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 …

Prediction of the precipitation profiles of weak base drugs in the small intestine using a simplified transfer (“dumping”) model coupled with in silico modeling and …

A Kambayashi, T Yasuji, JB Dressman - European Journal of …, 2016 - Elsevier
Background Precipitation of poorly soluble, weakly basic drugs upon entering the small
intestine may lead to poor bioavailability. It would be useful to be able to predict the extent of …

Miniaturized transfer models to predict the precipitation of poorly soluble weak bases upon entry into the small intestine

S Klein, NL Buchanan, CM Buchanan - AAPS PharmSciTech, 2012 - Springer
For poorly soluble weak bases, the possibility of drug precipitation upon entry into the small
intestine may affect the amount of drug available for uptake through the intestinal mucosa. A …

[HTML][HTML] Combining in vitro dissolution/permeation with microdialysis sampling: Capabilities and limitations for biopharmaceutical assessments of supersaturating drug …

FL Holzem, IH Jensen, JP Schaffland, C Stillhart… - European Journal of …, 2023 - Elsevier
Many novel small drug molecules are poorly water-soluble and thus, enabling drug
formulations may be required to ensure sufficient absorption upon oral administration …

Drug precipitation–permeation interplay: supersaturation in an absorptive environment

J Bevernage, J Brouwers, P Annaert… - European journal of …, 2012 - Elsevier
PURPOSE: The present study investigated the interplay between supersaturation,
absorption, precipitation, and excipient-mediated precipitation inhibition by comparing …

Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract

D Hörter, JB Dressman - Advanced drug delivery reviews, 2001 - Elsevier
The rate-limiting step to absorption of drugs from the gastrointestinal (GI) tract is often
dissolution from the dosage form. Consideration of the Noyes-Whitney dissolution model …

Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract

D Hörter, JB Dressman - Advanced Drug Delivery Reviews, 1997 - Elsevier
The rate-limiting step to absorption of drugs from the gastrointestinal (GI) tract is often
dissolution from the dosage form. Consideration of the Noyes-Whitney dissolution model …

Evaluation of dissolution in the lower intestine and its impact on the absorption process of high dose low solubility drugs

D Georgaka, J Butler, F Kesisoglou… - Molecular …, 2017 - ACS Publications
The purpose of this article was two-fold: first, to optimize a recently proposed two-stage
single-compartment in vitro test for the evaluation of dissolution in the lower intestine with …

Evaluation of gastrointestinal drug supersaturation and precipitation: strategies and issues

J Bevernage, J Brouwers, ME Brewster… - International journal of …, 2013 - Elsevier
Supersaturating drug delivery systems (SDDS) hold the promise of enabling intestinal
absorption for difficult-to-formulate, poorly soluble drug candidates based on a design …

In Vivo Predictive Dissolution (IPD) and Biopharmaceutical Modeling and Simulation: Future Use of Modern Approaches and Methodologies in a Regulatory Context

H Lennernas, A Lindahl, A Van Peer… - Molecular …, 2017 - ACS Publications
The overall objective of OrBiTo, a project within Innovative Medicines Initiative (IMI), is to
streamline and optimize the development of orally administered drug products through the …