Loading…
Detection of 1-Benzylpiperazine, 1-(3-Trifluoromethylphenyl)-piperazine, and 1-(3-Chlorophenyl)-piperazine in 3,4-Methylenedioxymethamphetamine-Positive Urine Samples
Historically, ecstasy tablets contained 3,4-methylenedioxymethamphetamine (MDMA) as the psychoactive component. In recent years, the Drug Enforcement Administration (DEA) and other law enforcement agencies have seized ecstasy tablets that are comprised of psychoactive drugs or drug mixtures other th...
Saved in:
Published in: | Journal of analytical toxicology 2010-10, Vol.34 (8), p.464-469 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c460t-44f7e156764316c4d2554c0ed0270a08cd1f71d7abfe6ba02ef2c97bd535dbbe3 |
---|---|
cites | |
container_end_page | 469 |
container_issue | 8 |
container_start_page | 464 |
container_title | Journal of analytical toxicology |
container_volume | 34 |
creator | Dickson, Amber J. Vorce, Shawn P. Holler, Justin M. Lyons, Timothy P. |
description | Historically, ecstasy tablets contained 3,4-methylenedioxymethamphetamine (MDMA) as the psychoactive component. In recent years, the Drug Enforcement Administration (DEA) and other law enforcement agencies have seized ecstasy tablets that are comprised of psychoactive drugs or drug mixtures other than MDMA. Many jurisdictions have reported the presence of piperazine derivatives including 1-benzylpiperazine (BZP), 1-(3-trifluoromethylphenyl)-piperazine (TFMPP), and 1-(3-chlorophenyl)-piperazine (mCPP) in ecstasy tablets. These piperazine derivatives produce stimulant and psychoactive effects similar to those produced by MDMA, amphetamine, and methamphetamine. In many countries, their use is not controlled, and therefore they have become a legal alternative to MDMA. For this study, a targeted population of 251 MDMA-positive urine samples were analyzed for designer drugs, including the piperazine derivatives. A basic liquid-liquid extraction followed by pentafluoropropionic anhydride (PFPA) derivatization and a full scan (m/z 42–550) gas chromatography-mass spectrometry analysis was used to screen the urine samples for 33 designer drugs. Overall, in 36% of the specimens analyzed, a stimulant or psychoactive compound other than MDMA and 3,4-methylenedioxyamphetamine (MDA) was detected. BZP, TFMPP, and mCPP were detected in 15%, 7%, and 1% of the samples, respectively. |
doi_str_mv | 10.1093/jat/34.8.464 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_902376594</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/jat/34.8.464</oup_id><sourcerecordid>893265303</sourcerecordid><originalsourceid>FETCH-LOGICAL-c460t-44f7e156764316c4d2554c0ed0270a08cd1f71d7abfe6ba02ef2c97bd535dbbe3</originalsourceid><addsrcrecordid>eNqF0UFv0zAYBmALgVgZ3DijXBAg1Z0dO3ZyhAIbqAgkOmniYjnOF9UjiYPtoHU_iN-JS8uGxGEnS_4ev_6kF6GnlCwoqdjJpY4njC_KBRf8HprRihc454TdRzNCucBcCnKEHoVwSQgVpWAP0VFOS1rJis7Qr7cQwUTrhsy1GcVvYLjedqMdwetrO8A83b1keO1t203Oux7iJs03MGy7V_hfp4dmb5ebLsH_SWaHjM05_vQnAgZorLva7gJ1n3TUfUL4iws22p-Qnfvdm69p1kF4jB60ugvw5HAeo_P379bLM7z6fPph-XqFDRckYs5bCbQQUnBGheFNXhTcEGhILokmpWloK2kjdd2CqDXJoc1NJeumYEVT18CO0Yt97ujdjwlCVL0NBrpOD-CmoCqSMymKit8py4rlomCEJTnfS-NdCB5aNXrba79VlKhdhSpVqBhXpUoVJv7sEDzVPTQ3-G9nCTw_AB2M7lqvB2PDrWN5SSQvbzd003jXl3gvbYhwdWO1_66EZLJQZxffVLU-Ldf044Vasd9VIsK0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>893265303</pqid></control><display><type>article</type><title>Detection of 1-Benzylpiperazine, 1-(3-Trifluoromethylphenyl)-piperazine, and 1-(3-Chlorophenyl)-piperazine in 3,4-Methylenedioxymethamphetamine-Positive Urine Samples</title><source>Oxford Journals Online</source><source>Alma/SFX Local Collection</source><creator>Dickson, Amber J. ; Vorce, Shawn P. ; Holler, Justin M. ; Lyons, Timothy P.</creator><creatorcontrib>Dickson, Amber J. ; Vorce, Shawn P. ; Holler, Justin M. ; Lyons, Timothy P.</creatorcontrib><description>Historically, ecstasy tablets contained 3,4-methylenedioxymethamphetamine (MDMA) as the psychoactive component. In recent years, the Drug Enforcement Administration (DEA) and other law enforcement agencies have seized ecstasy tablets that are comprised of psychoactive drugs or drug mixtures other than MDMA. Many jurisdictions have reported the presence of piperazine derivatives including 1-benzylpiperazine (BZP), 1-(3-trifluoromethylphenyl)-piperazine (TFMPP), and 1-(3-chlorophenyl)-piperazine (mCPP) in ecstasy tablets. These piperazine derivatives produce stimulant and psychoactive effects similar to those produced by MDMA, amphetamine, and methamphetamine. In many countries, their use is not controlled, and therefore they have become a legal alternative to MDMA. For this study, a targeted population of 251 MDMA-positive urine samples were analyzed for designer drugs, including the piperazine derivatives. A basic liquid-liquid extraction followed by pentafluoropropionic anhydride (PFPA) derivatization and a full scan (m/z 42–550) gas chromatography-mass spectrometry analysis was used to screen the urine samples for 33 designer drugs. Overall, in 36% of the specimens analyzed, a stimulant or psychoactive compound other than MDMA and 3,4-methylenedioxyamphetamine (MDA) was detected. BZP, TFMPP, and mCPP were detected in 15%, 7%, and 1% of the samples, respectively.</description><identifier>ISSN: 0146-4760</identifier><identifier>EISSN: 1945-2403</identifier><identifier>DOI: 10.1093/jat/34.8.464</identifier><identifier>PMID: 21819791</identifier><identifier>CODEN: JATOD3</identifier><language>eng</language><publisher>Niles, IL: Oxford University Press</publisher><subject>3,4-Methylenedioxyamphetamine - urine ; Biological and medical sciences ; Central Nervous System Stimulants - urine ; Designer Drugs - analysis ; Drug addictions ; Humans ; Medical sciences ; N-Methyl-3,4-methylenedioxyamphetamine - urine ; Piperazines - urine ; Reproducibility of Results ; Substance Abuse Detection - methods ; Toxicology ; Urinalysis</subject><ispartof>Journal of analytical toxicology, 2010-10, Vol.34 (8), p.464-469</ispartof><rights>2010</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c460t-44f7e156764316c4d2554c0ed0270a08cd1f71d7abfe6ba02ef2c97bd535dbbe3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23280748$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21819791$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dickson, Amber J.</creatorcontrib><creatorcontrib>Vorce, Shawn P.</creatorcontrib><creatorcontrib>Holler, Justin M.</creatorcontrib><creatorcontrib>Lyons, Timothy P.</creatorcontrib><title>Detection of 1-Benzylpiperazine, 1-(3-Trifluoromethylphenyl)-piperazine, and 1-(3-Chlorophenyl)-piperazine in 3,4-Methylenedioxymethamphetamine-Positive Urine Samples</title><title>Journal of analytical toxicology</title><addtitle>Journal of Analytical Toxicology</addtitle><addtitle>Journal of Analytical Toxicology</addtitle><description>Historically, ecstasy tablets contained 3,4-methylenedioxymethamphetamine (MDMA) as the psychoactive component. In recent years, the Drug Enforcement Administration (DEA) and other law enforcement agencies have seized ecstasy tablets that are comprised of psychoactive drugs or drug mixtures other than MDMA. Many jurisdictions have reported the presence of piperazine derivatives including 1-benzylpiperazine (BZP), 1-(3-trifluoromethylphenyl)-piperazine (TFMPP), and 1-(3-chlorophenyl)-piperazine (mCPP) in ecstasy tablets. These piperazine derivatives produce stimulant and psychoactive effects similar to those produced by MDMA, amphetamine, and methamphetamine. In many countries, their use is not controlled, and therefore they have become a legal alternative to MDMA. For this study, a targeted population of 251 MDMA-positive urine samples were analyzed for designer drugs, including the piperazine derivatives. A basic liquid-liquid extraction followed by pentafluoropropionic anhydride (PFPA) derivatization and a full scan (m/z 42–550) gas chromatography-mass spectrometry analysis was used to screen the urine samples for 33 designer drugs. Overall, in 36% of the specimens analyzed, a stimulant or psychoactive compound other than MDMA and 3,4-methylenedioxyamphetamine (MDA) was detected. BZP, TFMPP, and mCPP were detected in 15%, 7%, and 1% of the samples, respectively.</description><subject>3,4-Methylenedioxyamphetamine - urine</subject><subject>Biological and medical sciences</subject><subject>Central Nervous System Stimulants - urine</subject><subject>Designer Drugs - analysis</subject><subject>Drug addictions</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>N-Methyl-3,4-methylenedioxyamphetamine - urine</subject><subject>Piperazines - urine</subject><subject>Reproducibility of Results</subject><subject>Substance Abuse Detection - methods</subject><subject>Toxicology</subject><subject>Urinalysis</subject><issn>0146-4760</issn><issn>1945-2403</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqF0UFv0zAYBmALgVgZ3DijXBAg1Z0dO3ZyhAIbqAgkOmniYjnOF9UjiYPtoHU_iN-JS8uGxGEnS_4ev_6kF6GnlCwoqdjJpY4njC_KBRf8HprRihc454TdRzNCucBcCnKEHoVwSQgVpWAP0VFOS1rJis7Qr7cQwUTrhsy1GcVvYLjedqMdwetrO8A83b1keO1t203Oux7iJs03MGy7V_hfp4dmb5ebLsH_SWaHjM05_vQnAgZorLva7gJ1n3TUfUL4iws22p-Qnfvdm69p1kF4jB60ugvw5HAeo_P379bLM7z6fPph-XqFDRckYs5bCbQQUnBGheFNXhTcEGhILokmpWloK2kjdd2CqDXJoc1NJeumYEVT18CO0Yt97ujdjwlCVL0NBrpOD-CmoCqSMymKit8py4rlomCEJTnfS-NdCB5aNXrba79VlKhdhSpVqBhXpUoVJv7sEDzVPTQ3-G9nCTw_AB2M7lqvB2PDrWN5SSQvbzd003jXl3gvbYhwdWO1_66EZLJQZxffVLU-Ldf044Vasd9VIsK0</recordid><startdate>20101001</startdate><enddate>20101001</enddate><creator>Dickson, Amber J.</creator><creator>Vorce, Shawn P.</creator><creator>Holler, Justin M.</creator><creator>Lyons, Timothy P.</creator><general>Oxford University Press</general><general>Preston Publications</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><scope>7X8</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20101001</creationdate><title>Detection of 1-Benzylpiperazine, 1-(3-Trifluoromethylphenyl)-piperazine, and 1-(3-Chlorophenyl)-piperazine in 3,4-Methylenedioxymethamphetamine-Positive Urine Samples</title><author>Dickson, Amber J. ; Vorce, Shawn P. ; Holler, Justin M. ; Lyons, Timothy P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c460t-44f7e156764316c4d2554c0ed0270a08cd1f71d7abfe6ba02ef2c97bd535dbbe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>3,4-Methylenedioxyamphetamine - urine</topic><topic>Biological and medical sciences</topic><topic>Central Nervous System Stimulants - urine</topic><topic>Designer Drugs - analysis</topic><topic>Drug addictions</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>N-Methyl-3,4-methylenedioxyamphetamine - urine</topic><topic>Piperazines - urine</topic><topic>Reproducibility of Results</topic><topic>Substance Abuse Detection - methods</topic><topic>Toxicology</topic><topic>Urinalysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dickson, Amber J.</creatorcontrib><creatorcontrib>Vorce, Shawn P.</creatorcontrib><creatorcontrib>Holler, Justin M.</creatorcontrib><creatorcontrib>Lyons, Timothy P.</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><collection>MEDLINE - Academic</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of analytical toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dickson, Amber J.</au><au>Vorce, Shawn P.</au><au>Holler, Justin M.</au><au>Lyons, Timothy P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of 1-Benzylpiperazine, 1-(3-Trifluoromethylphenyl)-piperazine, and 1-(3-Chlorophenyl)-piperazine in 3,4-Methylenedioxymethamphetamine-Positive Urine Samples</atitle><jtitle>Journal of analytical toxicology</jtitle><stitle>Journal of Analytical Toxicology</stitle><addtitle>Journal of Analytical Toxicology</addtitle><date>2010-10-01</date><risdate>2010</risdate><volume>34</volume><issue>8</issue><spage>464</spage><epage>469</epage><pages>464-469</pages><issn>0146-4760</issn><eissn>1945-2403</eissn><coden>JATOD3</coden><abstract>Historically, ecstasy tablets contained 3,4-methylenedioxymethamphetamine (MDMA) as the psychoactive component. In recent years, the Drug Enforcement Administration (DEA) and other law enforcement agencies have seized ecstasy tablets that are comprised of psychoactive drugs or drug mixtures other than MDMA. Many jurisdictions have reported the presence of piperazine derivatives including 1-benzylpiperazine (BZP), 1-(3-trifluoromethylphenyl)-piperazine (TFMPP), and 1-(3-chlorophenyl)-piperazine (mCPP) in ecstasy tablets. These piperazine derivatives produce stimulant and psychoactive effects similar to those produced by MDMA, amphetamine, and methamphetamine. In many countries, their use is not controlled, and therefore they have become a legal alternative to MDMA. For this study, a targeted population of 251 MDMA-positive urine samples were analyzed for designer drugs, including the piperazine derivatives. A basic liquid-liquid extraction followed by pentafluoropropionic anhydride (PFPA) derivatization and a full scan (m/z 42–550) gas chromatography-mass spectrometry analysis was used to screen the urine samples for 33 designer drugs. Overall, in 36% of the specimens analyzed, a stimulant or psychoactive compound other than MDMA and 3,4-methylenedioxyamphetamine (MDA) was detected. BZP, TFMPP, and mCPP were detected in 15%, 7%, and 1% of the samples, respectively.</abstract><cop>Niles, IL</cop><pub>Oxford University Press</pub><pmid>21819791</pmid><doi>10.1093/jat/34.8.464</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0146-4760 |
ispartof | Journal of analytical toxicology, 2010-10, Vol.34 (8), p.464-469 |
issn | 0146-4760 1945-2403 |
language | eng |
recordid | cdi_proquest_miscellaneous_902376594 |
source | Oxford Journals Online; Alma/SFX Local Collection |
subjects | 3,4-Methylenedioxyamphetamine - urine Biological and medical sciences Central Nervous System Stimulants - urine Designer Drugs - analysis Drug addictions Humans Medical sciences N-Methyl-3,4-methylenedioxyamphetamine - urine Piperazines - urine Reproducibility of Results Substance Abuse Detection - methods Toxicology Urinalysis |
title | Detection of 1-Benzylpiperazine, 1-(3-Trifluoromethylphenyl)-piperazine, and 1-(3-Chlorophenyl)-piperazine in 3,4-Methylenedioxymethamphetamine-Positive Urine Samples |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T19%3A01%3A06IST&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=Detection%20of%201-Benzylpiperazine,%201-(3-Trifluoromethylphenyl)-piperazine,%20and%201-(3-Chlorophenyl)-piperazine%20in%203,4-Methylenedioxymethamphetamine-Positive%20Urine%20Samples&rft.jtitle=Journal%20of%20analytical%20toxicology&rft.au=Dickson,%20Amber%20J.&rft.date=2010-10-01&rft.volume=34&rft.issue=8&rft.spage=464&rft.epage=469&rft.pages=464-469&rft.issn=0146-4760&rft.eissn=1945-2403&rft.coden=JATOD3&rft_id=info:doi/10.1093/jat/34.8.464&rft_dat=%3Cproquest_cross%3E893265303%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c460t-44f7e156764316c4d2554c0ed0270a08cd1f71d7abfe6ba02ef2c97bd535dbbe3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=893265303&rft_id=info:pmid/21819791&rft_oup_id=10.1093/jat/34.8.464&rfr_iscdi=true |