Justification of disintegration testing beyond current FDA criteria using in vitro and in silico models

L Uebbing, L Klumpp, GK Webster… - Drug design …, 2017 - Taylor & Francis
Drug product performance testing is an important part of quality-by-design approaches, but
this process often lacks the underlying mechanistic understanding of the complex …

Equilibrium solubility measurement of compounds with low dissolution rate by Higuchi's Facilitated Dissolution Method. A validation study

K Takács-Novák, M Urac, P Horváth, G Völgyi… - European Journal of …, 2017 - Elsevier
Incubation time plays a critical role in the accurate measurement of equilibrium solubility of
compounds. Substances which dissolve very slowly generally need long incubation times …

Advances in experimental and mechanistic computational models to understand pulmonary exposure to inhaled drugs

P Bäckman, S Arora, W Couet, B Forbes… - European Journal of …, 2018 - Elsevier
Prediction of local exposure following inhalation of a locally acting pulmonary drug is central
to the successful development of novel inhaled medicines, as well as generic equivalents …

Cell-based multiscale computational modeling of small molecule absorption and retention in the lungs

J Yu, GR Rosania - Pharmaceutical research, 2010 - Springer
Purpose For optimizing the local, pulmonary targeting of inhaled medications, it is important
to analyze the relationship between the physicochemical properties of small molecules and …

Mathematical modeling of drug dissolution

J Siepmann, F Siepmann - International journal of pharmaceutics, 2013 - Elsevier
The dissolution of a drug administered in the solid state is a pre-requisite for efficient
subsequent transport within the human body. This is because only dissolved drug …

Modeling dissolution of sparingly soluble multisized powders

LP De Almeida, S Simões, P Brito, A Portugal… - Journal of …, 1997 - Elsevier
The dissolution of powder drugs, besides being a topic of utmost importance, especially for
the sparingly soluble ones, is far from being well-explained. The purpose of the present …

The isolated perfused lung for drug absorption studies

A Tronde, C Bosquillon, B Forbes - Drug absorption studies: In situ, in vitro …, 2008 - Springer
Over the past 20 years, the isolated perfused lung (IPL) technique has been developed for
the evaluation of pulmonary drug absorption and disposition. The procedure for establishing …

The development of a modified dissolution method suitable for investigating powder mixtures

LR Shaw, WJ Irwin, TJ Grattan… - Drug development and …, 2002 - Taylor & Francis
ABSTRACT A novel dissolution method was developed, suitable for powder mixtures, based
on the USP basket apparatus. The baskets were modified such that the powder mixtures …

Advances in in vivo predictive dissolution testing of solid oral formulations: how closer to in vivo performance?

M Shrivas, D Khunt, M Shrivas, M Choudhari… - Journal of …, 2020 - Springer
Dissolution has become an indispensable tool to predict the in vivo performance of dosage
form, especially in recent times, because of the increasing complexity of new drugs …

Integrating drug permeability with dissolution profile to develop IVIVC

R Takano, M Kataoka… - Biopharmaceutics & Drug …, 2012 - Wiley Online Library
In this review article, three different approaches to predict in vivo oral absorption based on
the in vitro data of drug permeability, solubility and dissolution were introduced. At the drug …