Three‐dimensional‐printed MPBI@β‐TCP scaffold promotes bone regeneration and impedes osteosarcoma under near‐infrared laser irradiation

Abstract

AbstractBeta‐tricalcium phosphate (β‐TCP) is considered as one of the most promising biomaterials for bone reconstruction. This study generated a functional molybdenum disulfide (MoS2)/polydopamine (PDA)/−bone morphogenetic protein 2 (BMP2)‐insulin‐like growth factor‐1 (IGF‐1) coating on the β‐TCP scaffold and analyzed the outcomes. The MoS2/PDA‐BMP2‐IGF‐1@β‐TCP (MPBI@β‐TCP) scaffold was prepared by 3D printing and physical adsorption, followed by characterization to validate its successful construction. The in vitro osteogenic effect of the MPBI@β‐TCP scaffold was evaluated. It was found that MPBI@β‐TCP augmented the adhesion, diffusion and proliferation of mesenchymal stem cells (MSCs). The alkaline phosphatase (ALP) activity, collagen secretion and extracellular matrix (ECM) mineralization along with the expression of Runx2, ALP and OCN were also enhanced in the presence of MPBI@β‐TCP. Additionally, MPBI@β‐TCP stimulated endothelial cells to secrete VEGF and promoted capillary‐like tubule formation. We then confirmed the biocompatibility of MPBI@β‐TCP to macrophages and its anti‐inflammatory effects. Furthermore, under near‐infrared (NIR) laser irradiation, MPBI@β‐TCP produced photothermal effect to not only kill MG‐63 osteosarcoma cells, but also enhance bone regeneration in vivo with biosafety. Overall, this work demonstrates that 3D‐printed MPBI@β‐TCP with enhanced osteogenic activity under NIR laser irradiation has a vast potential in the field of tissue defects.