Determination of N,N-dimethyltryptamine in beverages consumed in religious practices by headspace solid-phase microextraction followed by gas chromatography ion trap mass spectrometry
Alain Gaujac, Nicola M. Dempster, Sandro Navickiene, Simon D. Brandt, Jaílson B. de Andrade
Talanta February 1, 2013 DOI: 10.1016/j.talanta.2013.01.017 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Method development and validation Peer reviewed |
|---|---|
| Population | Ayahuasca and vinho da jurema samples from Brazilian religious groups |
| Topics | 5-MeO-DMT DMT |
| Keywords | Solid-phase microextraction Gas chromatography–mass spectrometry Ion trap Detection limit |
| Citations | 29 |
| Key points | The SPME/GC-IT-MS method accurately quantifies DMT in ayahuasca and vinho da jurema, with concentrations in real samples ranging from 0.10 to 1.81 g/L. |
Abstract
A novel analytical approach combining solid-phase microextraction (SPME)/gas chromatography ion trap mass spectrometry (GC-IT-MS) was developed for the detection and quantification N,N-dimethyltryptamine (DMT), a powerful psychoactive indole alkaloid present in a variety of South American indigenous beverages, such as ayahuasca and vinho da jurema. These particular plant products, often used within a religious context, are increasingly consumed throughout the world following an expansion of religious groups and the availability of plant material over the Internet and high street shops. The method described in the present study included the use of SPME in headspace mode combined GC-IT-MS and included the optimization of the SPME procedure using multivariate techniques. The method was performed with a polydimethylsiloxane/divinylbenzene (PDMS/DVB) fiber in headspace mode (70 min at 60 °C) which resulted in good precision (RSD<8.6%) and accuracy values (71-109%). Detection and quantification limits obtained for DMT were 0.78 and 9.5 mg L(-1), respectively and good linearity (1.56-300 mg L(-1), r(2)=0.9975) was also observed. In addition, the proposed method showed good robustness and allowed for the minimization of sample manipulation. Five jurema beverage samples were prepared in the laboratory in order to study the impact of temperature, pH and ethanol on the ability to extract DMT into solution. The developed method was then applied to the analysis of twelve real ayahuasca and vinho da jurema samples, obtained from Brazilian religious groups, which revealed DMT concentration levels between 0.10 and 1.81 g L(-1).
Citations in the library
Cited by 19
- Ayahuasca: Uses, Phytochemical and Biological Activities Natural Products and Bioprospecting May 27, 2019
- Biomedical analysis of New Psychoactive Substances (NPS) of natural origin. Journal of Pharmaceutical and Biomedical Analysis February 5, 2020
- Validation of an analytical method for the determination of the main ayahuasca active compounds and application to real ayahuasca samples from Brazil Journal of Chromatography B June 8, 2019
- Stability Evaluation of DMT and Harmala Alkaloids in Ayahuasca Tea Samples Molecules April 29, 2020
- Toxicological Aspects and Determination of the Main Components of Ayahuasca: A Critical Review Medicines October 18, 2019
and 14 more in the library
Cites 6
- Gas chromatographic analysis of dimethyltryptamine and β‐carboline alkaloids in ayahuasca, an amazonian psychoactive plant beverage Phytochemical Analysis January 12, 2009
- Identification of N,N‐dimethyltryptamine and β‐carbolines in psychotropic ayahuasca beverage Biomedical Chromatography May 27, 2008
- Application of analytical methods for the structural characterization and purity assessment of N,N-dimethyltryptamine, a potent psychedelic agent isolated from Mimosa tenuiflora inner barks Microchemical Journal April 5, 2012
- Consumption of Ayahuasca by Children and Pregnant Women: Medical Controversies and Religious Perspectives Journal of Psychoactive Drugs March 28, 2011
- Determination of N,N-dimethyltryptamine in Mimosa tenuiflora inner barks by matrix solid-phase dispersion procedure and GC–MS Journal of Chromatography B November 17, 2011
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