Strontium-Doped Bioglass-Laden Gelatin Methacryloyl Hydrogels for Vital Pulp Therapy

Author:

Aminmansour Sepideh1,Gomes de Carvalho Ana Beatriz12,Medeiros Cardoso Lais13ORCID,Anselmi Caroline14,Rahimnejad Maedeh1,Dal-Fabbro Renan1ORCID,Benavides Erika5,Campos Tiago Moreira Bastos6,Borges Alexandre Luiz Souto2ORCID,Bottino Marco C.17ORCID

Affiliation:

1. Department of Cariology, Restorative Sciences and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI 48109, USA

2. Department of Dental Materials and Prosthodontics, Sao Paulo State University, Sao Jose dos Campos 12245-000, SP, Brazil

3. Department of Dental Materials and Prosthodontics, Sao Paulo State University, Araraquara 14801-903, SP, Brazil

4. Department of Morphology and Pediatric Dentistry, Sao Paulo State University, Araraquara 14801-903, SP, Brazil

5. Department of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, MI 48109, USA

6. Department of Prosthodontics and Periodontology, Sao Paulo University, Bauru 17015-351, SP, Brazil

7. Department of Biomedical Engineering, College of Engineering, University of Michigan, Ann Arbor, MI 48109, USA

Abstract

This study aimed to develop gelatin methacryloyl (GelMA)-injectable hydrogels incorporated with 58S bioactive glass/BG-doped with strontium for vital pulp therapy applications. GelMA hydrogels containing 0% (control), 5%, 10%, and 20% BG (w/v) were prepared. Their morphological and chemical properties were evaluated by scanning electron microscopy/SEM, energy dispersive spectroscopy/EDS, and Fourier transform infrared spectroscopy/FTIR (n = 3). Their swelling capacity and degradation ratio were also measured (n = 4). Cell viability (n = 8), mineralized matrix formation, cell adhesion, and spreading (n = 6) on DPSCs were evaluated. Data were analyzed using ANOVA/post hoc tests (α = 5%). SEM and EDS characterization confirmed the incorporation of BG particles into the hydrogel matrix, showing GelMA’s (C, O) and BG’s (Si, Cl, Na, Sr) chemical elements. FTIR revealed the main chemical groups of GelMA and BG, as ~1000 cm−1 corresponds to Si-O and ~1440 cm−1 to C-H. All the formulations were degraded by day 12, with a lower degradation ratio observed for GelMA+BG20%. Increasing the concentration of BG resulted in a lower mass swelling ratio. Biologically, all the groups were compatible with cells (p > 0.6196), and cell adhesion increased over time, irrespective of BG concentration, indicating great biocompatibility. GelMA+BG5% demonstrated a higher deposition of mineral nodules over 21 days (p < 0.0001), evidencing the osteogenic potential of hydrogels. GelMA hydrogels incorporated with BG present great cytocompatibility, support cell adhesion, and have a clinically relevant degradation profile and suitable mineralization potential, supporting their therapeutic potential as promising biomaterials for pulp capping.

Funder

Sao Paulo Research Foundation

National Institutes of Health

Publisher

MDPI AG

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