Evidence map›Paper›PMID 40697327›Full record

ArticleJournal of mass spectrometry and advances in the clinical lab2025

Urine methamphetamine-to-amphetamine ratio by LC-MS/MS to differentiate methamphetamine use from pharmaceutical impurity in patients prescribed amphetamine.

Lindsey Contella, Phillip Kang, Clara E Wolf, Victoria L Thomas, Melissa Gildenberg, Marion L Snyder, Stacy E F Melanson, Nicole V Tolan

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Article in Journal of mass spectrometry and advances in the clinical lab, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Lindsey ContellaLuxor Scientific, Greenville, SC, USA.
Phillip KangDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Clara E WolfSt. Louis University School of Medicine, St. Louis, MO, USA.
Victoria L ThomasDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Melissa GildenbergDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Marion L SnyderLuxor Scientific, Greenville, SC, USA.
Stacy E F MelansonDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Nicole V TolanDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Patients compliant with prescribed amphetamine (AMPH) should not have detectable methamphetamine (METH) in their urine; detectable METH typically indicates illicit use. However, we have identified patients with results suggestive of METH as an impurity in prescribed AMPH. Objectives: Derive a METH:AMPH ratio cut-off from a training set of patients compliant with AMPH prescriptions to differentiate METH as an impurity from illicit use. Methods: Retrospective review of AMPH and METH-positive cases by liquid chromatography-tandem mass spectrometry (LC-MS/MS) at Brigham and Women's Hospital (BWH) and Luxor Scientific. Correlated results with clinical and medication history and compliance with prescribed medications. Results: The median ± interquartile range (IQR) METH:AMPH ratio for the Adderall training sets was 0.43 ± 0.31 % and 0.05 ± 0.040 %, with a maximum ratio of 1.125 % and 0.125 % at BWH and Luxor, respectively. The median ± IQR METH:AMPH ratio for the Luxor d-AMPH training set was 0.039 ± 0.028 %, with a maximum ratio of 0.09 %; not statistically different from the Adderall training set. Assessment of the BWH test set where METH < AMPH (n = 22) revealed that METH was likely due to an impurity (n = 10), distant METH mis/use (n = 11), or requiring further analysis (n = 1). METH was also detected by LC-MS/MS in a commercial AMPH calibrator and in Adderall XR. Discussion: METH may represent an impurity in the AMPH formulation. Laboratories are encouraged to define a METH:AMPH ratio below which an impurity is the likely explanation for METH and/or to increase the METH positivity cut-off to 50 or 100 ng/mL to reduce potential false-accusations of illicit METH use.

Indexed as

AmphetamineCompliance monitoringLiquid chromatography-tandem mass spectrometryMethamphetaminePharmaceutical impurityToxicology

Identifiers

PMID40697327
PMCPMC12280402

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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.