Drug delivery;
Drug release;
Drug adsorption;
Nanostructured drug delivery vehicles;
Functionalized mesoporous materials;
IN-VITRO RELEASE;
SILICA NANOPARTICLES;
ORGANIC MODIFICATION;
CONTROLLED DELIVERY;
MCM-41;
SBA-15;
IBUPROFEN;
INCLUSION;
PARTICLES;
SPHERES;
D O I:
10.1016/j.jssc.2009.03.034
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
The adsorption capacity and release properties of mesoporous materials for drug molecules can be improved by functionalizing their Surfaces with judiciously chosen organic groups. Functionalized ordered mesoporous materials containing various types of organic groups via a co-condensation synthetic method from 15% organosilane and by post-grafting organosilanes onto a pre-made mesoporous silica were synthesized. Comparative studies of their adsorption and release properties for various model drug molecules were then conducted. Functional groups including 3-aminopropyl, 3-mercaptopropyl, vinyl, and secondary amine groups were used to functionalize the mesoporous materials while rhodamine 6G and ibuprofen were utilized to investigate the materials' relative adsorption and release properties. The self-assembly of the mesoporous materials was carried out in the presence of cetyltrimethylammonium bromide (CTAB) surfactant, which produced MCM-41 type 2 materials with pore diameters of similar to 2.7-3.3 nm and moderate to high Surface areas up to similar to 1000 m(2)/g. The different functional groups introduced into the materials dictated their adsorption capacity and release properties. While mercaptopropyl and vinyl functionalized samples showed high adsorption capacity for rhodamine 6G, amine functionalized samples exhibited higher adsorption capacity for ibuprofen. While the diffusional release of ibuprofen was fitted on the Fickian diffusion model. the release of rhodamine 6G followed Super Case-II transport model. (C) 2009 Elsevier Inc. All rights reserved.
机构:
Purdue Univ, Ctr Paralysis Res, Sch Vet Med, W Lafayette, IN 47907 USAPurdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
Cho, Youngnam
Shi, Riyi
论文数: 0引用数: 0
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机构:
Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
Purdue Univ, Ctr Paralysis Res, Sch Vet Med, W Lafayette, IN 47907 USAPurdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
Shi, Riyi
Borgens, Richard B.
论文数: 0引用数: 0
h-index: 0
机构:
Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
Purdue Univ, Ctr Paralysis Res, Sch Vet Med, W Lafayette, IN 47907 USAPurdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
Borgens, Richard B.
Ivanisevic, Albena
论文数: 0引用数: 0
h-index: 0
机构:
Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
Purdue Univ, Dept Chem, W Lafayette, IN 47907 USAPurdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
机构:
Purdue Univ, Ctr Paralysis Res, Sch Vet Med, W Lafayette, IN 47907 USAPurdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
Cho, Youngnam
Shi, Riyi
论文数: 0引用数: 0
h-index: 0
机构:
Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
Purdue Univ, Ctr Paralysis Res, Sch Vet Med, W Lafayette, IN 47907 USAPurdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
Shi, Riyi
Borgens, Richard B.
论文数: 0引用数: 0
h-index: 0
机构:
Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
Purdue Univ, Ctr Paralysis Res, Sch Vet Med, W Lafayette, IN 47907 USAPurdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
Borgens, Richard B.
Ivanisevic, Albena
论文数: 0引用数: 0
h-index: 0
机构:
Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
Purdue Univ, Dept Chem, W Lafayette, IN 47907 USAPurdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA