Simultaneous quantification of acetaminophen and five acetaminophen metabolites in human plasma and urine by high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry: Method validation and application to a neonatal pharmacokinetic study.
Journal article

Simultaneous quantification of acetaminophen and five acetaminophen metabolites in human plasma and urine by high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry: Method validation and application to a neonatal pharmacokinetic study.

  • Cook SF Center for Human Toxicology, Department of Pharmacology and Toxicology, University of Utah, 30 South 2000 East, Suite 105, Salt Lake City, UT 84112, USA. Electronic address: cook.sarah@utah.edu.
  • King AD Center for Human Toxicology, Department of Pharmacology and Toxicology, University of Utah, 30 South 2000 East, Suite 105, Salt Lake City, UT 84112, USA.
  • van den Anker JN Division of Clinical Pharmacology, Children's National Health System, 111 Michigan Avenue, NW, Washington, DC 20010, USA; Departments of Pediatrics, Integrative Systems Biology, Pharmacology & Physiology, George Washington University School of Medicine and Health Sciences, 2300 Eye Street, NW, Washington, DC 20037, USA; Intensive Care and Department of Pediatric Surgery, Erasmus Medical Center-Sophia Children's Hospital, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands; Department of Paediatric Pharmacology, University Children's Hospital Basel, Spitalstrasse 33, 4056 Basel, Switzerland.
  • Wilkins DG Center for Human Toxicology, Department of Pharmacology and Toxicology, University of Utah, 30 South 2000 East, Suite 105, Salt Lake City, UT 84112, USA; Division of Medical Laboratory Sciences, Department of Pathology, University of Utah School of Medicine, 15 North Medical Drive, Salt Lake City, UT 84112, USA.
  • 2015-11-17
Published in:
  • Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. - 2015
English Drug metabolism plays a key role in acetaminophen (paracetamol)-induced hepatotoxicity, and quantification of acetaminophen metabolites provides critical information about factors influencing susceptibility to acetaminophen-induced hepatotoxicity in clinical and experimental settings. The aims of this study were to develop, validate, and apply high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry (HPLC-ESI-MS/MS) methods for simultaneous quantification of acetaminophen, acetaminophen-glucuronide, acetaminophen-sulfate, acetaminophen-glutathione, acetaminophen-cysteine, and acetaminophen-N-acetylcysteine in small volumes of human plasma and urine. In the reported procedures, acetaminophen-d4 and acetaminophen-d3-sulfate were utilized as internal standards (IS). Analytes and IS were recovered from human plasma (10μL) by protein precipitation with acetonitrile. Human urine (10μL) was prepared by fortification with IS followed only by sample dilution. Calibration concentration ranges were tailored to literature values for each analyte in each biological matrix. Prepared samples from plasma and urine were analyzed under the same HPLC-ESI-MS/MS conditions, and chromatographic separation was achieved through use of an Agilent Poroshell 120 EC-C18 column with a 20-min run time per injected sample. The analytes could be accurately and precisely quantified over 2.0-3.5 orders of magnitude. Across both matrices, mean intra- and inter-assay accuracies ranged from 85% to 112%, and intra- and inter-assay imprecision did not exceed 15%. Validation experiments included tests for specificity, recovery and ionization efficiency, inter-individual variability in matrix effects, stock solution stability, and sample stability under a variety of storage and handling conditions (room temperature, freezer, freeze-thaw, and post-preparative). The utility and suitability of the reported procedures were illustrated by analysis of pharmacokinetic samples collected from neonates receiving intravenous acetaminophen.
Language
  • English
Open access status
closed
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Persistent URL
https://sonar.ch/global/documents/17753
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