A method for analysis of wilfordmine in human plasma by liquid chromatography coupled with ion trap mass spectrometry
A simple and rapid liquid chromatography-ion trap mass spectrometric (LC-IT/MS) method has been developed and validated for quantification of wilfordmine in human plasma. After the protein precipitation was carried out by acetonitrile and the solution was cleaned by solid-phase extraction, the chrom...
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Veröffentlicht in: | Journal of chromatographic science 2015-01, Vol.53 (1), p.177-182 |
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creator | Zhou, Lixin Zhu, Hao Ouyang, Xiaokun Zhao, Jinshun Chen, Xiaohong |
description | A simple and rapid liquid chromatography-ion trap mass spectrometric (LC-IT/MS) method has been developed and validated for quantification of wilfordmine in human plasma. After the protein precipitation was carried out by acetonitrile and the solution was cleaned by solid-phase extraction, the chromatographic separation was performed on a Zorbax Plus RRHD C18 column by using a mixture of acetonitrile and 10.0 mmol/L ammonium acetate solution (70:30, v/v) as the mobile phase at a flow rate of 0.7 mL/min. Detection was performed on an atmospheric-pressure chemical ionization source in the positive multiple reaction monitoring mode using aconitine as an internal standard (IS) with transitions of m/z 806→710 for wilfordmine, and 646→586 for IS, respectively. The obtained calibration curve was linear (r = 0.9992) over the concentration range of 0.5-100.0 μg/L with a lower limit of quantification of 0.5 μg/L in plasma. The intra- and interday relative standard deviations were |
doi_str_mv | 10.1093/chromsci/bmu040 |
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After the protein precipitation was carried out by acetonitrile and the solution was cleaned by solid-phase extraction, the chromatographic separation was performed on a Zorbax Plus RRHD C18 column by using a mixture of acetonitrile and 10.0 mmol/L ammonium acetate solution (70:30, v/v) as the mobile phase at a flow rate of 0.7 mL/min. Detection was performed on an atmospheric-pressure chemical ionization source in the positive multiple reaction monitoring mode using aconitine as an internal standard (IS) with transitions of m/z 806→710 for wilfordmine, and 646→586 for IS, respectively. The obtained calibration curve was linear (r = 0.9992) over the concentration range of 0.5-100.0 μg/L with a lower limit of quantification of 0.5 μg/L in plasma. The intra- and interday relative standard deviations were <7.0 and 12.3%, respectively. The recoveries were between 86.0 and 97.0%. The proposed method was found to be applicable to clinical studies.</description><identifier>ISSN: 0021-9665</identifier><identifier>EISSN: 1945-239X</identifier><identifier>DOI: 10.1093/chromsci/bmu040</identifier><identifier>PMID: 24895446</identifier><language>eng</language><publisher>United States</publisher><subject>Acetonitrile ; Alkaloids - blood ; Chromatography ; Chromatography, High Pressure Liquid - methods ; Drugs, Chinese Herbal - analysis ; Extraction ; Flow rate ; Human ; Humans ; Ionization ; Liquid chromatography ; Mass Spectrometry - methods ; Standard deviation</subject><ispartof>Journal of chromatographic science, 2015-01, Vol.53 (1), p.177-182</ispartof><rights>Crown copyright 2014.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c292t-6576f74de49b286fcaa98823db30c6dbe4bc4a1467c2a9def02f0276af10958c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24895446$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Lixin</creatorcontrib><creatorcontrib>Zhu, Hao</creatorcontrib><creatorcontrib>Ouyang, Xiaokun</creatorcontrib><creatorcontrib>Zhao, Jinshun</creatorcontrib><creatorcontrib>Chen, Xiaohong</creatorcontrib><title>A method for analysis of wilfordmine in human plasma by liquid chromatography coupled with ion trap mass spectrometry</title><title>Journal of chromatographic science</title><addtitle>J Chromatogr Sci</addtitle><description>A simple and rapid liquid chromatography-ion trap mass spectrometric (LC-IT/MS) method has been developed and validated for quantification of wilfordmine in human plasma. After the protein precipitation was carried out by acetonitrile and the solution was cleaned by solid-phase extraction, the chromatographic separation was performed on a Zorbax Plus RRHD C18 column by using a mixture of acetonitrile and 10.0 mmol/L ammonium acetate solution (70:30, v/v) as the mobile phase at a flow rate of 0.7 mL/min. Detection was performed on an atmospheric-pressure chemical ionization source in the positive multiple reaction monitoring mode using aconitine as an internal standard (IS) with transitions of m/z 806→710 for wilfordmine, and 646→586 for IS, respectively. The obtained calibration curve was linear (r = 0.9992) over the concentration range of 0.5-100.0 μg/L with a lower limit of quantification of 0.5 μg/L in plasma. The intra- and interday relative standard deviations were <7.0 and 12.3%, respectively. The recoveries were between 86.0 and 97.0%. The proposed method was found to be applicable to clinical studies.</description><subject>Acetonitrile</subject><subject>Alkaloids - blood</subject><subject>Chromatography</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Drugs, Chinese Herbal - analysis</subject><subject>Extraction</subject><subject>Flow rate</subject><subject>Human</subject><subject>Humans</subject><subject>Ionization</subject><subject>Liquid chromatography</subject><subject>Mass Spectrometry - methods</subject><subject>Standard deviation</subject><issn>0021-9665</issn><issn>1945-239X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kEtLxDAUhYMozji6didZuqmTpGnaLAfxBQNuFNyVNA8baZpO0iD993acUbhwuYdzDpcPgGuM7jDi-Vq2wbso7bpxCVF0ApaY0yIjOf84BUuECM44Y8UCXMT4tT9xVZyDBaEVLyhlS5A20Omx9QoaH6DoRTdFG6E38Nt2s6Sc7TW0PWyTEz0cOhGdgM0EO7tLVsHfB8ToP4MY2glKn4ZOqzk8ttD6Ho6zDp2IEcZBy3E26zFMl-DMiC7qq-NegffHh7f752z7-vRyv9lmknAyZqwomSmp0pQ3pGJGCsGriuSqyZFkqtG0kVRgykpJBFfaIDJPyYSZ4RSVzFfg9tA7BL9LOo61s1HqrhO99inWuKwYQZQWdLauD1YZfIxBm3oI1okw1RjVe9b1H-v6wHpO3BzLU-O0-vf_wc1_AFZ4gHE</recordid><startdate>201501</startdate><enddate>201501</enddate><creator>Zhou, Lixin</creator><creator>Zhu, Hao</creator><creator>Ouyang, Xiaokun</creator><creator>Zhao, Jinshun</creator><creator>Chen, Xiaohong</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>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>201501</creationdate><title>A method for analysis of wilfordmine in human plasma by liquid chromatography coupled with ion trap mass spectrometry</title><author>Zhou, Lixin ; Zhu, Hao ; Ouyang, Xiaokun ; Zhao, Jinshun ; Chen, Xiaohong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c292t-6576f74de49b286fcaa98823db30c6dbe4bc4a1467c2a9def02f0276af10958c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acetonitrile</topic><topic>Alkaloids - blood</topic><topic>Chromatography</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Drugs, Chinese Herbal - analysis</topic><topic>Extraction</topic><topic>Flow rate</topic><topic>Human</topic><topic>Humans</topic><topic>Ionization</topic><topic>Liquid chromatography</topic><topic>Mass Spectrometry - methods</topic><topic>Standard deviation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Lixin</creatorcontrib><creatorcontrib>Zhu, Hao</creatorcontrib><creatorcontrib>Ouyang, Xiaokun</creatorcontrib><creatorcontrib>Zhao, Jinshun</creatorcontrib><creatorcontrib>Chen, Xiaohong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of chromatographic science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Lixin</au><au>Zhu, Hao</au><au>Ouyang, Xiaokun</au><au>Zhao, Jinshun</au><au>Chen, Xiaohong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A method for analysis of wilfordmine in human plasma by liquid chromatography coupled with ion trap mass spectrometry</atitle><jtitle>Journal of chromatographic science</jtitle><addtitle>J Chromatogr Sci</addtitle><date>2015-01</date><risdate>2015</risdate><volume>53</volume><issue>1</issue><spage>177</spage><epage>182</epage><pages>177-182</pages><issn>0021-9665</issn><eissn>1945-239X</eissn><abstract>A simple and rapid liquid chromatography-ion trap mass spectrometric (LC-IT/MS) method has been developed and validated for quantification of wilfordmine in human plasma. After the protein precipitation was carried out by acetonitrile and the solution was cleaned by solid-phase extraction, the chromatographic separation was performed on a Zorbax Plus RRHD C18 column by using a mixture of acetonitrile and 10.0 mmol/L ammonium acetate solution (70:30, v/v) as the mobile phase at a flow rate of 0.7 mL/min. Detection was performed on an atmospheric-pressure chemical ionization source in the positive multiple reaction monitoring mode using aconitine as an internal standard (IS) with transitions of m/z 806→710 for wilfordmine, and 646→586 for IS, respectively. The obtained calibration curve was linear (r = 0.9992) over the concentration range of 0.5-100.0 μg/L with a lower limit of quantification of 0.5 μg/L in plasma. The intra- and interday relative standard deviations were <7.0 and 12.3%, respectively. The recoveries were between 86.0 and 97.0%. The proposed method was found to be applicable to clinical studies.</abstract><cop>United States</cop><pmid>24895446</pmid><doi>10.1093/chromsci/bmu040</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetonitrile Alkaloids - blood Chromatography Chromatography, High Pressure Liquid - methods Drugs, Chinese Herbal - analysis Extraction Flow rate Human Humans Ionization Liquid chromatography Mass Spectrometry - methods Standard deviation |
title | A method for analysis of wilfordmine in human plasma by liquid chromatography coupled with ion trap mass spectrometry |
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