Fabrication of drug-eluting covered stents with micropores and differential coating of heparin and FK506

Yasuhide Nakayama , Shogo Nishi , Hatsue Ishibashi-Ueda
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引用次数: 29

Abstract

To reduce in-stent restenosis rates, we developed a novel drug-eluting covered stent with a microporous elastometric covered film, in which its luminal surface was flat and immobilized with heparin for anticoagulation and its outer surface immobilized with FK506 to prevent neointimal hyperplasia. One month after implantation into the bilateral common carotid arteries, all stented arteries were patent and the luminal surfaces were fully covered with a confluent of endothelial cells irrespective of the drug immobilization. In the control group, which consisted of covered stents without drug immobilization, intensive inflammatory cells adjacent to the stents and neointimal hyperplasia, indicating vascular injury, were observed. In contrast, in the developed drug-eluting stents, only a few inflammatory cells around the stent strut and covered film were observed, and there was no significant neointimal thickening.

肝素与FK506差异包被微孔药物洗脱支架的制备
为了降低支架内再狭窄的发生率,我们开发了一种新型药物洗脱覆盖支架,其微孔弹性覆盖膜,其腔面平坦,用肝素固定用于抗凝,外表面用FK506固定以防止内膜增生。植入双侧颈总动脉1个月后,所有支架动脉通畅,管腔表面完全被内皮细胞覆盖,与药物固定无关。对照组为未固定药物的覆盖支架组,支架周围炎症细胞密集,血管内膜增生,提示血管损伤。而在成熟的药物洗脱支架中,仅观察到支架支架支撑和覆盖膜周围的少量炎症细胞,未见明显的内膜增厚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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