Novel ketamine analogues cause a false positive phencyclidine immunoassay

Author:

Skaugen John M12,Scoccimarro Anthony3,Pizon Anthony F3,Rymer Jacqueline A2,Giannoutsos Spiros2,Ekins Sean4,Krasowski Matthew D5,Tamama Kenichi1267ORCID

Affiliation:

1. Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA

2. Clinical Laboratories, University of Pittsburgh Medical Center Presbyterian Hospital, Pittsburgh, PA, USA

3. Division of Medical Toxicology, Department of Emergency Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA

4. Collaborations Pharmaceuticals, Inc., Raleigh, North Carolina, USA

5. Department of Pathology, University of Iowa Hospital and Clinics, Iowa City, IA, USA

6. McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA, USA

7. Clinical Laboratory, Children’s Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA

Abstract

Background Immunoassays are commonly used to test for drugs of abuse in patients in a variety of settings. The increasing prevalence of ‘designer’ drugs causes difficulties for the toxicology laboratory and may result in unexpected false positives and identification of unfamiliar compounds. Within the past decade, there have been a variety of ketamine and phencyclidine analogues identified, particularly as drugs of abuse. Method We present a case of intoxication with a novel ketamine analogue, deschloro-N-ethyl-ketamine, causing a false positive phencyclidine immunoassay. Additionally, we performed spiking studies and 2D molecular similarity calculations for deschloro-N-ethyl-ketamine, ketamine and three other analogues on the Siemens Viva-E EMIT-II phencyclidine assay to assess their cross-reactivity. Results Four of the tested compounds (deschloro-N-ethyl-ketamine, 3-methoxy-phencyclidine, 3-methoxy-eticyclidine and methoxetamine) cause false positive phencyclidine immunoassay results, while ketamine gives a negative result. The cross-reactivity data are in accord with the similarity calculations of these molecules, further validating the ability of 2D molecular similarity analysis to predict the molecular cross-reactivity in immunoassays. Conclusions The cross-reactivity data of phencyclidine and ketamine analogues presented in this study could help toxicology laboratories and clinicians in evaluating unexpected results, particularly when novel PCP and ketamine analogues are being considered.

Publisher

SAGE Publications

Subject

Clinical Biochemistry,General Medicine

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Interpol Review of Drug Analysis 2019-2022;Forensic Science International: Synergy;2023

2. Laboratory Testing for Substance Misuse;Fundamentals of Analytical Toxicology;2020-06-05

3. Ketamine abuse;Reactions Weekly;2019-09-28

4. Newly Emerging Drugs of Abuse;Substance Use Disorders;2019

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