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Determination of the release mechanism of Theophylline from pellets coated with Surelease ® -A water dispersion of ethyl cellulose.

Authors :
Kazlauske J
Cafaro MM
Caccavo D
Marucci M
Lamberti G
Barba AA
Larsson A
Source :
International journal of pharmaceutics [Int J Pharm] 2017 Aug 07; Vol. 528 (1-2), pp. 345-353. Date of Electronic Publication: 2017 Jun 02.
Publication Year :
2017

Abstract

The aim of this study was to investigate the water transport over free standing films based on the aqueous ethyl cellulose (EC) coating Surelease <superscript>®</superscript> and the drug (Theophylline) release mechanism from coated pellets. It was found that the main drug release rate from pellets was controlled by a diffusion mechanism. However, the drug release rate was altered by addition of sodium chloride to the external release medium. A decrease in the drug release rate when sodium chloride is added to the release medium has traditionally been used to indicate an osmotic drug release mechanism. However, our findings that the release rate decreased by sodium chloride addition could be explained by sodium chloride diffusing through the coating layer into the inner parts of the pellets, decreasing the solubility of Theophylline. This gave a reduced drug concentration gradient over the coating layer and thus a slower release rate. Furthermore, this study shows, as expected, that the transport of water through Surelease <superscript>®</superscript> films into the pellets was faster than the transport out of Theophylline (approx. seven times), which was the reason why the pellets were swelling during the release. It was also shown that the drug release rate, determined for both whole dose release and for single pellets, decreased with increasing thickness (from 16 to 51μm) of the coating layer controlling the drug release rate.<br /> (Copyright © 2017. Published by Elsevier B.V.)

Details

Language :
English
ISSN :
1873-3476
Volume :
528
Issue :
1-2
Database :
MEDLINE
Journal :
International journal of pharmaceutics
Publication Type :
Academic Journal
Accession number :
28583332
Full Text :
https://doi.org/10.1016/j.ijpharm.2017.05.073