Prediction of the human oral bioavailability by using in vitro and in silico drug related parameters in a physiologically based absorption model.

Abstract:

:Estimates of the human oral absolute bioavailability were made by using a physiological-based pharmacokinetic model of absorption and the drug solubility at the gastrointestinal pH range 1.5-7.5, the apparent permeability (P(app)) in Caco-2 cells and the intrinsic clearance (Cl(int)) in human hepatocytes suspensions as major drug related parameters. The predictive ability of this approach was tested in 164 drugs divided in four levels of input data: (i) in vitro data for both P(app) and Cl(int); (ii) in vitro data for Cl(int) only; (iii) in vitro data for P(app) only and (iv) in silico data for both P(app) and Cl(int). In all scenarios, solubility was estimated in silico. Excellent predictive abilities were observed when in vitro data for both P(app) and Cl(int) were used, with 84% of drugs with oral bioavailability predictions within a±20% interval of the correct value. This predictive ability is reduced with the introduction of the in silico estimated parameters, particularly when Cl(int) is used. Performance of the model using only in silico data provided 53% of drugs with bioavailability predictions within a±20% acceptance interval. However, 74% of drugs in the same scenario resulted in bioavailability predictions within a±35% interval, which indicates that a qualitative prediction of the absolute bioavailability is still possible. This approach is a valuable way to estimate a fundamental pharmacokinetic parameter, using data typically collected in the drug discovery and early development phases, providing also mechanistic information of the limiting bioavailability steps of the drug.

journal_name

Int J Pharm

authors

Paixão P,Gouveia LF,Morais JA

doi

10.1016/j.ijpharm.2012.03.019

subject

Has Abstract

pub_date

2012-06-15 00:00:00

pages

84-98

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(12)00241-4

journal_volume

429

pub_type

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