A validated SPE–LC-MS/MS assay for Eplerenone and its hydrolyzed metabolite in human urine

• Published in: Journal of pharmaceutical and biomedical analysis 2003-02, Vol.31 (1), p.103-115
• Main Authors: Zhang, Ji Y, Fast, Douglas M, Breau, Alan P
• Format: Article
• Language: English
• Subjects: Analysis; Biological and medical sciences; Calibration; Chromatography, High Pressure Liquid; Chromatography, Liquid; Eplerenone; Freezing; General pharmacology; Humans; Hydrolysis; Indicators and Reagents; LC-MS/MS; Mass Spectrometry; Medical sciences; Mineralocorticoid Receptor Antagonists - pharmacokinetics; Mineralocorticoid Receptor Antagonists - urine; Pharmacology. Drug treatments; Quality Control; Reference Standards; Reproducibility of Results; Selective aldosterone receptor antagonist (SARA); Solid phase extraction; Spironolactone - analogs & derivatives; Spironolactone - pharmacokinetics; Spironolactone - urine
• ISSN: 0731-7085; 1873-264X
• DOI: 10.1016/S0731-7085(02)00595-2

An automated LC-MS/MS assay was validated to quantitate the first selective aldosterone blocker Eplerenone (I) and its hydrolyzed metabolite (II) in human urine. After the addition of the stable isotope labeled internal standards, human urine samples were extracted on a C 18 solid phase extraction (SPE) cartridge using a Zymark RapidTrace™ automation system. The extraction eluates were diluted with 20 mM ammonium acetate aqueous solution and directly injected onto the LC-MS/MS system. The chromatographic separation was performed on a reverse phase Zorbax XDB-C 8 HPLC column (2.1×50 mm, 5 μm) with a mobile phase of acetonitrile:water (40:60, v/v) containing 10 mM ammonium acetate (pH 7.4). I and II were ionized using positive and negative ionization mass spectrometry, respectively, to achieve the best sensitivity. The ionization polarity was switched during the run at approximately 2.5 min after the injection. Multiple reaction monitoring (MRM) with a tandem mass spectrometer was used to detect the analytes. The precursor to product ion transitions of m/ z 415→163 and m/ z 431→337 were used to measure I and II, respectively. The assay exhibited a linear dynamic range of 50–10 000 ng/ml of urine for both of I and II. The lower limit of quantitation (LLOQ) was 50 ng/ml for I and II. Acceptable precision and accuracy were obtained for concentrations over the standard curve range. Sample analysis time for each injection was 5 min; a throughput of 100 human urine standards and samples per run was achieved.