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Liquid Chromatography-Mass Spectrometric and Liquid Chromatography-Tandem Mass Spectrometric Determination of Hallucinogenic Indoles Psilocin and Psilocybin in “Magic Mushroom” Samples

Tohru Kamata, Masanobu Nishikawa, Munehiro Katagi, Hitoshi Tsuchihashi

Journal of Forensic Sciences March 1, 2005 DOI: 10.1520/jfs2004276 via OpenAlex

Summary

AI-generated from the abstract

Liquid chromatography-mass spectrometry (LC-MS) and liquid chromatography-tandem mass spectrometry (LC-MS-MS) can accurately and sensitively detect psilocin and psilocybin, the hallucinogens in magic mushrooms, without derivatization. Tandem mass spectrometry provides high specificity and accuracy. Detection limits range from 1 to 25 picograms by LC-MS in selected ion monitoring mode, with intra- and inter-day coefficients of variation of 4.21–5.93% by LC-MS-MS in selected reaction monitoring mode. Analysis of four real samples showed psilocin content from 0.60 to 1.4 mg/g dry weight and psilocybin content from 0.18 to 3.8 mg/g dry weight, varying widely between samples.

Study at a glance

Characteristics Analytical method development and validation Peer reviewed
Sample size 4
Population Magic mushroom samples
Topics Psilocybin
Keywords Liquid chromatography–mass spectrometry Selected reaction monitoring Tryptamine Tandem mass spectrometry
Citations 24
Key finding LC-MS and LC-MS-MS methods can detect psilocin and psilocybin with high sensitivity and specificity, and the contents of these compounds vary widely across mushroom samples.

Abstract

Abstract Accurate and sensitive analytical methods for psilocin (PC) and psilocybin (PB), tryptamine-type hallucinogens contained in “magic mushrooms,” were investigated using liquid chromatography-mass spectrometry (LC-MS) and liquid chromatography-tandem mass spectrometry (LC-MS-MS). The chromatographic separation on an ODS column and mass spectral information gave complete discrimination between PC and PB without derivatization. The mass spectrometric detection had a high sensitivity, and the tandem mass spectrometric detection provided more specificity and accuracy, as well as high sensitivity. The detection limits ranged from 1 to 25 pg by LC-MS in the selected ion monitoring mode, and the intra- and inter-day coefficients of variation were estimated to be 4.21–5.93% by LC-MS-MS in the selected reaction monitoring mode. By applying the present LC-MS-MS technique to four real samples, the contents of PC and PB were found to vary over a wide range (0.60–1.4 and 0.18–3.8 mg/g dry wt. for PC and PB, respectively) between samples.

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