Cargando…

A comparative evaluation of models to predict human intestinal metabolism from nonclinical data

Extensive gut metabolism is often associated with the risk of low and variable bioavailability. The prediction of the fraction of drug escaping gut wall metabolism as well as transporter‐mediated secretion (F (g)) has been challenged by the lack of appropriate preclinical models. The purpose of this...

Descripción completa

Detalles Bibliográficos
Autores principales: Yau, Estelle, Petersson, Carl, Dolgos, Hugues, Peters, Sheila Annie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412686/
https://www.ncbi.nlm.nih.gov/pubmed/28152562
http://dx.doi.org/10.1002/bdd.2068
Descripción
Sumario:Extensive gut metabolism is often associated with the risk of low and variable bioavailability. The prediction of the fraction of drug escaping gut wall metabolism as well as transporter‐mediated secretion (F (g)) has been challenged by the lack of appropriate preclinical models. The purpose of this study is to compare the performance of models that are widely employed in the pharmaceutical industry today to estimate F (g) and, based on the outcome, to provide recommendations for the prediction of human F (g) during drug discovery and early drug development. The use of in vitro intrinsic clearance from human liver microsomes (HLM) in three mechanistic models – the ADAM, Q (gut) and Competing Rates – was evaluated for drugs whose metabolism is dominated by CYP450s, assuming that the effect of transporters is negligible. The utility of rat as a model for human F (g) was also explored. The ADAM, Q (gut) and Competing Rates models had comparable prediction success (70%, 74%, 69%, respectively) and bias (AFE = 1.26, 0.74 and 0.81, respectively). However, the ADAM model showed better accuracy compared with the Q (gut) and Competing Rates models (RMSE =0.20 vs 0.30 and 0.25, respectively). Rat is not a good model (prediction success =32%, RMSE =0.48 and AFE = 0.44) as it seems systematically to under‐predict human F (g). Hence, we would recommend the use of rat to identify the need for F (g) assessment, followed by the use of HLM in simple models to predict human F (g). © 2017 Merck KGaA. Biopharmaceutics & Drug Disposition Published by John Wiley & Sons, Ltd.