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Sensitive determination of methomyl in blood using gas chromatography–mass spectrometry as its oxime tert.-butyldimethylsilyl derivative
A sensitive, selective and reliable method was developed to determine methomyl {methyl- N-[(methylcarbamoyl)oxy]thioacetimidate}, a carbamate insecticide in human blood, using gas chromatography–mass spectrometry. Dimethylglyoxime served as an internal standard (I.S.). Methomyl in the blood was conv...
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Published in: | Journal of chromatography. B, Biomedical sciences and applications Biomedical sciences and applications, 1998-08, Vol.713 (2), p.323-330 |
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container_title | Journal of chromatography. B, Biomedical sciences and applications |
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creator | Ito, Shinji Kudo, Keiko Imamura, Tohru Suzuki, Tsuneo Ikeda, Noriaki |
description | A sensitive, selective and reliable method was developed to determine methomyl {methyl-
N-[(methylcarbamoyl)oxy]thioacetimidate}, a carbamate insecticide in human blood, using gas chromatography–mass spectrometry. Dimethylglyoxime served as an internal standard (I.S.). Methomyl in the blood was converted to its oxime form by sodium hydroxide. The solution made acidic with hydrochloric acid was poured into a column packed with Extrelut. Methomyloxime and I.S. were eluted from the column with a mixture of dichloromethane–ethyl acetate–chloroform (65:25:10), transformed to
tert.-butyldimethylsilyl derivatives, and analyzed by gas chromatography–mass spectrometry in the electron impact mode. The calibration curves were linear in the concentration range from 1 ng/g to 100 ng/g and 100 ng/g to at least 5000 ng/g. The lower limit of detection was 0.5 ng/g. The absolute recoveries were 72–93% and within-day coefficients of variation were 3.1–5.6% at blood concentrations of 10 and 1000 ng/g. Two practical forensic applications are described. |
doi_str_mv | 10.1016/S0378-4347(98)00198-4 |
format | article |
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N-[(methylcarbamoyl)oxy]thioacetimidate}, a carbamate insecticide in human blood, using gas chromatography–mass spectrometry. Dimethylglyoxime served as an internal standard (I.S.). Methomyl in the blood was converted to its oxime form by sodium hydroxide. The solution made acidic with hydrochloric acid was poured into a column packed with Extrelut. Methomyloxime and I.S. were eluted from the column with a mixture of dichloromethane–ethyl acetate–chloroform (65:25:10), transformed to
tert.-butyldimethylsilyl derivatives, and analyzed by gas chromatography–mass spectrometry in the electron impact mode. The calibration curves were linear in the concentration range from 1 ng/g to 100 ng/g and 100 ng/g to at least 5000 ng/g. The lower limit of detection was 0.5 ng/g. The absolute recoveries were 72–93% and within-day coefficients of variation were 3.1–5.6% at blood concentrations of 10 and 1000 ng/g. Two practical forensic applications are described.</description><identifier>ISSN: 0378-4347</identifier><identifier>ISSN: 1387-2273</identifier><identifier>DOI: 10.1016/S0378-4347(98)00198-4</identifier><identifier>PMID: 9746247</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Acetamides ; Adult ; Biological and medical sciences ; Female ; Fluoroacetates ; Forensic Medicine - methods ; Gas Chromatography-Mass Spectrometry ; Humans ; Insecticides - analysis ; Insecticides - blood ; Insecticides - poisoning ; Male ; Medical sciences ; Methomyl ; Methomyl - analysis ; Methomyl - blood ; Methomyl - poisoning ; Middle Aged ; Organosilicon Compounds ; Plant poisons toxicology ; Reproducibility of Results ; Sensitivity and Specificity ; Toxicology</subject><ispartof>Journal of chromatography. B, Biomedical sciences and applications, 1998-08, Vol.713 (2), p.323-330</ispartof><rights>1998 Elsevier Science B.V.</rights><rights>1998 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-9a3daeeb3353cab6937b9b2a332c1ec59c278daf334d8c41ea3019f09ab76b913</citedby><cites>FETCH-LOGICAL-c389t-9a3daeeb3353cab6937b9b2a332c1ec59c278daf334d8c41ea3019f09ab76b913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2356392$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9746247$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ito, Shinji</creatorcontrib><creatorcontrib>Kudo, Keiko</creatorcontrib><creatorcontrib>Imamura, Tohru</creatorcontrib><creatorcontrib>Suzuki, Tsuneo</creatorcontrib><creatorcontrib>Ikeda, Noriaki</creatorcontrib><title>Sensitive determination of methomyl in blood using gas chromatography–mass spectrometry as its oxime tert.-butyldimethylsilyl derivative</title><title>Journal of chromatography. B, Biomedical sciences and applications</title><addtitle>J Chromatogr B Biomed Sci Appl</addtitle><description>A sensitive, selective and reliable method was developed to determine methomyl {methyl-
N-[(methylcarbamoyl)oxy]thioacetimidate}, a carbamate insecticide in human blood, using gas chromatography–mass spectrometry. Dimethylglyoxime served as an internal standard (I.S.). Methomyl in the blood was converted to its oxime form by sodium hydroxide. The solution made acidic with hydrochloric acid was poured into a column packed with Extrelut. Methomyloxime and I.S. were eluted from the column with a mixture of dichloromethane–ethyl acetate–chloroform (65:25:10), transformed to
tert.-butyldimethylsilyl derivatives, and analyzed by gas chromatography–mass spectrometry in the electron impact mode. The calibration curves were linear in the concentration range from 1 ng/g to 100 ng/g and 100 ng/g to at least 5000 ng/g. The lower limit of detection was 0.5 ng/g. The absolute recoveries were 72–93% and within-day coefficients of variation were 3.1–5.6% at blood concentrations of 10 and 1000 ng/g. 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N-[(methylcarbamoyl)oxy]thioacetimidate}, a carbamate insecticide in human blood, using gas chromatography–mass spectrometry. Dimethylglyoxime served as an internal standard (I.S.). Methomyl in the blood was converted to its oxime form by sodium hydroxide. The solution made acidic with hydrochloric acid was poured into a column packed with Extrelut. Methomyloxime and I.S. were eluted from the column with a mixture of dichloromethane–ethyl acetate–chloroform (65:25:10), transformed to
tert.-butyldimethylsilyl derivatives, and analyzed by gas chromatography–mass spectrometry in the electron impact mode. The calibration curves were linear in the concentration range from 1 ng/g to 100 ng/g and 100 ng/g to at least 5000 ng/g. The lower limit of detection was 0.5 ng/g. The absolute recoveries were 72–93% and within-day coefficients of variation were 3.1–5.6% at blood concentrations of 10 and 1000 ng/g. Two practical forensic applications are described.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>9746247</pmid><doi>10.1016/S0378-4347(98)00198-4</doi><tpages>8</tpages></addata></record> |
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subjects | Acetamides Adult Biological and medical sciences Female Fluoroacetates Forensic Medicine - methods Gas Chromatography-Mass Spectrometry Humans Insecticides - analysis Insecticides - blood Insecticides - poisoning Male Medical sciences Methomyl Methomyl - analysis Methomyl - blood Methomyl - poisoning Middle Aged Organosilicon Compounds Plant poisons toxicology Reproducibility of Results Sensitivity and Specificity Toxicology |
title | Sensitive determination of methomyl in blood using gas chromatography–mass spectrometry as its oxime tert.-butyldimethylsilyl derivative |
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