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Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations, Part 1: Method Parameterization and Comparison of In Vitro Digestion Profiles Across a Range of Representative Formulations

Journal of pharmaceutical sciences, 2012-09, Vol.101 (9), p.3360-3380

2012

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Solid lipid excipients - matrix agents for sustained drug delivery

Journal of controlled release, 2014-08, Vol.188, p.18-30

2014

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Development and evaluation of sustained-release Compritol® 888 ATO matrix mini-tablets

Drug development and industrial pharmacy, 2012-09, Vol.38 (9), p.1068-1076

2012

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Continuous twin screw melt granulation of glyceryl behenate: Development of controlled release tramadol hydrochloride tablets for improved safety

International journal of pharmaceutics, 2015-06, Vol.487 (1-2), p.72-80

2015

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High shear blending with glyceryl distearate provides individually coated drug particles for effective taste masking

Journal of drug delivery science and technology, 2018-12, Vol.48, p.437-449

2018

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Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations. 5. Lipolysis of Representative Formulations by Gastric Lipase

Pharmaceutical research, 2015-04, Vol.32 (4), p.1279-1287

2015

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Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations, Part 6: Effects of Varying Pancreatin and Calcium Levels

The AAPS journal, 2014-11, Vol.16 (6), p.1344-1357

2014

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Effect of Tablet Structure on Controlled Release from Supersaturating Solid Dispersions Containing Glyceryl Behenate

Molecular pharmaceutics, 2015-01, Vol.12 (1), p.120-126

2015

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Optimizing a wet granulation process to obtain high-dose sustained-release tablets with Compritol 888 ATO

Drug development and industrial pharmacy, 2015-01, Vol.41 (10), p.1738-1744

2015

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Preparation and characterization of Compritol 888 ATO matrix tablets for the sustained release of diclofenac sodium

Pharmaceutical development and technology, 2015-06, Vol.20 (4), p.507-512

2015

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An investigation into the mechanism of dissolution rate enhancement of poorly water-soluble drugs from spray chilled gelucire 50/13 microspheres

Journal of pharmaceutical sciences, 2010-01, Vol.99 (1), p.262-274

2010

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Solid dosage forms from self-emulsifying lipidic formulations

Pharmaceutical technology Europe, 2008-04, Vol.20 (4), p.46

2008

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Preparation and characterization of Compritol 888 ATO matrix tablets for the sustained release of diclofenac sodium

Pharmaceutical Development and Technology, 2015, Vol.20 (4), p.507-512

2015

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Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations, Part 1: Method Parameterization and Comparison of In Vitro Digestion Profiles Across a Range of Representative Formulations

Solid lipid excipients - matrix agents for sustained drug delivery

Development and evaluation of sustained-release Compritol® 888 ATO matrix mini-tablets

Continuous twin screw melt granulation of glyceryl behenate: Development of controlled release tramadol hydrochloride tablets for improved safety

High shear blending with glyceryl distearate provides individually coated drug particles for effective taste masking

Toward the Establishment of Standardized in Vitro Tests for Lipid-Based Formulations. 2. The Effect of Bile Salt Concentration and Drug Loading on the Performance of Type I, II, IIIA, IIIB, and IV Formulations during in Vitro Digestion

Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations. 5. Lipolysis of Representative Formulations by Gastric Lipase

Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations, Part 6: Effects of Varying Pancreatin and Calcium Levels

Effect of Tablet Structure on Controlled Release from Supersaturating Solid Dispersions Containing Glyceryl Behenate

Optimizing a wet granulation process to obtain high-dose sustained-release tablets with Compritol 888 ATO

Preparation and characterization of Compritol 888 ATO matrix tablets for the sustained release of diclofenac sodium

An investigation into the mechanism of dissolution rate enhancement of poorly water-soluble drugs from spray chilled gelucire 50/13 microspheres

Solid dosage forms from self-emulsifying lipidic formulations

Preparation and characterization of Compritol 888 ATO matrix tablets for the sustained release of diclofenac sodium

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