Key result
A micro-structurally detailed computational model of a polyethylene glycol hydrogel injectate in a rat biventricular geometry was successfully developed for multiscale simulations of MI therapies.
Provides a realistic micro-structurally detailed computational model of hydrogel injectate in a rat heart for studying therapies preventing adverse remodeling after myocardial infarction.
Provides platform for testing MI hydrogel therapies in silico; leaves open clinical translation from rat models.
Biomaterial injection-based therapies have showed cautious success in restoration of cardiac function and prevention of adverse remodelling into heart failure after myocardial infarction (MI). However, the underlying mechanisms are not well understood. Computational studies utilised simplified representations of the therapeutic myocardial injectates. Wistar rats underwent experimental infarction followed by immediate injection of polyethylene glycol hydrogel in the infarct region. Hearts were explanted, cryo-sectioned and the region with the injectate histologically analysed. Histological micrographs were used to reconstruct the dispersed hydrogel injectate. Cardiac magnetic resonance imaging data from a healthy rat were used to obtain an end-diastolic biventricular geometry which was subsequently adjusted and combined with the injectate model. The computational geometry of the injectate exhibited microscopic structural details found the in situ. The combination of injectate and cardiac geometry provides realistic geometries for multiscale computational studies of intra-myocardial injectate therapies for the rat model that has been widely used for MI research.
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Sirry et al. (2013) studied Myocardial infarction. Polyethylene glycol hydrogel injection was evaluated. A micro-structurally detailed computational model of a polyethylene glycol hydrogel injectate in a rat biventricular geometry was successfully developed for multiscale simulations of MI therapies.
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