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Rapid Biosynthesis of Silver Nanoparticles Using Pepino (Solanum muricatum) Leaf Extract and Their Cytotoxicity on HeLa Cells

机译:Pepino(Solanum muricatum)叶提取物快速生物合成银纳米粒子及其对HeLa细胞的细胞毒性

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摘要

Within nanotechnology, gold and silver nanostructures have unique physical, chemical, and electronic properties [,], which make them suitable for a number of applications. Moreover, biosynthetic methods are considered to be a safer alternative to conventional physicochemical procedures for both the environmental and biomedical applications, due to their eco-friendly nature and the avoidance of toxic chemicals in the synthesis. For this reason, employing bio routes in the synthesis of functionalized silver nanoparticles (FAgNP) have gained importance recently in this field. In the present study, we report the rapid synthesis of FAgNP through the extract of pepino (Solanum muricatum) leaves and employing microwave oven irradiation. The core-shell globular morphology and characterization of the different shaped and sized FAgNP, with a core of 20–50 nm of diameter is established using the UV-Visible spectroscopy (UV-vis), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and Zeta potential and dynamic light scanning (DLS) studies. Moreover, cytotoxic studies employing HeLa (human cervix carcinoma) cells were undertaken to understand FAgNP interactions with cells. HeLa cells showed significant dose dependent antiproliferative activity in the presence of FAgNP at relatively low concentrations. The calculated IC50 value was 37.5 µg/mL, similar to others obtained for FAgNPs against HeLa cells.
机译:在纳米技术中,金和银纳米结构具有独特的物理,化学和电子特性[,],使其适合多种应用。此外,由于生物合成方法的生态友好性以及在合成过程中避免使用有毒化学物质,因此在环境和生物医学应用中,生物合成方法被认为是常规物理化学方法的更安全替代方法。由于这个原因,在功能化银纳米颗粒(FAgNP)的合成中采用生物途径最近在该领域中变得越来越重要。在本研究中,我们报道了通过pepino(Solanum muricatum)叶提取物并利用微波炉辐射快速合成FAgNP。使用紫外-可见光谱(UV-vis),场发射扫描电子显微镜(FESEM),透射光谱确定了不同形状和大小的FAgNP的核-壳球形形态和特征,其直径为20–50 nm。电子显微镜(TEM)和Zeta电位及动态光扫描(DLS)研究。此外,进行了利用HeLa(人宫颈癌)细胞的细胞毒性研究,以了解FAgNP与细胞的相互作用。在相对低浓度的FAgNP存在下,HeLa细胞显示出显着的剂量依赖性抗增殖活性。计算出的IC50值为37.5 µg / mL,与针对HeLa细胞的FAgNPs获得的IC50值相似。

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