Simultaneous Immunoaffinity Column Cleanup and HPLC Analysis of Aflatoxins and Ochratoxin A in Spanish Bee Pollen

Bee pollen is a major substrate for mycotoxins growth when no prompt and adequate drying is performed by the beekeeper after collection by bees. Regulatory limits for aflatoxins and ochratoxin A are currently in force in the European Union for a rising list of foodstuffs, but not for this. An immuno...

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Bibliographic Details
Published in:Journal of agricultural and food chemistry Vol. 52; no. 24; pp. 7235 - 7239
Main Authors: Garcia-Villanova, Rafael J, Cordón, Carlos, González Paramás, Ana M, Aparicio, P, Garcia Rosales, M. Eugenia
Format: Journal Article
Language:English
Published: Washington, DC American Chemical Society 01-12-2004
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Summary:Bee pollen is a major substrate for mycotoxins growth when no prompt and adequate drying is performed by the beekeeper after collection by bees. Regulatory limits for aflatoxins and ochratoxin A are currently in force in the European Union for a rising list of foodstuffs, but not for this. An immunoaffinity column cleanup process has been applied prior to the analysis of aflatoxins B1, B2, G1, and G2 and ochratoxin A (OTA). Optimization of the HPLC conditions has envolved both a gradient elution and a wavelength program for the separation and fluorimetric quantitation of all five mycotoxins at their maximum excitation and emission values of wavelength in a single run. The higher limit of detection (μg/kg) was 0.49 for OTA and 0.20 for aflatoxin B1. Repeatability (RSDr) at the lower limit tested ranged from 9.85% for OTA to 6.23% for aflatoxin G2, and recoveries also at the lower spiked level were 73% for OTA and 81% for aflatoxin B1. None of the 20 samples assayed showed quantifiable values for the five mycotoxins. Keywords: Mycotoxins; aflatoxins; ochratoxin A; spanish bee pollen; immunoaffinity column; simultaneous food analysis
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ISSN:0021-8561
1520-5118
DOI:10.1021/jf048882z