共 72 条
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.
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页码:166 / 177
页数:12
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