Development of a standardized dissolution test method for inhaled pharmaceutical formulations
Authors:
- Jason T. McConvilleJMJason T. McConville
- 1 December 2009
- journal article
- Published by Elsevier in International Journal of Pharmaceutics
- Vol. 382 (1-2) , 15-22
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Preparation, characterization and applications of ultrathin cellulose acetate Langmuir–Blodgett filmsSoft Matter, 2007
- Inducing effect of liposomalization on the transdermal delivery of hydrocortisone: Creation of a drug supersaturated stateJournal of Controlled Release, 2006
- Modeling of dissolution-diffusion controlled drug release from planar polymeric systems with finite dissolution rate and arbitrary drug loadingJournal of Membrane Science, 2006
- Novel sustained release microspheres for pulmonary drug deliveryJournal of Controlled Release, 2005
- Synthesis, characterization and thermal studies on cellulose acetate membranes with additiveEuropean Polymer Journal, 2004
- Theophylline particle design using chitosan by the spray dryingInternational Journal of Pharmaceutics, 2003
- A novel method for assessing dissolution of aerosol inhaler productsInternational Journal of Pharmaceutics, 2003
- Application of In Vitro Dissolution Tests to Different Uranium Compounds and Comparison with In Vivo DataRadiation Protection Dosimetry, 1998
- Release kinetics of indomethacin from pressure sensitive adhesive matricesJournal of Controlled Release, 1997
- Analysis of Data on the Medicament Release from OintmentsJournal of Pharmaceutical Sciences, 1962