Abstract

Bone implants for clinical application should be endowed with antibacterial activity , biocompatibility, and even osteogenesis-promoting properties. In this work, metal–organic framework (MOF) based drug delivery platform was used to modify titanium implants for improved clinical applicability. Methyl [email protected] Imidazolate Framework-8 ( [email protected] ) was immobilized on the polydopamine (PDA) modified titanium. The sustainable release of the Zn 2+ and MV causes substantial oxidative damage to Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). The increased reactive oxygen species (ROS) significantly up-regulates the expression of oxidative stress and DNA damage response genes. Meanwhile, the structural disruption of lipid membranes caused by the ROS, the damage caused by Zinc active sites and the damage accelerated by the MV are both involved in inhibiting bacterial proliferation. The up-regulated expression of the osteogenic-related genes and proteins indicated that the [email protected] could effectively promote the osteogenic differentiation of the human bone mesenchymal stem cells (hBMSCs). RNA sequencing and Western blotting analysis revealed that the [email protected] coating activates the canonical Wnt/β-catenin signaling pathway through the regulation of tumor necrosis factor (TNF) pathway, thereby promoting the osteogenic differentiation of the hBMSCs. This work demonstrates a promising application of the MOF-based drug delivery platform in bone tissue engineering.