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Published:
Journal of Analytical Toxicology,
ISSN 0146-4760,
Volume 25,
Number 6 September 2001, pp. 450-455
Assessing
Chronic Exposure to Fumonisin Mycotoxins: The Use of Hair as a Suitable Noninvasive
Matrix
V.
Sewram*, J.J. Nair, T.W. Nieuwoudt, W.C.A. Gelderblom, W.F.O. Marasas, and
G.S. Shephard
PROMEC Unit, Medical Research Council, P.O. Box 19070, Tygerberg, 7505, South
Africa
This
study describes for the first time the accumulation of measurable levels of
fumonisin mycotoxins in the hair of nonhuman primates (vervet monkeys, Cercopithecus
aethiops) and rats exposed to contaminated feed. Hair was subjected to reflux
with methanol, and the resulting extract was cleaned up on strong anion exchange
(SAX) and C18 solid-phase sorbents. Fumonisins FB1, FB2, and FB3 as well as
their hydrolysis products commonly known as aminopolyols, AP1 and AP2, were
detected in monkey hair using high-performance liquid chromatography coupled
to electrospray ionization mass spectrometry (HPLCESI-MS). Despite matrix
interferences, the two-stage mass spectrometric process (MSMS) yielded
product ion mass spectra, which served as diagnostic indicators thus providing
unequivocal identification of FB1, FB2, and FB3 as well as AP1 and AP2. In
vervet monkeys, the levels of exposure related well to the levels of toxin
detected in hair, and levels as high as 5.98 mg FB1, 33.77 mg FB1, and 65.93
mg FB1/kg of hair were found in monkeys receiving control, low-dose, and high-dose
contaminated diets, respectively. Hair was also analyzed from rats given either
single gavage doses of 1 and 10 mg FB1/kg body weight or contaminated feed
(50 mg FB1/kg), resulting in an exposure of approximately 4.25 mg FB1/kg body
weight/day based on the measured daily feed intake. Analysis of rat hair over
a four-week period indicated that mean levels up to 34.50 mg/kg and 42.20
mg/kg were detectable by the fourth week in the rats treated by gavage (10
mg FB1/kg body weight) and those receiving contaminated feed, respectively.
This relationship indicates that hair can provide an easily applicable non-invasive
matrix for assessing chronic exposure to fumonisin mycotoxins.
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