Oral Controlled Release Dosage Forms. II. Glassy Polymers in Hydrophilic Matrices
- 1 January 1998
- journal article
- review article
- Published by Taylor & Francis in Drug Development and Industrial Pharmacy
- Vol. 24 (1) , 1-9
- https://doi.org/10.3109/03639049809082346
Abstract
Part I of this article reported general considerations of oral controlled release dosage forms and the applications of cellulose ether polymers in hydrophilic matrices. Part II of this study describes the advantages and disadvantages of limited swelling hydrophilic matrices, their preparation, mechanism, and parameters affecting drug release from these systems.Keywords
This publication has 31 references indexed in Scilit:
- Characterization of Compressibility and Compactibility of Poly(ethylene oxide) Polymers for Modified Release Application by Compaction SimulatorJournal of Pharmaceutical Sciences, 1996
- A study on permeation behavior of a liquid mixture through PVA membranes having a crosslinking gradient structure in pervaporationJournal of Applied Polymer Science, 1996
- Pervaporation performance of asymmetrically crosslinked PVA membranesJournal of Applied Polymer Science, 1995
- Preparation and characterization of two HEMA/PVA copolymers: Poly[HEMA-co-(PVA-AA)] and poly[HEMA-co-(PVA-MA)]Journal of Applied Polymer Science, 1992
- Modification of the dynamic swelling behavior of poly(2‐hydroxyethyl methacrylate) in waterJournal of Applied Polymer Science, 1991
- Consideration of Drug Load on the Swelling Kinetics of Glassy Gelatin MatricesJournal of Pharmaceutical Sciences, 1990
- Swelling of anionic and cationic starch‐based superabsorbents in water and saline solutionJournal of Applied Polymer Science, 1990
- Preparation, characterization, and properties of polylactide (PLA)–poly(ethylene glycol) (PEG) copolymers: A potential drug carrierJournal of Applied Polymer Science, 1990
- Crosslinked Poloxamers as a Versatile Monolithic Drug Delivery SystemDrug Development and Industrial Pharmacy, 1986
- Effect of non-uniform initial drug concentration distribution on the kinetics of drug release from glassy hydrogel matricesPolymer, 1984