Rescuing Cardiac Cells and Improving Cardiac Function by Targeted Delivery of Oxygen-Releasing Nanoparticles after or Even before Acute Myocardial Infarction.
Ya GuanHong NiuJiaxing WenYu DangMohamed ZayedJianjun GuanPublished in: ACS nano (2022)
Myocardial infarction (MI) causes massive cell death due to restricted blood flow and oxygen deficiency. Rapid and sustained oxygen delivery following MI rescues cardiac cells and restores cardiac function. However, current oxygen-generating materials cannot be administered during acute MI stage without direct injection or suturing methods, both of which risk rupturing weakened heart tissue. Here, we present infarcted heart-targeting, oxygen-releasing nanoparticles capable of being delivered by intravenous injection at acute MI stage, and specifically accumulating in the infarcted heart. The nanoparticles can also be delivered before MI, then gather at the injured area after MI. We demonstrate that the nanoparticles, delivered either pre-MI or post-MI, enhance cardiac cell survival, stimulate angiogenesis, and suppress fibrosis without inducing substantial inflammation and reactive oxygen species overproduction. Our findings demonstrate that oxygen-delivering nanoparticles can provide a nonpharmacological solution to rescue the infarcted heart during acute MI and preserve heart function.
Keyphrases
- heart failure
- left ventricular
- acute myocardial infarction
- liver failure
- cell death
- blood flow
- induced apoptosis
- cell cycle arrest
- respiratory failure
- reactive oxygen species
- atrial fibrillation
- drug induced
- endothelial cells
- cell proliferation
- endoplasmic reticulum stress
- mouse model
- cancer therapy
- extracorporeal membrane oxygenation
- replacement therapy