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Theoretical and practical approaches for prediction of drug-polymer miscibility and solubility

Pharmaceutical research, 2006-10, Vol.23 (10), p.2417-2426

2006

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Effect of excipient properties, water activity, and water content on the disproportionation of a pharmaceutical salt

International journal of pharmaceutics, 2018-07, Vol.546 (1-2), p.226-234

2018

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Osmotic-controlled release oral tablets: technology and functional insights

Trends in biotechnology (Regular ed.), 2022-05, Vol.40 (5), p.606-619

2022

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Improved protocol and data analysis for accelerated shelf-life estimation of solid dosage forms

Pharmaceutical research, 2007-04, Vol.24 (4), p.780-790

2007

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Characterization of the Time Scales of Molecular Motion in Pharmaceutically Important Glasses

The journal of physical chemistry. B, 1999-05, Vol.103 (20), p.4113-4121

1999

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Binary isobaric phase diagrams of stearyl alcohol-poloxamer 407 formulations in the molten and solid state

International journal of pharmaceutics, 2022-07, Vol.623, p.121908-121908, Article 121908

2022

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Evolution of the microstructure and the drug release upon annealing the drug loaded lipid-surfactant microspheres

European journal of pharmaceutical sciences, 2020-04, Vol.147, p.105278, Article 105278

2020

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Phase Behavior of Drug–Lipid–Surfactant Ternary Systems toward Understanding the Annealing-Induced Change

Molecular pharmaceutics, 2022-02, Vol.19 (2), p.532-546

2022

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Impact of Solid-State Form on the Disproportionation of Miconazole Mesylate

Molecular pharmaceutics, 2018-01, Vol.15 (1), p.40-52

2018

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Assessing the Risk of Salt Disproportionation Using Crystal Structure and Surface Topography Analysis

Crystal growth & design, 2018-11, Vol.18 (11), p.7027-7040

2018

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Coupling between chemical reactivity and structural relaxation in pharmaceutical glasses

Pharmaceutical research, 2006-10, Vol.23 (10), p.2254-2268

2006

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Pharmacoscintigraphy studies to assess the feasibility of a controlled release formulation of ziprasidone

Journal of controlled release, 2015-09, Vol.213, p.10-17

2015

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Impact of sertraline salt form on the oxidative stability in powder blends

International journal of pharmaceutics, 2014-01, Vol.461 (1-2), p.322-330

2014

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Correction to Discovery of the Hemifumarate and (α‑l‑Alanyloxy)methyl Ether as Prodrugs of an Antirheumatic Oxindole: Prodrugs for the Enolic OH Group

Journal of medicinal chemistry, 2018-04, Vol.61 (7), p.3237-3237

2018

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Molecular mobility of amorphous pharmaceuticals determined using differential scanning calorimetry

Thermochimica acta, 2001-12, Vol.380 (2), p.95-107

2001

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Enthalpy relaxation in binary amorphous mixtures containing sucrose

Pharmaceutical research, 1998-12, Vol.15 (12), p.1828-1834

1998

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The effects of absorbed water on the properties of amorphous mixtures containing sucrose

Pharmaceutical research, 1999-07, Vol.16 (7), p.1119-1124

1999

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The Glass Transition and Sub-Tg-Relaxation in Pharmaceutical Powders and Dried Proteins by Thermally Stimulated Current

Journal of pharmaceutical sciences, 2009-01, Vol.98 (1), p.81-93

2009

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Spontaneous Crystallinity Loss of Drugs in the Disordered Regions of Poly(Ethylene Oxide) in the Presence of Water

Journal of pharmaceutical sciences, 2008-08, Vol.97 (8), p.3182-3194

2008

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Discovery of the Hemifumarate and (α-l-Alanyloxy)methyl Ether as Prodrugs of an Antirheumatic Oxindole: Prodrugs for the Enolic OH Group

Journal of medicinal chemistry, 1996-01, Vol.39 (1), p.10-18

1996

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Polyamorphism: a pharmaceutical science perspective

Journal of pharmacy and pharmacology, 2002-08, Vol.54 (8), p.1151-1152

2002

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Direct Synthesis and Reactivity of Unsupported (.eta.3-Oxaallyl)rhodium(I) Complexes

Organometallics, 1994-03, Vol.13 (3), p.890-898

1994

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A pragmatic test of a simple calorimetric method for determining the fragility of some amorphous pharmaceutical materials

Pharmaceutical research, 1998-05, Vol.15 (5), p.762-767

1998

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Water vapor sorption by peptides, proteins and their formulations

European Journal of Pharmaceutics and Biopharmaceutics, 1998-05, Vol.45 (3), p.239-247

1998

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Molecular mobility of amorphous pharmaceutical solids below their glass transition temperatures

Pharmaceutical research, 1995-06, Vol.12 (6), p.799-806

1995

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Theoretical and practical approaches for prediction of drug-polymer miscibility and solubility

Effect of excipient properties, water activity, and water content on the disproportionation of a pharmaceutical salt

Osmotic-controlled release oral tablets: technology and functional insights

Improved protocol and data analysis for accelerated shelf-life estimation of solid dosage forms

Characterization of the Time Scales of Molecular Motion in Pharmaceutically Important Glasses

Binary isobaric phase diagrams of stearyl alcohol-poloxamer 407 formulations in the molten and solid state

Evolution of the microstructure and the drug release upon annealing the drug loaded lipid-surfactant microspheres

Phase Behavior of Drug–Lipid–Surfactant Ternary Systems toward Understanding the Annealing-Induced Change

Impact of Solid-State Form on the Disproportionation of Miconazole Mesylate

Assessing the Risk of Salt Disproportionation Using Crystal Structure and Surface Topography Analysis

Coupling between chemical reactivity and structural relaxation in pharmaceutical glasses

Pharmacoscintigraphy studies to assess the feasibility of a controlled release formulation of ziprasidone

Impact of sertraline salt form on the oxidative stability in powder blends

Correction to Discovery of the Hemifumarate and (α‑l‑Alanyloxy)methyl Ether as Prodrugs of an Antirheumatic Oxindole: Prodrugs for the Enolic OH Group

Molecular mobility of amorphous pharmaceuticals determined using differential scanning calorimetry

Enthalpy relaxation in binary amorphous mixtures containing sucrose

The effects of absorbed water on the properties of amorphous mixtures containing sucrose

The Glass Transition and Sub-Tg-Relaxation in Pharmaceutical Powders and Dried Proteins by Thermally Stimulated Current

Spontaneous Crystallinity Loss of Drugs in the Disordered Regions of Poly(Ethylene Oxide) in the Presence of Water

Discovery of the Hemifumarate and (α-l-Alanyloxy)methyl Ether as Prodrugs of an Antirheumatic Oxindole: Prodrugs for the Enolic OH Group

Polyamorphism: a pharmaceutical science perspective

Direct Synthesis and Reactivity of Unsupported (.eta.3-Oxaallyl)rhodium(I) Complexes

A pragmatic test of a simple calorimetric method for determining the fragility of some amorphous pharmaceutical materials

Water vapor sorption by peptides, proteins and their formulations

Molecular mobility of amorphous pharmaceutical solids below their glass transition temperatures

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