4.4 Article

Single-Laboratory Validation for the Determination of Aflatoxin B1, B2, G1, and G2 in Foods Based on Immunoaffinity Column and Liquid Chromatography with Postcolumn Derivatization and Fluorescence Detection

Journal

FOOD ANALYTICAL METHODS
Volume 6, Issue 1, Pages 36-44

Publisher

SPRINGER
DOI: 10.1007/s12161-012-9417-3

Keywords

Aflatoxin; HPLC; Immunoaffinity column; Validation

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This study presents a method validation procedure for the determination of aflatoxin B-1, B-2, G(1), and G(2) in hazelnut, hazelnut paste, walnut, peanut, pistachio, corn, and wheat. The method consisting of clean-up with immunoaffinity column, high performance liquid chromatography with postcolumn derivatization and fluorescence detection was validated in accordance with Commission Regulation 2004/882/EC. The selectivity, linearity, decision limit, detection capability, detection and quantification limits, precision, recovery, ruggedness, and measurement uncertainty of the method were determined. The limit of detection and limit of quantification values (mu g/kg) were: aflatoxin B-1, 0.02, 0.07; aflatoxin B-2, 0.01, 0.02; aflatoxin G(1), 0.02, 0.07; and aflatoxin G(2), 0.01, 0.03. The relative standard deviation values for the repeatability and within-laboratory reproducibility were below 4 and 5 %, respectively. The recovery values of the spiked samples ranged from 80 to 105 %. These results complied with minimum performance criteria established by regulation 2006/401/EC. Therefore, the procedure can be implemented for the routine analysis of aflatoxins in the studied matrices.

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