Intramyocardial injection of an alginate-based composite hydrogel releasing VEGF and BMP9 significantly reduced infarction size to 11.6% compared to 22.1% with PBS in a mouse model of myocardial infarction.
Does an injectable alginate-based composite hydrogel releasing VEGF and BMP9 improve angiogenesis, reduce infarct size, and improve heart function in a mouse model of myocardial infarction?
Dual-release of VEGF and BMP9 from an injectable composite hydrogel promotes angiogenesis and reduces infarct size in a preclinical mouse model of myocardial infarction.
Absolute Event Rate: 11.6% vs 22.1%
p-value: p=<0.001
Myocardial infarction (MI) is one of cardiovascular diseases that pose a serious threat to human health. The pathophysiology of MI is complex and contains several sequential phases including blockage of a coronary artery, necrosis of myocardial cells, inflammation, and myocardial fibrosis. Aiming at the treatment of different stages of MI, in this work, an injectable alginate based composite hydrogel is developed to load vascular endothelial active factor (VEGF) and silk fibroin (SF) microspheres containing bone morphogenetic protein 9 (BMP9) for releasing VEGF and BMP9 to realize their respective functions. The results of in vitro experiments indicate a rapid initial release of VEGF during the first few days and a relatively slow and sustained release of BMP9 for days, facilitating the formation of blood vessels in the early stage and inhibiting myocardial fibrosis in the long-term stage, respectively. Intramyocardial injection of such composite hydrogel into the infarct border zone of mice MI model via multiple points promotes angiogenesis and reduces the infarction size. Taken together, these results indicate that the dual-release of VEGF and BMP9 from the composite hydrogel results in a collaborative effect on the treatment of MI and improvement of heart function, showing a promising potential for cardiac clinical application.
Wu et al. (Fri,) conducted a other in Myocardial infarction (n=90). Alginate-based composite hydrogel loaded with VEGF and BMP9 (Gel + B/SF + V) vs. PBS was evaluated on Infarction size at 28 days (p=<0.001). Intramyocardial injection of an alginate-based composite hydrogel releasing VEGF and BMP9 significantly reduced infarction size to 11.6% compared to 22.1% with PBS in a mouse model of myocardial infarction.