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Improved dissolution behavior of lipophilic drugs by solid dispersions: the production process as starting point for formulation considerations

Expert opinion on drug delivery, 2011-09, Vol.8 (9), p.1121-1140

2011

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Bottom-Up Preparation Techniques for Nanocrystals of Lipophilic Drugs

Pharmaceutical research, 2011-05, Vol.28 (5), p.1220-1223

2011

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CLSM as Quantitative Method to Determine the Size of Drug Crystals in a Solid Dispersion

Pharmaceutical research, 2011-10, Vol.28 (10), p.2567-2574

2011

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Tailored protein release from biodegradable poly(ε-caprolactone-PEG)-b-poly(ε-caprolactone) multiblock-copolymer implants

European journal of pharmaceutics and biopharmaceutics, 2014-07, Vol.87 (2), p.329-337

2014

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Polymeric formulations for drug release prepared by hot melt extrusion: application and characterization

Drug discovery today, 2015-07, Vol.20 (7), p.812-823

2015

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Quality by design approach for optimizing the formulation and physical properties of extemporaneously prepared orodispersible films

International journal of pharmaceutics, 2015-05, Vol.485 (1-2), p.70-76

2015

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Orodispersible films in individualized pharmacotherapy: The development of a formulation for pharmacy preparations

International journal of pharmaceutics, 2015-01, Vol.478 (1), p.155-163

2015

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Inulin solid dispersion technology to improve the absorption of the BCS Class IV drug TMC240

European journal of pharmaceutics and biopharmaceutics, 2010-02, Vol.74 (2), p.233-238

2010

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Efficient production of solid dispersions by spray drying solutions of high solid content using a 3-fluid nozzle

European journal of pharmaceutics and biopharmaceutics, 2018-02, Vol.123, p.50-58

2018

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Characterization of a cyclosporine solid dispersion for inhalation

The AAPS journal, 2007-06, Vol.9 (2), p.E190-E199

2007

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Surface-Active Derivative of Inulin (Inutec® SP1) Is a Superior Carrier for Solid Dispersions with a High Drug Load

Journal of pharmaceutical sciences, 2011-06, Vol.100 (6), p.2333-2342

2011

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Controlled Crystallization of the Lipophilic Drug Fenofibrate During Freeze-Drying: Elucidation of the Mechanism by In-Line Raman Spectroscopy

The AAPS journal, 2010-12, Vol.12 (4), p.569-575

2010

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Nanoparticle formulation of a poorly soluble cannabinoid receptor 1 antagonist improves absorption by rat and human intestine

Drug metabolism and disposition, 2013-08, Vol.41 (8), p.1557

2013

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

Pharmaceutical development and technology, 2010-10, Vol.15 (5), p.460-468

2010

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Improved dissolution behavior of lipophilic drugs by solid dispersions: the production process as starting point for formulation considerations

Bottom-Up Preparation Techniques for Nanocrystals of Lipophilic Drugs

CLSM as Quantitative Method to Determine the Size of Drug Crystals in a Solid Dispersion

Tailored protein release from biodegradable poly(ε-caprolactone-PEG)-b-poly(ε-caprolactone) multiblock-copolymer implants

Polymeric formulations for drug release prepared by hot melt extrusion: application and characterization

Quality by design approach for optimizing the formulation and physical properties of extemporaneously prepared orodispersible films

Orodispersible films in individualized pharmacotherapy: The development of a formulation for pharmacy preparations

Inulin solid dispersion technology to improve the absorption of the BCS Class IV drug TMC240

Efficient production of solid dispersions by spray drying solutions of high solid content using a 3-fluid nozzle

Characterization of a cyclosporine solid dispersion for inhalation

Surface-Active Derivative of Inulin (Inutec® SP1) Is a Superior Carrier for Solid Dispersions with a High Drug Load

Controlled Crystallization of the Lipophilic Drug Fenofibrate During Freeze-Drying: Elucidation of the Mechanism by In-Line Raman Spectroscopy

Nanoparticle formulation of a poorly soluble cannabinoid receptor 1 antagonist improves absorption by rat and human intestine

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

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