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This work proposes an effective design of bioactive 3D-printed Ti-6Al-4V scaffold with the CaO-MgO-SiO 2 glass-ceramic coating to realize a comparable elastic modulus of bone tissue and boost osteogenic differentiation. The improved elastic modulus and stiffness of Ti alloy were achieved via effectively increasing surface area of Ti alloy to reduce stress shielding effect. A hydrophilic surface and bioactive glass-ceramic coating were conducted via chemical etching and heat-treatment under argon atmosphere to enhance cells attachment and boost cell proliferation and osteogenic differentiation. The expression of osteogenic genes in bioactive CaO-MgO-SiO 2 glass-ceramic was evaluated through ALP, OPN, Runx2, and Col1A1 gene markers to explore the mechanism of superior osteogenic differentiation. Significant increase in OPN expression level confirmed the effect of CaO-MgO-SiO 2 coating for the enhancement of osteogenic bioactivity. This work provides a feasible approach through surface etching and bioactive CaO-MgO-SiO 2 glass-ceramic coating on the Ti alloy surface to enhance bioactivity and osteogenesis. [Display omitted] • A compatible bone tissue of 3D-printed Ti-6Al-4V scaffold with the novel bioactive CaO-MgO-SiO 2 glass-ceramic coating. • A superior surface modification to enhance cells attachment and boost cell proliferation and osteogenic differentiation. • This work provides a feasible approach on the Ti-alloy surface to enhance bioactivity and osteogenesis. [ABSTRACT FROM AUTHOR]

[Display omitted] • Propose a high porosity bioglass preparation method. • Finding bioglass enhances mild magnetothermal therapy. • The mechanism relies on calcium ions during glass degradation. • The composite scaffold has superior biosafety and osteogenic effect. Bone defects and tumor cell residues after bone tumor resection have always been a challenge. We tried to investigate a kind of bioglass with both bone repair and tumor killing capability to achieve two birds with one stone. We used a Sol-Gel method to prepare the high porous magnetic bioglass (MBG) and then compounded the MBG with calcium sulfate (CS) bone cement to form the composite scaffold (CS-MBG). We found that the CS-MBG could reach about 43 °C under the condition of magnetic field in vitro. Under this condition, CS-MBG would release Ca2+ resulting in the cell death of calcium overload. Meanwhile, the suitable pH and osteogenic activity of CS-MBG can promote the postoperative bone repair and inhibit the growth of bone tumors. Our work has innovatively designed a magnetic bioglass and verified its mechanism of synergistic hyperthermia against tumor, providing a new idea for the treatment of tumor bone defects with magnetic bioglass. [ABSTRACT FROM AUTHOR]