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Analysis of the fusariotoxins zearalenone and vomitoxin (deoxynivalenol) in human foods and animal feeds by high-performance liquid chromatography (HPLC)
Authors:H Schweighardt  J Böhm  A M Abdelhamid  J Leibetseder  M Schuh  E Glawischnig
Institution:(1) Institut für Ernährung, Veterinärmedizinische Universität Wien, Linke Bahngasse 11, 1030 Wien, Austria;(2) II. Medizinische Universitätsklinik für Klauentiere, Veterinärmedizinische Universität Wien, Linke Bahngasse 11, 1030 Wien, Austria;(3) Institute of Animal Production, Faculty of Agriculture, Univ. of Mansoura, Egypt
Abstract:Summary HPLC procedures for analyses of the fusariotoxins zearalenone and vomitoxin in individual food- and feedstuffs as well as in mixed feed are described. Zearalenone is separated on a column with polar stationary phase (25 cm × 4.6 mm i.d., particle size 7 mgrm), eluted with a chloroform-isooctane (75/25, v/v)+1.5% methanol mixture and detected fluorometrically. The quantitative determination was possible in all analyzed samples with a detection limit of 2mgrg/kg with 70–80% recovery. Vomitoxin is fractionated by HPLC (C 18 1 column, 25 cm×4 mm i.d., 5 mgrm particle size) with water-methanol (60/40, v/v) mobile phase and determined by combining GLC or TLC with UV detection. The detection limit in mixed feed with interfering substances was 25 mgrg/kg (recovery 25–35%). The separation by HPLC makes preparation of pure vomitoxin possible. The described methods are fast, simple and low cost and are suitable for routine analyses.
Keywords:HPLC methods  Mycotoxins  Zearlenone  Vomitoxin (Deoxynivalenol)
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