Related references
Note: Only part of the references are listed.The elucidation of key factors for oral absorption enhancement of nanocrystal formulations: In vitro-in vivo correlation of nanocrystals
Masaaki Imono et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2020)
The Role of Functional Excipients in Solid Oral Dosage Forms to Overcome Poor Drug Dissolution and Bioavailability
Jannes van der Merwe et al.
PHARMACEUTICS (2020)
Toward Developing Discriminating Dissolution Methods for Formulations Containing Nanoparticulates in Solution: The Impact of Particle Drift and Drug Activity in Solution
Freddy A. Arce et al.
MOLECULAR PHARMACEUTICS (2020)
The Solubility-Permeability Interplay for Solubility-Enabling Oral Formulations
Nidhi Nainwal et al.
CURRENT DRUG TARGETS (2019)
Successful oral delivery of poorly water-soluble drugs both depends on the intraluminal behavior of drugs and of appropriate advanced drug delivery systems
Ben J. Boyd et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2019)
Intestinal Permeability and Drug Absorption: Predictive Experimental, Computational and In Vivo Approaches
David Dahlgren et al.
PHARMACEUTICS (2019)
Application of a Refined Developability Classification System
Julian Rosenberger et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2019)
Active intestinal drug absorption and the solubility-permeability interplay
Daniel Porat et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2018)
A Refined Developability Classification System
Julian Rosenberger et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2018)
Ranking Itraconazole Formulations Based on the Flux through Artificial Lipophilic Membrane
Konstantin Tsinman et al.
PHARMACEUTICAL RESEARCH (2018)
Dissolution Failure of Solid Oral Drug Products in Field Alert Reports
Dajun Sun et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2017)
In Vivo Predictive Dissolution (IPD) and Biopharmaceutical Modeling and Simulation: Future Use of Modern Approaches and Methodologies in a Regulatory Context
H. Lennernas et al.
MOLECULAR PHARMACEUTICS (2017)
The solubility-permeability interplay and oral drug formulation design: Two heads are better than one
Arik Dahan et al.
ADVANCED DRUG DELIVERY REVIEWS (2016)
Regulatory Considerations of Bioequivalence Studies for Oral Solid Dosage Forms in Japan
Ryosuke Kuribayashi et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2016)
Non-Sink Dissolution Conditions for Predicting Product Quality and In Vivo Performance of Supersaturating Drug Delivery Systems
Dajun D. Sun et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2016)
Advantage of the Dissolution/Permeation System for Estimating Oral Absorption of Drug Candidates in the Drug Discovery Stage
Yoshihiro Miyaji et al.
MOLECULAR PHARMACEUTICS (2016)
Haste Makes Waste: The Interplay Between Dissolution and Precipitation of Supersaturating Formulations
Dajun D. Sun et al.
AAPS JOURNAL (2015)
The use of captisol (SBE7-β-CD) in oral solubility-enabling formulations: Comparison to HPβCD and the solubility-permeability interplay
Avital Beig et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2015)
Gastrointestinal behavior of nano- and microsized fenofibrate: In vivo evaluation in man and in vitro simulation by assessment of the permeation potential
Bart Hens et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2015)
Impact of Solubilizing Additives on Supersaturation and Membrane Transport of Drugs
Shweta A. Raina et al.
PHARMACEUTICAL RESEARCH (2015)
Oral biopharmaceutics tools - Time for a new initiative - An introduction to the IMI project OrBiTo
H. Lennernas et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2014)
In vitro models for the prediction of in vivo performance of oral dosage forms
Edmund S. Kostewicz et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2014)
The Biopharmaceutics Classification System: Subclasses for in vivo predictive dissolution (IPD) methodology and IVIVC
Yasuhiro Tsume et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2014)
Quantification of Gastrointestinal Liquid Volumes and Distribution Following a 240 mL Dose of Water in the Fasted State
Deanna M. Mudie et al.
MOLECULAR PHARMACEUTICS (2014)
The interaction of nifedipine with selected cyclodextrins and the subsequent solubility-permeability trade-off
Avital Beig et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2013)
Correction: Oral Delivery of Lipophilic Drugs: The Tradeoff between Solubility Increase and Permeability Decrease When Using Cyclodextrin-Based Formulations
Avital Beig et al.
PLoS One (2013)
Strategies to Address Low Drug Solubility in Discovery and Development
Hywel D. Williams et al.
PHARMACOLOGICAL REVIEWS (2013)
The Solubility-Permeability Interplay and Its Implications in Formulation Design and Development for Poorly Soluble Drugs
Arik Dahan et al.
AAPS JOURNAL (2012)
Overcoming sink limitations in dissolution testing: a review of traditional methods and the potential utility of biphasic systems
Daniel J. Phillips et al.
JOURNAL OF PHARMACY AND PHARMACOLOGY (2012)
The Solubility-Permeability Interplay: Mechanistic Modeling and Predictive Application of the Impact of Micellar Solubilization on Intestinal Permeation
Jonathan M. Miller et al.
MOLECULAR PHARMACEUTICS (2011)
Possible reduction of effective thickness of intestinal unstirred water layer by particle drifting effect
Kiyohiko Sugano
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2010)
The Solubility-Permeability Interplay in Using Cyclodextrins as Pharmaceutical Solubilizers: Mechanistic Modeling and Application to Progesterone
Arik Dahan et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2010)
The Developability Classification System: Application of Biopharmaceutics Concepts to Formulation Development
James M. Butler et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2010)
Aqueous Boundary Layers Related to Oral Absorption of a Drug: From Dissolution of a Drug to Carrier Mediated Transport and Intestinal Wall Metabolism
Kiyohiko Sugano
MOLECULAR PHARMACEUTICS (2010)
Leakiness and Size Exclusion of Paracellular Channels in Cultured Epithelial Cell Monolayers-Interlaboratory Comparison
Alex Avdeef
PHARMACEUTICAL RESEARCH (2010)
Uptake of inert microparticles in normal and immune deficient mice
S. H. Smyth et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2008)
Rapid throughput solubility screening method for BCS class II drugs in animal GI fluids and simulated human GI fluids using a 96-well format
Jeremy Guo et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2008)
The asymmetry of the unstirred water layer in permeability experiments
Timo Korjamo et al.
PHARMACEUTICAL RESEARCH (2008)
Factors influencing intestinal microparticle uptake in vivo
M. Doyle-McCullough et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2007)
Intestinal fluid volumes and transit of dosage forms as assessed by magnetic resonance imaging
C Schiller et al.
ALIMENTARY PHARMACOLOGY & THERAPEUTICS (2005)
Share Paper
