萘普生
乙二胺
化学
热重分析
药物输送
Zeta电位
胺气处理
核化学
粉末衍射
热重分析
无机化学
有机化学
材料科学
纳米技术
结晶学
纳米颗粒
病理
替代医学
医学
作者
Miroslav Almáši,Vladimı́r Zeleňák,Peter Palotai,Eva Beňová,A. Zeleňáková
标识
DOI:10.1016/j.inoche.2018.05.007
摘要
Mesoporous metal-organic framework MIL-101(Fe)-NH2 was prepared and post-synthetically modified with amines of different chain lengths: ethylenediamine (en) and 1,2-bis(3-aminopropylamino)ethane (bap). Three prepared samples (MIL-101(Fe)-NH2, MIL-101(Fe)-NH2-en, MIL-101(Fe)-NH2-bap) were studied as carriers for drug delivery of non-steroidal antiinflamatory drug naproxen. The modification of MIL-101(Fe)-NH2, encapsulation of the drug and stability of the carriers were monitored by the combination of different analytical techniques such as elemental analysis (EA), infrared spectroscopy (IR), thermogravimetry (TG), measurements of zeta potential (ζ), high-energy powder X-ray diffraction (HE-PXRD), 1H NMR spectroscopy and N2 adsorption measurements. The naproxen release studies were performed into two simulated body fluids with different pH: the simulated gastric fluid (pH = 2) and the simulated intravenous solution (pH = 7.4). Results of naproxen release clearly showed the impact of pH and amine functional groups on the naproxen release. The number of amine groups in en and bap influenced the release process more significantly in solution with pH = 7.4 than pH = 2.
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