Photoactivated H<sub>2</sub> Nanogenerator for Enhanced Chemotherapy of Bladder Cancer.
basic_science · Level V
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- Record sourced from PubMed, PMID 32479062.
- Also identified by DOI 10.1021/acsnano.0c01300.
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Abstract
Hydrogen gas can mitigate oxidative stress in many diseases and is regarded to be safe and free of side effects. Inspired by a metalloenzyme in a variety of microorganisms, here, we propose a photoactivated H<sub>2</sub> nanogenerator that comprises a fluorinated chitosan (FCS), a chemotherapeutic drug (gemcitabine, GEM), and a catalyst of H<sub>2</sub> production ([FeFe]TPP) that can form self-assembled [FeFe]TPP/GEM/FCS nanoparticles (NPs). The [FeFe]TPP/GEM/FCS NPs exhibit excellent transmucosal and tumor cell penetration capacities after intravesical instillation into the bladder and can efficiently produce H<sub>2</sub> gas <i>in situ</i> upon 660 nm laser irradiation, which significantly enhances the efficacy of hydrogen chemotherapy of cancer <i>in vitro</i> and <i>in vivo</i>. Moreover, we discover that H<sub>2</sub> gas in hydrogen chemotherapy can inhibit mitochondrial function, hinder ATP synthesis, and cause a reduction of the P-gp efflux pump function, which finally attenuates P-gp protein drug transport capacity in cancer cells. This photoactivated H<sub>2</sub> evolution <i>in situ</i> to improve the therapeutic efficacy of chemotherapy of bladder cancer may present an effective hydrogen chemotherapy strategy for cancer treatment.
Medical subject headings
- Chitosan
- Nanoparticles
- Urinary Bladder Neoplasms