In silico evaluation of warfarin-bucolome therapy

Biopharm Drug Dispos. 2016 May;37(4):233-42. doi: 10.1002/bdd.2008.

Abstract

Purpose: Some reports have suggested that bucolome, an inhibitor of cytochrome P450 2C9, is useful for decreasing inter-patient variation in warfarin clearance. The purpose of the present study was to evaluate the utility of the concomitant administration of bucolome and warfarin using an in silico approach.

Methods: In vitro data regarding the enzymatic kinetics of (S)-warfarin and bucolome were collected from the literature. As a validation study, the geometric mean (GM) of the oral unbound clearance of (S)-warfarin and its inter-patient variation (assessed using the standard deviation of its natural logarithm (σ)) were predicted using a physiologically based population pharmacokinetic simulator (Simcyp(TM) ) and compared with clinical data. The utility of the concomitant administration was evaluated by comparing the GM and σ values predicted under various conditions (the prediction study).

Results and discussion: The σ values in the presence and absence of bucolome were predicted to be 0.73 and 0.68, respectively, suggesting that bucolome might increase the inter-patient variation, as clinically observed. In the prediction study, the σ value of the bucolome co-administered group was greater in almost all of the examined conditions. In conclusion, the concomitant administration of bucolome might not be useful for reducing the inter-patient variation of (S)-warfarin pharmacokinetics. Copyright © 2016 John Wiley & Sons, Ltd.

Keywords: CYP2C9; DDI; bucolomel; warfarin.

MeSH terms

  • Anticoagulants / pharmacokinetics*
  • Barbiturates / pharmacology*
  • Computer Simulation
  • Cytochrome P-450 CYP2C9 Inhibitors / pharmacology*
  • Drug Therapy, Combination
  • Fluconazole / pharmacology
  • Humans
  • Models, Biological*
  • Warfarin / pharmacokinetics*

Substances

  • Anticoagulants
  • Barbiturates
  • Cytochrome P-450 CYP2C9 Inhibitors
  • Warfarin
  • Fluconazole
  • bucolome