Overall, the ternary formulation showed higher peak compressive strength, significantly lower equilibrium swelling, favorable extract-based cytocompatibility, and preliminary antibacterial activity under the tested conditions, which support further investigation of this material as an antibacterial wound-dressing candidate following additional biological validation.
Abstract
The development of multifunctional hydrogels with balanced mechanical strength, swelling behavior, cytocompatibility, and antibacterial performance remains a key challenge in wound-dressing applications. In this study, a glyoxal-crosslinked acacia gum (AG) hydrogel reinforced with graphene oxide (GO) nanosheets and zinc ferrite (ZnFe₂O₄) nanoparticles was developed as a tri-component nanocomposite system. The incorporation of GO and ZnFe₂O₄ within the crosslinked AG network produced formulation-dependent structural and functional changes. The peak compressive strength was numerically higher in the final formulation (0.682 vs. 0.173 MPa), while the equilibrium swelling ratio decreased significantly from 463% to 292%. Rheological analysis showed elastic-dominant behavior, indicating stable gel-like viscoelastic properties under the tested conditions. Biological evaluation demonstrated high extract-based cytocompatibility toward MG-63 cells. Furthermore, preliminary antibacterial testing showed activity against
Staphylococcus aureus
and
Escherichia coli
, with inhibition values of 99.0% and 93.4%, respectively, in the representative CFU dataset. The proposed membrane-perturbation and oxidative-stress-related mechanisms are literature-supported and were not directly validated in this study. Overall, the ternary formulation showed higher peak compressive strength, significantly lower equilibrium swelling, favorable extract-based cytocompatibility, and preliminary antibacterial activity under the tested conditions. These findings support further investigation of this material as an antibacterial wound-dressing candidate following additional biological validation.
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