Publication | Open Access
Self‐Supply of O<sub>2</sub> and H<sub>2</sub>O<sub>2</sub> by a Nanocatalytic Medicine to Enhance Combined Chemo/Chemodynamic Therapy
362
Citations
28
References
2019
Year
Combined chemo/chemodynamic therapy is a promising strategy to achieve an improved anticancer effect. However, the hypoxic microenvironment and limited amount of H<sub>2</sub>O<sub>2</sub> in most solid tumors severely restrict the efficacy of this treatment. Herein, the construction of a nanocatalytic medicine, CaO<sub>2</sub>@DOX@ZIF-67, via a bottom-up approach is described. CaO<sub>2</sub>@DOX@ZIF-67 simultaneously supplies O<sub>2</sub> and H<sub>2</sub>O<sub>2</sub> to achieve improved chemo/chemodynamic therapy. In the weakly acidic environment within tumors, CaO<sub>2</sub>@DOX@ZIF-67 is broken down to rapidly release the Fenton-like catalyst Co<sup>2+</sup> and the chemotherapy drug doxorubicin (DOX). The unprotected CaO<sub>2</sub> reacts with H<sub>2</sub>O to generate both O<sub>2</sub> and H<sub>2</sub>O<sub>2</sub>. The generated O<sub>2</sub> relieves the hypoxia in the tumor and further improve the efficacy of DOX. Meanwhile, the generated H<sub>2</sub>O<sub>2</sub> reacts with Co<sup>2+</sup> ions to produce highly toxic •OH through a Fenton-like reaction, resulting in improved chemodynamic therapy.
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