<i>γ</i>‐Fe<sub>2</sub>O<sub>3</sub> Loading Mitoxantrone and Glucose Oxidase for pH‐Responsive Chemo/Chemodynamic/Photothermal Synergistic Cancer Therapy
Zhihao Zhong, Chao Liu, Yatao Xu, Weili Si, Wenjun Wang, Liping Zhong, Yongxiang Zhao, Xiaochen Dong
Abstract
Abstract Traditional cancer therapy is limited by poor prognosis and risk of recurrence. Emerging therapies offer alternatives to these problems. In addition, synergistic therapy can combine the advantages of multiple therapies to eliminate cancer cells while attenuating damage to normal tissues. Herein, a theranostic nanoplatform based on the chemotherapeutic drug mitoxantrone (MTO) and glucose oxidase (GOx) co‐loaded γ ‐Fe 2 O 3 nanoparticles (MTO‐GOx@ γ ‐Fe 2 O 3 NPs) is designed and prepared to realize photoacoustic imaging‐guided chemo/chemodynamic/photothermal (CT/CDT/PTT) synergistic cancer therapy. With a particle size of about 86.2 nm, the synthesized MTO‐GOx@ γ ‐Fe 2 O 3 NPs can selectively accumulate at tumor sites by enhanced permeability and retention (EPR) effects. After entering cancer cells by endocytosis, MTO‐GOx@ γ ‐Fe 2 O 3 NPs decompose into Fe 3+ ions and release cargo because of their pH‐responsive characteristic. As a Food and Drug Administration (FDA)‐approved chemotherapy drug, MTO shows strong DNA disruption ability and satisfying photothermal conversion ability under laser irradiation for photothermal therapy. Simultaneously, GOx catalyzes the decomposition of glucose and generates hydrogen peroxide (H 2 O 2 ) to enhance the chemodynamic therapy efficiency. In vitro and in vivo experiments reveal that MTO‐GOx@ γ ‐Fe 2 O 3 NPs possess a significant synergistic therapeutic effect in cancer treatment.