Mesoporous Silica as a Drug Delivery System for Naproxen: Influence of Surface Functionalization

被引:16
|
作者
Zid, Lukas [1 ]
Zelenak, Vladimir [1 ]
Almasi, Miroslav [1 ]
Zelenakova, Adriana [2 ]
Szucsova, Jaroslava [2 ]
Bednarcik, Jozef [2 ]
Sulekova, Monika [3 ]
Hudak, Alexander [3 ]
Vahovska, Lucia [3 ]
机构
[1] Safarik Univ, Dept Inorgan Chem, Fac Sci, Moyzesova 11, SK-04154 Kosice, Slovakia
[2] Safarik Univ, Inst Phys, Pk Angelinum 9, Kosice 04001, Slovakia
[3] Univ Vet Med & Pharm, Dept Chem Biochem & Biophys, Inst Pharmaceut Chem, Kosice 04181, Slovakia
来源
MOLECULES | 2020年 / 25卷 / 20期
关键词
drug delivery system; nanomaterials; mesoporous silica; naproxen; prolonged release; DIRECT CO-CONDENSATION; CONTROLLED-RELEASE; NANOPARTICLES; MCM-41;
D O I
10.3390/molecules25204722
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this work we describe the relationship between surface modification of hexagonally ordered mesoporous silica SBA-15 and loading/release characteristics of nonsteroidal anti-inflammatory drug (NSAID) naproxen. Mesoporous silica (MPS) was modified with 3-aminopropyl, phenyl and cyclohexyl groups by grafting method. Naproxen was adsorbed into pores of the prepared MPS from ethanol solution using a solvent evaporation method. The release of the drug was performed in buffer medium at pH 2 and physiological solution at pH 7.4. Parent MPSs as well as naproxen loaded MPSs were characterized using physicochemical techniques such as nitrogen adsorption/desorption, thermogravimetric analysis (TG), Zeta potential analysis, Fourier transform infrared spectroscopy (FT-IR), and elemental analysis. The amount of naproxen released from the MPSs into the medium was determined by high-performance liquid chromatography (HPLC). It was shown that the adsorption and desorption characteristics of naproxen are dependent on the pH of the solution and the surface functionalization of the host.
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页数:16
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