Detection and validated quantification of toxic alkaloids in human blood plasma-comparison of LC-APCI-MS with LC-ESI-MS/MS
Poisonings with toxic plants may occur after abuse, intentional or accidental ingestion of plants. For diagnosis of such poisonings, multianalyte procedures were developed for detection and validated quantification of the toxic alkaloids aconitine, atropine, colchicine, coniine, cytisine, nicotine a...
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description | Poisonings with toxic plants may occur after abuse, intentional or accidental ingestion of plants. For diagnosis of such poisonings, multianalyte procedures were developed for detection and validated quantification of the toxic alkaloids aconitine, atropine, colchicine, coniine, cytisine, nicotine and its metabolite cotinine, physostigmine, and scopolamine in plasma using LC‐APCI‐MS and LC‐ESI‐MS/MS. After mixed‐mode solid‐phase extraction of 1 ml of plasma, the analytes were separated using a C8 base select separation column and gradient elution (acetonitrile/ammonium formate, pH 3.5). Calibration curves were used for quantification with cotinine‐d3, benzoylecgonine‐d3, and trimipramine‐d3 as internal standards. The method was validated according to international guidelines. Both assays were selective for the tested compounds. No instability was observed after repeated freezing and thawing or in processed samples. The assays were linear for coniine, cytisine, nicotine and its metabolite cotinine, from 50 to 1000 ng/ml using LC‐APCI‐MS and 1 to 1000 ng/ml using LC‐ESI‐MS/MS, respectively, and for aconitine, atropine, colchicine, physostigmine, and scopolamine from 5 to 100 ng/ml for LC‐APCI‐MS and 0.1 to 100 ng/ml for LC‐ESI‐MS/MS, respectively. Accuracy ranged from − 38.6 to 14.0%, repeatability from 2.5 to 13.5%, and intermediate precision from 4.8 to 13.5% using LC‐APCI‐MS and from − 38.3 to 8.3% for accuracy, from 3.5 to 13.8%, for repeatability, and from 4.3 to 14.7% for intermediate precision using LC‐ESI‐MS/MS. The lower limit of quantification was fixed at the lowest calibrator in the linearity experiments. With the exception of the greater sensitivity and higher identification power, LC‐ESI‐MS/MS had no major advantages over LC‐APCI‐MS. Both presented assays were applicable for sensitive detection of all studied analytes and for accurate and precise quantification, with the exception of the rather volatile nicotine. The applicability of the assays was demonstrated by analysis of plasma samples from suspected poisoning cases. Copyright © 2007 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/jms.1191 |
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For diagnosis of such poisonings, multianalyte procedures were developed for detection and validated quantification of the toxic alkaloids aconitine, atropine, colchicine, coniine, cytisine, nicotine and its metabolite cotinine, physostigmine, and scopolamine in plasma using LC‐APCI‐MS and LC‐ESI‐MS/MS. After mixed‐mode solid‐phase extraction of 1 ml of plasma, the analytes were separated using a C8 base select separation column and gradient elution (acetonitrile/ammonium formate, pH 3.5). Calibration curves were used for quantification with cotinine‐d3, benzoylecgonine‐d3, and trimipramine‐d3 as internal standards. The method was validated according to international guidelines. Both assays were selective for the tested compounds. No instability was observed after repeated freezing and thawing or in processed samples. The assays were linear for coniine, cytisine, nicotine and its metabolite cotinine, from 50 to 1000 ng/ml using LC‐APCI‐MS and 1 to 1000 ng/ml using LC‐ESI‐MS/MS, respectively, and for aconitine, atropine, colchicine, physostigmine, and scopolamine from 5 to 100 ng/ml for LC‐APCI‐MS and 0.1 to 100 ng/ml for LC‐ESI‐MS/MS, respectively. Accuracy ranged from − 38.6 to 14.0%, repeatability from 2.5 to 13.5%, and intermediate precision from 4.8 to 13.5% using LC‐APCI‐MS and from − 38.3 to 8.3% for accuracy, from 3.5 to 13.8%, for repeatability, and from 4.3 to 14.7% for intermediate precision using LC‐ESI‐MS/MS. The lower limit of quantification was fixed at the lowest calibrator in the linearity experiments. With the exception of the greater sensitivity and higher identification power, LC‐ESI‐MS/MS had no major advantages over LC‐APCI‐MS. Both presented assays were applicable for sensitive detection of all studied analytes and for accurate and precise quantification, with the exception of the rather volatile nicotine. The applicability of the assays was demonstrated by analysis of plasma samples from suspected poisoning cases. Copyright © 2007 John Wiley & Sons, Ltd.</description><identifier>ISSN: 1076-5174</identifier><identifier>EISSN: 1096-9888</identifier><identifier>DOI: 10.1002/jms.1191</identifier><identifier>PMID: 17323418</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>alkaloids ; Alkaloids - analysis ; Alkaloids - blood ; Biological and medical sciences ; Chromatography, High Pressure Liquid ; determination ; Humans ; LC-MS ; LC-MS/MS ; Mass Spectrometry - methods ; Medical sciences ; Plant poisons toxicology ; Plants, Toxic - chemistry ; plasma ; Tandem Mass Spectrometry - methods ; Toxicology</subject><ispartof>Journal of mass spectrometry., 2007-05, Vol.42 (5), p.621-633</ispartof><rights>Copyright © 2007 John Wiley & Sons, Ltd.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3871-333d6decee787d3c97973e8310ae1f7ab9e218a69f838dcdbc2ef2d761bf676d3</citedby><cites>FETCH-LOGICAL-c3871-333d6decee787d3c97973e8310ae1f7ab9e218a69f838dcdbc2ef2d761bf676d3</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%2Fjms.1191$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjms.1191$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18743050$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17323418$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Beyer, Jochen</creatorcontrib><creatorcontrib>Peters, Frank T.</creatorcontrib><creatorcontrib>Kraemer, Thomas</creatorcontrib><creatorcontrib>Maurer, Hans H.</creatorcontrib><title>Detection and validated quantification of toxic alkaloids in human blood plasma-comparison of LC-APCI-MS with LC-ESI-MS/MS</title><title>Journal of mass spectrometry.</title><addtitle>J. Mass Spectrom</addtitle><description>Poisonings with toxic plants may occur after abuse, intentional or accidental ingestion of plants. For diagnosis of such poisonings, multianalyte procedures were developed for detection and validated quantification of the toxic alkaloids aconitine, atropine, colchicine, coniine, cytisine, nicotine and its metabolite cotinine, physostigmine, and scopolamine in plasma using LC‐APCI‐MS and LC‐ESI‐MS/MS. After mixed‐mode solid‐phase extraction of 1 ml of plasma, the analytes were separated using a C8 base select separation column and gradient elution (acetonitrile/ammonium formate, pH 3.5). Calibration curves were used for quantification with cotinine‐d3, benzoylecgonine‐d3, and trimipramine‐d3 as internal standards. The method was validated according to international guidelines. Both assays were selective for the tested compounds. No instability was observed after repeated freezing and thawing or in processed samples. The assays were linear for coniine, cytisine, nicotine and its metabolite cotinine, from 50 to 1000 ng/ml using LC‐APCI‐MS and 1 to 1000 ng/ml using LC‐ESI‐MS/MS, respectively, and for aconitine, atropine, colchicine, physostigmine, and scopolamine from 5 to 100 ng/ml for LC‐APCI‐MS and 0.1 to 100 ng/ml for LC‐ESI‐MS/MS, respectively. Accuracy ranged from − 38.6 to 14.0%, repeatability from 2.5 to 13.5%, and intermediate precision from 4.8 to 13.5% using LC‐APCI‐MS and from − 38.3 to 8.3% for accuracy, from 3.5 to 13.8%, for repeatability, and from 4.3 to 14.7% for intermediate precision using LC‐ESI‐MS/MS. The lower limit of quantification was fixed at the lowest calibrator in the linearity experiments. With the exception of the greater sensitivity and higher identification power, LC‐ESI‐MS/MS had no major advantages over LC‐APCI‐MS. Both presented assays were applicable for sensitive detection of all studied analytes and for accurate and precise quantification, with the exception of the rather volatile nicotine. The applicability of the assays was demonstrated by analysis of plasma samples from suspected poisoning cases. Copyright © 2007 John Wiley & Sons, Ltd.</description><subject>alkaloids</subject><subject>Alkaloids - analysis</subject><subject>Alkaloids - blood</subject><subject>Biological and medical sciences</subject><subject>Chromatography, High Pressure Liquid</subject><subject>determination</subject><subject>Humans</subject><subject>LC-MS</subject><subject>LC-MS/MS</subject><subject>Mass Spectrometry - methods</subject><subject>Medical sciences</subject><subject>Plant poisons toxicology</subject><subject>Plants, Toxic - chemistry</subject><subject>plasma</subject><subject>Tandem Mass Spectrometry - methods</subject><subject>Toxicology</subject><issn>1076-5174</issn><issn>1096-9888</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10MlOIzEQBmALDWKX5glGvow0Fwe7nXg5osAQUMIgheVoVXsRhl5CuwOEpydNWnCak6tUX7mkH6GfjA4YpdnxY5kGjGm2hfYY1YJopdSPrpaCjJgc7qL9lB4ppVoPxQ7aZZJnfMjUHno_9a23bawrDJXDL1BEB613-HkJVRtDtPA5rANu67doMRRPUNTRJRwr_LAsocJ5UdcOLwpIJRBblwtoYtrsTMfk5Hp8QWZz_Brbh64_m3ft8Wx-iLYDFMkf9e8Buv17djOekOm_84vxyZRYriQjnHMnnLfeSyUdt1pqyb3ijIJnQUKufcYUCB0UV8663GY-ZE4KlgchheMH6M_mX9vUKTU-mEUTS2hWhlHTxWfW8ZkuvjX9taGLZV569w37vNbgdw8gWShCA5WN6dspOeR0RNeObNxrLPzqvwfN5WzeH-59TK1_-_LQPBkhuRyZ-6tzw-7lZDa5uzKafwC3PJWC</recordid><startdate>200705</startdate><enddate>200705</enddate><creator>Beyer, Jochen</creator><creator>Peters, Frank T.</creator><creator>Kraemer, Thomas</creator><creator>Maurer, Hans H.</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</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></search><sort><creationdate>200705</creationdate><title>Detection and validated quantification of toxic alkaloids in human blood plasma-comparison of LC-APCI-MS with LC-ESI-MS/MS</title><author>Beyer, Jochen ; Peters, Frank T. ; Kraemer, Thomas ; Maurer, Hans H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3871-333d6decee787d3c97973e8310ae1f7ab9e218a69f838dcdbc2ef2d761bf676d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>alkaloids</topic><topic>Alkaloids - analysis</topic><topic>Alkaloids - blood</topic><topic>Biological and medical sciences</topic><topic>Chromatography, High Pressure Liquid</topic><topic>determination</topic><topic>Humans</topic><topic>LC-MS</topic><topic>LC-MS/MS</topic><topic>Mass Spectrometry - methods</topic><topic>Medical sciences</topic><topic>Plant poisons toxicology</topic><topic>Plants, Toxic - chemistry</topic><topic>plasma</topic><topic>Tandem Mass Spectrometry - methods</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beyer, Jochen</creatorcontrib><creatorcontrib>Peters, Frank T.</creatorcontrib><creatorcontrib>Kraemer, Thomas</creatorcontrib><creatorcontrib>Maurer, Hans H.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of mass spectrometry.</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beyer, Jochen</au><au>Peters, Frank T.</au><au>Kraemer, Thomas</au><au>Maurer, Hans H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection and validated quantification of toxic alkaloids in human blood plasma-comparison of LC-APCI-MS with LC-ESI-MS/MS</atitle><jtitle>Journal of mass spectrometry.</jtitle><addtitle>J. Mass Spectrom</addtitle><date>2007-05</date><risdate>2007</risdate><volume>42</volume><issue>5</issue><spage>621</spage><epage>633</epage><pages>621-633</pages><issn>1076-5174</issn><eissn>1096-9888</eissn><abstract>Poisonings with toxic plants may occur after abuse, intentional or accidental ingestion of plants. For diagnosis of such poisonings, multianalyte procedures were developed for detection and validated quantification of the toxic alkaloids aconitine, atropine, colchicine, coniine, cytisine, nicotine and its metabolite cotinine, physostigmine, and scopolamine in plasma using LC‐APCI‐MS and LC‐ESI‐MS/MS. After mixed‐mode solid‐phase extraction of 1 ml of plasma, the analytes were separated using a C8 base select separation column and gradient elution (acetonitrile/ammonium formate, pH 3.5). Calibration curves were used for quantification with cotinine‐d3, benzoylecgonine‐d3, and trimipramine‐d3 as internal standards. The method was validated according to international guidelines. Both assays were selective for the tested compounds. No instability was observed after repeated freezing and thawing or in processed samples. The assays were linear for coniine, cytisine, nicotine and its metabolite cotinine, from 50 to 1000 ng/ml using LC‐APCI‐MS and 1 to 1000 ng/ml using LC‐ESI‐MS/MS, respectively, and for aconitine, atropine, colchicine, physostigmine, and scopolamine from 5 to 100 ng/ml for LC‐APCI‐MS and 0.1 to 100 ng/ml for LC‐ESI‐MS/MS, respectively. Accuracy ranged from − 38.6 to 14.0%, repeatability from 2.5 to 13.5%, and intermediate precision from 4.8 to 13.5% using LC‐APCI‐MS and from − 38.3 to 8.3% for accuracy, from 3.5 to 13.8%, for repeatability, and from 4.3 to 14.7% for intermediate precision using LC‐ESI‐MS/MS. The lower limit of quantification was fixed at the lowest calibrator in the linearity experiments. With the exception of the greater sensitivity and higher identification power, LC‐ESI‐MS/MS had no major advantages over LC‐APCI‐MS. Both presented assays were applicable for sensitive detection of all studied analytes and for accurate and precise quantification, with the exception of the rather volatile nicotine. The applicability of the assays was demonstrated by analysis of plasma samples from suspected poisoning cases. Copyright © 2007 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>17323418</pmid><doi>10.1002/jms.1191</doi><tpages>13</tpages></addata></record> |
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subjects | alkaloids Alkaloids - analysis Alkaloids - blood Biological and medical sciences Chromatography, High Pressure Liquid determination Humans LC-MS LC-MS/MS Mass Spectrometry - methods Medical sciences Plant poisons toxicology Plants, Toxic - chemistry plasma Tandem Mass Spectrometry - methods Toxicology |
title | Detection and validated quantification of toxic alkaloids in human blood plasma-comparison of LC-APCI-MS with LC-ESI-MS/MS |
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