Skaggs Pharmaceutical Sciences Center, Department of Pharmacology & Toxicology, R. Ken Coit College of Pharmacy, The University of Arizona, Tucson, Arizona, 85721, USA.
NCI-designated University of Arizona Comprehensive Cancer Center, Tucson, Arizona, 85721, USA.
Biomater Sci. 2022 Sep 27;10(19):5459-5471. doi: 10.1039/d2bm00660j.
Atherosclerosis is a chronic and metabolic-related disease that is a serious threat to human health. Currently available diagnostic and therapeutic measures for atherosclerosis lack adequate efficiency which requires promising alternative approaches. Nanotechnology-based nano-delivery systems allow for new perspectives for atherosclerosis therapy. Surface-modified nanoparticles could achieve highly effective therapeutic effects by binding to specific receptors that are abnormally overexpressed in atherosclerosis, with less adverse effects on non-target tissues. The main purpose of this review is to summarize the research progress and design ideas to target atherosclerosis using a variety of ligand-modified nanoparticle systems, discuss the shortcomings of current vector design, and look at future development directions. We hope that this review will provide novel research strategies for the design and development of nanotherapeutics targeting atherosclerosis.
动脉粥样硬化是一种慢性代谢相关性疾病,严重威胁人类健康。目前针对动脉粥样硬化的诊断和治疗手段效果有限,需要有更有前景的替代方法。基于纳米技术的纳米递药系统为动脉粥样硬化治疗提供了新的思路。表面修饰的纳米颗粒可以通过与动脉粥样硬化中异常过表达的特定受体结合,实现高效的治疗效果,对非靶组织的不良反应较小。本文主要综述了利用多种配体修饰的纳米颗粒系统靶向动脉粥样硬化的研究进展和设计思路,讨论了目前载体设计的不足之处,并展望了未来的发展方向。希望本文的综述能为针对动脉粥样硬化的纳米药物设计和开发提供新的研究策略。
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