Evidence map›Paper›PMID 35562123›Full record

ArticleDrug testing and analysis2022

Trace residue identification, characterization, and longitudinal monitoring of the novel synthetic opioid β-U10, from discarded drug paraphernalia.

Henry West, John L Fitzgerald, Katherine L Hopkins, Michael G Leeming, Matthew DiRago, Dimitri Gerostamoulos, Nicolas Clark, Paul Dietze, Jonathan M White, James Ziogas and 1 more

Abstract read
In one paragraph

Article in Drug testing and analysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

11 authors.

Henry WestSchool of Chemistry, The University of Melbourne, Parkville, Victoria, Australia.
John L FitzgeraldSchool of Social and Political Science, The University of Melbourne, Parkville, Victoria, Australia.
Katherine L HopkinsSchool of Chemistry, The University of Melbourne, Parkville, Victoria, Australia.
Michael G LeemingMelbourne Mass Spectrometry and Proteomics Facility, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, Victoria, Australia.
Matthew DiRagoVictorian Institute of Forensic Medicine, Southbank, Victoria, Australia.
Dimitri GerostamoulosVictorian Institute of Forensic Medicine, Southbank, Victoria, Australia.ORCID https://orcid.org/0000-0002-7958-8235
Nicolas ClarkNorth Richmond Community Health, Richmond, Victoria, Australia.
Paul DietzeNational Drug Research Institute and enAble Institute, Curtin University, Melbourne, Victoria, Australia.
Jonathan M WhiteSchool of Chemistry, The University of Melbourne, Parkville, Victoria, Australia.
James ZiogasDepartment of Biochemistry and Pharmacology, The University of Melbourne, Parkville, Victoria, Australia.
Gavin E ReidSchool of Chemistry, The University of Melbourne, Parkville, Victoria, Australia.ORCID https://orcid.org/0000-0002-9675-1444

Funding

Victoria State Government Department of Health
6 · The paper itself

Abstract

Empirical data regarding dynamic alterations in illicit drug supply markets in response to the COVID-19 pandemic, including the potential for introduction of novel drug substances and/or increased poly-drug combination use at the "street" level, that is, directly proximal to the point of consumption, are currently lacking. Here, a high-throughput strategy employing ambient ionization-mass spectrometry is described for the trace residue identification, characterization, and longitudinal monitoring of illicit drug substances found within >6,600 discarded drug paraphernalia (DDP) samples collected during a pilot study of an early warning system for illicit drug use in Melbourne, Australia from August 2020 to February 2021, while significant COVID-19 lockdown conditions were imposed. The utility of this approach is demonstrated for the de novo identification and structural characterization of β-U10, a previously unreported naphthamide analog within the "U-series" of synthetic opioid drugs, including differentiation from its α-U10 isomer without need for sample preparation or chromatographic separation prior to analysis. Notably, β-U10 was observed with 23 other drug substances, most commonly in temporally distinct clusters with heroin, etizolam, and diphenhydramine, and in a total of 182 different poly-drug combinations. Longitudinal monitoring of the number and weekly "average signal intensity" (ASI) values of identified substances, developed here as a semi-quantitative proxy indicator of changes in availability, relative purity and compositions of street level drug samples, revealed that increases in the number of identifications and ASI for β-U10 and etizolam coincided with a 50% decrease in the number of positive detections and an order of magnitude decrease in the ASI for heroin.

Indexed as

COVID-19Illicit DrugsSubstance-Related DisordersAnalgesics, OpioidCommunicable Disease ControlHeroinHumansPandemicsPilot ProjectsAnalgesics, OpioidHeroinIllicit DrugsDARTmass spectrometrynovel synthetic opioidtrace residue analysisβ-U10

Identifiers

PMID35562123
PMCPMC9542064

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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.