Catheter-Deliverable Hydrogel Derived From Decellularized Ventricular Extracellular Matrix Increases Endogenous Cardiomyocytes and Preserves Cardiac Function Post-Myocardial Infarction

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

卷:59

Article

Singelyn, Jennifer M.¹  Sundaramurthy, Priya¹  Johnson, Todd D.¹  Schup-Magoffin, Pamela J.¹  Hu, Diane P.¹  Faulk, Denver M.¹  Wang, Jean¹  Mayle, Kristine M.¹  Bartels, Kendra²  Salvatore, Michael³  Kinsey, Adam M.³  DeMaria, Anthony N.²  Dib, Nabil²  Christman, Karen L.¹ 

[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA

[2] Univ Calif San Diego, Sch Med, La Jolla, CA 92093 USA

[3] Ventrix Inc, San Diego, CA USA

关键词: biomaterial;    extracellular matrix;    heart failure;    myocardial infarction;    scaffold;   

DOI  :  10.1016/j.jacc.2011.10.888

来源: Elsevier

【 摘 要 】

Objectives This study evaluated the use of an injectable hydrogel derived from ventricular extracellular matrix (ECM) for treating myocardial infarction (MI) and its ability to be delivered percutaneously. Background Injectable materials offer promising alternatives to treat MI. Although most of the examined materials have shown preserved or improved cardiac function in small animal models, none have been specifically designed for the heart, and few have translated to catheter delivery in large animal models. Methods We have developed a myocardial-specific hydrogel, derived from decellularized ventricular ECM, which self-assembles when injected in vivo. Female Sprague-Dawley rats underwent ischemia reperfusion followed by injection of the hydrogel or saline 2 weeks later. The implantation response was assessed via histology and immunohistochemistry, and the potential for arrhythmogenesis was examined using programmed electrical stimulation 1 week post-injection. Cardiac function was analyzed with magnetic resonance imaging 1 week pre-injection and 4 weeks post-MI. In a porcine model, we delivered the hydrogel using the NOGA-guided MyoStar catheter (Biologics Delivery Systems, Irwindale, California), and utilized histology to assess retention of the material. Results We demonstrate that injection of the material in the rat MI model increases endogenous cardiomyocytes in the infarct area and maintains cardiac function without inducing arrhythmias. Furthermore, we demonstrate feasibility of transendocardial catheter injection in a porcine model. Conclusions To our knowledge, this is the first in situ gelling material to be delivered via transendocardial injection in a large animal model, a critical step towards the translation of injectable materials for treating MI in humans. Our results warrant further study of this material in a large animal model of MI and suggest this may be a promising new therapy for treating MI. (J Am Coll Cardiol 2012;59:751-63) (C) 2012 by the American College of Cardiology Foundation

【 授权许可】

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