A Screening Procedure for the Determination of 13 Oral Anticoagulants and Rodenticides
Author(s) -
Hayat Lotfi,
M.-F Dreyfuss,
Pierre Marquet,
Jean Debord,
L. Merle,
Gérard Lachâtre
Publication year - 1996
Publication title -
journal of analytical toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.161
H-Index - 76
eISSN - 1945-2403
pISSN - 0146-4760
DOI - 10.1093/jat/20.2.93
Subject(s) - chromatography , detection limit , chemistry , elution , high performance liquid chromatography , calibration curve , extraction (chemistry) , acetonitrile , coefficient of variation , resolution (logic) , gradient elution , ether , analytical chemistry (journal) , organic chemistry , artificial intelligence , computer science
A technique for the simultaneous identification and quantitation of 13 hydroxycoumarin and indandione anticoagulant drugs and rodenticides from human serum by reversed-phase liquid chromatography with diode-array detection has been developed. High-performance liquid chromatography was performed using gradient elution with an acetonitrile and phosphate buffer on a Nucleosil ODS column. Ultraviolet spectra from 200 to 400 nm were recorded on-line during the analysis and compared with spectra stored in a library. For the spiked 2 mL of serum, acidic and alkaline liquid-liquid double extraction with diethylether-ether acetate (50:50, v/v) was conducted, and recoveries greater than 60% for most compounds were found. The detection limit was approximately 25 or 50 ng/mL for all components except for difethialone and fluindione, for which it was approximately 100 ng/mL. The standard calibration curves were linear from the detection limit to 5000 ng/mL. The within-run precision coefficient of variation (CV) was less than 10%, and the between-run precision CV was less than 20%.
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