Patrick O'Dwyer

Lecturer in Pharmaceutics

University College Cork

Ireland

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Patrick O'Dwyer is a Lecturer in Pharmaceutics at University College Cork, Ireland. His research primarily focuses on the development and analysis of lipid-based formulations and their interaction with various drug delivery systems. Recent articles highlight his work in machine learning applications for drug formulation and in vitro methodologies for assessing drug solubility and bioavailability.

Articles (12)

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2024

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2024

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2024

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2023

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2023

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2023

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2022

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2022

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2021

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2020

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2020

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2020

Collaborators (7)

Christos Reppas

National and Kapodistrian University of Athens

GREECE

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Harriet Bennett-Lenane

Lecturer in Clinical Pharmaceutics

University College Cork

IRELAND

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Joseph O’Shea

Lecturer in Pharmaceutics

University College Cork

IRELAND

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René Holm

Professor

University of Southern Denmark

DENMARK

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Martin Kuentz

University of Applied Sciences and Arts Northwestern Switzerland

SWITZERLAND

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Brendan Griffin

Professor at University College Cork

University College Cork

IRELAND

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Niklas Koehl

University College Cork National University of Ireland

IRELAND

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Patrick O'Dwyer

Research Interests

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Articles (12)

Comparative Analysis of Chemical Descriptors by Machine Learning Reveals Atomistic Insights into Solute–Lipid Interactions

Predictions of biorelevant solubility change during dispersion and digestion of lipid-based formulations

Predictive computational models for assessing the impact of co-milling on drug dissolution

Leveraging the use of in vitro and computational methods to support the development of enabling oral drug products: An InPharma commentary

Developing an in vitro lipolysis model for real-time analysis of drug concentrations during digestion of lipid-based formulations.

Advancing algorithmic drug product development: Recommendations for machine learning approaches in drug formulation.

On the usefulness of four in vitro methodologies in screening for product related differences in tacrolimus exposure after oral administration of amorphous solid dispersions with modified release characteristics in the fasted state

On the usefulness of four in vitro methods in assessing the intraluminal performance of poorly soluble, ionisable compounds in the fasted state

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

On the Usefulness of Two Small-Scale In Vitro Setups in the Evaluation of Luminal Precipitation of Lipophilic Weak Bases in Early Formulation Development

Applying Computational Predictions of Biorelevant Solubility Ratio Upon Self-Emulsifying Lipid-Based Formulations Dispersion to Predict Dose Number

Novel Biphasic Lipolysis Method to Predict in Vivo Performance of Lipid-Based Formulations

Collaborators (7)

Christos Reppas

Harriet Bennett-Lenane

Joseph O’Shea

René Holm

Martin Kuentz

Brendan Griffin

Niklas Koehl

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