Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs

E Galia, E Nicolaides, D Hörter, R Löbenberg… - Pharmaceutical …, 1998 - Springer
Purpose. In this paper we seek to verify the differences in dissolution behavior between
class I and class II drugs and to evaluate the suitability of two new physiologically based …

Forecasting the in vivo performance of four low solubility drugs from their in vitro dissolution data

E Nicolaides, E Galia, C Efthymiopoulos… - Pharmaceutical …, 1999 - Springer
Purpose. To assess the usefulness of biorelevant dissolution tests in predicting food and
formulation effects on the absorption of four poorly soluble, lipophilic drugs. Methods …

Evaluation of a three compartment in vitro gastrointestinal simulator dissolution apparatus to predict in vivo dissolution

S Takeuchi, Y Tsume, GE Amidon… - Journal of pharmaceutical …, 2014 - Elsevier
In vitro dissolution tests are performed for new formulations to evaluate in vivo performance,
which is affected by the change of gastrointestinal (GI) physiology, in the GI tract. Thus, those …

Dissolution testing as a prognostic tool for oral drug absorption: dissolution behavior of glibenclamide

R Löbenberg, J Krämer, VP Shah, GL Amidon… - Pharmaceutical …, 2000 - Springer
Purpose. The dissolution behavior of two commercially availableglibenclamide formulations
was tested in various media. The aim of thestudy was to investigate whether the use of …

In vivo in vitro correlations for a poorly soluble drug, danazol, using the flow-through dissolution method with biorelevant dissolution media

VH Sunesen, BL Pedersen, HG Kristensen… - European journal of …, 2005 - Elsevier
The purpose of the study was to design dissolution tests that were able to distinguish
between the behaviour of danazol under fasted and fed conditions, by using biorelevant …

In vitro–in vivo correlations for lipophilic, poorly water-soluble drugs

JB Dressman, C Reppas - European journal of pharmaceutical sciences, 2000 - Elsevier
Although several routes of administration can be considered for new drug entities, the most
popular remains the oral route. To predict the in vivo performance of a drug after oral …

pH-Dependent Dissolution in Vitro and Absorption in Vivo of Weakly Basic Drugs: Development of a Canine Model

R Zhou, P Moench, C Heran, X Lu, N Mathias… - Pharmaceutical …, 2005 - Springer
No Heading Purpose. The aim of this research was to develop a pH-dependent canine
absorption model for studying pH effect on both dissolution in vitro and pharmacokinetics in …

Validation of dissolution testing with biorelevant media: an OrBiTo study

J Mann, J Dressman, K Rosenblatt… - Molecular …, 2017 - ACS Publications
Dissolution testing with biorelevant media has become widespread in the pharmaceutical
industry as a means of better understanding how drugs and formulations behave in the …

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 testing as a prognostic tool for oral drug absorption: immediate release dosage forms

JB Dressman, GL Amidon, C Reppas, VP Shah - Pharmaceutical research, 1998 - Springer
Dissolution tests are used for many purposes in the pharmaceutical industry: in the
development of new products, for quality control and, to assist with the determination of …