Key result
Targeted nanoparticles reduce plaque inflammation and prevent atherogenesis in experimental models.
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.
No takes yet. Share an insight, caveat, or question.
Gorabi et al. (2019) conducted a review in Atherosclerosis. Nanoparticles (polymeric nanoparticles, liposomes, carbon nanotubes) vs. Traditional non-selective anti-inflammatory and immunosuppressive medications was evaluated on Atherosclerotic inflammation and atherogenesis. Nanoparticles offer a targeted strategy to deliver therapeutics to atherosclerotic lesions to reduce inflammation and prevent atherogenesis in experimental models.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: