J. Dressman

发表

Comparison of a miniaturized shake-flask solubility method with automated potentiometric acid/base titrations and calculated solubilities.

A. Glomme, J. März, J. Dressman, 2005, Journal of pharmaceutical sciences.

Absorption potential: estimating the fraction absorbed for orally administered compounds.

G. Amidon, J. Dressman, D. Fleisher, 1985, Journal of pharmaceutical sciences.

In vivo evaluation of a novel pH‐ and time‐based multiunit colonic drug delivery system

J. Dressman, H. Petereit, C. Bott, 2004, Alimentary pharmacology & therapeutics.

Upper Gastrointestinal (GI) pH in Young, Healthy Men and Women

J. Dressman, J. Barnett, R. Berardi, 1990, Pharmaceutical Research.

Characterization of the Human Upper Gastrointestinal Contents Under Conditions Simulating Bioavailability/Bioequivalence Studies

J. Dressman, B. Abrahamsson, L. Kalantzi, 2006, Pharmaceutical Research.

Current Challenges and Potential Opportunities for the Pharmaceutical Sciences to Make Global Impact: An FIP Perspective.

G. Tucker, J. Dressman, H. Sasaki, 2016, Journal of pharmaceutical sciences.

Predicting the precipitation of poorly soluble weak bases upon entry in the small intestine

J. Dressman, T. Bock, E. Kostewicz, 2004, The Journal of pharmacy and pharmacology.

Simulation of fasting gastric conditions and its importance for the in vivo dissolution of lipophilic compounds.

J. Dressman, C. Reppas, M. Vertzoni, 2005, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Dissolution Media Simulating Conditions in the Proximal Human Gastrointestinal Tract: An Update

J. Dressman, C. Reppas, E. Jantratid, 2008, Pharmaceutical Research.

An In Vitro Methodology for Forecasting Luminal Concentrations and Precipitation of Highly Permeable Lipophilic Weak Bases in the Fasted Upper Small Intestine

J. Dressman, C. Reppas, D. Busby, 2012, Pharmaceutical Research.

Comparison of in vitro tests at various levels of complexity for the prediction of in vivo performance of lipid-based formulations: case studies with fenofibrate.

B. Griffin, J. Dressman, M. Kuentz, 2014, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Oral Drug Absorption: Prediction and Assessment

H. Lennernäs, J. Dressman, 2000 .

Evolution of a detailed physiological model to simulate the gastrointestinal transit and absorption process in humans, part 1: oral solutions.

J. Dressman, J. Lippert, R. Burghaus, 2011, Journal of pharmaceutical sciences.

A physiological model for the estimation of the fraction dose absorbed in humans.

Walter Schmitt, Stefan Willmann, Jörg Keldenich, 2004, Journal of medicinal chemistry.

Classification of orally administered drugs on the World Health Organization Model list of Essential Medicines according to the biopharmaceutics classification system.

Jennifer B Dressman, Sabine Kopp, J. Dressman, 2004, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Utilizing in vitro and PBPK tools to link ADME characteristics to plasma profiles: case example nifedipine immediate release formulation.

Stefan Willmann, Arzu Selen, Christian Wagner, 2013, Journal of pharmaceutical sciences.

Evolution of a detailed physiological model to simulate the gastrointestinal transit and absorption process in humans, part II: extension to describe performance of solid dosage forms.

Stefan Willmann, Jennifer B Dressman, Jörg Lippert, 2012, Journal of pharmaceutical sciences.

Analysis of nifedipine absorption from soft gelatin capsules using PBPK modeling and biorelevant dissolution testing.

J. Dressman, J. Lippert, S. Willmann, 2010, Journal of pharmaceutical sciences.

Whole‐body physiologically based pharmacokinetic population modelling of oral drug administration: inter‐individual variability of cimetidine absorption

Stefan Willmann, Andrea N. Edginton, J. Dressman, 2009 .

Development and Validation of a Physiology-based Model for the Prediction of Oral Absorption in Monkeys

Stefan Willmann, Andrea N. Edginton, J. Dressman, 2007, Pharmaceutical Research.

Physiologically Based Pharmacokinetic/Pharmacodynamic Modeling to Predict the Impact of CYP2C9 Genetic Polymorphisms, Co-Medication and Formulation on the Pharmacokinetics and Pharmacodynamics of Flurbiprofen

M. Jamei, J. Dressman, Rodrigo Cristofoletti, 2020, Pharmaceutics.

An in silico approach to determine challenges in the bioavailability of ciprofloxacin, a poorly soluble weak base with borderline solubility and permeability characteristics

Yoshihiro Miyaji, Jennifer Dressman, J. Dressman, 2018, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

IMI – Oral biopharmaceutics tools project – Evaluation of bottom‐up PBPK prediction success part 3: Identifying gaps in system parameters by analysing In Silico performance across different compound classes

Amitava Mitra, Jian Lin, Mai Anh Nguyen, 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Forecasting oral absorption across biopharmaceutics classification system classes with physiologically based pharmacokinetic models

Leon Aarons, Alison Margolskee, Jennifer Dressman, 2016, The Journal of pharmacy and pharmacology.

Exploratory Investigation of the Limiting Steps of Oral Absorption of Fluconazole and Ketoconazole in Children Using an In Silico Pediatric Absorption Model.

Naseem A. Charoo, J. Dressman, Rodrigo Cristofoletti, 2016, Journal of pharmaceutical sciences.

Differences in Food Effects for 2 Weak Bases With Similar BCS Drug-Related Properties: What Is Happening in the Intestinal Lumen?

Rodrigo Cristofoletti, Jennifer B Dressman, Nikunjkumar Patel, 2016, Journal of pharmaceutical sciences.

Use of physiologically based pharmacokinetic models coupled with pharmacodynamic models to assess the clinical relevance of current bioequivalence criteria for generic drug products containing Ibuprofen.

J. Dressman, Rodrigo Cristofoletti, 2014, Journal of pharmaceutical sciences.

Mechanism-based prediction of particle size-dependent dissolution and absorption: cilostazol pharmacokinetics in dogs.

Stefan Willmann, Jennifer B Dressman, Jörg Lippert, 2010, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

IMI – Oral biopharmaceutics tools project – Evaluation of bottom‐up PBPK prediction success part 2: An introduction to the simulation exercise and overview of results

Amitava Mitra, Jian Lin, Mai Anh Nguyen, 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Early pharmaceutical profiling to predict oral drug absorption: current status and unmet needs.

Mark McAllister, René Holm, Christel A. S. Bergström, 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

The BCS: Where Do We Go from Here?

J. Dressman, C. Reppas, J. Butler, 2001 .

Estimation of the Increase in Solubility of Drugs as a Function of Bile Salt Concentration

J. Dressman, Jennifer B. Dressman, S. Mithani, 2004, Pharmaceutical Research.

Evaluation of Various Dissolution Media for Predicting In Vivo Performance of Class I and II Drugs

R. Löbenberg, J. Dressman, C. Reppas, 1998, Pharmaceutical Research.

Comparison of the Adsorption of Several Drugs to Typical Filter Materials

J. Dressman, M. Lindenberg, C. Wiegand, 2005 .

Characterization of fasted‐state human intestinal fluids collected from duodenum and jejunum

Patrick Augustijns, Jan Tack, Jennifer Dressman, 2006, The Journal of pharmacy and pharmacology.

Characterization of Solid Dispersions of Itraconazole and Hydroxypropylmethylcellulose Prepared by Melt Extrusion, Part II

Christian Leuner, Jules Mullens, Jennifer Dressman, 2003, Pharmaceutical Research.

Pair distribution function X-ray analysis explains dissolution characteristics of felodipine melt extrusion products.

J Dressman, M. Schmidt, J. Dressman, 2009, Journal of pharmaceutical sciences.

Application of a ternary HP-β-CD-complex approach to improve the dissolution performance of a poorly soluble weak acid under biorelevant conditions.

Jennifer B Dressman, J. Dressman, T. Zoeller, 2012, International journal of pharmaceutics.

Mechanistic investigation of the negative food effect of modified release zolpidem

Xavier Pepin, Christos Reppas, Jennifer B Dressman, 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Predicting the oral pharmacokinetic profiles of multiple-unit (pellet) dosage forms using a modeling and simulation approach coupled with biorelevant dissolution testing: case example diclofenac sodium.

Atsushi Kambayashi, Jennifer B Dressman, J. Dressman, 2014, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans.

Filippos Kesisoglou, Christos Reppas, Jennifer B Dressman, 2010, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

A Physiologic Model for Simulating Gastrointestinal Flow and Drug Absorption in Rats

W. Schmitt, J. Dressman, J. Keldenich, 2003, Pharmaceutical Research.

The developability classification system: application of biopharmaceutics concepts to formulation development.

Jennifer B Dressman, James M Butler, J. Dressman, 2010, Journal of pharmaceutical sciences.

In vitro models for the prediction of in vivo performance of oral dosage forms.

Anette Müllertz, Patrick Augustijns, Bertil Abrahamsson, 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Biorelevant in vitro dissolution testing of products containing micronized or nanosized fenofibrate with a view to predicting plasma profiles.

Christos Reppas, Christian Wagner, Jennifer B Dressman, 2011, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

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

J. Dressman, C. Reppas, J B Dressman, 2000, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

On the Use of the Quasi-Equilibrium Assumption for Drug Dissolution

B. Palsson, J. Dressman, S. Ozturk, 1990, Pharmaceutical Research.

Measuring pH and Buffer Capacity in Fluids Aspirated from the Fasted Upper Gastrointestinal Tract of Healthy Adults

J. Dressman, C. Reppas, M. Vertzoni, 2020, Pharmaceutical Research.

Composition and physicochemical properties of fasted-state human duodenal and jejunal fluid: a critical evaluation of the available data.

J. Dressman, A. Fuchs, 2014, Journal of pharmaceutical sciences.

Dissolution media simulating the proximal canine gastrointestinal tract in the fasted state.

J. Dressman, C. Reppas, N. Parrott, 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Biorelevant Media to Simulate Fluids in the Ascending Colon of Humans and Their Usefulness in Predicting Intracolonic Drug Solubility

J. Dressman, B. Abrahamsson, C. Reppas, 2010, Pharmaceutical Research.

Canine Intestinal Contents vs. Simulated Media for the Assessment of Solubility of Two Weak Bases in the Human Small Intestinal Contents

J. Dressman, B. Abrahamsson, L. Kalantzi, 2006, Pharmaceutical Research.

Media to simulate the postprandial stomach I. Matching the physicochemical characteristics of standard breakfasts

J. Dressman, C. Reppas, S. Klein, 2004, The Journal of pharmacy and pharmacology.

Absorption of ACE inhibitors from small intestine and colon.

J. Dressman, D. Fleisher, J. Kim, 1994, Journal of pharmaceutical sciences.

Effects of medicines used to treat gastrointestinal diseases on the pharmacokinetics of coadministered drugs: a PEARRL Review

J. Dressman, N. Fotaki, E. Kostewicz, 2018, The Journal of pharmacy and pharmacology.

Dissolution of lonizable Drugs in Buffered and Unbuffered Solutions

B. Palsson, J. Dressman, S. Ozturk, 1988, Pharmaceutical Research.

Characterization of the Ascending Colon Fluids in Ulcerative Colitis

J. Dressman, B. Abrahamsson, K. Goumas, 2010, Pharmaceutical Research.

Opportunities for Successful Stabilization of Poor Glass-Forming Drugs: A Stability-Based Comparison of Mesoporous Silica Versus Hot Melt Extrusion Technologies

D. J. Price, J. Dressman, M. Kuentz, 2019, Pharmaceutics.

Mesoporous silica‐based dosage forms improve bioavailability of poorly soluble drugs in pigs: case example fenofibrate

B. Griffin, J. Dressman, C. O’Driscoll, 2017, The Journal of pharmacy and pharmacology.

Application of the relationship between pharmacokinetics and pharmacodynamics in drug development and therapeutic equivalence: a PEARRL review

J. Dressman, N. Fotaki, M. McAllister, 2019, The Journal of pharmacy and pharmacology.

FIP/AAPS Guidelines for Dissolution/In Vitro Release Testing of Novel/Special Dosage Forms*

Cynthia K. Brown, V. Shah, J. Dressman, 2003 .

Cyclodextrin-water soluble polymer ternary complexes enhance the solubility and dissolution behaviour of poorly soluble drugs. Case example: itraconazole.

J. Dressman, S. Klein, C. M. Buchanan, 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Biowaiver monographs for immediate release solid oral dosage forms: furosemide.

D M Barends, H E Junginger, D. Barends, 2010, Journal of pharmaceutical sciences.

The impact of the EMA change in definition of "dose" on the BCS dose-solubility ratio: a review of the biowaiver monographs.

J. Dressman, P. Langguth, M. Kubbinga, 2014, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: prednisolone.

D. Barends, H. Junginger, S. Stavchansky, 2007, Journal of pharmaceutical sciences.

Rediguieri CF, Porta V, Nunes DSG, Nunes TM, Junginger HE, Kopp S, Midha KK, Shah VP, Stavchansky S, Dressman JB, Barends DM. 2011. Biowaiver monographs for immediate‐release solid oral dosage forms: Metronidazole. J Pharm Sci 100:1618–1627.

D. Barends, H. Junginger, S. Stavchansky, 2011 .

Online monitoring of dissolution tests using dedicated potentiometric sensors in biorelevant media.

Jennifer B Dressman, Koen Vanhoutte, Hugo Bohets, 2011, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Practical Considerations When Using Fiber Optics for Dissolution Testing

J. Dressman, M. Wunderlich, T. Way, 2003 .

Selection of excipient, solvent and packaging to optimize the performance of spray-dried formulations: case example fenofibrate

J. Dressman, K. Kunath, M. Hugo, 2013, Drug development and industrial pharmacy.

FIP/AAPS guidelines to dissolution/in vitro release testing of novel/special dosage forms

Cynthia K. Brown, John C. Kraemer, J. Crison, 2008, AAPS PharmSciTech.

Kinetics of Release from Enteric-Coated Tablets

B. Palsson, J. Dressman, S. Ozturk, 1988, Pharmaceutical Research.

Diffusion of phenol in the presence of a complexing agent, tetrahydrofuran.

J. Dressman, K. Himmelstein, T. Higuchi, 1983, Journal of pharmaceutical sciences.

Simultaneous self-association and diffusion of phenol in isooctane.

J. Dressman, K. Himmelstein, T. Higuchi, 1982, Journal of pharmaceutical sciences.

Comparison of gastrointestinal pH in dogs and humans: implications on the use of the beagle dog as a model for oral absorption in humans.

G. Amidon, J. Dressman, D. Fleisher, 1986, Journal of pharmaceutical sciences.

Bridging the Gap Between In Vitro Dissolution and the Time Course of Ibuprofen-Mediating Pain Relief.

J. Dressman, Rodrigo Cristofoletti, 2016, Journal of pharmaceutical sciences.

Evolution of Dissolution Media Over the Last Twenty Years

J. Dressman, 2014 .

Comparison of US Pharmacopeia Simulated Intestinal Fluid TS (without pancreatin) and Phosphate Standard Buffer pH 6.8, TS of the International Pharmacopoeia with Respect to Their Use in In Vitro Dissolution Testing

Erika S. Stippler, J. Dressman, S. Kopp, 2004 .

Instant FaSSIF and FeSSIF—Biorelevance Meets Practicality

J. Dressman, J.W.Pape Wolfgang, J. Boni, 2009 .

Ability of two comestible formulations of hydroxypropylmethylcellulose to lower serum cholesterol concentrations

J. Dressman, J. Barnett, C. Reppas, 1996 .

New formulation approaches to improve solubility and drug release from fixed dose combinations: case examples pioglitazone/glimepiride and ezetimibe/simvastatin.

J. Dressman, S. Klein, Thomas Taupitz, 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Combining biorelevant in vitro and in silico tools to investigate the in vivo performance of the amorphous solid dispersion formulation of etravirine in the fed state.

J. Dressman, M. Kuentz, R. Holm, 2020, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Predicting the Intestinal Solubility of Poorly Soluble Drugs

A. Glomme, J. März, J. Dressman, 2007 .

Investigation of Dissolution Performance of Hard Gelatin Capsule Products Using Various Sinkers

J. Dressman, Yaser Mansuroglu, 2020 .

Biowaiver Monograph for Immediate-Release Solid Oral Dosage Forms: Sitagliptin phosphate monohydrate.

Naseem A. Charoo, J. Polli, A. Parr, 2021, Journal of pharmaceutical sciences.

Radiotelemetric method for evaluating enteric coatings in vivo.

G. Amidon, J. Dressman, 1984, Journal of pharmaceutical sciences.

Comparison of gastrointestinal pH in cystic fibrosis and healthy subjects

G. Amidon, J. Dressman, R. Berardi, 1987, Digestive Diseases and Sciences.

FaSSIF-V3, but not compendial media, appropriately detects differences in the peak and extent of exposure between reference and test formulations of ibuprofen.

J. Dressman, Rodrigo Cristofoletti, 2016, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Towards virtual bioequivalence studies for oral dosage forms containing poorly water-soluble drugs: a physiologically based biopharmaceutics modeling (PBBM) approach.

J. Dressman, A. Kambayashi, 2021, Journal of pharmaceutical sciences.

Biowaiver Monograph for Immediate-Release Solid Oral Dosage Forms: Moxifloxacin hydrochloride.

Naseem A. Charoo, J. Polli, A. Parr, 2020, Journal of pharmaceutical sciences.

Can dosage form-dependent food effects be predicted using biorelevant dissolution tests? Case example extended release nifedipine.

J. Dressman, W. Mueck, U. Muenster, 2016, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Poor-Quality and Counterfeit Drugs: A Systematic Assessment of Prevalence and Risks Based on Data Published From 2007 to 2016.

J. Dressman, Andreas Koczwara, 2017, Journal of pharmaceutical sciences.

Are counterfeit or substandard anti-infective products the cause of treatment failure in Papua New Guinea?

J. Dressman, R. Jähnke, A. Nair, 2011, Journal of pharmaceutical sciences.

Biowaiver monograph for immediate-release solid oral dosage forms: fluconazole.

Naseem A. Charoo, J. Polli, V. Shah, 2014, Journal of pharmaceutical sciences.

Effect of size and density on canine gastric emptying of nondigestible solids.

G. Amidon, J. Meyer, J. Dressman, 1985, Gastroenterology.

Mechanism of Acyclovir Uptake in Rat Jejunum

J. Dressman, Kem C. Meadows, 1990, Pharmaceutical Research.

Applications of Physiologically Based Biopharmaceutics Modeling (PBBM) to support Drug Product Quality: A Workshop Summary Report.

Gustavo Mendes Lima Santos, J. Dressman, A. Babiskin, 2020, Journal of pharmaceutical sciences.

Meeting report: International workshop on implementation of biowaivers based on the biopharmaceutics classification system (BCS)

J. Polli, V. Shah, J. Dressman, 2015 .

Review of global regulations concerning biowaivers for immediate release solid oral dosage forms.

D. Barends, R. A. Lipper, V. Shah, 2006, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Differences in drug quality between South Africa and Germany

J. Dressman, A. Lehmann, Martin Hofsäß, 2018, The Journal of pharmacy and pharmacology.

Biowaiver Monographs for Immediate Release Solid Oral Dosage Forms: Levetiracetam.

J. Polli, V. Shah, J. Dressman, 2015, Journal of pharmaceutical sciences.

Comparison of WHO and US FDA biowaiver dissolution test conditions using bioequivalent doxycycline hyclate drug products

J. Dressman, E. Jantratid, S. Strauch, 2009 .

SOME DETERMINANTS OF MORPHOLOGY AND RELEASE RATE FROM POLY(L)LACTIC ACID MICROSPHERES

J. Dressman, A. Kishida, S. Yoshioka, 1990 .

Absorption of Flurbiprofen in the Fed and Fasted States

J. Wagner, J. Dressman, G. Elta, 1992, Pharmaceutical Research.

Modification of gastric pH in the fasted dog

J. Dressman, B. Abrahamsson, Britta I. Polentarutti, 2010, The Journal of pharmacy and pharmacology.

A new 5-aminosalicylic acid multi-unit dosage form for the therapy of ulcerative colitis.

J. Dressman, H. Petereit, T. Beckert, 2001, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Effects of viscosity and fluid outflow on postcibal gastric emptying of solids.

J. Elashoff, G. Amidon, J. Meyer, 1986, The American journal of physiology.

Biorelevant two-stage in vitro testing for rDCS classification and in PBPK modelling - Case example ritonavir.

J. Dressman, S. Arora, P. Augustijns, 2020, Journal of pharmaceutical sciences.

Prediction of oral absorption of cinnarizine--a highly supersaturating poorly soluble weak base with borderline permeability.

J. Dressman, W. Baumann, M. Berlin, 2014, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Current State and Future Expectations of Translational Modeling Strategies to Support Drug Product Development, Manufacturing Changes and Controls: A Workshop Summary Report.

Amitava Mitra, Sandra Suarez-Sharp, Andrew Babiskin, 2020, Journal of pharmaceutical sciences.

Gastrointestinal parameters that influence oral medications.

W. Ritschel, J. Dressman, E. Ziv, 1993, Journal of pharmaceutical sciences.

Improving drug solubility for oral delivery using solid dispersions.

J Dressman, J. Dressman, C Leuner, 2000, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Biowaiver monographs for immediate-release solid oral dosage forms: Zidovudine (azidothymidine).

K. C. Soares, J. Polli, V. Shah, 2013, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: ibuprofen.

D. Barends, H. Junginger, K. Midha, 2005, Journal of pharmaceutical sciences.

Trends in active pharmaceutical ingredient salt selection based on analysis of the Orange Book database.

Jennifer B Dressman, Christoph Saal, J. Dressman, 2007, Journal of medicinal chemistry.

A comparative analysis of biopharmaceutics classification system and biopharmaceutics drug disposition classification system: a cross-sectional survey with 500 bioequivalence studies.

Chang Chiann, J. Dressman, Rodrigo Cristofoletti, 2013, Journal of pharmaceutical sciences.

Dissolution enhancement of fenofibrate by micronization, cogrinding and spray-drying: comparison with commercial preparations.

Jennifer B Dressman, J. Dressman, K. Kunath, 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Site‐specific delivery of anti‐inflammatory drugs in the gastrointestinal tract: an in‐vitro release model

Jennifer Dressman, J. Dressman, S. Klein, 2005, The Journal of pharmacy and pharmacology.

Biowaiver monographs for immediate release solid oral dosage forms: levofloxacin.

D. Barends, H. Junginger, S. Stavchansky, 2011, Journal of pharmaceutical sciences.

Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract.

J. Dressman, J B Dressman, D. Hörter, 1997, Advanced drug delivery reviews.

In vitro tools for evaluating novel dosage forms of poorly soluble, weakly basic drugs: case example ketoconazole.

J. Dressman, S. Klein, Thomas Taupitz, 2013, Journal of pharmaceutical sciences.

Dissolution improvement of four poorly water soluble drugs by cogrinding with commonly used excipients.

Jennifer B Dressman, J. Dressman, K. Kunath, 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Biorelevant dissolution testing of St John's wort products

J. Dressman, M. Schubert-Zsilavecz, M. Wurglics, 2002, The Journal of pharmacy and pharmacology.

Forecasting the Oral Absorption Behavior of Poorly Soluble Weak Bases Using Solubility and Dissolution Studies in Biorelevant Media

J. Dressman, E. Kostewicz, U. Brauns, 2002, Pharmaceutical Research.

Biorelevant Dissolution Testing to Predict the Plasma Profile of Lipophilic Drugs After Oral Administration

Christos Reppas, J. Dressman, C. Reppas, 2001, Pharmaceutical Research.

Forecasting the In Vivo Performance of Four Low Solubility Drugs from Their In Vitro Dissolution Data

Christos Reppas, J. Dressman, C. Reppas, 1999, Pharmaceutical Research.

Dissolution Testing as a Prognostic Tool for Oral Drug Absorption: Immediate Release Dosage Forms

Christos Reppas, Vinod P. Shah, Gordon L. Amidon, 2004, Pharmaceutical Research.

Assessment of Bioequivalence of Weak Base Formulations Under Various Dosing Conditions Using Physiologically Based Pharmacokinetic Simulations in Virtual Populations. Case Examples: Ketoconazole and Posaconazole.

N. Patel, J. Dressman, Rodrigo Cristofoletti, 2017, Journal of pharmaceutical sciences.

Physiochemical and physiological mechanisms for the effects of food on drug absorption: the role of lipids and pH.

J. Dressman, C. Porter, W. Charman, 1997, Journal of pharmaceutical sciences.

Risk assessment for extending the Biopharmaceutics Classification System‐based biowaiver of immediate release dosage forms of fluconazole in adults to the paediatric population

Naseem A. Charoo, J. Dressman, Rodrigo Cristofoletti, 2015, The Journal of pharmacy and pharmacology.

Thermal Properties of Hot-Stage Extrudates of Itraconazole and Eudragit E100. Phase separation and polymorphism

J. Dressman, G. Verreck, P. Augustijns, 2002 .

Upper Gastrointestinal pH in Seventy-Nine Healthy, Elderly, North American Men and Women

J. Dressman, J. Barnett, R. Berardi, 1993, Pharmaceutical Research.

Animal models for oral drug absorption

J. Dressman, J. B. Dressman, K. Yamada, 1991 .

Biowaiver Monographs for Immediate Release Solid Oral Dosage Forms: Ribavirin

J. Polli, V. Shah, J. Dressman, 2016, Journal of Pharmaceutical Sciences.

Sustained-release hot melt extrudates of the weak acid TMP-001: A case study using PBB modelling.

J. Dressman, M. Schmidt, E. Alig, 2021, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Analysis of the enhanced oral bioavailability of fenofibrate lipid formulations in fasted humans using an in vitro-in silico-in vivo approach.

Jennifer B Dressman, Edmund S Kostewicz, J. Dressman, 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Biowaiver monographs for immediate release solid oral dosage forms: efavirenz.

J. Polli, V. Shah, J. Dressman, 2013, Journal of pharmaceutical sciences.

Biowaiver Monographs for Immediate Release Solid Oral Dosage Forms: Cephalexin Monohydrate.

J. Polli, A. Parr, V. Shah, 2020, Journal of pharmaceutical sciences.

J. Wagner, J. Dressman, J. Barnett, 2004, Pharmaceutical Research.

Dissolution media simulating the intralumenal composition of the small intestine: physiological issues and practical aspects

Christos Reppas, Erika S. Stippler, Christian Leuner, 2004, The Journal of pharmacy and pharmacology.

Introduction to the OrBiTo decision tree to select the most appropriate in vitro methodology for release testing of solid oral dosage forms during development.

B Abrahamsson, P Augustijns, J Dressman, 2018, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Gastric juice as a dissolution medium: Surface tension and pH

J. Dressman, M. Efentakis, 1998, European Journal of Drug Metabolism and Pharmacokinetics.

PBPK models for the prediction of in vivo performance of oral dosage forms.

Martin Bergstrand, Xavier Pepin, Erik Sjögren, 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

In vitro biorelevant models for evaluating modified release mesalamine products to forecast the effect of formulation and meal intake on drug release.

J. Dressman, C. Reppas, C. Markopoulos, 2015, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Application of biorelevant dissolution tests to the prediction of in vivo performance of diclofenac sodium from an oral modified-release pellet dosage form.

Jennifer B Dressman, J. Dressman, M. Vertzoni, 2009, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Dissolution Methods to Increasing Discriminatory Power of In Vitro Dissolution Testing for Ibuprofen Free Acid and Its Salts.

J. Dressman, Rodrigo Cristofoletti, 2017, Journal of pharmaceutical sciences.

Dissolution Testing as a Prognostic Tool for Oral Drug Absorption: Dissolution Behavior of Glibenclamide

Raimar Löbenberg, Vinod P. Shah, Johannes Krämer, 2000, Pharmaceutical Research.

Biorelevant Dissolution Media Simulating the Proximal Human Gastrointestinal Tract: An Update

J. Dressman, E. Jantratid, Ekarat Jantratid, 2009 .

Comparison of Drug Release From Metoprolol Modified Release Dosage Forms in Single Buffer versus a pH-Gradient Dissolution Test

J. Dressman, S. Klein, Jennifer B. Dressman, 2006 .

Biowaiver monographs for immediate release solid oral dosage forms: acetazolamide.

D. Barends, H. Junginger, S. Stavchansky, 2008, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: isoniazid.

D. Barends, G. Amidon, H. Junginger, 2007, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: diclofenac sodium and diclofenac potassium.

D. Barends, J. Polli, G. Amidon, 2009, Journal of pharmaceutical sciences.

A comparative study of different release apparatus in generating in vitro-in vivo correlations for extended release formulations.

J Dressman, C Reppas, N Fotaki, 2009, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Biowaiver monographs for immediate release solid oral dosage forms: aciclovir.

D. Barends, G. Amidon, M. Bermejo, 2008, Journal of pharmaceutical sciences.

Development, current applications and future roles of biorelevant two‐stage in vitro testing in drug development

Jennifer Dressman, Tom Fiolka, J. Dressman, 2018, The Journal of pharmacy and pharmacology.

Drug solubility: how to measure it, how to improve it☆

J. Dressman, C. Reppas, 2007 .

Biowaiver monographs for immediate release solid oral dosage forms: ciprofloxacin hydrochloride.

D. Barends, H. Junginger, S. Stavchansky, 2011, Journal of pharmaceutical sciences.

Can the USP paddle method be used to represent in‐vivo hydrodynamics?

Bertil Abrahamsson, Jennifer B Dressman, Edmund Kostewicz, 2003, The Journal of pharmacy and pharmacology.

MECHANISM OF RELEASE FROM PELLETS COATED WITH AN ETHYLCELLULOSE-BASED FILM

B. Palsson, J. Dressman, S. Ozturk, 1990 .

An update on computational oral absorption simulation

Stefan Willmann, Jennifer B Dressman, Kirstin Thelen, 2011, Expert opinion on drug metabolism & toxicology.

Biowaiver Monographs for Immediate-Release Solid Oral Dosage Forms: Folic Acid.

J. Polli, A. Parr, V. Shah, 2017, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: quinidine sulfate.

D. Barends, J. Polli, H. Junginger, 2009, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: quinidine sulfate.

D. Barends, H. Junginger, S. Stavchansky, 2009, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: acetaminophen (paracetamol).

D. Barends, G. Amidon, H. Junginger, 2006, Journal of pharmaceutical sciences.

The impact of food intake on the luminal environment and performance of oral drug products with a view to in vitro and in silico simulations: a PEARRL review

J. Dressman, C. Reppas, M. Vertzoni, 2018, The Journal of pharmacy and pharmacology.

Pharmaceutics, Drug Delivery and Pharmaceutical Technology Dissolution Methods to Increasing Discriminatory Power of In Vitro Dissolution Testing for Ibuprofen Free Acid and Its Salts

J. Dressman, Rodrigo Cristofoletti, 2017 .

Is bicarbonate buffer suitable as a dissolution medium?

J. Dressman, J. Boni, R. Brickl, 2007, The Journal of pharmacy and pharmacology.

Biowaiver monographs for immediate release solid oral dosage forms: metronidazole.

D. Barends, H. Junginger, S. Stavchansky, 2011, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: lamivudine.

D. Barends, H. Junginger, S. Stavchansky, 2011, Journal of pharmaceutical sciences.

Human postprandial gastric emptying of 1-3-millimeter spheres.

J. Elashoff, G. Amidon, J. Meyer, 1988, Gastroenterology.

The delayed dissolution of paracetamol products in the canine fed stomach can be predicted in vitro but it does not affect the onset of plasma levels.

J. Dressman, B. Abrahamsson, L. Kalantzi, 2005, International journal of pharmaceutics.

Biowaiver monographs for immediate release solid oral dosage forms: pyrazinamide.

D. Barends, G. Amidon, H. Junginger, 2008, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate-release solid oral dosage forms: stavudine.

D. Barends, H. Junginger, S. Stavchansky, 2012, Journal of pharmaceutical sciences.

In‐vitro–in‐silico investigation of the negative food effect of zolpidem when administered as immediate‐release tablets

J. Dressman, D. Turner, C. J. Andreas, 2019, The Journal of pharmacy and pharmacology.

Physicochemical model for dose-dependent drug absorption.

G. Amidon, J. Dressman, D. Fleisher, 1984, Journal of pharmaceutical sciences.

Intestinal Uptake of Cimetidine and Ranitidine in Rats

J. Dressman, V. Mummaneni, 1994, Pharmaceutical Research.

In vitro models for the prediction of in vivo performance of oral dosage forms: Recent progress from partnership through the IMI OrBiTo collaboration

Anette Müllertz, Filippos Kesisoglou, Christos Reppas, 2019, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Oral biopharmaceutics tools: recent progress from partnership through the Pharmaceutical Education and Research with Regulatory Links collaboration.

B. Griffin, J. Dressman, C. Reppas, 2021, The Journal of pharmacy and pharmacology.

Prediction of in‐vivo pharmacokinetic profile for immediate and modified release oral dosage forms of furosemide using an in‐vitro–in‐silico–in‐vivo approach

Arzu Selen, Christian Wagner, Jennifer Dressman, 2015, The Journal of pharmacy and pharmacology.

Biowaiver monographs for immediate release solid oral dosage forms: rifampicin.

D. Barends, H. Junginger, S. Stavchansky, 2009, Journal of pharmaceutical sciences.

Solubilization and Wetting Effects of Bile Salts on the Dissolution of Steroids

J. Dressman, V. Bakatselou, R. C. Oppenheim, 1991, Pharmaceutical Research.

Unusual solubility behaviour of cyclosporin A in aqueous media

J. Dressman, C. Reppas, P. Macheras, 1991, The Journal of pharmacy and pharmacology.

Impact of acid-reducing agents on gastrointestinal physiology and design of biorelevant dissolution tests to reflect these changes.

J. Dressman, D. Carlile, Eva M. Karlsson, 2019, Journal of pharmaceutical sciences.

Gastric emptying of nondigestible solids in dogs: a hydrodynamic correlation.

G. Amidon, J. Meyer, J. Dressman, 1990, The American journal of physiology.

In-vitro simulation of luminal conditions for evaluation of performance of oral drug products: Choosing the appropriate test media.

Christos Reppas, Jennifer Dressman, J. Dressman, 2015, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Establishing virtual bioequivalence and clinically relevant specifications using in vitro biorelevant dissolution testing and physiologically-based population pharmacokinetic modeling. Case example: Naproxen.

Rodrigo Cristofoletti, David B Turner, Nikoletta Fotaki, 2019, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Approaches to increase mechanistic understanding and aid in the selection of precipitation inhibitors for supersaturating formulations – a PEARRL review

Martin Kuentz, René Holm, Jennifer B Dressman, 2019, The Journal of pharmacy and pharmacology.

Biowaiver monographs for immediate release solid oral dosage forms: mefloquine hydrochloride.

D. Barends, J. Polli, H. Junginger, 2011, Journal of pharmaceutical sciences.

Cytochrome P450‐mediated metabolism in the human gut wall

J. Dressman, K. Thelen, Kirstin Thelen, 2009 .

Cytochrome P450-mediated metabolism in the human gut wall.

J. Dressman, K. Thelen, 2009, The Journal of pharmacy and pharmacology.

Comparison of Canine and Human Gastrointestinal Physiology

J. Dressman, Jennifer B. Dressman, 1986, Pharmaceutical Research.

Biowaiver Monographs for Immediate Release Solid Oral Dosage Forms: Proguanil Hydrochloride.

J. Polli, A. Parr, V. Shah, 2018, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate-release solid oral dosage forms: primaquine phosphate.

D. Barends, J. Polli, V. Shah, 2012, Journal of pharmaceutical sciences.

Human Postprandial Gastric l-3-Millimeter Spheres Emptying of

J. Elashoff, G. Amidon, J. Dressman, 1988 .

Predicting the Changes in Oral Absorption of Weak Base Drugs Under Elevated Gastric pH Using an In Vitro-In Silico-In Vivo Approach: Case Examples-Dipyridamole, Prasugrel, and Nelfinavir.

J. Dressman, A. Kambayashi, 2019, Journal of pharmaceutical sciences.

Coupling biorelevant dissolution methods with physiologically based pharmacokinetic modelling to forecast in‐vivo performance of solid oral dosage forms

Jennifer Dressman, J. Dressman, Yasushi Shono, 2013, The Journal of pharmacy and pharmacology.

Drug Release Characteristics of Different Mesalazine Products Using USP Apparatus 3 to Simulate Passage Through the GI Tract

J. Dressman, M. Rudolph, S. Klein, 2002 .

Biowaiver monographs for immediate-release solid oral dosage forms: ketoprofen.

D. Barends, J. Polli, V. Shah, 2012, Journal of pharmaceutical sciences.

PBPK modeling coupled with biorelevant dissolution to forecast the oral performance of amorphous solid dispersion formulations.

J. Dressman, A. Kambayashi, Tsuyoshi Kiyota, 2019, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Forecasting gastrointestinal precipitation and oral pharmacokinetics of dantrolene in dogs using an in vitro precipitation testing coupled with in silico modeling and simulation

J. Dressman, A. Kambayashi, 2017, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Understanding the in vivo performance of enteric coated tablets using an in vitro-in silico-in vivo approach: case example diclofenac.

Atsushi Kambayashi, Jennifer Dressman, J. Dressman, 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

An in vitro-in silico-in vivo approach to predicting the oral pharmacokinetic profile of salts of weak acids: case example dantrolene.

J. Dressman, A. Kambayashi, 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Prediction of the precipitation profiles of weak base drugs in the small intestine using a simplified transfer ("dumping") model coupled with in silico modeling and simulation approach.

Atsushi Kambayashi, Jennifer B Dressman, J. Dressman, 2016, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Advances and challenges in PBPK modeling--Analysis of factors contributing to the oral absorption of atazanavir, a poorly soluble weak base.

Wei Xu, Filippos Kesisoglou, Jennifer B Dressman, 2015, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Precipitation in the small intestine may play a more important role in the in vivo performance of poorly soluble weak bases in the fasted state: case example nelfinavir.

Jennifer B Dressman, J. Dressman, E. Jantratid, 2011, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

In vitro methods to assess drug precipitation in the fasted small intestine – a PEARRL review

Martin Kuentz, Christos Reppas, Jennifer B Dressman, 2018, The Journal of pharmacy and pharmacology.

Study of a Standardized Taurocholate- Lecithin Powder for Preparing the Biorelevant Media FeSSIF and FaSSIF

Martin Kuentz, J. Dressman, M. Kuentz, 2010 .

Development of Dissolution Tests on the Basis of Gastrointestinal Physiology

Erika S. Stippler, Erika Stippler, J. Dressman, 2005 .

Calculation of drug‐polymer mixing enthalpy as a new screening method of precipitation inhibitors for supersaturating pharmaceutical formulations

Daniel J. Price, J. Dressman, M. Kuentz, 2019, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Albendazole Generics—A Comparative In Vitro Study

J. Dressman, J. Horton, E. Galia, 1999, Pharmaceutical Research.

The biopharmaceutics risk assessment roadmap for optimizing clinical drug product performance.

Anette Müllertz, Arzu Selen, Hans Lennernäs, 2014, Journal of pharmaceutical sciences.

Prediction of food effects on the absorption of celecoxib based on biorelevant dissolution testing coupled with physiologically based pharmacokinetic modeling.

Filippos Kesisoglou, Christos Reppas, Jennifer B Dressman, 2009, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Release of phenylpropanolamine HCI from ethylcellulose-coated pellets in biorelevant media

J. Dressman, N. Fotaki, C. Reppas, 2001 .

Biowaiver monographs for immediate release solid oral dosage forms: ranitidine hydrochloride.

D M Barends, H E Junginger, D. Barends, 2005, Journal of pharmaceutical sciences.

Solubility of Mefenamic Acid Under Simulated Fed- and Fasted-State Conditions

J. Dressman, V. Bakatselou, C. Tenhoor, 1991, Pharmaceutical Research.

Mechanisms of release from coated pellets

B. Palsson, J. Dressman, S. Ozturk, 1994 .

Biowaiver monograph for immediate-release solid oral dosage forms: bisoprolol fumarate.

Naseem A. Charoo, J. Polli, V. Shah, 2014, Journal of pharmaceutical sciences.

Combining biorelevant in vitro and in silico tools to simulate and better understand the in vivo performance of a nano-sized formulation of aprepitant in the fasted and fed states.

N. Patel, J. Dressman, M. Kuentz, 2019, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Biowaiver monographs for immediate release solid oral dosage forms: ethambutol dihydrochloride.

D. Barends, G. Amidon, H. Junginger, 2008, Journal of pharmaceutical sciences.

Past, Present, and Future of Bioequivalence: Improving Assessment and Extrapolation of Therapeutic Equivalence for Oral Drug Products.

Malcolm Rowland, Rodrigo Cristofoletti, Amin Rostami-Hodjegan, 2018, Journal of pharmaceutical sciences.

Matching phosphate and maleate buffer systems for dissolution of weak acids: Equivalence in terms of buffer capacity of bulk solution or surface pH?

J. Dressman, Rodrigo Cristofoletti, 2016, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Characterization of the Contents of Ascending Colon to Which Drugs are Exposed After Oral Administration to Healthy Adults

Christos Reppas, Bertil Abrahamsson, Jennifer Dressman, 2009, Pharmaceutical Research.

Characterization of a new solvate of risedronate.

J. Dressman, M. Schmidt, E. Alig, 2011, Journal of pharmaceutical sciences.

Analytical methods for dissolution testing of nanosized drugs

J. Dressman, D. Juenemann, 2012, The Journal of pharmacy and pharmacology.

Convenient and rapid determination of cimetidine in human plasma using perchloric acid-mediated plasma protein precipitation and high-performance liquid chromatography.

J. Dressman, J. Foley, E. Jantratid, 2007, Biomedical chromatography : BMC.

Enteric coated aspirin circumventing gastric retention.

G. Amidon, J. Dressman, 1985, The Journal of rheumatology.

Prediction of plasma profiles of a weakly basic drug after administration of omeprazole using PBPK modeling.

J. Dressman, Eva M. Karlsson, J. Mann, 2020, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Oral absorption of peptides and proteins

J. Dressman, C. Tenhoor, 1992 .

Biowaiver Monographs for Immediate-Release Solid Oral Dosage Forms: Enalapril.

J. Polli, R. Löbenberg, I. Kanfer, 2017, Journal of pharmaceutical sciences.

Biowaiver Monographs for Immediate Release Solid Oral Dosage Forms: Metformin Hydrochloride.

J. Polli, A. Parr, V. Shah, 2021, Journal of pharmaceutical sciences.

Use of the BioDis to generate a physiologically relevant IVIVC.

Jennifer B Dressman, Hans-Ulrich Petereit, J. Dressman, 2008, Journal of controlled release : official journal of the Controlled Release Society.

Oral biopharmaceutics tools - time for a new initiative - an introduction to the IMI project OrBiTo.

H Lennernäs, A Lindahl, B Abrahamsson, 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

The dispersion releaser technology is an effective method for testing drug release from nanosized drug carriers

J. Dressman, W. Mäntele, M. Wacker, 2017, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Biowaiver Monograph for Immediate-Release Solid Oral Dosage Forms: Amoxicillin Trihydrate.

J. Polli, A. Parr, V. Shah, 2017, Journal of pharmaceutical sciences.

Prediction of blood-brain barrier penetration of poorly soluble drug candidates using surface activity profiling.

J. Dressman, M. Brewster, J. Mensch, 2010, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Biowaiver Monographs for Immediate-Release Solid Oral Dosage Forms: Nifedipine.

J. Polli, V. Shah, J. Dressman, 2015, Journal of pharmaceutical sciences.

Biowaiver Monograph for Immediate-Release Solid Oral Dosage Forms: Ondansetron.

J. Polli, A. Parr, V. Shah, 2019, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: metoclopramide hydrochloride.

D. Barends, H. Junginger, S. Stavchansky, 2008, Journal of pharmaceutical sciences.

A Refined Developability Classification System.

Jennifer Dressman, Julian Rosenberger, James Butler, 2018, Journal of pharmaceutical sciences.

Advances in the design of fasted state simulating intestinal fluids: FaSSIF-V3.

J. Dressman, A. Fuchs, Alexander Fuchs, 2015, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Dissolution of steroids in bile salt solutions is modified by the presence of lecithin

N. Weiner, J. Dressman, N. Rodríguez-Hornedo, 1995 .

Biowaiver monographs for immediate release solid oral dosage forms: prednisone.

D. Barends, H. Junginger, S. Stavchansky, 2007, Journal of pharmaceutical sciences.

Solubility Determination of Active Pharmaceutical Ingredients Which Have Been Recently Added to the List of Essential Medicines in the Context of the Biopharmaceutics Classification System-Biowaiver.

J. Dressman, Martin Hofsäß, G. Plöger, 2018, Journal of pharmaceutical sciences.

The Discriminatory Power of the BCS-Based Biowaiver: A Retrospective With Focus on Essential Medicines.

Jennifer B Dressman, Martin A Hofsäss, J. Dressman, 2019, Journal of pharmaceutical sciences.

Use of 1-Methyl-Pyrrolidone as a Solubilizing Agent for Determining the Uptake of Poorly Soluble Drugs

J. Dressman, U. Hesse, Antje S. Uch, 1999, Pharmaceutical Research.

Incorporation of HPMCAS during loading of glibenclamide onto mesoporous silica improves dissolution and inhibits precipitation.

Daniel J. Price, J. Dressman, M. Kuentz, 2019, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Biowaiver Monograph for Immediate-Release Solid Oral Dosage Forms: Levocetirizine dihydrochloride.

Naseem A. Charoo, J. Polli, A. Parr, 2022, Journal of pharmaceutical sciences.

Comparison of the Mechanism of Dissolution of Hydrocortisone in Simple and Mixed Micelle Systems

J. Dressman, V. Bakatselou, L. J. Naylor, 1993, Pharmaceutical Research.

Measuring pH and Buffer Capacity in Fluids Aspirated from the Fasted Upper Gastrointestinal Tract of Healthy Adults

J. Dressman, C. Reppas, M. Vertzoni, 2020, Pharmaceutical Research.

Designing biorelevant dissolution tests for lipid formulations: case example--lipid suspension of RZ-50.

Jennifer B Dressman, Hitesh Chokshi, J. Dressman, 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Biorelevant dissolution testing of a weak base: Interlaboratory reproducibility and investigation of parameters controlling in vitro precipitation.

J. Dressman, P. Augustijns, J. Butler, 2019, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Dissolution behavior of various drugs in different FaSSIF versions.

J. Dressman, M. Leigh, L. Klumpp, 2019, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Stability of Biorelevant Media Under Various Storage Conditions

Jennifer Dressman, J. Dressman, A. Seybert, 2019, Dissolution Technologies.

Validation of Dissolution Testing with Biorelevant Media: An OrBiTo Study.

Patrick Augustijns, René Holm, Paul Hutchins, 2017, Molecular pharmaceutics.

In Vitro–In Silico Tools to Predict Pharmacokinetics of Poorly Soluble Drug Compounds

J. Dressman, C. Wagner, 2014 .

Development of an in vitro/in vivo correlation for lipid formulations of EMD 50733, a poorly soluble, lipophilic drug substance.

J. Dressman, Sven Schreder, Karen Schamp, 2006, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

New media discriminate dissolution properties of poorly soluble drugs

J. Dressman, C. Reppas, E. Galia, 1996 .

Application of a Refined Developability Classification System.

Jennifer Dressman, Julian Rosenberger, James Butler, 2019, Journal of pharmaceutical sciences.

The use of PBPK/PD to establish clinically relevant dissolution specifications for zolpidem immediate release tablets.

J. Dressman, N. Fotaki, M. McAllister, 2020, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Biowaiver monographs for immediate release solid oral dosage forms: mefloquine hydrochloride.

D. Barends, H. Junginger, S. Stavchansky, 2011, Journal of pharmaceutical sciences.

The biowaiver procedure: its application to antituberculosis products in the WHO prequalification programme.

J. Dressman, M. Stahl, E. Jantratid, 2011, Journal of pharmaceutical sciences.

Comparison of WHO and US FDA biowaiver dissolution test conditions using bioequivalent doxycycline hyclate drug products.

J. Dressman, E. Jantratid, S. Strauch, 2009, The Journal of pharmacy and pharmacology.

Biowaiver monographs for immediate release solid oral dosage forms: cimetidine.

D. Barends, G. Amidon, H. Junginger, 2006, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: amitriptyline hydrochloride.

D. Barends, G. Amidon, V. Shah, 2006, Journal of pharmaceutical sciences.

Feasibility of Biowaiver Extension to Biopharmaceutics Classification System Class III Drug Products

Jennifer B Dressman, Gordon L Amidon, G. Amidon, 2006, Clinical Pharmacokinetics.

Dissolution: a Continuing Perspective

V. Shah, J. Dressman, T. Foster, 2004 .

Towards Quantitative Prediction of Oral Drug Absorption

J. Dressman, E. Jantratid, K. Thelen, 2008, Clinical pharmacokinetics.

Gastric pH Influences the Appearance of Double Peaks in the Plasma Concentration-Time Profiles of Cimetidine After Oral Administration in Dogs

Gordon L. Amidon, G. Amidon, J. Dressman, 1995, Pharmaceutical Research.

flP Guidelines for Dissolution Testing of Solid Oral Products Joint Report of the Section for O"icial laboratories and Medicines Control Services and the Section of Industrial Pharmacists of the FIP

L. Lesko, V. Shah, J. Dressman, 1997 .

Suitability of the z-Factor for Dissolution Simulation of Solid Oral Dosage Forms: Potential Pitfalls and Refinements.

J. Dressman, Martin Hofsäß, 2020, Journal of pharmaceutical sciences.

Evaluation of Differences in Dosage Form Performance of Generics using BCS-Based Biowavier Specifications and Biopharmaceutical Modeling - Case Examples Amoxicillin and Doxycycline.

J. Dressman, Martin Hofsäß, 2020, Journal of pharmaceutical sciences.

Characteristics of contents in the upper gastrointestinal lumen after a standard high-calorie high-fat meal and implications for the in vitro drug product performance testing conditions.

J. Dressman, K. Goumas, C. Reppas, 2020, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

In Vitro Biopredictive Methods: A Workshop Summary Report.

Amitava Mitra, Sandra Suarez-Sharp, Erik Sjögren, 2020, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: piroxicam.

D. Barends, J. Polli, V. Shah, 2014, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: Doxycycline hyclate.

D. Barends, G. Amidon, H. Junginger, 2010, Journal of pharmaceutical sciences.

Mixing-tank model for predicting dissolution rate control or oral absorption.

J. Dressman, D. Fleisher, J B Dressman, 1986, Journal of pharmaceutical sciences.

Integrating drug- and formulation-related properties with gastrointestinal tract variability using a product-specific particle size approach: case example ibuprofen.

N. Patel, J. Dressman, B. Hens, 2019, Journal of pharmaceutical sciences.

Biorelevant in vitro tools and in silico modelling to assess pH-dependent drug-drug interactions for salts of weak acids: case example potassium raltegravir.

J. Dressman, Eva M. Karlsson, J. Mann, 2021, Journal of pharmaceutical sciences.

Evaluating the impact of acid-reducing agents on drug absorption using biorelevant in vitro tools and PBPK modeling - Case example dipyridamole.

J. Dressman, S. Arora, Ric Barker, 2021, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Biowaiver Monograph for Immediate-Release Solid Oral Dosage Forms: Carbamazepine.

J. Polli, A. Parr, V. Shah, 2021, Journal of pharmaceutical sciences.

Comment on "In Silico Modeling of Gastrointestinal Drug Absorption: Predictive Performance of Three Physiologically-Based Absorption Models".

N. Patel, M. Jamei, S. Polak, 2017, Molecular pharmaceutics.

An In Vitro Methodology for Forecasting Luminal Concentrations and Precipitation of Highly Permeable Lipophilic Weak Bases in the Fasted Upper Small Intestine

J. Dressman, C. Reppas, D. Busby, 2012, Pharmaceutical Research.

Influence of Hydrodynamics and Particle Size on the Absorption of Felodipine in Labradors

J. Dressman, A. Ungell, B. Abrahamsson, 2004, Pharmaceutical Research.

Mesoporous silica‐based dosage forms improve release characteristics of poorly soluble drugs: case example fenofibrate

J. Dressman, D. Lubda, E. Herbert, 2016, The Journal of pharmacy and pharmacology.

A simplified method to screen for in‐vivo performance of oral lipid formulations

Jennifer Dressman, J. Dressman, Murat Kilic, 2014, The Journal of pharmacy and pharmacology.

Biowaiver monographs for immediate-release solid oral dosage forms: codeine phosphate.

J. Polli, G. Amidon, V. Shah, 2014, Journal of pharmaceutical sciences.

Biowaiver monograph for immediate-release solid oral dosage forms: acetylsalicylic acid.

D. Barends, J. Polli, V. Shah, 2012, Journal of pharmaceutical sciences.

PQRI Workshop Report: Application of IVIVC in Formulation Development

Anthony J. DeStefano, Sandra Suarez-Sharp, Maziar Kakhi, 2014 .

Cogrinding enhances the oral bioavailability of EMD 57033, a poorly water soluble drug, in dogs.

J. Dressman, K. Kunath, C. Reppas, 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Estimate of Volume/Flow Ratio of Gastrointestinal (GI) Fluids in Humans Using Pharmacokinetic Data

J. Dressman, C. Reppas, P. Macheras, 1990, Pharmaceutical Research.

Particle diffusional layer thickness in a USP dissolution apparatus II: a combined function of particle size and paddle speed.

G. Amidon, J. Dressman, P. Sirois, 2008, Journal of pharmaceutical sciences.

Harmonization of regulatory approaches for evaluating therapeutic equivalence and interchangeability of multisource drug products: workshop summary report.

Lawrence X. Yu, V. Shah, J. Dressman, 2011, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

A novel in vivo predictive dissolution testing coupled with a modeling and simulation for hydrogel matrix monolithic extended release oral dosage forms.

J. Dressman, A. Kambayashi, 2019, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Salt screening and characterization for poorly soluble, weak basic compounds: case study albendazole.

J. Dressman, C. Saal, G. S. Paulekuhn, 2013, Die Pharmazie.

Physiologically Based Pharmacokinetic/Pharmacodynamic Modeling to Support Waivers of In Vivo Clinical Studies: Current Status, Challenges, and Opportunities.

J. Dressman, Ioannis Loisios-Konstantinidis, 2020, Molecular Pharmaceutics.

Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract.

J. Dressman, D. Hörter, 1997, Advanced drug delivery reviews.

Evaluation of Drug Adsorption to Membrane Filters under Biowaiver Test Conditions

J. Dressman, Kevin Kiehm, 2008 .

Harmonization of Regulatory Approaches for Evaluating Therapeutic Equivalence and Interchangeability of Multisource Drug Products: Workshop Summary Report

Lawrence X. Yu, J. Dressman, T. Hyslop, 2011, The AAPS Journal.

Dissolved Oxygen as a Measure for De- and Reaeration of Aqueous Media for Dissolution Testing

J. Dressman, S. Diebold, 1998 .

Drug Quality in South Africa: A Field Test.

J. Dressman, A. Lehmann, D. Katerere, 2018, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate-release solid oral dosage forms: quinine sulfate.

D. Barends, J. Polli, V. Shah, 2012, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: amodiaquine hydrochloride.

D. Barends, J. Polli, V. Shah, 2012, Journal of pharmaceutical sciences.

Estimating drug solubility in the gastrointestinal tract.

J. Dressman, K. Goumas, C. Reppas, 2007, Advanced drug delivery reviews.

Early pharmaceutical profiling to predict oral drug absorption: current status and unmet needs.

Christel A. S. Bergström, Kung-I Feng, P. Artursson, 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Dissolution media simulating the proximal canine gastrointestinal tract in the fasted state.

J. Dressman, C. Reppas, N. Parrott, 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Modification of gastric pH in the fasted dog

J. Dressman, B. Abrahamsson, Britta I. Polentarutti, 2010, The Journal of pharmacy and pharmacology.

Effect of hydroxypropylmethylcellulose on gastrointestinal transit and luminal viscosity in dogs.

J. Meyer, J. Dressman, P. Sirois, 1991, Gastroenterology.

Lipid‐Based Oral Formulations

J. Dressman, C. Reppas, M. Kilic, 2019, In Vitro Drug Release Testing of Special Dosage Forms.

Intestinal Permeability: Prediction from Theory

Hans Lennernäs, H. Lennernäs, J. Dressman, 2000 .

Advances in the design of fasted state simulating intestinal fluids: FaSSIF-V3.

J. Dressman, A. Fuchs, M. Leigh, 2015, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Application of biorelevant dissolution tests to the prediction of in vivo performance of diclofenac sodium from an oral modified-release pellet dosage form.

J. Dressman, M. Vertzoni, Vincenzo De Maio, 2009, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Biowaiver monographs for immediate release solid oral dosage forms: ciprofloxacin hydrochloride.

D. Barends, H. Junginger, S. Stavchansky, 2011, Journal of pharmaceutical sciences.

Mesoporous silica‐based dosage forms improve release characteristics of poorly soluble drugs: case example fenofibrate

J. Dressman, D. Lubda, C. Saal, 2016, The Journal of pharmacy and pharmacology.

Prediction of oral absorption of cinnarizine--a highly supersaturating poorly soluble weak base with borderline permeability.

J. Dressman, W. Baumann, M. Berlin, 2014, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

J. Dressman, A. Kambayashi, H. Blume, 2014, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Estimation of intragastric drug solubility in the fed state: comparison of various media with data in aspirates

J. Dressman, C. Reppas, M. Vertzoni, 2009, Biopharmaceutics & drug disposition.

Effect of elevated viscosity in the upper gastrointestinal tract on drug absorption in dogs.

J. Dressman, C. Reppas, J. Dressman, 1998, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Biowaiver monographs for immediate release solid oral dosage forms: acetaminophen (paracetamol).

D. Barends, G. Amidon, H. Junginger, 2006, Journal of pharmaceutical sciences.

The effect of HPMC—a cholesterol‐lowering agent—on oral drug absorption in dogs

J. Dressman, C. Reppas, Moira Symillides, 1998, Biopharmaceutics & drug disposition.

Validation of Dissolution Testing with Biorelevant Media: An OrBiTo Study.

J. Dressman, P. Augustijns, R. Holm, 2017, Molecular pharmaceutics.

Application of a ternary HP-β-CD-complex approach to improve the dissolution performance of a poorly soluble weak acid under biorelevant conditions.

J. Dressman, T. Zoeller, S. Klein, 2012, International journal of pharmaceutics.

Biowaiver Monographs for Immediate-Release Solid Oral Dosage Forms: Folic Acid.

J. Polli, A. Parr, V. Shah, 2017, Journal of pharmaceutical sciences.

Colloidal carriers for controlled drug delivery and targeting: Modification, characterization and in vivo distribution : by Rainer H. Muller, Wissenschaftliche Verlagsgesellschaft, Stuttgart, Germany, 1991,227 figures, DM168

J. Dressman, 1992 .

Elevation of gastric pH with ranitidine does not affect the release characteristics of sustained release ibuprofen tablets

J. Dressman, G. Elta, R. Berardi, 1988, Biopharmaceutics & drug disposition.

Biowaiver monographs for immediate release solid oral dosage forms: isoniazid.

D. Barends, G. Amidon, H. Junginger, 2007, Journal of Pharmacy and Science.

A comparative analysis of biopharmaceutics classification system and biopharmaceutics drug disposition classification system: a cross-sectional survey with 500 bioequivalence studies.

Chang Chiann, J. Dressman, Rodrigo Cristofoletti, 2013, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: furosemide.

D. Barends, H. Junginger, S. Stavchansky, 2010, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: acetazolamide.

D. Barends, H. Junginger, S. Stavchansky, 2008, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: pyrazinamide.

D. Barends, H. Junginger, S. Stavchansky, 2008, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: amitriptyline hydrochloride.

D. Barends, J. Dressman, M. E. Olivera, 2006, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate release solid oral dosage forms: metronidazole.

D. Barends, H. Junginger, S. Stavchansky, 2011, Journal of pharmaceutical sciences.

Biowaiver monographs for immediate-release solid oral dosage forms: Zidovudine (azidothymidine).

K. C. Soares, J. Polli, V. Shah, 2013, Journal of pharmaceutical sciences.

Highlights from the 2020 AAPS 360 Annual Meeting

J. Dressman, N. Fotaki, Y. Tsume, 2021, Dissolution Technologies.

Surface Activity Profiling (SAP): A potential means of predicting intestinal membrane permeability.

J. Dressman, K. Schäfer, K. Schmid, 2019, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Dissolution/In Vitro Release Testing of Special Dosage Forms*

Cynthia K. Brown, Vinod P. Shah, V. Shah, 2002 .