Structure elucidation and identification of a common metabolite for naphthoylindole-based synthetic cannabinoids using LC-TOF and comparison to a synthetic reference standard

Abstract The identification of a predominate metabolite found in urine specimens which test positive for naphthoylindole-based synthetic cannabinoids is reported. The presence of this new metabolite was detected at the Air Force Drug Testing Lab Investigations Division during screening analysis for...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Forensic science international 2013-03, Vol.226 (1), p.81-87
Hauptverfasser: Lovett, Dennis P, Yanes, Enrique G, Herbelin, Travis W, Knoerzer, Timm A, Levisky, Joseph A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 87
container_issue 1
container_start_page 81
container_title Forensic science international
container_volume 226
creator Lovett, Dennis P
Yanes, Enrique G
Herbelin, Travis W
Knoerzer, Timm A
Levisky, Joseph A
description Abstract The identification of a predominate metabolite found in urine specimens which test positive for naphthoylindole-based synthetic cannabinoids is reported. The presence of this new metabolite was detected at the Air Force Drug Testing Lab Investigations Division during screening analysis for metabolites of JWH-018 and JWH-073, because it shares the same MRM transitions as the JWH-073 N -(3-hydroxybutyl) metabolite. However, the detected peak is chromatographically distinguished from other metabolites due to differences in retention time. This metabolite appears to be a common metabolite for select naphthoylindole-based synthetic cannabinoids that could potentially be used as a common biomarker for their qualitative and quantitative analyses. The new metabolite has been successfully identified as 3-(3-(1-naphthoyl)-1 H -indol-1-yl) propanoic acid ( 1 , JWH 072 N -propanoic acid metabolite, Fig. 1 ) by using various mass spectrometric and liquid chromatographic techniques as well as chemical derivatization. The metabolite identity was confirmed through the comparison of authentic positive urine and a chemically synthesized metabolite standard. Both materials shared the same chromatographic retention time on two separate chromatographic systems, mass fragmentation pattern and exact mass. Full characterization of the synthetic reference material and intermediates by1 H NMR,13 C NMR, IR and HRMS was also conducted.
doi_str_mv 10.1016/j.forsciint.2012.12.012
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1762132342</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S037907381200549X</els_id><sourcerecordid>1365153721</sourcerecordid><originalsourceid>FETCH-LOGICAL-c553t-95cd977f3afc4d7fa60a88960b2dea8c5da11a4d3ff68204058a2880cac869683</originalsourceid><addsrcrecordid>eNqNkt9qFDEUhwdR7Fp9BQ14482s-TOTydwIZbEqLPSiFbwL2eSMm3U2WZOMsC_lM3rGrS30pkLghOE7vzNJvqp6w-iSUSbf75ZDTNl6H8qSU8aXuLA8qRZMdbyWXImn1YKKrq9pJ9RZ9SLnHaW0bbl8Xp1xIZiQlC2q39clTbZMCQiMk_XOFB8DMcER7yAUP3h7-hQHYoiN-z3u91DMJo6-AMH_IMEctmUbj6MPLo5Qb0wGR_IxlC0Ub4k1IZiND9G7TKbsw3eyXtU3V5d_52DmwSSfMbdEnHHfl2CABMECyQVJk9zL6tlgxgyvbut59fXy483qc72--vRldbGubduKUvetdX3XDcIMtnHdYCQ1SvWSbrgDo2zrDGOmcWIYpOK0oa0yXClqjVWyl0qcV-9OuYcUf06Qi977bGEcTYA4Zc06yZngouGPo0K2rBUd8o-jrGtor1iP6NsH6C5OKeCZZ0q2TcNlh1R3omyKOeN16UPye5OOmlE9i6J3-k4UPYuicWHBzte3-dNmD-6u758ZCFycAMBr_uUhaUyZ38L5BLZoF_1_DPnwIMOiIijU-AOOkO9PpDM26OvZ11lXxtHUpv8m_gAnIes7</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1316544267</pqid></control><display><type>article</type><title>Structure elucidation and identification of a common metabolite for naphthoylindole-based synthetic cannabinoids using LC-TOF and comparison to a synthetic reference standard</title><source>Elsevier ScienceDirect Journals</source><source>ProQuest Central UK/Ireland</source><creator>Lovett, Dennis P ; Yanes, Enrique G ; Herbelin, Travis W ; Knoerzer, Timm A ; Levisky, Joseph A</creator><creatorcontrib>Lovett, Dennis P ; Yanes, Enrique G ; Herbelin, Travis W ; Knoerzer, Timm A ; Levisky, Joseph A</creatorcontrib><description>Abstract The identification of a predominate metabolite found in urine specimens which test positive for naphthoylindole-based synthetic cannabinoids is reported. The presence of this new metabolite was detected at the Air Force Drug Testing Lab Investigations Division during screening analysis for metabolites of JWH-018 and JWH-073, because it shares the same MRM transitions as the JWH-073 N -(3-hydroxybutyl) metabolite. However, the detected peak is chromatographically distinguished from other metabolites due to differences in retention time. This metabolite appears to be a common metabolite for select naphthoylindole-based synthetic cannabinoids that could potentially be used as a common biomarker for their qualitative and quantitative analyses. The new metabolite has been successfully identified as 3-(3-(1-naphthoyl)-1 H -indol-1-yl) propanoic acid ( 1 , JWH 072 N -propanoic acid metabolite, Fig. 1 ) by using various mass spectrometric and liquid chromatographic techniques as well as chemical derivatization. The metabolite identity was confirmed through the comparison of authentic positive urine and a chemically synthesized metabolite standard. Both materials shared the same chromatographic retention time on two separate chromatographic systems, mass fragmentation pattern and exact mass. Full characterization of the synthetic reference material and intermediates by1 H NMR,13 C NMR, IR and HRMS was also conducted.</description><identifier>ISSN: 0379-0738</identifier><identifier>EISSN: 1872-6283</identifier><identifier>DOI: 10.1016/j.forsciint.2012.12.012</identifier><identifier>PMID: 23313601</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Analytical chemistry ; Chromatography ; Common biomarker ; Drug testing ; Drugs ; Forensic science ; Forensic sciences ; JWH-072 metabolite ; LC-TOF ; Metabolites ; NMR ; Nuclear magnetic resonance ; Pathology ; Quantitative analysis ; Synthetic cannabinoid metabolites ; UPLC ; Urine</subject><ispartof>Forensic science international, 2013-03, Vol.226 (1), p.81-87</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2012 Elsevier Ireland Ltd</rights><rights>Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.</rights><rights>Copyright Elsevier Limited Mar 10, 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c553t-95cd977f3afc4d7fa60a88960b2dea8c5da11a4d3ff68204058a2880cac869683</citedby><cites>FETCH-LOGICAL-c553t-95cd977f3afc4d7fa60a88960b2dea8c5da11a4d3ff68204058a2880cac869683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1316544267?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976,64364,64366,64368,72218</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23313601$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lovett, Dennis P</creatorcontrib><creatorcontrib>Yanes, Enrique G</creatorcontrib><creatorcontrib>Herbelin, Travis W</creatorcontrib><creatorcontrib>Knoerzer, Timm A</creatorcontrib><creatorcontrib>Levisky, Joseph A</creatorcontrib><title>Structure elucidation and identification of a common metabolite for naphthoylindole-based synthetic cannabinoids using LC-TOF and comparison to a synthetic reference standard</title><title>Forensic science international</title><addtitle>Forensic Sci Int</addtitle><description>Abstract The identification of a predominate metabolite found in urine specimens which test positive for naphthoylindole-based synthetic cannabinoids is reported. The presence of this new metabolite was detected at the Air Force Drug Testing Lab Investigations Division during screening analysis for metabolites of JWH-018 and JWH-073, because it shares the same MRM transitions as the JWH-073 N -(3-hydroxybutyl) metabolite. However, the detected peak is chromatographically distinguished from other metabolites due to differences in retention time. This metabolite appears to be a common metabolite for select naphthoylindole-based synthetic cannabinoids that could potentially be used as a common biomarker for their qualitative and quantitative analyses. The new metabolite has been successfully identified as 3-(3-(1-naphthoyl)-1 H -indol-1-yl) propanoic acid ( 1 , JWH 072 N -propanoic acid metabolite, Fig. 1 ) by using various mass spectrometric and liquid chromatographic techniques as well as chemical derivatization. The metabolite identity was confirmed through the comparison of authentic positive urine and a chemically synthesized metabolite standard. Both materials shared the same chromatographic retention time on two separate chromatographic systems, mass fragmentation pattern and exact mass. Full characterization of the synthetic reference material and intermediates by1 H NMR,13 C NMR, IR and HRMS was also conducted.</description><subject>Analytical chemistry</subject><subject>Chromatography</subject><subject>Common biomarker</subject><subject>Drug testing</subject><subject>Drugs</subject><subject>Forensic science</subject><subject>Forensic sciences</subject><subject>JWH-072 metabolite</subject><subject>LC-TOF</subject><subject>Metabolites</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Pathology</subject><subject>Quantitative analysis</subject><subject>Synthetic cannabinoid metabolites</subject><subject>UPLC</subject><subject>Urine</subject><issn>0379-0738</issn><issn>1872-6283</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkt9qFDEUhwdR7Fp9BQ14482s-TOTydwIZbEqLPSiFbwL2eSMm3U2WZOMsC_lM3rGrS30pkLghOE7vzNJvqp6w-iSUSbf75ZDTNl6H8qSU8aXuLA8qRZMdbyWXImn1YKKrq9pJ9RZ9SLnHaW0bbl8Xp1xIZiQlC2q39clTbZMCQiMk_XOFB8DMcER7yAUP3h7-hQHYoiN-z3u91DMJo6-AMH_IMEctmUbj6MPLo5Qb0wGR_IxlC0Ub4k1IZiND9G7TKbsw3eyXtU3V5d_52DmwSSfMbdEnHHfl2CABMECyQVJk9zL6tlgxgyvbut59fXy483qc72--vRldbGubduKUvetdX3XDcIMtnHdYCQ1SvWSbrgDo2zrDGOmcWIYpOK0oa0yXClqjVWyl0qcV-9OuYcUf06Qi977bGEcTYA4Zc06yZngouGPo0K2rBUd8o-jrGtor1iP6NsH6C5OKeCZZ0q2TcNlh1R3omyKOeN16UPye5OOmlE9i6J3-k4UPYuicWHBzte3-dNmD-6u758ZCFycAMBr_uUhaUyZ38L5BLZoF_1_DPnwIMOiIijU-AOOkO9PpDM26OvZ11lXxtHUpv8m_gAnIes7</recordid><startdate>20130310</startdate><enddate>20130310</enddate><creator>Lovett, Dennis P</creator><creator>Yanes, Enrique G</creator><creator>Herbelin, Travis W</creator><creator>Knoerzer, Timm A</creator><creator>Levisky, Joseph A</creator><general>Elsevier Ireland Ltd</general><general>Elsevier Limited</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20130310</creationdate><title>Structure elucidation and identification of a common metabolite for naphthoylindole-based synthetic cannabinoids using LC-TOF and comparison to a synthetic reference standard</title><author>Lovett, Dennis P ; Yanes, Enrique G ; Herbelin, Travis W ; Knoerzer, Timm A ; Levisky, Joseph A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c553t-95cd977f3afc4d7fa60a88960b2dea8c5da11a4d3ff68204058a2880cac869683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Analytical chemistry</topic><topic>Chromatography</topic><topic>Common biomarker</topic><topic>Drug testing</topic><topic>Drugs</topic><topic>Forensic science</topic><topic>Forensic sciences</topic><topic>JWH-072 metabolite</topic><topic>LC-TOF</topic><topic>Metabolites</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Pathology</topic><topic>Quantitative analysis</topic><topic>Synthetic cannabinoid metabolites</topic><topic>UPLC</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lovett, Dennis P</creatorcontrib><creatorcontrib>Yanes, Enrique G</creatorcontrib><creatorcontrib>Herbelin, Travis W</creatorcontrib><creatorcontrib>Knoerzer, Timm A</creatorcontrib><creatorcontrib>Levisky, Joseph A</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Toxicology Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Forensic science international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lovett, Dennis P</au><au>Yanes, Enrique G</au><au>Herbelin, Travis W</au><au>Knoerzer, Timm A</au><au>Levisky, Joseph A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure elucidation and identification of a common metabolite for naphthoylindole-based synthetic cannabinoids using LC-TOF and comparison to a synthetic reference standard</atitle><jtitle>Forensic science international</jtitle><addtitle>Forensic Sci Int</addtitle><date>2013-03-10</date><risdate>2013</risdate><volume>226</volume><issue>1</issue><spage>81</spage><epage>87</epage><pages>81-87</pages><issn>0379-0738</issn><eissn>1872-6283</eissn><abstract>Abstract The identification of a predominate metabolite found in urine specimens which test positive for naphthoylindole-based synthetic cannabinoids is reported. The presence of this new metabolite was detected at the Air Force Drug Testing Lab Investigations Division during screening analysis for metabolites of JWH-018 and JWH-073, because it shares the same MRM transitions as the JWH-073 N -(3-hydroxybutyl) metabolite. However, the detected peak is chromatographically distinguished from other metabolites due to differences in retention time. This metabolite appears to be a common metabolite for select naphthoylindole-based synthetic cannabinoids that could potentially be used as a common biomarker for their qualitative and quantitative analyses. The new metabolite has been successfully identified as 3-(3-(1-naphthoyl)-1 H -indol-1-yl) propanoic acid ( 1 , JWH 072 N -propanoic acid metabolite, Fig. 1 ) by using various mass spectrometric and liquid chromatographic techniques as well as chemical derivatization. The metabolite identity was confirmed through the comparison of authentic positive urine and a chemically synthesized metabolite standard. Both materials shared the same chromatographic retention time on two separate chromatographic systems, mass fragmentation pattern and exact mass. Full characterization of the synthetic reference material and intermediates by1 H NMR,13 C NMR, IR and HRMS was also conducted.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>23313601</pmid><doi>10.1016/j.forsciint.2012.12.012</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0379-0738
ispartof Forensic science international, 2013-03, Vol.226 (1), p.81-87
issn 0379-0738
1872-6283
language eng
recordid cdi_proquest_miscellaneous_1762132342
source Elsevier ScienceDirect Journals; ProQuest Central UK/Ireland
subjects Analytical chemistry
Chromatography
Common biomarker
Drug testing
Drugs
Forensic science
Forensic sciences
JWH-072 metabolite
LC-TOF
Metabolites
NMR
Nuclear magnetic resonance
Pathology
Quantitative analysis
Synthetic cannabinoid metabolites
UPLC
Urine
title Structure elucidation and identification of a common metabolite for naphthoylindole-based synthetic cannabinoids using LC-TOF and comparison to a synthetic reference standard
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T16%3A15%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Structure%20elucidation%20and%20identification%20of%20a%20common%20metabolite%20for%20naphthoylindole-based%20synthetic%20cannabinoids%20using%20LC-TOF%20and%20comparison%20to%20a%20synthetic%20reference%20standard&rft.jtitle=Forensic%20science%20international&rft.au=Lovett,%20Dennis%20P&rft.date=2013-03-10&rft.volume=226&rft.issue=1&rft.spage=81&rft.epage=87&rft.pages=81-87&rft.issn=0379-0738&rft.eissn=1872-6283&rft_id=info:doi/10.1016/j.forsciint.2012.12.012&rft_dat=%3Cproquest_cross%3E1365153721%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1316544267&rft_id=info:pmid/23313601&rft_els_id=1_s2_0_S037907381200549X&rfr_iscdi=true