Variability in the bioavailability of phenytoin capsules in males and females

Citation
Mc. Meyer et al., Variability in the bioavailability of phenytoin capsules in males and females, PHARM RES, 18(3), 2001, pp. 394-397
Citations number
13
Categorie Soggetti
Pharmacology & Toxicology
Journal title
PHARMACEUTICAL RESEARCH
ISSN journal
07248741 → ACNP
Volume
18
Issue
3
Year of publication
2001
Pages
394 - 397
Database
ISI
SICI code
0724-8741(200103)18:3<394:VITBOP>2.0.ZU;2-B
Abstract
Purpose. To determine inter-lot and intra-subject variability in the bioava ilability of the 100 mg extended phenytoin sodium capsules. In addition, to determine the effect of gender and menstrual cycle on phenytoin bioavailab ility. Methods. Three different lots of extended phenytoin sodium capsules wen giv en to 12 healthy male and 12 healthy female subjects in a crossover fashion . One of the lots was also given a second time to each subject. Plasma phen ytoin was determined, using an HPLC assay, in samples collected over a 73-h r period after each dose. Results.The mean Cmax for the four administrations ranged from 1.71-1.79 mu g/ml and mean AUC(0-infinity) values from ranged 53.0-54.1 mug,hr/ml. The e limination half-life was 3 hr shorter, and the AUC(0-infinity) adjusted for the mg/kg dose was 30% lower for females. Average bioequivalence was demon strated between the three lots for both Cmax and AUC(0-infinity) based on t he BE limit of 80-125%. Further, all confidence intervals of AUC(0-infinity ) fell within the limit of 90-111%. There were no differences in the confid ence limits for Cmax and AUC(0-infinity) determined separately for males an d females. Also, there was no difference in the mean Cmax or AUC(0-infinity ) for females when analyzed as a function of the week of their menstrual cy cle. Individual bioequivalence was demonstrated between three lots of pheny toin using the constant-scaled method, but not the reference-scaled method. Conclusions. There was very little difference in the bioavailability of the three lots of phenytoin. Females exhibited a lower AUC(0-infinity) than ma les after adjustment of dose for body weight, but their inclusion in the st udy did not affect the assessment of bioequivalence. When dose was not adju sted for body weight, no difference in AUC(0-infinity) was seen between mal es and females.