The Suitability of an in Situ Perfusion Model for Permeability Determinations: Utility for BCS Class I Biowaiver Requests
- 4 October 2006
- journal article
- research article
- Published by American Chemical Society (ACS) in Molecular Pharmaceutics
- Vol. 3 (6) , 686-694
- https://doi.org/10.1021/mp060042f
Abstract
The FDA has published recommendations for sponsors who wish to request a waiver of in vivo bioavailability (BA) or bioequivalence (BE) studies for immediate release (IR) solid oral dosage forms based on the Biopharmaceutics Classification System (BCS). Biowaivers can be requested for IR formulations in which the active ingredient is shown to be a BCS class I drug: that is, a drug showing high permeability and high solubility over a pH range of 1−7.5. For permeability determinations, a variety of experimental methods can be used, such as the rat in situ single pass perfusion or Caco-2 cell culture models, once the suitability of the particular method is established. Following the recommended procedure for assessing the suitability of permeability determinations, we determined the permeability of 20 test drugs using the in situ single pass perfusion model in rats. The test compounds were coperfused through jejunal intestinal segments with an internal permeability reference standard (metoprolol) over a 90 min time period. Sample analysis was performed by HPLC, and the ratio of the effective permeability, Peff (cm/s), of test compound to that of metoprolol was determined. To address the question of test drug permeabilities that approach that of the internal standard, we propose that a statistical analysis such as the “0.8−1.25 rule” used for in vivo or in vitro bioequivalence studies provide guidance for permeability classification using the in situ single pass perfusion model. We developed a method using the 90% confidence interval of the permeability ratio of the test to internal reference standard in order to differentiate between high and low permeability compounds. This analysis allowed for the proper permeability classification of all of the test compounds and suggests a robust means for assessing drug permeability classification. Keywords: Biopharmaceutics Classification System; bioavailability; in situ rat perfusion; permeability; confidence intervalKeywords
This publication has 21 references indexed in Scilit:
- Summary workshop report: Biopharmaceutics classification system—implementation challenges and extension opportunitiesJournal of Pharmaceutical Sciences, 2004
- Molecular Properties of WHO Essential Drugs and Provisional Biopharmaceutical ClassificationMolecular Pharmaceutics, 2003
- The Site-Specific Transport and Metabolism of Tacrolimus in Rat Small IntestineThe Journal of Pharmacology and Experimental Therapeutics, 2003
- The effect of amiloride on the in vivo effective permeability of amoxicillin in human jejunum: experience from a regional perfusion techniqueEuropean Journal of Pharmaceutical Sciences, 2002
- In vitro prediction of gastrointestinal absorption and bioavailability: an experts' meeting report.European Journal of Clinical Pharmacology, 2001
- Correlation of Human Jejunal Permeability (in Vivo) of Drugs with Experimentally and Theoretically Derived Parameters. A Multivariate Data Analysis ApproachJournal of Medicinal Chemistry, 1998
- Intestinal drug absorption during induced net water absorption in man; a mechanistic study using antipyrine, atenolol and enalaprilat.British Journal of Clinical Pharmacology, 1994
- Nonlinearity of amoxicillin absorption kinetics in humanEuropean Journal of Clinical Pharmacology, 1992
- Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cellsBiochemical and Biophysical Research Communications, 1991
- Pharmacokinetic studies on the selectiveβ 1-receptor antagonist metoprolol in manJournal of Pharmacokinetics and Biopharmaceutics, 1974