4.8 Article

One-pot synthesis of AuPd@FexOy nanoagent with the activable Fe species for enhanced Chemodynamic-photothermal synergetic therapy

Journal

BIOMATERIALS
Volume 274, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2021.120821

Keywords

Fenton reaction; Metastable Fe-based oxide; Chemodynamic-photothermal synergetic; therapy; Nanotheranostic agent

Funding

  1. Department of Science and Technology of Jilin Province [20190701052 GH]
  2. National Natural Science Foundation of China [21775145]

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The study demonstrates that facile fabrication of Fe-based nanotheranostic agents with enhanced Chemodynamic therapy effects and multiple functions is achievable using a simple redox self-assembly strategy. The core-shell nanoparticles exhibited enhanced production of center dot OH in Fenton reaction when activated, along with a favorable photothermal effect and pH-responsive properties. This work provides an attractive route to prepare versatile nanotheranostic agents for oncotherapy.
Facile fabrication of Fe-based nanotheranostic agents with the enhanced Chemodynamic therapy (CDT) effect and multiple functions is important for oncotherapy. In this report, noble-metal@FexOy core-shell nanoparticles (Au@FexOy NPs, AuRu@FexOy NPs, AuPt@FexOy NPs and AuPd@FexOy NPs) are one-pot constructed by a simply redox self-assembly strategy. As a typical example, AuPd@FexOy NPs are applied for oncotherapy. Compared to their crystalline counterparts (e.g., AuPd@c-Fe2O3 nanocrystals (NCs)), AuPd@FexOy NPs with the metastable FexOy shell can be activated by a small amount of NaBH4 to obviously enhance the production of center dot OH in subsequent Fenton reaction (these activated products are termed as r-AuPd@FexOy NPs). In addition, a favorable photothermal effect (63.5% photothermal conversion efficiency) of r-AuPd@FexOy NPs can further promote the center dot OH generation. Moreover, r-AuPd@FexOy NPs also show a pH-responsive T1-weighted MRI contrast property, CT imaging capacity and the function of regulating tumor microenvironment. This work presents an attractive route to prepare versatile nanotheranostic agents.

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