4.7 Article

Tumor microenvironment self-regulation: Bimetallic metal nanozyme-derived multifunctional nanodrug for optimizable cascade catalytic reaction-synergetic anti-tumor theranostics

期刊

CHEMICAL ENGINEERING JOURNAL
卷 442, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.136096

关键词

Nanozyme; Tumor microenvironment (TME); Cascade catalytic reaction; Multimodal imaging; Synergistic therapy

资金

  1. National Natural Science Foundation of China [21674085]
  2. Postdoctoral Science Foundation of China [2020M670073ZX, 2021M702557]
  3. Natural Science Basic Research Plan in Shaanxi Province of China [2022JQ-472]
  4. Young Talent Support Program of Xi?an Science and Technology Association [095920211303]
  5. Laboratory Construction Program of Xi?an Municipal Bureau of Science and Technology [201805056ZD7CG40]
  6. Institutional Foundation of The First Affiliated Hospital of Xi?an Jiaotong University [2020QN-22]

向作者/读者索取更多资源

The construction of a well-defined nanodrug with tumor microenvironment-responsive properties has been achieved in this study. The nanodrug demonstrated tumor-specific cytotoxicity and potent antitumor efficacy, highlighting its importance in effective tumor therapy.
The tumor microenvironment (TME) responsive multimodal theranostic nanoplatforms have attracted great attentions for precision medicine. To design well-defined cascade catalytic therapy and achieve the synergistic effect of different components in a nanoplatform, herein a spindle-shaped nanodrug termed as FeCu-GOx PNzyme-MTO was constructed by in-situ growth of bimetallic metal nanozyme (FeCu PNzyme), and simultaneous encapsulation of glucose oxidase (GOx) as well as fluorescent and chemotherapeutic mitoxanthrone (MTO). Interestingly, the obtained FeCu-GOx PNzyme is able to efficiently upregulate endogenous H(2)O2 level and down-regulate acidity via inducing the catalytic decomposition of intratumoral glucose to gluconic acid and H2O2 in TME, which is benefit to the cascade catalytic reactions for chemodynamic therapy (CDT). After efficient loading of MTO, such intelligent nanozyme triggers reactive oxygen species (ROS) generation in situ with tumor stimuli, self-augment ROS level upon intrinsic photothermal-conversion efficiency (53.05%) and glutathione (GSH) depletion, and specifically TME-responsive release of MTO to achieve high chemotherapeutic efficacy and biosafety. Both in vitro cellular assays and in vivo tumor-xenograft experiments proved that the tumor-specific cytotoxicity, biodegradability and potent antitumor efficiency of nanodrug, with co-contributions from highly cytotoxic ROS generated and precise drug delivery within tumors. This work thus presents the friendly construction of biocompatible FeCu-GOx PNzyme-MTO as effective nanodrug to provided a promising strategy for a new perspective on effective tumor therapy.

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