Int. Journal of Clinical Pharmacology and Therapeutics, Volume 58 (2020) - August (426 - 438)

Determination of atomoxetine or escitalopram in human plasma by HPLC: Applications in neuroscience research studies

Jens Teichert1, James B. Rowe2, 3, Karen D. Ersche4, Nikolina Skandali2, 4, 5, Julia Sacher6, 7, 8, Achim Aigner1, Ralf Regenthal1
1 Division of Clinical Pharmacology, Rudolf-Boehm-Institute of Pharmacology and Toxicology, Medical Faculty, University of Leipzig, Leipzig, Germany, 2 Medical Research Council/Wellcome Trust Behavioural and Clinical Neuroscience Institute, 3 Department of Clinical Neurosciences, 4 Department of Psychiatry, University of Cambridge, 5 Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK, 6 Emotion NeuroimaGinG(EGG)-Lab, 7 Department of Neurology, Max Planck Institute for Cognitive and Brain Sciences, and 8 Clinic for Cognitive Neurology, University of Leipzig, Leipzig, Germany

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DOI 10.5414/CP203705

Abstract

Background: Atomoxetine and escitalopram are potent and selective drugs approved for noradrenergic or serotonergic modulation of neuronal networks in attention-deficit hyperactivity disorder (ADHD) or depression, respectively. High-performance liquid chromatography (HPLC) methods still play an important role in the therapeutic drug monitoring (TDM) of psychopharmacological drugs, and coupled with tandem mass spectrometry are the gold standard for the quantification of drugs in biological matrices, but not available everywhere. The aim of this work was to develop and validate a HPLC method for neuroscientific studies using atomoxetine or escitalopram as a test drug.
Materials and methods: A HPLC method from routine TDM determination of atomoxetine or citalopram in plasma was adapted and validated for use in neuroscientific research. Using photo diode array detection with UV absorption at 205 nm, the variation of internal standard within one chromatographic method enables separate drug monitoring for concentration-controlled explorative studies in healthy humans and patients with Parkinson’s disease.
Results: The method described here was found to be linear in the range of 0.002 – 1.4 mg/L for atomoxetine and 0.0012 – 0.197 mg/L for escitalopram, with overall mean intra-day and inter-day imprecision and accuracy bias < 10% for both drugs. The method was successfully applied in concentration-controlled neuroimaging studies in populations of healthy humans and patients with Parkinson’s disease.
Conclusion: A simple, sensitive, robust HPLC method capable of monitoring escitalopram and atomoxetine is presented and validated, as a useful tool for drug monitoring and the study of pharmacokinetics in neuroscientific study applications.

Author Details

Authors

Departments

  • 1 Division of Clinical Pharmacology, Rudolf-Boehm-Institute of Pharmacology and Toxicology, Medical Faculty, University of Leipzig, Leipzig, Germany,
  • 2 Medical Research Council/Wellcome Trust Behavioural and Clinical Neuroscience Institute,
  • 3 Department of Clinical Neurosciences,
  • 4 Department of Psychiatry, University of Cambridge,
  • 5 Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK,
  • 6 Emotion NeuroimaGinG(EGG)-Lab,
  • 7 Department of Neurology, Max Planck Institute for Cognitive and Brain Sciences, and
  • 8 Clinic for Cognitive Neurology, University of Leipzig, Leipzig, Germany

Address


Dr. Ralf Regenthal
Division of Clinical Pharmacology
Rudolf-Boehm-Institute of Pharmacology and Toxicology
University of Leipzig, Medical Faculty
04107 Leipzig, Germany
Email: ralf.regenthal@
medizin.uni-leipzig.de

Citation

Jens Teichert, James B. Rowe, Karen D. Ersche, Nikolina Skandali, Julia Sacher, Achim Aigner, and Ralf Regenthal.Determination of atomoxetine or escitalopram in human plasma by HPLC: Applications in neuroscience research studies
. Int J Clin Pharmacol Ther. 2020; 58: 426-438. doi: 10.5414/CP203705.

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