Document Type
Article
Publication Date
6-1-2023
Publication Title
Heliyon
Keywords
COVID-19, Cardiovascular disease, Drug delivery, Hypertension, Nanoparticles, Renin-angiotensin system
ISSN
2405-8440
Volume
9
Issue/No.
6
First Page
e16951
Abstract
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.
Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 4.0 International License.
NSUWorks Citation
Hettiarachchi, Sajini D.; Kwon, Young M.; Omidi, Yadollah; and Speth, Robert C., "Nanoparticle approaches for the renin-angiotensin system" (2023). HPD Articles. 32.
https://nsuworks.nova.edu/hpd_facarticles/32
ORCID ID
0000-0002-4063-1355; 0000-0002-9935-4866; 0000-0003-0067-2475; 0000-0002-6434-2136
DOI
10.1016/j.heliyon.2023.e16951
Copyright
© 2023 Published by Elsevier Ltd.