Evidence map›Paper›PMID 40076839›Full record

ArticleInternational journal of molecular sciences2025

Drug-Checking and Monitoring New Psychoactive Substances: Identification of the U-48800 Synthetic Opioid Using Mass Spectrometry, Nuclear Magnetic Resonance Spectroscopy, and Bioinformatic Tools.

Maria Beatriz Pereira, Carlos Família, Daniel Martins, Mar Cunha, Mário Dias, Nuno R Neng, Helena Gaspar, Alexandre Quintas

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Interpol review of forensic drug chemistry, 2022-2025.Forensic science international. Synergy · 2026
    Review
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

8 authors.

Maria Beatriz PereiraCentro de Investigação Interdisciplinar Egas Moniz, Cooperativa de Ensino Egas Moniz, 2825-084 Caparica, Portugal.
Carlos FamíliaCentro de Investigação Interdisciplinar Egas Moniz, Cooperativa de Ensino Egas Moniz, 2825-084 Caparica, Portugal.ORCID 0000-0001-5059-2487
Daniel MartinsKosmicare, Rua de São Dionísio, 17, 4000-027 Porto, Portugal.ORCID 0000-0002-1317-2819
Mar CunhaKosmicare, Rua de São Dionísio, 17, 4000-027 Porto, Portugal.ORCID 0000-0001-9999-5885
Mário DiasCentro de Investigação Interdisciplinar Egas Moniz, Cooperativa de Ensino Egas Moniz, 2825-084 Caparica, Portugal.
Nuno R NengCentro de Investigação Interdisciplinar Egas Moniz, Cooperativa de Ensino Egas Moniz, 2825-084 Caparica, Portugal.ORCID 0000-0001-9879-1565
Helena GasparBioISI-Biosystems & Integrative Sciences Institute, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade de Lisboa, Campo Grande, 1749-016 Lisboa, Portugal.ORCID 0000-0002-1613-7023
Alexandre QuintasCentro de Investigação Interdisciplinar Egas Moniz, Cooperativa de Ensino Egas Moniz, 2825-084 Caparica, Portugal.ORCID 0000-0002-5188-0453

Funding

BioISI-BioSystems and Integrative Sciences Institute UID/04046/2025the CiiEM research AService-Cannabis 105030223Understanding the dynamics and consequences of New Psychoactive Substances use in a rapidly changing (online) drug market 861834
6 · The paper itself

Abstract

The misuse of opioids and opiates has remained a persistent issue since the 19th century. The recent resurgence of non-fentanyl synthetic opioids, such as U-type opioids and nitazenes, has further exacerbated the ongoing crisis. Identifying these synthetic opioids presents many challenges, including the emergence of new substances, the lack of standards, and the presence of structural isomers. This highlights the need for a robust structural characterisation strategy in forensic laboratories. To address these challenges, we developed a methodology to identify a U-type opioid sample received by Kosmicare from the European Union-funded SCANNER project, which was suspected to be either U-48800 or U-51754. Our innovative approach combined gas chromatography coupled with mass spectrometry (GC-MS), nuclear magnetic resonance spectroscopy (NMR), and molecular dynamics to characterise the questioned sample unequivocally. While the GC-MS analysis suggested a potential match with the mass spectrum of U-51754 and its structural isomer U-48800, NMR analysis confirmed the presence of U-48800 in the sample, which was further validated through molecular dynamics experiments. These experiments provided additional insights, confirming the structural features underlying the obtained NMR profile. The presented methodology offers a valuable solution for cases involving the identification of isomers, which are currently one of the most significant challenges in identifying new psychoactive substances.

Indexed as

Analgesics, OpioidComputational BiologyHydroxybutyratesPsychotropic DrugsBenzamidesGas Chromatography-Mass SpectrometryHumansIllicit DrugsMagnetic Resonance SpectroscopyMolecular Dynamics SimulationAnalgesics, OpioidBenzamidesHydroxybutyratesIllicit DrugsPsychotropic DrugsU-47700gas chromatography coupled with mass spectrometrymolecular dynamicsnuclear magnetic resonanceU-48800U-51754U-type opioids

Identifiers

PMID40076839
PMCPMC11900529

What OpenQuestion holds

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Registered trials

None linked

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.