Biomaterial-induced mild alkaline microenvironments can positively affect osteoblast activity, contributing to bone regeneration. However, the challenge associated with silicate bioactive glasses, including melt-derived 45S5 Bioglass (45S5-Glass) and sol–gel bioactive glasses, lies in the rapid release of cations in the early stage, resulting in a significant increase in the local pH, which could induce inflammatory reactions and even hinder the process of bone regeneration. Therefore, it is crucial to develop bioactive glass with mild alkaline capacity and a moderate release rate of bioactive ions. In this study, a novel class of bioactive glass (SP-Glass, CaTiSiO₅ glass) is fabricated via a containerless melting approach to avoid phase separation and heterogeneous nucleation during the glass formation process. Compared with 45S5-Glass, the network structure of SP-Glass is more stable, resulting in a significant reduction in the pH value and release rate of bioactive ions. SP-Glass creates a favorable mildly alkaline microenvironment for promoting the osteogenic differentiation of osteoblasts while inhibiting osteoclastic activity. Moreover, SP-Glass facilitates the shift of macrophages from the proinflammatory M1 state to the anti-inflammatory M2 state and promotes bone regeneration in vivo. Therefore, containerless melting-prepared bioactive glasses with mild alkalinity combine excellent biocompatibility and bone-forming bioactivity, representing a new class of bioactive materials for tissue regeneration.

Bioglass (BG) microspheres with a constitution of CaO–SiO₂–P₂O₅ demonstrate promising applications in bone repair. It has been proved that the cerium ion incorporation in bioglass structure can provide materials with additional antioxidant, anti-inflammatory and angiogenesis functions. In this study, cerium-incorporated bioglass (Ce–BG) microspheres were prepared via a spray drying process. The effects of Ce content on the phase composition, degradation performance and in vitro bioactivity of Ce–BG microspheres were investigated. The results show that all microspheres are uniform in element distribution with relatively smooth surfaces and a high degree of sphericity. The Ce incorporation introduces a small amount of CePO₄ and CeO₂ crystalline phases. Along with the increase of Ce content, the degradation rate of Ce–BG microspheres slows down, and the effect of degradation products on the increase of environmental pH value is alleviated, and the pH value was found to be the lowest after 7 d of immersion for Ce–BG microspheres with mole ratio of Ce and Ce+Ca of 0.03:1.00 in Tris-HCl buffer. Ce–BG microspheres with different Ce content have good ability to induce apatite deposition in vitro.