Platelet-rich fibrin (PRF) modified nano-hydroxyapatite/chitosan/gelatin/ alginate scaffolds increase adhesion and viability of human dental pulp stem cells (DPSC) and osteoblasts derived from DPSC
Keywords: Platelet-rich fibrin, Cell survival, Bone regeneration, 3D scaffolds, Adult stem cells
Abstract
Bone tissue regeneration strategies have incorporated the use of natural polymers, such as hydroxyapatite (nHA), chitosan (CH), gelatin (GEL), or alginate (ALG). Additionally, platelet concentrates, such as platelet-rich fibrin (PRF) have been suggested to improve scaffold biocompatibility. This study aimed to develop scaffolds composed of nHA, GEL, and CH, with or without ALG and lyophilized PRF, to evaluate the scaffold's properties, growth factor release, and dental pulp stem cells (DPSC), and osteoblast (OB) derived from DPSC viability. Four scaffold variations were synthesized and lyophilized. Then, degradation, swelling profiles, and morphological analysis were performed. Furthermore, PDGF-BB and FGF-B growth factors release were quantified by ELISA, and cytotoxicity and cell viability were evaluated. The swelling and degradation profiles were similar in all scaffolds, with pore sizes ranging between 100 and 250 μm. FGF-B and PDGF-BB release was evidenced after 24 h of scaffold immersion in cell culture medium. DPSC and OB-DPSC viability was notably increased in PRFsupplemented scaffolds. The nHA-CH-GEL-PRF scaffold demonstrated optimal physical-biological characteristics for stimulating DPSC and OB-DPSC cell viability. These results suggest lyophilized PRF improves scaffold biocompatibility for bone tissue regeneration purposes.
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Título de la Revista: | INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES |
Volumen: | 273 |
Número: | Part 1 |
Editorial: | Elsevier |
Fecha de publicación: | 2024 |
Página de inicio: | 133064 |
Página final: | 233076 |
Idioma: | Inglés |
Financiamiento/Sponsor: | FONDECYT |
URL: | https://www.sciencedirect.com/science/article/pii/S0141813024038698?via%3Dihub |
DOI: |
https://doi.org/10.1016/j.ijbiomac.2024.133064 |
Notas: | ISI |