Extracellular Matrix‐Mediated Crosslinking of Adhesive Hyaluronic Acid Patch for Treating Volumetric Muscle Injury

The treatment of volumetric muscle loss (VML) is challenging owing to the deficiency of appropriate bioscaffolds and ineffective therapeutic outcomes with conventional approaches. Adhesive hydrogels have emerged as potential tools for promoting tissue regeneration, offering effective integration with damaged tissues. However, technical procedures requiring non-biocompatible crosslinking methods, mechanical mismatches, or the absence of tissue-specific microenvironments in conventional adhesive hydrogels have hindered their successful application in tissue reconstruction. In this study, a patch-type adhesive hydrogel is developed by combining a muscle tissue-derived extracellular matrix (MEM) and catechol-conjugated hyaluronic acid (HA-CA). This MEM-containing HA-CA (HCM) patch hydrogel utilizes MEM as both a biocompatible crosslinker and a therapeutic substance. The HCM patch hydrogel, crosslinked through a combination of covalent and non-covalent interactions via MEM and catechol in the composite, not only provides stable physical support but also develops muscle tissue-specific biochemical cues, mediating the recruitment and maturation of muscular cells. In animal models of VML, the HCM patch hydrogel effectively stimulates satellite cells and supports de novo muscle regeneration with functional restoration. This study emphasizes the efficacy and ready-to-use convenience of HCM patch hydrogels for muscle regeneration.

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Publication Details

Journal
Advanced Healthcare Materials
Published
2025-04-24
DOI
https://doi.org/10.1002/adhm.202403747
Citations
3
Primary Topic
Tissue Engineering and Regenerative Medicine
Type
article
Field-Weighted Citation Impact
6.02

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article

Extracellular Matrix‐Mediated Crosslinking of Adhesive Hyaluronic Acid Patch for Treating Volumetric Muscle Injury

Soohwan An, Seung Yeop Han, Seung‐Woo Cho, Eunseon Jeong et al.
3 citations
Advanced Healthcare Materials
Tissue Engineering and Regenerative Medicine
6.02
article

Extracellular Matrix‐Mediated Crosslinking of Adhesive Hyaluronic Acid Patch for Treating Volumetric Muscle Injury

Soohwan An, Seung Yeop Han, Seung‐Woo Cho, Eunseon Jeong, Jung Seung Lee, Eun Je Jeon, Young Seok Song
article en
3 citations

Abstract

The treatment of volumetric muscle loss (VML) is challenging owing to the deficiency of appropriate bioscaffolds and ineffective therapeutic outcomes with conventional approaches. Adhesive hydrogels have emerged as potential tools for promoting tissue regeneration, offering effective integration with damaged tissues. However, technical procedures requiring non-biocompatible crosslinking methods, mechanical mismatches, or the absence of tissue-specific microenvironments in conventional adhesive hydrogels have hindered their successful application in tissue reconstruction. In this study, a patch-type adhesive hydrogel is developed by combining a muscle tissue-derived extracellular matrix (MEM) and catechol-conjugated hyaluronic acid (HA-CA). This MEM-containing HA-CA (HCM) patch hydrogel utilizes MEM as both a biocompatible crosslinker and a therapeutic substance. The HCM patch hydrogel, crosslinked through a combination of covalent and non-covalent interactions via MEM and catechol in the composite, not only provides stable physical support but also develops muscle tissue-specific biochemical cues, mediating the recruitment and maturation of muscular cells. In animal models of VML, the HCM patch hydrogel effectively stimulates satellite cells and supports de novo muscle regeneration with functional restoration. This study emphasizes the efficacy and ready-to-use convenience of HCM patch hydrogels for muscle regeneration.

Advanced Healthcare MaterialsVol. 14(14)
Yonsei University (KR), Institute for Basic Science (KR), Sungkyunkwan University (KR)
Ministry of Trade, Industry and Energy, Ministry of Health and Welfare, Ministry of Science and ICT, South Korea
Openalex Percentile: Top 4%
Tissue Engineering and Regenerative Medicine
6.02
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