PT  - JOURNAL ARTICLE
AU  - S. J. Roffey
AU  - S. Cole
AU  - P. Comby
AU  - D. Gibson
AU  - S. G. Jezequel
AU  - A. N. R. Nedderman
AU  - D. A. Smith
AU  - D. K. Walker
AU  - N. Wood
TI  - THE DISPOSITION OF VORICONAZOLE IN MOUSE, RAT, RABBIT, GUINEA PIG, DOG, AND HUMAN
AID  - 10.1124/dmd.31.6.731
DP  - 2003 Jun 01
TA  - Drug Metabolism and Disposition
PG  - 731--741
VI  - 31
IP  - 6
4099  - http://dmd.aspetjournals.org/content/31/6/731.short
4100  - http://dmd.aspetjournals.org/content/31/6/731.full
SO  - Drug Metab Dispos2003 Jun 01; 31
AB  - Voriconazole is a new triazole antifungal agent with potent, wide-spectrum activity. Its pharmacokinetics and metabolism have been studied in mouse, rat, rabbit, dog, guinea pig, and humans after single and multiple administration by both oral and intravenous routes. Absorption of voriconazole is essentially complete in all species. The elimination of voriconazole is characterized by non-linear pharmacokinetics in all species. Consequently, pharmacokinetic parameters are dependent upon dose, and a superproportional increase in area under the curve is seen with increasing dose in rat and dog toxicology studies. Following multiple administration, there is a decrease in systemic exposure. This is most pronounced in mouse and rat, less so in dog, and not observed in guinea pig or rabbit. Repeat-dose toxicology studies in mouse, rat, and dog have demonstrated that induction of cytochrome P450 by voriconazole (autoinduction of metabolism) is responsible for the decreased exposure in these species. Autoinduction of metabolism is not observed in humans, and plasma steady-state concentrations remain constant with time. Voriconazole is extensively metabolized in all species. The major pathways in humans involve fluoropyrimidine N-oxidation, fluoropyrimidine hydroxylation, and methyl hydroxylation. Also, N-oxidation facilitates cleavage of the molecule, resulting in loss of the fluoropyrimidine moiety and subsequent conjugation with glucuronic acid. Major pathways are represented in animal species. The major circulating metabolite in rat, dog, and human is the N-oxide of voriconazole. It is not thought to contribute to efficacy since it is at least 100-fold less potent than voriconazole against fungal pathogens in vitro. The American Society for Pharmacology and Experimental Therapeutics