Hybrid mesoporous silica with controlled drug release
Author(s) -
László Almásy,
Ana-Maria Putz,
Qiang Tian,
Г. П. Копица,
Т. В. Хамова,
Réka Barabás,
M. O. Rigo,
Attila Bóta,
András Wacha,
Marius Mirica,
Bogdan-Ovidiu Țăranu,
Cecilia Savii
Publication year - 2019
Publication title -
journal of the serbian chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.227
H-Index - 45
eISSN - 1820-7421
pISSN - 0352-5139
DOI - 10.2298/jsc181109009a
Subject(s) - mesoporous material , mesoporous silica , ammonium bromide , chemical engineering , materials science , nitric acid , porosity , microstructure , drug delivery , adsorption , ketoprofen , fourier transform infrared spectroscopy , catalysis , nuclear chemistry , chemistry , organic chemistry , chromatography , nanotechnology , composite material , pulmonary surfactant , engineering , metallurgy
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.
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