The utility of rat jejunal permeability for biopharmaceutics classification system

P Zakeri-Milani, H Valizadeh… - Drug development …, 2009 - Taylor & Francis
Purpose: The biopharmaceutical classification system has been developed to provide a
scientific approach for classifying drug compounds based on their dose/solubility ratio and …

ADME evaluation: 2. A computer model for the prediction of intestinal absorption in humans

G Klopman, LR Stefan, RD Saiakhov - European journal of pharmaceutical …, 2002 - Elsevier
Purpose: To develop a computational method to rapidly evaluate human intestinal
absorption, one of the drug properties included in the term ADME (Absorption, Distribution …

A topological sub-structural approach for predicting human intestinal absorption of drugs

MAC Pérez, MB Sanz, LR Torres, RG Ávalos… - European journal of …, 2004 - Elsevier
The human intestinal absorption (HIA) of drugs was studied using a topological sub-
structural approach (TOPS-MODE). The drugs were divided into three classes according to …

Prediction of the in vitro permeability determined in Caco-2 cells by using artificial neural networks

P Paixão, LF Gouveia, JAG Morais - European Journal of Pharmaceutical …, 2010 - Elsevier
Caco-2 cells are currently the most used in vitro tool for prediction of the potential oral
absorption of new drugs. The existence of computational models based on this data may …

Current and evolving approaches for improving the oral permeability of BCS Class III or analogous molecules

VS Dave, D Gupta, M Yu, P Nguyen… - Drug development …, 2017 - Taylor & Francis
Abstract The Biopharmaceutics Classification System (BCS) classifies pharmaceutical
compounds based on their aqueous solubility and intestinal permeability. The BCS Class III …

The role of permeability in drug ADME/PK, interactions and toxicity—presentation of a permeability-based classification system (PCS) for prediction of ADME/PK in …

U Fagerholm - Pharmaceutical research, 2008 - Springer
Purpose The objective was to establish in vitro passive permeability (P e) vs in vivo fraction
absorbed (fa)-relationships for each passage through the human intestine, liver, renal tubuli …

Prediction of drug bioavailability based on molecular structure

JV Turner, BD Glass, S Agatonovic-Kustrin - Analytica Chimica Acta, 2003 - Elsevier
Oral dosing is the most common method of drug administration, and final plasma
concentrations of the drug depend upon its bioavailability. In the current study, a quantitative …

Provisional in-silico biopharmaceutics classification (BCS) to guide oral drug product development

O Wolk, R Agbaria, A Dahan - Drug design, development and …, 2014 - Taylor & Francis
The main objective of this work was to investigate in-silico predictions of physicochemical
properties, in order to guide oral drug development by provisional biopharmaceutics …

Biopharmaceutical Classification System: a strategic tool in pharmaceutical formulation

TG Agnihotri, PK Paradia, A Jain - Dosage Forms, Formulation …, 2024 - Elsevier
In recent years, the pharmaceutical sector has been viewed as one of the most revenue-
generating fields which primarily deals with all the activities ranging from approving …

In silico prediction of intestinal permeability by hierarchical support vector regression

MH Lee, GH Ta, CF Weng, MK Leong - International Journal of Molecular …, 2020 - mdpi.com
The vast majority of marketed drugs are orally administrated. As such, drug absorption is
one of the important drug metabolism and pharmacokinetics parameters that should be …