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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Biosynthesis, characterization of magnetic iron oxide nanoparticles and evaluations of the cytotoxicity and DNA damage of human breast carcinoma cell lines
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Biosynthesis, characterization of magnetic iron oxide nanoparticles and evaluations of the cytotoxicity and DNA damage of human breast carcinoma cell lines

机译:磁性氧化铁纳米粒子的生物合成,表征以及对人乳腺癌细胞系的细胞毒性和DNA损伤的评估

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Abstract Magnetic iron oxide nanoparticles (MNPs) were synthesized using Albizia adianthifolia leaf extract as reducing and protecting agent. Colour changing, UV–Vis spectrum, X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM) confirmed the biosynthesis and characterization of MNPs. The XRD pattern revealed that MNPs are crystalline in nature. FT-IR spectral analysis showed that MNPs was capped with plant constituents. From SEM analysis, the MNPs were generally found to be spherical in shape and the size was ranged 32–100?nm. Free radical scavenging potentials of the MNPs against DPPH were confirmed based on its stable anti-oxidant effects. The synthesized MNPs were used to capture Staphylococcus aureus under the magnetic field effect. Further, it was observed that the MNPs are able to exert cytotoxic effect towards human breast (AMJ-13) and (MCF-7) cancer cells. The anti-proliferative effect of this treatment is due to cell death and inducing apoptosis. Mitochondrial membrane potential, acridine orange-propidium iodide staining assays as well as single cell and DNA gel electrophoresis analyses indicated that MNPs induce cell death only by apoptosis. The findings of present study suggest that the MNPs might be used for medicinal applications particularly for cancer therapeutics.
机译:摘要以白花铁皮叶提取物为还原剂和保护剂,合成了磁性氧化铁纳米颗粒(MNPs)。颜色变化,UV-Vis光谱,X射线衍射(XRD),傅里叶变换红外(FT-IR)光谱和扫描电子显微镜(SEM)证实了MNP的生物合成和特征。 XRD图谱表明MNP本质上是晶体。 FT-IR光谱分析表明,MNPs具有植物成分。根据SEM分析,通常发现MNP呈球形,大小范围为32–100?nm。基于其稳定的抗氧化作用,证实了MNP对DPPH的清除自由基的能力。合成的MNPs在磁场作用下被用于捕获金黄色葡萄球菌。此外,已经观察到MNP能够对人乳腺癌(AMJ-13)和(MCF-7)癌细胞发挥细胞毒性作用。该治疗的抗增殖作用归因于细胞死亡和诱导细胞凋亡。线粒体膜电位,a啶橙-碘化丙啶染色分析以及单细胞和DNA凝胶电泳分析表明MNP仅通过凋亡诱导细胞死亡。本研究的发现表明,MNPs可用于医学应用,特别是用于癌症治疗。

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