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Ranking Itraconazole Formulations Based on the Flux through Artificial Lipophilic Membrane

Pharmaceutical research, 2018-08, Vol.35 (8), p.161-13, Article 161

2018

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Prediction of Bioequivalence and Food Effect Using Flux- and Solubility-Based Methods

Molecular pharmaceutics, 2019-10, Vol.16 (10), p.4121-4130

2019

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P-glycoprotein deficient mouse in situ blood–brain barrier permeability and its prediction using an in combo PAMPA model

European journal of pharmaceutical sciences, 2009-09, Vol.38 (2), p.121-137

2009

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The Permeation of Amphoteric Drugs through Artificial Membranes − An in Combo Absorption Model Based on Paracellular and Transmembrane Permeability

Journal of medicinal chemistry, 2010-01, Vol.53 (1), p.392-401

2010

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Miniaturized Rotating Disk Intrinsic Dissolution Rate Measurement: Effects of Buffer Capacity in Comparisons to Traditional Wood’s Apparatus

Pharmaceutical research, 2008-11, Vol.25 (11), p.2613-2627

2008

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Using pH Gradient Dissolution with In-Situ Flux Measurement to Evaluate Bioavailability and DDI for Formulated Poorly Soluble Drug Products

AAPS PharmSciTech, 2018-10, Vol.19 (7), p.2898-2907

2018

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Physicochemical Selectivity of the BBB Microenvironment Governing Passive Diffusion--Matching with a Porcine Brain Lipid Extract Artificial Membrane Permeability Model

Pharmaceutical research, 2011-02, Vol.28 (2), p.337-363

2011

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The effect of formulation additives on in vitro dissolution-absorption profile and in vivo bioavailability of telmisartan from brand and generic formulations

European journal of pharmaceutical sciences, 2018-03, Vol.114, p.310-317

2018

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Powder Dissolution Method for Estimating Rotating Disk Intrinsic Dissolution Rates of Low Solubility Drugs

Pharmaceutical research, 2009-09, Vol.26 (9), p.2093-2100

2009

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Acid-Base Cosolvent Method for Determining Aqueous Permeability of Amiodarone, Itraconazole, Tamoxifen, Terfenadine and Other Very Insoluble Molecules

Chemical and Pharmaceutical Bulletin, 2004, Vol.52(5), pp.561-565

2004

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Food effect risk assessment in preformulation stage using material sparing µFLUX methodology

ADMET & DMPK, 2022-10

2022

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Dissolution Rate and Apparent Solubility of Poorly Soluble Drugs in Biorelevant Dissolution Media

Molecular pharmaceutics, 2010-10, Vol.7 (5), p.1419-1430

2010

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Spectrophotometric pKa determination of ionizable pharmaceuticals: Resolution of molecules with weak pH-dependent spectral shift

Journal of pharmaceutical and biomedical analysis, 2015-10, Vol.114, p.88-96

2015

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Investigation and Mathematical Description of the Real Driving Force of Passive Transport of Drug Molecules from Supersaturated Solutions

Molecular pharmaceutics, 2016-11, Vol.13 (11), p.3816-3826

2016

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Skin–PAMPA: A new method for fast prediction of skin penetration

European journal of pharmaceutical sciences, 2012-04, Vol.45 (5), p.698-707

2012

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PAMPA : A drug absorption in vitro model 13. chemical selectivity due to membrane hydrogen bonding: In combo comparisons of HDM-, DOPC-, and DS-PAMPA models

European journal of pharmaceutical sciences, 2006-05, Vol.28 (1-2), p.43-50

2006

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Flux-Based Formulation Development—A Proof of Concept Study

The AAPS journal, 2022-01, Vol.24 (1), p.22-22, Article 22

2022

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Solubility-excipient classification gradient maps

Pharmaceutical research, 2007-03, Vol.24 (3), p.530-545

2007

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Effect of Formulation Additives on Drug Transport through Size-Exclusion Membranes

Molecular pharmaceutics, 2018-08, Vol.15 (8), p.3308-3317

2018

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PAMPA—a drug absorption in vitro model: 11. Matching the in vivo unstirred water layer thickness by individual-well stirring in microtitre plates

European journal of pharmaceutical sciences, 2004-08, Vol.22 (5), p.365-374

2004

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Miniaturization of Powder Dissolution Measurement and Estimation of Particle Size

Chemistry & biodiversity, 2009-11, Vol.6 (11), p.1796-1811

2009

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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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Membrane-Water partitioning, membrane permeability, and baseline toxicity of the parasiticides ivermectin, albendazole, and morantel

Environmental toxicology and chemistry, 2008-04, Vol.27 (4), p.909-918

2008

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PAMPA—A drug absorption in vitro model

European journal of pharmaceutical sciences, 2006-05, Vol.28 (1), p.43-50

2006

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PAMPA-excipient classification gradient map

Pharmaceutical research, 2006-11, Vol.23 (11), p.2525-2535

2006

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Ranking Itraconazole Formulations Based on the Flux through Artificial Lipophilic Membrane

Prediction of Bioequivalence and Food Effect Using Flux- and Solubility-Based Methods

P-glycoprotein deficient mouse in situ blood–brain barrier permeability and its prediction using an in combo PAMPA model

The Permeation of Amphoteric Drugs through Artificial Membranes − An in Combo Absorption Model Based on Paracellular and Transmembrane Permeability

Miniaturized Rotating Disk Intrinsic Dissolution Rate Measurement: Effects of Buffer Capacity in Comparisons to Traditional Wood’s Apparatus

Using pH Gradient Dissolution with In-Situ Flux Measurement to Evaluate Bioavailability and DDI for Formulated Poorly Soluble Drug Products

Physicochemical Selectivity of the BBB Microenvironment Governing Passive Diffusion--Matching with a Porcine Brain Lipid Extract Artificial Membrane Permeability Model

The effect of formulation additives on in vitro dissolution-absorption profile and in vivo bioavailability of telmisartan from brand and generic formulations

Powder Dissolution Method for Estimating Rotating Disk Intrinsic Dissolution Rates of Low Solubility Drugs

Acid-Base Cosolvent Method for Determining Aqueous Permeability of Amiodarone, Itraconazole, Tamoxifen, Terfenadine and Other Very Insoluble Molecules

Food effect risk assessment in preformulation stage using material sparing µFLUX methodology

Dissolution Rate and Apparent Solubility of Poorly Soluble Drugs in Biorelevant Dissolution Media

Spectrophotometric pKa determination of ionizable pharmaceuticals: Resolution of molecules with weak pH-dependent spectral shift

Investigation and Mathematical Description of the Real Driving Force of Passive Transport of Drug Molecules from Supersaturated Solutions

Skin–PAMPA: A new method for fast prediction of skin penetration

PAMPA : A drug absorption in vitro model 13. chemical selectivity due to membrane hydrogen bonding: In combo comparisons of HDM-, DOPC-, and DS-PAMPA models

Flux-Based Formulation Development—A Proof of Concept Study

Solubility-excipient classification gradient maps

Effect of Formulation Additives on Drug Transport through Size-Exclusion Membranes

PAMPA—a drug absorption in vitro model: 11. Matching the in vivo unstirred water layer thickness by individual-well stirring in microtitre plates

Miniaturization of Powder Dissolution Measurement and Estimation of Particle Size

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

Membrane-Water partitioning, membrane permeability, and baseline toxicity of the parasiticides ivermectin, albendazole, and morantel

PAMPA—A drug absorption in vitro model

PAMPA-excipient classification gradient map

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