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A highly efficient, high-throughput lipidomics platform for the quantitative detection of eicosanoids in human whole blood
We have developed an ultra-performance liquid chromatography–multiple reaction monitoring/mass spectrometry (UPLC–MRM/MS)-based, high-content, high-throughput platform that enables simultaneous profiling of multiple lipids produced ex vivo in human whole blood (HWB) on treatment with calcium ionopho...
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Published in: | Analytical biochemistry 2013-02, Vol.433 (2), p.181-188 |
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creator | Song, Jiao Liu, Xuejun Wu, Jiejun Meehan, Michael J. Blevitt, Jonathan M. Dorrestein, Pieter C. Milla, Marcos E. |
description | We have developed an ultra-performance liquid chromatography–multiple reaction monitoring/mass spectrometry (UPLC–MRM/MS)-based, high-content, high-throughput platform that enables simultaneous profiling of multiple lipids produced ex vivo in human whole blood (HWB) on treatment with calcium ionophore and its modulation with pharmacological agents. HWB samples were processed in a 96-well plate format compatible with high-throughput sample processing instrumentation. We employed a scheduled MRM (sMRM) method, with a triple–quadrupole mass spectrometer coupled to a UPLC system, to measure absolute amounts of 122 distinct eicosanoids using deuterated internal standards. In a 6.5-min run, we resolved and detected with high sensitivity (lower limit of quantification in the range of 0.4–460pg) all targeted analytes from a very small HWB sample (2.5μl). Approximately 90% of the analytes exhibited a dynamic range exceeding 1000. We also developed a tailored software package that dramatically sped up the overall data quantification and analysis process with superior consistency and accuracy. Matrix effects from HWB and precision of the calibration curve were evaluated using this newly developed automation tool. This platform was successfully applied to the global quantification of changes on all 122 eicosanoids in HWB samples from healthy donors in response to calcium ionophore stimulation. |
doi_str_mv | 10.1016/j.ab.2012.10.022 |
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HWB samples were processed in a 96-well plate format compatible with high-throughput sample processing instrumentation. We employed a scheduled MRM (sMRM) method, with a triple–quadrupole mass spectrometer coupled to a UPLC system, to measure absolute amounts of 122 distinct eicosanoids using deuterated internal standards. In a 6.5-min run, we resolved and detected with high sensitivity (lower limit of quantification in the range of 0.4–460pg) all targeted analytes from a very small HWB sample (2.5μl). Approximately 90% of the analytes exhibited a dynamic range exceeding 1000. We also developed a tailored software package that dramatically sped up the overall data quantification and analysis process with superior consistency and accuracy. Matrix effects from HWB and precision of the calibration curve were evaluated using this newly developed automation tool. This platform was successfully applied to the global quantification of changes on all 122 eicosanoids in HWB samples from healthy donors in response to calcium ionophore stimulation.</description><identifier>ISSN: 0003-2697</identifier><identifier>EISSN: 1096-0309</identifier><identifier>DOI: 10.1016/j.ab.2012.10.022</identifier><identifier>PMID: 23103340</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Automated software ; automation ; blood ; calcium ; Calcium Ionophores - pharmacology ; Chromatography, High Pressure Liquid - instrumentation ; Chromatography, High Pressure Liquid - methods ; computer software ; Eicosanoids ; Eicosanoids - blood ; High-throughput platform ; Human whole blood ; Humans ; instrumentation ; Lipidomics ; mass spectrometry ; Metabolomics - instrumentation ; Metabolomics - methods ; monitoring ; spectrometers ; UPLC–MRM/MS</subject><ispartof>Analytical biochemistry, 2013-02, Vol.433 (2), p.181-188</ispartof><rights>2012 Elsevier Inc.</rights><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c374t-5e3c1ec97b3d9b1ff2ef9b64653a7867966043708a8e6d980d384ee075d814063</citedby><cites>FETCH-LOGICAL-c374t-5e3c1ec97b3d9b1ff2ef9b64653a7867966043708a8e6d980d384ee075d814063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23103340$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Song, Jiao</creatorcontrib><creatorcontrib>Liu, Xuejun</creatorcontrib><creatorcontrib>Wu, Jiejun</creatorcontrib><creatorcontrib>Meehan, Michael J.</creatorcontrib><creatorcontrib>Blevitt, Jonathan M.</creatorcontrib><creatorcontrib>Dorrestein, Pieter C.</creatorcontrib><creatorcontrib>Milla, Marcos E.</creatorcontrib><title>A highly efficient, high-throughput lipidomics platform for the quantitative detection of eicosanoids in human whole blood</title><title>Analytical biochemistry</title><addtitle>Anal Biochem</addtitle><description>We have developed an ultra-performance liquid chromatography–multiple reaction monitoring/mass spectrometry (UPLC–MRM/MS)-based, high-content, high-throughput platform that enables simultaneous profiling of multiple lipids produced ex vivo in human whole blood (HWB) on treatment with calcium ionophore and its modulation with pharmacological agents. HWB samples were processed in a 96-well plate format compatible with high-throughput sample processing instrumentation. We employed a scheduled MRM (sMRM) method, with a triple–quadrupole mass spectrometer coupled to a UPLC system, to measure absolute amounts of 122 distinct eicosanoids using deuterated internal standards. In a 6.5-min run, we resolved and detected with high sensitivity (lower limit of quantification in the range of 0.4–460pg) all targeted analytes from a very small HWB sample (2.5μl). Approximately 90% of the analytes exhibited a dynamic range exceeding 1000. We also developed a tailored software package that dramatically sped up the overall data quantification and analysis process with superior consistency and accuracy. Matrix effects from HWB and precision of the calibration curve were evaluated using this newly developed automation tool. This platform was successfully applied to the global quantification of changes on all 122 eicosanoids in HWB samples from healthy donors in response to calcium ionophore stimulation.</description><subject>Automated software</subject><subject>automation</subject><subject>blood</subject><subject>calcium</subject><subject>Calcium Ionophores - pharmacology</subject><subject>Chromatography, High Pressure Liquid - instrumentation</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>computer software</subject><subject>Eicosanoids</subject><subject>Eicosanoids - blood</subject><subject>High-throughput platform</subject><subject>Human whole blood</subject><subject>Humans</subject><subject>instrumentation</subject><subject>Lipidomics</subject><subject>mass spectrometry</subject><subject>Metabolomics - instrumentation</subject><subject>Metabolomics - methods</subject><subject>monitoring</subject><subject>spectrometers</subject><subject>UPLC–MRM/MS</subject><issn>0003-2697</issn><issn>1096-0309</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp1kUFv1DAQRi0EotvCnRP4yIEs4zjrxNyqCgpSJQ7Qs-XY441XSZzaTqvy6_GyhRsXjzx68430hpA3DLYMmPh42Op-WwOry3cLdf2MbBhIUQEH-ZxsAIBXtZDtGTlP6QDAWLMTL8lZzRlw3sCG_Lqkg98P4yNF57zxOOcPfzpVHmJY98OyZjr6xdsweZPoMursQpxoeWgekN6tes4-6-zvkVrMaLIPMw2Oojch6Tl4m6if6bBOeqYPQxiR9mMI9hV54fSY8PVTvSC3Xz7_vPpa3Xy__nZ1eVMZ3ja52iE3DI1se25lz5yr0cleNGLHdduJVgoBDW-h0x0KKzuwvGsQod3ZjjUg-AV5f8pdYrhbMWU1-WRwHPWMYU2K1W1Z1EoJBYUTamJIKaJTS_STjo-KgToaVwele3U0fuwU42Xk7VP62k9o_w38VVyAdyfA6aD0Pvqkbn-UBFGuU4umkYX4dCKwWLj3GFU6HsKg9bHoVDb4_-__DdP6mnI</recordid><startdate>20130215</startdate><enddate>20130215</enddate><creator>Song, Jiao</creator><creator>Liu, Xuejun</creator><creator>Wu, Jiejun</creator><creator>Meehan, Michael J.</creator><creator>Blevitt, Jonathan M.</creator><creator>Dorrestein, Pieter C.</creator><creator>Milla, Marcos E.</creator><general>Elsevier Inc</general><scope>FBQ</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>20130215</creationdate><title>A highly efficient, high-throughput lipidomics platform for the quantitative detection of eicosanoids in human whole blood</title><author>Song, Jiao ; Liu, Xuejun ; Wu, Jiejun ; Meehan, Michael J. ; Blevitt, Jonathan M. ; Dorrestein, Pieter C. ; Milla, Marcos E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c374t-5e3c1ec97b3d9b1ff2ef9b64653a7867966043708a8e6d980d384ee075d814063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Automated software</topic><topic>automation</topic><topic>blood</topic><topic>calcium</topic><topic>Calcium Ionophores - pharmacology</topic><topic>Chromatography, High Pressure Liquid - instrumentation</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>computer software</topic><topic>Eicosanoids</topic><topic>Eicosanoids - blood</topic><topic>High-throughput platform</topic><topic>Human whole blood</topic><topic>Humans</topic><topic>instrumentation</topic><topic>Lipidomics</topic><topic>mass spectrometry</topic><topic>Metabolomics - instrumentation</topic><topic>Metabolomics - methods</topic><topic>monitoring</topic><topic>spectrometers</topic><topic>UPLC–MRM/MS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Song, Jiao</creatorcontrib><creatorcontrib>Liu, Xuejun</creatorcontrib><creatorcontrib>Wu, Jiejun</creatorcontrib><creatorcontrib>Meehan, Michael J.</creatorcontrib><creatorcontrib>Blevitt, Jonathan M.</creatorcontrib><creatorcontrib>Dorrestein, Pieter C.</creatorcontrib><creatorcontrib>Milla, Marcos E.</creatorcontrib><collection>AGRIS</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>Analytical biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Song, Jiao</au><au>Liu, Xuejun</au><au>Wu, Jiejun</au><au>Meehan, Michael J.</au><au>Blevitt, Jonathan M.</au><au>Dorrestein, Pieter C.</au><au>Milla, Marcos E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A highly efficient, high-throughput lipidomics platform for the quantitative detection of eicosanoids in human whole blood</atitle><jtitle>Analytical biochemistry</jtitle><addtitle>Anal Biochem</addtitle><date>2013-02-15</date><risdate>2013</risdate><volume>433</volume><issue>2</issue><spage>181</spage><epage>188</epage><pages>181-188</pages><issn>0003-2697</issn><eissn>1096-0309</eissn><abstract>We have developed an ultra-performance liquid chromatography–multiple reaction monitoring/mass spectrometry (UPLC–MRM/MS)-based, high-content, high-throughput platform that enables simultaneous profiling of multiple lipids produced ex vivo in human whole blood (HWB) on treatment with calcium ionophore and its modulation with pharmacological agents. HWB samples were processed in a 96-well plate format compatible with high-throughput sample processing instrumentation. We employed a scheduled MRM (sMRM) method, with a triple–quadrupole mass spectrometer coupled to a UPLC system, to measure absolute amounts of 122 distinct eicosanoids using deuterated internal standards. In a 6.5-min run, we resolved and detected with high sensitivity (lower limit of quantification in the range of 0.4–460pg) all targeted analytes from a very small HWB sample (2.5μl). Approximately 90% of the analytes exhibited a dynamic range exceeding 1000. We also developed a tailored software package that dramatically sped up the overall data quantification and analysis process with superior consistency and accuracy. Matrix effects from HWB and precision of the calibration curve were evaluated using this newly developed automation tool. This platform was successfully applied to the global quantification of changes on all 122 eicosanoids in HWB samples from healthy donors in response to calcium ionophore stimulation.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23103340</pmid><doi>10.1016/j.ab.2012.10.022</doi><tpages>8</tpages></addata></record> |
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subjects | Automated software automation blood calcium Calcium Ionophores - pharmacology Chromatography, High Pressure Liquid - instrumentation Chromatography, High Pressure Liquid - methods computer software Eicosanoids Eicosanoids - blood High-throughput platform Human whole blood Humans instrumentation Lipidomics mass spectrometry Metabolomics - instrumentation Metabolomics - methods monitoring spectrometers UPLC–MRM/MS |
title | A highly efficient, high-throughput lipidomics platform for the quantitative detection of eicosanoids in human whole blood |
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