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Studying the effect of solubilizing agents on drug diffusion through the unstirred water layer (UWL) by localized spectroscopy

European journal of pharmaceutics and biopharmaceutics, 2019-06, Vol.139, p.205-212

2019

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Analysis of Non-linear Pharmacokinetics of P-Glycoprotein Substrates in a Microfluidic Device Using a Mathematical Model that Includes an Unstirred Water Layer (UWL) Compartment

Pharmaceutical research, 2021-06, Vol.38 (6), p.1031-1039

2021

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Towards a better mechanistic comprehension of drug permeation and absorption: Introducing the diffusion-partitioning interplay

International journal of pharmaceutics, 2021-10, Vol.608, p.121116-121116, Article 121116

2021

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Effect of surface charge, particle size, and modification by polyethylene glycol of liposomes on their association with Caco-2 cells across an unstirred water layer

Pharmazie, 2018-01, Vol.73 (1), p.3-8

2018

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In vitro-in vivo correlation in the effect of cyclodextrin on oral absorption of poorly soluble drugs

International journal of pharmaceutics, 2021-05, Vol.600, p.120494-120494, Article 120494

2021

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Nasal powders of quercetin-β-cyclodextrin derivatives complexes with mannitol/lecithin microparticles for Nose-to-Brain delivery: In vitro and ex vivo evaluation

International journal of pharmaceutics, 2021-09, Vol.607, p.121016-121016, Article 121016

2021

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Bridging in vitro dissolution and in vivo exposure for acalabrutinib. Part I. Mechanistic modelling of drug product dissolution to derive a P-PSD for PBPK model input

European journal of pharmaceutics and biopharmaceutics, 2019-09, Vol.142, p.421-434

2019

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Dose-Dependent Solubility-Permeability Interplay for Poorly Soluble Drugs under Non-Sink Conditions

Pharmaceutics, 2021-03, Vol.13 (3), p.323

2021

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Experimental estimation of the effective unstirred water layer thickness in the human jejunum, and its importance in oral drug absorption

European journal of pharmaceutical sciences, 1995-10, Vol.3 (5), p.247-253

1995

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The elucidation of key factors for oral absorption enhancement of nanocrystal formulations: In vitro–in vivo correlation of nanocrystals

European journal of pharmaceutics and biopharmaceutics, 2020-01, Vol.146, p.84-92

2020

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Non-Effective Improvement of Absorption for Some Nanoparticle Formulations Explained by Permeability under Non-Sink Conditions

Pharmaceutics, 2022-04, Vol.14 (4), p.816

2022

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Interaction with biliary and pancreatic fluids drives supersaturation and drug absorption from lipid-based formulations of low (saquinavir) and high (fenofibrate) permeability poorly soluble drugs

Journal of controlled release, 2021-03, Vol.331, p.45-61

2021

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In vitro dissolution testing of respirable size anti-tubercular drug particles using a small volume dissolution apparatus

International journal of pharmaceutics, 2019-03, Vol.559, p.235-244

2019

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Understanding peroral absorption: regulatory aspects and contemporary approaches to tackling solubility and permeability hurdles

Acta pharmaceutica Sinica. B, 2017-05, Vol.7 (3), p.260-280

2017

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Identification of Staphylococcus aureus Cellular Pathways Affected by the Stilbenoid Lead Drug SK-03-92 Using a Microarray

Antibiotics (Basel), 2017-09, Vol.6 (3), p.17

2017

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In vitro measurement of drug transport using a new diffusion chamber compatible with Millicell® culture supports: Performance with caco-2 monolayers

International journal of pharmaceutics, 1996-05, Vol.133 (1), p.47-58

1996

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The use of bioadhesives in targeted delivery within the gastrointestinal tract

Advanced drug delivery reviews, 1993-09, Vol.11 (3), p.221-251

Helliwell, Mark

1993

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Commercially Available Cell-Free Permeability Tests for Industrial Drug Development: Increased Sustainability through Reduction of In Vivo Studies

Pharmaceutics, 2023-02, Vol.15 (2), p.592

2023

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Drug Permeability Profiling Using the Novel Permeapad® 96-Well Plate

Pharmaceutical research, 2020-05, Vol.37 (6), p.93-93, Article 93

2020

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The Effect of Anesthetic Regimens on Intestinal Absorption of Passively Absorbed Drugs in Rats

Pharmaceutical research, 2020-05, Vol.37 (5), p.87-87, Article 87

2020

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Mechanistic Insight in Permeability through Different Membranes in the Presence of Pharmaceutical Excipients: A Case of Model Hydrophobic Carbamazepine

Pharmaceutics, 2024-01, Vol.16 (2), p.184

2024

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Mucins are Involved in the Intestinal Permeation of Lipophilic Drugs in the Proximal Region of Rat Small Intestine

Pharmaceutical research, 2019-11, Vol.36 (11), p.1-11, Article 162

2019

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Intestinal Absorption Study: Challenges and Absorption Enhancement Strategies in Improving Oral Drug Delivery

Pharmaceuticals (Basel, Switzerland), 2022-08, Vol.15 (8), p.975

2022

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Versatile Nasal Application of Cyclodextrins: Excipients and/or Actives?

Pharmaceutics, 2021-07, Vol.13 (8), p.1180

2021

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Mucin-Protected Caco-2 Assay to Study Drug Permeation in the Presence of Complex Biorelevant Media

Pharmaceutics, 2022-03, Vol.14 (4), p.699

2022

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Studying the effect of solubilizing agents on drug diffusion through the unstirred water layer (UWL) by localized spectroscopy

Analysis of Non-linear Pharmacokinetics of P-Glycoprotein Substrates in a Microfluidic Device Using a Mathematical Model that Includes an Unstirred Water Layer (UWL) Compartment

Towards a better mechanistic comprehension of drug permeation and absorption: Introducing the diffusion-partitioning interplay

Effect of surface charge, particle size, and modification by polyethylene glycol of liposomes on their association with Caco-2 cells across an unstirred water layer

In vitro-in vivo correlation in the effect of cyclodextrin on oral absorption of poorly soluble drugs

Nasal powders of quercetin-β-cyclodextrin derivatives complexes with mannitol/lecithin microparticles for Nose-to-Brain delivery: In vitro and ex vivo evaluation

Bridging in vitro dissolution and in vivo exposure for acalabrutinib. Part I. Mechanistic modelling of drug product dissolution to derive a P-PSD for PBPK model input

Dose-Dependent Solubility-Permeability Interplay for Poorly Soluble Drugs under Non-Sink Conditions

Experimental estimation of the effective unstirred water layer thickness in the human jejunum, and its importance in oral drug absorption

The elucidation of key factors for oral absorption enhancement of nanocrystal formulations: In vitro–in vivo correlation of nanocrystals

Non-Effective Improvement of Absorption for Some Nanoparticle Formulations Explained by Permeability under Non-Sink Conditions

Interaction with biliary and pancreatic fluids drives supersaturation and drug absorption from lipid-based formulations of low (saquinavir) and high (fenofibrate) permeability poorly soluble drugs

In vitro dissolution testing of respirable size anti-tubercular drug particles using a small volume dissolution apparatus

Understanding peroral absorption: regulatory aspects and contemporary approaches to tackling solubility and permeability hurdles

Identification of Staphylococcus aureus Cellular Pathways Affected by the Stilbenoid Lead Drug SK-03-92 Using a Microarray

In vitro measurement of drug transport using a new diffusion chamber compatible with Millicell® culture supports: Performance with caco-2 monolayers

The use of bioadhesives in targeted delivery within the gastrointestinal tract

Commercially Available Cell-Free Permeability Tests for Industrial Drug Development: Increased Sustainability through Reduction of In Vivo Studies

Drug Permeability Profiling Using the Novel Permeapad® 96-Well Plate

The Effect of Anesthetic Regimens on Intestinal Absorption of Passively Absorbed Drugs in Rats

Mechanistic Insight in Permeability through Different Membranes in the Presence of Pharmaceutical Excipients: A Case of Model Hydrophobic Carbamazepine

Mucins are Involved in the Intestinal Permeation of Lipophilic Drugs in the Proximal Region of Rat Small Intestine

Intestinal Absorption Study: Challenges and Absorption Enhancement Strategies in Improving Oral Drug Delivery

Versatile Nasal Application of Cyclodextrins: Excipients and/or Actives?

Mucin-Protected Caco-2 Assay to Study Drug Permeation in the Presence of Complex Biorelevant Media

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