Synthesis and characterization of ZIF-8 nanoparticles for controlled release of 6-mercaptopurine drug

纳米颗粒 药物输送 沸石咪唑盐骨架 材料科学 傅里叶变换红外光谱 控制释放 化学工程 粒径 核化学 纳米技术 毒品携带者 化学 有机化学 金属有机骨架 吸附 工程类
作者
Harpreet Kaur,Girish C. Mohanta,Vandana Gupta,Deepak Kukkar,Sachin Tyagi
出处
期刊:Journal of Drug Delivery Science and Technology [Elsevier]
卷期号:41: 106-112 被引量:297
标识
DOI:10.1016/j.jddst.2017.07.004
摘要

Zeolitic imidazolate framework (ZIF-8) has been synthesized at room temperature in aqueous medium. Their suitability as potential drug carrier for delivery of an anti-leukemia drug, 6-mercaptopurine (6-MP) is examined. 6-MP was loaded in situ into the ZIF-8 nanoparticles during synthesis. Both ZIF-8 and [email protected] have been characterized using various characterization tools. The structural integrity and phase purity of [email protected] nanoparticles was obtained through X-ray diffraction pattern and was comparable to that of sodalite type ZIF-8. FESEM micrographs of pure ZIF-8 showed hexagonal nanocrystals with well-developed facets and uniform particle size distribution of around 80–100 nm. Encapsulation of 6-MP into ZIF-8 resulted into a nearly two fold increase of size while preserving the well-developed facets and hexagonal morphology. The encapsulation of 6-MP was confirmed by UV-Visible and FTIR spectroscopy studies. Furthermore, the release kinetics of 6-MP drug from [email protected] has been investigated in phosphate buffer saline 37 °C at two different pH values 7.4 and 5.0. The [email protected] exhibited much faster release of drug in acidic pH as compared with release in pH 7.4 owing to the decomposition of ZIF-8 structure, thus, indicating the potential of ZIF-8 to be used as a carrier for controlled delivery of 6-MP against cancerous cells.
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