We report a qualitative liquid chromatography-tandem mass spectrometry (LC/MS/MS) method for the simultaneous analysis of the three known N,N-dimethyltryptamine endogenous hallucinogens, their precursors and metabolites, as well as melatonin and its metabolic precursors. The method was characterized using artificial cerebrospinal fluid (aCSF) as the matrix and was subsequently applied to the analysis of rat brain pineal gland-aCSF microdialysate. The method describes the simultaneous analysis of 23 chemically diverse compounds plus a deuterated internal standard by direct injection, requiring no dilution or extraction of the samples. The results demonstrate that this is a simple, sensitive, specific and direct approach to the qualitative analysis of these compounds in this matrix. The protocol also employs stringent MS confirmatory criteria for the detection and confirmation of the compounds examined, including exact mass measurements. The excellent limits of detection and broad scope make it a valuable research tool for examining the endogenous hallucinogen pathways in the central nervous system. We report here, for the first time, the presence of N,N-dimethyltryptamine in pineal gland microdialysate obtained from the rat.
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http://dx.doi.org/10.1002/bmc.2981 | DOI Listing |
Sci Rep
November 2024
Department of Chemical Engineering, Military Institute of Engineering, Rio de Janeiro, RJ, Brazil.
Talanta
January 2025
Department of Chemical and Geological Sciences, University of Modena and Reggio Emilia, via G. Campi 103, 41125, Modena, Italy; Interdepartmental Research Centre of the University of Modena and Reggio Emilia BIOGEST-SITEIA, Piazzale Europa 1, 42124, Reggio Emilia, Italy. Electronic address:
In this work, we investigated the ability of an electrochemical sensor to recognize Cannabis sativa L. samples with different total content of Δ-tetrahydrocannabinol (Δ-THC), determined by the levels of the psychoactive cannabinoid and of its biosynthetic precursor Δ-tetrahydrocannabinolic acid (Δ-THCA), using a multivariate approach. The voltammetric responses recorded with screen-printed electrodes modified with carbon black reflected the compositional differences from the different samples, in terms of cannabinoids of the vegetal material.
View Article and Find Full Text PDFJ Anal Toxicol
September 2024
Office of the Chief Medical Examiner, 1 Newhall Street, San Francisco, California, United States.
A streamlined LC-MS/MS method utilizing protein precipitation and filtration extraction was developed to consolidate analyses for drug-facilitated crime (DFC), postmortem investigations, and driving under the influence of drugs (DUID) testing. Fifty-seven target drug and metabolite analytes eluted in under 6-minutes and compromised of GHB precursors (1), hallucinogens (3), muscle relaxants (3), anticonvulsants (7), antidepressants (20), antihistamines (5), antipsychotics (11), antihypertensives and alpha-adrenergics (3), analgesics and anesthetics (3), and miscellaneous (1) in blood (quantitatively) and urine (qualitatively). Limits of detection were set to meet the more challenging sensitivity requirements for DFC, and are therefore also suitable for postmortem investigations, and other forensic casework, including DUID.
View Article and Find Full Text PDFSensors (Basel)
August 2024
School of Applied Systems Biology, La Trobe University, Bundoora, VIC 3083, Australia.
Cannabis is cultivated for therapeutic and recreational purposes where delta-9 tetrahydrocannabinol (THC) is a main target for its therapeutic effects. As the global cannabis industry and research into cannabinoids expands, more efficient and cost-effective analysis methods for determining cannabinoid concentrations will be beneficial to increase efficiencies and maximize productivity. The utilization of machine learning tools to develop near-infrared (NIR) spectroscopy-based prediction models, which have been validated from accurate and sensitive chemical analysis, such as gas chromatography (GC) or liquid chromatography mass spectroscopy (LCMS), is essential.
View Article and Find Full Text PDFYakugaku Zasshi
July 2024
Division of Pharmacognosy, Phytochemistry and Narcotics, National Institute of Health Sciences.
Since around 2021, products claiming to contain a Δ-tetrahydrocannabinol (THC) analog with different lengths of alkyl chain at C-3 position have been sold on the internet in Japan. Δ-THC has a pentyl group derived from the precursor olivetol at the C-3 position. These products include liquid cartridges for electronic cigarettes, herbal products, and gummy products.
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