Table 2.
Application of nanoparticles in regulating cardiac homeostasis.
Types of Nanoparticles | Payload | Target | Animal Model | Outcomes | Ref. |
---|---|---|---|---|---|
Polyethylene glycol nanoparticles | Bilirubin | Infarcted myocardium | Myocardial infarction (ischemia-reperfusion, mice) | Inhibition of cell apoptosis and reduction of myocardial infarction size | [107] |
Liposome nanoparticles | Methotrexate | Infarcted myocardium | Myocardial infarction (permanent occlusion, mice) | Reduced infarct size and promoted a significant improvement in left ventricular systolic function | [108] |
Micellar nanoparticles | 2,2,6,6-tetramethylpiperidine-1-oxyl | Infarcted myocardium | Myocardial infarction (ischemia-reperfusion, dog) | Reduced myocardial infarct size and myocardial apoptosis | [109] |
PEG modification of solid lipid nanoparticles | Schisandrin B | SOD/GSH-Px | Myocardial infarction (permanent occlusion, rat) | Reduction in infarct size | [110] |
PEG-graphene quantum dot nanoparticles | Curcumin | Infarcted myocardium | Myocardial infarction (permanent occlusion, rat) | Reduction of myocardial infarct size and fibrosis | [111] |
Liposome nanoparticles | MI antigen and rapamycin | T cell | Myocardial infarction (permanent occlusion, mice) | Infarct size and fibrosis area were reduced | [112] |
MSN conjugated to CD11b anti-body | Panax notoginseng saponins R1 | Monocytes and neutrophils | Myocardial infarction (permanent occlusion, mice) | Improves local inflammation of injured myocardium and reduces myocardial infarction area | [113] |
Methacrylic acid, N-isopropyl acrylamide hydrogel | Visnagin | Infarcted myocardium | Myocardial infarction (ischemia-reperfusion, rat) | Reduce myocardial infarction area and improve cardiac dysfunction | [114] |