4.8 Article

Tumor-Specific Endogenous FeII-Activated, MRI-Guided Self-Targeting Gadolinium-Coordinated Theranostic Nanoplatforms for Amplification of ROS and Enhanced Chemodynamic Chemotherapy

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 12, 期 13, 页码 14884-14904

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c00970

关键词

tumor-specific endogenous Fe-II ions; coordination nanoplatforms; chemodynamic chemotherapy; tumor self-targeting; MRI imaging

资金

  1. Fundamental Research Funds for the Central Universities [20720190150]
  2. Health Commission of Jiangsu Province of China [H2018070]

向作者/读者索取更多资源

Low drug payload and lack of tumor-targeting for chemodynamic therapy (CDT) result in an insufficient reactive oxygen species (ROS) generation, which seriously hinders its further clinical application. Therefore, how to improve the drug payload and tumor targeting for amplification of ROS and combine it with chemotherapy has been a huge challenge in CDT. Herein, methotrexate (MTX), gadolinium (Gd), and artesunate (ASA) were used as theranostic building blocks to be coordinately assembled into tumor-specific endogenous Fe-II-activated and magnetic resonance imaging (MRI)-guided self-targeting carrierfree nanoplatforms (NPs) for amplification of ROS and enhanced chemodynamic chemotherapy. The obtained ASA-MTX-Gd-III NPs exhibited extremely high drug payload (similar to 96 wt %), excellent physiological stability, long circulating ability (half-time: similar to 12 h), and outstanding tumor accumulation. Moreover, ASA-MTX-Gd-III NPs could be specifically uptaken by tumor cells via folate (FA) receptors and subsequently be disassembled via lysosomal acidity-induced coordination breakage, resulting in drug burst release. Most strikingly, the produced ASA could be catalyzed by tumor-specific overexpressed endogenous Fe-II ions to generate sufficient ROS for enhancing the main chemodynamic efficacy, which could exert a synergistic effect with the assistant chemotherapy of MTX. Interestingly, ASA-MTX-Gd-III NPs caused a lower ROS generation and toxicity on normal cell lines that seldom expressed endogenous Fe-II ions. Under MRI guidance with assistance of self-targeting, significantly superior synergistic tumor therapy was performed on FA receptor-overexpressed tumor-bearing mice with a higher ROS generation and an almost complete elimination of tumor. This work highlights ASA-MTX-Gd-III NPs as an efficient chemodynamic-chemotherapeutic agent for MRI imaging and tumor theranostics.

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