4.7 Article

Nanoenzyme Reactor-Based Oxidation-Induced Reaction for Quantitative SERS Analysis of Food Antiseptics

Journal

BIOSENSORS-BASEL
Volume 12, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/bios12110988

Keywords

nanoenzyme reactor; oxidation-induced reaction; SERS; food antiseptics

Funding

  1. National Natural Science Foundation of China
  2. special project of the Marine and Fishery Department of Xiamen
  3. [22004105]
  4. [19CZB001HJ03]

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In this study, a double wing with one body strategy was developed to establish a reduced food antiseptic sensing method using shell-isolated colloidal plasmonic nanomaterials. The cascade reactor generated center dot OH with high oxidative capacity toward acid preservatives, and the introduction of the signal molecule DA improved the sensitivity of the analysis. Additionally, the stable shell-isolated structure enabled a reproducible and quantitative SERS analysis method.
Nanoenzyme reactors based on shell-isolated colloidal plasmonic nanomaterials are well-established and widely applied in catalysis and surface-enhanced Raman scattering (SERS) sensing. In this study, a double wing with one body strategy was developed to establish a reduced food antiseptic sensing method using shell-isolated colloidal plasmonic nanomaterials. Gold nano particles (Au NPs) were used to synthesize the colloidal plasmonic nanomaterials, which was achieved by attaching ferrous ions (Fe2+), ferric ions (Fe3+), nitroso (NO-) group, cyanogen (CN-) group, and dopamine (DA) via coordinative interactions. The oxidation-induced reaction was utilized to generate center dot OH following the Fe2+-mediated Fenton reaction with the shell-isolated colloidal plasmonic nanomaterials. The center dot OH generated in the cascade reactor had a high oxidative capacity toward acid preservatives. Importantly, with the introduction of the signal molecule DA, the cascade reactor exhibited also induced a Raman signal change by reaction with the oxidation product (malondialdehyde) which improved the sensitivity of the analysis. In addition, the stable shell-isolated structure was effective in realizing a reproducible and quantitative SERS analysis method, which overcomes previous limitations and could extend the use of nanoenzymes to various complex sensing applications.

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