Simultaneous determination of six alkaloids in tobacco and tobacco products by direct analysis of real‐time triple quadrupole mass spectrometry with a modified pretreatment method
In order to determine six alkaloids (mass fraction) of nicotine, nornicotine, myosmine, anatabine, anabasine, and nicotyrine in tobacco and tobacco products quickly, accurately, and simultaneously, a novel method based on direct analysis of real‐time model in situ ionization technique combined tande...
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Veröffentlicht in: | Journal of separation science 2020-04, Vol.43 (8), p.1603-1613 |
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creator | Li, Chao Li, E'xian Ma, Ming Liu, Xiuming You, Junheng Wu, Yiqin Jiang, Wei Liu, Zhihua Qin, Yunhua |
description | In order to determine six alkaloids (mass fraction) of nicotine, nornicotine, myosmine, anatabine, anabasine, and nicotyrine in tobacco and tobacco products quickly, accurately, and simultaneously, a novel method based on direct analysis of real‐time model in situ ionization technique combined tandem mass spectrometry with a modified sample pretreatment was established, in which experimental parameters such as the type and amount of extraction solvent and injection rate were optimized, respectively. The samples of five commercial cigarettes and five kinds of tobacco leaves were analyzed by the established method, and the determined values were compared with those obtained using a gas chromatography with mass spectrometry method: (1) Under optimized conditions (30 mL ultrapure water as extraction solvent and with extraction rate of 0.6 mm/s), analysis could be completed within 10 min. (2) The linear range of the method was 0.002–2000 μg/g withR2=0.9957, the recovery ranged from 86.8 to 105.6%, and the limit of detection and the limit of quantification were 0.004–0.835 μg/g and 0.013–2.787 μg/g, respectively. (3) The relative standard deviation between direct analysis of real‐time method and the gas chromatography with mass spectrometry method was 0.34–8.83%. The established method is rapid, reliable, and suitable for the ultrafast determination of six alkaloids in tobacco and tobacco products. |
doi_str_mv | 10.1002/jssc.201900946 |
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The samples of five commercial cigarettes and five kinds of tobacco leaves were analyzed by the established method, and the determined values were compared with those obtained using a gas chromatography with mass spectrometry method: (1) Under optimized conditions (30 mL ultrapure water as extraction solvent and with extraction rate of 0.6 mm/s), analysis could be completed within 10 min. (2) The linear range of the method was 0.002–2000 μg/g withR2=0.9957, the recovery ranged from 86.8 to 105.6%, and the limit of detection and the limit of quantification were 0.004–0.835 μg/g and 0.013–2.787 μg/g, respectively. (3) The relative standard deviation between direct analysis of real‐time method and the gas chromatography with mass spectrometry method was 0.34–8.83%. The established method is rapid, reliable, and suitable for the ultrafast determination of six alkaloids in tobacco and tobacco products.</description><identifier>ISSN: 1615-9306</identifier><identifier>ISSN: 1615-9314</identifier><identifier>EISSN: 1615-9314</identifier><identifier>DOI: 10.1002/jssc.201900946</identifier><identifier>PMID: 32034866</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Alkaloids ; Alkaloids - analysis ; Chromatography ; Cigarettes ; direct analysis ; Gas chromatography ; Ions ; Mass Spectrometry ; Nicotine ; Parameter modification ; Pretreatment ; Quadrupoles ; Scientific imaging ; Solvents ; Spectroscopy ; Time Factors ; Tobacco ; Tobacco Products - analysis ; ultrapure water</subject><ispartof>Journal of separation science, 2020-04, Vol.43 (8), p.1603-1613</ispartof><rights>2020 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4053-cb138407f5764bb30156602fca0d50e23b57b1115fd9d5943854bee0adb59bf83</citedby><cites>FETCH-LOGICAL-c4053-cb138407f5764bb30156602fca0d50e23b57b1115fd9d5943854bee0adb59bf83</cites><orcidid>0000-0003-2730-0794</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%2Fjssc.201900946$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjssc.201900946$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32034866$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Chao</creatorcontrib><creatorcontrib>Li, E'xian</creatorcontrib><creatorcontrib>Ma, Ming</creatorcontrib><creatorcontrib>Liu, Xiuming</creatorcontrib><creatorcontrib>You, Junheng</creatorcontrib><creatorcontrib>Wu, Yiqin</creatorcontrib><creatorcontrib>Jiang, Wei</creatorcontrib><creatorcontrib>Liu, Zhihua</creatorcontrib><creatorcontrib>Qin, Yunhua</creatorcontrib><title>Simultaneous determination of six alkaloids in tobacco and tobacco products by direct analysis of real‐time triple quadrupole mass spectrometry with a modified pretreatment method</title><title>Journal of separation science</title><addtitle>J Sep Sci</addtitle><description>In order to determine six alkaloids (mass fraction) of nicotine, nornicotine, myosmine, anatabine, anabasine, and nicotyrine in tobacco and tobacco products quickly, accurately, and simultaneously, a novel method based on direct analysis of real‐time model in situ ionization technique combined tandem mass spectrometry with a modified sample pretreatment was established, in which experimental parameters such as the type and amount of extraction solvent and injection rate were optimized, respectively. The samples of five commercial cigarettes and five kinds of tobacco leaves were analyzed by the established method, and the determined values were compared with those obtained using a gas chromatography with mass spectrometry method: (1) Under optimized conditions (30 mL ultrapure water as extraction solvent and with extraction rate of 0.6 mm/s), analysis could be completed within 10 min. (2) The linear range of the method was 0.002–2000 μg/g withR2=0.9957, the recovery ranged from 86.8 to 105.6%, and the limit of detection and the limit of quantification were 0.004–0.835 μg/g and 0.013–2.787 μg/g, respectively. (3) The relative standard deviation between direct analysis of real‐time method and the gas chromatography with mass spectrometry method was 0.34–8.83%. The established method is rapid, reliable, and suitable for the ultrafast determination of six alkaloids in tobacco and tobacco products.</description><subject>Alkaloids</subject><subject>Alkaloids - analysis</subject><subject>Chromatography</subject><subject>Cigarettes</subject><subject>direct analysis</subject><subject>Gas chromatography</subject><subject>Ions</subject><subject>Mass Spectrometry</subject><subject>Nicotine</subject><subject>Parameter modification</subject><subject>Pretreatment</subject><subject>Quadrupoles</subject><subject>Scientific imaging</subject><subject>Solvents</subject><subject>Spectroscopy</subject><subject>Time Factors</subject><subject>Tobacco</subject><subject>Tobacco Products - analysis</subject><subject>ultrapure water</subject><issn>1615-9306</issn><issn>1615-9314</issn><issn>1615-9314</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkbuO1DAUhiMEYpeFlhJZoqGZ4TiOnaREI65aiWKgjnw50Xqw46ztaEnHI_AyvBBPgkezTEFD5V_2dz7J56-q5xS2FKB-fUhJb2ugPUDfiAfVJRWUb3pGm4fnDOKiepLSAYC2XQ-PqwtWA2s6IS6rX3vrF5flhGFJxGDG6O0ksw0TCSNJ9juR7pt0wZpE7ERyUFLrQORkznmOwSw6J6JWYmxEncuzdGuy6eiIKN3vHz-z9UhytLNDcrtIE5c5lOhlSiTNZSgGjzmu5M7mGyKJD8aOFk3Rl2uU2eOUSUFugnlaPRqlS_js_ryqvr57-2X3YXP9-f3H3ZvrjW6As41WlHUNtCNvRaMUA8qFgHrUEgwHrJniraKU8tH0hvcN63ijEEEaxXs1duyqenXyli_eLpjy4G3S6NxpX0PNeC14x3hf0Jf_oIewxLKGI9W3nDLKeaG2J0rHkFLEcZij9TKuA4XhWOhwLHQ4F1oGXtxrF-XRnPG_DRagOQF31uH6H93wab_fiZYz9gdGwbGg</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>Li, Chao</creator><creator>Li, E'xian</creator><creator>Ma, Ming</creator><creator>Liu, Xiuming</creator><creator>You, Junheng</creator><creator>Wu, Yiqin</creator><creator>Jiang, Wei</creator><creator>Liu, Zhihua</creator><creator>Qin, Yunhua</creator><general>Wiley Subscription Services, Inc</general><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>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2730-0794</orcidid></search><sort><creationdate>202004</creationdate><title>Simultaneous determination of six alkaloids in tobacco and tobacco products by direct analysis of real‐time triple quadrupole mass spectrometry with a modified pretreatment method</title><author>Li, Chao ; Li, E'xian ; Ma, Ming ; Liu, Xiuming ; You, Junheng ; Wu, Yiqin ; Jiang, Wei ; Liu, Zhihua ; Qin, Yunhua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4053-cb138407f5764bb30156602fca0d50e23b57b1115fd9d5943854bee0adb59bf83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Alkaloids</topic><topic>Alkaloids - analysis</topic><topic>Chromatography</topic><topic>Cigarettes</topic><topic>direct analysis</topic><topic>Gas chromatography</topic><topic>Ions</topic><topic>Mass Spectrometry</topic><topic>Nicotine</topic><topic>Parameter modification</topic><topic>Pretreatment</topic><topic>Quadrupoles</topic><topic>Scientific imaging</topic><topic>Solvents</topic><topic>Spectroscopy</topic><topic>Time Factors</topic><topic>Tobacco</topic><topic>Tobacco Products - analysis</topic><topic>ultrapure water</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Chao</creatorcontrib><creatorcontrib>Li, E'xian</creatorcontrib><creatorcontrib>Ma, Ming</creatorcontrib><creatorcontrib>Liu, Xiuming</creatorcontrib><creatorcontrib>You, Junheng</creatorcontrib><creatorcontrib>Wu, Yiqin</creatorcontrib><creatorcontrib>Jiang, Wei</creatorcontrib><creatorcontrib>Liu, Zhihua</creatorcontrib><creatorcontrib>Qin, Yunhua</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of separation science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Chao</au><au>Li, E'xian</au><au>Ma, Ming</au><au>Liu, Xiuming</au><au>You, Junheng</au><au>Wu, Yiqin</au><au>Jiang, Wei</au><au>Liu, Zhihua</au><au>Qin, Yunhua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous determination of six alkaloids in tobacco and tobacco products by direct analysis of real‐time triple quadrupole mass spectrometry with a modified pretreatment method</atitle><jtitle>Journal of separation science</jtitle><addtitle>J Sep Sci</addtitle><date>2020-04</date><risdate>2020</risdate><volume>43</volume><issue>8</issue><spage>1603</spage><epage>1613</epage><pages>1603-1613</pages><issn>1615-9306</issn><issn>1615-9314</issn><eissn>1615-9314</eissn><abstract>In order to determine six alkaloids (mass fraction) of nicotine, nornicotine, myosmine, anatabine, anabasine, and nicotyrine in tobacco and tobacco products quickly, accurately, and simultaneously, a novel method based on direct analysis of real‐time model in situ ionization technique combined tandem mass spectrometry with a modified sample pretreatment was established, in which experimental parameters such as the type and amount of extraction solvent and injection rate were optimized, respectively. The samples of five commercial cigarettes and five kinds of tobacco leaves were analyzed by the established method, and the determined values were compared with those obtained using a gas chromatography with mass spectrometry method: (1) Under optimized conditions (30 mL ultrapure water as extraction solvent and with extraction rate of 0.6 mm/s), analysis could be completed within 10 min. (2) The linear range of the method was 0.002–2000 μg/g withR2=0.9957, the recovery ranged from 86.8 to 105.6%, and the limit of detection and the limit of quantification were 0.004–0.835 μg/g and 0.013–2.787 μg/g, respectively. (3) The relative standard deviation between direct analysis of real‐time method and the gas chromatography with mass spectrometry method was 0.34–8.83%. The established method is rapid, reliable, and suitable for the ultrafast determination of six alkaloids in tobacco and tobacco products.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32034866</pmid><doi>10.1002/jssc.201900946</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-2730-0794</orcidid></addata></record> |
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subjects | Alkaloids Alkaloids - analysis Chromatography Cigarettes direct analysis Gas chromatography Ions Mass Spectrometry Nicotine Parameter modification Pretreatment Quadrupoles Scientific imaging Solvents Spectroscopy Time Factors Tobacco Tobacco Products - analysis ultrapure water |
title | Simultaneous determination of six alkaloids in tobacco and tobacco products by direct analysis of real‐time triple quadrupole mass spectrometry with a modified pretreatment method |
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