A rapid UPLC-MS/MS method for the determination of oleanolic acid in rat plasma and liver tissue: application to plasma and liver pharmacokinetics
A reliable high‐throughput ultra‐high performance liquid chromatography–tandem mass spectrometry (UPLC‐MS/MS) method was developed and validated for oleanolic acid (OA) determination in rat plasma and liver tissue using glycyrrhetic acid as the internal standard (IS). Plasma and liver homogenate sam...
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Veröffentlicht in: | Biomedical chromatography 2016-04, Vol.30 (4), p.520-527 |
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creator | Li, Tian-xue Chu, Chao-sen Zhu, Jia-yu Yang, Tian-yi Zhang, Jie Hu, Yu-tao Yang, Xing-hao |
description | A reliable high‐throughput ultra‐high performance liquid chromatography–tandem mass spectrometry (UPLC‐MS/MS) method was developed and validated for oleanolic acid (OA) determination in rat plasma and liver tissue using glycyrrhetic acid as the internal standard (IS). Plasma and liver homogenate samples were prepared using solid‐phase extraction. Chromatographic separation was achieved on a C18 column using an isocratic mobile phase system. The detection was performed by multiple reaction monitoring mode via positive electrospray ionization interface. The calibration curves showed good linearity (R2 > 0.9997) within the tested concentration ranges. The lower limit of quantification for plasma and liver tissue was ≤0.75 ng/mL. The intra‐ and inter‐day precision and accuracy deviations were within ±15% in plasma and liver tissue. The mean extraction recoveries ranged from 80.8 to 87.0%. In addition, the carryover, matrix effect, stability and robustness involved in the method were also validated. The method was successfully applied to the plasma and hepatic pharmacokinetics of OA after oral administration to rats. Copyright © 2015 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/bmc.3577 |
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Plasma and liver homogenate samples were prepared using solid‐phase extraction. Chromatographic separation was achieved on a C18 column using an isocratic mobile phase system. The detection was performed by multiple reaction monitoring mode via positive electrospray ionization interface. The calibration curves showed good linearity (R2 > 0.9997) within the tested concentration ranges. The lower limit of quantification for plasma and liver tissue was ≤0.75 ng/mL. The intra‐ and inter‐day precision and accuracy deviations were within ±15% in plasma and liver tissue. The mean extraction recoveries ranged from 80.8 to 87.0%. In addition, the carryover, matrix effect, stability and robustness involved in the method were also validated. The method was successfully applied to the plasma and hepatic pharmacokinetics of OA after oral administration to rats. Copyright © 2015 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0269-3879</identifier><identifier>EISSN: 1099-0801</identifier><identifier>DOI: 10.1002/bmc.3577</identifier><identifier>PMID: 26234772</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Animals ; bio-analysis ; Chromatography, High Pressure Liquid - methods ; Limit of Detection ; Liquid-Liquid Extraction - methods ; Liver - chemistry ; liver tissue ; Male ; oleanolic acid ; Oleanolic Acid - analysis ; Oleanolic Acid - blood ; Rats ; Rats, Sprague-Dawley ; Reproducibility of Results ; solid-phase extraction ; Tandem Mass Spectrometry - methods ; UPLC-MS/MS</subject><ispartof>Biomedical chromatography, 2016-04, Vol.30 (4), p.520-527</ispartof><rights>Copyright © 2015 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4297-aac2b644da3cd37604a4ee575646355deb4e266b6463f8b72e3f01d5cf2d94183</citedby><cites>FETCH-LOGICAL-c4297-aac2b644da3cd37604a4ee575646355deb4e266b6463f8b72e3f01d5cf2d94183</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.3577$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbmc.3577$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26234772$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Tian-xue</creatorcontrib><creatorcontrib>Chu, Chao-sen</creatorcontrib><creatorcontrib>Zhu, Jia-yu</creatorcontrib><creatorcontrib>Yang, Tian-yi</creatorcontrib><creatorcontrib>Zhang, Jie</creatorcontrib><creatorcontrib>Hu, Yu-tao</creatorcontrib><creatorcontrib>Yang, Xing-hao</creatorcontrib><title>A rapid UPLC-MS/MS method for the determination of oleanolic acid in rat plasma and liver tissue: application to plasma and liver pharmacokinetics</title><title>Biomedical chromatography</title><addtitle>Biomed. Chromatogr</addtitle><description>A reliable high‐throughput ultra‐high performance liquid chromatography–tandem mass spectrometry (UPLC‐MS/MS) method was developed and validated for oleanolic acid (OA) determination in rat plasma and liver tissue using glycyrrhetic acid as the internal standard (IS). Plasma and liver homogenate samples were prepared using solid‐phase extraction. Chromatographic separation was achieved on a C18 column using an isocratic mobile phase system. The detection was performed by multiple reaction monitoring mode via positive electrospray ionization interface. The calibration curves showed good linearity (R2 > 0.9997) within the tested concentration ranges. The lower limit of quantification for plasma and liver tissue was ≤0.75 ng/mL. The intra‐ and inter‐day precision and accuracy deviations were within ±15% in plasma and liver tissue. The mean extraction recoveries ranged from 80.8 to 87.0%. In addition, the carryover, matrix effect, stability and robustness involved in the method were also validated. The method was successfully applied to the plasma and hepatic pharmacokinetics of OA after oral administration to rats. Copyright © 2015 John Wiley & Sons, Ltd.</description><subject>Animals</subject><subject>bio-analysis</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Limit of Detection</subject><subject>Liquid-Liquid Extraction - methods</subject><subject>Liver - chemistry</subject><subject>liver tissue</subject><subject>Male</subject><subject>oleanolic acid</subject><subject>Oleanolic Acid - analysis</subject><subject>Oleanolic Acid - blood</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reproducibility of Results</subject><subject>solid-phase extraction</subject><subject>Tandem Mass Spectrometry - methods</subject><subject>UPLC-MS/MS</subject><issn>0269-3879</issn><issn>1099-0801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10c1u1DAUBWALgehQkHgC5CWbtP6LnbBrB2iRZgqoVCytG_tGY5rEqZ0B-ho8MRnNUBaIlXWl75yFDyEvOTvhjInTpncnsjTmEVlwVtcFqxh_TBZM6LqQlamPyLOcvzHGai3MU3IktJDKGLEgv85ogjF4evNptSzW16fra9rjtImetjHRaYPU44SpDwNMIQ40tjR2CEPsgqPg5mQY5oqJjh3kHigMnnbhO87ZkPMW31AYx9nu01P8140bSD24eBsGnILLz8mTFrqMLw7vMbl5_-7L8rJYfbz4sDxbFU6J2hQATjRaKQ_SeWk0U6AQS1NqpWVZemwUCq2b3dlWjREoW8Z96Vrha8UreUxe73vHFO-2mCfbh-yw62DAuM2WG8MqzY1Qf6lLMeeErR1T6CHdW87sbgE7L2B3C8z01aF12_ToH-CfL59BsQc_Qof3_y2y5-vlofDgQ57w54OHdGu1kaa0X68u7NVnreq3q3N7KX8DR8-fWA</recordid><startdate>201604</startdate><enddate>201604</enddate><creator>Li, Tian-xue</creator><creator>Chu, Chao-sen</creator><creator>Zhu, Jia-yu</creator><creator>Yang, Tian-yi</creator><creator>Zhang, Jie</creator><creator>Hu, Yu-tao</creator><creator>Yang, Xing-hao</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>201604</creationdate><title>A rapid UPLC-MS/MS method for the determination of oleanolic acid in rat plasma and liver tissue: application to plasma and liver pharmacokinetics</title><author>Li, Tian-xue ; Chu, Chao-sen ; Zhu, Jia-yu ; Yang, Tian-yi ; Zhang, Jie ; Hu, Yu-tao ; Yang, Xing-hao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4297-aac2b644da3cd37604a4ee575646355deb4e266b6463f8b72e3f01d5cf2d94183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>bio-analysis</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Limit of Detection</topic><topic>Liquid-Liquid Extraction - methods</topic><topic>Liver - chemistry</topic><topic>liver tissue</topic><topic>Male</topic><topic>oleanolic acid</topic><topic>Oleanolic Acid - analysis</topic><topic>Oleanolic Acid - blood</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reproducibility of Results</topic><topic>solid-phase extraction</topic><topic>Tandem Mass Spectrometry - methods</topic><topic>UPLC-MS/MS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Tian-xue</creatorcontrib><creatorcontrib>Chu, Chao-sen</creatorcontrib><creatorcontrib>Zhu, Jia-yu</creatorcontrib><creatorcontrib>Yang, Tian-yi</creatorcontrib><creatorcontrib>Zhang, Jie</creatorcontrib><creatorcontrib>Hu, Yu-tao</creatorcontrib><creatorcontrib>Yang, Xing-hao</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>Li, Tian-xue</au><au>Chu, Chao-sen</au><au>Zhu, Jia-yu</au><au>Yang, Tian-yi</au><au>Zhang, Jie</au><au>Hu, Yu-tao</au><au>Yang, Xing-hao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A rapid UPLC-MS/MS method for the determination of oleanolic acid in rat plasma and liver tissue: application to plasma and liver pharmacokinetics</atitle><jtitle>Biomedical chromatography</jtitle><addtitle>Biomed. Chromatogr</addtitle><date>2016-04</date><risdate>2016</risdate><volume>30</volume><issue>4</issue><spage>520</spage><epage>527</epage><pages>520-527</pages><issn>0269-3879</issn><eissn>1099-0801</eissn><abstract>A reliable high‐throughput ultra‐high performance liquid chromatography–tandem mass spectrometry (UPLC‐MS/MS) method was developed and validated for oleanolic acid (OA) determination in rat plasma and liver tissue using glycyrrhetic acid as the internal standard (IS). Plasma and liver homogenate samples were prepared using solid‐phase extraction. Chromatographic separation was achieved on a C18 column using an isocratic mobile phase system. The detection was performed by multiple reaction monitoring mode via positive electrospray ionization interface. The calibration curves showed good linearity (R2 > 0.9997) within the tested concentration ranges. The lower limit of quantification for plasma and liver tissue was ≤0.75 ng/mL. The intra‐ and inter‐day precision and accuracy deviations were within ±15% in plasma and liver tissue. The mean extraction recoveries ranged from 80.8 to 87.0%. In addition, the carryover, matrix effect, stability and robustness involved in the method were also validated. The method was successfully applied to the plasma and hepatic pharmacokinetics of OA after oral administration to rats. Copyright © 2015 John Wiley & Sons, Ltd.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>26234772</pmid><doi>10.1002/bmc.3577</doi><tpages>8</tpages></addata></record> |
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subjects | Animals bio-analysis Chromatography, High Pressure Liquid - methods Limit of Detection Liquid-Liquid Extraction - methods Liver - chemistry liver tissue Male oleanolic acid Oleanolic Acid - analysis Oleanolic Acid - blood Rats Rats, Sprague-Dawley Reproducibility of Results solid-phase extraction Tandem Mass Spectrometry - methods UPLC-MS/MS |
title | A rapid UPLC-MS/MS method for the determination of oleanolic acid in rat plasma and liver tissue: application to plasma and liver pharmacokinetics |
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