In-situ freeze-drying - forming amorphous solids directly within capsules: An investigation of dissolution enhancement for a poorly soluble drug

Amorphous solid dispersions: Rational selection of a manufacturing process

(2016) Teófilo Vasconcelos et al.   ADVANCED DRUG DELIVERY REVIEWS

Wetting Kinetics: an Alternative Approach Towards Understanding the Enhanced Dissolution Rate for Amorphous Solid Dispersion of a Poorly Soluble Drug

(2015) Sanjay Verma et al.   AAPS PHARMSCITECH

FTIR Spectroscopic Study of Poly(Ethylene Glycol)–Nifedipine Dispersion Stability in Different Relative Humidities

(2015) Waleed S. Iqbal et al.   JOURNAL OF PHARMACEUTICAL SCIENCES

Description of the Upcoming Change in Data Analysis for USP Dissolution Performance Verification Tests

(2015) Walter W. Hauck et al.   DISSOLUTION TECHNOLOGIES

Selecting oral bioavailability enhancing formulations during drug discovery and development

(2014) Sorin Emilian Leucuta   Expert Opinion on Drug Discovery

Factors Influencing Crystal Growth Rates from Undercooled Liquids of Pharmaceutical Compounds

(2014) Niraj S. Trasi et al.   JOURNAL OF PHYSICAL CHEMISTRY B

Impact of Polymers on the Crystallization and Phase Transition Kinetics of Amorphous Nifedipine during Dissolution in Aqueous Media

(2014) Shweta A. Raina et al.   MOLECULAR PHARMACEUTICS

The Role of Drug–Polymer Hydrogen Bonding Interactions on the Molecular Mobility and Physical Stability of Nifedipine Solid Dispersions

(2014) Khushboo Kothari et al.   MOLECULAR PHARMACEUTICS

Dissolution Studies of Poorly Soluble Drug Nanosuspensions in Non-sink Conditions

(2013) Peng Liu et al.   AAPS PHARMSCITECH

Preparation of carbamazepine–Soluplus® solid dispersions by hot-melt extrusion, and prediction of drug–polymer miscibility by thermodynamic model fitting

(2013) Jelena Djuris et al.   EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS

Development of Photothermal FTIR Microspectroscopy as a Novel Means of Spatially Identifying Amorphous and Crystalline Salbutamol Sulfate on Composite Surfaces

(2013) Louise C. Grisedale et al.   MOLECULAR PHARMACEUTICS

Polymorphism of Nifedipine: Crystal Structure and Reversible Transition of the Metastable β Polymorph

(2012) Erica Gunn et al.   CRYSTAL GROWTH & DESIGN

A Review on Freeze Drying of Drugs withtert-Butanol (TBA) + Water Systems: Characteristics, Advantages, Drawbacks

(2012) Séverine Vessot et al.   DRYING TECHNOLOGY

Solvent-mediated amorphous-to-crystalline transformation of nitrendipine in amorphous particle suspensions containing polymers

(2012) Dengning Xia et al.   EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES

In situlyophilisation of nifedipine directly in hard gelatine capsules

(2012) Matthew Crum et al.   PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY

The technologies used for developing orally disintegrating tablets: A review

(2011) Bhatu Badgujar et al.   ACTA PHARMACEUTICA

DEVELOPMENT AND VALIDATION OF A RAPID AND SIMPLE STABILITY-INDICATING LC METHOD FOR NIFEDIPINE

(2010) Gislaine Kuminek et al.   JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES

Phase Behavior of Poly(vinylpyrrolidone) Containing Amorphous Solid Dispersions in the Presence of Moisture

(2009) Alfred C. F. Rumondor et al.   MOLECULAR PHARMACEUTICS

Effect of drug-carrier interaction on the dissolution behavior of solid dispersion tablets

(2009) Parinda Srinarong et al.   PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY

Prediction of glass transition temperatures: Binary blends and copolymers

(2008) Witold Brostow et al.   MATERIALS LETTERS

Challenges and opportunities in the encapsulation of liquid and semi-solid formulations into capsules for oral administration

(2007) Ewart T. Cole et al.   ADVANCED DRUG DELIVERY REVIEWS