Comparative study of sample preparation procedures to determine the main compounds in ayahuasca beverages by QuEChERS and high‐performance liquid chromatography analysis

Author:

Gonçalves Joana12,Rosado Tiago12,Barroso Mário3,Restolho José4,Fernández Nicolás5,Luís Ângelo12,Gallardo Eugenia12ORCID,Duarte Ana Paula12

Affiliation:

1. Centro de Investigação em Ciências da Saúde (CICS‐UBI) Universidade da Beira Interior Covilhã Portugal

2. Laboratório de Fármaco‐Toxicologia, UBIMedical Universidade da Beira Interior Covilhã Portugal

3. Serviço de Química e Toxicologia Forenses Instituto Nacional de Medicina Legal e Ciências Forenses, Delegação do Sul Lisbon Portugal

4. Eurofins Forensic Services (Heathrow) Feltham UK

5. Cátedra de Toxicología y Química Legal, Laboratorio de Asesoramiento Toxicológico Analítico (CENATOXA), Facultad de Farmacia y Bioquímica Universidad de Buenos Aires Ciudad Autónoma de Buenos Aires Argentina

Abstract

AbstractIntroductionAyahuasca is a psychoactive drink originally consumed by indigenous people of the Amazon. The lack of regulation of this drink leads to uncontrolled consumption, and it is often consumed in religious contexts.ObjectiveThe aim of this work is to compare three miniaturised extraction techniques for extracting the main ayahuasca compounds from beverages.MethodologyThree sample pretreatment techniques were evaluated (dispersive liquid–liquid microextraction [DLLME], microextraction by packed sorbent [MEPS] and QuEChERS [Quick, Easy, Cheap, Effective, Rugged and Safe]) for the simultaneous extraction of N,N‐dimethyltryptamine (DMT), tetrahydroharmine (THH), harmine, harmaline, harmol and harmalol from ayahuasca beverage samples. Then, the most promising technique (QuEChERS) was chosen to pre‐concentrate the analytes, subsequently detected by high‐performance liquid chromatography coupled to a diode array detector (HPLC‐DAD).ResultsThe procedure was optimised, with the final conditions being 500 μL of extractor solvent, 85 mg of primary secondary amine (PSA) and 4 s of vortexing. The analytical method was validated, showing to be linear between 0.16 and 10 μg/mL for β‐carbolines and between 0.016 and 1 μg/mL for DMT, with coefficients of determination (R2) between 0.9968 and 0.9993. The limit of detection (LOD) and lower limit of quantification (LLOQ) were 0.16 μg/mL for all compounds, except for DMT (0.016 μg/mL) and extraction efficiencies varied between 60.2% and 88.0%.ConclusionThe analytical methodology proved to be accurate and precise, with good linearity, LODs and LLOQs. This method has been fully validated and successfully applied to ayahuasca beverage samples.

Funder

Fundação para a Ciência e a Tecnologia

European Regional Development Fund

Publisher

Wiley

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