A Method for the Simultaneous Identification and Quantitation of Five Superwarfarin Rodenticides in Human Serum

A high-performance liquid chromatographic method with ultraviolet (UV) and fluorescence detection was developed for the analysis of one indandione and four hydroxycoumarin anticoagulant rodenticides in human serum. The superwarfarin rodenticides, chlorophacinone, bromadiolone, difenacoum, brodifacou...

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Veröffentlicht in:Journal of analytical toxicology 1995-11, Vol.19 (7), p.557-562
Hauptverfasser: Kuijpers, Eugenie A.P., Hartigh, Jan den, Savelkoul, T. Jean F., de Wolff, Frederik A.
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container_end_page 562
container_issue 7
container_start_page 557
container_title Journal of analytical toxicology
container_volume 19
creator Kuijpers, Eugenie A.P.
Hartigh, Jan den
Savelkoul, T. Jean F.
de Wolff, Frederik A.
description A high-performance liquid chromatographic method with ultraviolet (UV) and fluorescence detection was developed for the analysis of one indandione and four hydroxycoumarin anticoagulant rodenticides in human serum. The superwarfarin rodenticides, chlorophacinone, bromadiolone, difenacoum, brodifacoum, and difethialone, can be identified and quantitated simultaneously with this method. After adding a buffer (pH 5.5), the anticoagulants were extracted from serum with chloroform-acetone. The organic phase was separated and evaporated to dryness, and the residue was subjected to chromatographic analysis. The anticoagulants were separated by reversed-phase chromatography and detected by UV absorption at 285 nm and by fluorescence at an excitation wavelength of 265 nm and an emission wavelength of 400 nm. Extraction efficiencies from 55 to 131% were obtained. The within-run precision ranged from 2.0 to 7.1% for UV detection and from 0.0 to 4.8% for fluorescence detection. Between-run precision ranged from 1.3 to 16.0% for UV detection and from 1.8 to 9.0% for fluorescence detection. The anticoagulants can be quantitated at serum concentrations down to 3–12 ng/mL for fluorescence detection and down to 20–75 ng/mL for UV detection. No interferences were observed with the related compounds warfarin and vitamin K1.
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Jean F.</creatorcontrib><creatorcontrib>de Wolff, Frederik A.</creatorcontrib><title>A Method for the Simultaneous Identification and Quantitation of Five Superwarfarin Rodenticides in Human Serum</title><title>Journal of analytical toxicology</title><addtitle>Journal of Analytical Toxicology</addtitle><description>A high-performance liquid chromatographic method with ultraviolet (UV) and fluorescence detection was developed for the analysis of one indandione and four hydroxycoumarin anticoagulant rodenticides in human serum. The superwarfarin rodenticides, chlorophacinone, bromadiolone, difenacoum, brodifacoum, and difethialone, can be identified and quantitated simultaneously with this method. After adding a buffer (pH 5.5), the anticoagulants were extracted from serum with chloroform-acetone. The organic phase was separated and evaporated to dryness, and the residue was subjected to chromatographic analysis. The anticoagulants were separated by reversed-phase chromatography and detected by UV absorption at 285 nm and by fluorescence at an excitation wavelength of 265 nm and an emission wavelength of 400 nm. Extraction efficiencies from 55 to 131% were obtained. The within-run precision ranged from 2.0 to 7.1% for UV detection and from 0.0 to 4.8% for fluorescence detection. Between-run precision ranged from 1.3 to 16.0% for UV detection and from 1.8 to 9.0% for fluorescence detection. The anticoagulants can be quantitated at serum concentrations down to 3–12 ng/mL for fluorescence detection and down to 20–75 ng/mL for UV detection. 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Jean F. ; de Wolff, Frederik A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c332t-9a58515e22117e128af39c9db93bc8fce85a151c3816a7fae5f9a9ce7c63d3623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>4-Hydroxycoumarins - blood</topic><topic>Absorption</topic><topic>Acetone - chemistry</topic><topic>Anticoagulants</topic><topic>Anticoagulants - blood</topic><topic>Biological and medical sciences</topic><topic>Chloroform - chemistry</topic><topic>Chromatography</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Drug Interactions</topic><topic>Fluorescence</topic><topic>Humans</topic><topic>Hydrogen-Ion Concentration</topic><topic>Indans - blood</topic><topic>Medical sciences</topic><topic>Pesticides, fertilizers and other agrochemicals toxicology</topic><topic>pH effects</topic><topic>Quantitation</topic><topic>Reference Standards</topic><topic>Rodenticides</topic><topic>Rodenticides - blood</topic><topic>Spectrometry, Fluorescence</topic><topic>Toxicology</topic><topic>U.V. radiation</topic><topic>Vitamin K 1 - blood</topic><topic>Vitamins</topic><topic>Warfarin</topic><topic>Warfarin - blood</topic><topic>Wavelength</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuijpers, Eugenie A.P.</creatorcontrib><creatorcontrib>Hartigh, Jan den</creatorcontrib><creatorcontrib>Savelkoul, T. 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Jean F.</au><au>de Wolff, Frederik A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Method for the Simultaneous Identification and Quantitation of Five Superwarfarin Rodenticides in Human Serum</atitle><jtitle>Journal of analytical toxicology</jtitle><addtitle>Journal of Analytical Toxicology</addtitle><date>1995-11</date><risdate>1995</risdate><volume>19</volume><issue>7</issue><spage>557</spage><epage>562</epage><pages>557-562</pages><issn>0146-4760</issn><eissn>1945-2403</eissn><coden>JATOD3</coden><abstract>A high-performance liquid chromatographic method with ultraviolet (UV) and fluorescence detection was developed for the analysis of one indandione and four hydroxycoumarin anticoagulant rodenticides in human serum. The superwarfarin rodenticides, chlorophacinone, bromadiolone, difenacoum, brodifacoum, and difethialone, can be identified and quantitated simultaneously with this method. After adding a buffer (pH 5.5), the anticoagulants were extracted from serum with chloroform-acetone. The organic phase was separated and evaporated to dryness, and the residue was subjected to chromatographic analysis. The anticoagulants were separated by reversed-phase chromatography and detected by UV absorption at 285 nm and by fluorescence at an excitation wavelength of 265 nm and an emission wavelength of 400 nm. Extraction efficiencies from 55 to 131% were obtained. The within-run precision ranged from 2.0 to 7.1% for UV detection and from 0.0 to 4.8% for fluorescence detection. Between-run precision ranged from 1.3 to 16.0% for UV detection and from 1.8 to 9.0% for fluorescence detection. The anticoagulants can be quantitated at serum concentrations down to 3–12 ng/mL for fluorescence detection and down to 20–75 ng/mL for UV detection. 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subjects 4-Hydroxycoumarins - blood
Absorption
Acetone - chemistry
Anticoagulants
Anticoagulants - blood
Biological and medical sciences
Chloroform - chemistry
Chromatography
Chromatography, High Pressure Liquid
Drug Interactions
Fluorescence
Humans
Hydrogen-Ion Concentration
Indans - blood
Medical sciences
Pesticides, fertilizers and other agrochemicals toxicology
pH effects
Quantitation
Reference Standards
Rodenticides
Rodenticides - blood
Spectrometry, Fluorescence
Toxicology
U.V. radiation
Vitamin K 1 - blood
Vitamins
Warfarin
Warfarin - blood
Wavelength
title A Method for the Simultaneous Identification and Quantitation of Five Superwarfarin Rodenticides in Human Serum
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