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Crosslinked Polyphosphazene Nanospheres with Anticancer Quercetin: Synthesis, Spectroscopic, Thermal Properties, and Controlled Drug Release

机译:具有抗癌槲皮素的交联多磷腈纳米球:合成,光谱,热性能和受控药物释放

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摘要

In this study, novel cross-linked inorganic-organic hybrid polyphosphazene nanospheres were synthesized via self-assembly precipitation polymerization between hexachlorocyclotriphosphazene (HCCP) as a crosslinker molecule and anticancer featured quercetin (QCT). The technique used for synthesizing QCT nanospheres is quite simple and rapid, and has some advantages like using just ultrasonic power. Furthermore, it does not require any surfactant or stabilizer. Growth of nanospheres and reaction time effect on the formation of QCT nanospheres were investigated. Quercetin and 4′,7-dihydroxyflavone were compared for the formation of nanospheres. The particle size of the spheres was determined to be approximately 434 nm by DLS (dynamic light scattering) measurements in 3 hours reaction time. The structure and morphology of synthesized QCT nanospheres were investigated by SEMEDX (scanning electron microscope) and XRD (X-ray diffractometer). The spectroscopic and thermal properties of cyclomatrix polyphosphazene QCT nanospheres were investigated by FTIR (Fourier transform infrared spectroscopy), UV-vis (ultraviolet-visible), fluorescence, and TGA (thermogravimetric analysis). Moreover, QCT nanospheres were used for controlled release of acriflavine which had been chosen as a model drug.
机译:在该研究中,通过作为交联剂分子和抗癌的己烷分子和抗癌特征槲皮素(QCT)通过自组装沉淀聚合来合成新的交联无机 - 有机杂种聚磷腈纳米球。用于合成QCT纳米球的技术非常简单且快速,并且具有仅使用超声波的一些优点。此外,它不需要任何表面活性剂或稳定剂。研究了纳米球的生长和对QCT纳米球形成的反应时间效应。比较槲皮素和4',比较7-二羟基氟拉拉夫酮,形成纳米球。在3小时反应时间内测定球体的粒度约为434nm(动态光散射)测量。通过Semredx(扫描电子显微镜)和XRD(X射线衍射仪)研究了合成QCT纳米球的结构和形态。通过FTIR(傅里叶变换红外光谱),UV-Vis(紫外 - 可见),荧光和TGA(热重分析)研究了Cyclomatrix多磷腈QCT纳米球的光谱和热性能。此外,Qct纳米球用于被选自模型药物的Acriflavine的控制释放。

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