Key result
CorMatrix P-ECM delivery system achieves controlled intramyocardial injection depth and volume in heart failure models.
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Biomaterials with direct intramyocardial injection devices have been developed and are being investigated as a potential cardiac regenerative therapy for end-stage ischemic heart failure. Decellularized extracellular matrix (ECM) has been shown to improve cardiac function and attenuate or reverse pathologic remodeling cascades. CorMatrix Cardiovascular, Inc. has developed a porcine small intestinal submucosa-derived particulate extracellular matrix (P-ECM) and ECM Delivery System to provide uniform and controlled intramyocardial delivery of the injectable P-ECM material into infarcted regions. The CorMatrix ECM Delivery System is composed of a Multi-Needle P-ECM Syringe Assembly, Automated Injection Controller, and Tissue Depth Measurement System (portable ultrasound). Feasibility of the P-ECM delivery system was tested intraoperatively in a chronic ischemic heart failure bovine model (n = 11), and demonstrated the ability to control injection volume (0.1-1.0 ml) and depth of penetration (3-5 mm) under regulated injection pressure (150 psi CO2) into the ischemic region. Targeted intramyocardial delivery of P-ECM may improve efficacy and enable development of novel patient-specific therapy.
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Slaughter et al. (2014) studied Chronic ischemic heart failure (bovine model) (n=11). CorMatrix ECM Delivery System with porcine small intestinal submucosa-derived particulate extracellular matrix (P-ECM) was evaluated on Feasibility of controlled intramyocardial injection volume and depth of penetration. The CorMatrix P-ECM delivery system controlled intramyocardial injection volume (0.1-1.0 ml) and depth (3-5 mm) at 150 psi CO2 in a bovine ischemic heart failure model (n=11).
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