Novel IAC-LC-ESI-MS2 analytical set-up for ochratoxin A determination in pork

被引:14
作者
Duarte, S. C. [1 ,2 ]
Lino, C. M. [1 ]
Pena, A. [1 ]
机构
[1] Univ Coimbra, Fac Pharm, Ctr Pharmaceut Studies, Grp Hlth Surveillance, P-3000548 Coimbra, Portugal
[2] Escola Univ Vasco da Gama, Dept Vet Med, P-3040714 Coimbra, Portugal
关键词
Ochratoxin A; Pork; Mass spectrometry; Immunoaffinity columns; LC-MS/MS; IMMUNOAFFINITY COLUMN CLEANUP; MYCOTOXIN ANALYSIS; PERFORMANCE; FOOD; EXTRACTION; PRODUCTS; CEREALS; TISSUES; ACID;
D O I
10.1016/j.foodchem.2012.11.071
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
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.
引用
收藏
页码:1055 / 1061
页数:7
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