1. Department of Cardiology, Institute of Cardiovascular Diseases, the First Affiliated Hospital, Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
2. Department of Molecular Biology, Medical Scientific Research Center, Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Theranostics. 2014 Jan 8;4(2):175-200. doi: 10.7150/thno.7210. eCollection 2014.
Percutaneous coronary intervention (PCI) has become the most common revascularization procedure for coronary artery disease. The use of stents has reduced the rate of restenosis by preventing elastic recoil and negative remodeling. However, in-stent restenosis remains one of the major drawbacks of this procedure. Drug-eluting stents (DESs) have proven to be effective in reducing the risk of late restenosis, but the use of currently marketed DESs presents safety concerns, including the non-specificity of therapeutics, incomplete endothelialization leading to late thrombosis, the need for long-term anti-platelet agents, and local hypersensitivity to polymer delivery matrices. In addition, the current DESs lack the capacity for adjustment of the drug dose and release kinetics appropriate to the disease status of the treated vessel. The development of efficacious therapeutic strategies to prevent and inhibit restenosis after PCI is critical for the treatment of coronary artery disease. The administration of drugs using biodegradable polymer nanoparticles as carriers has generated immense interest due to their excellent biocompatibility and ability to facilitate prolonged drug release. Despite the potential benefits of nanoparticles as smart drug delivery and diagnostic systems, much research is still required to evaluate potential toxicity issues related to the chemical properties of nanoparticle materials, as well as to their size and shape. This review describes the molecular mechanism of coronary restenosis, the use of DESs, and progress in nanoparticle drug- or gene-eluting stents for the prevention and treatment of coronary restenosis.
经皮冠状动脉介入治疗(PCI)已成为治疗冠状动脉疾病最常用的血运重建方法。支架的使用通过防止弹性回缩和负性重构,降低了再狭窄的发生率。然而,支架内再狭窄仍然是该手术的主要缺点之一。药物洗脱支架(DES)已被证明可有效降低晚期再狭窄的风险,但目前市场上的 DES 的使用存在安全性问题,包括治疗的非特异性、不完全内皮化导致的晚期血栓形成、需要长期抗血小板药物以及对聚合物传递基质的局部过敏。此外,目前的 DES 缺乏根据治疗血管的疾病状态调整药物剂量和释放动力学的能力。开发有效的治疗策略来预防和抑制 PCI 后的再狭窄对于治疗冠状动脉疾病至关重要。使用可生物降解聚合物纳米颗粒作为载体的药物给药引起了极大的兴趣,因为它们具有出色的生物相容性和促进药物延长释放的能力。尽管纳米颗粒作为智能药物输送和诊断系统具有潜在的优势,但仍需要大量研究来评估与纳米颗粒材料的化学性质以及其大小和形状相关的潜在毒性问题。本文综述了冠状动脉再狭窄的分子机制、DES 的应用以及用于预防和治疗冠状动脉再狭窄的纳米颗粒药物或基因洗脱支架的进展。