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Signal Enhancement in the HPLC-ESI-MS/MS analysis of spironolactone and its metabolites using HFIP and NH4F as eluent additives

Takkis, Kalev (författare)
Institute of Chemistry, University of Tartu, Tartu, Estonia
Aro, Rudolf, 1992- (författare)
Institute of Chemistry, University of Tartu, Tartu, Estonia
Kõrgvee, Lenne-Triin (författare)
Children’s Clinic, Tartu University Hospital, Tartu, Estonia; Institute of Biomedicine and Translational Medicine, Department of Pharmacology, University of Tartu, Tartu, Estonia
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Varendi, Heili (författare)
Children’s Clinic, Tartu University Hospital, Tartu, Estonia
Lass, Jana (författare)
Pharmacy Department, Tartu University Hospital, Tartu, Estonia; Institute of Biomedicine and Translational Medicine, Department of Microbiology, University of Tartu, Tartu, Estonia
Herodes, Koit (författare)
Institute of Chemistry, University of Tartu, Tartu, Estonia
Kipper, Karin (författare)
Institute of Chemistry, University of Tartu, Tartu, Estonia; Paediatric Infectious Diseases Research Group, Institute for Infection and Immunity, St. George’s, University of London, London, United Kingdom
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 (creator_code:org_t)
2017-02-21
2017
Engelska.
Ingår i: Analytical and Bioanalytical Chemistry. - : Springer. - 1618-2642 .- 1618-2650. ; 409:12, s. 3145-3151
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • This paper describes an LC-MS/MS method to determine the concentration of spironolactone and its metabolites 7-alpha-methylthiospironolactone and canrenone in blood plasma samples. The resulting assay is simple (using protein precipitation for sample preparation) and sensitive (the lower limit of quantification is close to 0.5 ng/ml) while requiring only 50 mu l of plasma, making it especially suitable for analyzing samples obtained from pediatric and neonatal patients where sample sizes are limited. The sensitivity is achieved by using ammonium fluoride as an eluent additive, which in our case amplifies the signal from our analytes in the plasma solution on average about 70 times. The method is fully validated according to the European Medicines Agency's guideline and used for the measurement of pediatric patients' samples in clinical trials for evaluating oral spironolactone's and its metabolites' pharmacokinetics in children up to 2 years of age.

Ämnesord

NATURVETENSKAP  -- Kemi -- Analytisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Analytical Chemistry (hsv//eng)

Nyckelord

Spironolactone; Ammonium fluoride; Signal enhancement; Liquid chromatography-mass spectrometry; Ionization efficiency; Hexafluoroisopropanol
Analytical Chemistry
Analytisk kemi

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