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Acellular dermal matrix integration in hydrogel scaffolds: A novel approach to cartilage tissue engineering

Authors
Park, HojinKim, Min-SookLee, Tae-YulSong, Han-SangKim, Deok-Woo
Issue Date
Jul-2025
Publisher
Elsevier BV
Keywords
Chondrocytes; Extracellular matrix; Hydrogels; Scaffold; Tissue engineering
Citation
Journal of Plastic, Reconstructive and Aesthetic Surgery, v.106, pp 393 - 400
Pages
8
Indexed
SCIE
SCOPUS
Journal Title
Journal of Plastic, Reconstructive and Aesthetic Surgery
Volume
106
Start Page
393
End Page
400
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/77657
DOI
10.1016/j.bjps.2025.05.038
ISSN
1748-6815
1878-0539
Abstract
Background: Scaffold materials impact engineered cartilage properties, but current options like hydrogels and PCL have limitations, including insufficient strength and inflammatory responses. This study explored the efficacy of integrating hydrogel scaffolds with an acellular dermal matrix (ADM) to enhance structural integrity and chondrogenesis. Methods: Human third costal cartilage was obtained and processed to isolate chondrocytes, which were assessed via flow cytometry for surface markers (CD44, CD54, CD31, CD45). Chondrocytes were cultured in a gelatin scaffold with (ADM group) or without ADM sheets (Hydrogel group), then implanted in BALB/c nude mice for 12 weeks. Histological staining and ECM analyses, including GAG and type II collagen ELISA, were conducted on harvested constructs. Results: The rectangular shape was better preserved in the ADM group compared to the hydrogel group, indicating less contraction and deformation. The scaffold width in the ADM group was significantly greater (9.20±0.23 mm) than that in the hydrogel group (7.40±0.93 mm, p<0.05). Histological analysis revealed an enhanced ECM formation in the ADM group with uniform ECM distribution. The quantitative assays demonstrated significantly higher glycosaminoglycan content (3.3±0.7 μg/mg) and type II collagen levels (11.3±1.6 μg/mg) in the ADM group compared to the hydrogel group (2.2±0.2 μg/mg and 4.6±0.4 μg/mg, respectively; p<0.05). Conclusion: The ADM-covered hydrogel scaffold effectively maintained its structural integrity and volume in vivo, promoting ECM production compared with the hydrogel-only scaffold. These findings indicate that the ADM-covered hydrogel scaffolds have significant potential for cartilage tissue engineering and reconstructive surgery. © 2025
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Kim, Deok Woo
Ansan Hospital (Department of Plastic and Reconstructive Surgery, Ansan Hospital)
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