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Formulation and Characterization of an Effervescent Hydrogen-Generating Tablet

Pharmaceuticals (Basel, Switzerland), 2021-12, Vol.14 (12), p.1327

2021

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Oral Solid Dosage Form Disintegration Testing — The Forgotten Test

Journal of pharmaceutical sciences, 2015-09, Vol.104 (9), p.2664-2675

2015

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Simulated, biorelevant, clinically relevant or physiologically relevant dissolution media: The hidden role of bicarbonate buffer

European journal of pharmaceutics and biopharmaceutics, 2019-09, Vol.142, p.8-19

2019

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Floating and Sustained-Release Characteristics of Effervescent Tablets Prepared with a Mixed Matrix of Eudragit L-100-55 and Eudragit E PO

Chemical and Pharmaceutical Bulletin, 2011/02/01, Vol.59(2), pp.155-160

2011

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In Vitro Evaluation of Enteric-Coated HPMC Capsules—Effect of Formulation Factors on Product Performance

Pharmaceutics, 2020-07, Vol.12 (8), p.696

2020

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Mass Transport Analysis of the Enhanced Buffer Capacity of the Bicarbonate–CO2 Buffer in a Phase-Heterogenous System: Physiological and Pharmaceutical Significance

Molecular pharmaceutics, 2018-11, Vol.15 (11), p.5291-5301

2018

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In Vitro Methodologies for Evaluating Colon-Targeted Pharmaceutical Products and Industry Perspectives for Their Applications

Pharmaceutics, 2022-01, Vol.14 (2), p.291

2022

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Enteric Hard Capsules for Targeting the Small Intestine: Positive Correlation between In Vitro Disintegration and Dissolution Times

Pharmaceutics, 2020-02, Vol.12 (2), p.123

2020

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Hybrid Biopolymer and Lipid Nanoparticles with Improved Transfection Efficacy for mRNA

Cells (Basel, Switzerland), 2020-09, Vol.9 (9), p.2034

2020

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Novel food drug interaction mechanism involving acyclovir, chitosan and endogenous mucus

Drug metabolism and pharmacokinetics, 2023-04, Vol.49, p.100491-100491, Article 100491

2023

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Toward Mechanistic Design of Surrogate Buffers for Dissolution Testing of pH-Dependent Drug Delivery Systems

Pharmaceutics, 2020-12, Vol.12 (12), p.1197

2020

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Biphasic Dissolution as an Exploratory Method During Early Drug Product Development

Pharmaceutics, 2020-05, Vol.12 (5), p.420

2020

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Exploring Bioequivalence of Dexketoprofen Trometamol Drug Products with the Gastrointestinal Simulator (GIS) and Precipitation Pathways Analyses

Pharmaceutics, 2019-03, Vol.11 (3), p.122

2019

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Corrigendum to Novel analytical solutions for convolution in compartmental pharmacokinetic models and application to non-bioequivalent formulations [European Journal of Pharmaceutical Sciences 202 (2024) 1–10/106892]

European journal of pharmaceutical sciences, 2024-09, p.106909, Article 106909

2024

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Effect of Calcium Ions on the Disintegration of Enteric-Coated Solid Dosage Forms

Journal of pharmaceutical sciences, 2016-02, Vol.105 (2), p.509-511

2016

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Novel analytical solutions for convolution in compartmental pharmacokinetic models and application to non-bioequivalent formulations

European journal of pharmaceutical sciences, 2024-11, Vol.202, p.106892, Article 106892

2024

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Unpredictable Performance of pH-Dependent Coatings Accentuates the Need for Improved Predictive in Vitro Test Systems

Molecular pharmaceutics, 2017-12, Vol.14 (12), p.4209-4219

2017

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Solubility vs Dissolution in Physiological Bicarbonate Buffer

Pharmaceutical research, 2024-05, Vol.41 (5), p.937-945

2024

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Mass Transport Analysis of Bicarbonate Buffer: Effect of the CO2–H2CO3 Hydration–Dehydration Kinetics in the Fluid Boundary Layer and the Apparent Effective pK a Controlling Dissolution of Acids and Bases

Molecular pharmaceutics, 2019-06, Vol.16 (6), p.2626-2635

2019

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Mass Transport Analysis of Bicarbonate Buffer: Effect of the CO2-H2CO3 Hydration-Dehydration Kinetics in the Fluid Boundary Layer and the Apparent Effective p Ka Controlling Dissolution of Acids and Bases

Molecular pharmaceutics, 2019-06, Vol.16 (6), p.2626-2635

2019

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Comparative Evaluation of Dissolution Performance in a USP 2 Setup and Alternative Stirrers and Vessel Designs: A Systematic Computational Investigation

Molecular pharmaceutics, 2024-05, Vol.21 (5), p.2406-2414

2024

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Floating and Sustained-Release Characteristics of Effervescent Tablets Prepared with a Mixed Matrix of Eudragit L-100-55 and Eudragit E PO

Chemical & Pharmaceutical Bulletin, 2011, Vol.59 (2), p.155-160

2011

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Mechanistic understanding of underperforming enteric coated products: Opportunities to add clinical relevance to the dissolution test

Journal of controlled release, 2020-09, Vol.325, p.323-334

2020

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Hierarchical Mass Transfer Analysis of Drug Particle Dissolution, Highlighting the Hydrodynamics, pH, Particle Size, and Buffer Effects for the Dissolution of Ionizable and Nonionizable Drugs in a Compendial Dissolution Vessel

Molecular pharmaceutics, 2020-10, Vol.17 (10), p.3870-3884

2020

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Assessing the utility of in silico tools in early drug development: The case of a pharmaceutically relevant formulation of the prodrug psilocybin

Journal of drug delivery science and technology, 2024-02, Vol.92, p.105305, Article 105305

2024

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Formulation and Characterization of an Effervescent Hydrogen-Generating Tablet

Oral Solid Dosage Form Disintegration Testing — The Forgotten Test

Simulated, biorelevant, clinically relevant or physiologically relevant dissolution media: The hidden role of bicarbonate buffer

Floating and Sustained-Release Characteristics of Effervescent Tablets Prepared with a Mixed Matrix of Eudragit L-100-55 and Eudragit E PO

In Vitro Evaluation of Enteric-Coated HPMC Capsules—Effect of Formulation Factors on Product Performance

Mass Transport Analysis of the Enhanced Buffer Capacity of the Bicarbonate–CO2 Buffer in a Phase-Heterogenous System: Physiological and Pharmaceutical Significance

In Vitro Methodologies for Evaluating Colon-Targeted Pharmaceutical Products and Industry Perspectives for Their Applications

Enteric Hard Capsules for Targeting the Small Intestine: Positive Correlation between In Vitro Disintegration and Dissolution Times

Hybrid Biopolymer and Lipid Nanoparticles with Improved Transfection Efficacy for mRNA

Novel food drug interaction mechanism involving acyclovir, chitosan and endogenous mucus

Toward Mechanistic Design of Surrogate Buffers for Dissolution Testing of pH-Dependent Drug Delivery Systems

Biphasic Dissolution as an Exploratory Method During Early Drug Product Development

Exploring Bioequivalence of Dexketoprofen Trometamol Drug Products with the Gastrointestinal Simulator (GIS) and Precipitation Pathways Analyses

Corrigendum to Novel analytical solutions for convolution in compartmental pharmacokinetic models and application to non-bioequivalent formulations [European Journal of Pharmaceutical Sciences 202 (2024) 1–10/106892]

Effect of Calcium Ions on the Disintegration of Enteric-Coated Solid Dosage Forms

Novel analytical solutions for convolution in compartmental pharmacokinetic models and application to non-bioequivalent formulations

Unpredictable Performance of pH-Dependent Coatings Accentuates the Need for Improved Predictive in Vitro Test Systems

Solubility vs Dissolution in Physiological Bicarbonate Buffer

Mass Transport Analysis of Bicarbonate Buffer: Effect of the CO2–H2CO3 Hydration–Dehydration Kinetics in the Fluid Boundary Layer and the Apparent Effective pK a Controlling Dissolution of Acids and Bases

Mass Transport Analysis of Bicarbonate Buffer: Effect of the CO2-H2CO3 Hydration-Dehydration Kinetics in the Fluid Boundary Layer and the Apparent Effective p Ka Controlling Dissolution of Acids and Bases

Comparative Evaluation of Dissolution Performance in a USP 2 Setup and Alternative Stirrers and Vessel Designs: A Systematic Computational Investigation

Floating and Sustained-Release Characteristics of Effervescent Tablets Prepared with a Mixed Matrix of Eudragit L-100-55 and Eudragit E PO

Mechanistic understanding of underperforming enteric coated products: Opportunities to add clinical relevance to the dissolution test

Hierarchical Mass Transfer Analysis of Drug Particle Dissolution, Highlighting the Hydrodynamics, pH, Particle Size, and Buffer Effects for the Dissolution of Ionizable and Nonionizable Drugs in a Compendial Dissolution Vessel

Assessing the utility of in silico tools in early drug development: The case of a pharmaceutically relevant formulation of the prodrug psilocybin

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