In Vitro Release Mechanisms of Doxorubicin From a Clinical Bead Drug-Delivery System
Open Access
- 1 November 2016
- journal article
- research article
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 105 (11) , 3387-3398
Abstract
No abstract availableKeywords
Funding Information
- Swedish Research Council (521-2011-373)
This publication has 47 references indexed in Scilit:
- Controlling Cellular Uptake of Nanoparticles with pH-Sensitive PolymersScientific Reports, 2013
- Radiopaque Drug-Eluting Beads for Transcatheter Embolotherapy: Experimental Study of Drug Penetration and Coverage in SwineJournal of Vascular and Interventional Radiology, 2012
- New Insights into the Mechanisms of the Interactions Between Doxorubicin and the Ion-Exchange Hydrogel DC Bead™ for Use in Transarterial Chemoembolization (TACE)Journal of Biomaterials Science, Polymer Edition, 2012
- Accelerated in vitro release testing of implantable PLGA microsphere/PVA hydrogel composite coatingsInternational Journal of Pharmaceutics, 2012
- FIP/AAPS Joint Workshop Report: Dissolution/In Vitro Release Testing of Novel/Special Dosage FormsAAPS PharmSciTech, 2011
- Effect of Chemical Nature of 1,1-Salt on Structure of Polyelectrolyte Gel−Surfactant ComplexesThe Journal of Physical Chemistry B, 2001
- Visible absorption and proton nuclear magnetic resonance studies on the self-association of doxorubicin in aqueous solution.Chemical and Pharmaceutical Bulletin, 1991
- Phase equilibria in a three-component water-soap-alcohol system. A thermodynamic modelThe Journal of Physical Chemistry, 1987
- A Fickian diffusion transport process with features of transport catalysis. Doxorubicin transport in human red blood cells.Journal of General Physiology, 1981
- The Exchange Adsorption of Ions from Aqueous Solutions by Organic Zeolites. II. Kinetics1Journal of the American Chemical Society, 1947