Journal
JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES
Volume 25, Issue 12, Pages 1821-1833Publisher
MARCEL DEKKER INC
DOI: 10.1081/JLC-120005876
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This paper investigates the suitability of 37 reaction partners for the derivatization of fumonisins with o-phthaldialdehyde (OPA). All resulting fumonisin derivatives were compared for stability by UV-absorption. Subsequently, the relative fluorescence and retention times of derivatives found to be stable in UV-absorption were investigated by high performance liquid chromatography (HPLC), using well-established chromatographic conditions for fumonisin analysis. Several alternatives to 2-mercaptoethanol could be identified to be superior derivatization agents (3-mercapto-propionic acid, N-acetyl-cystein and thioglycerol). Those are especially valid when immunoaffinity column clean up is used prior to derivatization. The structure of the fumonisin B1-derivative obtained from the most suitable derivatization agent N-acetyl-cystein was verified by HPLC-MS.
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