Dissolution rate and apparent solubility of poorly soluble drugs in biorelevant dissolution media
JH Fagerberg, O Tsinman, N Sun… - Molecular …, 2010 - ACS Publications
A series of poorly soluble BCS class II compounds with “grease ball” characteristics were
assessed for solubility and dissolution rate in biorelevant dissolution media (BDM) with the …
assessed for solubility and dissolution rate in biorelevant dissolution media (BDM) with the …
The particle has landed—characterizing the fate of inhaled pharmaceuticals
Although there is a modest body of literature on the absorption of inhaled pharmaceuticals
by normal lungs and some limited information from diseased lungs, there is still a surprising …
by normal lungs and some limited information from diseased lungs, there is still a surprising …
Assessment of absorption potential of poorly water-soluble drugs by using the dissolution/permeation system
M Kataoka, K Yano, Y Hamatsu, Y Masaoka… - European Journal of …, 2013 - Elsevier
This study aims to assess the absorption potential of oral absorption of poorly water-soluble
drugs by using the dissolution/permeation system (D/P system). The D/P system can be …
drugs by using the dissolution/permeation system (D/P system). The D/P system can be …
Development of an Aerosol Dose Collection Apparatus for In Vitro Dissolution Measurements of Orally Inhaled Drug Products
The aim of the study was to develop a robust and standardized in vitro dissolution
methodology for orally inhaled drug products (OIDPs). An aerosol dose collection (ADC) …
methodology for orally inhaled drug products (OIDPs). An aerosol dose collection (ADC) …
Simultaneous Evaluation of Dissolution and Permeation of Oral Drug Solid Formulations for Predicting Absorption Rate–Limiting Factors and In Vitro–In Vivo …
Z Li, X He, S Tian, G Feng, C Huang, M Xun, Z Wu… - AAPS …, 2019 - Springer
Combined dissolution and permeation systems are designed to simultaneously assess the
dissolution of a pharmaceutical dosage form and the permeation of dissolved drugs …
dissolution of a pharmaceutical dosage form and the permeation of dissolved drugs …
Integration of In Silico Pharmacokinetic Modeling Approaches Into In Vitro Dissolution Profiles to Predict Bioavailability of a Poorly Soluble Compound
T Kato, T Watanabe, K Nakamura, S Ando - Journal of Pharmaceutical …, 2019 - Elsevier
The objective of present study is to develop pharmacokinetic (PK) prediction methods using
in silico PK model for oral immediate release drug products (ie solution, suspension, and …
in silico PK model for oral immediate release drug products (ie solution, suspension, and …
Toxicity of orally inhaled drug formulations at the alveolar barrier: parameters for initial biological screening
E Fröhlich - Drug Delivery, 2017 - Taylor & Francis
Oral delivery is the most common mode of systemic drug application. Inhalation is mainly
used for local therapy of lung diseases but may also be a promising route for systemic …
used for local therapy of lung diseases but may also be a promising route for systemic …
Dissolution Techniques for In Vitro Testing of Dry Powders for Inhalation
S May, B Jensen, M Wolkenhauer, M Schneider… - Pharmaceutical …, 2012 - Springer
Purpose To evaluate different dissolution testing methods and subsequently develop a
simple to perform but reproducible and discriminating dissolution technique for inhalative …
simple to perform but reproducible and discriminating dissolution technique for inhalative …
In vitro dissolution/permeation system to predict the oral absorption of poorly water-soluble drugs: effect of food and dose strength on it
M Kataoka, S Itsubata, Y Masaoka… - Biological and …, 2011 - jstage.jst.go.jp
The aim of the present work was to confirm the usefulness of the dissolution/permeation
system (D/P system) in the estimation of human oral absorption of poorly water-soluble …
system (D/P system) in the estimation of human oral absorption of poorly water-soluble …
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 …
this process often lacks the underlying mechanistic understanding of the complex …