Tabletted polylactide microspheres prepared by a w/o emulsion-spray drying method
- 1 January 2000
- journal article
- research article
- Published by Taylor & Francis in Journal of Microencapsulation
- Vol. 17 (6), 711-720
- https://doi.org/10.1080/02652040050161701
Abstract
An emulsification-spray drying technique is used to prepare poly(D, L-lactic acid) (PDLLA) microparticles loaded with a water soluble, non-steroidal antiinflammatory drug (NSAID), sodium naproxen (NaNPX). The method involves the preparation of a w/o emulsion in which the water soluble drug is dissolved in the aqueous dispersed phase, while the polymer is dissolved in the organic continuous phase. As a comparison, microparticles were prepared by spraying a suspension of the drug into an organic solution of the polymer. The spray-dried particles were characterized using SEM, DSC, XRD and in vitro release tests. The spray-dried product was then compressed (direct compression) to obtain controlled release matrix tablets. All microparticles release NaNPX within 30min. The matrix tablets release the drug in 8-10h; the matrix tablets characterized by the presence of surfactant (due to the emulsion used to obtain the microparticles) have the highest release rate.Keywords
This publication has 7 references indexed in Scilit:
- A new method for the synthesis of smooth, round, hydrophilic protein microspheres using low concentrations of polymeric dispersing agentsJournal of Microencapsulation, 1995
- Preparation and Evaluation of Controlled Release Indomethacin MicrospheresDrug Development and Industrial Pharmacy, 1984
- Morphological changes of ethylene/vinyl acetate-based controlled delivery systems during release of water-soluble solutesJournal of Membrane Science, 1983
- Letters to the Editor: Linearization of dissolution rate curves by the Weibull distributionJournal of Pharmacy and Pharmacology, 1972
- Drug Release from Wax Matrices IIJournal of Pharmaceutical Sciences, 1968
- Mechanism of sustained‐action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matricesJournal of Pharmaceutical Sciences, 1963
- A New Oral Gelatinized Sustained-Release Dosage FormJournal of Pharmaceutical Sciences, 1963