Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs

CJH Porter, NL Trevaskis, WN Charman - Nature reviews Drug …, 2007 - nature.com
Highly potent, but poorly water-soluble, drug candidates are common outcomes of
contemporary drug discovery programmes and present a number of challenges to drug …

Enhancing intestinal drug solubilisation using lipid-based delivery systems

CJH Porter, CW Pouton, JF Cuine… - Advanced drug delivery …, 2008 - Elsevier
Lipid-based delivery systems are finding increasing application in the oral delivery of poorly
water-soluble, lipophilic drugs. Whilst lipidic dose forms may improve oral bioavailability via …

Dissolution media simulating conditions in the proximal human gastrointestinal tract: an update

E Jantratid, N Janssen, C Reppas… - Pharmaceutical …, 2008 - Springer
Purpose The aim of this study was to update the compositions of biorelevant media to
represent the composition and physical chemical characteristics of the gastrointestinal fluids …

The developability classification system: application of biopharmaceutics concepts to formulation development

JM Butler, JB Dressman - Journal of pharmaceutical sciences, 2010 - Elsevier
A revised classification system for oral drugs was developed using the biopharmaceutics
classification system (BCS) as a starting point. The revised system is designed to have a …

PBPK models for the prediction of in vivo performance of oral dosage forms

ES Kostewicz, L Aarons, M Bergstrand… - European Journal of …, 2014 - Elsevier
Drug absorption from the gastrointestinal (GI) tract is a highly complex process dependent
upon numerous factors including the physicochemical properties of the drug, characteristics …

When poor solubility becomes an issue: from early stage to proof of concept

S Stegemann, F Leveiller, D Franchi, H De Jong… - European journal of …, 2007 - Elsevier
Drug absorption, sufficient and reproducible bioavailability and/or pharmacokinetic profile in
humans are recognized today as one of the major challenges in oral delivery of new drug …

In vivo methods for drug absorption–comparative physiologies, model selection, correlations with in vitro methods (IVIVC), and applications for formulation/API …

E Sjögren, B Abrahamsson, P Augustijns… - European Journal of …, 2014 - Elsevier
This review summarizes the current knowledge on anatomy and physiology of the human
gastrointestinal tract in comparison with that of common laboratory animals (dog, pig, rat and …

Gut instincts: explorations in intestinal physiology and drug delivery

EL McConnell, HM Fadda, AW Basit - International journal of pharmaceutics, 2008 - Elsevier
We need to look beyond our gut instincts to use information on “simple” intestinal
physiological parameters as they have been presented to us in the past. Here we present a …

Early pharmaceutical profiling to predict oral drug absorption: current status and unmet needs

CAS Bergström, R Holm, SA Jørgensen… - European Journal of …, 2014 - Elsevier
Preformulation measurements are used to estimate the fraction absorbed in vivo for orally
administered compounds and thereby allow an early evaluation of the need for enabling …

Biopharmaceutical parameters to consider in order to alter the fate of nanocarriers after oral delivery

E Roger, F Lagarce, E Garcion, JP Benoit - Nanomedicine, 2010 - Taylor & Francis
Oral route is the most common route for the delivery of drugs because it is simple to
implement and improves patient compliance and quality of life. However, oral absorption is …