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Performance of multilayered particles: influence of a thin cushioning layer
O Chambin1, A Rota, M-H Rochat-Gonthier
1Pharmaceutical Powder Technology Group, IMSAPS Team, EA 581, University of Burgundy, School of Pharmacy, Dijon Cedex, France. odile.chambin@u-bourgogne.fr
Adding a HydroxyPropylMethyl Cellulose (HPMC) cushioning layer to coated theophylline particles protects polymer coats during tablet compression. This layer also enhances drug release rates, requiring careful evaluation for controlled oral drug delivery systems.
Area of Science:
- Pharmaceutical Technology
- Materials Science
- Drug Delivery Systems
Background:
- Controlled release oral dosage forms are increasingly important.
- Polymer coating of drug particles is a common method for controlling drug release.
- Coating integrity is often compromised during tablet compression, altering drug release.
Purpose of the Study:
- To investigate the impact of a HydroxyPropylMethyl Cellulose (HPMC) cushioning layer on coated theophylline particles.
- To assess the effects on particle characteristics, tablet properties, and dissolution performance.
- To understand how HPMC cushioning influences coating integrity and drug release during compression.
Main Methods:
- Coating theophylline particles with a polymer.
- Applying a thin HydroxyPropylMethyl Cellulose (HPMC) cushioning layer.
- Compressing coated particles into tablets.
- Evaluating particle characteristics, tablet properties (e.g., cohesiveness), and drug release profiles.
Main Results:
- The HPMC cushioning layer did not significantly affect particle characteristics.
- Tablet cohesiveness was reduced due to the cushioning effect of HPMC.
- The theophylline release rate increased, attributed to HPMC's water-solubility and channel formation.
- The cushioning layer protected polymer coats from fracture during compression.
Conclusions:
- A thin HPMC cushioning layer effectively protects polymer coats from damage during tablet compression.
- While protecting coats, the HPMC layer can increase drug release rates due to its properties.
- Both the protective effect on coating integrity and the impact on drug release must be evaluated for such drug delivery systems.
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