4.6 Article

Rapid microwave-assisted dispersive micro-solid phase extraction of mycotoxins in food using zirconia nanoparticles

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1561, Issue -, Pages 1-12

Publisher

ELSEVIER
DOI: 10.1016/j.chroma.2018.05.031

Keywords

Mycotoxins; Nano zirconia; Microwave-assisted dispersive micro-solid phase extraction; Ultra-high-performance liquid chromatography; Quadrupole time-of-flight tandem mass spectrometry

Funding

  1. National Natural Science Foundation of China [81573552]
  2. public welfare research project of Zhejiang Province [LGF18H280006]
  3. Projects for Study Abroad Returnees of Hangzhou (China)
  4. Hangzhou 131 middle-aged and young talent training plan (China)
  5. Hangzhou Social Development of Scientific Research projects [20150533B05]

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Mycotoxins are a group of secondary fungi metabolites present in foods that cause adverse effects in humans and animals. The objective of this study was to develop and validate a reliable and sensitive method to determine the presence of fumonisin B1, aflatoxin Bl, ochratoxin B, T-2 toxin, ochratoxin A and zearalenone. A rapid, effective process, which involves microwave-assisted dispersive micro-solid phase extraction (MA-D-mu-SPE), has been proposed for the extraction and detection of 6 mycotoxins in peach seed, milk powder, corn flour and beer sample matrixes, for subsequent analysis by ultra-highperformance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry (UHPLC-Q-TOF/MS). Several experimental parameters (type of dispersant, concentration of dispersant, vortex time, type of desorption solvent and pH) affecting the extraction efficiency were systematically studied and optimized. The optimum extraction conditions involved immersing 2.5 mu g/mL of nano zirconia (as dispersant) in a 5 mL sample solution. After 2 min of extraction by vigorous shaking, the target analytes were desorbed by 100 mu L of chloroform at pH 4.5. The results indicated good linearity in the range of 0.0074-3.6 mu g/mL (r >= 0.9982), low limits of detection (0.0036-0.033 mu g/kg for solid samples and 0.0022-0.017 ng/mL for beer), acceptable reproducibility (relative standard deviation (RSD%) 2.08-2.76% for retention time and 3.51-4.59% for peak area, n = 3), and satisfactory spiked recoveries (84.27-104.96%) for studied mycotoxins in sample matrixes, which demonstrated that MA-D-mu-SPE coupled with UHPLC-Q-TOF/MS is a useful tool for analysis of multi-mycotoxin. (C) 2018 Elsevier B.V. All rights reserved.

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