Liquid chromatography-tandem mass spectrometry for determination of fingolimod and its active metabolite fingolimod phosphate in whole blood of patients with multiple sclerosis
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
Grant support
SGS12/LF/2021
Ministry of Education, Youth, and Sports of the Czech Republic
MH CZ-DRO (FNOs/2023)
University Hospital Ostrava
PubMed
38932506
DOI
10.1002/bmc.5947
Knihovny.cz E-resources
- Keywords
- fingolimod, fingolimod phosphate, liquid chromatography, mass spectrometry, multiple sclerosis,
- MeSH
- Chromatography, Liquid methods MeSH
- Adult MeSH
- Fingolimod Hydrochloride * blood pharmacokinetics therapeutic use chemistry MeSH
- Immunosuppressive Agents blood pharmacokinetics MeSH
- Humans MeSH
- Limit of Detection MeSH
- Linear Models MeSH
- Reproducibility of Results MeSH
- Multiple Sclerosis blood drug therapy MeSH
- Tandem Mass Spectrometry * methods MeSH
- Chromatography, High Pressure Liquid methods MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Fingolimod Hydrochloride * MeSH
- Immunosuppressive Agents MeSH
Fingolimod is an oral drug for the escalation of treatment of relapsing-remitting multiple sclerosis in patients with persistent disease activity on first-line drugs or in patients with rapidly progressive severe relapsing-remitting multiple sclerosis. An ultra-high-performance liquid chromatography-tandem mass spectrometry method for determining the concentrations of fingolimod and its active metabolite fingolimod phosphate in whole blood has been developed and validated. The advantages of this method are the easy, fast and cheap sample preparation using protein precipitation from blood with a mixture of acetonitrile-methanol (40:60, v/v). Chromatographic separation was performed on a ultra-high performance liquid chromatography BEH C18 1.7 μm (100 × 2.1 mm) column. Two modes of ionization, electrospray ionization and atmospheric pressure chemical ionization, were tested and compared. For validation, the electrospray ionization mode was chosen. As internal standard, isotopically labeled fingolimod-D4 was used to quantify the analytes. The method was validated according to the rules of the European Medicines Agency. The coefficients of variation for fingolimod were in the range of 1.13-11.88%, and the recovery was 98.80-106.00%. The coefficients of variation for fingolimod phosphate were in the range of 2.73-9.31%, and the recovery was 90.08-107.00%. The method is quite easy and fast and can be used for routine analysis.
Department of Clinical Pharmacology Faculty of Medicine University of Ostrava Ostrava Czech Republic
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