再狭窄
血管成形术
离体
西罗莫司
体内
气球
冠状动脉
肝素
医学
动脉
化学
心脏病学
内科学
体外
支架
生物
生物化学
生物技术
作者
Jayesh V Betala,Sooneon Bae,Eugene M. Langan,Martine LaBerge,Jeoung Soo Lee
出处
期刊:Nanomedicine
日期:2020-05-01
卷期号:15 (12): 1205-1220
被引量:3
标识
DOI:10.2217/nnm-2020-0028
摘要
Aim: To develop poly(lactide-co-glycolide)-graft-polyethylenimine (PgP) as a dual drug-delivery carrier for sirolimus (SR) and heparin (Hep) to inhibit restenosis after balloon angioplasty. Materials & methods: SR was loaded in the hydrophobic core and negatively charged Hep complexed with the positively charged hydrophilic shell of PgP. SR- and Hep-loaded PgP was tested on rat aortic smooth muscle cells in vitro and injured porcine coronary arteries after balloon angioplasty ex vivo. Results & conclusion: SR and Hep loading efficiency in PgP were approximately 37 and 82%, respectively. SR- and Hep-loaded PgP treatment decreased smooth muscle cell proliferation up to 14 days post-treatment and decreased proliferation, collagen deposition and neointimal thickness and increased patency in porcine coronary arteries after balloon angioplasty ex vivo.
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