TABLE 2.
Studies in the last 5 years using injectable hydrogels combined with cells for treating myocardial infarction.
Biomaterial | Type of cells | Animal model | Type of MI model/Processing time point after successful MI model | End-point after treatment | Injection site | Results compared to control | References |
HA | Endothelial progenitor cell | Rats | Immediate acute myocardial infarction model | 1/4 weeks | Myocardium | Minimize postischemic remodeling | Gaffey et al., 2015, 2019 |
FA | iPS | Mice | Immediate acute myocardial infarction model | 1, 2, 4 weeks | Myocardium | Improved the retention and survival of iPS; less adverse heart remodeling and stimulation of neovascularization | Li H. et al., 2018 |
Chitosan | MSCs | Rats | 1 weeks acute myocardial infarction model | 24 h | Myocardium | Increased graft size and cell retention, promoted MSCs to differentiate into cardiomyocytes and increased the effects of MSCs on neovas-culature formation | Xu et al., 2017 |
HA, hyaluronic acid; FA, folic acid; iPS, induced pluripotent stem cells; MSCs, mesenchymal stem cells.