A high-throughput LC–MS/MS assay for quantification of artesunate and its metabolite dihydroartemisinin in human plasma and saliva

Author:

Birgersson Sofia1,Ericsson Therese1,Blank Antje2,Hagens Cornelia von3,Ashton Michael1,Hoffmann Kurt-Jürgen1

Affiliation:

1. Unit for Pharmacokinetics & Drug Metabolism, Department of Pharmacology, Sahlgrenska Academy at the University of Gothenburg, Sweden

2. Heidelberg University Hospital, Department of Clinical Pharmacology & Pharmacoepidemiology, Heidelberg, Germany

3. University Women's Hospital Heidelberg, Department of Gynecological Endocrinology & Reproductive Medicine, Naturopathy & Integrative Medicine, Heidelberg, Germany

Abstract

Aim: Saliva is an alternative sampling matrix to plasma, offering a noninvasive technique, but requires a highly sensitive bioanalytical method. Materials & methods: An API 3000 triple quadrupole mass spectrometer with an electrospray ionization source operated in the positive ion mode was used for the analysis. Results: A high-throughput LC–MS/MS method using SPE for the quantification of artesunate and dihydroartemisinin in plasma and saliva has been optimized and validated according to US FDA guidelines. For both analytes the LLOQ was determined to 5 ng/ml and the calibration range was 5–1000 ng/ml for artesunate and 5–2000 ng/ml for dihydroartemisinin. Conclusion: For the first time, a bioanalytical method for determination of artesunate and dihydroartemisinin in human saliva has been described, showing possible applicability in clinical saliva samples in addition to plasma samples.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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