Ethyl glucuronide: Unusual distribution between head hair and pubic hair
Abstract Ethyl glucuronide (EtG) is a minor metabolite of ethanol that can be detected in hair. In some specific situations, head hair can be missing, and therefore, alternative anatomical locations of hair are of interest. In this study, paired hair specimens (head hair and pubic hair) from eight s...
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description | Abstract Ethyl glucuronide (EtG) is a minor metabolite of ethanol that can be detected in hair. In some specific situations, head hair can be missing, and therefore, alternative anatomical locations of hair are of interest. In this study, paired hair specimens (head hair and pubic hair) from eight social drinkers were analyzed for EtG. Each sample was decontaminated by two dichloromethane bathes (5 ml) for 2 min. After cutting into small pieces, about 50 mg of hair was incubated in 2 ml water in the presence of 10 ng of EtG-d5 , used as internal standard and submitted to ultra-sonication for 2 h. The aqueous phase was extracted by SPE using Oasis MAX columns. The hair extract was separated on an ACQUITY BEH HILIC column using a gradient of acetonitrile and formate buffer. Detection was based on two daughter ions: transitions m / z 221–85 and 75 and m / z 226–75 for EtG and the IS, respectively. This laboratory is using a positive cut-off at 50 pg/mg. All eight head hair specimens were negative for EtG at a limit of quantitation fixed at 10 pg/mg. Surprisingly, EtG was identified at high concentrations in pubic hair, in the range 12–1370 pg/mg. It appears, therefore, that it is not possible to document the drinking status of a subject by simply switching from head hair to pubic hair. |
doi_str_mv | 10.1016/j.forsciint.2007.08.012 |
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In some specific situations, head hair can be missing, and therefore, alternative anatomical locations of hair are of interest. In this study, paired hair specimens (head hair and pubic hair) from eight social drinkers were analyzed for EtG. Each sample was decontaminated by two dichloromethane bathes (5 ml) for 2 min. After cutting into small pieces, about 50 mg of hair was incubated in 2 ml water in the presence of 10 ng of EtG-d5 , used as internal standard and submitted to ultra-sonication for 2 h. The aqueous phase was extracted by SPE using Oasis MAX columns. The hair extract was separated on an ACQUITY BEH HILIC column using a gradient of acetonitrile and formate buffer. Detection was based on two daughter ions: transitions m / z 221–85 and 75 and m / z 226–75 for EtG and the IS, respectively. This laboratory is using a positive cut-off at 50 pg/mg. All eight head hair specimens were negative for EtG at a limit of quantitation fixed at 10 pg/mg. Surprisingly, EtG was identified at high concentrations in pubic hair, in the range 12–1370 pg/mg. It appears, therefore, that it is not possible to document the drinking status of a subject by simply switching from head hair to pubic hair.</description><identifier>ISSN: 0379-0738</identifier><identifier>EISSN: 1872-6283</identifier><identifier>DOI: 10.1016/j.forsciint.2007.08.012</identifier><identifier>PMID: 17997064</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Adult ; Alcohol ; Alcohol Drinking ; Child custody ; Child, Preschool ; Children & youth ; Ethanol ; Ethyl glucuronide ; Female ; Forensic sciences ; Forensic Toxicology ; Gas Chromatography-Mass Spectrometry ; Genitalia ; Glucuronates - analysis ; Hair ; Hair - chemistry ; Humans ; LC-MS/MS ; Male ; Middle Aged ; Pathology ; Pediatrics ; Puberty ; Scalp ; Substance Abuse Detection</subject><ispartof>Forensic science international, 2008-03, Vol.176 (1), p.87-90</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2007 Elsevier Ireland Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c452t-6cb5b982a7d0e3d73ad3f4b4c2539f4992ab93e9f70892c554c45e60b2ccfe1d3</citedby><cites>FETCH-LOGICAL-c452t-6cb5b982a7d0e3d73ad3f4b4c2539f4992ab93e9f70892c554c45e60b2ccfe1d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1034454890?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,3541,27915,27916,45986,64374,64378,72230</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17997064$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kintz, Pascal</creatorcontrib><creatorcontrib>Villain, Marion</creatorcontrib><creatorcontrib>Vallet, Emilie</creatorcontrib><creatorcontrib>Etter, Mathieu</creatorcontrib><creatorcontrib>Salquebre, Guillaume</creatorcontrib><creatorcontrib>Cirimele, Vincent</creatorcontrib><title>Ethyl glucuronide: Unusual distribution between head hair and pubic hair</title><title>Forensic science international</title><addtitle>Forensic Sci Int</addtitle><description>Abstract Ethyl glucuronide (EtG) is a minor metabolite of ethanol that can be detected in hair. In some specific situations, head hair can be missing, and therefore, alternative anatomical locations of hair are of interest. In this study, paired hair specimens (head hair and pubic hair) from eight social drinkers were analyzed for EtG. Each sample was decontaminated by two dichloromethane bathes (5 ml) for 2 min. After cutting into small pieces, about 50 mg of hair was incubated in 2 ml water in the presence of 10 ng of EtG-d5 , used as internal standard and submitted to ultra-sonication for 2 h. The aqueous phase was extracted by SPE using Oasis MAX columns. The hair extract was separated on an ACQUITY BEH HILIC column using a gradient of acetonitrile and formate buffer. Detection was based on two daughter ions: transitions m / z 221–85 and 75 and m / z 226–75 for EtG and the IS, respectively. This laboratory is using a positive cut-off at 50 pg/mg. All eight head hair specimens were negative for EtG at a limit of quantitation fixed at 10 pg/mg. Surprisingly, EtG was identified at high concentrations in pubic hair, in the range 12–1370 pg/mg. It appears, therefore, that it is not possible to document the drinking status of a subject by simply switching from head hair to pubic hair.</description><subject>Adult</subject><subject>Alcohol</subject><subject>Alcohol Drinking</subject><subject>Child custody</subject><subject>Child, Preschool</subject><subject>Children & youth</subject><subject>Ethanol</subject><subject>Ethyl glucuronide</subject><subject>Female</subject><subject>Forensic sciences</subject><subject>Forensic Toxicology</subject><subject>Gas Chromatography-Mass Spectrometry</subject><subject>Genitalia</subject><subject>Glucuronates - analysis</subject><subject>Hair</subject><subject>Hair - chemistry</subject><subject>Humans</subject><subject>LC-MS/MS</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pathology</subject><subject>Pediatrics</subject><subject>Puberty</subject><subject>Scalp</subject><subject>Substance Abuse Detection</subject><issn>0379-0738</issn><issn>1872-6283</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><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>eNqNkU1v1DAQhq0K1C6FvwCROCdM_BHHHJCqqrRIlTi0PVv-mLBeUmexk6L993i7Kypx4mRZet9nNM8Q8qGFpoW2-7RphillF0KcGwogG-gbaOkJWbW9pHVHe_aKrIBJVYNk_Rl5k_MGAISg3Sk5a6VSEjq-IjdX83o3Vj_GxS1pisHj5-ohLnkxY-VDnlOwyxymWFmcfyPGao3GV2sTUmWir7aLDe75-5a8HsyY8d3xPScPX6_uL2_q2-_X3y4vbmvHBZ3rzllhVU-N9IDMS2Y8G7jljgqmBq4UNVYxVIOEXlEnBC897MBS5wZsPTsnHw_cbZp-LZhnvZmWFMtI3QLjXPBeQUnJQ8qlKeeEg96m8GjSroT03qDe6L8G9d6ghl4Xg6X5_shf7CP6l95RWQlcHAJYtnwKmHShYHToQ0I3az-F_xjy5R-GG0MMzow_cYf5ZSOdqQZ9tz_k_o4gC6Tjgv0BzLWbeA</recordid><startdate>20080321</startdate><enddate>20080321</enddate><creator>Kintz, Pascal</creator><creator>Villain, Marion</creator><creator>Vallet, Emilie</creator><creator>Etter, Mathieu</creator><creator>Salquebre, Guillaume</creator><creator>Cirimele, Vincent</creator><general>Elsevier Ireland Ltd</general><general>Elsevier Limited</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>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></search><sort><creationdate>20080321</creationdate><title>Ethyl glucuronide: Unusual distribution between head hair and pubic hair</title><author>Kintz, Pascal ; 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In some specific situations, head hair can be missing, and therefore, alternative anatomical locations of hair are of interest. In this study, paired hair specimens (head hair and pubic hair) from eight social drinkers were analyzed for EtG. Each sample was decontaminated by two dichloromethane bathes (5 ml) for 2 min. After cutting into small pieces, about 50 mg of hair was incubated in 2 ml water in the presence of 10 ng of EtG-d5 , used as internal standard and submitted to ultra-sonication for 2 h. The aqueous phase was extracted by SPE using Oasis MAX columns. The hair extract was separated on an ACQUITY BEH HILIC column using a gradient of acetonitrile and formate buffer. Detection was based on two daughter ions: transitions m / z 221–85 and 75 and m / z 226–75 for EtG and the IS, respectively. This laboratory is using a positive cut-off at 50 pg/mg. All eight head hair specimens were negative for EtG at a limit of quantitation fixed at 10 pg/mg. Surprisingly, EtG was identified at high concentrations in pubic hair, in the range 12–1370 pg/mg. It appears, therefore, that it is not possible to document the drinking status of a subject by simply switching from head hair to pubic hair.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>17997064</pmid><doi>10.1016/j.forsciint.2007.08.012</doi><tpages>4</tpages></addata></record> |
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subjects | Adult Alcohol Alcohol Drinking Child custody Child, Preschool Children & youth Ethanol Ethyl glucuronide Female Forensic sciences Forensic Toxicology Gas Chromatography-Mass Spectrometry Genitalia Glucuronates - analysis Hair Hair - chemistry Humans LC-MS/MS Male Middle Aged Pathology Pediatrics Puberty Scalp Substance Abuse Detection |
title | Ethyl glucuronide: Unusual distribution between head hair and pubic hair |
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