Hybrid mesoporous silica with controlled drug release

被引:9
|
作者
Almasy, Laszlo [1 ,2 ]
Putz, Ana-Maria [3 ]
Tian, Qiang [1 ]
Kopitsa, Gennady P. [4 ,5 ]
Khamova, Tamara, V [5 ]
Barabas, Reka [6 ]
Rigo, Melinda [6 ]
Bota, Attila [7 ]
Wacha, Andras [7 ]
Mirica, Marius [8 ]
Taranu, Bogdan [8 ]
Savii, Cecilia [3 ]
机构
[1] Southwest Univ Sci & Technol, State Key Lab Environm Friendly Energy Mat, Mianyang 621010, Sichuan, Peoples R China
[2] Hungarian Acad Sci, Wigner Res Ctr Phys, Inst Solid State Phys & Opt, POB 49, H-1525 Budapest, Hungary
[3] Romanian Acad, Coriolan Dragulescu Inst Chem Timisoara, Bv Mihai Viteazul 24, RO-300223 Timisoara, Romania
[4] RAS, Inst Silicate Chem, Nab Makarova 2, St Petersburg 199034, Russia
[5] Petersburg Nucl Phys Inst, PNPI 1, Gatchina 188300, Leningrad Regio, Russia
[6] Babes Bolyai Univ, Fac Chem & Chem Engn, Dept Chem & Chem Engn Hungarian Line Study, Arany Janos Str 11, RO-400028 Cluj Napoca, Romania
[7] Hungarian Acad Sci, Res Ctr Nat Sci, POB 286, H-1519 Budapest, Hungary
[8] Natl Inst Res & Dev Electrochem & Condensed Matte, Dr Aurel Paunescu Podeanu Str 144, RO-300569 Timisoara, Romania
关键词
sol-gel process; ketoprofen; hybrid material; SAXS; STRUCTURAL-PROPERTIES; MCM-41; METHYLTRIETHOXYSILANE; FUNCTIONALIZATION; NANOCOMPOSITE; ADSORPTION; IBUPROFEN; POROSITY; SPHERES; WATER;
D O I
10.2298/JSC181109009A
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The mesoporous silica particles were prepared by the sol-gel method in one-step synthesis, in acidic conditions, from tetraethoxysilane (TEOS) and methyltriethoxysilane (MTES), varying the mole ratio of the silica precursors. Nitric acid was used as catalyst at room temperature and hexadecyltrimethyl ammonium bromide (CTAB) as structure directing agent. Optical properties, porosity and microstructure of the materials in function of the MTES/TEOS ratio were evaluated using infrared spectroscopy, nitrogen adsorption and small angle X-ray scattering. All materials showed the ordered pore structure and the high specific surfaces, making them suitable as the drug delivery systems. Drug loading and release tests using ketoprofen were performed to assess their performance for drug delivery applications. The amount of the methylated precursor used in the synthesis had little effect on the drug loading capacity, but had a strong influence on the initial rate of the drug release.
引用
收藏
页码:1027 / 1039
页数:13
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