Robert Taylor: Automated Measurements of Lipolysis, Supersaturation & Biphasic Dissolution

Surface dissolution imaging to investigate the influence of common ion effect on Papaverine hydrochloride

Interplay between Ketoconazole Cocrystal Supersaturation and Trans-membrane Flux Behavior In Simulated Intestinal Fluids

Application of In Situ Potentiometric Sensors to Study Dissolution-Precipitation Behavior of Electrospray-Generated Loperamide Nanoparticles

Cyclodextrin-Based Orally Fast Dissolving Drug Delivery System of Aripiprazole and Its In Vitro Dissolution-Permeation Testing Using µFLUX

Dissolution, Free Drug Concentration and Permeability of Crystalline Nanoparticle Formulation Study Using In Situ Fiber Optic and Potentiometric Techniques

Real Time Dissolution Monitoring of Dual Component Drug Product Using Fiber Optic System

MacroFLUX An Integration of Absorption Chamber with USP II Dissolution Apparatus

Dissolution Rate and Apparent Solubility of Poorly Soluble Compounds in Biorelevant Fluids

Universal Potentiometric Sensors Fast Determination of Free Ionized Drug Concentration in Micellar Solutions

Universal Potentiometric Sensors: Application for Real Time Concentration Monitoring in Surfactant Containing

Determination of the Intrinsic Dissolution Rate (IDR) from a Powder and using a Miniaturized Wood’s Apparatus

Penetration Enhancer Effect of Sucrose Esters

Prediction of Caco-2 pH-Dependent Permeability based on High Quality in vitro Training Set

Comparison of Miniaturized Intrinsic Dissolution Rate Measurement to Traditional Wood’s Apparatus

Novel in vitro PK (non-animal PK) Assay for Excipient/Vehicle Formulation Studies

Drug Permeation in Skin PAMPA and Franz Cell Model

In Situ Solubility and Dissolution of Concentrated Solutions

Powder Intrinsic Dissolution Rate Measurement: When is it Possible?

Prediction of in situ Blood-Brain Barrier Permeability using BBB PAMPA Model

Impact of Biorelevant Media on Apparent Solubility and Biopharmaceutical Classification of Poorly Soluble Compounds

Very Thin PAMPA Membranes Indicate Higher Antipyrene Permeability but are Fragile and Contain Leaky Water Pores

Nanoparticle Formulation of Gresiofulvin

Universal Potentiometric Sensors Protein Binding

In Vitro-In Vivo Correlation (IVIVC): Prediction of pK a at 37°C, From the Measured Value at 25°C

Human Jejunal Permeability Predicted from Caco-2 Assay - A Biophysical Model Applied to Fluoroquinolone Antimicrobials

Novel Device and Method for in situ UV Dissolution and Precipitation Monitoring in 96-well Plate

Evaluation of Optimized Caco-2 Permeability Measurements

Developing Skin PAMPA for Transdermal Patches

Supersaturation and Transmembrane Flux of Meloxicam

Universal Potentiometric Sensors Food Matrixes

Preparation, Physical Characterization and Solubility-Dissolution Testing of Loratidine Hot Melt Extrudates Prepared on a Laboratory Mixing Extruder

Evaluating Drug Salt Dissolution and Precipitation Processes for Rational Formulation Strategies

Skin-PAMPA: A New Method for Fast Prediction of Skin Penetration

Monitoring Supersaturation State of Solid Dispersions of Low Solubility Compounds

Skin-PAMPA: Fast Prediction of Skin Penetration

Comparison of Naproxen Release from Nano- and Microsuspensions with Its Dissolution from Untreated and Micronized Powder

Soluplus® Maintains the Supersaturation of Carbamazepine from Amorphous Solid Dispersions

In Situ Monitoring of Supersaturation State for Solid Dispersions of Low Soluble Compounds

Application of Skin PAMPA to Differentiate Between Topical Pharmaceutical Formulations of Ibuprofen

Dissolution and Precipitation Monitoring of Crystalline Salts

Assessment of Transdermal Penetration Enhancement by Topical Pharmaceutical Excipients Using Skin PAMPA Method

Universal Potentiometric Sensors: Application for Real Time Concentration Monitoring in Complex Biorelevant Media

Real Time Monitoring of Dissolution, Supersaturation and Precipitation Processes in Dynamically Changing Biorelevant Media

Dissolution-Permeability Apparatus with Integrated In Situ Concentration Monitoring of both Donor and Receiver Compartments

Novel HT Method for Parallel Excipient/Vehicle Formulation Studies

Using Skin PAMPA For Transdermal Patch Testing

In Situ Method for Monitoring Free Drug Concentration Released from Nanoparticles

Degree and Extent of Supersaturation of Amorphous Pharmaceuticals and Their Flux through Lipophilic Membranes

Progress in pKa Determination Technology: Case Studies in Low and High Soluble Flavonoids

Using flux experiments through artificial lipophilic membranes for predicting food effect for BCS Class 2 Compounds

Application of simultaneous dissolution-absorption apparatus for screening formulations before bioequivalence studies

Using Integrated Absorption Chamber with USP II Dissolution Apparatus to Predict Risk of Drug-Drug Interaction from pH Modifying Agents: Poster

Biorelevant drug release of Metformin dosage forms using complementary in vitro tools

Differentiating itraconazole formulations based on the flux through artificial lipophilic membranes

Utilization of pH-Metric Titration

Application of Skin Pampa to Cosmetic Solvent Screening

Karl Box Sunrise Presentation

Application of MacroFLUX™ Apparatus for Screening Formulations before Bioequivalent Studies

Supersaturation in additives and GI fluids

Determination of Polymer Effectiveness

In-situ Solubility Measurements of Ionizable Drugs

Determination of pKa values and Solubility pH Profiles of Selected ß blockers

Validation of titrimetric measurement of pKa, logP and solubility

Measuring the solubility of salts of basic drugs

The intrinsic solubility of indomethacin

A low volume method for screening Plasdone polymers

Determination of Aqueous Solubility by Extrapolation

Behavior of Basic Compounds in the Presence of Plasdone Polymers

Characteristics of Felodipine ‐ HPMCAS Solid Dispersions

Dissolution Performance of Inhaled Products in Simulated Lung Fluid

Automated Measurements of Precipitation, Supersaturation and Biphasic Dissolution

Biphasic dissolution studies of Aripiprazole

Biphasic dissolution studies: Impact of concentration and particle size on partition rate

Improvements in biphasic dissolution

Solubilities of morphine analogs

Solubility measurement by extrapolation

Simulated Lung Fluid media

Physicochemical Studies of Triclosan

Supersaturation & precipitation of ionizable drugs with cellulose polymers

Solubility of drugs in the presence of excipients in lipid based formulations

Small volume dissolution of a poorly soluble drug as solid dispersions

Application of the SDI in Pharmaceuticals - Mei Wong (Pfizer)

In-situ pH change on a biphasic dissolution model in the presence of SIFs

Use of SDI to assess dissolution characteristics - John Comer (Pion)

Dissolution Experiments in Lipid Layers

Small scale assays for studying dissolution of cocrystals

Dissolution & precipitation studies of carbamazepine cocrystals with small scale assays

Dissolution of a drug in the presence of additives and biorelevant media

Dissolution in presence of lipid to mimic absorption

Biphasic dissolution studies of Felodipine

Biorelevant dissolution - the quest for simple in-vitro experiments

Visualising the release patterns of promethazine across microparticulate systems

AAPS 2017 Flo-Vitro poster KBox

AAPS Understanding drug release mechanisms of metformin using complementary in vitro dissolution tools

AAPS 2017 Supersaturation modelling poster KBox

AAPS 2017 Supersaturation excipients poster KBox

Supersaturation time with CheqSol using different excipients

Faster Dissolution Methods of Pharmaceutical salts

Low Volume Dissolution Assays