Metabolic profiling of valproic acid in patients using negative-ion chemical ionization gas chromatography-mass spectrometry

J Chromatogr. 1990 May 18;527(2):327-41. doi: 10.1016/s0378-4347(00)82116-7.

Abstract

A negative-ion chemical ionization gas chromatographic-mass spectrometric method for the determination of valproic acid (VPA) and fourteen of its metabolites in a single chromatographic run is reported. The assay features the use of four internal standards and is applicable to the analysis of small serum and urine volumes. A combination of pentafluorobenzyl and trimethylsilyl derivatization resulted in the [M - 181]- ion as the base peak for all the metabolites measured. When these ions were monitored sensitivities in the low picogram levels were achieved. The VPA metabolite profile was determined in pediatric patients on VPA monotherapy and on combined VPA therapy with either carbamazepine or clobazam. The recently characterized diene metabolite, (E,E)-2,3'-diene-VPA, was found to be a major serum metabolite of VPA. In the patient groups taking VPA in combination with carbamazepine, the induction of omega and omega-1 pathways of VPA metabolism was apparent, while the levels of the beta-oxidation products were significantly decreased.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Anti-Anxiety Agents*
  • Benzodiazepines*
  • Benzodiazepinones / therapeutic use
  • Carbamazepine / therapeutic use
  • Child
  • Child, Preschool
  • Clobazam
  • Drug Therapy, Combination
  • Fluorobenzenes
  • Gas Chromatography-Mass Spectrometry / methods*
  • Humans
  • Infant
  • Kinetics
  • Saliva / metabolism
  • Seizures / drug therapy
  • Valproic Acid / blood
  • Valproic Acid / metabolism*
  • Valproic Acid / therapeutic use
  • Valproic Acid / urine

Substances

  • Anti-Anxiety Agents
  • Benzodiazepinones
  • Fluorobenzenes
  • Benzodiazepines
  • pentafluorobenzyl bromide
  • Clobazam
  • Carbamazepine
  • Valproic Acid