An investigation into the use of low quantities of functional additives to control drug release from hot melt extruded solid dispersions for poorly soluble drug delivery
Authors:
- 1 April 2020
- journal article
- research article
- Published by Elsevier in International Journal of Pharmaceutics
- Vol. 579, 119172
Abstract
No abstract availableKeywords
Funding Information
- European Regional Development Fund (2S01-059_IMODE)
This publication has 29 references indexed in Scilit:
- A discriminatory intrinsic dissolution study using UV area imaging analysis to gain additional insights into the dissolution behaviour of active pharmaceutical ingredientsInternational Journal of Pharmaceutics, 2012
- Behaviour of HPMC compacts investigated using UV-imagingInternational Journal of Pharmaceutics, 2012
- Critical factors in the release of drugs from sustained release hydrophilic matricesJournal of Controlled Release, 2011
- The influence of crystallization inhibition of HPMC and HPMCAS on model substance dissolution and release in swellable matrix tabletsEuropean Journal of Pharmaceutics and Biopharmaceutics, 2011
- An investigation into the mechanism of dissolution rate enhancement of poorly water-soluble drugs from spray chilled gelucire 50/13 microspheresJournal of Pharmaceutical Sciences, 2010
- Effects of Moisture on the Growth Rate of Felodipine Crystals in the Presence and Absence of PolymersCrystal Growth & Design, 2009
- Hydroxypropyl Methylcellulose Acetate Succinate-Based Spray-Dried Dispersions: An OverviewMolecular Pharmaceutics, 2008
- Pharmaceutical Applications of Hot-Melt Extrusion: Part IDrug Development and Industrial Pharmacy, 2007
- Controlled Release of a Poorly Water-Soluble Drug from Hot-Melt Extrudates Containing Acrylic PolymersDrug Development and Industrial Pharmacy, 2006
- Relationship between the glass transition temperature and the interaction parameter of miscible binary polymer blendsMacromolecules, 1992