利用 Drimia indica 绿色合成硒纳米粒子:对抗癌和抗菌活性的启示。

IF 2 3区 工程技术 Q2 ANATOMY & MORPHOLOGY
Fuad Ameen, Norah Salem Almalki, Rawan Alshalan, Penislusshiyan Sakayanathan
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引用次数: 0

摘要

硒纳米粒子(SeNPs)作为抗癌和抗菌剂引起了人们的极大兴趣。研究人员利用药用植物 Drimia indica 叶子(DI-LAE)的水提取物合成了 SeNPs(DI-SeNPs),并通过紫外可见吸收率、TEM、EDX、XRD、zeta 电位测量和傅立叶变换红外光谱对其进行了广泛表征。DI-SeNPs 对人类肺腺癌细胞系(A549;IC50 为 43.21 μg/mL)具有剂量依赖性毒性。DI-SeNPs 增加了 A549 细胞中活性氧(ROS)的生成。DI-SeNPs 使 A549 细胞的细胞周期停滞在 G2/M 期,DNA 损伤增加,最终导致这些细胞凋亡。在 A549 细胞中,DI-SeNPs 能明显提高 p53 的水平,降低 Akt 的水平,提高裂解的 caspase 3 的水平。此外,DI-SeNPs 还对多种细菌和真菌具有抗菌活性。这些研究结果表明,DI-SeNPs 具有显著的抗癌和抗菌特性,其机制涉及 ROS 生成、细胞周期停滞和细胞凋亡诱导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Green Synthesis of Selenium Nanoparticles Utilizing Drimia indica: Insights Into Anticancer and Antimicrobial Activities.

Selenium nanoparticles (SeNPs) have garnered significant interest as anticancer and antimicrobial agents. The aqueous extract of medicinal plant Drimia indica leaves (DI-LAE) was used to synthesize SeNPs (DI-SeNPs) that were extensively characterized by UV-visible absorbance, TEM, EDX, XRD, zeta potential measurements, and FTIR. DI-SeNPs exhibited dose-dependent toxicity against the human lung adenocarcinoma cell line (A549; IC50 of 43.21 μg/mL). DI-SeNPs increased reactive oxygen species (ROS) generation in A549 cells. DI-SeNPs caused cell cycle arrest in the G2/M phase and increased DNA damage in A549 cells, ultimately driving these cells toward apoptosis. DI-SeNPs significantly increased p53 levels, decreasing Akt levels and elevating cleaved caspase 3 levels in A549 cells. Additionally, DI-SeNPs exhibited antimicrobial activity against various bacteria and fungi. These findings suggest that DI-SeNPs possess significant anticancer and antimicrobial properties, mediated through mechanisms involving ROS generation, cell cycle arrest, and apoptosis induction.

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来源期刊
Microscopy Research and Technique
Microscopy Research and Technique 医学-解剖学与形态学
CiteScore
5.30
自引率
20.00%
发文量
233
审稿时长
4.7 months
期刊介绍: Microscopy Research and Technique (MRT) publishes articles on all aspects of advanced microscopy original architecture and methodologies with applications in the biological, clinical, chemical, and materials sciences. Original basic and applied research as well as technical papers dealing with the various subsets of microscopy are encouraged. MRT is the right form for those developing new microscopy methods or using the microscope to answer key questions in basic and applied research.
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