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Application of Empore C-8 Extraction Disks for Screening Urine in Systematic Toxicological Analysis
Solid-phase extraction (SPE) by means of disposable columns has become a widely accepted technique for sample pretreatment in toxicology, both for directed analyses and for screening analyses. However, the sample capacity in SPE is usually limited to a few millilitres. Therefore, we have investigate...
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Published in: | Journal of forensic sciences 1992-03, Vol.37 (2), p.460-466 |
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creator | Ensing, K Franke, JP Temmink, A Chen, X-H de Zeeuw, RA |
description | Solid-phase extraction (SPE) by means of disposable columns has become a widely accepted technique for sample pretreatment in toxicology, both for directed analyses and for screening analyses. However, the sample capacity in SPE is usually limited to a few millilitres. Therefore, we have investigated to what extent these problems can be overcome by using Empore extraction disks, consisting of chemically modified C-8 reversed-phase silica, embedded in an inert polytetrafluoroethylene (PTFE) matrix. Human urine was selected as the matrix and dexetimide and mepyramine were initially used as test drugs because these drugs were available in tritiated form. Additional drugs investigated included codeine, hexobarbital, imipramine, methamphetamine, and nitrazepam. In these investigations, the sample capacity for untreated urine was at least 25 mL, and analyte quantities up to 250 μg could be retained by these filters. Washing with water/methanol mixtures was successful in removing substantial amounts of endogenous interferences, and methanol proved to be an acceptable eluent. Thus, these disks seem to have interesting potential for toxicological analysis in that sample concentration and cleanup can be achieved at the same time. |
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However, the sample capacity in SPE is usually limited to a few millilitres. Therefore, we have investigated to what extent these problems can be overcome by using Empore extraction disks, consisting of chemically modified C-8 reversed-phase silica, embedded in an inert polytetrafluoroethylene (PTFE) matrix. Human urine was selected as the matrix and dexetimide and mepyramine were initially used as test drugs because these drugs were available in tritiated form. Additional drugs investigated included codeine, hexobarbital, imipramine, methamphetamine, and nitrazepam. In these investigations, the sample capacity for untreated urine was at least 25 mL, and analyte quantities up to 250 μg could be retained by these filters. Washing with water/methanol mixtures was successful in removing substantial amounts of endogenous interferences, and methanol proved to be an acceptable eluent. Thus, these disks seem to have interesting potential for toxicological analysis in that sample concentration and cleanup can be achieved at the same time.</description><identifier>ISSN: 0022-1198</identifier><identifier>EISSN: 1556-4029</identifier><identifier>DOI: 10.1520/JFS13255J</identifier><identifier>PMID: 1354247</identifier><identifier>CODEN: JFSCAS</identifier><language>eng</language><publisher>United States: Callaghan and Co</publisher><subject><![CDATA[Barbiturates - chemistry ; Barbiturates - isolation & purification ; Barbiturates - urine ; Codeine - chemistry ; Codeine - isolation & purification ; Codeine - urine ; Dexetimide - chemistry ; Dexetimide - isolation & purification ; Dexetimide - urine ; Filtration ; Hexobarbital - chemistry ; Hexobarbital - isolation & purification ; Hexobarbital - urine ; Humans ; Imipramine - chemistry ; Imipramine - isolation & purification ; Imipramine - urine ; Methamphetamine - chemistry ; Methamphetamine - isolation & purification ; Methamphetamine - urine ; Molecular Structure ; Nitrazepam - chemistry ; Nitrazepam - isolation & purification ; Nitrazepam - urine ; Pharmacology ; Prazepam - chemistry ; Prazepam - isolation & purification ; Prazepam - urine ; Pyrilamine - chemistry ; Pyrilamine - isolation & purification ; Pyrilamine - urine ; Toxicology ; Urinalysis]]></subject><ispartof>Journal of forensic sciences, 1992-03, Vol.37 (2), p.460-466</ispartof><rights>All rights reserved. This material may not be reproduced or copied, in whole or in part, in any printed, mechanical, electronic, film, or other distribution and storage media, without the written consent of the publisher.</rights><rights>Copyright American Society for Testing and Materials Mar 1992</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a480t-56259ed34a8aed0ed40c28fd1fefe18e4e2af40965bc93b4547bf821b3e0bc8c3</citedby><cites>FETCH-LOGICAL-a480t-56259ed34a8aed0ed40c28fd1fefe18e4e2af40965bc93b4547bf821b3e0bc8c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,9791,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1354247$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ensing, K</creatorcontrib><creatorcontrib>Franke, JP</creatorcontrib><creatorcontrib>Temmink, A</creatorcontrib><creatorcontrib>Chen, X-H</creatorcontrib><creatorcontrib>de Zeeuw, RA</creatorcontrib><title>Application of Empore C-8 Extraction Disks for Screening Urine in Systematic Toxicological Analysis</title><title>Journal of forensic sciences</title><addtitle>J Forensic Sci</addtitle><description>Solid-phase extraction (SPE) by means of disposable columns has become a widely accepted technique for sample pretreatment in toxicology, both for directed analyses and for screening analyses. However, the sample capacity in SPE is usually limited to a few millilitres. Therefore, we have investigated to what extent these problems can be overcome by using Empore extraction disks, consisting of chemically modified C-8 reversed-phase silica, embedded in an inert polytetrafluoroethylene (PTFE) matrix. Human urine was selected as the matrix and dexetimide and mepyramine were initially used as test drugs because these drugs were available in tritiated form. Additional drugs investigated included codeine, hexobarbital, imipramine, methamphetamine, and nitrazepam. In these investigations, the sample capacity for untreated urine was at least 25 mL, and analyte quantities up to 250 μg could be retained by these filters. Washing with water/methanol mixtures was successful in removing substantial amounts of endogenous interferences, and methanol proved to be an acceptable eluent. Thus, these disks seem to have interesting potential for toxicological analysis in that sample concentration and cleanup can be achieved at the same time.</description><subject>Barbiturates - chemistry</subject><subject>Barbiturates - isolation & purification</subject><subject>Barbiturates - urine</subject><subject>Codeine - chemistry</subject><subject>Codeine - isolation & purification</subject><subject>Codeine - urine</subject><subject>Dexetimide - chemistry</subject><subject>Dexetimide - isolation & purification</subject><subject>Dexetimide - urine</subject><subject>Filtration</subject><subject>Hexobarbital - chemistry</subject><subject>Hexobarbital - isolation & purification</subject><subject>Hexobarbital - urine</subject><subject>Humans</subject><subject>Imipramine - chemistry</subject><subject>Imipramine - isolation & purification</subject><subject>Imipramine - urine</subject><subject>Methamphetamine - chemistry</subject><subject>Methamphetamine - isolation & purification</subject><subject>Methamphetamine - urine</subject><subject>Molecular Structure</subject><subject>Nitrazepam - chemistry</subject><subject>Nitrazepam - isolation & purification</subject><subject>Nitrazepam - urine</subject><subject>Pharmacology</subject><subject>Prazepam - chemistry</subject><subject>Prazepam - isolation & purification</subject><subject>Prazepam - urine</subject><subject>Pyrilamine - chemistry</subject><subject>Pyrilamine - isolation & purification</subject><subject>Pyrilamine - urine</subject><subject>Toxicology</subject><subject>Urinalysis</subject><issn>0022-1198</issn><issn>1556-4029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><recordid>eNp1kE1PGzEQhi1UlKbQAz-gktVKlTgs-HNjH6M0FBAShyRny-sdI9Pd9dbeSKS_vkuDmgNwmsP7zDOjF6EzSi6oZOTy9mpFOZPy9ghNqZRlIQjTH9CUEMYKSrX6iD7l_EgIKWlJJ2hCuRRMzKbIzfu-Cc4OIXY4erxs-5gALwqFl09Dsu5f8CPkXxn7mPDKJYAudA94k0IHOHR4tcsDtKPB4XV8Ci428WE0Nnje2WaXQz5Fx942GT6_zBO0uVquF9fF3f3Pm8X8rrBCkaGQJZMaai6sslATqAVxTPmaevBAFQhg1guiS1k5zSshxazyitGKA6mccvwEfd17-xR_byEP5jFu0_hENozqUgkt9Qh9ew-inKiSa14-U-d7yqWYcwJv-hRam3aGEvNcuflf-ch-eTFuqxbqA7nveMxn-9zmoT1cGwWGzwwzf0L_2mr62o-b39_afP3CX6fVmRI</recordid><startdate>19920301</startdate><enddate>19920301</enddate><creator>Ensing, K</creator><creator>Franke, JP</creator><creator>Temmink, A</creator><creator>Chen, X-H</creator><creator>de Zeeuw, RA</creator><general>Callaghan and Co</general><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>IOIBA</scope><scope>K30</scope><scope>PAAUG</scope><scope>PAWHS</scope><scope>PAWZZ</scope><scope>PAXOH</scope><scope>PBHAV</scope><scope>PBQSW</scope><scope>PBYQZ</scope><scope>PCIWU</scope><scope>PCMID</scope><scope>PCZJX</scope><scope>PDGRG</scope><scope>PDWWI</scope><scope>PETMR</scope><scope>PFVGT</scope><scope>PGXDX</scope><scope>PIHIL</scope><scope>PISVA</scope><scope>PJCTQ</scope><scope>PJTMS</scope><scope>PLCHJ</scope><scope>PMHAD</scope><scope>PNQDJ</scope><scope>POUND</scope><scope>PPLAD</scope><scope>PQAPC</scope><scope>PQCAN</scope><scope>PQCMW</scope><scope>PQEME</scope><scope>PQHKH</scope><scope>PQMID</scope><scope>PQNCT</scope><scope>PQNET</scope><scope>PQSCT</scope><scope>PQSET</scope><scope>PSVJG</scope><scope>PVMQY</scope><scope>PZGFC</scope><scope>K7.</scope></search><sort><creationdate>19920301</creationdate><title>Application of Empore C-8 Extraction Disks for Screening Urine in Systematic Toxicological Analysis</title><author>Ensing, K ; Franke, JP ; Temmink, A ; Chen, X-H ; de Zeeuw, RA</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a480t-56259ed34a8aed0ed40c28fd1fefe18e4e2af40965bc93b4547bf821b3e0bc8c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Barbiturates - chemistry</topic><topic>Barbiturates - isolation & purification</topic><topic>Barbiturates - urine</topic><topic>Codeine - chemistry</topic><topic>Codeine - isolation & purification</topic><topic>Codeine - urine</topic><topic>Dexetimide - chemistry</topic><topic>Dexetimide - isolation & purification</topic><topic>Dexetimide - urine</topic><topic>Filtration</topic><topic>Hexobarbital - chemistry</topic><topic>Hexobarbital - isolation & purification</topic><topic>Hexobarbital - urine</topic><topic>Humans</topic><topic>Imipramine - chemistry</topic><topic>Imipramine - isolation & purification</topic><topic>Imipramine - urine</topic><topic>Methamphetamine - chemistry</topic><topic>Methamphetamine - isolation & purification</topic><topic>Methamphetamine - urine</topic><topic>Molecular Structure</topic><topic>Nitrazepam - chemistry</topic><topic>Nitrazepam - isolation & purification</topic><topic>Nitrazepam - urine</topic><topic>Pharmacology</topic><topic>Prazepam - chemistry</topic><topic>Prazepam - isolation & purification</topic><topic>Prazepam - urine</topic><topic>Pyrilamine - chemistry</topic><topic>Pyrilamine - isolation & purification</topic><topic>Pyrilamine - urine</topic><topic>Toxicology</topic><topic>Urinalysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ensing, K</creatorcontrib><creatorcontrib>Franke, JP</creatorcontrib><creatorcontrib>Temmink, A</creatorcontrib><creatorcontrib>Chen, X-H</creatorcontrib><creatorcontrib>de Zeeuw, RA</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Periodicals Index Online Segment 29</collection><collection>Periodicals Index Online</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - West</collection><collection>Primary Sources Access (Plan D) - International</collection><collection>Primary Sources Access & Build (Plan A) - 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However, the sample capacity in SPE is usually limited to a few millilitres. Therefore, we have investigated to what extent these problems can be overcome by using Empore extraction disks, consisting of chemically modified C-8 reversed-phase silica, embedded in an inert polytetrafluoroethylene (PTFE) matrix. Human urine was selected as the matrix and dexetimide and mepyramine were initially used as test drugs because these drugs were available in tritiated form. Additional drugs investigated included codeine, hexobarbital, imipramine, methamphetamine, and nitrazepam. In these investigations, the sample capacity for untreated urine was at least 25 mL, and analyte quantities up to 250 μg could be retained by these filters. Washing with water/methanol mixtures was successful in removing substantial amounts of endogenous interferences, and methanol proved to be an acceptable eluent. Thus, these disks seem to have interesting potential for toxicological analysis in that sample concentration and cleanup can be achieved at the same time.</abstract><cop>United States</cop><pub>Callaghan and Co</pub><pmid>1354247</pmid><doi>10.1520/JFS13255J</doi><tpages>7</tpages></addata></record> |
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subjects | Barbiturates - chemistry Barbiturates - isolation & purification Barbiturates - urine Codeine - chemistry Codeine - isolation & purification Codeine - urine Dexetimide - chemistry Dexetimide - isolation & purification Dexetimide - urine Filtration Hexobarbital - chemistry Hexobarbital - isolation & purification Hexobarbital - urine Humans Imipramine - chemistry Imipramine - isolation & purification Imipramine - urine Methamphetamine - chemistry Methamphetamine - isolation & purification Methamphetamine - urine Molecular Structure Nitrazepam - chemistry Nitrazepam - isolation & purification Nitrazepam - urine Pharmacology Prazepam - chemistry Prazepam - isolation & purification Prazepam - urine Pyrilamine - chemistry Pyrilamine - isolation & purification Pyrilamine - urine Toxicology Urinalysis |
title | Application of Empore C-8 Extraction Disks for Screening Urine in Systematic Toxicological Analysis |
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