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Effect of stents coated with a combination of sirolimus and alpha-lipoic acid in a porcine coronary restenosis model

机译:西罗莫司和α-硫辛酸复合涂层支架在猪冠状动脉再狭窄模型中的作用

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摘要

The aim of this study was to evaluate antiproliferative sirolimus- and antioxidative alpha-lipoic acid (ALA)-eluting stents using biodegradable polymer [poly-L-lactic acid (PLA)] in a porcine coronary overstretch restenosis model. Forty coronary arteries of 20 pigs were randomized into four groups in which the coronary arteries had a bare metal stent (BMS, n = 10), ALA-eluting stent with PLA (AES, n = 10), sirolimus-eluting stent with PLA (SES, n = 10), or sirolimus- and ALA-eluting stent with PLA (SAS, n = 10). A histopathological analysis was performed 28 days after the stenting. The ALA and sirolimus released slowly over 30 days. There were no significant differences between groups in the injury or inflammation score; however, there were significant differences in the percent area of stenosis (56.2 +/- 11.78 % in BMS vs. 51.5 +/- 12.20 % in AES vs. 34.7 +/- 7.23 % in SES vs. 28.7 +/- 7.30 % in SAS, P < 0.0001) and fibrin score [1.0 (range 1.0-1.0) in BMS vs. 1.0 (range 1.0-1.0) in AES vs. 2.0 (range 2.0-2.0) in SES vs. 2.0 (range 2.0-2.0) in SAS, P < 0.0001] between the four groups. The percent area of stenosis based on micro-computed tomography corresponded with the restenosis rates based on histopathological stenosis in different proportions in the four groups (54.8 +/- 7.88 % in BMS vs. 50.4 +/- 14.87 % in AES vs. 34.5 +/- 7.22 % in SES vs. 28.9 +/- 7.22 % in SAS, P < 0.05). SAS showed a better neointimal inhibitory effect than BMS, AES, and SES at 1 month after stenting in a porcine coronary restenosis model. Therefore, SAS with PLA can be a useful drug combination for coronary stent coating to suppress neointimal hyperplasia.
机译:这项研究的目的是在猪冠状动脉过度拉伸再狭窄模型中使用可生物降解的聚合物[聚-L-乳酸(PLA)]评估抗增殖的西罗莫司和抗氧化的α-硫辛酸(ALA)洗脱支架。将20只猪的40条冠状动脉随机分为四组,其中冠状动脉具有裸金属支架(BMS,n = 10),带有PLA的ALA洗脱支架(AES,n = 10),具有PLA的西罗莫司洗脱支架( SES,n = 10),或具有PLA的西罗莫司和ALA洗脱支架(SAS,n = 10)。支架置入术后28天进行组织病理学分析。 ALA和西罗莫司在30天内缓慢释放。损伤或炎症评分在两组之间无显着差异。然而,狭窄区域的百分比存在显着差异(BMS为56.2 +/- 11.78%,AES为51.5 +/- 12.20%,SES为34.7 +/- 7.23%,而SES为28.7 +/- 7.30% SAS,P <0.0001)和BMS纤维蛋白评分[1.0(1.0-1.0范围)vs AES 1.0(2.0-2.0范围)1.0(SES 2.0)(2.0-2.0范围)2.0(2.0-2.0)在SAS中,四组之间的P <0.0001]。四组中基于微计算机断层扫描的狭窄百分比面积与基于组织病理狭窄的再狭窄率相对应(BMS为54.8 +/- 7.88%,AES为50.4 +/- 14.87%,AES为34.5 + /-SES为7.22%,而SAS为28.9 +/- 7.22%,P <0.05)。在猪冠状动脉再狭窄模型中置入支架后1个月,SAS显示出比BMS,AES和SES更好的新内膜抑制作用。因此,SAS与PLA可以成为用于冠状动脉支架涂层抑制新内膜增生的有用药物组合。

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  • 来源
    《Journal of materials science》 |2016年第4期|66.1-66.10|共10页
  • 作者单位

    Korea Cardiovasc Stent Inst, Jangsung, South Korea|Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea|Chonnam Natl Univ Hosp, Cardiovasc Res Ctr, 671 Dong Gu, Gwangju 501757, South Korea;

    Sunchon Natl Univ, Dept Polymer Sci & Engn, Sunchon, South Korea;

    Korea Cardiovasc Stent Inst, Jangsung, South Korea|Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea|Chonnam Natl Univ Hosp, Cardiovasc Res Ctr, 671 Dong Gu, Gwangju 501757, South Korea|Chonnam Natl Univ, Regener Res Ctr, Gwangju, South Korea;

    Korea Cardiovasc Stent Inst, Jangsung, South Korea|Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea;

    Sunchon Natl Univ, Dept Polymer Sci & Engn, Sunchon, South Korea;

    Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea|Chonnam Natl Univ Hosp, Cardiovasc Res Ctr, 671 Dong Gu, Gwangju 501757, South Korea;

    Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea|Chonnam Natl Univ Hosp, Cardiovasc Res Ctr, 671 Dong Gu, Gwangju 501757, South Korea;

    Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea|Chonnam Natl Univ Hosp, Cardiovasc Res Ctr, 671 Dong Gu, Gwangju 501757, South Korea;

    Korea Cardiovasc Stent Inst, Jangsung, South Korea|Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea;

    Korea Cardiovasc Stent Inst, Jangsung, South Korea|Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea;

    Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea|Chonnam Natl Univ Hosp, Cardiovasc Res Ctr, 671 Dong Gu, Gwangju 501757, South Korea;

    Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea|Chonnam Natl Univ Hosp, Cardiovasc Res Ctr, 671 Dong Gu, Gwangju 501757, South Korea;

    Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea|Chonnam Natl Univ Hosp, Cardiovasc Res Ctr, 671 Dong Gu, Gwangju 501757, South Korea;

    Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea|Chonnam Natl Univ Hosp, Cardiovasc Res Ctr, 671 Dong Gu, Gwangju 501757, South Korea;

    Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea|Chonnam Natl Univ Hosp, Cardiovasc Res Ctr, 671 Dong Gu, Gwangju 501757, South Korea;

    Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea|Chonnam Natl Univ Hosp, Cardiovasc Res Ctr, 671 Dong Gu, Gwangju 501757, South Korea;

    Korea Minist Hlth & Welf, Cardiovasc Convergence Res Ctr, Gwangju, South Korea|Chonnam Natl Univ Hosp, Cardiovasc Res Ctr, 671 Dong Gu, Gwangju 501757, South Korea;

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