Efficacy and Safety Evaluation of Tacrolimus-Eluting Stent in a Porcine Coronary Artery Model.

IF 4.4 4区 医学 Q2 CELL & TISSUE ENGINEERING Tissue engineering and regenerative medicine Pub Date : 2024-07-01 Epub Date: 2024-06-04 DOI:10.1007/s13770-024-00646-0
Dae Sung Park, Mi Hyang Na, Myung Ho Jeong, Doo Sun Sim, Yu Jeong Jin, Hae Jin Kee, Mun Ki Kim, Jeong Ha Kim, Young Joon Hong, Kyung Hoon Cho, Dae Young Hyun, Seok Oh, Kyung Seob Lim, Dae-Heung Byeon, Jeong Hun Kim
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Abstract

Background: A drug-eluting stent (DES) is a highly beneficial medical device used to widen or unblock narrowed blood vessels. However, the drugs released by the implantation of DES may hinder the re-endothelialization process, increasing the risk of late thrombosis. We have developed a tacrolimus-eluting stent (TES) that as acts as a potent antiproliferative and immunosuppressive agent, enhancing endothelial regeneration. In addition, we assessed the safety and efficacy of TES through both in vitro and in vivo tests.

Methods: Tacrolimus and Poly(lactic-co-glycolic acid) (PLGA) were applied to the metal stent using electrospinning equipment. The surface morphology of the stent was examined before and after coating using a scanning electron microscope (SEM) and energy dispersive X-rays (EDX). The drug release test was conducted through high-performance liquid chromatography (HPLC). Cell proliferation and migration assays were performed using smooth muscle cells (SMC). The stent was then inserted into the porcine coronary artery and monitored for a duration of 4 weeks.

Results: SEM analysis confirmed that the coating surface was uniform. Furthermore, EDX analysis showed that the surface was coated with both polymer and drug components. The HPCL analysis of TCL at a wavelength of 215 nm revealed that the drug was continuously released over a period of 4 weeks. Smooth muscle cell migration was significantly decreased in the tacrolimus group (54.1% ± 11.90%) compared to the non-treated group (90.1% ± 4.86%). In animal experiments, the stenosis rate was significantly reduced in the TES group (29.6% ± 7.93%) compared to the bare metal stent group (41.3% ± 10.18%). Additionally, the fibrin score was found to be lower in the TES group compared to the group treated with a sirolimus-eluting stent (SES).

Conclusion: Similar to SES, TES reduces neointimal proliferation in a porcine coronary artery model, specifically decreasing the fibrins score. Therefore, tacrolimus could be considered a promising drug for reducing restenosis and thrombosis.

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他克莫司洗脱支架在猪冠状动脉模型中的疗效和安全性评估
背景:药物洗脱支架(DES药物洗脱支架(DES)是一种非常有益的医疗设备,用于拓宽或疏通狭窄的血管。然而,药物洗脱支架植入后释放的药物可能会阻碍血管再内皮化过程,增加后期血栓形成的风险。我们已经开发出一种他克莫司洗脱支架(TES),它可以作为一种强效的抗增生剂和免疫抑制剂,促进内皮再生。此外,我们还通过体外和体内试验评估了 TES 的安全性和有效性:方法:使用电纺丝设备将他克莫司和聚乳酸(PLGA)应用于金属支架。使用扫描电子显微镜(SEM)和能量色散 X 射线(EDX)对涂覆前后的支架表面形态进行了检测。药物释放测试通过高效液相色谱法(HPLC)进行。使用平滑肌细胞(SMC)进行了细胞增殖和迁移试验。然后将支架插入猪冠状动脉并监测 4 周:扫描电子显微镜分析证实涂层表面均匀一致。此外,EDX 分析表明表面涂有聚合物和药物成分。在 215 纳米波长下对 TCL 进行的 HPCL 分析表明,药物在 4 周内持续释放。与未处理组(90.1% ± 4.86%)相比,他克莫司组(54.1% ± 11.90%)的平滑肌细胞迁移率明显降低。在动物实验中,与裸金属支架组(41.3% ± 10.18%)相比,他克莫司组(29.6% ± 7.93%)的血管狭窄率明显降低。此外,与西罗莫司洗脱支架(SES)治疗组相比,TES治疗组的纤维蛋白评分更低:结论:与 SES 相似,TES 也能减少猪冠状动脉模型中的新内膜增生,特别是降低纤维蛋白评分。因此,他克莫司被认为是一种有希望减少再狭窄和血栓形成的药物。
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来源期刊
Tissue engineering and regenerative medicine
Tissue engineering and regenerative medicine CELL & TISSUE ENGINEERING-ENGINEERING, BIOMEDICAL
CiteScore
6.80
自引率
5.60%
发文量
83
审稿时长
6-12 weeks
期刊介绍: Tissue Engineering and Regenerative Medicine (Tissue Eng Regen Med, TERM), the official journal of the Korean Tissue Engineering and Regenerative Medicine Society, is a publication dedicated to providing research- based solutions to issues related to human diseases. This journal publishes articles that report substantial information and original findings on tissue engineering, medical biomaterials, cells therapy, stem cell biology and regenerative medicine.
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