Modification of a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method targeting lysergic acid diethylamide (LSD) and its primary metabolite (OH-LSD) to include nine LSD analogs.

Autor: Patton AL; Division of Forensic Toxicology, Armed Forces Medical Examiner System, Dover, Delaware, USA.; SNA International, LLC, Contractor Supporting the Armed Forces Medical Examiner System, Alexandria, Virginia, USA., Karschner EL; Division of Forensic Toxicology, Armed Forces Medical Examiner System, Dover, Delaware, USA., Walterscheid JP; Division of Forensic Toxicology, Armed Forces Medical Examiner System, Dover, Delaware, USA., Garcia JM; Division of Forensic Toxicology, Armed Forces Medical Examiner System, Dover, Delaware, USA.
Jazyk: angličtina
Zdroj: Journal of forensic sciences [J Forensic Sci] 2024 Sep; Vol. 69 (5), pp. 1789-1798. Date of Electronic Publication: 2024 Jun 27.
DOI: 10.1111/1556-4029.15572
Abstrakt: A variety of LSD analogs have emerged in recent years with dual purposes of avoiding prosecution from possession while providing new options for those willing to experiment with hallucinogenic drugs. In this study, a previously published automated sample preparation method for LSD and its primary metabolite (OH-LSD) was utilized to extract LSD, OH-LSD, and nine LSD analogs from urine. The liquid chromatography tandem mass spectrometry (LC-MS/MS) method was modified from the previously published LC conditions to utilize a different analytical column and gradient elution program. Mobile phases of 10 mM ammonium formate with 0.1% formic acid in deionized water (mobile phase A) and 0.1% formic acid in methanol (mobile phase B) were employed. The method was validated to ANSI/ASB Standard 036 with a 0.1 ng/mL limit of detection for all analytes and was utilized for the analysis of 325 urine specimens. Although no LSD analogs were observed in the samples analyzed, this validated method was demonstrated to be suitable for the analysis of these compounds in laboratories seeking to expand their testing scope. Automated sample preparation allows for the efficient analysis of these analytically challenging compounds with minimal manual handling. Additionally, there was no increased analytical time burden when the LC column and gradient were modified to target nine additional analytes. Detection may improve as new reference standards are developed to allow laboratories to focus on the metabolic products of these analogs. For now, this validated procedure can assist with the routine analysis and surveillance of these emerging substances.
(Published 2024. This article is a U.S. Government work and is in the public domain in the USA.)
Databáze: MEDLINE
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