SIMULTANEOUS DETERMINATION OF FLUPYRAZOFOS AND ITS METABOLITE 1-PHENYL-3-TRIFLUOROMETHYL-5-HYDROXYPYRAZOLE AND FLUPYRAZOFOS OXON IN RAT PLASMA BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH ULTRAVIOLET ABSORBENCY DETECTION
Hc. Shin et al., SIMULTANEOUS DETERMINATION OF FLUPYRAZOFOS AND ITS METABOLITE 1-PHENYL-3-TRIFLUOROMETHYL-5-HYDROXYPYRAZOLE AND FLUPYRAZOFOS OXON IN RAT PLASMA BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH ULTRAVIOLET ABSORBENCY DETECTION, Journal of chromatography B. Biomedical sciences and applications, 718(1), 1998, pp. 61-68
Citations number
11
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
Journal title
Journal of chromatography B. Biomedical sciences and applications
An isocratic high-performance liquid chromatography (HPLC) system with
UV detection was developed for simultaneous determination of flupyraz
ofos and its metabolites, 1-phenyl-3-trifluoromethyl-5-hydroxypyrazole
and flupyrazofos oxon, in rat plasma. Optimal analytical conditions i
nvolved an analytical cartridge column consisting of a phenyl bonded p
hase, a mobile phase of 50 mM phosphate buffer (pH3.0)-acetonitrile (4
0:60, v/v) and a UV detection wavelength of 232 nm. Under these condit
ions the peaks of flupyrazofos and its metabolites were all well separ
ated and the total time for complete separation was less than 12 min.
The limit of quantitation was 40 ng/ml for flupyrazofos and 20 ng/ml f
or PTMHP. Recoveries from rat plasma were higher than 90%. Following i
ntravenous administration of flupyrazofos, the method has been success
fully applied in a toxicokinetic study in rats involving plasma sample
s. Therefore, the current method is a valuable analytical tool for inv
estigating the metabolism and toxicokinetics of flupyrazofos. (C) 1998
Elsevier Science B.V. All rights reserved.