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U.S. Department of Energy
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Metabolism, mass spectral analysis and mode of action of trichothecene mycotoxins. Final report, 15 July 1985-14 July 1989

Technical Report ·
OSTI ID:6832996
Methods of analysis for T-2 toxin, HT-2 and T-2-tetraol in blood and urine were developed using hybrid tandem mass spectrometry, more specifically, Multiple Reaction Monitoring (MRM). Essentially, the mass spectra of the above toxins were obtained in electron impact, the fragments studied for selection of appropriate parent and daughters were generated with the objective of using them analytically. As an example, m/z 478 of the trifluoroacetate derivative of T-2 toxin was reacted in the collision chamber (field free region three) with argon and 23 eV to produce daughters 12, 138 and 180. These were used in method development so that T-2 was detected in a biological matrix with a sensitivity of 1 part per billion. A field method of urine collection was developed for the analysis of T-2 toxin. An attempt was made to find toxic isolates of Fusarium in soils of the Arctic of Norway that would explain some of the hemorrhagic activity noted with this genus. More specifically, descriptions of toxicity of biological warfare agents originating in Southeast Asia included extreme hemorrhaging. To this end, toxic isolates were found that caused extreme hemorrhaging in rats. The natural product responsible for the toxicity was isolated, purified and characterized as wortmannin. Wortmannin was shown to cause hemorrhaging in the heart, bladder, stomach and thymus. The chemistry, NMR and mass spectra of wortmannin are presented.
Research Organization:
Minnesota Univ., St. Paul, MN (USA). Dept. of Plant Pathology
OSTI ID:
6832996
Report Number(s):
AD-A-218488/5/XAB
Country of Publication:
United States
Language:
English