Self-nano-emulsifying drug-delivery systems: From the development to the current applications and challenges in oral drug delivery

AB Buya, A Beloqui, PB Memvanga, V Préat - Pharmaceutics, 2020 - mdpi.com
Approximately one third of newly discovered drug molecules show insufficient water
solubility and therefore low oral bio-availability. Self-nano-emulsifying drug-delivery systems …

Improving drug solubility for oral delivery using solid dispersions

C Leuner, J Dressman - European journal of Pharmaceutics and …, 2000 - Elsevier
The solubility behaviour of drugs remains one of the most challenging aspects in formulation
development. With the advent of combinatorial chemistry and high throughput screening, the …

[图书][B] Drug-like properties: concepts, structure design and methods from ADME to toxicity optimization

L Di, EH Kerns - 2015 - books.google.com
Of the thousands of novel compounds that a drug discovery project team invents and that
bind to the therapeutic target, only a fraction have sufficient ADME (absorption, distribution …

[HTML][HTML] Computational prediction of drug solubility in water-based systems: Qualitative and quantitative approaches used in the current drug discovery and …

CAS Bergström, P Larsson - International journal of pharmaceutics, 2018 - Elsevier
In this review we will discuss recent advances in computational prediction of solubility in
water-based solvents. Our focus is set on recent advances in predictions of biorelevant …

The biopharmaceutics classification system (BCS) and the biopharmaceutics drug disposition classification system (BDDCS): beyond guidelines

A Charalabidis, M Sfouni, C Bergström… - International journal of …, 2019 - Elsevier
The recent impact of the Biopharmaceutics Classification System (BCS) and the
Biopharmaceutics Drug Disposition Classification System (BDDCS) on relevant scientific …

In vitro models for the prediction of in vivo performance of oral dosage forms

ES Kostewicz, B Abrahamsson, M Brewster… - European Journal of …, 2014 - Elsevier
Accurate prediction of the in vivo biopharmaceutical performance of oral drug formulations is
critical to efficient drug development. Traditionally, in vitro evaluation of oral drug …

[HTML][HTML] Drug permeability profiling using cell-free permeation tools: Overview and applications

P Berben, A Bauer-Brandl, M Brandl, B Faller… - European Journal of …, 2018 - Elsevier
Cell-free permeation systems are gaining interest in drug discovery and development as
tools to obtain a reliable prediction of passive intestinal absorption without the …

The Use of Biorelevant Dissolution Media to Forecast the In Vivo Performance of a Drug

S Klein - The AAPS journal, 2010 - Springer
Simulation of gastrointestinal conditions is essential to adequately predict the in vivo
behavior of drug formulations. To reduce the size and number of human studies required to …

Physiological Parameters for Oral Delivery and in Vitro Testing

DM Mudie, GL Amidon, GE Amidon - Molecular pharmaceutics, 2010 - ACS Publications
Pharmaceutical solid oral dosage forms must undergo dissolution in the intestinal fluids of
the gastrointestinal tract before they can be absorbed and reach the systemic circulation …

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 …