Evaluation of liquid chromatography-ion trap-time of flight hybrid mass spectrometry on the quantitative analysis for ginsenosides
ABSTRACTIt is ideal and desirable for a single instrument to meet the requirement of both qualitative and quantitative analysis of complicated components in pharmacokinetic research for herbal medicine. Liquid chromatography combined with hybrid ion trap and time‐of‐flight mass spectrometry (LCMS‐IT...
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| Veröffentlicht in: | Biomedical chromatography 2014-07, Vol.28 (7), p.1003-1010 |
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| container_title | Biomedical chromatography |
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| creator | Xing, Lu Xie, Lin Liang, Yan Xing, Rong Rao, Tai Zhou, Lijun Wang, Qian Fu, Hanxu Ye, Wei Wang, Guangji |
| description | ABSTRACTIt is ideal and desirable for a single instrument to meet the requirement of both qualitative and quantitative analysis of complicated components in pharmacokinetic research for herbal medicine. Liquid chromatography combined with hybrid ion trap and time‐of‐flight mass spectrometry (LCMS‐IT‐TOF) was recently confirmed as a very powerful tool for the qualitative analysis of both target and nontarget components in herbal medicines. The present study was designed to investigate the feasibility of LCMS‐IT‐TOF on quantitative analysis of ginsenosides in biological matrices. A simple liquid–liquid extraction procedure was followed by injection of the extracts onto a C18 column with gradient elution and detection based on LCMS‐IT‐TOF system in negative scan mode. The developed method was validated with respect to the limit of quantification, linear dynamic range, precision, accuracy, matrix effects and stabilities. All the results suggested that the presently developed method was sufficiently sensitive and robust enough to simultaneously monitor 15 ginsenosides with diverse properties and a large range of concentration differences. Therefore, this method would be expected to be highly useful for comprehensive studies of ginsenosides in complicated matrix. Copyright © 2014 John Wiley & Sons, Ltd. |
| doi_str_mv | 10.1002/bmc.3108 |
| format | Article |
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Liquid chromatography combined with hybrid ion trap and time‐of‐flight mass spectrometry (LCMS‐IT‐TOF) was recently confirmed as a very powerful tool for the qualitative analysis of both target and nontarget components in herbal medicines. The present study was designed to investigate the feasibility of LCMS‐IT‐TOF on quantitative analysis of ginsenosides in biological matrices. A simple liquid–liquid extraction procedure was followed by injection of the extracts onto a C18 column with gradient elution and detection based on LCMS‐IT‐TOF system in negative scan mode. The developed method was validated with respect to the limit of quantification, linear dynamic range, precision, accuracy, matrix effects and stabilities. All the results suggested that the presently developed method was sufficiently sensitive and robust enough to simultaneously monitor 15 ginsenosides with diverse properties and a large range of concentration differences. Therefore, this method would be expected to be highly useful for comprehensive studies of ginsenosides in complicated matrix. Copyright © 2014 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0269-3879</identifier><identifier>EISSN: 1099-0801</identifier><identifier>DOI: 10.1002/bmc.3108</identifier><identifier>PMID: 24420027</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Animals ; Chromatography, Liquid - methods ; ginsenosides ; Ginsenosides - blood ; Ginsenosides - chemistry ; Ginsenosides - isolation & purification ; Ginsenosides - pharmacokinetics ; herbal medicine ; LCMS-IT-TOF ; Linear Models ; Liquid-Liquid Extraction ; Male ; Mass Spectrometry - methods ; pharmacokinetics ; Rats ; Rats, Sprague-Dawley ; Reproducibility of Results ; Sensitivity and Specificity</subject><ispartof>Biomedical chromatography, 2014-07, Vol.28 (7), p.1003-1010</ispartof><rights>Copyright © 2014 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4298-8f165e443e0e37a0e303b9d1d9a5129210387a417fbfb9aaf30aae164147388e3</citedby><cites>FETCH-LOGICAL-c4298-8f165e443e0e37a0e303b9d1d9a5129210387a417fbfb9aaf30aae164147388e3</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%2Fbmc.3108$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbmc.3108$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24420027$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xing, Lu</creatorcontrib><creatorcontrib>Xie, Lin</creatorcontrib><creatorcontrib>Liang, Yan</creatorcontrib><creatorcontrib>Xing, Rong</creatorcontrib><creatorcontrib>Rao, Tai</creatorcontrib><creatorcontrib>Zhou, Lijun</creatorcontrib><creatorcontrib>Wang, Qian</creatorcontrib><creatorcontrib>Fu, Hanxu</creatorcontrib><creatorcontrib>Ye, Wei</creatorcontrib><creatorcontrib>Wang, Guangji</creatorcontrib><title>Evaluation of liquid chromatography-ion trap-time of flight hybrid mass spectrometry on the quantitative analysis for ginsenosides</title><title>Biomedical chromatography</title><addtitle>Biomed. Chromatogr</addtitle><description>ABSTRACTIt is ideal and desirable for a single instrument to meet the requirement of both qualitative and quantitative analysis of complicated components in pharmacokinetic research for herbal medicine. Liquid chromatography combined with hybrid ion trap and time‐of‐flight mass spectrometry (LCMS‐IT‐TOF) was recently confirmed as a very powerful tool for the qualitative analysis of both target and nontarget components in herbal medicines. The present study was designed to investigate the feasibility of LCMS‐IT‐TOF on quantitative analysis of ginsenosides in biological matrices. A simple liquid–liquid extraction procedure was followed by injection of the extracts onto a C18 column with gradient elution and detection based on LCMS‐IT‐TOF system in negative scan mode. The developed method was validated with respect to the limit of quantification, linear dynamic range, precision, accuracy, matrix effects and stabilities. All the results suggested that the presently developed method was sufficiently sensitive and robust enough to simultaneously monitor 15 ginsenosides with diverse properties and a large range of concentration differences. Therefore, this method would be expected to be highly useful for comprehensive studies of ginsenosides in complicated matrix. Copyright © 2014 John Wiley & Sons, Ltd.</description><subject>Animals</subject><subject>Chromatography, Liquid - methods</subject><subject>ginsenosides</subject><subject>Ginsenosides - blood</subject><subject>Ginsenosides - chemistry</subject><subject>Ginsenosides - isolation & purification</subject><subject>Ginsenosides - pharmacokinetics</subject><subject>herbal medicine</subject><subject>LCMS-IT-TOF</subject><subject>Linear Models</subject><subject>Liquid-Liquid Extraction</subject><subject>Male</subject><subject>Mass Spectrometry - methods</subject><subject>pharmacokinetics</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><issn>0269-3879</issn><issn>1099-0801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10M1u1DAUBWALUdGhIPEEyEs2KXbsceIlnZa2qIUNP0vrJrmZGJJ4xnYK2fLkOOq0rLqxLfm7R7qHkDecnXLG8vfVUJ8KzspnZMWZ1hkrGX9OVixXOhNloY_JyxB-Msa0yosX5DiXMk9zxYr8vbiDfoJo3UhdS3u7n2xD6867AaLbeth1c7Z8xvTMoh1wYW1vt12k3Vz5pAcIgYYd1jFNYfQzXXyHdD_BGG1M6XdIYYR-DjbQ1nm6tWPA0QXbYHhFjlroA74-3Cfk28eLr5ur7ObL5fXmw01Wy1yXWdlytUYpBTIUBaSDiUo3vNGw5rnOOUubguRFW7WVBmgFA0CuJJeFKEsUJ-Tdfe7Ou_2EIZrBhhr7HkZ0UzB8LZQqpZDqP629C8Fja3beDuBnw5lZGjepcbM0nujbQ-pUDdg8woeKE8juwW_b4_xkkDm73RwCD96GiH8ePfhfRhWiWJsfny_Nd6U-nauz3DDxD7x-m0s</recordid><startdate>201407</startdate><enddate>201407</enddate><creator>Xing, Lu</creator><creator>Xie, Lin</creator><creator>Liang, Yan</creator><creator>Xing, Rong</creator><creator>Rao, Tai</creator><creator>Zhou, Lijun</creator><creator>Wang, Qian</creator><creator>Fu, Hanxu</creator><creator>Ye, Wei</creator><creator>Wang, Guangji</creator><general>Blackwell Publishing 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><scope>7X8</scope></search><sort><creationdate>201407</creationdate><title>Evaluation of liquid chromatography-ion trap-time of flight hybrid mass spectrometry on the quantitative analysis for ginsenosides</title><author>Xing, Lu ; Xie, Lin ; Liang, Yan ; Xing, Rong ; Rao, Tai ; Zhou, Lijun ; Wang, Qian ; Fu, Hanxu ; Ye, Wei ; Wang, Guangji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4298-8f165e443e0e37a0e303b9d1d9a5129210387a417fbfb9aaf30aae164147388e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Chromatography, Liquid - methods</topic><topic>ginsenosides</topic><topic>Ginsenosides - blood</topic><topic>Ginsenosides - chemistry</topic><topic>Ginsenosides - isolation & purification</topic><topic>Ginsenosides - pharmacokinetics</topic><topic>herbal medicine</topic><topic>LCMS-IT-TOF</topic><topic>Linear Models</topic><topic>Liquid-Liquid Extraction</topic><topic>Male</topic><topic>Mass Spectrometry - methods</topic><topic>pharmacokinetics</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xing, Lu</creatorcontrib><creatorcontrib>Xie, Lin</creatorcontrib><creatorcontrib>Liang, Yan</creatorcontrib><creatorcontrib>Xing, Rong</creatorcontrib><creatorcontrib>Rao, Tai</creatorcontrib><creatorcontrib>Zhou, Lijun</creatorcontrib><creatorcontrib>Wang, Qian</creatorcontrib><creatorcontrib>Fu, Hanxu</creatorcontrib><creatorcontrib>Ye, Wei</creatorcontrib><creatorcontrib>Wang, Guangji</creatorcontrib><collection>Istex</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>Biomedical chromatography</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xing, Lu</au><au>Xie, Lin</au><au>Liang, Yan</au><au>Xing, Rong</au><au>Rao, Tai</au><au>Zhou, Lijun</au><au>Wang, Qian</au><au>Fu, Hanxu</au><au>Ye, Wei</au><au>Wang, Guangji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of liquid chromatography-ion trap-time of flight hybrid mass spectrometry on the quantitative analysis for ginsenosides</atitle><jtitle>Biomedical chromatography</jtitle><addtitle>Biomed. Chromatogr</addtitle><date>2014-07</date><risdate>2014</risdate><volume>28</volume><issue>7</issue><spage>1003</spage><epage>1010</epage><pages>1003-1010</pages><issn>0269-3879</issn><eissn>1099-0801</eissn><abstract>ABSTRACTIt is ideal and desirable for a single instrument to meet the requirement of both qualitative and quantitative analysis of complicated components in pharmacokinetic research for herbal medicine. Liquid chromatography combined with hybrid ion trap and time‐of‐flight mass spectrometry (LCMS‐IT‐TOF) was recently confirmed as a very powerful tool for the qualitative analysis of both target and nontarget components in herbal medicines. The present study was designed to investigate the feasibility of LCMS‐IT‐TOF on quantitative analysis of ginsenosides in biological matrices. A simple liquid–liquid extraction procedure was followed by injection of the extracts onto a C18 column with gradient elution and detection based on LCMS‐IT‐TOF system in negative scan mode. The developed method was validated with respect to the limit of quantification, linear dynamic range, precision, accuracy, matrix effects and stabilities. All the results suggested that the presently developed method was sufficiently sensitive and robust enough to simultaneously monitor 15 ginsenosides with diverse properties and a large range of concentration differences. Therefore, this method would be expected to be highly useful for comprehensive studies of ginsenosides in complicated matrix. Copyright © 2014 John Wiley & Sons, Ltd.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24420027</pmid><doi>10.1002/bmc.3108</doi><tpages>8</tpages></addata></record> |
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| subjects | Animals Chromatography, Liquid - methods ginsenosides Ginsenosides - blood Ginsenosides - chemistry Ginsenosides - isolation & purification Ginsenosides - pharmacokinetics herbal medicine LCMS-IT-TOF Linear Models Liquid-Liquid Extraction Male Mass Spectrometry - methods pharmacokinetics Rats Rats, Sprague-Dawley Reproducibility of Results Sensitivity and Specificity |
| title | Evaluation of liquid chromatography-ion trap-time of flight hybrid mass spectrometry on the quantitative analysis for ginsenosides |
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