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Eye function of Mysidacea (Crustacea) in the northern Baltic Sea

Journal of experimental marine biology and ecology, 2000-03, Vol.246 (1), p.85-101

Lindstroem, M

2000

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Chronic obstructive pulmonary disease outpatients bear risks of both unplanned weight loss and obesity

Clinical nutrition ESPEN, 2022-06, Vol.49, p.246-251

2022

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Unstirred Water Layers and the Kinetics of Organic Cation Transport

Pharmaceutical research, 2015-09, Vol.32 (9), p.2937-2949

2015

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Albumin-mediated transport phenomenon' observed for ligands with high membrane permeability : effect of the unstirred water layer in the Disse's space of rat liver

Journal of hepatology, 1992-09, Vol.16 (1-2), p.38-49

1992

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The Solubility–Permeability Interplay in Using Cyclodextrins as Pharmaceutical Solubilizers: Mechanistic Modeling and Application to Progesterone

Journal of pharmaceutical sciences, 2010-06, Vol.99 (6), p.2739-2749

2010

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Lipid Absorption Triggers Drug Supersaturation at the Intestinal Unstirred Water Layer and Promotes Drug Absorption from Mixed Micelles

Pharmaceutical research, 2013-12, Vol.30 (12), p.3045-3058

2013

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Practical Approach to Modeling the Impact of Amorphous Drug Nanoparticles on the Oral Absorption of Poorly Soluble Drugs

Molecular pharmaceutics, 2020-01, Vol.17 (1), p.180-189

2020

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Effect of Mechanical Agitation on Cationic Liposome Transport across an Unstirred Water Layer in Caco-2 Cells

Biological and Pharmaceutical Bulletin, 2016/08/01, Vol.39(8), pp.1293-1299

2016

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Possible reduction of effective thickness of intestinal unstirred water layer by particle drifting effect

International journal of pharmaceutics, 2010-03, Vol.387 (1), p.103-109

Sugano, Kiyohiko

2010

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An evaluation of the relative roles of the unstirred water layer and receptor sink in limiting the in-vitro intestinal permeability of drug compounds of varying lipophilicity

Journal of pharmacy and pharmacology, 2008-10, Vol.60 (10), p.1311-1319

2008

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Pharmaceutical applications of cyclodextrins: effects on drug permeation through biological membranes

Journal of pharmacy and pharmacology, 2011-09, Vol.63 (9), p.1119-1135

2011

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Oral delivery of lipophilic drugs: the tradeoff between solubility increase and permeability decrease when using cyclodextrin-based formulations

PloS one, 2013-07, Vol.8 (7), p.e68237-e68237

2013

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Combined effects of the drug distribution and mucus diffusion properties of self-microemulsifying drug delivery systems on the oral absorption of fenofibrate

International journal of pharmaceutics, 2018-07, Vol.546 (1-2), p.263-271

2018

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The Solubility–Permeability Interplay: Mechanistic Modeling and Predictive Application of the Impact of Micellar Solubilization on Intestinal Permeation

Molecular pharmaceutics, 2011-10, Vol.8 (5), p.1848-1856

2011

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Prediction of food effect by bile micelles on oral drug absorption considering free fraction in intestinal fluid

European journal of pharmaceutical sciences, 2010-05, Vol.40 (2), p.118-124

2010

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The Solubility–Permeability Interplay When Using Cosolvents for Solubilization: Revising the Way We Use Solubility-Enabling Formulations

Molecular pharmaceutics, 2012-03, Vol.9 (3), p.581-590

2012

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Drug permeation through biomembranes: cyclodextrins and the unstirred water layer

Pharmazie, 2012-05, Vol.67 (5), p.363-370

Loftsson, T

2012

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Analysis of Unstirred Water Layer in In Vitro Permeability Experiments

Journal of pharmaceutical sciences, 2009-12, Vol.98 (12), p.4469-4479

2009

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Antimicrobial Resistance Patterns of Fecal Escherichia coli in Wildlife, Urban Wildlife, and Livestock in the Eastern Region of Sri Lanka, and Differences between Carnivores, Omnivores, and Herbivores

Journal of wildlife diseases, 2022-04, Vol.58 (2), p.380-383

2022

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Methacrylate-Copolymer Eudragit EPO as a Solubility-Enabling Excipient for Anionic Drugs: Investigation of Drug Solubility, Intestinal Permeability, and Their Interplay

Molecular pharmaceutics, 2019-07, Vol.16 (7), p.2884-2891

2019

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Impact of Drug-Rich Colloids of Itraconazole and HPMCAS on Membrane Flux in Vitro and Oral Bioavailability in Rats

Molecular pharmaceutics, 2017-07, Vol.14 (7), p.2437-2449

2017

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PAMPA—a drug absorption in vitro model: 7. Comparing rat in situ, Caco-2, and PAMPA permeability of fluoroquinolones

European journal of pharmaceutical sciences, 2004-03, Vol.21 (4), p.429-441

2004

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Theoretical investigation of passive intestinal membrane permeability using Monte Carlo method to generate drug-like molecule population

International journal of pharmaceutics, 2009-05, Vol.373 (1), p.55-61

Sugano, Kiyohiko

2009

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Quantitative Investigation of Intestinal Drug Absorption Enhancement by Drug-Rich Nanodroplets Generated via Liquid–Liquid Phase Separation

Molecular pharmaceutics, 2024-04, Vol.21 (4), p.1745-1755

2024

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In vitro digestion models to evaluate lipid based drug delivery systems; present status and current trends

Advanced drug delivery reviews, 2019-03, Vol.142, p.35-49

2019

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Eye function of Mysidacea (Crustacea) in the northern Baltic Sea

Chronic obstructive pulmonary disease outpatients bear risks of both unplanned weight loss and obesity

Unstirred Water Layers and the Kinetics of Organic Cation Transport

Albumin-mediated transport phenomenon' observed for ligands with high membrane permeability : effect of the unstirred water layer in the Disse's space of rat liver

The Solubility–Permeability Interplay in Using Cyclodextrins as Pharmaceutical Solubilizers: Mechanistic Modeling and Application to Progesterone

Lipid Absorption Triggers Drug Supersaturation at the Intestinal Unstirred Water Layer and Promotes Drug Absorption from Mixed Micelles

Practical Approach to Modeling the Impact of Amorphous Drug Nanoparticles on the Oral Absorption of Poorly Soluble Drugs

Effect of Mechanical Agitation on Cationic Liposome Transport across an Unstirred Water Layer in Caco-2 Cells

Possible reduction of effective thickness of intestinal unstirred water layer by particle drifting effect

An evaluation of the relative roles of the unstirred water layer and receptor sink in limiting the in-vitro intestinal permeability of drug compounds of varying lipophilicity

Pharmaceutical applications of cyclodextrins: effects on drug permeation through biological membranes

Oral delivery of lipophilic drugs: the tradeoff between solubility increase and permeability decrease when using cyclodextrin-based formulations

Combined effects of the drug distribution and mucus diffusion properties of self-microemulsifying drug delivery systems on the oral absorption of fenofibrate

The Solubility–Permeability Interplay: Mechanistic Modeling and Predictive Application of the Impact of Micellar Solubilization on Intestinal Permeation

Prediction of food effect by bile micelles on oral drug absorption considering free fraction in intestinal fluid

The Solubility–Permeability Interplay When Using Cosolvents for Solubilization: Revising the Way We Use Solubility-Enabling Formulations

Drug permeation through biomembranes: cyclodextrins and the unstirred water layer

Analysis of Unstirred Water Layer in In Vitro Permeability Experiments

Antimicrobial Resistance Patterns of Fecal Escherichia coli in Wildlife, Urban Wildlife, and Livestock in the Eastern Region of Sri Lanka, and Differences between Carnivores, Omnivores, and Herbivores

Methacrylate-Copolymer Eudragit EPO as a Solubility-Enabling Excipient for Anionic Drugs: Investigation of Drug Solubility, Intestinal Permeability, and Their Interplay

Impact of Drug-Rich Colloids of Itraconazole and HPMCAS on Membrane Flux in Vitro and Oral Bioavailability in Rats

PAMPA—a drug absorption in vitro model: 7. Comparing rat in situ, Caco-2, and PAMPA permeability of fluoroquinolones

Theoretical investigation of passive intestinal membrane permeability using Monte Carlo method to generate drug-like molecule population

Quantitative Investigation of Intestinal Drug Absorption Enhancement by Drug-Rich Nanodroplets Generated via Liquid–Liquid Phase Separation

In vitro digestion models to evaluate lipid based drug delivery systems; present status and current trends

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