再狭窄
体内
材料科学
涂层
脂质体
一氧化氮
生物医学工程
控制释放
支架
纳米技术
医学
外科
内科学
生物
生物技术
作者
Mahmoud A. Elnaggar,Seong Ho Seo,Samy Gobaa,Kyung Seob Lim,In‐Ho Bae,Myung Ho Jeong,Dong Keun Han,Yoon Ki Joung
出处
期刊:Small
[Wiley]
日期:2016-09-13
卷期号:12 (43): 6012-6023
被引量:50
标识
DOI:10.1002/smll.201600337
摘要
The sustained or controlled release of nitric oxide (NO) can be the most promising approach for the suppression or prevention of restenosis and thrombosis caused by stent implantation. The aim of this study is to investigate the feasibility in the potential use of layer-by-layer (LBL) coating with a NO donor-containing liposomes to control the release rate of NO from a metallic stent. Microscopic observation and surface characterizations of LBL-modified stents demonstrate successful LBL coating with liposomes on a stent. Release profiles of NO show that the release rate is sustained up to 5 d. In vitro cell study demonstrates that NO release significantly enhances endothelial cell proliferation, whereas it markedly inhibits smooth muscle cell proliferation. Finally, in vivo study conducted with a porcine coronary injury model proves the therapeutic efficacy of the NO-releasing stents coated by liposomal LBL technique, supported by improved results in luminal healing, inflammation, and neointimal thickening except thrombo-resistant effect. As a result, all these results demonstrate that highly optimized release rate and therapeutic dose of NO can be achieved by LBL coating and liposomal encapsulation, followed by significantly efficacious outcome in vivo.
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