Photo‐crosslinkable hydrogel incorporated with bone matrix particles for advancements in dentin tissue engineering

Author:

da Silva Isabela Sanches Pompeo1ORCID,Bordini Ester Alves Ferreira1ORCID,Bronze‐Uhle Erika Soares1ORCID,de Stuani Vitor1ORCID,Costa Matheus Castro1ORCID,de Carvalho Letícia Alves Martins2ORCID,Cassiano Fernanda Balestrero1ORCID,de Azevedo Silva Lucas José3ORCID,Borges Ana Flávia Sanches1ORCID,Soares Diana Gabriela1ORCID

Affiliation:

1. Department of Operative Dentistry, Endodontics, and Dental Materials, School of Dentistry University of São Paulo—USP Bauru Brazil

2. Department of Anatomy, Biology Institute University of Campinas—IB/Unicamp São Paulo Brazil

3. Department of Prosthodontics and Periodontics, Bauru School of Dentistry University of São Paulo—USP Bauru Brazil

Abstract

AbstractThe objective of this study was to create injectable photo‐crosslinkable biomaterials, using gelatin methacryloyl (GelMA) hydrogel, combined with a decellularized bone matrix (BMdc) and a deproteinized (BMdp) bovine bone matrix. These were intended to serve as bioactive scaffolds for dentin regeneration. The parameters for GelMA hydrogel fabrication were initially selected, followed by the incorporation of BMdc and BMdp at a 1% (w/v) ratio. Nano‐hydroxyapatite (nHA) was also included as a control. A physicochemical characterization was conducted, with FTIR analysis indicating that the mineral phase was complexed with GelMA, and BMdc was chemically bonded to the amide groups of gelatin. The porous structure was preserved post‐BMdc incorporation, with bone particles incorporated alongside the pores. Conversely, the mineral phase was situated inside the pore opening, affecting the degree of porosity. The mineral phase did not modify the degradability of GelMA, even under conditions of type I collagenase‐mediated enzymatic challenge, allowing hydrogel injection and increased mechanical strength. Subsequently, human dental pulp cells (HDPCs) were seeded onto the hydrogels. The cells remained viable and proliferative, irrespective of the GelMA composition. All mineral phases resulted in a significant increase in alkaline phosphatase activity and mineralized matrix deposition. However, GelMA‐BMdc exhibited higher cell expression values, significantly surpassing those of all other formulations. In conclusion, our results showed that GelMA‐BMdc produced a porous and stable hydrogel, capable of enhancing odontoblastic differentiation and mineral deposition when in contact with HDPCs, thereby showing potential for dentin regeneration.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Wiley

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