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Analytical Chemistry

ISSN 0003-2700

7 papers in the library · 282 citations · publishing 1988-2025

Papers

On-Line Immunoaffinity Extraction-Coupled Column Capillary Liquid Chromatography/Tandem Mass Spectrometry: Trace Analysis of LSD Analogs and Metabolites in Human Urine

Analytical Chemistry January 1, 1996 Jianyi Cai, Jack D. Henion 112 citations

An on-line immunoaffinity extraction-coupled column capillary liquid chromatography/tandem mass spectrometry method was developed to detect LSD and its analogs and metabolites in human urine. The system uses three columns and allows direct analysis of diluted urine without pretreatment, eliminating sample handling steps. Concentrations as low as 2.5 parts per trillion of LSD and several analogs were detected in spiked human urine, which is 20-fold lower than the previous limit of detection using solid phase extraction and liquid chromatography/tandem mass spectrometry. The method was also applied to urine specimens from LSD users.

Quantification of LSD and N-demethyl-LSD in urine by gas chromatography/resonance electron capture ionization mass spectrometry

Analytical Chemistry July 15, 1988 Hyun Kyoon Lim, David M. Andrenyak, Paula Francom et al. 68 citations

A gas chromatography/resonance electron capture ionization mass spectrometry method was developed to quantify LSD and its metabolite N-demethyl-LSD in urine. The method achieved detection limits of 0.1 ng/mL for LSD and 0.2 ng/mL for N-demethyl-LSD, with linear calibration curves over a range of 0.5 to 20 ng/mL. The technique was applied to urine samples from human subjects administered known doses of LSD, demonstrating reliable identification and measurement of both compounds. The approach offers improved sensitivity and specificity for forensic and clinical detection of LSD use.

Determination of lysergic acid diethylamide (LSD), iso-LSD, and N-demethyl-LSD in body fluids by gas chromatography/tandem mass spectrometry

Analytical Chemistry July 15, 1992 Chad C. Nelson, Rodger L. Foltz 64 citations

Capillary gas chromatography/tandem mass spectrometry (GC/MS/MS) methods can detect and quantify LSD, iso-LSD, and N-demethyl-LSD in urine or blood at low-pg/mL concentrations. Derivatization, sample introduction, and ionization techniques were evaluated for efficiency and specificity. Fragmentation pathways from collision-induced dissociation show principal losses from the amide and piperidine-ring moieties. Positive-ion ammonia chemical ionization with MS/MS analysis of trimethylsilyl derivatives provides high specificity for identifying these compounds. Negative-ion chemical ionization with GC/MS/MS of the trifluoroacetyl derivative is suited for trace-level identification of N-demethyl-LSD, a metabolite.

Setup of a Serotonin 2A Receptor (5-HT2AR) Bioassay: Demonstration of Its Applicability To Functionally Characterize Hallucinogenic New Psychoactive Substances and an Explanation Why 5-HT2AR Bioassays Are Not Suited for Universal Activity-Based Screening of Biofluids for New Psychoactive Substances

Analytical Chemistry November 14, 2019 Eline Pottie, Annelies Cannaert, Katleen van Uytfanghe et al. 29 citations

Classic hallucinogens, which activate the serotonin 2A receptor (5-HT2AR), represent the third largest category of new psychoactive substances. A new bioassay was developed that measures receptor activation by monitoring β-arrestin2 recruitment using a split-luciferase system. The assay determined potency and efficacy for various hallucinogens, including LSD, 5-MeO-DALT, mescaline, and several 2C compounds and their NBOMe derivatives, with EC50 values ranging from subnanomolar (NBOMes) to micromolar (mescaline) levels. When applied to plasma screening, blank samples showed pronounced receptor activation due to endogenous serotonin, confirmed by its elimination with a 5-HT2AR antagonist or MAO-A treatment, and by LC-HRMS analysis. The bioassay's main application is characterizing poorly understood serotonergic hallucinogens, as MAO-A metabolism of some compounds could bias detection in biofluids.

Photothermal Desorption and Reagent-Assisted Low-Temperature Plasma Ionization Miniature IT-MS/MS for On-Site Analysis of Illicit Drugs in Saliva and Urine.

Analytical Chemistry February 11, 2025 Yun Wu, Mei Li, Ruidong Liu et al. 6 citations

A new portable mass spectrometry device, PDRA-LTP-ITMS, can detect illicit drugs in saliva or urine within 5 seconds using only 10 microliters of sample. The method improves sensitivity up to 10-fold compared to some other techniques and achieves detection limits for MDMA, MDA, methamphetamine, amphetamine, ketamine, and cocaine ranging from 4.5 to 20 picograms per microliter in saliva, meeting Chinese national standards. The device's performance approaches that of a high-end laboratory mass spectrometer, offering a rapid on-site tool for identifying drug-impaired drivers.

Rapid Screening of Illicit Drugs from Biofluid via Dried Blood/Urine Spot and Ultrasonic Desorption-Assisted Low-Temperature Arc Plasma Ionization Mass Spectrometry.

Analytical Chemistry April 29, 2025 Zhongbao Han, Zhongyu Zhao, Meiyun Pan et al. 3 citations

A new method for quickly detecting illicit drugs in biological fluids uses paper-based sample collection combined with ultrasonic desorption and low-temperature plasma ionization mass spectrometry. Optimized with ketamine, the technique achieves detection limits of 10 to 20 ng per mL, linear ranges with R² above 0.99, and recovery rates over 91% in complex fluids. It performs reliably even with drug mixtures and under varied storage conditions. Analysis takes only 3 seconds, making it suitable for high-throughput point-of-care testing and forensic screening.

Rapid Screening Method for New Psychoactive Substances of Forensic Interest: Electrochemistry and Analytical Determination of Phenethylamines Derivatives (NBOMe) via Cyclic and Differential Pulse Voltammetry.

Analytical Chemistry February 7, 2017 Ana Flávia B. Andrade, Samuel Kasahun Mamo, Jose Gonzalez-Rodriguez

NBOMe derivatives are phenethylamines related to the 2C class of hallucinogens. Few human pharmacologic studies exist, but several intoxication cases and deaths have been reported. These compounds are not part of routine drug screening for many police forces, and no rapid immunoassay tests can detect them. For the first time, the voltammetric behavior of 25B-NBOMe and 25I-NBOMe was investigated, and their electroanalytical characteristics were determined. A novel, fast, and sensitive screening method was developed to identify these two most common NBOMes in real samples. The method uses electrochemical oxidation to produce an analytical signal related to concentration, with an average lower limit of quantitation of 0.01 mg/mL for both. It is selective enough to identify each compound individually despite their structural similarity.