Two nonlinear pharmacokinetic models were simulated to investigate the relationship between single and multiple dose bioequivalency parameters for drugs such as phenytoin and propranolol which exhibit either saturable elimination kinetics or a capacity limited first pass effect. Mean T,,,, C, , , an
Prediction of steady-state bioequivalence relationships using single dose data I-linear kinetics
✍ Scribed by André J. Jackson
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 693 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0142-2782
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✦ Synopsis
Simulated data using a linear one-and two-compartment body model with different absorption characteristics were used to evaluate the ability of single dose bioavailability data to predict the relationships that exist at steady state. This was done by comparing the confidence intervals obtained from single and multiple dose data sets for the parameters of T,,,, C,,;,,, and area under the curve from time zero to infinity (AUC[&,). As a consequence of T,;,, and C,;,, decreasing and increasing from single to multiple dosing regimens, the confidence intervals for these parameters reflected these changes. The 90 per cent confidence interval expressed as a percentage of the reference mean increased or decreased for T,;,, dependent upon the ratio of K., testiK,, reference, and decreased for C,,, while the interval for AUC,&, exhibited no predictable pattern and appeared to be influenced by the amount of error in the data set. Alteration of either the dosing interval or the fraction absorbed did not affect the pattern of change in the confidence intervals for T,,, and C,;,,, but the latter did result in a decrease in the interval for AUC+=. Analysis of the confidence intervals for T,,,, C,,, and AUC,&, in bioequivalency studies for quinidine gluconate and procainamide hydrochloride following administration of single and multiple doses to different subjects appeared to be consistent with the patterns observed for the simulated data sets.
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