Alfred E. Mann Department of Biomedical Engineering, University of Southern California, Los Angeles, California, USA.
Department of Medicine, Division of Nephrology and Hypertension, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
J Biomed Mater Res A. 2024 Jun;112(6):895-913. doi: 10.1002/jbm.a.37668. Epub 2024 Jan 12.
Although cardiovascular diseases (CVD) are the leading cause of global mortality, there is a lack of therapies that target and revert underlying pathological processes. Mitochondrial dysfunction is involved in the pathophysiology of CVD, and thus is a potential target for therapeutic development. To target the mitochondria and improve therapeutic efficacy, nanoparticle-based delivery systems have been proposed as promising strategies for the delivery of therapeutic agents to the mitochondria. This review will first discuss how mitochondrial dysfunction is related to the progression of several CVD and then delineate recent progress in mitochondrial targeting using nanoparticle-based delivery systems including peptide-based nanosystems, polymeric nanoparticles, liposomes, and lipid nanoparticles. In addition, we summarize the advantages of these nanocarriers and remaining challenges in targeting the mitochondria as a therapeutic strategy for CVD treatment.
虽然心血管疾病 (CVD) 是全球死亡的主要原因,但目前缺乏针对潜在病理过程的治疗方法。线粒体功能障碍与 CVD 的病理生理学有关,因此是治疗开发的潜在靶点。为了靶向线粒体并提高治疗效果,基于纳米粒子的递药系统已被提出作为将治疗剂递送到线粒体的有前途的策略。本综述首先讨论了线粒体功能障碍如何与几种 CVD 的进展相关,然后描述了使用基于纳米粒子的递药系统靶向线粒体的最新进展,包括基于肽的纳米系统、聚合物纳米粒子、脂质体和脂纳米粒子。此外,我们总结了这些纳米载体的优点以及作为 CVD 治疗的治疗策略靶向线粒体的剩余挑战。