One-pot synthesis of AuPd@Fe<sub>x</sub>O<sub>y</sub> nanoagent with the activable Fe species for enhanced Chemodynamic-photothermal synergetic therapy.

Sun, Yanhong; Chen, Hongda; Huang, Ying; Xu, Fengqin; Liu, Guifeng; Ma, Lina; Wang, Zhenxin · Biomaterials · 2021

basic_science · Level V

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Abstract

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@Fe<sub>x</sub>O<sub>y</sub> core-shell nanoparticles (Au@Fe<sub>x</sub>O<sub>y</sub> NPs, AuRu@Fe<sub>x</sub>O<sub>y</sub> NPs, AuPt@Fe<sub>x</sub>O<sub>y</sub> NPs and AuPd@Fe<sub>x</sub>O<sub>y</sub> NPs) are one-pot constructed by a simply redox self-assembly strategy. As a typical example, AuPd@Fe<sub>x</sub>O<sub>y</sub> NPs are applied for oncotherapy. Compared to their crystalline counterparts (e.g., AuPd@c-Fe<sub>2</sub>O<sub>3</sub> nanocrystals (NCs)), AuPd@Fe<sub>x</sub>O<sub>y</sub> NPs with the metastable Fe<sub>x</sub>O<sub>y</sub> shell can be activated by a small amount of NaBH<sub>4</sub> to obviously enhance the production of ·OH in subsequent Fenton reaction (these activated products are termed as r-AuPd@Fe<sub>x</sub>O<sub>y</sub> NPs). In addition, a favorable photothermal effect (63.5% photothermal conversion efficiency) of r-AuPd@Fe<sub>x</sub>O<sub>y</sub> NPs can further promote the ·OH generation. Moreover, r-AuPd@Fe<sub>x</sub>O<sub>y</sub> NPs also show a pH-responsive T<sub>1</sub>-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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