ZnO-5FU纳米颗粒对乳腺癌细胞系的细胞毒性研究前景广阔

M. Sanad, Shimaa Nabih, Goda Ma
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引用次数: 13

摘要

在这项研究中,我们提出了一种新的方法修饰5-FU药物,该药物通过抑制必要的生物过程来治疗癌症。最近对5-FU治疗机制的了解导致了提高其活性的新方法的发展。本文通过与氧化锌的结合修饰药物的功能,这是近10年来抗癌药物开发领域中备受关注的。氧化锌的抗癌活性揭示了活性氧和离子的产生。采用溶胶-凝胶法设计氧化锌。利用x射线、高分辨率过渡电子显微镜和扫描电子显微镜对样品的结构和形貌进行表征。应用DPPH、SOD和GPx自由基清除活性研究其抗氧化活性。通过MTT、流式细胞术和RT-PCR检测MCF-7的细胞毒性,证实(ZnO-5-FU)将成为治疗乳腺癌的有效药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Lot of Promise for ZnO-5FU Nanoparticles Cytotoxicity against Breast Cancer Cell Lines
In this study we present an approach for new modification of 5-FU drug, which widely used for treatment of cancer by inhibiting essential biological processes. Recently understanding of the treating mechanism of 5-FU has led to the development of new ways that raises its activity. Herein, we modify the drug function by combination with ZnO which get a lot of attention in the past 10 years in the field of anticancer drug development. Anticancer activity of ZnO reveals to production of Reactive Oxygen and ions. Zinc Oxide were designed by Sol-Gel. X-ray, High resolution transition electron microscope and scanning electron microscope used to characterize the structure and morphology of samples. DPPH, SOD and GPx radical scavenging activity applied to investigate the antioxidant activity. Cytotoxicity of MCF-7 was determined by MTT assay, flow cytometry and RT-PCR which confirms that (ZnO-5-FU) will be promising efficient drug for treatment of breast cancer.
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