Metabolite profiling in rat urine by liquid chromatography/electrospray ion trap mass spectrometry. Application to the study of heavy metal toxicity
This work reports the use of reverse‐phase liquid chromatography coupled to electrospray ion trap (QIT) mass spectrometry for the analysis of the metabolome in rat urine. An injection of 20 μL of urine into the chromatographic system is followed by a slow gradient elution and mass spectrometric dete...
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creator | Lafaye, Alexandra Junot, Christophe Gall, Béatrice Ramounet-Le Fritsch, Paul Tabet, Jean-Claude Ezan, Eric |
description | This work reports the use of reverse‐phase liquid chromatography coupled to electrospray ion trap (QIT) mass spectrometry for the analysis of the metabolome in rat urine. An injection of 20 μL of urine into the chromatographic system is followed by a slow gradient elution and mass spectrometric detection in the scanning mode from m/z 100–1000 in both positive and negative modes. Over a time scale of 90 min, 30 and 20 resolved peaks were observed in the positive and the negative modes, respectively, corresponding to the presence of a few hundred m/z ratios. By using a QIT analyzer, data‐dependent tandem mass spectrometry of selected m/z ratios identified several compounds in rat urine and characterized various chemical families, including carboxylic acids, amines, sulfated compounds, glucuronides and glycosides, by the observation of characteristic fragment ions or neutral losses. The method has been applied to the investigation of the chronic toxicity of heavy metals in rat urine. A few tens of m/z ratios, differing in intensity more than threefold from control values, were observed in both positive and negative modes. The time variations for some selected ions suggest that LC/ESI‐MS could allow selective characterization of biomarkers in response to specific toxic compounds. Copyright © 2003 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/rcm.1243 |
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Over a time scale of 90 min, 30 and 20 resolved peaks were observed in the positive and the negative modes, respectively, corresponding to the presence of a few hundred m/z ratios. By using a QIT analyzer, data‐dependent tandem mass spectrometry of selected m/z ratios identified several compounds in rat urine and characterized various chemical families, including carboxylic acids, amines, sulfated compounds, glucuronides and glycosides, by the observation of characteristic fragment ions or neutral losses. The method has been applied to the investigation of the chronic toxicity of heavy metals in rat urine. A few tens of m/z ratios, differing in intensity more than threefold from control values, were observed in both positive and negative modes. The time variations for some selected ions suggest that LC/ESI‐MS could allow selective characterization of biomarkers in response to specific toxic compounds. Copyright © 2003 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0951-4198</identifier><identifier>EISSN: 1097-0231</identifier><identifier>DOI: 10.1002/rcm.1243</identifier><identifier>PMID: 14608626</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Amino Acids - urine ; Animals ; Cadmium - toxicity ; Chromatography, High Pressure Liquid ; DNA - urine ; Metals, Heavy - toxicity ; Metals, Heavy - urine ; Peptide Mapping ; Rats ; Spectrometry, Mass, Electrospray Ionization ; Uranium - toxicity ; Vitamins - urine</subject><ispartof>Rapid communications in mass spectrometry, 2003-01, Vol.17 (22), p.2541-2549</ispartof><rights>Copyright © 2003 John Wiley & Sons, Ltd.</rights><rights>Copyright 2003 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4213-ff249b3c29b573b5670f4c35b178ace093572c67feeeff24fc053dd8ff9c484c3</citedby><cites>FETCH-LOGICAL-c4213-ff249b3c29b573b5670f4c35b178ace093572c67feeeff24fc053dd8ff9c484c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Frcm.1243$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Frcm.1243$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14608626$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lafaye, Alexandra</creatorcontrib><creatorcontrib>Junot, Christophe</creatorcontrib><creatorcontrib>Gall, Béatrice Ramounet-Le</creatorcontrib><creatorcontrib>Fritsch, Paul</creatorcontrib><creatorcontrib>Tabet, Jean-Claude</creatorcontrib><creatorcontrib>Ezan, Eric</creatorcontrib><title>Metabolite profiling in rat urine by liquid chromatography/electrospray ion trap mass spectrometry. Application to the study of heavy metal toxicity</title><title>Rapid communications in mass spectrometry</title><addtitle>Rapid Commun. Mass Spectrom</addtitle><description>This work reports the use of reverse‐phase liquid chromatography coupled to electrospray ion trap (QIT) mass spectrometry for the analysis of the metabolome in rat urine. An injection of 20 μL of urine into the chromatographic system is followed by a slow gradient elution and mass spectrometric detection in the scanning mode from m/z 100–1000 in both positive and negative modes. Over a time scale of 90 min, 30 and 20 resolved peaks were observed in the positive and the negative modes, respectively, corresponding to the presence of a few hundred m/z ratios. By using a QIT analyzer, data‐dependent tandem mass spectrometry of selected m/z ratios identified several compounds in rat urine and characterized various chemical families, including carboxylic acids, amines, sulfated compounds, glucuronides and glycosides, by the observation of characteristic fragment ions or neutral losses. The method has been applied to the investigation of the chronic toxicity of heavy metals in rat urine. A few tens of m/z ratios, differing in intensity more than threefold from control values, were observed in both positive and negative modes. The time variations for some selected ions suggest that LC/ESI‐MS could allow selective characterization of biomarkers in response to specific toxic compounds. Copyright © 2003 John Wiley & Sons, Ltd.</description><subject>Amino Acids - urine</subject><subject>Animals</subject><subject>Cadmium - toxicity</subject><subject>Chromatography, High Pressure Liquid</subject><subject>DNA - urine</subject><subject>Metals, Heavy - toxicity</subject><subject>Metals, Heavy - urine</subject><subject>Peptide Mapping</subject><subject>Rats</subject><subject>Spectrometry, Mass, Electrospray Ionization</subject><subject>Uranium - toxicity</subject><subject>Vitamins - urine</subject><issn>0951-4198</issn><issn>1097-0231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10NtO3DAQBmALFZWFVuIJqrnsTRYf4hwu6aqFSkDFoarUG8txxqzbZBNsL-D36AOTZVftVa9Gmvn0S_MTcszonFHKT7zp54znYo_MGK3LjHLB3pAZrSXLclZXB-QwhF-UMiY5fUsOWF7QquDFjPy5xKiboXMRYfSDdZ1b3YNbgdcR1t6tEJoEnXtYuxbM0g-9jsO91-MynWCHJvohjF4ncMMK4rSHXocAYXw99Rh9msPpOHbO6PhqBohLhBDXbYLBwhL1Y4IJ6m66PTvjYnpH9q3uAr7fzSPy_cvnu8V5dvHt7Ovi9CIzOWcis5bndSMMrxtZikYWJbW5EbJhZaUN0lrIkpuitIi4sdZQKdq2srY2eTXJI_Jxm2umL4JHq0bveu2TYlRtilVTsWpT7EQ_bOm4bnps_8FdkxPItuDJdZj-G6RuFpe7wJ13IeLzX6_9b1WUopTqx9WZkp_ubq-vft6qWrwA4UqV1A</recordid><startdate>20030101</startdate><enddate>20030101</enddate><creator>Lafaye, Alexandra</creator><creator>Junot, Christophe</creator><creator>Gall, Béatrice Ramounet-Le</creator><creator>Fritsch, Paul</creator><creator>Tabet, Jean-Claude</creator><creator>Ezan, Eric</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</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></search><sort><creationdate>20030101</creationdate><title>Metabolite profiling in rat urine by liquid chromatography/electrospray ion trap mass spectrometry. 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By using a QIT analyzer, data‐dependent tandem mass spectrometry of selected m/z ratios identified several compounds in rat urine and characterized various chemical families, including carboxylic acids, amines, sulfated compounds, glucuronides and glycosides, by the observation of characteristic fragment ions or neutral losses. The method has been applied to the investigation of the chronic toxicity of heavy metals in rat urine. A few tens of m/z ratios, differing in intensity more than threefold from control values, were observed in both positive and negative modes. The time variations for some selected ions suggest that LC/ESI‐MS could allow selective characterization of biomarkers in response to specific toxic compounds. Copyright © 2003 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>14608626</pmid><doi>10.1002/rcm.1243</doi><tpages>9</tpages></addata></record> |
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subjects | Amino Acids - urine Animals Cadmium - toxicity Chromatography, High Pressure Liquid DNA - urine Metals, Heavy - toxicity Metals, Heavy - urine Peptide Mapping Rats Spectrometry, Mass, Electrospray Ionization Uranium - toxicity Vitamins - urine |
title | Metabolite profiling in rat urine by liquid chromatography/electrospray ion trap mass spectrometry. Application to the study of heavy metal toxicity |
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