Determination of moniliformin using SAX column clean-up and HPLC/DAD-detection

This work describes a method for the determination of theFusarium mycotoxin moniliformin (MON) in cereals. In addition to the optimization of the clean-up and the HPLC determination the most efficient extraction mode was investigated on natural contaminated samples. The method was validated for maize and wheat using a calibration range from 57 to 2300 μg/kg. Due to the ionic nature of the toxin the clean-up of the extracts was carried out with strong-anion-exchange columns. Moniliformin was separated by reversed phase ion-pair-chromatography (RP-Ion pair-HPLC) and detected by DAD. The validated method yielded recoveries of 76%±9% (maize) and 87%±5% (wheat) and detection limits of 39 μg/kg and 30 μg/kg, respectively. The suitability of the developed method was demonstrated on natural contaminated samples. Presented at the 25^th Mykotoxin Workshop in Giessen, Germany, May 19–21, 2003