LC–MS/MS method for determination of kansuinine a in rat plasma and its application to a rat pharmacokinetic study
Kansuinine A is a macrocyclic jatrophane diterpene isolated from the plant Euphorbia kansui Liou. It exhibits many pharmacological activities including cytoxic, antitumor, antiallergic and proinflammatory effects. In the present study, a simple and sensitive LC–MS/MS method was established and valid...
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description | Kansuinine A is a macrocyclic jatrophane diterpene isolated from the plant Euphorbia kansui Liou. It exhibits many pharmacological activities including cytoxic, antitumor, antiallergic and proinflammatory effects. In the present study, a simple and sensitive LC–MS/MS method was established and validated for the determination of kansuinine A in rat plasma. After methanol‐mediated protein precipitation, chromatographic separation was achieved on an Acquity BEH C18 column (2.1 × 100 mm, 1.7 μm) using acetonitrile and 0.1% formic acid in water as mobile phase by gradient elution. Kansuinine A and IS were quantified in negative multiple reaction monitoring mode with ion transitions at m/z 731.1–693.2 for kansuinine A and m/z 723.2–623.1 for IS. The method showed excellent linearity over the range 1–500 ng/ml. The intra‐ and inter‐day precisions (relative standard deviation) were 2.13–4.28 and 3.83–7.67%, respectively, whereas accuracy (relative error) ranged from −4.17 to 3.73%. The extraction recovery, stability and matrix effect met the requirement of the regulations issued by the US Food and Drug Administration. The validated method was successfully applied to the pre‐clinical pharmacokinetic study of kansuinine A in rats after oral administration (20 mg/kg) and intravenous administration (2 mg/kg). This study provides valuable reference for the further study of E. kansui liou, especially for the drug development and clinical application of kansuinine A. |
doi_str_mv | 10.1002/bmc.5282 |
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It exhibits many pharmacological activities including cytoxic, antitumor, antiallergic and proinflammatory effects. In the present study, a simple and sensitive LC–MS/MS method was established and validated for the determination of kansuinine A in rat plasma. After methanol‐mediated protein precipitation, chromatographic separation was achieved on an Acquity BEH C18 column (2.1 × 100 mm, 1.7 μm) using acetonitrile and 0.1% formic acid in water as mobile phase by gradient elution. Kansuinine A and IS were quantified in negative multiple reaction monitoring mode with ion transitions at m/z 731.1–693.2 for kansuinine A and m/z 723.2–623.1 for IS. The method showed excellent linearity over the range 1–500 ng/ml. The intra‐ and inter‐day precisions (relative standard deviation) were 2.13–4.28 and 3.83–7.67%, respectively, whereas accuracy (relative error) ranged from −4.17 to 3.73%. The extraction recovery, stability and matrix effect met the requirement of the regulations issued by the US Food and Drug Administration. The validated method was successfully applied to the pre‐clinical pharmacokinetic study of kansuinine A in rats after oral administration (20 mg/kg) and intravenous administration (2 mg/kg). This study provides valuable reference for the further study of E. kansui liou, especially for the drug development and clinical application of kansuinine A.</description><identifier>ISSN: 0269-3879</identifier><identifier>EISSN: 1099-0801</identifier><identifier>DOI: 10.1002/bmc.5282</identifier><identifier>PMID: 34806205</identifier><language>eng</language><publisher>England</publisher><subject>Animals ; bioavailability ; Chromatography, High Pressure Liquid - methods ; Chromatography, Liquid - methods ; kansuinine A ; LC–MS/MS ; Linear Models ; pharmacokinetic ; Rats ; Rats, Sprague-Dawley ; Reproducibility of Results ; Tandem Mass Spectrometry - methods</subject><ispartof>Biomedical chromatography, 2022-03, Vol.36 (3), p.e5282-n/a</ispartof><rights>2021 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3212-fea7f1755fb7f8da574869187fad58895f7417e9d1d3b77e4b118aac75625a223</citedby><cites>FETCH-LOGICAL-c3212-fea7f1755fb7f8da574869187fad58895f7417e9d1d3b77e4b118aac75625a223</cites><orcidid>0000-0002-9032-6543</orcidid></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.5282$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbmc.5282$$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/34806205$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jiang, Xianglan</creatorcontrib><creatorcontrib>Liu, Qingwang</creatorcontrib><creatorcontrib>Xue, Shiyang</creatorcontrib><title>LC–MS/MS method for determination of kansuinine a in rat plasma and its application to a rat pharmacokinetic study</title><title>Biomedical chromatography</title><addtitle>Biomed Chromatogr</addtitle><description>Kansuinine A is a macrocyclic jatrophane diterpene isolated from the plant Euphorbia kansui Liou. It exhibits many pharmacological activities including cytoxic, antitumor, antiallergic and proinflammatory effects. In the present study, a simple and sensitive LC–MS/MS method was established and validated for the determination of kansuinine A in rat plasma. After methanol‐mediated protein precipitation, chromatographic separation was achieved on an Acquity BEH C18 column (2.1 × 100 mm, 1.7 μm) using acetonitrile and 0.1% formic acid in water as mobile phase by gradient elution. Kansuinine A and IS were quantified in negative multiple reaction monitoring mode with ion transitions at m/z 731.1–693.2 for kansuinine A and m/z 723.2–623.1 for IS. The method showed excellent linearity over the range 1–500 ng/ml. The intra‐ and inter‐day precisions (relative standard deviation) were 2.13–4.28 and 3.83–7.67%, respectively, whereas accuracy (relative error) ranged from −4.17 to 3.73%. The extraction recovery, stability and matrix effect met the requirement of the regulations issued by the US Food and Drug Administration. The validated method was successfully applied to the pre‐clinical pharmacokinetic study of kansuinine A in rats after oral administration (20 mg/kg) and intravenous administration (2 mg/kg). This study provides valuable reference for the further study of E. kansui liou, especially for the drug development and clinical application of kansuinine A.</description><subject>Animals</subject><subject>bioavailability</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Chromatography, Liquid - methods</subject><subject>kansuinine A</subject><subject>LC–MS/MS</subject><subject>Linear Models</subject><subject>pharmacokinetic</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reproducibility of Results</subject><subject>Tandem Mass Spectrometry - methods</subject><issn>0269-3879</issn><issn>1099-0801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kLtO5DAYRi20CIaLxBOsXG4TsJ04tsvdETdpRhQDdfQntoWXJA62IzQd78Ab8iRkGC4V1dec7xQHoRNKTikh7KzumlPOJNtBM0qUyogk9BeaEVaqLJdC7aODGP8TQlTJxB7azwtJSkb4DKXF_PX5Zbk6W65wZ9K919j6gLVJJnSuh-R8j73FD9DH0fWuNxiw63GAhIcWYgcYeo1dihiGoXXN9pH8hL0z9xA6aPzD9EyuwTGNen2Edi200Rx_7CG6uzi_nV9li5vL6_nfRdbkjLLMGhCWCs5tLazUwEUhS0WlsKC5lIpbUVBhlKY6r4UwRU2pBGgELxkHxvJD9GfrHYJ_HE1MVediY9oWeuPHWLGSEEklV8U32gQfYzC2GoLrIKwrSqpN42pqXG0aT-jvD-tYd0Z_gZ9RJyDbAk-uNesfRdW_5fxd-AbeyIZa</recordid><startdate>202203</startdate><enddate>202203</enddate><creator>Jiang, Xianglan</creator><creator>Liu, Qingwang</creator><creator>Xue, Shiyang</creator><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><orcidid>https://orcid.org/0000-0002-9032-6543</orcidid></search><sort><creationdate>202203</creationdate><title>LC–MS/MS method for determination of kansuinine a in rat plasma and its application to a rat pharmacokinetic study</title><author>Jiang, Xianglan ; Liu, Qingwang ; Xue, Shiyang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3212-fea7f1755fb7f8da574869187fad58895f7417e9d1d3b77e4b118aac75625a223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>bioavailability</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Chromatography, Liquid - methods</topic><topic>kansuinine A</topic><topic>LC–MS/MS</topic><topic>Linear Models</topic><topic>pharmacokinetic</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reproducibility of Results</topic><topic>Tandem Mass Spectrometry - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiang, Xianglan</creatorcontrib><creatorcontrib>Liu, Qingwang</creatorcontrib><creatorcontrib>Xue, Shiyang</creatorcontrib><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>Jiang, Xianglan</au><au>Liu, Qingwang</au><au>Xue, Shiyang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LC–MS/MS method for determination of kansuinine a in rat plasma and its application to a rat pharmacokinetic study</atitle><jtitle>Biomedical chromatography</jtitle><addtitle>Biomed Chromatogr</addtitle><date>2022-03</date><risdate>2022</risdate><volume>36</volume><issue>3</issue><spage>e5282</spage><epage>n/a</epage><pages>e5282-n/a</pages><issn>0269-3879</issn><eissn>1099-0801</eissn><abstract>Kansuinine A is a macrocyclic jatrophane diterpene isolated from the plant Euphorbia kansui Liou. It exhibits many pharmacological activities including cytoxic, antitumor, antiallergic and proinflammatory effects. In the present study, a simple and sensitive LC–MS/MS method was established and validated for the determination of kansuinine A in rat plasma. After methanol‐mediated protein precipitation, chromatographic separation was achieved on an Acquity BEH C18 column (2.1 × 100 mm, 1.7 μm) using acetonitrile and 0.1% formic acid in water as mobile phase by gradient elution. Kansuinine A and IS were quantified in negative multiple reaction monitoring mode with ion transitions at m/z 731.1–693.2 for kansuinine A and m/z 723.2–623.1 for IS. The method showed excellent linearity over the range 1–500 ng/ml. The intra‐ and inter‐day precisions (relative standard deviation) were 2.13–4.28 and 3.83–7.67%, respectively, whereas accuracy (relative error) ranged from −4.17 to 3.73%. The extraction recovery, stability and matrix effect met the requirement of the regulations issued by the US Food and Drug Administration. The validated method was successfully applied to the pre‐clinical pharmacokinetic study of kansuinine A in rats after oral administration (20 mg/kg) and intravenous administration (2 mg/kg). This study provides valuable reference for the further study of E. kansui liou, especially for the drug development and clinical application of kansuinine A.</abstract><cop>England</cop><pmid>34806205</pmid><doi>10.1002/bmc.5282</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-9032-6543</orcidid></addata></record> |
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subjects | Animals bioavailability Chromatography, High Pressure Liquid - methods Chromatography, Liquid - methods kansuinine A LC–MS/MS Linear Models pharmacokinetic Rats Rats, Sprague-Dawley Reproducibility of Results Tandem Mass Spectrometry - methods |
title | LC–MS/MS method for determination of kansuinine a in rat plasma and its application to a rat pharmacokinetic study |
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