Criteria for Determining Purity of Fusarium Mycotoxins
Abstract Physical and chemical properties that may be used to determine the purity of several Fusarlum mycotoxins have been investigated. A combination of analytical procedures, which include high performance thin-layer chromatography (HPTLC), liquid chromatography (LC), gas chromatography (GC), gas chromatography/mass spectrometry (GC/MS), ultraviolet spectrometry (UV), and nuclear magnetic resonance (NMR) spectrometry have been used to examine mycotoxin standards obtained from commercial sources and from laboratory fermentations. Results of this investigation indicate that commercially available standards are greater than 90 % pure, but the label weight of purchased reference standards in individual containers should be verified. Mycotoxin standards, determined to be greater than 98 % pure by HPTLC, LC, and GC/MS, were examined by UV spectrometry and the coefficients of extinction were determined. An interlaboratory study, involving 5 collaborators who determined coefficients of extinction (in methanol) for identical samples, gave the following results: α-zearalenol (λ236 = 28 538 ± 558); β- zearalenol (λ238 = 24 963 ± 747); deoxynivalenol (λ219 = 6395 ± 349, lot 1), (6020 ± 228, lot 2); and T-2 toxin (λ202 = 3681 ± 255). UV maxima and coefficients of extinction are also reported for HT-2 toxin (λ202 = 1959), diacetoxyscirpenol (λ203 = 2487), neosolaniol (λ203 = 2644), nivalenol (λ220 = 5142), and fusarenon-X (λ217 = 5997).