Hybrid mesoporous silica with controlled drug release

Author:

Almásy László1,Putz Ana-Maria2,Tian Qiang3,Kopitsa Gennady4,Khamova Tamara5,Barabás Réka6,Rigó Melinda6,Bóta Attila7,Wacha András7,Mirica Marius8,Ţăranu Bogdan8,Savii Cecilia2

Affiliation:

1. State Key Laboratory of Environment-Friendly Energy Materials, Southwest University of Science and Technology, Mianyang, China + Institute for Solid State Physics and Optics, Wigner Research Centre for Physics, Hungarian Academy of Sciences, POB Budapest,

2. Institute of Chemistry Timisoara of Romanian Academy, Timisoara, Romania

3. State Key Laboratory of Environment-Friendly Energy Materials, Southwest University of Science and Technology, Mianyang, China

4. Institute of Silicate Chemistry of RAS, St. Petersburg, Russia + Petersburg Nuclear Physics Institute, PNPI, Gatchina, Leningrad region, Russia

5. Petersburg Nuclear Physics Institute, PNPI, Gatchina, Leningrad region, Russia

6. Babeș-Bolyai University, Faculty of Chemistry and Chemical Engineering, Department of Chemistry and Chemical Engineering of Hungarian Line of Study, Cluj-Napoca, Romania

7. Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary

8. National Institute for Research and Development in Electrochemistry and Condensed Matter, Timisoara, Romania

Abstract

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.

Publisher

National Library of Serbia

Subject

General Chemistry

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