Evidence map›Paper›PMID 34443578›Full record

ArticleMolecules (Basel, Switzerland)2021

Untargeted Metabolomics in Forensic Toxicology: A New Approach for the Detection of Fentanyl Intake in Urine Samples.

Eleonora Amante, Eugenio Alladio, Rebecca Rizzo, Daniele Di Corcia, Pierre Negri, Lia Visintin, Michela Guglielmotto, Elena Tamagno, Marco Vincenti, Alberto Salomone

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Review
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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

10 authors.

Eleonora AmanteDipartimento di Chimica, Università di Torino, 10125 Torino, Italy.
Eugenio AlladioDipartimento di Chimica, Università di Torino, 10125 Torino, Italy.
Rebecca RizzoDipartimento di Chimica, Università di Torino, 10125 Torino, Italy.
Daniele Di CorciaCentro Regionale Antidoping e di Tossicologia, 10043 Orbassano, Italy.
Pierre NegriAB SCIEX, Redwood City, CA 01701, USA.
Lia VisintinDipartimento di Chimica, Università di Torino, 10125 Torino, Italy.ORCID 0000-0001-7747-2901
Michela GuglielmottoDipartimento di Neuroscienze Rita Levi Montalcini, Università di Torino, 10126 Torino, Italy.
Elena TamagnoDipartimento di Neuroscienze Rita Levi Montalcini, Università di Torino, 10126 Torino, Italy.
Marco VincentiDipartimento di Chimica, Università di Torino, 10125 Torino, Italy.ORCID 0000-0002-6275-7194
Alberto SalomoneDipartimento di Chimica, Università di Torino, 10125 Torino, Italy.ORCID 0000-0002-8501-4799

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The misuse of fentanyl, and novel synthetic opioids (NSO) in general, has become a public health emergency, especially in the United States. The detection of NSO is often challenged by the limited diagnostic time frame allowed by urine sampling and the wide range of chemically modified analogues, continuously introduced to the recreational drug market. In this study, an untargeted metabolomics approach was developed to obtain a comprehensive "fingerprint" of any anomalous and specific metabolic pattern potentially related to fentanyl exposure. In recent years, in vitro models of drug metabolism have emerged as important tools to overcome the limited access to positive urine samples and uncertainties related to the substances actually taken, the possible combined drug intake, and the ingested dose. In this study, an in vivo experiment was designed by incubating HepG2 cell lines with either fentanyl or common drugs of abuse, creating a cohort of 96 samples. These samples, together with 81 urine samples including negative controls and positive samples obtained from recent users of either fentanyl or "traditional" drugs, were subjected to untargeted analysis using both UHPLC reverse phase and HILIC chromatography combined with QTOF mass spectrometry. Data independent acquisition was performed by SWATH in order to obtain a comprehensive profile of the urinary metabolome. After extensive processing, the resulting datasets were initially subjected to unsupervised exploration by principal component analysis (PCA), yielding clear separation of the fentanyl positive samples with respect to both controls and samples positive to other drugs. The urine datasets were then systematically investigated by supervised classification models based on soft independent modeling by class analogy (SIMCA) algorithms, with the end goal of identifying fentanyl users. A final single-class SIMCA model based on an RP dataset and five PCs yielded 96% sensitivity and 74% specificity. The distinguishable metabolic patterns produced by fentanyl in comparison to other opioids opens up new perspectives in the interpretation of the biological activity of fentanyl.

Indexed as

FentanylForensic ToxicologyMetabolomicsAnalgesics, OpioidChromatography, High Pressure LiquidHep G2 CellsHumansMaleMetabolomeSubstance Abuse DetectionAnalgesics, OpioidFentanylfentanylforensic toxicologyHepG2 cell linesmetabolomicsmultivariate data analysisnovel synthetic opioids (NSO)PCASIMCAurine samples

Identifiers

PMID34443578
PMCPMC8398448

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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.