Bromadiolone poisoning: LC-MS method and pharmacokinetic data

J Forensic Sci. 2008 Jul;53(4):993-6. doi: 10.1111/j.1556-4029.2008.00737.x.

Abstract

Poisoning with superwarfarins, like bromadiolone, is a growing public health problem, and the mortality is high. Pharmacokinetic data on bromadiolone in humans are however scarce, and there are no reports following repeated exposures to bromadiolone. We have developed a method for quantification of bromadiolone in whole blood, using liquid chromatography-mass spectrometry (LC-MS). The analytical method is reported. Limit of detection was 0.005 mg/L and limit of quantification was 0.01 mg/L. The concentrations of bromadiolone in whole blood and plasma in serial samples from a 62-year-old woman were measured. The half-life of bromadiolone in blood was estimated to be about 6 days in the initial phase of elimination and about 10-13 days in the terminal phase. The mean plasma/blood ratio of bromadiolone was 1.7 +/- 0.6. Stability testing of bromadiolone in whole blood samples after two cycles of freeze and thaw revealed that bromadiolone concentrations decreased.

MeSH terms

  • 4-Hydroxycoumarins / blood
  • 4-Hydroxycoumarins / pharmacokinetics*
  • 4-Hydroxycoumarins / poisoning*
  • Anticoagulants / blood
  • Anticoagulants / pharmacokinetics*
  • Anticoagulants / poisoning*
  • Chromatography, Liquid
  • Drug Stability
  • Female
  • Forensic Toxicology
  • Half-Life
  • Humans
  • Mass Spectrometry
  • Middle Aged
  • Molecular Structure

Substances

  • 4-Hydroxycoumarins
  • Anticoagulants
  • bromadiolone