Preparation and release behaviour of mesoporous silica/ethylcellulose sustained-release mini-matrix.
- Author:
Qiao-li WU
;
Gui-lan QUAN
;
Yu HONG
;
Lin-na WU
;
You-mei ZENG
;
Ge LI
;
Xin PAN
;
Chuan-bin WU
- Publication Type:Journal Article
- MeSH:
Adsorption;
Calorimetry, Differential Scanning;
Cellulose;
analogs & derivatives;
Delayed-Action Preparations;
Drug Carriers;
chemistry;
Particle Size;
Porosity;
Powder Diffraction;
Powders;
Silicon Dioxide;
Solubility;
X-Ray Diffraction
- From:
Acta Pharmaceutica Sinica
2015;50(4):492-499
- CountryChina
- Language:Chinese
-
Abstract:
Hot-melt extrusion was applied to prepare mesoporous silica/ethylcellulose mini-matrix for sustained release, and fenofibrate was used as a model drug, ethylcellulose and xanthan gum were chosen as sustained-release agent and releasing moderator, respectively. This novel matrix obtained the controlled release ability by combining mesoporous silica drug delivery system and hot-melt extrusion technology. And mesoporous silica particle (SBA-15) was chosen as drug carrier to increase the dissolution rate of fenofibrate in this martix. Scanning electron microscope, transmission electron microscope, small angle X-ray powder diffraction and N2 adsorption-desorption were introduced to determine the particle morphology, particle size and pore structure of the synthesized SBA-15. The results showed that SBA-15 had a very high Brunauer-Emmett-Teller specific surface area, a narrow pore size distribution, large pore volume and a ordered two-dimensional hexagonal structure of p6mm symmetry. Differential scanning calorimetry and X-ray powder diffraction results demonstrated that fenofibrate dispersed in an amorphous state inside the pores of the mesoporous silica which contributed to the improvement in the dissolution rate. The drug release of mini-matrices was influenced by ethylcellulose viscosity grades and xanthan gum concentration, which increased with the increasing of xanthan gum concentration and decreasing of ethylcellulose viscosity. Mini-matrix containing 22% xanthan gum exhibited a good sustained release performance, and the drug release behavior followed the first-order kinetics.
