TY - JOUR
T1 - Trace residue identification, characterization, and longitudinal monitoring of the novel synthetic opioid β-U10, from discarded drug paraphernalia
AU - West, Henry
AU - Fitzgerald, John L.
AU - Hopkins, Katherine L.
AU - Leeming, Michael G.
AU - Di Rago, Matthew
AU - Gerostamoulos, Dimitri
AU - Clark, Nicolas
AU - Dietze, Paul
AU - White, Jonathan M.
AU - Ziogas, James
AU - Reid, Gavin E.
N1 - Funding Information:
We would like to acknowledge Dr. Yukie O'Bryan and the Melbourne Trace Analysis for Chemical, Earth and Environmental Sciences (TrACEES) Platform at the University of Melbourne for acquiring the GC–MS data reported in this study. Funding for this study was provided from the Victoria State Government Department of Health. Open access publishing facilitated by The University of Melbourne, as part of the Wiley ‐ The University of Melbourne agreement via the Council of Australian University Librarians.
Publisher Copyright:
© 2022 The Authors. Drug Testing and Analysis published by John Wiley & Sons Ltd.
PY - 2022/9
Y1 - 2022/9
N2 - 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.
AB - 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.
KW - DART
KW - mass spectrometry
KW - novel synthetic opioid
KW - trace residue analysis
KW - β-U10
UR - http://www.scopus.com/inward/record.url?scp=85130255938&partnerID=8YFLogxK
U2 - 10.1002/dta.3284
DO - 10.1002/dta.3284
M3 - Article
C2 - 35562123
AN - SCOPUS:85130255938
SN - 1942-7603
VL - 14
SP - 1576
EP - 1586
JO - Drug Testing and Analysis
JF - Drug Testing and Analysis
IS - 9
ER -