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An Investigation of the Cytotoxicity and Caspase-Mediated Apoptotic Effect of Green Synthesized Zinc Oxide Nanoparticles Using Eclipta prostrata on Human Liver Carcinoma Cells

机译:墨旱莲绿色合成氧化锌纳米粒子对人肝癌细胞的细胞毒性和半胱天冬酶介导的凋亡作用的研究

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摘要

Cancer is a leading cause of death worldwide and sustained focus is on the discovery and development of newer and better tolerated anticancer drugs, especially from plants. In the present study, a simple, eco-friendly, and inexpensive approach was followed for the synthesis of zinc oxide nanoparticles (ZnO NPs) using the aqueous leaf extract of Eclipta prostrata. The synthesized ZnO NPs were characterized by UV-visible absorption spectroscopy, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX), High-resolution transmission electron microscopy (HRTEM), and Selected area (electron) diffraction (SAED). The HRTEM images confirmed the presence of triangle, radial, hexagonal, rod, and rectangle, shaped with an average size of 29 ± 1.3 nm. The functional groups for synthesized ZnO NPs were 3852 cm−1 for H-H weak peak, 3138 cm−1 for aromatic C-H extend, and 1648 cm−1 for Aromatic ring stretch. The 3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT), caspase and DNA fragmentation assays were carried out using various concentrations of ZnO NPs ranging from 1 to 100 mg/mL. The synthesized ZnO NPs showed dose dependent cytopathic effects in the Hep-G2 cell line. At 100 mg/mL concentration, the synthesized ZnO NPs exhibited significant cytotoxic effects and the apoptotic features were confirmed through caspase-3 activation and DNA fragmentation assays.
机译:癌症是全球死亡的主要原因,持续关注的是发现和开发耐受性更高的新型抗癌药物,尤其是来自植物的抗癌药物。在本研究中,遵循了一种简单,环保且廉价的方法,使用Eclipta prostrata的水性叶提取物合成氧化锌纳米颗粒(ZnO NPs)。通过紫外可见吸收光谱,X射线衍射(XRD),傅立叶变换红外光谱(FTIR),扫描电子显微镜和能量色散X射线光谱(SEM-EDX),高分辨率透射电子对ZnO NPs进行了表征显微镜(HRTEM)和选定区域(电子)衍射(SAED)。 HRTEM图像确认存在三角形,径向,六边形,杆形和矩形,它们的形状平均尺寸为29±1.3 nm。合成的ZnO NPs的官能团在HH弱峰处为3852 cm -1 ,在芳香族CH中为3138 cm -1 ,1648 cm −1 用于芳香环拉伸。使用浓度范围为1至100 mg / mL的各种ZnO NP进行3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物(MTT),胱天蛋白酶和DNA片段化分析。合成的ZnO NP在Hep-G2细胞系中显示出剂量依赖性的细胞病变作用。在100 mg / mL的浓度下,合成的ZnO NPs表现出显着的细胞毒性作用,并且通过caspase-3活化和DNA片段化分析证实了其凋亡特征。

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