Defective S‐TiO2−x/CeO2 Heterojunction for Mutual Reinforcing Chemodynamic/Sonocatalytic Antibacterial Therapy and Sonoelectric/Ion‐Activated Bone Regeneration

Abstract

AbstractSonocatalysis and chemodynamics have attracted widespread attention in antibacterial therapy. The transfer efficiency of electrons plays an important role in sonocatalysis and chemodynamics, and how to regulate electron transfer and achieve mutual‐reinforcement between sonocatalysis and chemodynamic to achieve efficient antibacterial therapy is a difficult problem. Here, this study develops a defective S‐doped TiO2 and CeO2 heterojunction(S‐TiO2−x/CeO2）sonosensitizer that can enhance chemodynamic therapy by regulating valence transitions of CeIII/CeIV by sonoelectrons, and enhancing sonocatalytic therapy by creating heterojunctions to accelerate the transfer of interface electron, thereby achieving mutual reinforcement of sonocatalysis and chemodynamic. It could kill 99.3% of S. aureus under ultrasound (US) irradiation . Due to the presence of mixed valence states CeIII/CeIV in CeO2, S‐TiO2−x/CeO2 could be as oxy‐substrates. Ce4+ can deplete glutathione and reacts with H2O2 in bacteria to produce reactive oxygen species (ROS). These activities combines with ROS generated from sonocatalysis, resulting in bacterial death. Meanwhile, the electrical signal generated by S‐TiO2−x/CeO2 under US stimulation and the cerium ions could activate the Wnt/β‐catenin signaling pathway to induce hBMSCs to differentiate into osteoblast. S‐TiO2−x/CeO2 successfully treats osteomyelitis under US irradiation by effectively clearing infection, suppressing inflammatory, and promoting bone regeneration, and it provides effective treatment for patients with deep infection.