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Development and validation of a solid‐phase extraction method coupled with LC–MS/MS for the simultaneous determination of 16 antibiotic residues in duck meat
The present study was carried out to determine 16 antibiotics belonging to seven different groups (tetracyclines, sulfonamides, penicillins, fluoroquinolones, macrolides, lincosamides and trimethoprims) in duck meat. A solid‐phase extraction method based on Oasis HLB cartridges coupled with liquid c...
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Published in: | Biomedical chromatography 2019-05, Vol.33 (5), p.e4501-n/a |
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creator | Zheng, Weijia Abd El‐Aty, A. M. Kim, Seong‐Kwan Choi, Jeong‐Min Park, Da‐Hee Yoo, Kyung‐Hee Kang, Young‐Sun Jeon, Jong‐Sup Hacımüftüoğlu, Ahmet Shim, Jae‐Han Shin, Ho‐Chul |
description | The present study was carried out to determine 16 antibiotics belonging to seven different groups (tetracyclines, sulfonamides, penicillins, fluoroquinolones, macrolides, lincosamides and trimethoprims) in duck meat. A solid‐phase extraction method based on Oasis HLB cartridges coupled with liquid chromatography–electrospray ionization tandem mass spectrometry was developed. Solutions of 0.1 m ethylenediaminetetraacetic acid disodium salt and 2% trifluoroacetic acid were used for the preliminary extraction of the target antibiotics from duck meat and n‐hexane was used for purification prior to solid‐phase extraction. Mobile phases composed of 0.1% trifluoroacetic acid in distilled water (solvent A) and 0.1% trifluoroacetic acid in methanol (solvent B), combined with a reversed‐phase C18 analytical column, provided the optimal separation and signal intensity. The linearity of the method was assessed using six concentrations (5, 10, 20, 30, 40, and 50 μg/kg), and the recoveries, which were calculated at three spiking concentrations (5, 10 and 20 μg/kg), were in the range 69.8–103.3% with relative standard deviations (RSDs) ≤ 6.9% for the 16 tested antibiotics. Matrix effects ranging from −47.2 to −13.5% were observed for all the analytes, and the limits of quantitation (LOQ), which ranged from 4.93 to 26.21 μg/kg, were much lower than the maximum residue limits (MRLs) set by various regulatory authorities. Ten samples from a market were tested, and none of the target analytes were detected. Thus, a simple and versatile protocol has been developed to detect and quantify 16 antibiotics in duck meat samples. |
doi_str_mv | 10.1002/bmc.4501 |
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M. ; Kim, Seong‐Kwan ; Choi, Jeong‐Min ; Park, Da‐Hee ; Yoo, Kyung‐Hee ; Kang, Young‐Sun ; Jeon, Jong‐Sup ; Hacımüftüoğlu, Ahmet ; Shim, Jae‐Han ; Shin, Ho‐Chul</creator><creatorcontrib>Zheng, Weijia ; Abd El‐Aty, A. M. ; Kim, Seong‐Kwan ; Choi, Jeong‐Min ; Park, Da‐Hee ; Yoo, Kyung‐Hee ; Kang, Young‐Sun ; Jeon, Jong‐Sup ; Hacımüftüoğlu, Ahmet ; Shim, Jae‐Han ; Shin, Ho‐Chul</creatorcontrib><description>The present study was carried out to determine 16 antibiotics belonging to seven different groups (tetracyclines, sulfonamides, penicillins, fluoroquinolones, macrolides, lincosamides and trimethoprims) in duck meat. A solid‐phase extraction method based on Oasis HLB cartridges coupled with liquid chromatography–electrospray ionization tandem mass spectrometry was developed. Solutions of 0.1 m ethylenediaminetetraacetic acid disodium salt and 2% trifluoroacetic acid were used for the preliminary extraction of the target antibiotics from duck meat and n‐hexane was used for purification prior to solid‐phase extraction. Mobile phases composed of 0.1% trifluoroacetic acid in distilled water (solvent A) and 0.1% trifluoroacetic acid in methanol (solvent B), combined with a reversed‐phase C18 analytical column, provided the optimal separation and signal intensity. The linearity of the method was assessed using six concentrations (5, 10, 20, 30, 40, and 50 μg/kg), and the recoveries, which were calculated at three spiking concentrations (5, 10 and 20 μg/kg), were in the range 69.8–103.3% with relative standard deviations (RSDs) ≤ 6.9% for the 16 tested antibiotics. Matrix effects ranging from −47.2 to −13.5% were observed for all the analytes, and the limits of quantitation (LOQ), which ranged from 4.93 to 26.21 μg/kg, were much lower than the maximum residue limits (MRLs) set by various regulatory authorities. Ten samples from a market were tested, and none of the target analytes were detected. Thus, a simple and versatile protocol has been developed to detect and quantify 16 antibiotics in duck meat samples.</description><identifier>ISSN: 0269-3879</identifier><identifier>EISSN: 1099-0801</identifier><identifier>DOI: 10.1002/bmc.4501</identifier><identifier>PMID: 30702178</identifier><language>eng</language><publisher>England</publisher><subject>analysis ; antibiotics ; duck meat ; LC–MS/MS ; residues ; solid‐phase extraction</subject><ispartof>Biomedical chromatography, 2019-05, Vol.33 (5), p.e4501-n/a</ispartof><rights>2019 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3211-80696006de41a2c17b4b33ce7c7adf487dd95559c64462f99ef785bb6c1caddf3</citedby><cites>FETCH-LOGICAL-c3211-80696006de41a2c17b4b33ce7c7adf487dd95559c64462f99ef785bb6c1caddf3</cites><orcidid>0000-0001-5500-3901 ; 0000-0002-5361-2903 ; 0000-0001-6596-7907</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30702178$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zheng, Weijia</creatorcontrib><creatorcontrib>Abd El‐Aty, A. M.</creatorcontrib><creatorcontrib>Kim, Seong‐Kwan</creatorcontrib><creatorcontrib>Choi, Jeong‐Min</creatorcontrib><creatorcontrib>Park, Da‐Hee</creatorcontrib><creatorcontrib>Yoo, Kyung‐Hee</creatorcontrib><creatorcontrib>Kang, Young‐Sun</creatorcontrib><creatorcontrib>Jeon, Jong‐Sup</creatorcontrib><creatorcontrib>Hacımüftüoğlu, Ahmet</creatorcontrib><creatorcontrib>Shim, Jae‐Han</creatorcontrib><creatorcontrib>Shin, Ho‐Chul</creatorcontrib><title>Development and validation of a solid‐phase extraction method coupled with LC–MS/MS for the simultaneous determination of 16 antibiotic residues in duck meat</title><title>Biomedical chromatography</title><addtitle>Biomed Chromatogr</addtitle><description>The present study was carried out to determine 16 antibiotics belonging to seven different groups (tetracyclines, sulfonamides, penicillins, fluoroquinolones, macrolides, lincosamides and trimethoprims) in duck meat. A solid‐phase extraction method based on Oasis HLB cartridges coupled with liquid chromatography–electrospray ionization tandem mass spectrometry was developed. Solutions of 0.1 m ethylenediaminetetraacetic acid disodium salt and 2% trifluoroacetic acid were used for the preliminary extraction of the target antibiotics from duck meat and n‐hexane was used for purification prior to solid‐phase extraction. Mobile phases composed of 0.1% trifluoroacetic acid in distilled water (solvent A) and 0.1% trifluoroacetic acid in methanol (solvent B), combined with a reversed‐phase C18 analytical column, provided the optimal separation and signal intensity. The linearity of the method was assessed using six concentrations (5, 10, 20, 30, 40, and 50 μg/kg), and the recoveries, which were calculated at three spiking concentrations (5, 10 and 20 μg/kg), were in the range 69.8–103.3% with relative standard deviations (RSDs) ≤ 6.9% for the 16 tested antibiotics. Matrix effects ranging from −47.2 to −13.5% were observed for all the analytes, and the limits of quantitation (LOQ), which ranged from 4.93 to 26.21 μg/kg, were much lower than the maximum residue limits (MRLs) set by various regulatory authorities. Ten samples from a market were tested, and none of the target analytes were detected. Thus, a simple and versatile protocol has been developed to detect and quantify 16 antibiotics in duck meat samples.</description><subject>analysis</subject><subject>antibiotics</subject><subject>duck meat</subject><subject>LC–MS/MS</subject><subject>residues</subject><subject>solid‐phase extraction</subject><issn>0269-3879</issn><issn>1099-0801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kDtOxDAQQC0EguUjcQLkkiYwzseOS1i-0q4ogDpy7InWkMRR7PDpOAISJ-BqnITAAh3VaDRPb6RHyC6DAwYQH5aNPkgzYCtkwkDKCHJgq2QCMZdRkgu5QTa9vwMAyWOxTjYSEBAzkU_I-wk-YO26BttAVWvog6qtUcG6lrqKKurduH-8vHYL5ZHiU-iV_r42GBbOUO2GrkZDH21Y0Nn04-Vtfn04v6aV62lYIPW2GeqgWnSDpwYD9o1t__yMj0-DLa0LVtMevTUDempbagZ9P_5QYZusVar2uPMzt8jt2enN9CKaXZ1fTo9mkU5ixqIcuOQA3GDKVKyZKNMySTQKLZSp0lwYI7Msk5qnKY8rKbESeVaWXDOtjKmSLbK_9Oreed9jVXS9bVT_XDAovioXY-Xiq_KI7i3RbigbNH_gb9YRiJbAo63x-V9RcTyffgs_AT5viww</recordid><startdate>201905</startdate><enddate>201905</enddate><creator>Zheng, Weijia</creator><creator>Abd El‐Aty, A. 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M. ; Kim, Seong‐Kwan ; Choi, Jeong‐Min ; Park, Da‐Hee ; Yoo, Kyung‐Hee ; Kang, Young‐Sun ; Jeon, Jong‐Sup ; Hacımüftüoğlu, Ahmet ; Shim, Jae‐Han ; Shin, Ho‐Chul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3211-80696006de41a2c17b4b33ce7c7adf487dd95559c64462f99ef785bb6c1caddf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>analysis</topic><topic>antibiotics</topic><topic>duck meat</topic><topic>LC–MS/MS</topic><topic>residues</topic><topic>solid‐phase extraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zheng, Weijia</creatorcontrib><creatorcontrib>Abd El‐Aty, A. M.</creatorcontrib><creatorcontrib>Kim, Seong‐Kwan</creatorcontrib><creatorcontrib>Choi, Jeong‐Min</creatorcontrib><creatorcontrib>Park, Da‐Hee</creatorcontrib><creatorcontrib>Yoo, Kyung‐Hee</creatorcontrib><creatorcontrib>Kang, Young‐Sun</creatorcontrib><creatorcontrib>Jeon, Jong‐Sup</creatorcontrib><creatorcontrib>Hacımüftüoğlu, Ahmet</creatorcontrib><creatorcontrib>Shim, Jae‐Han</creatorcontrib><creatorcontrib>Shin, Ho‐Chul</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Biomedical chromatography</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zheng, Weijia</au><au>Abd El‐Aty, A. M.</au><au>Kim, Seong‐Kwan</au><au>Choi, Jeong‐Min</au><au>Park, Da‐Hee</au><au>Yoo, Kyung‐Hee</au><au>Kang, Young‐Sun</au><au>Jeon, Jong‐Sup</au><au>Hacımüftüoğlu, Ahmet</au><au>Shim, Jae‐Han</au><au>Shin, Ho‐Chul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development and validation of a solid‐phase extraction method coupled with LC–MS/MS for the simultaneous determination of 16 antibiotic residues in duck meat</atitle><jtitle>Biomedical chromatography</jtitle><addtitle>Biomed Chromatogr</addtitle><date>2019-05</date><risdate>2019</risdate><volume>33</volume><issue>5</issue><spage>e4501</spage><epage>n/a</epage><pages>e4501-n/a</pages><issn>0269-3879</issn><eissn>1099-0801</eissn><abstract>The present study was carried out to determine 16 antibiotics belonging to seven different groups (tetracyclines, sulfonamides, penicillins, fluoroquinolones, macrolides, lincosamides and trimethoprims) in duck meat. A solid‐phase extraction method based on Oasis HLB cartridges coupled with liquid chromatography–electrospray ionization tandem mass spectrometry was developed. Solutions of 0.1 m ethylenediaminetetraacetic acid disodium salt and 2% trifluoroacetic acid were used for the preliminary extraction of the target antibiotics from duck meat and n‐hexane was used for purification prior to solid‐phase extraction. Mobile phases composed of 0.1% trifluoroacetic acid in distilled water (solvent A) and 0.1% trifluoroacetic acid in methanol (solvent B), combined with a reversed‐phase C18 analytical column, provided the optimal separation and signal intensity. The linearity of the method was assessed using six concentrations (5, 10, 20, 30, 40, and 50 μg/kg), and the recoveries, which were calculated at three spiking concentrations (5, 10 and 20 μg/kg), were in the range 69.8–103.3% with relative standard deviations (RSDs) ≤ 6.9% for the 16 tested antibiotics. Matrix effects ranging from −47.2 to −13.5% were observed for all the analytes, and the limits of quantitation (LOQ), which ranged from 4.93 to 26.21 μg/kg, were much lower than the maximum residue limits (MRLs) set by various regulatory authorities. Ten samples from a market were tested, and none of the target analytes were detected. Thus, a simple and versatile protocol has been developed to detect and quantify 16 antibiotics in duck meat samples.</abstract><cop>England</cop><pmid>30702178</pmid><doi>10.1002/bmc.4501</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-5500-3901</orcidid><orcidid>https://orcid.org/0000-0002-5361-2903</orcidid><orcidid>https://orcid.org/0000-0001-6596-7907</orcidid></addata></record> |
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title | Development and validation of a solid‐phase extraction method coupled with LC–MS/MS for the simultaneous determination of 16 antibiotic residues in duck meat |
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