Griess reaction-based paper strip for colorimetric/fluorescent/SERS triple sensing of nitrite.

Biosens Bioelectron

Shanghai Key Laboratory of Functional&School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, PR China. Electronic address:

Published: January 2018

AI Article Synopsis

  • This study presents a new method for detecting nitrite using a combination of colorimetric, fluorescent, and SERS (surface-enhanced Raman scattering) techniques through the assembly of gold nanorods and nanoparticles.
  • The assembly process involves the excitation of gold nanorods modified with specific molecules, leading to a color change from orange-yellow to purple, and a decrease in fluorescence upon nitrite addition, allowing for easy visual detection.
  • The method has a low detection limit for nitrite—0.05μM via colorimetry, 0.01μM via fluorescence, and 0.8nM for SERS—making it suitable for practical applications such as on-site testing of human urine and meat products.

Article Abstract

This study demonstrates a novel strategy for colorimetric/fluorescent/surface enhanced Raman scattering (SERS) triple-mode sensing of nitrite based on Griess reaction modulated gold nanorods (GNRs)-Azo-gold nanoparticles (GNPs) (GNRs-Azo-GNPs) assembly. The p-aminothiophenol (PATP)-capped GNRs (GNRs@PATP) and 1,8-diaminonaphthalene (DAP)-modified GNPs (GNPs@DAP) are first synthesized through Au-S and Au-N bonds, respectively. Upon being excited at 365nm, the dispersion of GNRs-GNPs (GNRs@PATP and GNPs@DAP) emits cyan fluorescence. Next, the addition of nitrite into the GNRs-GNPs induces the formation of GNRs-Azo-GNPs assembly, resulting in the enhancement of color and decrease of fluorescence. Therefore, the GNRs-Azo-GNPs assembly can not only be used as a naked-eye indicator of nitrite changed from orange-yellow to purple, but also as a highly selective ''fluorescence quenching'' probe due to the fluorescence resonance energy transfer (FRET) between azo-moiety and DAP. The limit of detection (LOD) for nitrite is 0.05μM by colorimetry and 0.01μM by fluorescence. Meanwhile, the GNRs-Azo-GNPs assembly possesses controllable core-satellites nanostructures and enables on-field SERS detection of nitrite with the LOD of 0.8nM. More importantly, the GNRs-GNPs sensing system can not only be used as a paper-based test strip for on-site fast screening of nitrite with a high sensitivity and selectivity, but also as a SERS substrate for reliable quantitative analysis of nitrite. This study offers a new method for on-site visual detection of nitrite in human urine and meat products, as well as provides a strategy for designing multi-mode sensing platform for various applications.

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Source
http://dx.doi.org/10.1016/j.bios.2017.08.008DOI Listing

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