6533b7d3fe1ef96bd12600ba

RESEARCH PRODUCT

Determination of benperidol and its reduced metabolite in human plasma by high-performance liquid chromatography and electrochemical detection.

A. HillertWalther SeilerGünter SchöllnhammerChristoph HiemkeStephan SüssHermann Wetzel

subject

ChromatographySilica gelMetaboliteBenperidolExtraction (chemistry)General ChemistryHigh-performance liquid chromatographychemistry.chemical_compoundBenperidolColumn chromatographychemistryBlood plasmamedicineElectrochemistryHumansAcetonitrileChromatography High Pressure Liquidmedicine.drug

description

An isocratic high-performance liquid chromatographic method with electrochemical detection for the quantification of benperidol and its suggested reduced metabolite TVX Q 5402 in human plasma is described. The method included a two-step solid-phase extraction on reversed-phase and cation-exchange material, followed by separation on a cyanopropyl silica gel column (5 microns; 250 mm x 4.6 mm I.D.). The eluent was 0.15 M acetate buffer (pH 4.7) containing 25% acetonitrile (w/w). Spiperone served as internal standard. The inclusion of the cation-exchange step provided sample purity higher than those achieved with other methods. After extraction of 1 ml of plasma, concentrations as low as 0.5 ng/ml were detectable for both benperidol and the metabolite. In plasma samples collected from a schizophrenic patient treated with a single oral dose of 6 mg of benperidol, plasma levels of benperidol and of the metabolite could be measured from 20 min to at least 12 h after administration.

10.1016/0378-4347(91)80397-uhttps://pubmed.ncbi.nlm.nih.gov/1874880