A. Orinak, DETERMINATION OF UNCHANGED RESIDUES OF A PYRETHROID INSECTICIDE, PYR-VU-TO2, IN SHEEP INTERNAL ORGAN-TISSUES, Pesticide science, 37(1), 1993, pp. 1-7
During subacute toxicological testing of PYR-VU-TO2, a novel cypermeth
rin-like pyrethroid with a high (150:1) cis: trans ratio, its distribu
tion in skeletal muscle and internal organ tissues of two groups of ex
perimental sheep was investigated after oral administration of two dif
ferent doses (1/10 and 1/20 of the LD50). Residual levels of PYR-VU-TO
2 were also observed in sheep blood after administration of a single d
ose of the compound. Homogenized internal organ tissues and blood samp
les were extracted in light petroleum distillate + acetone for 15 min.
After filtration. the extract was cleaned up on a 'Florisil'(R) and s
odium sulfate layer. The pyrethroid elution was processed with acetone
-light petroleum distillate (2 + 98 by volume). Recoveries ranged from
80.7 to 93.5%. Unchanged PYR-VU-TO2 residues were determined on a 1.5
-m stainless steel packed column under isothermal conditions with an e
lectron-capture detector. The results were evaluated by the calibratio
n curve method. The coefficients of variation were generally lower tha
n 5% and determination limit for PYR-VU-TO2 was 20 mug kg-1. Mean unch
anged PYR-VU-TO2 residues lay within a wide range. After six weeks of
treatment the following order of tissue residue levels could be stated
: heart > lung > muscle > spleen > kidney > liver > brain, and spleen
> muscle > lung > heart > liver > kidney > brain for experiment groups
I and II, respectively Only small differences between the residues in
the tissues of males and females were found in the first group (daily
PYR-VU-TO2 dose of 50 mg kg-1 live weight). The experimental females
of the second group (daily PYR-VU-TO2 dose of 200 mg kg-1 body weight)
revealed higher levels (other than spleen) than did the males. Maximu
m PYR-VU-TO2 residues in sheep blood were found 24 h after administrat
ion of a single dose. Confirmation of the results was carried out by d
etermination of -dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic aci
d methyl ester by capillary GC.