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Diffusion-Controlled Drug Release From the Mesoporous Magnesium Carbonate Upsalite(®)
Peng Zhang1, Teresa Zardán Gómez de la Torre1, Johan Forsgren1
1Division of Nanotechnology and Functional Materials, Department of Engineering Sciences, Uppsala University, Uppsala SE-751 21, Sweden.
Mesoporous magnesium carbonate Upsalite® enhances ibuprofen dissolution and enables sustained release. Particle size controls initial release, while material properties facilitate extended drug delivery over 24 hours.
Area of Science:
- Materials Science
- Pharmaceutical Sciences
- Chemical Engineering
Background:
- Mesoporous materials are investigated for drug delivery applications.
- Upsalite®, a mesoporous magnesium carbonate, shows potential as a drug carrier.
- Ibuprofen, a Biopharmaceutics Classification System class II drug, exhibits poor solubility.
Purpose of the Study:
- To investigate in vitro drug release of ibuprofen from Upsalite®.
- To evaluate the effect of particle size on drug release kinetics.
- To determine the diffusion parameters of ibuprofen within the Upsalite® matrix.
Main Methods:
- In vitro drug release studies using well-defined particle-size fractions of Upsalite®.
- Drug loading quantification and characterization of ibuprofen state (amorphous/crystalline).
- Analysis of diffusion parameters including diffusion coefficient, constrictivity, and tortuosity.
Main Results:
- Ibuprofen was loaded at 30% w/w, with 80% pore filling, in an amorphous state.
- Initial release rate was particle-size dependent, with dissolution over four times faster than crystalline ibuprofen.
- An extended release of approximately 24 hours was observed, influenced by drug concentration.
Conclusions:
- Upsalite® enhances the dissolution rate of ibuprofen.
- The material's high tortuosity (15) supports its use in sustained-release formulations.
- Particle size engineering of Upsalite® can optimize drug release profiles for enhanced and sustained delivery.
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