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蜂蜜和柠檬酸盐稳定的金纳米粒子的比较分析:与蛋白质的体外相互作用和毒性研究。

Comparative analysis of honey and citrate stabilized gold nanoparticles: In vitro interaction with proteins and toxicity studies.

机构信息

National Institute for Research and Development in Microtechnologies (IMT Bucharest), 126A Erou Iancu Nicolae Street, 72996 Bucharest, Romania.

National Institute for Research and Development in Microtechnologies (IMT Bucharest), 126A Erou Iancu Nicolae Street, 72996 Bucharest, Romania.

出版信息

J Photochem Photobiol B. 2019 Aug;197:111519. doi: 10.1016/j.jphotobiol.2019.111519. Epub 2019 Jun 5.

Abstract

Gold nanoparticles of comparable size were synthetized using honey mediated green method (AuNPs@honey) and citrate mediated Turkevich method (AuNPs@citrate). Their colloidal behavior in two cell media DMEM and RPMI, both supplemented with 10% FBS, was systematically investigated with different characterization techniques in order to evidence how the composition of the media influences their stability and the development of protein/NP complex. We revealed the formation of the protein corona which individually covers the nanoparticles in RPMI media, like a dielectric spacer according to UV-Vis spectroscopy, while DMEM promotes more abundant agglomerations, clustering together the nanoparticles, according to TEM investigations. In order to evaluate the biological impact of nanoparticles, B16 melanoma and L929 mouse fibroblasts cells were used to carry out the viability assays. Generally, the L929 cells were more sensitive than B16 cells to the presence of gold nanoparticles. Measurements of cell viability, proliferation and apoptotic activities of B16 cells indicated that the effects induced by AuNPs@honey were slightly similar to those induced by AuNPs@citrate, however, the toxic response improved in the L929 fibroblast cells following the treatment with AuNPs@honey within the same concentration range from 1 μg/ml to 15 μg/ml for 48 h. Results showed that honey mediated synthesis generates nanoparticles with reduced toxicity trends depending on the cell type, concentration of nanoparticles and exposure time toward various biomedical applications.

摘要

采用蜂蜜介导的绿色方法(AuNPs@honey)和柠檬酸钠介导的 Turkevich 方法(AuNPs@citrate)合成了具有相似尺寸的金纳米粒子。使用不同的表征技术系统地研究了它们在两种细胞培养基 DMEM 和 RPMI 中的胶体行为,以证明培养基的组成如何影响它们的稳定性和蛋白质/纳米颗粒复合物的形成。我们揭示了蛋白质冠的形成,根据紫外可见光谱,它单独覆盖了 RPMI 培养基中的纳米颗粒,就像介电间隔物一样,而根据 TEM 研究,DMEM 促进了更丰富的团聚,将纳米颗粒聚集在一起。为了评估纳米颗粒的生物学影响,使用 B16 黑色素瘤和 L929 小鼠成纤维细胞进行了细胞活力测定。通常,L929 细胞比 B16 细胞对金纳米颗粒的存在更敏感。B16 细胞活力、增殖和凋亡活性的测量表明,AuNPs@honey 诱导的作用与 AuNPs@citrate 诱导的作用略有相似,然而,在相同浓度范围内(1μg/ml 至 15μg/ml),AuNPs@honey 在 48 h 内处理 L929 成纤维细胞时,毒性反应得到改善。结果表明,根据细胞类型、纳米颗粒浓度和暴露时间,蜂蜜介导的合成产生了毒性趋势降低的纳米颗粒,可用于各种生物医学应用。

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