Detection and quantification of codeine-6-glucuronide, hydromorphone-3-glucuronide, oxymorphone-3-glucuronide, morphine 3-glucuronide and morphine-6-glucuronide in human hair from opioid users by LC–MS-MS
Abstract Current hair testing methods that rely solely on quantification of parent drug compounds are unable to definitively distinguish between drug use and external contamination. One possible solution to this problem is to confirm the presence of unique drug metabolites that cannot be present thr...
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Veröffentlicht in: | Journal of analytical toxicology 2018-03, Vol.42 (2), p.115-125 |
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creator | Grabenauer, Megan Bynum, Nichole D Moore, Katherine N White, Robert M Mitchell, John M Hayes, Eugene D Flegel, Ronald |
description | Abstract
Current hair testing methods that rely solely on quantification of parent drug compounds are unable to definitively distinguish between drug use and external contamination. One possible solution to this problem is to confirm the presence of unique drug metabolites that cannot be present through contamination, such as phase II glucuronide conjugates. This work demonstrates for the first time that codeine-6-glucuronide, hydromorphone-3-glucuronide, oxymorphone-3-glucuronide, morphine-3-glucuronide and morphine-6-glucuronide are present at sufficient concentrations to be quantifiable in hair of opioid users and that their concentrations generally increase as the concentrations of the corresponding parent compounds increase. Here, we present a validated liquid chromatography tandem mass spectrometry method to quantify codeine-6-glucuronide, dihydrocodeine-6-glucuronide, hydromorphone-3-glucuronide, morphine-3-glucuronide, morphine-6-glucuronide, oxymorphone-3-glucuronide, codeine, dihydrocodeine, dihydromorphine, hydrocodone, hydromorphone, morphine, oxycodone, oxymorphone and 6-acetylmorphine in human hair. The method was used to analyze 46 human hair samples from known drug users that were confirmed positive for opioids by an independent laboratory. Glucuronide concentrations in samples positive for parent analytes ranged from ~1 to 25 pg/mg, and most samples had glucuronide concentrations in the range of ~1 to 5 pg/mg. Relative to the parent concentrations, the average concentrations of the four detected glucuronides were as follows: codeine-6-glucuronide, 2.33%; hydromorphone-3-glucuronide, 0.94%; oxymorphone-3-glucuronide, 0.77%; morphine 3-glucuronide, 0.59%; and morphine-6-glucuronide, 0.93%. |
doi_str_mv | 10.1093/jat/bkx086 |
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Current hair testing methods that rely solely on quantification of parent drug compounds are unable to definitively distinguish between drug use and external contamination. One possible solution to this problem is to confirm the presence of unique drug metabolites that cannot be present through contamination, such as phase II glucuronide conjugates. This work demonstrates for the first time that codeine-6-glucuronide, hydromorphone-3-glucuronide, oxymorphone-3-glucuronide, morphine-3-glucuronide and morphine-6-glucuronide are present at sufficient concentrations to be quantifiable in hair of opioid users and that their concentrations generally increase as the concentrations of the corresponding parent compounds increase. Here, we present a validated liquid chromatography tandem mass spectrometry method to quantify codeine-6-glucuronide, dihydrocodeine-6-glucuronide, hydromorphone-3-glucuronide, morphine-3-glucuronide, morphine-6-glucuronide, oxymorphone-3-glucuronide, codeine, dihydrocodeine, dihydromorphine, hydrocodone, hydromorphone, morphine, oxycodone, oxymorphone and 6-acetylmorphine in human hair. The method was used to analyze 46 human hair samples from known drug users that were confirmed positive for opioids by an independent laboratory. Glucuronide concentrations in samples positive for parent analytes ranged from ~1 to 25 pg/mg, and most samples had glucuronide concentrations in the range of ~1 to 5 pg/mg. Relative to the parent concentrations, the average concentrations of the four detected glucuronides were as follows: codeine-6-glucuronide, 2.33%; hydromorphone-3-glucuronide, 0.94%; oxymorphone-3-glucuronide, 0.77%; morphine 3-glucuronide, 0.59%; and morphine-6-glucuronide, 0.93%.</description><identifier>ISSN: 0146-4760</identifier><identifier>EISSN: 1945-2403</identifier><identifier>DOI: 10.1093/jat/bkx086</identifier><identifier>PMID: 29186453</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Chromatography, Liquid ; Codeine - analogs & derivatives ; Codeine - analysis ; Glucuronates - analysis ; Hair - chemistry ; Humans ; Hydromorphone - analogs & derivatives ; Hydromorphone - analysis ; Limit of Detection ; Morphine Derivatives - analysis ; Opioid-Related Disorders - diagnosis ; Reproducibility of Results ; Specimen Handling ; Substance Abuse Detection - methods ; Tandem Mass Spectrometry</subject><ispartof>Journal of analytical toxicology, 2018-03, Vol.42 (2), p.115-125</ispartof><rights>The Author 2017. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c379t-10c9923974778378e32b2655099b1a72402e7609028cafe7b43ca02f05bd804d3</citedby><cites>FETCH-LOGICAL-c379t-10c9923974778378e32b2655099b1a72402e7609028cafe7b43ca02f05bd804d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,1585,27928,27929</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29186453$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grabenauer, Megan</creatorcontrib><creatorcontrib>Bynum, Nichole D</creatorcontrib><creatorcontrib>Moore, Katherine N</creatorcontrib><creatorcontrib>White, Robert M</creatorcontrib><creatorcontrib>Mitchell, John M</creatorcontrib><creatorcontrib>Hayes, Eugene D</creatorcontrib><creatorcontrib>Flegel, Ronald</creatorcontrib><title>Detection and quantification of codeine-6-glucuronide, hydromorphone-3-glucuronide, oxymorphone-3-glucuronide, morphine 3-glucuronide and morphine-6-glucuronide in human hair from opioid users by LC–MS-MS</title><title>Journal of analytical toxicology</title><addtitle>J Anal Toxicol</addtitle><description>Abstract
Current hair testing methods that rely solely on quantification of parent drug compounds are unable to definitively distinguish between drug use and external contamination. One possible solution to this problem is to confirm the presence of unique drug metabolites that cannot be present through contamination, such as phase II glucuronide conjugates. This work demonstrates for the first time that codeine-6-glucuronide, hydromorphone-3-glucuronide, oxymorphone-3-glucuronide, morphine-3-glucuronide and morphine-6-glucuronide are present at sufficient concentrations to be quantifiable in hair of opioid users and that their concentrations generally increase as the concentrations of the corresponding parent compounds increase. Here, we present a validated liquid chromatography tandem mass spectrometry method to quantify codeine-6-glucuronide, dihydrocodeine-6-glucuronide, hydromorphone-3-glucuronide, morphine-3-glucuronide, morphine-6-glucuronide, oxymorphone-3-glucuronide, codeine, dihydrocodeine, dihydromorphine, hydrocodone, hydromorphone, morphine, oxycodone, oxymorphone and 6-acetylmorphine in human hair. The method was used to analyze 46 human hair samples from known drug users that were confirmed positive for opioids by an independent laboratory. Glucuronide concentrations in samples positive for parent analytes ranged from ~1 to 25 pg/mg, and most samples had glucuronide concentrations in the range of ~1 to 5 pg/mg. Relative to the parent concentrations, the average concentrations of the four detected glucuronides were as follows: codeine-6-glucuronide, 2.33%; hydromorphone-3-glucuronide, 0.94%; oxymorphone-3-glucuronide, 0.77%; morphine 3-glucuronide, 0.59%; and morphine-6-glucuronide, 0.93%.</description><subject>Chromatography, Liquid</subject><subject>Codeine - analogs & derivatives</subject><subject>Codeine - analysis</subject><subject>Glucuronates - analysis</subject><subject>Hair - chemistry</subject><subject>Humans</subject><subject>Hydromorphone - analogs & derivatives</subject><subject>Hydromorphone - analysis</subject><subject>Limit of Detection</subject><subject>Morphine Derivatives - analysis</subject><subject>Opioid-Related Disorders - diagnosis</subject><subject>Reproducibility of Results</subject><subject>Specimen Handling</subject><subject>Substance Abuse Detection - methods</subject><subject>Tandem Mass Spectrometry</subject><issn>0146-4760</issn><issn>1945-2403</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9O3DAYxa2qqAy0mx4AeVOpQqR8jh07XqIp_6RBXdCuI8dxOoZJHOxYmtlxB-7FITgJZgaQZtFubOm9n96TvofQVwI_CEh6fKPG4_p2CSX_gCZEsiLLGdCPaAKE8YwJDrtoL4QbAMJLTj-h3VySkrOCTtDjTzMaPVrXY9U3-C6qfrSt1WotuRZr1xjbm4xnfxdRR-9625gjPF813nXOD3OXTLptuuXqX9ZaT3l4S193v1nbVdj2eB47lV5lPW5TK3aDdbbBMRgfcL3Cs-nT_cPVdXZ1_RnttGoRzJfXfx_9OTv9Pb3IZr_OL6cns0xTIceMgJYyp1IwIUoqSkPzOudFAVLWRIl0vtyks0nIS61aI2pGtYK8haJuSmAN3UffN7mDd3fRhLHqbNBmsVC9cTFURArgDKAgCT3coNq7ELxpq8HbTvlVRaB62a9K-1Wb_RJ88Job68407-jbYAn4tgFcHP4X9AyU4Kfq</recordid><startdate>20180301</startdate><enddate>20180301</enddate><creator>Grabenauer, Megan</creator><creator>Bynum, Nichole D</creator><creator>Moore, Katherine N</creator><creator>White, Robert M</creator><creator>Mitchell, John M</creator><creator>Hayes, Eugene D</creator><creator>Flegel, Ronald</creator><general>Oxford University Press</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>7X8</scope></search><sort><creationdate>20180301</creationdate><title>Detection and quantification of codeine-6-glucuronide, hydromorphone-3-glucuronide, oxymorphone-3-glucuronide, morphine 3-glucuronide and morphine-6-glucuronide in human hair from opioid users by LC–MS-MS</title><author>Grabenauer, Megan ; Bynum, Nichole D ; Moore, Katherine N ; White, Robert M ; Mitchell, John M ; Hayes, Eugene D ; Flegel, Ronald</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379t-10c9923974778378e32b2655099b1a72402e7609028cafe7b43ca02f05bd804d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Chromatography, Liquid</topic><topic>Codeine - analogs & derivatives</topic><topic>Codeine - analysis</topic><topic>Glucuronates - analysis</topic><topic>Hair - chemistry</topic><topic>Humans</topic><topic>Hydromorphone - analogs & derivatives</topic><topic>Hydromorphone - analysis</topic><topic>Limit of Detection</topic><topic>Morphine Derivatives - analysis</topic><topic>Opioid-Related Disorders - diagnosis</topic><topic>Reproducibility of Results</topic><topic>Specimen Handling</topic><topic>Substance Abuse Detection - methods</topic><topic>Tandem Mass Spectrometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grabenauer, Megan</creatorcontrib><creatorcontrib>Bynum, Nichole D</creatorcontrib><creatorcontrib>Moore, Katherine N</creatorcontrib><creatorcontrib>White, Robert M</creatorcontrib><creatorcontrib>Mitchell, John M</creatorcontrib><creatorcontrib>Hayes, Eugene D</creatorcontrib><creatorcontrib>Flegel, Ronald</creatorcontrib><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><jtitle>Journal of analytical toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grabenauer, Megan</au><au>Bynum, Nichole D</au><au>Moore, Katherine N</au><au>White, Robert M</au><au>Mitchell, John M</au><au>Hayes, Eugene D</au><au>Flegel, Ronald</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection and quantification of codeine-6-glucuronide, hydromorphone-3-glucuronide, oxymorphone-3-glucuronide, morphine 3-glucuronide and morphine-6-glucuronide in human hair from opioid users by LC–MS-MS</atitle><jtitle>Journal of analytical toxicology</jtitle><addtitle>J Anal Toxicol</addtitle><date>2018-03-01</date><risdate>2018</risdate><volume>42</volume><issue>2</issue><spage>115</spage><epage>125</epage><pages>115-125</pages><issn>0146-4760</issn><eissn>1945-2403</eissn><abstract>Abstract
Current hair testing methods that rely solely on quantification of parent drug compounds are unable to definitively distinguish between drug use and external contamination. One possible solution to this problem is to confirm the presence of unique drug metabolites that cannot be present through contamination, such as phase II glucuronide conjugates. This work demonstrates for the first time that codeine-6-glucuronide, hydromorphone-3-glucuronide, oxymorphone-3-glucuronide, morphine-3-glucuronide and morphine-6-glucuronide are present at sufficient concentrations to be quantifiable in hair of opioid users and that their concentrations generally increase as the concentrations of the corresponding parent compounds increase. Here, we present a validated liquid chromatography tandem mass spectrometry method to quantify codeine-6-glucuronide, dihydrocodeine-6-glucuronide, hydromorphone-3-glucuronide, morphine-3-glucuronide, morphine-6-glucuronide, oxymorphone-3-glucuronide, codeine, dihydrocodeine, dihydromorphine, hydrocodone, hydromorphone, morphine, oxycodone, oxymorphone and 6-acetylmorphine in human hair. The method was used to analyze 46 human hair samples from known drug users that were confirmed positive for opioids by an independent laboratory. Glucuronide concentrations in samples positive for parent analytes ranged from ~1 to 25 pg/mg, and most samples had glucuronide concentrations in the range of ~1 to 5 pg/mg. Relative to the parent concentrations, the average concentrations of the four detected glucuronides were as follows: codeine-6-glucuronide, 2.33%; hydromorphone-3-glucuronide, 0.94%; oxymorphone-3-glucuronide, 0.77%; morphine 3-glucuronide, 0.59%; and morphine-6-glucuronide, 0.93%.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>29186453</pmid><doi>10.1093/jat/bkx086</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Chromatography, Liquid Codeine - analogs & derivatives Codeine - analysis Glucuronates - analysis Hair - chemistry Humans Hydromorphone - analogs & derivatives Hydromorphone - analysis Limit of Detection Morphine Derivatives - analysis Opioid-Related Disorders - diagnosis Reproducibility of Results Specimen Handling Substance Abuse Detection - methods Tandem Mass Spectrometry |
title | Detection and quantification of codeine-6-glucuronide, hydromorphone-3-glucuronide, oxymorphone-3-glucuronide, morphine 3-glucuronide and morphine-6-glucuronide in human hair from opioid users by LC–MS-MS |
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