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The Therapeutic Potential of Nanoparticles to Reduce Inflammation in Atherosclerosis Publisher Pubmed



Gorabi AM1 ; Kiaie N1 ; Reiner Z2 ; Carbone F3, 4, 5 ; Montecucco F3, 4, 5, 6 ; Sahebkar A7, 8, 9
Authors
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Authors Affiliations
  1. 1. Research Center for Advanced Technologies in Cardiovascular Medicine, Tehran Heart Center, Tehran University of Medical Sciences, Tehran, 1411713138, Iran
  2. 2. University Hospital Centre Zagreb, School of Medicine University of Zagreb, Department of Internal Medicine, Zagreb, 1000, Croatia
  3. 3. First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, 16132, Italy
  4. 4. IRCCS Ospedale Policlinico San Martino Genoa - Italian Cardiovascular Network, Genoa, 16132, Italy
  5. 5. First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, 16132, Italy
  6. 6. Centre of Excellence for Biomedical Research (CEBR), University of Genoa, Genoa, 16132, Italy
  7. 7. Neurogenic Inflammation Research Center, Mashhad University of Medical Sciences, Mashhad, 9177948564, Iran
  8. 8. Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, 9177948564, Iran
  9. 9. School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, 9177948564, Iran

Source: Biomolecules Published:2019


Abstract

Chronic inflammation is one of the main determinants of atherogenesis. The traditional medications for treatment of atherosclerosis are not very efficient in targeting atherosclerotic inflammation. Most of these drugs are non-selective, anti-inflammatory and immunosuppressive agents that have adverse effects and very limited anti-atherosclerotic effects, which limits their systemic administration. New approaches using nanoparticles have been investigated to specifically deliver therapeutic agents directly on atherosclerotic lesions. The use of drug delivery systems, such as polymeric nanoparticles, liposomes, and carbon nanotubes are attractive strategies, but some limitations exist. For instance, nanoparticles may alter the drug kinetics, based on the pathophysiological mechanisms of the diseases. In this review, we will update pathophysiological evidence for the use of nanoparticles to reduce inflammation and potentially prevent atherogenesis in different experimental models. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.
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