Journal
JOURNAL OF CHROMATOGRAPHY A
Volume 1292, Issue -, Pages 111-120Publisher
ELSEVIER
DOI: 10.1016/j.chroma.2012.10.071
Keywords
Salting-out liquid-liquid extraction; LC-MS/MS; Pig urine; Mycotoxins; Biomarker
Funding
- Belgian Federal Science Policy Office
- Marie Curie Actions from the European Commission
- Linking Sino-European Universities Through Mobility (LISUM)
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Direct determination of urinary mycotoxins is a better approach to assess individual's exposure than the indirect estimation from average dietary intakes. In this study, a new analytical method was developed and validated for simultaneous analysis of aflatoxin B-1, deoxynivalenol, fumonisin B-1, ochratoxin A, zear-alenone and T2 toxin and their metabolites in pig urine. In total 12 analytes were selected. A salting-out assisted liquid-liquid extraction procedure was used for sample preparation. High performance liquid chromatography/tandem mass spectrometry was used for the separation and detection of all the analytes. The extraction recoveries were in a range of 70-108%, with the intra-day relative standard deviation and inter-day relative standard deviation lower than 25% for most of the compounds at 3 different concentration levels. Meanwhile the method bias for all the analytes did not exceed 20%. The limits of quantification ranged from 0.07 ng mL(-1) for ochratoxin A to 3.3 ng mL(-1) for deoxynivalenol. Matrix effect was evaluated in this study and matrix-matched calibration was used for quantification. The developed method was also validated for human urine as an extension of its application. Finally, the developed method was applied in a pilot study to analyze 28 pig urine samples. Deoxynivalenol, aflatoxin B-1, fumonisin B-1 and ochratoxin A were detected in these samples. (C) 2012 Elsevier B.V. All rights reserved.
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