Magnesium/sodium co-doping enhances hemocompatibility and antibacterial properties of hydroxyapatite bone graft
Human bone is primarily composed of hydroxyapatite (HA) with magnesium (Mg) and sodium (Na) as trace elements. This study aims to investigate the individual and combined effects of Mg and Na doping in HA to better mimic human bone and to evaluate its biological activity. Mg–Na–HA was synthesized by chemical precipitation and characterized by X-ray diffraction, transmission electron microscopy, X-ray fluorescence, and Fourier-transform infrared spectroscopy. An assay using simulated body fluid was performed to examine ion release and the materials’ potential charge. Biological assessments were performed using MC3T3-E1 cells for cytotoxicity and osteopontin (OPN) protein level assessments, as well as antibacterial and hemocompatibility evaluations. Characterizations confirmed the successful formation of HA with a hexagonal structure, particle size of approximately 100 nm, and the presence of Mg and Na in the doped materials. Antibacterial assays demonstrated that Mg–Na–HA exhibited the strongest antimicrobial activity toward Staphylococcus aureus and Escherichia coli, attributed to the combined ionic effects. Assessments using MC3T3-E1 cells confirmed the material’s biocompatibility and showed that Mg–Na–HA significantly increased OPN protein level relative to HA. Moreover, hemocompatibility testing revealed that all co-doped materials induced <20% hemolysis, with Na–HA and Mg–Na– HA showing excellent compatibility, inducing <5% hemolysis. Mg–Na–HA is biocompatible and shows strong potential as a bone graft material, offering enhanced osteogenic and antibacterial properties to improve bone regeneration and prevent infections.
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