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Updated: Jun 2, 2026

Porous Silicon Microparticles for Delivery of siRNA Therapeutics
Published on: January 15, 2015
Novel amorphous microporous silica spheres for controlled release applications
Els Verraedt1, Guy Van den Mooter, Johan A Martens
1Centre for Surface Chemistry and Catalysis, K.U. Leuven, Kasteelpark Arenberg, Leuven, Belgium.
Researchers developed amorphous microporous silica (AMS) spheres for drug delivery. These particles enable slow, controlled release of ibuprofen for up to 14 days, showing potential for long-term medication management.
Area of Science:
- Materials Science
- Nanotechnology
- Pharmaceutical Sciences
Background:
- Developing advanced drug delivery systems is crucial for sustained therapeutic effects.
- Microporous materials offer potential for controlled release applications due to their high surface area and tunable pore structures.
Purpose of the Study:
- To synthesize novel spherical amorphous microporous silica (AMS) particles.
- To investigate the loading and in vitro release of ibuprofen from these AMS particles.
- To evaluate the potential of AMS spheres for long-term controlled drug delivery.
Main Methods:
- Synthesis of spherical amorphous microporous silica (AMS) particles using an oil drop method.
- Loading of molten ibuprofen into the prepared AMS particles.
- In vitro drug release studies to determine release kinetics and diffusion coefficients.
Main Results:
- Successfully synthesized spherical AMS particles (approx. 100 µm diameter, <2 nm pore diameter).
- Achieved successful loading of ibuprofen into the AMS pores.
- Demonstrated a slow pore diffusion-controlled release of ibuprofen lasting up to 14 days.
- Determined ibuprofen diffusion coefficients in the range of 10(-15) -10(-16) m(2) s(-1).
Conclusions:
- Amorphous microporous silica (AMS) spheres are effective carriers for controlled release of small drug molecules.
- The pore diffusion mechanism facilitates long-term drug release profiles.
- The spherical morphology of AMS particles enhances powder flow and ensures reliable release, beneficial for pharmaceutical formulations.
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Modified-Release Drug Delivery Systems: Rate-Programmed I
Modified-Release Drug Delivery Systems: Rate-Programmed II
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