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Antibacterial and Bioactive 3D-Printed Hexagonal Boron Nitride Incorporated Gelatin/Methyl Cellulose Scaffolds for Bone Tissue Engineering Applications

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Volume Title

dc.identifier.issn

1438-7492
1439-2054

dc.identifier.doi

10.1002/mame.70198

dc.identifier.other

dc.description.volume

311

dc.description.issue

2

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WILEY-V C H VERLAG GMBH

DOI

10.1002/mame.70198
10.1002/mame.70198

Abstract

In this study, we fabricated 3D-printed scaffolds based on gelatin (GEL), methylcellulose (MC), and varying concentrations of hexagonal boron nitride h-BN nanoplatelets. The GEL/MC/BN hydrogel inks were prepared with optimized rheological properties for extrusion-based 3D printing and chemically crosslinked using EDC/NHS. The printability, pore fidelity, and strut geometry of the scaffolds were characterized, revealing consistent architectures with adequate mechanical robustness. FTIR, swelling behavior, degradation, and contact angle measurements demonstrated successful h-BN nanoplatelet incorporation and favorable hydrogel network stability. Mechanical tests indicated that h-BN nanoplatelet addition preserved the compressive modulus and flexibility. In vitro assays using MC3T3-E1 pre-osteoblasts demonstrated that the scaffolds supported % cell viability and proliferation. Remarkably, h-BN nanoplatelet incorporation triggered calcium phosphate formation both in SBF and Alizarin Red staining studies. FTIR and SEM-EDS analysis demonstrated that apatite formation was triggered with h-BN. Apatite formation is possibly due to the negative charge of h-BN nanoplatelets in the medium which triggered calcium phosphate deposition. Antibacterial testing against Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus revealed a significant, species-specific bactericidal effect at >= 5% BN content, especially against Gram-negative strains. Overall, these findings indicate the potential of h-BN-incorporated GEL/MC scaffolds as a promising platform for infection-resistant, cytocompatible, and structurally stable bone grafts.

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