Login / Signup

Titanium Sulfide Nanosheets Serve as Cascade Bioreactors for H<sub>2</sub> S-Mediated Programmed Gas-Sonodynamic Cancer Therapy.

Guangqiang LiHuali LeiYuqi YangXiaoyan ZhongFei GongYuehan GongYangkai ZhouYuqi ZhangHaibin ShiZhidong XiaoZhiqiang DongLiang Cheng
Published in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2022)
Gas-mediated sonodynamic therapy (SDT) has the potential to become an effective strategy to improve the therapeutic outcome and survival rate of cancer patients. Herein, titanium sulfide nanosheets (TiS<sub>X</sub> NSs) are prepared as cascade bioreactors for sequential gas-sonodynamic cancer therapy. TiS<sub>X</sub> NSs themselves as hydrogen sulfide (H<sub>2</sub> S) donors can burst release H<sub>2</sub> S gas. Following H<sub>2</sub> S generation, TiS<sub>X</sub> NSs are gradually degraded to become S-defective and partly oxidized into TiO<sub>X</sub> on their surface, which endows TiS<sub>X</sub> NSs with high sonodynamic properties under ultrasound (US) irradiation. In vitro and in vivo experiments show the excellent therapeutic effects of TiS<sub>X</sub> NSs. In detail, large amounts of H<sub>2</sub> S gas and reactive oxygen species (ROS) can simultaneously inhibit mitochondrial respiration and ATP synthesis, leading to cancer cell apoptosis. Of note, H<sub>2</sub> S gas also plays important roles in modulating and activating the immune system to effectively inhibit pulmonary metastasis. Finally, the metabolizable TiS<sub>X</sub> NSs are excreted out of the body without inducing any significant long-term toxicity. Collectively, this work establishes a cascade bioreactor of TiS<sub>X</sub> NSs with satisfactory H<sub>2</sub> S release ability and excellent ROS generation properties under US irradiation for programmed gas-sonodynamic cancer therapy.
Keyphrases