Deuterated ritanserin analysis by gas chromatography/mass spectrometry: a sensitive technique to study human ritanserin pharmacokinetics

Biomed Environ Mass Spectrom. 1989 Jul;18(7):498-502. doi: 10.1002/bms.1200180709.

Abstract

Ritanserin, a new selective serotonin-S2 antagonist, was labelled in one 4-fluorophenyl moiety to obtain a (2H4)-labelled analogue having the following isotopic distribution: 2H0: 0.0%, 2H1: 0.1%, 2H2: 1.9%, 2H3: 5.8%, 2H4: 92.2%. (2H0/2H4) Ritanserin and the internal standard were isolated from the plasma by liquid/liquid extraction and analysed by selected-ion monitoring gas chromatography/mass spectrometry in the 70 eV electron impact mode. A detection limit of 0.1 ng ml-1 could be obtained for both (2H0) and (2H4)ritanserin. The precision (per cent coefficient of variation) and accuracy (per cent relative error) of the method were 4.1% and 4.1%, respectively. The method was used to determine the plasma levels of ritanserin and tetradeuterated ritanserin in three healthy male subjects receiving an equimolar mixture of 5:5 mg (2H0/2H4)ritanserin. The pharmacokinetics of both isotopomers proved to be identical, indicating the absence of an isotope effect, so that this technique might be very promising for use in bioequivalence studies.

MeSH terms

  • Gas Chromatography-Mass Spectrometry
  • Humans
  • Isotope Labeling
  • Piperidines / analysis*
  • Piperidines / pharmacokinetics
  • Ritanserin
  • Serotonin Antagonists / analysis*
  • Serotonin Antagonists / pharmacokinetics

Substances

  • Piperidines
  • Serotonin Antagonists
  • Ritanserin