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Ibuprofen release from hydrophilic ceramic-polymer composites
D Arcos1, M V Cabanas, C V Ragel
1Departamento de Química Inorgánica y Bioinorgánica, Facultad de Farmacia, UCM, Madrid, Spain.
Biomaterials
|September 23, 1997
Summary
This study developed novel composite materials for drug delivery. The alpha-Al2O3 ceramic component controlled swelling and ibuprofen release from polymer matrices, preventing premature drug burst.
Area of Science:
- Materials Science
- Polymer Chemistry
- Biomedical Engineering
Background:
- Advanced composite materials are crucial for controlled drug delivery systems.
- Poly(methyl methacrylate) (PMMA) and poly(vinyl pyrrolidone) (PVP) are common polymers in biomedical applications.
- Alpha-alumina (alpha-Al2O3) offers unique properties for composite material design.
Purpose of the Study:
- To synthesize and characterize novel alpha-Al2O3/polymer composites for drug delivery.
- To investigate the influence of hydrophilic components on composite hydration and swelling.
- To evaluate the drug release kinetics of ibuprofen from the developed composite systems.
Main Methods:
- Free radical polymerization was used to prepare the composite systems.
- Spectroscopic techniques, thermogravimetric analysis (TGA), and differential thermal analysis (DTA) were employed for characterization.
- Hydration behavior and ibuprofen release were analyzed in buffered solutions at pH 7.4 and 37°C using UV spectroscopy.
Main Results:
- Composite swelling was significantly influenced by the hydrophilic content and the presence of alpha-Al2O3.
- The release of ibuprofen was modulated by the composite components.
- A controlled drug release profile was observed, notably lacking the typical 'burst' effect seen in purely hydrophilic systems.
Conclusions:
- The developed alpha-Al2O3/polymer composites demonstrate tunable hydration and drug release properties.
- The incorporation of alpha-Al2O3 effectively controls swelling and modulates ibuprofen release kinetics.
- These findings suggest potential for these composites in advanced drug delivery applications requiring sustained release.