Departmental Papers (BE)

Document Type

Journal Article

Date of this Version

5-19-2010

Abstract

A recent trend has emerged that involves myocardial injection of biomaterials, containing cells or acellular, following myocardial infarction (MI) to influence the remodeling response through both biological and mechanical effects. Despite the number of different materials injected in these approaches, there has been little investigation into the importance of material properties on therapeutic outcomes. This work focuses on the investigation of injectable hyaluronic acid (MeHA) hydrogels that have tunable mechanics and gelation behavior. Specifically, two MeHA formulations that exhibit similar degradation and tissue distribution upon injection but have differential moduli (∼8 versus ∼43 kPa) were injected into a clinically relevant ovine MI model to evaluate the associated salutary effect of intramyocardial hydrogel injection on the remodeling response based on hydrogel mechanics. Treatment with both hydrogels significantly increased the wall thickness in the apex and basilar infarct regions compared with the control infarct. However, only the higher-modulus (MeHA High) treatment group had a statistically smaller infarct area compared with the control infarct group. Moreover, reductions in normalized end-diastolic and end-systolic volumes were observed for the MeHA High group. This group also tended to have better functional outcomes (cardiac output and ejection fraction) than the low-modulus (MeHA Low) and control infarct groups. This study provides fundamental information that can be used in the rational design of therapeutic materials for treatment of MI.

Comments

Suggested Citation:
Ifkovits, J.L. et. al. (2010). "Injectable hydrogel properties influence infact expansion and extent of postinfarction left ventricular remodeling in an ovine model." Proceedings of the National Academy of Sciences. Vol. 107(25). pp. 11507-11512.

www.pnas.org/cgi/doi/10.1073/pnas.1004097107

Keywords

infarction, cardiac, mechanics, polymer, biomaterial

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Date Posted: 30 November 2010

This document has been peer reviewed.