Amine-functionalized mesoporous silica KIT 6 as a controlled release drug delivery carrier

被引:74
作者
Ayad, Mohamad M. [1 ,2 ]
Salahuddin, Nehal A. [1 ]
Abu El-Nasr, Ahmed [1 ]
Torad, Nagy L. [1 ]
机构
[1] Tanta Univ, Fac Sci, Dept Chem, Tanta, Egypt
[2] Egypt Japan Univ Sci & Technol, Sch Basic & Appl Sci, New Borg El Arab City 21934, Alexandria, Egypt
关键词
Mesoporous silica KIT-6; Sol-gel method; Drug delivery; Quartz crystal microbalance (QCM); TRIBLOCK COPOLYMER; MOLECULAR-SIEVE; NANOPARTICLES; CARBON; ADSORPTION; SYSTEMS; EPOXIDATION; COMPLEXES; CATALYSTS; DESIGN;
D O I
10.1016/j.micromeso.2016.04.029
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Mesoporous silica KIT-6, has been prepared through the sol-gel method followed by a chemical modification using 3-aminopropyl triethoxysilane (APTS) to obtain KIT-6-NH2 as a drug delivery carrier. The mesostructure properties was fully characterized by transmission electron microscope (TEM), N-2 sorption isotherm, Fourier transform infrared (FT-IR), low-angel X-ray diffraction (XRD) and small-angel x-ray scattering (SAXS). Loading of ketoprofen (KP) and 5-flurouracil (5-FU) drugs as models into KIT-6 and KIT-6-NH2 was studied using quartz crystal microbalance (QCM) and UV visible spectroscopy. The loading uptake and release behaviors of KP and 5-FU were highly dependent on the textural properties of KIT-6 and KIT-6-NH2. The release of drugs was carefully studied in simulated gastric fluid (pH 2) and in simulated intestinal fluid (pH 7.4). First order, Higuchi, Hixson-Crowell and Korsmeyer-Peppas release kinetic models were applied to the experimental data and the release was found to obey a first-order rate kinetic. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:166 / 177
页数:12
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