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Published on: December 23, 2013
Matrix polymeric excipients: comparing a novel interpolyelectrolyte complex with hydroxypropylmethylcellulose
Zhilei Lu1, Weiyang Chen, Eugene Olivier
1Department of Pharmaceutical Sciences, Tshwane University of Technology, Pretoria, South Africa.
This study compared hydroxypropylmethylcellulose matrix systems with chitosan-polycarbophil complex systems for drug release. The chitosan-polycarbophil complex demonstrated slower drug release and approached zero-order kinetics, indicating improved controlled drug delivery.
Area of Science:
- Pharmaceutical Sciences
- Polymer Science
Background:
- Hydrophilic polymers like hydroxypropylmethylcellulose are widely used in monolithic matrix systems for controlled drug release.
- Chitosan and polycarbophil can form interpolyelectrolyte complexes with potential applications in drug delivery.
Purpose of the Study:
- To compare the in vitro dissolution, swelling, and erosion behavior of hydroxypropylmethylcellulose (HPMC) matrix systems with those containing a chitosan-polycarbophil interpolyelectrolyte complex.
- To evaluate the drug release mechanisms and kinetics from these two types of matrix systems.
Main Methods:
- Preparation of monolithic matrix tablets containing either HPMC or a chitosan-polycarbophil complex.
- In vitro dissolution, swelling, and erosion studies were conducted.
- Kinetic analysis of drug release profiles was performed.
Main Results:
- Both matrix systems exhibited a combination of swelling and erosion as drug release mechanisms.
- Matrix systems containing the chitosan-polycarbophil complex showed higher mean dissolution times, indicating slower drug release compared to HPMC systems.
- Zero-order release kinetics were approached for some formulations with the chitosan-polycarbophil complex, but not for HPMC formulations.
Conclusions:
- The chitosan-polycarbophil interpolyelectrolyte complex is a promising alternative to HPMC for developing monolithic matrix systems with controlled drug release properties.
- The observed slower drug release and potential for zero-order kinetics from chitosan-polycarbophil matrices offer advantages for optimizing drug delivery profiles.
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