首页> 美国卫生研究院文献>International Journal of Nanomedicine >Green synthesis of selenium nanoparticles using Acinetobacter sp. SW30: optimization characterization and its anticancer activity in breast cancer cells
【2h】

Green synthesis of selenium nanoparticles using Acinetobacter sp. SW30: optimization characterization and its anticancer activity in breast cancer cells

机译:使用不动杆菌属绿色合成硒纳米颗粒。 SW30:乳腺癌细胞的优化表征及其抗癌活性

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The aim of this study was to synthesize selenium nanoparticles (SeNPs) using cell suspension and total cell protein of Acinetobacter sp. SW30 and optimize its synthesis by studying the influence of physiological and physicochemical parameters. Also, we aimed to compare its anticancer activity with that of chemically synthesized SeNPs in breast cancer cells. Cell suspension of Acinetobacter sp. SW30 was exposed to various physiological and physicochemical conditions in the presence of sodium selenite to study their effects on the synthesis and morphology of SeNPs. Breast cancer cells (4T1, MCF-7) and noncancer cells (NIH/3T3, HEK293) were exposed to different concentrations of SeNPs. The 18 h grown culture with 2.7×109 cfu/mL could synthesize amorphous nanospheres of size 78 nm at 1.5 mM and crystalline nanorods at above 2.0 mM Na2SeO3 concentration. Polygonal-shaped SeNPs of average size 79 nm were obtained in the supernatant of 4 mg/mL of total cell protein of Acinetobacter sp. SW30. Chemical SeNPs showed more anticancer activity than SeNPs synthesized by Acinetobacter sp. SW30 (BSeNPs), but they were found to be toxic to noncancer cells also. However, BSeNPs were selective against breast cancer cells than chemical ones. Results suggest that BSeNPs are a good choice of selection as anticancer agents.
机译:这项研究的目的是利用不动杆菌属的细胞悬浮液和总细胞蛋白合成硒纳米颗粒(SeNPs)。 SW30并通过研究生理和理化参数的影响来优化其合成。此外,我们旨在比较其抗癌活性与化学合成的SeNPs在乳腺癌细胞中的抗癌活性。不动杆菌属的细胞悬液。 SW30在亚硒酸钠存在下暴露于多种生理和物理化学条件下,以研究其对SeNPs合成和形态的影响。乳腺癌细胞(4T1,MCF-7)和非癌细胞(NIH / 3T3,HEK293)暴露于不同浓度的SeNPs。在2.7×10 9 cfu / mL的条件下培养18 h,可以合成1.5 mM的78 nm非晶态纳米球和2.0 mM以上的Na2SeO3浓度的晶体纳米棒。在不动杆菌属总细胞蛋白4 mg / mL的上清液中获得平均大小为79 nm的多边形SeNP。 SW30。化学SeNPs显示出比不动杆菌属合成的SeNPs更多的抗癌活性。 SW30(BSeNPs),但也发现它们对非癌细胞也有毒性。但是,BSeNPs对乳腺癌细胞的选择性高于化学细胞。结果表明,BSeNPs是抗癌药物的良好选择。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号