved the entity of zwitterions on the surface of DLC-PEG-N-S. Meanwhile, the adsorption of blood proteins such as, human serum albumin (HSA) and fibrinogen was found considerably down-regulated in DLC-PEG-N-S, due mainly to the protein-repellant effect of PEG and zwitterion. Microscopic observation also revealed that as compared with the other substrates without zwitterion, the degree of platelet adhesion was the lowest with DLC-PEG-N-S. In addition, DLC-PEG-N-S retained an extended blood coagulation time as measured by activated partial thromboplastin time (APTT). The present results suggested that surface grafting of zwitterionic PEG derivatives could substantially enhance the blood compatibility of TiNi-DLC stent. In conclusion, anti-fouling properties of PEG and zwitterions are expected to be very useful in advancing overall stent performance.
引用
收藏
页码:507 / 514
页数:7
相关论文
共 241 条
  • [1] Assali A(1998)Coronary stent deployment without predilation: prevention of complications of venous graft angioplasty Angiology 49 613-617
  • [2] Adler Y(2004)Increased C-reactive protein level after renal stent implantation in patients with atherosclerotic renal stenosis Angiology. 55 479-484
  • [3] Solodky A(2005)Hehrlein C Particle debris from a nanoporous stent coating obscures potential antiproliferative effects of tacrolimus-eluting stents in a porcine model of restenosis.Catheter Cardiovasc Interv. 64 85-90
  • [4] Shor N(2004)Clinical, angiographic, and procedural predictors of angiographic restenosis after sirolimus-eluting stent implantation in complex patients: an evaluation from the rapamycin-eluting stent evaluated at rotterdam cardiology hospital (RESEARCH) study Circulation. 109 1366-1370
  • [5] Ben-Gal T(2005)Short- and long-term clinical outcome after drug-eluting stent implantation for the percutaneous treatment of left main coronary artery disease: insights from the rapamycin-eluting and taxus stent evaluated at rotterdam cardiology hospital registries (RESEARCH and T-SEARCH) Circulation. 111 1383-1389
  • [6] Sclarovsky S(2005)A prospective randomized comparison between paclitaxel and sirolimus stents in the real world of interventional cardiology: The TAXi trial J Am Coll Cardiol 45 308-311
  • [7] Pardes A(2009)Paclitaxel-eluting stents versus bare-metal stents in acute myocardial infarction N Engl J Med 360 1946-1959
  • [8] Herz I(2003)Sirolimus-eluting stents versus standard stents in patients with stenosis in a native coronary artery N Engl J Med 349 1315-1323
  • [9] Li J-J(1995)Low-dose radioactive endovascular stents prevent smooth muscle cell proliferation and neointimal hyperplasia in rabbits Circulation. 92 1570-1575
  • [10] Fang C-H(2003)Inhibition of neointimal proliferation with Radiology. 229 847-854