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Matrices of water-soluble drug using natural polymer and direct compression method
Nery L Rosario1, Evone S Ghaly
1School of Pharmacy, University of Puerto Rico, P.O. Box 365067, San Juan, Puerto Rico 00936-5067.
Drug Development and Industrial Pharmacy
|October 16, 2002
Summary
Carrageenan matrices prepared by direct compression offer controlled theophylline release. Formulation optimization, including polymer concentration and dissolution media, is key to achieving desired drug delivery properties.
Area of Science:
- Pharmaceutical Sciences
- Materials Science
- Drug Delivery
Background:
- Carrageenan is a natural polymer with potential for pharmaceutical applications.
- Direct compression offers an efficient manufacturing method for solid dosage forms.
- Controlling drug release from polymer matrices is crucial for effective therapy.
Purpose of the Study:
- To optimize Carrageenan matrix formulations for controlled theophylline release.
- To evaluate the impact of Carrageenan concentration and excipients on drug release and physical properties.
- To investigate the influence of dissolution media and apparatus parameters on drug release kinetics.
Main Methods:
- Preparation of theophylline-loaded Carrageenan matrices using direct compression.
- Evaluation of drug release profiles in various dissolution media (water, HCl, phosphate buffer).
- Assessment of dissolution rate under different rotational speeds and apparatus types.
Main Results:
- Increased Carrageenan concentration reduced theophylline release.
- Dissolution media (pH 7.4 phosphate buffer, 0.1 N HCl) enhanced drug release.
- Higher rotational speeds increased drug release by affecting the gel layer integrity.
- Drug release followed a diffusion model up to 90 minutes, then a zero-order model.
Conclusions:
- Carrageenan matrices can be successfully manufactured via direct compression.
- Formulation parameters significantly influence drug release characteristics.
- Carrageenan matrices show potential for developing controlled-release drug delivery systems.