Liquid-chromatographic determination of amitryptyline and its metabolites in serum, with adsorption onto glass minimized

Clin Chem. 1982 Oct;28(10):2143-8.

Abstract

To study correlations between the concentrations, in serum, of amitriptyline and its most important metabolites with clinical response in patients, we developed a "high-performance" liquid-chromatographic method for routine determination of amitriptyline, nortriptyline, total 10-hydroxy-amitriptyline, desmethylnortriptyline, and E(trans)- and Z(cis)-10-hydroxynortriptyline. These compounds are extracted from 1 mL of alkalinized serum into hexane/isoamyl alcohol (99/1 by vol). Perazine is the internal standard. To minimize irreversible adsorption of the drugs onto the glassware, 5 micrograms of maprotiline is added to the organic phase just before evaporation. After a 10-min resolution on a silica column eluted with acetonitrile/methanol/NH4OH (1 mol/L), absorbance is measured at 240 nm. Only chlorimipramine, doxepin, procainamide, and N-acetylprocainamide may interfere with assay of the compounds that probably are therapeutically relevant: amitriptyline, nortriptyline, and E-10-hydroxynortriptyline. Uremia, lipemia, and icterus also do not affect the analysis.

MeSH terms

  • Adsorption
  • Amitriptyline / blood*
  • Binding, Competitive
  • Chromatography, High Pressure Liquid / methods
  • Depressive Disorder / blood
  • Evaluation Studies as Topic
  • Glass
  • Humans
  • Hydroxylation
  • Maprotiline / blood
  • Stereoisomerism

Substances

  • Amitriptyline
  • Maprotiline