Hettiarachchi Sajini D, Kwon Young M, Omidi Yadollah, Speth Robert C
Department of Pharmaceutical Sciences, Barry and Judy College of Pharmacy, Nova Southeastern University, 3200 S University Dr, Davie, FL, 33328 USA.
Department of Pharmacology and Physiology, School of Medicine Georgetown University, 3900 Reservoir Rd. NW, Washington, DC, 20057, USA.
Heliyon. 2023 Jun 2;9(6):e16951. doi: 10.1016/j.heliyon.2023.e16951. eCollection 2023 Jun.
The renin-angiotensin system (RAS) is a hormonal cascade that contributes to several disorders: systemic hypertension, heart failure, kidney disease, and neurodegenerative disease. Activation of the RAS can promote inflammation and fibrosis. Drugs that target the RAS can be classified into 3 categories, AT1 angiotensin receptor blockers (ARBs), angiotensin-converting enzyme (ACE) inhibitors, and renin inhibitors. The therapeutic efficacy of current RAS-inhibiting drugs is limited by poor penetration across the blood-brain barrier, low bioavailability, and to some extent, short half-lives. Nanoparticle-mediated drug delivery systems (DDSs) are possible emerging alternatives to overcome such limitations. Nanoparticles are ideally 1-100 nm in size and are considered efficient DDSs mainly due to their unique characteristics, including water dispersity, prolonged half-life in blood circulation, smaller size, and biocompatibility. Nano-scale DDSs can reduce the drug dosage frequency and acute toxicity of drugs while enhancing therapeutic success. Different types of nanoparticles, such as chitosan, polymeric, and nanofibers, have been examined in RAS-related studies, especially in hypertension, cardiovascular disease, and COVID-19. In this review article, we summarize the physical and chemical characteristics of each nanoparticle to elaborate on their potential use in RAS-related nano-drug delivery research and clinical application.
肾素-血管紧张素系统(RAS)是一种激素级联反应,与多种疾病相关:系统性高血压、心力衰竭、肾脏疾病和神经退行性疾病。RAS的激活可促进炎症和纤维化。作用于RAS的药物可分为三类:AT1血管紧张素受体阻滞剂(ARBs)、血管紧张素转换酶(ACE)抑制剂和肾素抑制剂。目前抑制RAS的药物的治疗效果受到血脑屏障穿透性差、生物利用度低以及在一定程度上半衰期短的限制。纳米颗粒介导的药物递送系统(DDSs)可能是克服这些限制的新兴替代方案。纳米颗粒的理想尺寸为1-100纳米,被认为是高效的DDSs,主要是由于其独特的特性,包括水分散性、血液循环中半衰期延长、尺寸更小以及生物相容性。纳米级DDSs可以减少药物给药频率和药物的急性毒性,同时提高治疗成功率。在RAS相关研究中,特别是在高血压、心血管疾病和COVID-19研究中,已经对不同类型的纳米颗粒,如壳聚糖、聚合物和纳米纤维进行了研究。在这篇综述文章中,我们总结了每种纳米颗粒的物理和化学特性,以阐述它们在RAS相关纳米药物递送研究和临床应用中的潜在用途。