Simultaneous determination of (fluoro)quinolones antibacterials residues in bovine milk using ultra performance liquid chromatography–tandem mass spectrometry

The ultra performance liquid chromatography–tandem mass spectrometry (UPLC) method had been developed for 22 (fluoro)quinolone(QNs) antibacterials in milk with multiple reaction monitoring (MRM) as acquisition mode. The analytes were extracted from the sample using Mcllvaine buffer by ultrasonic bat...

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Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 2009-02, Vol.49 (2), p.367-374
Hauptverfasser: Zhang, Hong, Ren, Yiping, Bao, Xiaoli
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Ren, Yiping
Bao, Xiaoli
description The ultra performance liquid chromatography–tandem mass spectrometry (UPLC) method had been developed for 22 (fluoro)quinolone(QNs) antibacterials in milk with multiple reaction monitoring (MRM) as acquisition mode. The analytes were extracted from the sample using Mcllvaine buffer by ultrasonic bath, and purified by solid-phase extraction (SPE) cartridge. The residue were dried under nitrogen and dissolved in mobile phase before UPLC–MS/MS final analysis. The calibration curve of six concentrations for 22 QNs showed good linearity and the good correlation coefficients ( r ≥ 0.9851) were achieved. The limit range of quantification was 0.008–0.339 μg/kg. The recovery range was 63.1–94.6% except flumequine, nalidixic acid and nadifloxacin. The method was precise: the relative standard deviations of the method for milk were not more than 13.12%. The accuracies and sensitivity of the method were good for simultaneous determination of 22 QNs.
doi_str_mv 10.1016/j.jpba.2008.10.043
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The analytes were extracted from the sample using Mcllvaine buffer by ultrasonic bath, and purified by solid-phase extraction (SPE) cartridge. The residue were dried under nitrogen and dissolved in mobile phase before UPLC–MS/MS final analysis. The calibration curve of six concentrations for 22 QNs showed good linearity and the good correlation coefficients ( r ≥ 0.9851) were achieved. The limit range of quantification was 0.008–0.339 μg/kg. The recovery range was 63.1–94.6% except flumequine, nalidixic acid and nadifloxacin. The method was precise: the relative standard deviations of the method for milk were not more than 13.12%. 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The analytes were extracted from the sample using Mcllvaine buffer by ultrasonic bath, and purified by solid-phase extraction (SPE) cartridge. The residue were dried under nitrogen and dissolved in mobile phase before UPLC–MS/MS final analysis. The calibration curve of six concentrations for 22 QNs showed good linearity and the good correlation coefficients ( r ≥ 0.9851) were achieved. The limit range of quantification was 0.008–0.339 μg/kg. The recovery range was 63.1–94.6% except flumequine, nalidixic acid and nadifloxacin. The method was precise: the relative standard deviations of the method for milk were not more than 13.12%. 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Drug treatments</subject><subject>Quinolone antibacterials</subject><subject>Sensitivity and Specificity</subject><subject>Solid Phase Extraction</subject><subject>Spectrometry, Mass, Electrospray Ionization - methods</subject><subject>Tandem Mass Spectrometry - methods</subject><subject>Ultrasonics</subject><subject>UPLC–MS/MS</subject><issn>0731-7085</issn><issn>1873-264X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2O1DAQhS0EYpqBC7BA3oBgkcaOnT-JDRrxJ43EApDYWY5TmakmtjN2MlLvuAMX4GychGq6BTs2tlT1-bnqPcYeS7GVQtYvd9vd3NttKURLha3Q6g7byLZRRVnrr3fZRjRKFo1oqzP2IOedEKKSnb7PzmQn61KXasN-fkK_TosNENfMB1ggeQx2wRh4HPnzcVpjii9uVgxxigEyt2HB3joC0U6ZJ8g4rFTHwPt4iwG4x-kbXzOGK07SyfIZ0hiTt8EBn5C0Bu6uU_R2iVfJztf7X99_0AgDeO5tzjzP4Bbqw5L2D9m9kf6BR6f7nH15--bzxfvi8uO7DxevLwunZbUUdaU0NPLPQWvX49BB2yrbWGU7Tfs2sqVGVfdOj6BcXdZda4Vzle2Fkr06Z8-OunOKN7TPYjxmB9N0tMaUolIdWUZgeQRdijknGM2c0Nu0N1KYQy5mZw65mEMuhxrlQo-enNTX3sPw78kpCAKengCbnZ3GRGZh_suVsqyrVnfEvTpyQF7cIiSTHQIZO2Ai08wQ8X9z_AbA-bGF</recordid><startdate>20090220</startdate><enddate>20090220</enddate><creator>Zhang, Hong</creator><creator>Ren, Yiping</creator><creator>Bao, Xiaoli</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20090220</creationdate><title>Simultaneous determination of (fluoro)quinolones antibacterials residues in bovine milk using ultra performance liquid chromatography–tandem mass spectrometry</title><author>Zhang, Hong ; Ren, Yiping ; Bao, Xiaoli</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-6534e7134e710736fd9e883a7a3a9419171810756bc4fe3c62698a0cc5ab031b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Analysis</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Anti-Bacterial Agents - analysis</topic><topic>Biological and medical sciences</topic><topic>Bovine milk</topic><topic>Buffers</topic><topic>Calibration</topic><topic>Cattle</topic><topic>Chromatography, Liquid - instrumentation</topic><topic>Chromatography, Liquid - methods</topic><topic>Drug Residues - analysis</topic><topic>Female</topic><topic>Fluoroquinolones - analysis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General pharmacology</topic><topic>Medical sciences</topic><topic>Milk - chemistry</topic><topic>Pharmacology. Drug treatments</topic><topic>Quinolone antibacterials</topic><topic>Sensitivity and Specificity</topic><topic>Solid Phase Extraction</topic><topic>Spectrometry, Mass, Electrospray Ionization - methods</topic><topic>Tandem Mass Spectrometry - methods</topic><topic>Ultrasonics</topic><topic>UPLC–MS/MS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Hong</creatorcontrib><creatorcontrib>Ren, Yiping</creatorcontrib><creatorcontrib>Bao, Xiaoli</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Hong</au><au>Ren, Yiping</au><au>Bao, Xiaoli</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous determination of (fluoro)quinolones antibacterials residues in bovine milk using ultra performance liquid chromatography–tandem mass spectrometry</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><addtitle>J Pharm Biomed Anal</addtitle><date>2009-02-20</date><risdate>2009</risdate><volume>49</volume><issue>2</issue><spage>367</spage><epage>374</epage><pages>367-374</pages><issn>0731-7085</issn><eissn>1873-264X</eissn><coden>JPBADA</coden><abstract>The ultra performance liquid chromatography–tandem mass spectrometry (UPLC) method had been developed for 22 (fluoro)quinolone(QNs) antibacterials in milk with multiple reaction monitoring (MRM) as acquisition mode. The analytes were extracted from the sample using Mcllvaine buffer by ultrasonic bath, and purified by solid-phase extraction (SPE) cartridge. The residue were dried under nitrogen and dissolved in mobile phase before UPLC–MS/MS final analysis. The calibration curve of six concentrations for 22 QNs showed good linearity and the good correlation coefficients ( r ≥ 0.9851) were achieved. The limit range of quantification was 0.008–0.339 μg/kg. The recovery range was 63.1–94.6% except flumequine, nalidixic acid and nadifloxacin. The method was precise: the relative standard deviations of the method for milk were not more than 13.12%. The accuracies and sensitivity of the method were good for simultaneous determination of 22 QNs.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>19162423</pmid><doi>10.1016/j.jpba.2008.10.043</doi><tpages>8</tpages></addata></record>
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subjects Analysis
Analytical, structural and metabolic biochemistry
Animals
Anti-Bacterial Agents - analysis
Biological and medical sciences
Bovine milk
Buffers
Calibration
Cattle
Chromatography, Liquid - instrumentation
Chromatography, Liquid - methods
Drug Residues - analysis
Female
Fluoroquinolones - analysis
Fundamental and applied biological sciences. Psychology
General pharmacology
Medical sciences
Milk - chemistry
Pharmacology. Drug treatments
Quinolone antibacterials
Sensitivity and Specificity
Solid Phase Extraction
Spectrometry, Mass, Electrospray Ionization - methods
Tandem Mass Spectrometry - methods
Ultrasonics
UPLC–MS/MS
title Simultaneous determination of (fluoro)quinolones antibacterials residues in bovine milk using ultra performance liquid chromatography–tandem mass spectrometry
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