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合成的银纳米粒子抑制甲状腺癌细胞系 (TPC1) 的增殖并诱导 ROS 介导的细胞凋亡。

synthesized silver nanoparticles inhibit cell proliferation and induce ROS mediated apoptosis in thyroid cancer cell line (TPC1).

机构信息

Physical Examination Center, The First Affiliated Hospital of Kunming Medical University, Kunming, China.

Physical Examination Center, The Fourth Affiliated Hospital of Kunming Medical University, Kunming, China.

出版信息

Artif Cells Nanomed Biotechnol. 2020 Dec;48(1):800-809. doi: 10.1080/21691401.2019.1687495.

Abstract

We used cell-free culture filtrate of as a reducing mediator of AgNO to silvernanoparticles (AgNPs) and possibly used as a potential anticancer agent against thyroid cancer cells (TPC1). The bio-generation of AgNPs was firmly established by taking a UV spectrum at 380-500 nm wavelength. The Fourier transform spectrum analysis reveals the association of alcohol, phenol and aromatic functional groups with synthesized AgNPs (-AgNPs). By observing under transmission electron microscopy (TEM), the size and structure of the -AgNPs were characterized as the size was 30-70 nm and spherical in shape. The concentration-dependent cytotoxicity of -AgNPs on TPC1 cells was observed and IC50 value was calculated. The alteration of oxidative and antioxidant biomarkers in Ps-AgNPs treated cells were observed. The induced apoptosis was determined by staining the -AgNPs treated cells with DCFH-DA, Rh-123 dye, Acridine Orange (AO) and ethidium bromide (EtBr). Increased level of intracellular reactive oxygen species (ROS) generation and decreased level of mitochondrial membrane potential was observed in -AgNPs treated TPC1 cells. Moreover, the apoptotic morphological changes were explored, which indicates increased apoptosis by inducing cell membrane damage in -AgNPs treated cells. This biogenic approach will enable an effective and significant improvement in nano-oncotherapy.

摘要

我们使用无细胞培养滤液作为 AgNO 的还原剂来生成银纳米颗粒 (AgNPs),并可能将其用作治疗甲状腺癌细胞 (TPC1) 的潜在抗癌剂。通过在 380-500nm 波长处获取 UV 光谱,牢固地确立了 AgNPs 的生物生成。傅里叶变换光谱分析揭示了醇、酚和芳香族官能团与合成的 AgNPs (-AgNPs) 的关联。通过透射电子显微镜 (TEM) 观察,-AgNPs 的大小和结构被表征为大小为 30-70nm 且呈球形。观察了 -AgNPs 对 TPC1 细胞的浓度依赖性细胞毒性,并计算了 IC50 值。观察了 Ps-AgNPs 处理细胞中氧化和抗氧化生物标志物的变化。通过用 DCFH-DA、Rh-123 染料、吖啶橙 (AO) 和溴化乙锭 (EtBr) 染色处理的 -AgNPs 来确定诱导的细胞凋亡。在 -AgNPs 处理的 TPC1 细胞中观察到细胞内活性氧 (ROS) 生成水平增加和线粒体膜电位降低。此外,还探索了凋亡的形态变化,这表明通过在 -AgNPs 处理的细胞中诱导细胞膜损伤来增加细胞凋亡。这种生物发生方法将使纳米肿瘤治疗得到有效和显著的改善。

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