A confirmatory analysis of malachite green residues in rainbow trout with liquid chromatography–electrospray tandem mass spectrometry
A quantitative liquid chromatography–tandem mass spectrometric (LC–MS/MS) method has been developed for the determination of malachite green (MG) and its metabolite leucomalachite green (LMG) in fish. Residues were extracted with an acetonitrile–acetate buffer and purified using the automated solid-...
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Veröffentlicht in: | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2007, Vol.845 (1), p.74-79 |
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creator | Halme, Kirsi Lindfors, Erja Peltonen, Kimmo |
description | A quantitative liquid chromatography–tandem mass spectrometric (LC–MS/MS) method has been developed for the determination of malachite green (MG) and its metabolite leucomalachite green (LMG) in fish. Residues were extracted with an acetonitrile–acetate buffer and purified using the automated solid-phase extraction (ASPEC). Residues were analyzed with a reversed-phase LC–MS/MS using a positive-ion electrospray ionisation (ESI). Isotope-labelled leucomalachite green (LMG-D5) was used as an internal standard for the quantification of LMG residues. The related dye, brilliant green (BG) was used as an instrumental standard. Identification and quantification of analytes were based on the ion transitions monitored by multiple reaction monitoring (MRM). The decision limit (CCα) for MG and LMG was 0.13 and 0.16
μg
kg
−1. The respective detection capabilities (CCβ) were 0.22 and 0.27
μg
kg
−1. The absolute recovery (repeatability SD
r) was in the range of 58–65% (7.8–11.2%) for MG and 59–68% (9.7–16.9%) for LMG. LMG was quantified also based on the internal standard, giving a recovery (repeatability SD
r) of 103–110% (4.8–9.3%). The method was further evaluated by analyzing a total of 34 fish residue monitoring samples, of which eight samples were found to be non-compliant containing low residues of LMG. |
doi_str_mv | 10.1016/j.jchromb.2006.07.048 |
format | Article |
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μg
kg
−1. The respective detection capabilities (CCβ) were 0.22 and 0.27
μg
kg
−1. The absolute recovery (repeatability SD
r) was in the range of 58–65% (7.8–11.2%) for MG and 59–68% (9.7–16.9%) for LMG. LMG was quantified also based on the internal standard, giving a recovery (repeatability SD
r) of 103–110% (4.8–9.3%). The method was further evaluated by analyzing a total of 34 fish residue monitoring samples, of which eight samples were found to be non-compliant containing low residues of LMG.</description><identifier>ISSN: 1570-0232</identifier><identifier>EISSN: 1873-376X</identifier><identifier>DOI: 10.1016/j.jchromb.2006.07.048</identifier><identifier>PMID: 16931188</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Analysis ; Analytical, structural and metabolic biochemistry ; Animals ; Antifungal Agents - analysis ; Biological and medical sciences ; Chromatography, Liquid - methods ; Confirmation ; Fish ; Fundamental and applied biological sciences. Psychology ; General pharmacology ; LC–MS/MS ; Leucomalachite green ; Malachite green ; Medical sciences ; Oncorhynchus mykiss ; Pharmacology. Drug treatments ; Rosaniline Dyes - analysis ; Spectrometry, Mass, Electrospray Ionization - methods ; Tandem Mass Spectrometry - methods</subject><ispartof>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2007, Vol.845 (1), p.74-79</ispartof><rights>2006 Elsevier B.V.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-863bbb768dfa0c434adda7b9cdeaa79962d1a962b68423554f396341ffc01eaf3</citedby><cites>FETCH-LOGICAL-c422t-863bbb768dfa0c434adda7b9cdeaa79962d1a962b68423554f396341ffc01eaf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1570023206006465$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,4009,27902,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18430012$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16931188$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Halme, Kirsi</creatorcontrib><creatorcontrib>Lindfors, Erja</creatorcontrib><creatorcontrib>Peltonen, Kimmo</creatorcontrib><title>A confirmatory analysis of malachite green residues in rainbow trout with liquid chromatography–electrospray tandem mass spectrometry</title><title>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</title><addtitle>J Chromatogr B Analyt Technol Biomed Life Sci</addtitle><description>A quantitative liquid chromatography–tandem mass spectrometric (LC–MS/MS) method has been developed for the determination of malachite green (MG) and its metabolite leucomalachite green (LMG) in fish. Residues were extracted with an acetonitrile–acetate buffer and purified using the automated solid-phase extraction (ASPEC). Residues were analyzed with a reversed-phase LC–MS/MS using a positive-ion electrospray ionisation (ESI). Isotope-labelled leucomalachite green (LMG-D5) was used as an internal standard for the quantification of LMG residues. The related dye, brilliant green (BG) was used as an instrumental standard. Identification and quantification of analytes were based on the ion transitions monitored by multiple reaction monitoring (MRM). The decision limit (CCα) for MG and LMG was 0.13 and 0.16
μg
kg
−1. The respective detection capabilities (CCβ) were 0.22 and 0.27
μg
kg
−1. The absolute recovery (repeatability SD
r) was in the range of 58–65% (7.8–11.2%) for MG and 59–68% (9.7–16.9%) for LMG. LMG was quantified also based on the internal standard, giving a recovery (repeatability SD
r) of 103–110% (4.8–9.3%). The method was further evaluated by analyzing a total of 34 fish residue monitoring samples, of which eight samples were found to be non-compliant containing low residues of LMG.</description><subject>Analysis</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Antifungal Agents - analysis</subject><subject>Biological and medical sciences</subject><subject>Chromatography, Liquid - methods</subject><subject>Confirmation</subject><subject>Fish</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General pharmacology</subject><subject>LC–MS/MS</subject><subject>Leucomalachite green</subject><subject>Malachite green</subject><subject>Medical sciences</subject><subject>Oncorhynchus mykiss</subject><subject>Pharmacology. Drug treatments</subject><subject>Rosaniline Dyes - analysis</subject><subject>Spectrometry, Mass, Electrospray Ionization - methods</subject><subject>Tandem Mass Spectrometry - methods</subject><issn>1570-0232</issn><issn>1873-376X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1TAQhS0EoqXwCCBv6C7BjnPtZIWqij-pEhuQ2FkTe9zrqyRO7aRVduz6ALwhT4LbG6lLNvZI_mbm-BxC3nJWcsblh0N5MPsYhq6sGJMlUyWrm2fklDdKFELJX89zvVOsYJWoTsirlA6MccWUeElOuGwF501zSu4vqAmj83GAOcSVwgj9mnyiwdEBejB7PyO9jogjjZi8XTBRn2vwYxfu6BzDMtM7P-9p728Wb-mjqjzsOsK0X__-_oM9moylKcJKZxgtDnl0SjRNjw8DznF9TV446BO-2e4z8vPzpx-XX4ur71--XV5cFaauqrlopOi6TsnGOmCmFjVYC6prjUUA1bayshzy2cmmrsRuVzvRSlFz5wzjCE6ckfPj3CmGm_yXWQ8-Gex7GDEsSctGyLYVIoO7I2iy9BTR6Sn6AeKqOdMPCeiD3hLQDwlopnROIPe92xYs3YD2qWuzPAPvNwCSgd5FGI1PT1xTixxUlbmPRw6zHbceo07G42jQ-ph90zb4_0j5BxMhrPQ</recordid><startdate>2007</startdate><enddate>2007</enddate><creator>Halme, Kirsi</creator><creator>Lindfors, Erja</creator><creator>Peltonen, Kimmo</creator><general>Elsevier B.V</general><general>Elsevier Science</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>7X8</scope></search><sort><creationdate>2007</creationdate><title>A confirmatory analysis of malachite green residues in rainbow trout with liquid chromatography–electrospray tandem mass spectrometry</title><author>Halme, Kirsi ; Lindfors, Erja ; Peltonen, Kimmo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-863bbb768dfa0c434adda7b9cdeaa79962d1a962b68423554f396341ffc01eaf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Analysis</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Antifungal Agents - analysis</topic><topic>Biological and medical sciences</topic><topic>Chromatography, Liquid - methods</topic><topic>Confirmation</topic><topic>Fish</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General pharmacology</topic><topic>LC–MS/MS</topic><topic>Leucomalachite green</topic><topic>Malachite green</topic><topic>Medical sciences</topic><topic>Oncorhynchus mykiss</topic><topic>Pharmacology. Drug treatments</topic><topic>Rosaniline Dyes - analysis</topic><topic>Spectrometry, Mass, Electrospray Ionization - methods</topic><topic>Tandem Mass Spectrometry - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Halme, Kirsi</creatorcontrib><creatorcontrib>Lindfors, Erja</creatorcontrib><creatorcontrib>Peltonen, Kimmo</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>MEDLINE - Academic</collection><jtitle>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Halme, Kirsi</au><au>Lindfors, Erja</au><au>Peltonen, Kimmo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A confirmatory analysis of malachite green residues in rainbow trout with liquid chromatography–electrospray tandem mass spectrometry</atitle><jtitle>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</jtitle><addtitle>J Chromatogr B Analyt Technol Biomed Life Sci</addtitle><date>2007</date><risdate>2007</risdate><volume>845</volume><issue>1</issue><spage>74</spage><epage>79</epage><pages>74-79</pages><issn>1570-0232</issn><eissn>1873-376X</eissn><abstract>A quantitative liquid chromatography–tandem mass spectrometric (LC–MS/MS) method has been developed for the determination of malachite green (MG) and its metabolite leucomalachite green (LMG) in fish. Residues were extracted with an acetonitrile–acetate buffer and purified using the automated solid-phase extraction (ASPEC). Residues were analyzed with a reversed-phase LC–MS/MS using a positive-ion electrospray ionisation (ESI). Isotope-labelled leucomalachite green (LMG-D5) was used as an internal standard for the quantification of LMG residues. The related dye, brilliant green (BG) was used as an instrumental standard. Identification and quantification of analytes were based on the ion transitions monitored by multiple reaction monitoring (MRM). The decision limit (CCα) for MG and LMG was 0.13 and 0.16
μg
kg
−1. The respective detection capabilities (CCβ) were 0.22 and 0.27
μg
kg
−1. The absolute recovery (repeatability SD
r) was in the range of 58–65% (7.8–11.2%) for MG and 59–68% (9.7–16.9%) for LMG. LMG was quantified also based on the internal standard, giving a recovery (repeatability SD
r) of 103–110% (4.8–9.3%). The method was further evaluated by analyzing a total of 34 fish residue monitoring samples, of which eight samples were found to be non-compliant containing low residues of LMG.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>16931188</pmid><doi>10.1016/j.jchromb.2006.07.048</doi><tpages>6</tpages></addata></record> |
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subjects | Analysis Analytical, structural and metabolic biochemistry Animals Antifungal Agents - analysis Biological and medical sciences Chromatography, Liquid - methods Confirmation Fish Fundamental and applied biological sciences. Psychology General pharmacology LC–MS/MS Leucomalachite green Malachite green Medical sciences Oncorhynchus mykiss Pharmacology. Drug treatments Rosaniline Dyes - analysis Spectrometry, Mass, Electrospray Ionization - methods Tandem Mass Spectrometry - methods |
title | A confirmatory analysis of malachite green residues in rainbow trout with liquid chromatography–electrospray tandem mass spectrometry |
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