Simultaneous determination of four secoiridoid and iridoid glycosides in rat plasma by ultra performance liquid chromatography-tandem mass spectrometry and its application to a comparative pharmacokinetic study
A simple, reliable and rapid ultra‐performance liquid chromatography–tandem mass spectrometry method was developed and validated for the simultaneous quantification of four secoiridoid (gentiopicroside, swertiamarin, sweroside) and iridoid glycosides (loganic acid), the bio‐active ingredients in rat...
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Veröffentlicht in: | Biomedical chromatography 2016-02, Vol.30 (2), p.97-104 |
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description | A simple, reliable and rapid ultra‐performance liquid chromatography–tandem mass spectrometry method was developed and validated for the simultaneous quantification of four secoiridoid (gentiopicroside, swertiamarin, sweroside) and iridoid glycosides (loganic acid), the bio‐active ingredients in rat plasma. After liquid–liquid extraction, chromatographic separation was accomplished on a Shim‐pack XR‐ODS column with a mobile phase consisting of methanol and 0.1% formic acid in water. A triple quadrupole tandem mass spectrometry equipped with an electrospray ionization source was used as detector operating both in positive and negative ionization mode and operated by multiple‐reaction monitoring scanning. The lower limits of quantitation were 0.25–30 ng/mL for all the analytes. Both intra‐day and inter‐day precision and accuracy of analytes were well within acceptance criteria (±15%). The mean extraction recoveries of analytes and internal standard (amygdalin) from rat plasma were all >71.4%. The validated method was successfully applied to a comparative pharmacokinetic study of four analytes in rat plasma between normal and arthritic rats after oral administration of Huo Luo Xiao Ling Dan and Gentiana macrophylla extract, respectively. Results showed significant differences in pharmacokinetic properties of the analytes among the different groups. Copyright © 2015 John Wiley & Sons, Ltd. |
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After liquid–liquid extraction, chromatographic separation was accomplished on a Shim‐pack XR‐ODS column with a mobile phase consisting of methanol and 0.1% formic acid in water. A triple quadrupole tandem mass spectrometry equipped with an electrospray ionization source was used as detector operating both in positive and negative ionization mode and operated by multiple‐reaction monitoring scanning. The lower limits of quantitation were 0.25–30 ng/mL for all the analytes. Both intra‐day and inter‐day precision and accuracy of analytes were well within acceptance criteria (±15%). The mean extraction recoveries of analytes and internal standard (amygdalin) from rat plasma were all >71.4%. The validated method was successfully applied to a comparative pharmacokinetic study of four analytes in rat plasma between normal and arthritic rats after oral administration of Huo Luo Xiao Ling Dan and Gentiana macrophylla extract, respectively. Results showed significant differences in pharmacokinetic properties of the analytes among the different groups. Copyright © 2015 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0269-3879</identifier><identifier>EISSN: 1099-0801</identifier><identifier>DOI: 10.1002/bmc.3519</identifier><identifier>PMID: 26014753</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Administration, Oral ; Animals ; arthritis ; Arthritis, Experimental ; comparative pharmacokinetics ; Drugs, Chinese Herbal - administration & dosage ; Drugs, Chinese Herbal - pharmacokinetics ; Huo Luo Xiao Ling Dan ; Iridoid Glycosides - blood ; Iridoid Glycosides - chemistry ; Iridoid Glycosides - isolation & purification ; Iridoid Glycosides - pharmacokinetics ; Linear Models ; Male ; rat plasma ; Rats ; Rats, Sprague-Dawley ; Reproducibility of Results ; Sensitivity and Specificity ; UPLC-MS/MS</subject><ispartof>Biomedical chromatography, 2016-02, Vol.30 (2), p.97-104</ispartof><rights>Copyright © 2015 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4299-19c4b95a12e493858f936cc3f7f7160738703e4167f065f35937b057133877623</citedby><cites>FETCH-LOGICAL-c4299-19c4b95a12e493858f936cc3f7f7160738703e4167f065f35937b057133877623</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.3519$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbmc.3519$$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/26014753$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Yun</creatorcontrib><creatorcontrib>Ai, Yu</creatorcontrib><creatorcontrib>Wang, Fenrong</creatorcontrib><creatorcontrib>Ma, Wen</creatorcontrib><creatorcontrib>Bian, Qiaoxia</creatorcontrib><creatorcontrib>Lee, David Y.-W.</creatorcontrib><creatorcontrib>Dai, Ronghua</creatorcontrib><title>Simultaneous determination of four secoiridoid and iridoid glycosides in rat plasma by ultra performance liquid chromatography-tandem mass spectrometry and its application to a comparative pharmacokinetic study</title><title>Biomedical chromatography</title><addtitle>Biomed. Chromatogr</addtitle><description>A simple, reliable and rapid ultra‐performance liquid chromatography–tandem mass spectrometry method was developed and validated for the simultaneous quantification of four secoiridoid (gentiopicroside, swertiamarin, sweroside) and iridoid glycosides (loganic acid), the bio‐active ingredients in rat plasma. After liquid–liquid extraction, chromatographic separation was accomplished on a Shim‐pack XR‐ODS column with a mobile phase consisting of methanol and 0.1% formic acid in water. A triple quadrupole tandem mass spectrometry equipped with an electrospray ionization source was used as detector operating both in positive and negative ionization mode and operated by multiple‐reaction monitoring scanning. The lower limits of quantitation were 0.25–30 ng/mL for all the analytes. Both intra‐day and inter‐day precision and accuracy of analytes were well within acceptance criteria (±15%). The mean extraction recoveries of analytes and internal standard (amygdalin) from rat plasma were all >71.4%. The validated method was successfully applied to a comparative pharmacokinetic study of four analytes in rat plasma between normal and arthritic rats after oral administration of Huo Luo Xiao Ling Dan and Gentiana macrophylla extract, respectively. Results showed significant differences in pharmacokinetic properties of the analytes among the different groups. Copyright © 2015 John Wiley & Sons, Ltd.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>arthritis</subject><subject>Arthritis, Experimental</subject><subject>comparative pharmacokinetics</subject><subject>Drugs, Chinese Herbal - administration & dosage</subject><subject>Drugs, Chinese Herbal - pharmacokinetics</subject><subject>Huo Luo Xiao Ling Dan</subject><subject>Iridoid Glycosides - blood</subject><subject>Iridoid Glycosides - chemistry</subject><subject>Iridoid Glycosides - isolation & purification</subject><subject>Iridoid Glycosides - pharmacokinetics</subject><subject>Linear Models</subject><subject>Male</subject><subject>rat plasma</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</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>eNp1kcFuFSEUhidGY2-riU9gWLqZCsMAw1JvtNVUXagx6YZwmTO92GGgwGjnNX0iaea2rlxBcj6-Q_6_ql4QfEowbl7vnDmljMhH1YZgKWvcYfK42uCGy5p2Qh5Vxyn9xBhL3oin1VHDMWkFo5vqz1fr5jHrCfycUA8ZorOTztZPyA9o8HNECYy30fbe9khPPbq_X42L8cn2kJCdUNQZhVEnp9FuQcUZNQoQBx-dngyg0d7M5ZHZR-909ldRh_1Sl809OOR0SigFMLlMIcdlXZQT0iGM1qwfyh5pZLwLuiyzvwCFvS5246_tBNkalPLcL8-qJ4MeEzw_nCfV9_fvvm3P64svZx-2by5q0zYlIyJNu5NMkwZaSTvWDZJyY-ggBkE4FiU3TKElXAyYs4EyScUOM0FomQje0JPq1eoN0d_MkLJyNhkYxzVMRQTHHWs5Yf9QE31KEQYVonU6LopgddegKg2quwYL-vJgnXcO-gfwvrIC1Cvw246w_Fek3n7aHoQH3qYMtw-8jteKCyqY-vH5TDWX9CNtxbm6pH8BuyK5Bw</recordid><startdate>201602</startdate><enddate>201602</enddate><creator>Wu, Yun</creator><creator>Ai, Yu</creator><creator>Wang, Fenrong</creator><creator>Ma, Wen</creator><creator>Bian, Qiaoxia</creator><creator>Lee, David Y.-W.</creator><creator>Dai, Ronghua</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>201602</creationdate><title>Simultaneous determination of four secoiridoid and iridoid glycosides in rat plasma by ultra performance liquid chromatography-tandem mass spectrometry and its application to a comparative pharmacokinetic study</title><author>Wu, Yun ; Ai, Yu ; Wang, Fenrong ; Ma, Wen ; Bian, Qiaoxia ; Lee, David Y.-W. ; Dai, Ronghua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4299-19c4b95a12e493858f936cc3f7f7160738703e4167f065f35937b057133877623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>arthritis</topic><topic>Arthritis, Experimental</topic><topic>comparative pharmacokinetics</topic><topic>Drugs, Chinese Herbal - administration & dosage</topic><topic>Drugs, Chinese Herbal - pharmacokinetics</topic><topic>Huo Luo Xiao Ling Dan</topic><topic>Iridoid Glycosides - blood</topic><topic>Iridoid Glycosides - chemistry</topic><topic>Iridoid Glycosides - isolation & purification</topic><topic>Iridoid Glycosides - pharmacokinetics</topic><topic>Linear Models</topic><topic>Male</topic><topic>rat plasma</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>UPLC-MS/MS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Yun</creatorcontrib><creatorcontrib>Ai, Yu</creatorcontrib><creatorcontrib>Wang, Fenrong</creatorcontrib><creatorcontrib>Ma, Wen</creatorcontrib><creatorcontrib>Bian, Qiaoxia</creatorcontrib><creatorcontrib>Lee, David Y.-W.</creatorcontrib><creatorcontrib>Dai, Ronghua</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>Wu, Yun</au><au>Ai, Yu</au><au>Wang, Fenrong</au><au>Ma, Wen</au><au>Bian, Qiaoxia</au><au>Lee, David Y.-W.</au><au>Dai, Ronghua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous determination of four secoiridoid and iridoid glycosides in rat plasma by ultra performance liquid chromatography-tandem mass spectrometry and its application to a comparative pharmacokinetic study</atitle><jtitle>Biomedical chromatography</jtitle><addtitle>Biomed. Chromatogr</addtitle><date>2016-02</date><risdate>2016</risdate><volume>30</volume><issue>2</issue><spage>97</spage><epage>104</epage><pages>97-104</pages><issn>0269-3879</issn><eissn>1099-0801</eissn><abstract>A simple, reliable and rapid ultra‐performance liquid chromatography–tandem mass spectrometry method was developed and validated for the simultaneous quantification of four secoiridoid (gentiopicroside, swertiamarin, sweroside) and iridoid glycosides (loganic acid), the bio‐active ingredients in rat plasma. After liquid–liquid extraction, chromatographic separation was accomplished on a Shim‐pack XR‐ODS column with a mobile phase consisting of methanol and 0.1% formic acid in water. A triple quadrupole tandem mass spectrometry equipped with an electrospray ionization source was used as detector operating both in positive and negative ionization mode and operated by multiple‐reaction monitoring scanning. The lower limits of quantitation were 0.25–30 ng/mL for all the analytes. Both intra‐day and inter‐day precision and accuracy of analytes were well within acceptance criteria (±15%). The mean extraction recoveries of analytes and internal standard (amygdalin) from rat plasma were all >71.4%. The validated method was successfully applied to a comparative pharmacokinetic study of four analytes in rat plasma between normal and arthritic rats after oral administration of Huo Luo Xiao Ling Dan and Gentiana macrophylla extract, respectively. Results showed significant differences in pharmacokinetic properties of the analytes among the different groups. Copyright © 2015 John Wiley & Sons, Ltd.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>26014753</pmid><doi>10.1002/bmc.3519</doi><tpages>8</tpages></addata></record> |
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subjects | Administration, Oral Animals arthritis Arthritis, Experimental comparative pharmacokinetics Drugs, Chinese Herbal - administration & dosage Drugs, Chinese Herbal - pharmacokinetics Huo Luo Xiao Ling Dan Iridoid Glycosides - blood Iridoid Glycosides - chemistry Iridoid Glycosides - isolation & purification Iridoid Glycosides - pharmacokinetics Linear Models Male rat plasma Rats Rats, Sprague-Dawley Reproducibility of Results Sensitivity and Specificity UPLC-MS/MS |
title | Simultaneous determination of four secoiridoid and iridoid glycosides in rat plasma by ultra performance liquid chromatography-tandem mass spectrometry and its application to a comparative pharmacokinetic study |
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