Paintable Decellularized‐ECM Hydrogel for Preventing Cardiac Tissue Damage

Author:

Lee Jaewoo1,Lee Seul‐Gi2,Kim Beom‐seok34,Park Shinhye2,Sundaram M. Nivedhitha1,Kim Byung‐gee456,Kim C‐Yoon7,Hwang Nathaniel S.136ORCID

Affiliation:

1. School of Chemical and Biological Engineering, Institute of Chemical Processes Seoul National University Seoul 151–742 Republic of Korea

2. Department of Stem Cell Biology School of Medicine Konkuk University Seoul 143–701 Republic of Korea

3. Interdisciplinary Program in Bioengineering Seoul National University Seoul 151–742 Republic of Korea

4. Research Division EGC Therapeutics Seoul 08790 Republic of Korea

5. Institute of Molecular Biology and Genetics, Institute for Sustainable Development (ISD) Seoul National University Seoul 08826 Republic of Korea

6. Bio‐MAX/N‐Bio Institute of BioEngineering Seoul National University Seoul 08826 Republic of Korea

7. College of Veterinary Medicine Konkuk University Seoul 05029 Republic of Korea

Abstract

AbstractThe tissue‐specific heart decellularized extracellular matrix (hdECM) demonstrates a variety of therapeutic advantages, including fibrosis reduction and angiogenesis. Consequently, recent research for myocardial infarction (MI) therapy has utilized hdECM with various delivery techniques, such as injection or patch implantation. In this study, a novel approach for hdECM delivery using a wet adhesive paintable hydrogel is proposed. The hdECM‐containing paintable hydrogel (pdHA_t) is simply applied, with no theoretical limit to the size or shape, making it highly beneficial for scale‐up. Additionally, pdHA_t exhibits robust adhesion to the epicardium, with a minimal swelling ratio and sufficient adhesion strength for MI treatment when applied to the rat MI model. Moreover, the adhesiveness of pdHA_t can be easily washed off to prevent undesired adhesion with nearby organs, such as the rib cages and lungs, which can result in stenosis. During the 28 days of in vivo analysis, the pdHA_t not only facilitates functional regeneration by reducing ventricular wall thinning but also promotes neo‐vascularization in the MI region. In conclusion, the pdHA_t presents a promising strategy for MI treatment and cardiac tissue regeneration, offering the potential for improved patient outcomes and enhanced cardiac function post‐MI.

Funder

National Research Foundation of Korea

Publisher

Wiley

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