Determination of N,N-dimethyltryptamine in Mimosa tenuiflora inner barks by matrix solid-phase dispersion procedure and GC–MS
Alain Gaujac, Adriano Aquino, Sandro Navickiene, Jaílson B. de Andrade
Journal of Chromatography B November 17, 2011 DOI: 10.1016/j.jchromb.2011.11.014 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Method optimization and validation Peer reviewed |
|---|---|
| Sample size | 24 |
| Population | Mimosa tenuiflora inner bark samples obtained locally |
| Topics | Ayahuasca 5-MeO-DMT DMT |
| Keywords | Detection limit Chromatography Matrix chemical analysis Stationary phase Context archaeology Traditional medicine |
| Citations | 30 |
| Key points | The optimized MSPD-GC-MS method successfully quantified DMT in Mimosa tenuiflora bark, with concentrations ranging from 1.26 to 9.35 mg/g across 24 samples. |
Abstract
N,N-dimethyltryptamine (DMT) is a potent hallucinogen found in beverages consumed in religion rituals and neo-shamanic practices over the world. Two of these religions, Santo Daime and União do Vegetal (UDV), are represented in countries including Australia, the United States and several European nations. In some of this countries there have been legal disputes concerning the legalization of ayahuasca consumption during religious rituals, a beverage rich in DMT. In Brazil, even children and pregnant women are legally authorized to consume ayahuasca in a religious context. A simple and low-cost method based on matrix solid-phase dispersion (MSPD) and gas chromatography with mass spectrometric detection (GC-MS) has been optimized for the determination of N,N-dimethyltryptamine in Mimosa tenuiflora inner bark. The experimental variables that affect the MSPD method, such as the amounts of solid-phase and herbal sample, solvent nature, eluate volume and NaOH concentration were optimized using an experimental design. The method showed good linearity (r = 0.9962) and repeatability (RSD < 7.4%) for DMT compound, with detection limit of 0.12 mg/g. The proposed method was used to analyze 24 samples obtained locally. The results showed that concentrations of the target compound in M. tenuiflora barks, ranged from 1.26 to 9.35 mg/g for these samples.
Citations in the library
Cited by 14
- Neuropharmacology of N,N-dimethyltryptamine Brain Research Bulletin April 30, 2016
- Developments in harmine pharmacology — Implications for ayahuasca use and drug-dependence treatment Progress in Neuro-Psychopharmacology and Biological Psychiatry June 10, 2012
- Bioinspired total synthesis and structural revision of yuremamine, an alkaloid from the entheogenic plant Mimosa tenuiflora Chemical Communications 2015
- Determination of N,N-dimethyltryptamine in beverages consumed in religious practices by headspace solid-phase microextraction followed by gas chromatography ion trap mass spectrometry Talanta February 1, 2013
- Detection and Quantification of Psychoactive N,N-Dimethyltryptamine in Ayahuasca Brews by Ambient Ionization High-Resolution Mass Spectrometry ACS Omega October 27, 2020
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Cites 10
- Pharmahuasca: Human Pharmacology of Oral DMT Plus Harmine Journal of Psychoactive Drugs April 1, 1999
- Gas chromatographic analysis of dimethyltryptamine and β‐carboline alkaloids in ayahuasca, an amazonian psychoactive plant beverage Phytochemical Analysis January 12, 2009
- Direct analysis of psychoactive tryptamine and harmala alkaloids in the Amazonian botanical medicine ayahuasca by liquid chromatography-electrospray ionization-tandem mass spectrometry. Journal of Chromatography A December 18, 2009
- Analytical chemistry of synthetic routes to psychoactive tryptamines : Part II. Characterisation of the Speeter and Anthony synthetic route to N,N-dialkylated tryptamines using GC-EI-ITMS, ESI-TQ-MS-MS and NMR The Analyst 2005
- A general approach to the screening and confirmation of tryptamines and phenethylamines by mass spectral fragmentation. Talanta January 15, 2008
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