Analytical Chemistry · 2014 · 263 citations · 27 references
PharmacyToxicologyAnalytical ToxicologyDiagnostic ToxicologyMycotoxicologyBioanalytical Method ValidationEnzyme-linked Immunosorbent AssayImmunoassay AnalysisImmunoassay DevelopmentLateral Flow ImmunoassaysMycotoxinsAflatoxin ContaminationAflatoxin DetectionAnalytical Methods For MycotoxinsDeoxynivalenol ContaminationImmunoassay Cross-reactivityMultiplex Lateral Flow AssaysMycotoxin QuantificationZearalenone Contamination
A new lateral flow immunoassay (LFA) is proposed for qualitative and/or semiquantitative determination of aflatoxin B1 (AFB1), zearalenone (ZEA), deoxynivalenol (DON), and their analogues (AFs, ZEAs, DONs) in cereal samples. Each of the mycotoxin specific antibody was class specific and there was no cross reactivity to other groups of compounds. The visual limits of detection (vLOD) of the strip were 0.03, 1.6, and 10 μg/kg for AFB1, ZEA and DON, respectively. The calculated limits of detection (cLOD) were 0.05, 1, and 3 μg/kg, respectively. Meanwhile the cutoff values were achieved at 1, 50, and 60 μg/kg for AFB1, ZEA and DON, respectively. Recoveries ranged from 80% to 122% and RSD from 5% to 20%. Both the vLOD and cLOD for the three mycotoxins were lower than the EU maximum levels. Analysis of naturally contaminated maize samples resulted in a good agreement between the multiplex LFA and LC-MS/MS (100% for DONs and AFs, and 81% for ZEAs). Careful analysis of the results further explained the general overestimation of LFA compared to chromatographic methods for quantification of mycotoxins.
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Human exposure to mycotoxins and their masked forms through cereal-based foods in Belgium
Marthe De Boevre, Liesbeth Jacxsens, Carl Lachat et al. · Toxicology Letters · 2013 · 158 citations · Full text
Pharmacy, Food Science, Toxicology +13