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Matrices containing NaCMC and HPMC 2. Swelling and release mechanism study
1Department of Pharmaceutical Chemistry, Via Taramelli, 12, I-27100 Pavia, Italy. stefania.conti@unipv.it
This study explores how swelling in hydroxypropylmethylcellulose (HPMC) and sodium carboxymethylcellulose (NaCMC) matrices affects drug release. Results show specific swelling behaviors at different pH levels, influencing drug delivery.
Area of Science:
- Pharmaceutical Sciences
- Materials Science
Background:
- Controlled drug release systems utilize polymer matrices to modulate drug delivery.
- Hydroxypropylmethylcellulose (HPMC) and sodium carboxymethylcellulose (NaCMC) are widely used hydrophilic polymers in oral dosage forms.
Purpose of the Study:
- To investigate the swelling behavior of combined HPMC and NaCMC matrix systems (MB) with a model drug.
- To correlate the morphological changes during swelling with the drug release performance across different pH environments.
- To understand the gel layer characteristics and their impact on drug release kinetics.
Main Methods:
- Tablets containing a drug-polymer mixture (MB) and reference tablets with individual polymers were prepared.
- Swelling studies were conducted at three different pH values (acidic and neutral).
- Morphological analysis of the gel layer and drug release profiles were evaluated.
Main Results:
- MB matrices exhibited similar swelling at pH 4.5 and 6.8 but different behavior in acidic conditions.
- At pH 1, NaCMC formed a rigid, partially crosslinked gel, while HPMC and MB formed physical, non-crosslinked gels.
- At pH 4.5 and 6.8, all systems showed physical gel formation, with MB matrices achieving constant drug release via diffusion and erosion.
Conclusions:
- The pH-dependent swelling behavior of HPMC/NaCMC matrices significantly influences drug release mechanisms.
- MB matrices demonstrate potential for zero-order drug release at neutral pH due to stable gel layer formation and combined diffusion-erosion mechanisms.
- Understanding polymer-drug interactions and matrix morphology is crucial for designing effective controlled-release formulations.
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