Rapid Extraction and Qualitative Screening of 30 Drugs in Oral Fluid at Concentrations Recommended for the Investigation of DUID Cases.


Journal

Journal of analytical toxicology
ISSN: 1945-2403
Titre abrégé: J Anal Toxicol
Pays: England
ID NLM: 7705085

Informations de publication

Date de publication:
14 Oct 2022
Historique:
received: 03 03 2022
revised: 04 04 2022
accepted: 30 05 2022
pubmed: 1 6 2022
medline: 19 10 2022
entrez: 31 5 2022
Statut: ppublish

Résumé

A rapid, simple extraction method followed by qualitative screening using liquid chromatography-tandem mass spectrometry (LC-MS-MS) for drugs in oral fluid is presented. The decision points were selected to be at, or lower, than those recommended as Tier I compounds by the National Safety Council's Alcohol, Drugs and Impairment Division for toxicological investigation of driving under the influence of drug (DUID) cases and were also at, or lower, than those recommended by Substance Abuse and Mental Health Service Administration and the Department of Transportation for Federal workplace drug testing programs. The method included 30 drugs: delta-9-tetrahydrocannabinol, amphetamine, methamphetamine, 3,4-methylenedioxymethamphetamine, 3,4-methylenedioxyamphetamine, cocaine, benzoylecgonine, carisoprodol, meprobamate, zolpidem, alprazolam, clonazepam, 7-aminoclonazepam, diazepam, nordiazepam, lorazepam, oxazepam, temazepam, codeine, morphine, 6-acetylmorphine, buprenorphine, fentanyl, hydrocodone, hydromorphone, oxycodone, oxymorphone, methadone, tramadol and phencyclidine. Phencyclidine was included because it is in the Federal workplace program even though it is considered a Tier II drug for DUID cases. A liquid-liquid extraction method using isopropanol, hexane and ethyl acetate to extract drugs from the oral fluid-buffer mix collected in a Quantisal™ device, followed by LC-MS-MS screening, was developed and validated according to ANSI/ASB 2019 Standard Practices for Method Validation in Forensic Toxicology. Interference studies, limit of detection, precision at the decision point, ionization suppression/enhancement and processed sample stability were determined for each drug. The method was successfully applied to proficiency specimens and routine samples received in the laboratory.

Identifiants

pubmed: 35640884
pii: 6595855
doi: 10.1093/jat/bkac031
doi:

Substances chimiques

Amphetamines 0
Hexanes 0
Morphine Derivatives 0
Pharmaceutical Preparations 0
Carisoprodol 21925K482H
Tramadol 39J1LGJ30J
Buprenorphine 40D3SCR4GZ
Methamphetamine 44RAL3456C
3,4-Methylenedioxyamphetamine 4764-17-4
Clonazepam 5PE9FDE8GB
Nordazepam 67220MCM01
Oxazepam 6GOW6DWN2A
Hydrocodone 6YKS4Y3WQ7
Dronabinol 7J8897W37S
Zolpidem 7K383OQI23
Meprobamate 9I7LNY769Q
Oxymorphone 9VXA968E0C
Oxycodone CD35PMG570
Temazepam CHB1QD2QSS
Cocaine I5Y540LHVR
Phencyclidine J1DOI7UV76
N-Methyl-3,4-methylenedioxyamphetamine KE1SEN21RM
2-Propanol ND2M416302
Lorazepam O26FZP769L
Hydromorphone Q812464R06
Methadone UC6VBE7V1Z
Fentanyl UF599785JZ
Codeine UX6OWY2V7J
Alprazolam YU55MQ3IZY

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

899-904

Subventions

Organisme : CSAP SAMHSA HHS
ID : HHSS277201800001C
Pays : United States

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Cynthia Coulter (C)

9-Delta Analytical LLC, 4365 E. Lowell Street, Suite E, Ontario, CA 91761, USA.

Margaux Garnier (M)

9-Delta Analytical LLC, 4365 E. Lowell Street, Suite E, Ontario, CA 91761, USA.

Christine Moore (C)

9-Delta Analytical LLC, 4365 E. Lowell Street, Suite E, Ontario, CA 91761, USA.

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Classifications MeSH