生物相容性
再狭窄
涂层
支架
新生内膜增生
药物输送
聚合物
生物医学工程
材料科学
血管成形术
纳米技术
医学
外科
内科学
冶金
复合材料
作者
Ayala Hezi‐Yamit,C. Roger Sullivan,Jennifer Wong,Laura David,Mingfei Chen,Pei‐Wen Cheng,David Shumaker,Josiah N. Wilcox,Kishore Udipi
出处
期刊:Combinatorial Chemistry & High Throughput Screening
[Bentham Science]
日期:2009-08-01
卷期号:12 (7): 664-676
被引量:17
标识
DOI:10.2174/138620709788923674
摘要
The development of stents has been a major advancement over balloon angioplasty, improving vessel revascularization in obstructive coronary artery disease. The development of drug-eluting stents (DES) was the next breakthrough, designed to prevent the development of neointimal hyperplasia (restenosis) following percutaneous coronary interventions (PCI). Several DES are currently in various stages of clinical development; these DES use different stent platforms, different antiproliferative drugs and different polymeric coatings that carry the drugs and control their delivery kinetics. Following DES implantation, when the entire drug is released, the polymeric coating is still retained on the stent and can influence subsequent tissue response and vascular healing. Therefore, the biocompatibility of the polymeric coatings is an important component of DES safety and needs to be thoroughly evaluated. Here we describe the development of a high throughput screening platform for the evaluation of polymer biocompatibility, assaying whether a polymeric coating triggers inflammation in vascular cells. The data generated by these assays provides a structure-activity relationship (SAR) that can guide polymer chemists in polymer design. We have also applied this methodology to evaluate the components of a novel polymer system (BioLinx polymer system) designed in-house. In addition, we assayed other polymeric coatings similar to those currently used on various DES. The results of this evaluation reveal a remarkable correlation between polymer hydrophobicity and its ability to provoke inflammatory response.
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