A universal multi-wavelength fluorescence polarization immunoassay for multiplexed detection of mycotoxins in maize

Biosens Bioelectron. 2016 May 15:79:258-65. doi: 10.1016/j.bios.2015.12.033. Epub 2015 Dec 17.

Abstract

Multi-analyte immunoassays have attracted increasing attention due to their short assay times, low sample consumption, and reduced detection costs per assay. In this work, we describe a homologous and high-throughput multi-wavelength fluorescence polarization immunoassay (MWFPIA) for the multiplexed detection of mycotoxins. Three typical Fusarium mycotoxins, deoxynivalenol (DON), T-2 toxin and fumonisin B1 (FB1), were labeled with different dyes. Tracers and specific monoclonal antibodies (mAbs) were employed in the MWFPIA to simultaneously detect the three mycotoxins. Under optimal conditions, the limits of detection using MWFPIA were 242.0 μg kg(-1) for DON, 17.8 μg kg(-1) for T-2 toxin and 331.5 μg kg(-1) for FB1, providing sufficient sensitivity to meet the action levels of these three contaminants in maize as set by the European Union. The use of a methanol/water (2:3, v/v) mixture for sample pretreatment allowed recoveries ranging from 76.5-106.3%, with coefficients of variation less than 21.7%. The total time of analysis, including sample preparation, was less than 30 min. Twenty naturally contaminated maize samples were tested using MWFPIA and HPLC-MS/MS, with correlation coefficients (R(2)) of 0.97 for DON and 0.99 for FB1. By changing the targets of interest, homologous MWFPIA, a method with high sensitivity, a simple procedure and a short analysis time, can easily be extended to other chemical contaminants. Thus, MWFPIA represents a versatile strategy for food safety analysis.

Keywords: Fluorescence polarization immunoassay; Homologous; Maize; Multi-wavelength; Multiplexed detection; Mycotoxins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biosensing Techniques*
  • Chromatography, High Pressure Liquid
  • Fluorescence
  • Fluorescence Polarization Immunoassay / methods
  • Food Contamination
  • Fumonisins / isolation & purification*
  • Humans
  • Limit of Detection
  • T-2 Toxin / isolation & purification*
  • Tandem Mass Spectrometry
  • Trichothecenes / isolation & purification*
  • Zea mays / microbiology

Substances

  • Fumonisins
  • Trichothecenes
  • fumonisin B1
  • T-2 Toxin
  • deoxynivalenol