Characterization of extensive 2-fluorodeschloroketamine metabolism in pooled human liver microsomes, urine and hair from an addicted patient using high-resolution accurate mass spectrometry.
Delphine Joseph, Camille Lesueur, Fanny Zerizer, Alexia Fenot, Jean Claude Alvarez, Islam Amine Larabi
Journal of analytical toxicology July 22, 2023 DOI: 10.1093/jat/bkad030 via PubMed
Summary
AI-generated from the abstractTwenty-six potential metabolites of the ketamine derivative 2-fluorodeschloroketamine (2F-DCK) were identified, with 15 reported for the first time. Thirteen metabolites were detected in pooled human liver microsomes, 10 were confirmed in both urine and hair from a chronic user, and all were found in at least one of those samples. Nor-2F-DCK is confirmed as a reliable target analyte; OH-dihydro-nor-2F-DCK and dehydro-nor-2F-DCK are suggested as new target analytes in urine and hair, respectively. Deschloroketamine (DCK) was identified as a 2F-DCK metabolite for the first time, with concentrations in hair segments A (0–3 cm), B (3–6 cm), and C (6–9 cm) of 885, 1,500, and 1,850 pg/mg, respectively. Two seized crystals contained 2F-DCK at 67% and 96% with traces of DCK (0.4% and 0.6%) from cross-contamination.
Study at a glance
| Characteristics | In vitro metabolism study with authentic sample analysis Peer reviewed |
|---|---|
| Sample size | 1 |
| Population | One chronic drug user providing urine and hair samples |
| Citations | 8 |
| Key finding | Twenty-six metabolites of 2F-DCK were identified; nor-2F-DCK is a reliable target analyte, and DCK was confirmed as a metabolite for the first time with concentrations in hair ranging from 885 to 1,850 pg/mg. |
Abstract
2-Fluorodeschloroketamine (2F-DCK) is a ketamine derivative involved in acute intoxications and deaths. The aim of this study is to investigate its metabolism using pooled human liver microsomes (pHLMs) and to apply it to authentic samples (urine, hair and seized materials) from a drug user. 2F-DCK (100 µM) incubates with pHLMs were analyzed by liquid chromatography-high-resolution accurate mass (LC-HRAM; Q-Exactive, Thermo Fisher Scientific®) according to a previously published protocol. Spectra annotation was performed using Compound Discoverer® software and the metabolic scheme was drawn using ChemDraw software. Urine (200 µL) and hair (previously decontaminated using dichloromethane and segmented into three segments: A, 0-3 cm; B, 3-6 cm; C, 6-9 cm) were extracted with a mixture of hexane:ethyl acetate (1:1) and chloroform:isopropanol (4:1). About 10 µL of both reconstituted residues were analyzed by LC-HRAM. Hair was also analyzed by LC-MS-MS (TSQ Vantage, Thermo Fisher Scientific®) for 2F-DCK and deschloroketamine (DCK) quantification. The two presumed 2F-DCK crystals consumed by the patient were dissolved in methanol (1 mg/mL) and 10 µL were analyzed by LC-MS-MS (Quantum Access Max, Thermo Fisher Scientific®). Twenty-six putative 2F-DCK metabolites were identified, 15 being reported for the first time. Thirteen metabolites were detected in pHLMs, 10 confirmed in both the patient's urine and hair and all were found in at least one of the two samples. Twenty-three metabolites were detected in urine and 20 in hair. Our research confirms the reliability of nor-2F-DCK as a target analyte and suggests OH-dihydro-nor-2F-DCK and dehydro-nor-2F-DCK as new target analytes in urine and hair, respectively. This is the first study to report DCK as a 2F-DCK metabolite using pHLMs and to determine its concentrations in hair (A/B/C, 885/1,500/1,850 pg/mg) following chronic use. Finally, the two seized crystals contained 2F-DCK at 67% and 96% with traces of DCK (0.4% and 0.6%) related to cross-contamination by container exchange.