Identification of phenobarbital and other barbiturates in forensic drug screening using positive electrospray ionization liquid chromatography−high resolution mass spectrometry

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Standard

Identification of phenobarbital and other barbiturates in forensic drug screening using positive electrospray ionization liquid chromatography−high resolution mass spectrometry. / Høj, Lars Jakobsen; Mollerup, Christian Brinch; Rasmussen, Brian Schou; Johansen, Sys Stybe; Linnet, Kristian; Dalsgaard, Petur Weihe.

I: Drug Testing and Analysis, Bind 11, Nr. 8, 08.2019, s. 1258-1263.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Høj, LJ, Mollerup, CB, Rasmussen, BS, Johansen, SS, Linnet, K & Dalsgaard, PW 2019, 'Identification of phenobarbital and other barbiturates in forensic drug screening using positive electrospray ionization liquid chromatography−high resolution mass spectrometry', Drug Testing and Analysis, bind 11, nr. 8, s. 1258-1263. https://doi.org/10.1002/dta.2603

APA

Høj, L. J., Mollerup, C. B., Rasmussen, B. S., Johansen, S. S., Linnet, K., & Dalsgaard, P. W. (2019). Identification of phenobarbital and other barbiturates in forensic drug screening using positive electrospray ionization liquid chromatography−high resolution mass spectrometry. Drug Testing and Analysis, 11(8), 1258-1263. https://doi.org/10.1002/dta.2603

Vancouver

Høj LJ, Mollerup CB, Rasmussen BS, Johansen SS, Linnet K, Dalsgaard PW. Identification of phenobarbital and other barbiturates in forensic drug screening using positive electrospray ionization liquid chromatography−high resolution mass spectrometry. Drug Testing and Analysis. 2019 aug.;11(8):1258-1263. https://doi.org/10.1002/dta.2603

Author

Høj, Lars Jakobsen ; Mollerup, Christian Brinch ; Rasmussen, Brian Schou ; Johansen, Sys Stybe ; Linnet, Kristian ; Dalsgaard, Petur Weihe. / Identification of phenobarbital and other barbiturates in forensic drug screening using positive electrospray ionization liquid chromatography−high resolution mass spectrometry. I: Drug Testing and Analysis. 2019 ; Bind 11, Nr. 8. s. 1258-1263.

Bibtex

@article{777abcfd20b342aa9b49aff04541d0e7,
title = "Identification of phenobarbital and other barbiturates in forensic drug screening using positive electrospray ionization liquid chromatography−high resolution mass spectrometry",
abstract = "Comprehensive drug-screening performed by liquid chromatography−high resolution mass spectrometry (LC−HRMS) enables identification of hundreds to thousands of drug compounds in a single analysis. Forensic drug screening is generally performed with positive electrospray ionization (ESI+), targeting basic drugs; however, a few toxicologically important drugs such as barbiturates, may require analysis by negative ESI. In this work, screening targets for barbiturates were determined using our LC−HRMS screening with ESI+. For several years, our forensic whole blood samples have been analyzed using the LC−HRMS−ESI+ screening in parallel with a multi-target LC–MS/MS−ESI− method. From 2014 to 2018, 23 samples were positive for phenobarbital (0.5−81 mg/kg). Retrospective data analysis of 4816 blood samples (15 positive) revealed several potential screening targets for phenobarbital. The targets were tentatively identified by exact mass and isotopic pattern as uncommon adducts of phenobarbital and as a decomposition product of phenobarbital N-glucoside (C17H24N2O7). Analysis of a test set containing eight positive (0.5–65 mg/kg phenobarbital) and 31 negative samples supported the use of the observed target m/z 323.0614 at 5.14 minutes, corresponding to the [M + HCOONa+Na]+ adduct of phenobarbital. The [M + HCOONa+Na]+ adduct was confirmed as a screening target for common barbiturates, by analysis of barbiturate reference standards in ESI+/ESI−. The [M + HCOONa+Na]+ adduct allowed retrospective analysis with 91% sensitivity (n = 23) and 100% specificity (n = 4855) for phenobarbital in our existing LC−HRMS−ESI+ screening. The two negative results were the two whole-blood samples with the lowest phenobarbital concentration (<1.8 mg/kg). Thus, a specialized screening is not necessary and use of this adduct likely enables screening for other barbiturates.",
keywords = "forensic screening, forensic toxicology, phenobarbital, retrospective analysis",
author = "H{\o}j, {Lars Jakobsen} and Mollerup, {Christian Brinch} and Rasmussen, {Brian Schou} and Johansen, {Sys Stybe} and Kristian Linnet and Dalsgaard, {Petur Weihe}",
year = "2019",
month = aug,
doi = "10.1002/dta.2603",
language = "English",
volume = "11",
pages = "1258--1263",
journal = "Drug Testing and Analysis",
issn = "1942-7603",
publisher = "JohnWiley & Sons Ltd",
number = "8",

}

RIS

TY - JOUR

T1 - Identification of phenobarbital and other barbiturates in forensic drug screening using positive electrospray ionization liquid chromatography−high resolution mass spectrometry

AU - Høj, Lars Jakobsen

AU - Mollerup, Christian Brinch

AU - Rasmussen, Brian Schou

AU - Johansen, Sys Stybe

AU - Linnet, Kristian

AU - Dalsgaard, Petur Weihe

PY - 2019/8

Y1 - 2019/8

N2 - Comprehensive drug-screening performed by liquid chromatography−high resolution mass spectrometry (LC−HRMS) enables identification of hundreds to thousands of drug compounds in a single analysis. Forensic drug screening is generally performed with positive electrospray ionization (ESI+), targeting basic drugs; however, a few toxicologically important drugs such as barbiturates, may require analysis by negative ESI. In this work, screening targets for barbiturates were determined using our LC−HRMS screening with ESI+. For several years, our forensic whole blood samples have been analyzed using the LC−HRMS−ESI+ screening in parallel with a multi-target LC–MS/MS−ESI− method. From 2014 to 2018, 23 samples were positive for phenobarbital (0.5−81 mg/kg). Retrospective data analysis of 4816 blood samples (15 positive) revealed several potential screening targets for phenobarbital. The targets were tentatively identified by exact mass and isotopic pattern as uncommon adducts of phenobarbital and as a decomposition product of phenobarbital N-glucoside (C17H24N2O7). Analysis of a test set containing eight positive (0.5–65 mg/kg phenobarbital) and 31 negative samples supported the use of the observed target m/z 323.0614 at 5.14 minutes, corresponding to the [M + HCOONa+Na]+ adduct of phenobarbital. The [M + HCOONa+Na]+ adduct was confirmed as a screening target for common barbiturates, by analysis of barbiturate reference standards in ESI+/ESI−. The [M + HCOONa+Na]+ adduct allowed retrospective analysis with 91% sensitivity (n = 23) and 100% specificity (n = 4855) for phenobarbital in our existing LC−HRMS−ESI+ screening. The two negative results were the two whole-blood samples with the lowest phenobarbital concentration (<1.8 mg/kg). Thus, a specialized screening is not necessary and use of this adduct likely enables screening for other barbiturates.

AB - Comprehensive drug-screening performed by liquid chromatography−high resolution mass spectrometry (LC−HRMS) enables identification of hundreds to thousands of drug compounds in a single analysis. Forensic drug screening is generally performed with positive electrospray ionization (ESI+), targeting basic drugs; however, a few toxicologically important drugs such as barbiturates, may require analysis by negative ESI. In this work, screening targets for barbiturates were determined using our LC−HRMS screening with ESI+. For several years, our forensic whole blood samples have been analyzed using the LC−HRMS−ESI+ screening in parallel with a multi-target LC–MS/MS−ESI− method. From 2014 to 2018, 23 samples were positive for phenobarbital (0.5−81 mg/kg). Retrospective data analysis of 4816 blood samples (15 positive) revealed several potential screening targets for phenobarbital. The targets were tentatively identified by exact mass and isotopic pattern as uncommon adducts of phenobarbital and as a decomposition product of phenobarbital N-glucoside (C17H24N2O7). Analysis of a test set containing eight positive (0.5–65 mg/kg phenobarbital) and 31 negative samples supported the use of the observed target m/z 323.0614 at 5.14 minutes, corresponding to the [M + HCOONa+Na]+ adduct of phenobarbital. The [M + HCOONa+Na]+ adduct was confirmed as a screening target for common barbiturates, by analysis of barbiturate reference standards in ESI+/ESI−. The [M + HCOONa+Na]+ adduct allowed retrospective analysis with 91% sensitivity (n = 23) and 100% specificity (n = 4855) for phenobarbital in our existing LC−HRMS−ESI+ screening. The two negative results were the two whole-blood samples with the lowest phenobarbital concentration (<1.8 mg/kg). Thus, a specialized screening is not necessary and use of this adduct likely enables screening for other barbiturates.

KW - forensic screening

KW - forensic toxicology

KW - phenobarbital

KW - retrospective analysis

UR - http://www.scopus.com/inward/record.url?scp=85066912923&partnerID=8YFLogxK

U2 - 10.1002/dta.2603

DO - 10.1002/dta.2603

M3 - Journal article

C2 - 30993867

AN - SCOPUS:85066912923

VL - 11

SP - 1258

EP - 1263

JO - Drug Testing and Analysis

JF - Drug Testing and Analysis

SN - 1942-7603

IS - 8

ER -

ID: 226264994