Journal
FOOD CHEMISTRY
Volume 138, Issue 2-3, Pages 1055-1061Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.foodchem.2012.11.071
Keywords
Ochratoxin A; Pork; Mass spectrometry; Immunoaffinity columns; LC-MS/MS
Funding
- Portuguese Fundacao para a Ciencia e Tecnologia (FCT) [SFRH/BD/37409/2007, vPEst-OE/SAU/UI0177/2011]
- Fundação para a Ciência e a Tecnologia [SFRH/BD/37409/2007] Funding Source: FCT
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A reliable exposure assessment of mycotoxin contamination relies on their unambiguous identification and accurate quantification. With such purpose, a new analytical methodology was developed for evaluation of ochratoxin A (OTA) contamination in pork. Briefly OTA extraction from minced muscle samples involved the use of acidified methanol, ultrasound treatment and centrifugation, followed by an immunoaffinity column (IAC) clean-up step before mass spectrometric detection (precursor-to-fragment transitions: m/z 404 -> m/z 358 and m/z 404 -> m/z 386) in positive ESI mode using SRM scanning. The method combines green chemistry principles (e.g. absence of highly toxic solvents commonly used in this matrix) with a validation according to the guidelines laid down by the 2002/657/EC European Decision parameters: recoveries varied between 98.5% and 100.6%, limits of detection (LOD) and quantification (LOQ) were estimated at 0.06 and 0.19 mu g/kg, whereas decision limit (CC alpha) and detection capability (CC beta) were 0.01 and 0.50 mu g/kg, respectively. The proposed analytical set-up was successfully applied to twenty pork samples commercially acquired. (C) 2012 Elsevier Ltd. All rights reserved.
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