Large Differences in Urinary Benzene Metabolite S-Phenylmercapturic Acid Quantitation: A Comparison of Five LC-MS-MS Methods

Denise S. Tevis, Andrew Willmore, Deepak Bhandari, Brett Bowman, Chloe Biren, Brandon M. Kenwood, Peyton Jacob, Jia Liu, Kristina Bello, Stephen S. Hecht, Steven G. Carmella, Menglan Chen, Eric Gaudreau, Jean François Bienvenu, Benjamin C. Blount, Víctor R. De Jesús

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Benzene is a known genotoxic carcinogen linked to many hematological abnormalities. S-phenylmercapturic acid (PHMA, N-acetyl-S-(phenyl)-L-cysteine, CAS# 4775-80-8) is a urinary metabolite of benzene and is used as a biomarker to assess benzene exposure. Pre-S-phenylmercapturic acid (pre-PHMA) is a PHMA precursor that dehydrates to PHMA at acidic pH. Published analytical methods that measure urinary PHMA adjust urine samples to a wide range of pH values using several types of acid, potentially leading to highly variable results depending on the concentration of pre-PHMA in a sample. Information is lacking on the variation in sample preparation among laboratories regularly measuring PHMA and the effect of those differences on PHMA quantitation in human urine samples. To investigate the differences in PHMA quantitation, we conducted an inter-laboratory comparison that included the analysis of 50 anonymous human urine samples (25 self-identified smokers and 25 self-identified non-smokers), quality control samples and commercially available reference samples in five laboratories using different analytical methods. Observed urinary PHMA concentrations were proportionally higher at lower pH, and results for anonymous urine samples varied widely among the methods. The method with the neutral preparation pH yielded results about 60% lower than the method using the most acidic conditions. Samples spiked with PHMA showed little variation, suggesting that the variability in results in human urine samples across methods is driven by the acid-mediated conversion of pre-PHMA to PHMA.

Original languageEnglish (US)
Pages (from-to)657-665
Number of pages9
JournalJournal of Analytical Toxicology
Volume45
Issue number7
DOIs
StatePublished - Oct 7 2020

Bibliographical note

Publisher Copyright:
© 2020 Published by Oxford University Press. This work is written by (a) US Government employee(s) and is in the public domain in the US.

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