[PDF][PDF] Dissolution media simulating fasted and fed states
M Marques - Dissolution Technologies, 2004 - researchgate.net
When dissolution testing is used to forecast the in vivo performance of a drug, it is critical that
the in vitro test mimic the conditions in vivo as closely as possible. A team of researchers, led …
the in vitro test mimic the conditions in vivo as closely as possible. A team of researchers, led …
The Use of Biorelevant Dissolution Media to Forecast the In Vivo Performance of a Drug
S Klein - The AAPS journal, 2010 - Springer
Simulation of gastrointestinal conditions is essential to adequately predict the in vivo
behavior of drug formulations. To reduce the size and number of human studies required to …
behavior of drug formulations. To reduce the size and number of human studies required to …
Dissolution media simulating conditions in the proximal human gastrointestinal tract: an update
E Jantratid, N Janssen, C Reppas… - Pharmaceutical …, 2008 - Springer
Purpose The aim of this study was to update the compositions of biorelevant media to
represent the composition and physical chemical characteristics of the gastrointestinal fluids …
represent the composition and physical chemical characteristics of the gastrointestinal fluids …
Biorelevant dissolution methods and their applications in in vitro-in vivo correlations for oral formulations
N Fotaki, M Vertzoni - The Open Drug Delivery Journal, 2010 - benthamopen.com
Dissolution tests that can predict the in vivo performance of drug products are usually called
biorelevant dissolution tests. Biorelevant dissolution testing can be used to guide …
biorelevant dissolution tests. Biorelevant dissolution testing can be used to guide …
Dynamic dissolution: a step closer to predictive dissolution testing?
M McAllister - Molecular pharmaceutics, 2010 - ACS Publications
The use of compendial dissolution techniques to characterize the performance of oral drug
delivery systems is an established area of pharmaceutical science. However, compendial …
delivery systems is an established area of pharmaceutical science. However, compendial …
[PDF][PDF] In vitro dissolution curve comparisons: a critique of current practice
D LeBlond, S Altan, S Novick, J Peterson… - Dissolution …, 2016 - dissolutiontech.com
Many pharmacologically active molecules are formulated as solid dosage form drug
products. Following oral administration, the diffusion of an active molecule from the …
products. Following oral administration, the diffusion of an active molecule from the …
[PDF][PDF] Simplified biorelevant media for screening dissolution performance of poorly soluble drugs
T Zoeller, S Klein - Dissolution Technol, 2007 - dissolutiontech.com
Simulation of gastrointestinal conditions is essential to adequately predict the in vivo
behavior of poorly soluble drugs. Simulating small intestinal conditions with biorelevant …
behavior of poorly soluble drugs. Simulating small intestinal conditions with biorelevant …
Unconventional dissolution methodologies
V Pillay, R Fassihi - Journal of pharmaceutical sciences, 1999 - Elsevier
In line with the key focus of recent publications1-3 emerging from the labs of Dressman,
Amidon, and Shah, and in conjunction with the aims of both the FDA and US …
Amidon, and Shah, and in conjunction with the aims of both the FDA and US …
[PDF][PDF] Biorelevant dissolution: methodology and application in drug development
Dissolution testing can play an important role in several areas for drug products as a quality
control tool to monitor batch-to-batch consistency of drug release from a dosage form and as …
control tool to monitor batch-to-batch consistency of drug release from a dosage form and as …
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 …
the gastrointestinal tract before they can be absorbed and reach the systemic circulation …