[HTML][HTML] Current challenges and future perspectives in oral absorption research: An opinion of the UNGAP network

Z Vinarov, B Abrahamsson, P Artursson… - Advanced Drug Delivery …, 2021 - Elsevier
Although oral drug delivery is the preferred administration route and has been used for
centuries, modern drug discovery and development pipelines challenge conventional …

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 …

The Biopharmaceutics Classification System: subclasses for in vivo predictive dissolution (IPD) methodology and IVIVC

Y Tsume, DM Mudie, P Langguth, GE Amidon… - European Journal of …, 2014 - Elsevier
Abstract The Biopharmaceutics Classification System (BCS) has found widespread utility in
drug discovery, product development and drug product regulatory sciences. The …

Formulation of a danazol cocrystal with controlled supersaturation plays an essential role in improving bioavailability

SL Childs, P Kandi, SR Lingireddy - Molecular pharmaceutics, 2013 - ACS Publications
Cocrystals have become an established and adopted approach for creating crystalline
solids with improved physical properties, but incorporating cocrystals into enabling pre …

In vitro methods to assess drug precipitation in the fasted small intestine – a PEARRL review

PJ O'Dwyer, C Litou, KJ Box… - Journal of Pharmacy …, 2019 - academic.oup.com
Objectives Drug precipitation in vivo poses a significant challenge for the pharmaceutical
industry. During the drug development process, the impact of drug supersaturation or …

Spray congealing: An emerging technology to prepare solid dispersions with enhanced oral bioavailability of poorly water soluble drugs

S Bertoni, B Albertini, N Passerini - Molecules, 2019 - mdpi.com
The low and variable oral bioavailability of poorly water soluble drugs remains a major
concern for the pharmaceutical industry. Spray congealing is an emerging technology for the …

Toward successful cyclodextrin based solubility-enabling formulations for oral delivery of lipophilic drugs: solubility–permeability trade-off, biorelevant dissolution, and …

N Fine-Shamir, A Beig, M Zur, D Lindley… - Molecular …, 2017 - ACS Publications
The purpose of this work was to investigate key factors dictating the success/failure of
cyclodextrin-based solubility-enabling formulations for oral delivery of low-solubility drugs …

In Vitroin Vivo Correlation of the Effect of Supersaturation on the Intestinal Absorption of BCS Class 2 Drugs

H Higashino, T Hasegawa, M Yamamoto… - Molecular …, 2014 - ACS Publications
The aim of this study was to establish an in vitro method for evaluating the effect of
supersaturation on oral absorption of poorly water-soluble drugs in vivo. Albendazole …

Dissolution challenges associated with the surface pH of drug particles: integration into mechanistic oral absorption modeling

B Hens, N Seegobin, M Bermejo, Y Tsume, N Clear… - The AAPS Journal, 2022 - Springer
The present work aimed to differentiate between in vitro dissolution profiles of ibuprofen as
input for GastroPlus™ and to see the impact on systemic exposure. In vitro dissolution …

Oral controlled release dosage forms: dissolution versus diffusion

M Bermejo, B Sanchez-Dengra… - Expert Opinion on …, 2020 - Taylor & Francis
Introduction Controlled release (CR) dosage forms comprise a wide range of technologies,
which modify the drug pharmacokinetic (PK) profile by avoiding the immediate release (IR) …