Simultaneous determination of 5 psychotropic drugs of various types in an autopsy case of acute multiple drug poisoning

Abstract We attempted the simultaneous determination of 5 drugs, mirtazapine, sertraline, chlorpromazine, amoxapine and zolpidem, detected in a gas chromatography–mass spectrometry screening test in an autopsy case. The solid-phase extraction of the analytes from biological samples was achieved usin...

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Veröffentlicht in:Forensic science international 2013-04, Vol.227 (1), p.90-94
Hauptverfasser: Sasaki, Chizuko, Shinozuka, Tatsuo, Murakami, Chikako, Irie, Wataru, Maeda, Kazuho, Watanabe, Toshimasa, Nakamaru, Naomi, Furukawa, Masataka, Nakamura, Shigeki, Kurihara, Katsuyoshi
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container_issue 1
container_start_page 90
container_title Forensic science international
container_volume 227
creator Sasaki, Chizuko
Shinozuka, Tatsuo
Murakami, Chikako
Irie, Wataru
Maeda, Kazuho
Watanabe, Toshimasa
Nakamaru, Naomi
Furukawa, Masataka
Nakamura, Shigeki
Kurihara, Katsuyoshi
description Abstract We attempted the simultaneous determination of 5 drugs, mirtazapine, sertraline, chlorpromazine, amoxapine and zolpidem, detected in a gas chromatography–mass spectrometry screening test in an autopsy case. The solid-phase extraction of the analytes from biological samples was achieved using Oasis® HLB cartridges (Waters, Milford, MA, USA). Gas chromatography was performed on a HP-5MS fused silica capillary column (30 m × 0.25 mm i.d., 0.25 μm film thickness, Agilent Technologies). The mass spectrometer was operated with an electron energy of 70 eV in electron impact mode. The qualitative and quantitative analyses were performed in full-scan mode and the selected ion monitoring mode, respectively. The total ion chromatogram showed good separation of these drugs. Linear graphs were obtained with good correlation coefficients for these drugs from 0.001 to 2.0 μg/mL ( r2 = 0.9909–0.9986) using imipramine-d6 as an internal standard. The recoveries of these drugs were found to be 62.8–88.0% in spiked whole blood. Mirtazapine, sertraline, chlorpromazine, amoxapine and zolpidem were found in post-mortem samples of the deceased at concentrations of 2.67, 0.07, 0.25, 0.32 and 0.68 μg/mL, respectively. The concentration of mirtazapine was within the lethal level and those of amoxapine and zolpidem were within the toxic level. We diagnosed that the cause of death was acute multiple drug poisoning. The simple and practical procedure used in this study is useful for the simultaneous determination of psychotropic drugs of various types in post-mortem biological samples.
doi_str_mv 10.1016/j.forsciint.2012.11.015
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The solid-phase extraction of the analytes from biological samples was achieved using Oasis® HLB cartridges (Waters, Milford, MA, USA). Gas chromatography was performed on a HP-5MS fused silica capillary column (30 m × 0.25 mm i.d., 0.25 μm film thickness, Agilent Technologies). The mass spectrometer was operated with an electron energy of 70 eV in electron impact mode. The qualitative and quantitative analyses were performed in full-scan mode and the selected ion monitoring mode, respectively. The total ion chromatogram showed good separation of these drugs. Linear graphs were obtained with good correlation coefficients for these drugs from 0.001 to 2.0 μg/mL ( r2 = 0.9909–0.9986) using imipramine-d6 as an internal standard. The recoveries of these drugs were found to be 62.8–88.0% in spiked whole blood. Mirtazapine, sertraline, chlorpromazine, amoxapine and zolpidem were found in post-mortem samples of the deceased at concentrations of 2.67, 0.07, 0.25, 0.32 and 0.68 μg/mL, respectively. The concentration of mirtazapine was within the lethal level and those of amoxapine and zolpidem were within the toxic level. We diagnosed that the cause of death was acute multiple drug poisoning. 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The solid-phase extraction of the analytes from biological samples was achieved using Oasis® HLB cartridges (Waters, Milford, MA, USA). Gas chromatography was performed on a HP-5MS fused silica capillary column (30 m × 0.25 mm i.d., 0.25 μm film thickness, Agilent Technologies). The mass spectrometer was operated with an electron energy of 70 eV in electron impact mode. The qualitative and quantitative analyses were performed in full-scan mode and the selected ion monitoring mode, respectively. The total ion chromatogram showed good separation of these drugs. Linear graphs were obtained with good correlation coefficients for these drugs from 0.001 to 2.0 μg/mL ( r2 = 0.9909–0.9986) using imipramine-d6 as an internal standard. The recoveries of these drugs were found to be 62.8–88.0% in spiked whole blood. Mirtazapine, sertraline, chlorpromazine, amoxapine and zolpidem were found in post-mortem samples of the deceased at concentrations of 2.67, 0.07, 0.25, 0.32 and 0.68 μg/mL, respectively. The concentration of mirtazapine was within the lethal level and those of amoxapine and zolpidem were within the toxic level. We diagnosed that the cause of death was acute multiple drug poisoning. The simple and practical procedure used in this study is useful for the simultaneous determination of psychotropic drugs of various types in post-mortem biological samples.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>23266306</pmid><doi>10.1016/j.forsciint.2012.11.015</doi><tpages>5</tpages></addata></record>
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subjects Adult
Amoxapine - analysis
Amoxapine - poisoning
Calibration
Chlorpromazine - analysis
Chlorpromazine - poisoning
Drug dosages
Female
Forensic sciences
Forensic Toxicology
Gas Chromatography-Mass Spectrometry - methods
Gastrointestinal Contents - chemistry
GC–MS
Humans
Mianserin - analogs & derivatives
Mianserin - analysis
Mianserin - poisoning
Mirtazapine
Multiple drug poisoning
Pathology
Poisoning
Psychotropic drugs
Psychotropic Drugs - analysis
Psychotropic Drugs - poisoning
Pyridines - analysis
Pyridines - poisoning
Sertraline - analysis
Sertraline - poisoning
Simultaneous determination
Solid Phase Extraction
title Simultaneous determination of 5 psychotropic drugs of various types in an autopsy case of acute multiple drug poisoning
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