Abstract
It is urgent to develop an alternative dynamic therapy-based method to overcome the limited efficacy of traditional therapy methods for bladder cancer and the damage caused to patients. Sonodynamic therapy (SDT) has the advantages of high tissue penetration, high spatiotemporal selectivity, and being non-invasive, representing an emerging method for eradicating deep solid tumors. However, the effectiveness of SDT is often hindered by the inefficient production of reactive oxygen species and the nondegradability of the sonosensitizer. To improve the anti-tumor effect of SDT on bladder cancer, herein, a BP-based heterojunction sonosensitizer (BFeSe(2)) was synthesized by anchoring FeSe(2) onto BP via P-Se bonding to enhance the stability and the effect of SDT. As a result, BFeSe(2) showed great cytotoxicity to bladder cancer cells under ultrasound (US) irradiation. BFeSe(2) led to a notable inhibition effect on tumor growth in subcutaneous tumor models and orthotopic tumor models under US irradiation. In addition, BFeSe(2) could also enhance T2-weighted magnetic resonance imaging (MRI) to achieve monitoring and guide treatment of bladder cancer. In general, BFeSe(2) sonosensitizer integrates MRI functions for precise treatment, promising great clinical potential for the theranostics of bladder cancer.