Cascaded Antitumor Therapy Excited by Dual Nanozymes Based on Energy Restriction and Photocatalysis

In nanocatalytic medicine, drugs can be transformed into toxic components through highly selective and highly specific catalytic reactions in the tumor microenvironment, avoiding toxic side effects on normal tissues. Due to the coexistence of Ce 3+ and Ce 4+, CeO 2 is endowed with dual nanozyme activities. Herein, CeO 2 nanoparticles served as templates to construct a biomimetic nanodrug delivery system (C/CeO 2 @M) by electrostatic adsorption of carbon quantum dots (CQDs) and coating a homologous tumor cytomembrane. After homologous targeting to tumors, the CQDs emitted 350–600 nm light under 660 nm laser irradiation by upconversion luminescence, which caused a CeO 2 -mediated photocatalytic reaction to generate reactive oxygen species. The catalase-like activity of CeO 2 -enabled converting excess H 2 O 2 to O 2, which not only alleviated tumor hypoxia and promoted intratumor drug delivery but also provided substrates for subsequent catalytic reactions. Meanwhile, the phosphatase activity of CeO 2 could consume adenosine triphosphate (ATP) to block the energy supply for tumor cells, thus limiting cell proliferation and metastasis. The strategy of energy restriction and photocatalysis of dual nanozyme stimulation offers great potentials in enhancing drug penetration and eradicating solid tumors.