Preprint Article Version 1 Preserved in Portico This version is not peer-reviewed

Fabrication and Characterization of Porous PEGDA Hydrogels for Articular Cartilage Regeneration

Version 1 : Received: 18 April 2024 / Approved: 18 April 2024 / Online: 18 April 2024 (07:51:42 CEST)

How to cite: Gonella, S.; Domingues, M.F.; Miguel, F.; Moura, C.S.; Rodrigues, C.A.; Ferreira, F.C.; Silva, J.C. Fabrication and Characterization of Porous PEGDA Hydrogels for Articular Cartilage Regeneration. Preprints 2024, 2024041210. https://doi.org/10.20944/preprints202404.1210.v1 Gonella, S.; Domingues, M.F.; Miguel, F.; Moura, C.S.; Rodrigues, C.A.; Ferreira, F.C.; Silva, J.C. Fabrication and Characterization of Porous PEGDA Hydrogels for Articular Cartilage Regeneration. Preprints 2024, 2024041210. https://doi.org/10.20944/preprints202404.1210.v1

Abstract

Functional articular cartilage regeneration remains an unmet medical challenge, increasing the interest for innovative biomaterial-based tissue engineering (TE) strategies. Hydrogels, 3D macromolecular networks with hydrophilic groups, present articular cartilage-like features such as high water content and load-bearing capacity. In this study, 3D porous polyethylene glycol diacrylate (PEGDA) hydrogels were fabricated combining the gas foaming technique and an UV-based crosslinking strategy. The 3D porous PEGDA hydrogels were characterized in terms of their physical, structural and mechanical properties. Our results showed that the size of the hydrogels pores can be modulated by varying the initiator concentration. In vitro cytotoxicity tests showed that 3D porous PEGDA hydrogels presented high biocompatibility both with human chondrocytes and osteoblast-like cells. Importantly, the 3D porous PEGDA hydrogels supported the viability and chondrogenic differentiation of human bone marrow-derived mesenchymal stem/stromal cells (hBM-MSCs)-based spheroids as demonstrated by the positive staining of typical cartilage extracellular matrix (ECM) (glycosaminoglycans (GAGs)) and upregulation of chondrogenesis marker genes. Overall, the produced 3D porous PEGDA hydrogels presented cartilage-like mechanical properties and supported MSC-spheroid chondrogenesis, highlighting their potential as suitable scaffolds for cartilage TE or disease modelling strategies.

Keywords

Articular cartilage tissue engineering; Biocompatibility tests; Chondrogenic differentiation; Gas foaming; Hydrogels; Mesenchymal stem/stromal cells; Polyethylene glycol diacrylate

Subject

Engineering, Bioengineering

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