Single-step multiresidue determination of ten multiclass veterinary drugs in pork, milk, and eggs using liquid chromatography with tandem mass spectrometry

A multiclass, multiresidue determination method is reported for the detection of ten veterinary drugs, including scopolamine, metoclopramide, acriflavine, berberine, tripelennamine, diphenhydramine, acrinol, triamcinolone, loperamide, and roxithromycin in pork, milk, and eggs. The method involves a...

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Veröffentlicht in:Journal of separation science 2015-08, Vol.38 (16), p.2772-2780
Hauptverfasser: Park, Jin-A, Zhang, Dan, Kim, Dong-Soon, Kim, Seong-Kwan, Cho, Kyeong-Su, Jeong, Dana, Shim, Jae-Han, Kim, Jin-Suk, Abd El-Aty, A. M., Shin, Ho-Chul
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container_end_page 2780
container_issue 16
container_start_page 2772
container_title Journal of separation science
container_volume 38
creator Park, Jin-A
Zhang, Dan
Kim, Dong-Soon
Kim, Seong-Kwan
Cho, Kyeong-Su
Jeong, Dana
Shim, Jae-Han
Kim, Jin-Suk
Abd El-Aty, A. M.
Shin, Ho-Chul
description A multiclass, multiresidue determination method is reported for the detection of ten veterinary drugs, including scopolamine, metoclopramide, acriflavine, berberine, tripelennamine, diphenhydramine, acrinol, triamcinolone, loperamide, and roxithromycin in pork, milk, and eggs. The method involves a simple extraction using 0.1% formic acid in acetonitrile, followed by defatting with n‐hexane, centrifugation, and filtration prior to liquid chromatography with tandem mass spectrometric analysis. As ion suppression and enhancement effects are reported, matrix‐matched calibrations are used for quantification, with determination coefficients ≥0.9765. For the majority of the tested analytes, the intra‐ and interday accuracy (expressed as recovery %) range from 70.6 to 94.6% and from 70.1 to 93.3%, respectively, and the precision (expressed as relative standard deviation) ranges from 0.5 to 19.8% and from 2.8 to 18.4% in all matrices. The limits of quantification range between 0.5 and 10 ng/g. The validated tandem mass spectrometry method is successfully applied to market samples; the target analytes are not detected in any of the tested samples. In terms of accuracy, no extract cleanup is deemed necessary. The developed method is feasible for the simultaneous detection of the tested analytes in pork, milk, and eggs.
doi_str_mv 10.1002/jssc.201500501
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For the majority of the tested analytes, the intra‐ and interday accuracy (expressed as recovery %) range from 70.6 to 94.6% and from 70.1 to 93.3%, respectively, and the precision (expressed as relative standard deviation) ranges from 0.5 to 19.8% and from 2.8 to 18.4% in all matrices. The limits of quantification range between 0.5 and 10 ng/g. The validated tandem mass spectrometry method is successfully applied to market samples; the target analytes are not detected in any of the tested samples. In terms of accuracy, no extract cleanup is deemed necessary. 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M.</creatorcontrib><creatorcontrib>Shin, Ho-Chul</creatorcontrib><title>Single-step multiresidue determination of ten multiclass veterinary drugs in pork, milk, and eggs using liquid chromatography with tandem mass spectrometry</title><title>Journal of separation science</title><addtitle>J. Sep. Science</addtitle><description>A multiclass, multiresidue determination method is reported for the detection of ten veterinary drugs, including scopolamine, metoclopramide, acriflavine, berberine, tripelennamine, diphenhydramine, acrinol, triamcinolone, loperamide, and roxithromycin in pork, milk, and eggs. The method involves a simple extraction using 0.1% formic acid in acetonitrile, followed by defatting with n‐hexane, centrifugation, and filtration prior to liquid chromatography with tandem mass spectrometric analysis. As ion suppression and enhancement effects are reported, matrix‐matched calibrations are used for quantification, with determination coefficients ≥0.9765. 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M.</creator><creator>Shin, Ho-Chul</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>201508</creationdate><title>Single-step multiresidue determination of ten multiclass veterinary drugs in pork, milk, and eggs using liquid chromatography with tandem mass spectrometry</title><author>Park, Jin-A ; Zhang, Dan ; Kim, Dong-Soon ; Kim, Seong-Kwan ; Cho, Kyeong-Su ; Jeong, Dana ; Shim, Jae-Han ; Kim, Jin-Suk ; Abd El-Aty, A. 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M.</au><au>Shin, Ho-Chul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single-step multiresidue determination of ten multiclass veterinary drugs in pork, milk, and eggs using liquid chromatography with tandem mass spectrometry</atitle><jtitle>Journal of separation science</jtitle><addtitle>J. Sep. Science</addtitle><date>2015-08</date><risdate>2015</risdate><volume>38</volume><issue>16</issue><spage>2772</spage><epage>2780</epage><pages>2772-2780</pages><issn>1615-9306</issn><eissn>1615-9314</eissn><abstract>A multiclass, multiresidue determination method is reported for the detection of ten veterinary drugs, including scopolamine, metoclopramide, acriflavine, berberine, tripelennamine, diphenhydramine, acrinol, triamcinolone, loperamide, and roxithromycin in pork, milk, and eggs. The method involves a simple extraction using 0.1% formic acid in acetonitrile, followed by defatting with n‐hexane, centrifugation, and filtration prior to liquid chromatography with tandem mass spectrometric analysis. As ion suppression and enhancement effects are reported, matrix‐matched calibrations are used for quantification, with determination coefficients ≥0.9765. For the majority of the tested analytes, the intra‐ and interday accuracy (expressed as recovery %) range from 70.6 to 94.6% and from 70.1 to 93.3%, respectively, and the precision (expressed as relative standard deviation) ranges from 0.5 to 19.8% and from 2.8 to 18.4% in all matrices. The limits of quantification range between 0.5 and 10 ng/g. The validated tandem mass spectrometry method is successfully applied to market samples; the target analytes are not detected in any of the tested samples. In terms of accuracy, no extract cleanup is deemed necessary. The developed method is feasible for the simultaneous detection of the tested analytes in pork, milk, and eggs.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>26033853</pmid><doi>10.1002/jssc.201500501</doi><tpages>9</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Analytical chemistry
Animal food products
Animals
Cattle
Chickens
Chromatography
Chromatography, High Pressure Liquid - methods
Drug Residues - chemistry
Drugs
Eggs
Eggs - analysis
Liquid chromatography
Liquid-phase extraction
Mass spectrometry
Meat - analysis
Milk
Milk - chemistry
Multiresidue analysis
Pork
Scientific imaging
Swine
Tandem mass spectrometry
Tandem Mass Spectrometry - methods
Veterinary
Veterinary drugs
Veterinary Drugs - chemistry
Veterinary medicine
title Single-step multiresidue determination of ten multiclass veterinary drugs in pork, milk, and eggs using liquid chromatography with tandem mass spectrometry
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