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Cyclodextrins as Functional Excipients: Methods to Enhance Complexation Efficiency

Journal of pharmaceutical sciences, 2012-09, Vol.101 (9), p.3019-3032

2012

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Pharmaceutical applications of cyclodextrins: basic science and product development

Journal of pharmacy and pharmacology, 2010-11, Vol.62 (11), p.1607-1621

2010

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Cyclodextrins as pharmaceutical solubilizers

Advanced drug delivery reviews, 2007-07, Vol.59 (7), p.645-666

2007

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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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Cyclodextrin-based pharmaceutics: past, present and future

Nature reviews. Drug discovery, 2004-12, Vol.3 (12), p.1023-1035

2004

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Evaluation of gastrointestinal drug supersaturation and precipitation: Strategies and issues

International journal of pharmaceutics, 2013-08, Vol.453 (1), p.25-35

2013

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Supersaturating Drug Delivery Systems: Fast is Not Necessarily Good Enough

Journal of pharmaceutical sciences, 2012-01, Vol.101 (1), p.7-9

2012

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Supersaturating Drug Delivery Systems: The Answer to Solubility-Limited Oral Bioavailability?

Journal of pharmaceutical sciences, 2009-08, Vol.98 (8), p.2549-2572

2009

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Self-Association of Cyclodextrins and Cyclodextrin Complexes

Journal of pharmaceutical sciences, 2004-05, Vol.93 (5), p.1091-1099

2004

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Effects of Cyclodextrins on Drug Delivery Through Biological Membranes

Journal of pharmaceutical sciences, 2007-10, Vol.96 (10), p.2532-2546

2007

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High speed electrospinning for scaled-up production of amorphous solid dispersion of itraconazole

International journal of pharmaceutics, 2015-03, Vol.480 (1-2), p.137-142

2015

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In vitro models for the prediction of in vivo performance of oral dosage forms

European journal of pharmaceutical sciences, 2014-06, Vol.57, p.342-366

2014

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Early pharmaceutical profiling to predict oral drug absorption: Current status and unmet needs

European journal of pharmaceutical sciences, 2014-06, Vol.57, p.173-199

2014

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Evaluation of various PAMPA models to identify the most discriminating method for the prediction of BBB permeability

European journal of pharmaceutics and biopharmaceutics, 2010-03, Vol.74 (3), p.495-502

2010

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Comparative interaction of 2-hydroxypropyl-β-cyclodextrin and sulfobutylether-β-cyclodextrin with itraconazole: Phase-solubility behavior and stabilization of supersaturated drug solutions

European journal of pharmaceutical sciences, 2008-07, Vol.34 (2), p.94-103

2008

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Self-assembly of cyclodextrin complexes: Aggregation of hydrocortisone/cyclodextrin complexes

International journal of pharmaceutics, 2011-04, Vol.407 (1), p.174-183

2011

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Use of a screening method to determine excipients which optimize the extent and stability of supersaturated drug solutions and application of this system to solid formulation design

International journal of pharmaceutics, 2007-09, Vol.342 (1), p.168-175

2007

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Self-assembly of cyclodextrins: The effect of the guest molecule

International journal of pharmaceutics, 2011-04, Vol.408 (1-2), p.235-247

2011

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Preparation and characterization of nanofibers containing amorphous drug dispersions generated by electrostatic spinning

Pharmaceutical research, 2003-05, Vol.20 (5), p.810-817

2003

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Incorporation of drugs in an amorphous state into electrospun nanofibers composed of a water-insoluble, nonbiodegradable polymer

Journal of controlled release, 2003-10, Vol.92 (3), p.349-360

2003

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Evaluation of Three Amorphous Drug Delivery Technologies to Improve the Oral Absorption of Flubendazole

Journal of pharmaceutical sciences, 2016-09, Vol.105 (9), p.2782-2793

2016

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Effect of the unstirred water layer on permeability enhancement by hydrophilic cyclodextrins

International journal of pharmaceutics, 2007-09, Vol.342 (1), p.250-253

2007

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Novel generic UPLC/MS/MS method for high throughput analysis applied to permeability assessment in early Drug Discovery

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2007-03, Vol.847 (2), p.182-187

2007

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Active and passive tumor targeting of a novel poorly soluble cyclin dependent kinase inhibitor, JNJ-7706621

International journal of pharmaceutics, 2010-06, Vol.392 (1), p.20-28

2010

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Physicochemical Properties of the Amorphous Drug, Cast Films, and Spray Dried Powders to Predict Formulation Probability of Success for Solid Dispersions: Etravirine

Journal of pharmaceutical sciences, 2011-01, Vol.100 (1), p.260-274

2011

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Cyclodextrins as Functional Excipients: Methods to Enhance Complexation Efficiency

Pharmaceutical applications of cyclodextrins: basic science and product development

Cyclodextrins as pharmaceutical solubilizers

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

Cyclodextrin-based pharmaceutics: past, present and future

Evaluation of gastrointestinal drug supersaturation and precipitation: Strategies and issues

Supersaturating Drug Delivery Systems: Fast is Not Necessarily Good Enough

Supersaturating Drug Delivery Systems: The Answer to Solubility-Limited Oral Bioavailability?

Self-Association of Cyclodextrins and Cyclodextrin Complexes

Effects of Cyclodextrins on Drug Delivery Through Biological Membranes

High speed electrospinning for scaled-up production of amorphous solid dispersion of itraconazole

In vitro models for the prediction of in vivo performance of oral dosage forms

Early pharmaceutical profiling to predict oral drug absorption: Current status and unmet needs

Evaluation of various PAMPA models to identify the most discriminating method for the prediction of BBB permeability

Comparative interaction of 2-hydroxypropyl-β-cyclodextrin and sulfobutylether-β-cyclodextrin with itraconazole: Phase-solubility behavior and stabilization of supersaturated drug solutions

Self-assembly of cyclodextrin complexes: Aggregation of hydrocortisone/cyclodextrin complexes

Use of a screening method to determine excipients which optimize the extent and stability of supersaturated drug solutions and application of this system to solid formulation design

Self-assembly of cyclodextrins: The effect of the guest molecule

Preparation and characterization of nanofibers containing amorphous drug dispersions generated by electrostatic spinning

Incorporation of drugs in an amorphous state into electrospun nanofibers composed of a water-insoluble, nonbiodegradable polymer

Evaluation of Three Amorphous Drug Delivery Technologies to Improve the Oral Absorption of Flubendazole

Effect of the unstirred water layer on permeability enhancement by hydrophilic cyclodextrins

Novel generic UPLC/MS/MS method for high throughput analysis applied to permeability assessment in early Drug Discovery

Active and passive tumor targeting of a novel poorly soluble cyclin dependent kinase inhibitor, JNJ-7706621

Physicochemical Properties of the Amorphous Drug, Cast Films, and Spray Dried Powders to Predict Formulation Probability of Success for Solid Dispersions: Etravirine

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