Reactive Oxygen Species Scavenging Nanomedicine for the Treatment of Ischemic Heart Disease
- PMID: 35470476
- DOI: 10.1002/adma.202202169
Reactive Oxygen Species Scavenging Nanomedicine for the Treatment of Ischemic Heart Disease
Abstract
Ischemic heart disease (IHD) is the leading cause of disability and mortality worldwide. Reactive oxygen species (ROS) have been shown to play key roles in the progression of diabetes, hypertension, and hypercholesterolemia, which are independent risk factors that lead to atherosclerosis and the development of IHD. Engineered biomaterial-based nanomedicines are under extensive investigation and exploration, serving as smart and multifunctional nanocarriers for synergistic therapeutic effect. Capitalizing on cell/molecule-targeting drug delivery, nanomedicines present enhanced specificity and safety with favorable pharmacokinetics and pharmacodynamics. Herein, the roles of ROS in both IHD and its risk factors are discussed, highlighting cardiovascular medications that have antioxidant properties, and summarizing the advantages, properties, and recent achievements of nanomedicines that have ROS scavenging capacity for the treatment of diabetes, hypertension, hypercholesterolemia, atherosclerosis, ischemia/reperfusion, and myocardial infarction. Finally, the current challenges of nanomedicines for ROS-scavenging treatment of IHD and possible future directions are discussed from a clinical perspective.
Keywords: cardiovascular disease; diabetes; hypercholesterolemia; hypertension; ischemia heart disease; nanomedicine; reactive oxygen species.
© 2022 The Authors. Advanced Materials published by Wiley-VCH GmbH.
References
-
- M. A. Khan, M. J. Hashim, H. Mustafa, M. Y. Baniyas, S. Al Suwaidi, R. AlKatheeri, F. M. K. Alblooshi, M. Almatrooshi, M. E. H. Alzaabi, R. S. Al Darmaki, S. Lootah, Cureus 2020, 12, e9349.
-
- L. Milkovic, A. Cipak Gasparovic, M. Cindric, P. A. Mouthuy, N. Zarkovic, Cells 2019, 8, 793.
-
- a) M. Qiu, A. Singh, D. Wang, J. L. Qu, M. Swihart, H. Zhang, P. N. Prasad, Nano Today 2019, 25, 135;
-
- b) M. E. Lobatto, V. Fuster, Z. A. Fayad, W. J. M. Mulder, Nat. Rev. Drug Discovery 2011, 10, 835;
-
- c) E. K. H. Chow, D. Ho, Sci. Transl. Med. 2013, 5, 216rv4.
Publication types
MeSH terms
Substances
Grants and funding
- 32171318/National Natural Science Foundation of China
- 0109/2018/A3/Science and Technology Development Fund, Macau SAR
- 0011/2019/AKP/Science and Technology Development Fund, Macau SAR
- 0113/2019/A2/Science and Technology Development Fund, Macau SAR
- 0103/2021/A/Science and Technology Development Fund, Macau SAR
- 0002/2021/AKP/Science and Technology Development Fund, Macau SAR
- Shenzhen Science and Technology Innovation Commission
- SGDX20201103093600004/Shenzhen-Hong Kong-Macau Science and Technology Plan C
- MOH-000014/Singapore National Medical Research Council Clinician Scientist Award
- NHG-LKC/National Healthcare Group-Lee Kong Chian School of Medicine
- OFIRG20nov-0123/Singapore National Medical Research Council
- NMRC/OFYIRG/0081/2018/Singapore National Medical Research Council
- NUHSRO/2020/133/Startup/08/National University of Singapore
- NUHSRO/2021/034/TRP/09/Nanomedicine/NUS School of Medicine Nanomedicine Translational Research Programme
- CG21APR1005/National Medical Council Center Grant
LinkOut - more resources
Full Text Sources