Evidence map›Paper›PMID 40931322›Full record

ArticleJournal of mass spectrometry : JMS2025

A Sensitive and Comprehensive LC-MS/MS Method for the Analysis of Hallucinogens, Synthetic Cathinones, and Synthetic Cannabinoids in Urine Samples.

Bruno Pereira Dos Santos, Letícia Birk, Vítor Camargo Pôrto, Sabrina Nunes Nascimento, Viviane Cristina Sebben, Sarah Eller, Tiago Franco de Oliveira

Abstract read
In one paragraph

Article in Journal of mass spectrometry : JMS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Bruno Pereira Dos SantosGraduate Program in Health Sciences, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande do Sul, Brazil.ORCID https://orcid.org/0000-0002-7624-5966
Letícia BirkGraduate Program in Health Sciences, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande do Sul, Brazil.ORCID https://orcid.org/0000-0002-9229-5840
Vítor Camargo PôrtoGraduate Program in Health Sciences, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande do Sul, Brazil.ORCID https://orcid.org/0009-0009-1645-0667
Sabrina Nunes NascimentoToxicological Information Center of Rio Grande do Sul (CIT-RS), Rio Grande do Sul State Center for Health Surveillance (CEVS), Porto Alegre, Rio Grande do Sul, Brazil.ORCID https://orcid.org/0000-0001-5936-3074
Viviane Cristina SebbenToxicological Information Center of Rio Grande do Sul (CIT-RS), Rio Grande do Sul State Center for Health Surveillance (CEVS), Porto Alegre, Rio Grande do Sul, Brazil.ORCID https://orcid.org/0000-0001-9388-4105
Sarah EllerGraduate Program in Health Sciences, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande do Sul, Brazil.ORCID https://orcid.org/0000-0003-2200-6959
Tiago Franco de OliveiraGraduate Program in Health Sciences, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande do Sul, Brazil.ORCID https://orcid.org/0000-0003-2594-8415

Funding

Coordination for the Improvement of Higher Education Personnel
6 · The paper itself

Abstract

The laboratory analysis of new psychoactive substances and related drugs is crucial for accurate clinical and forensic diagnosis of poisonings. Given this, a new LC-MS/MS method for analyzing hallucinogens, synthetic cathinones, and synthetic cannabinoids in urine was developed. Urine samples were extracted using a liquid-liquid extraction protocol optimized via a multivariate experimental design. An aliquot of 400 μL of urine was enzymatically hydrolyzed with β-glucuronidase and extracted with 700 μL of ethyl acetate. The resulting extracts were analyzed using LC-MS/MS, with a total chromatographic run time of 8 min. The method was validated according to the ANSI/ASB Standard 036 guideline and was applied to 24 samples from suspected poisoning cases. The lower limits of quantification ranged from 0.1 to 1 ng/mL. Within-run and between-run precision (CV) were < 16%, and bias ranged from -12.8% to 19.8%. Nine of the 20 analytes investigated showed significant ionization suppression or enhancement (> 25%). Only two analytes (2C-E and 2-oxo-3-OH-LSD) had a recovery rate lower than 70%. Among the 24 analyzed urine samples, one tested positive for 25B-NBOH, one for LSD, and two for 2-oxo-3-OH-LSD. The developed method enables the simultaneous quantification of 20 illicit drugs, serving as an efficient diagnostic tool for clinical and forensic laboratories.

Indexed as

AlkaloidsCannabinoidsHallucinogensTandem Mass SpectrometryChromatography, LiquidHumansLimit of DetectionLinear ModelsLiquid Chromatography-Mass SpectrometryLiquid-Liquid ExtractionReproducibility of ResultsAlkaloidsCannabinoidscathinoneHallucinogensdrug analysisLC‐MS/MSnew psychoactive substancesurine

Identifiers

PMID40931322
PMCPMC12423360

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.