Understanding sensitivity and cross‐reactivity of xylazine lateral flow immunoassay test strips for drug checking applications

Author:

Sisco Edward1ORCID,Nestadt Danielle F.2,Bloom Madeline B.3,Schneider Kristin E.2,Elkasabany Rae A.2,Rouhani Saba4,Sherman Susan G.2

Affiliation:

1. National Institute of Standards and Technology Gaithersburg Maryland USA

2. Department of Health, Behavior and Society Johns Hopkins Bloomberg School of Public Health Baltimore Maryland USA

3. Department of Forensic Sciences George Washington University Washington DC USA

4. Department of Epidemiology New York University School of Global Public Health New York New York USA

Abstract

AbstractThe continued prevalence of xylazine in the illicit drug market has necessitated development of quick and simple methods for identification, including lateral flow immunoassays (also known as “test strips”), like those frequently used to detect fentanyl. This study explored the drug checking applicability of the first publicly available xylazine test strips (XTS) using four sub‐studies: reproducibility (i.e., consistency of positive results in a highly‐concentrated xylazine solution); limit of detection on a calibration curve of xylazine concentrations; cross‐reactivity against 77 commonly encountered drugs, cutting agents, and other structurally similar compounds; and applicability for analyzing community‐acquired samples—where 100 drug residue samples were analyzed using XTS, direct analysis in real time mass spectrometry (DART‐MS), and gas chromatography tandem mass spectrometry (GC–MS/MS). XTS consistently detected xylazine at concentrations ≥2.5 μg/ml, and XTS results were reproducible. Sensitivity and specificity of XTS were calculated by comparing expected versus obtained results based on xylazine concentration of community‐acquired samples measured by GC‐MS/MS. XTS consistently detected xylazine in samples with concentration >2 μg/ml and yielded a sensitivity of 0.974, specificity of 1.00, and overall accuracy of 0.986. Cross‐reactivity with lidocaine, a common cutting agent, and lack of XTS reactivity with other α2‐agonists found in the illicit drug supply highlight the need to offer consumers comprehensive drug checking services that identify a range of substances and better inform them about drug contents.

Publisher

Wiley

Subject

Spectroscopy,Pharmaceutical Science,Environmental Chemistry,Analytical Chemistry

Reference18 articles.

1. Drug Enforcement Administration.Xylazine. Accessed February 21 2023 https://www.deadiversion.usdoj.gov/drug_chem_info/Xylazine.pdf

2. Biden–Harris administration designates fentanyl combined with xylazine as an emerging threat to the United States.2023. Accessed May 2 2023.https://www.whitehouse.gov/ondcp/briefing-room/2023/04/12/biden-harris-administration-designates-fentanyl-combined-with-xylazine-as-an-emerging-threat-to-the-united-states/

3. Xylazine spreads across the US: A growing component of the increasingly synthetic and polysubstance overdose crisis

4. Notes from the Field: Xylazine Detection and Involvement in Drug Overdose Deaths — United States, 2019

5. Maryland Xylazine Workgroup.Xylazine in Maryland: an initial report of the Maryland Xylazine Workgroup 2022.2023.

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