利用山楂“tejocote”的生物合成铜纳米粒子和正常细胞和癌细胞的细胞毒性

Gilmer David Cab-Torres , Lluvia López , Daniela Salado-Leza , Gabriela Navarro-Tovar
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摘要

利用植物提取物生物合成金属纳米颗粒(MNPs)是一种简单、低成本的方法,可以增强这些MNPs的抗菌和抗癌性能,这表明植物提取物盖层也可以提高生物安全性。本文以富含多酚和黄酮类化合物的红山楂提取物为原料,合成了直径为86±46 nm的铜纳米颗粒,并分别在人角质形成细胞HaCaT细胞(健康细胞)和前列腺肿瘤PC-3细胞中进行了毒性和抗肿瘤活性评价。在实验浓度下,植物提取物对HaCaT和PC-3细胞均无或有轻微的细胞毒性作用。在HaCaT细胞中,用玫瑰提取物合成的CuNPs的IC50为120±1.13µg/mL,而在肿瘤PC-3细胞中,IC50为491±1.06µg/mL。研究表明,C. rosei capping不足以调节暴露于高浓度CuNPs的健康细胞的氧化应激,并且需要较高浓度的CuNPs才能使肿瘤PC-3细胞的细胞活力降低70%。因此,对不同生物源合成的CuNPs粒径的进一步研究可以确定对同一模型的不同影响。与其他癌细胞和生物标志物进行体外分析也具有相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Harnessing Crataegus rosei “tejocote” for biogenic synthesis of copper nanoparticles and cytotoxicity in normal and cancer cells
The biogenic synthesis of metallic nanoparticles (MNPs) using plant extracts has been proposed as a facile and low-cost process that can enhance the antimicrobial and anticancer properties of those MNPs, suggesting that the plant extract capping can also improve biosafety. In this work, copper nanoparticles (CuNPs) (86 ± 46 nm) were synthesized using a Crataegus rosei “tejocote” extract (rich in polyphenols and flavonoids), and the obtained particles were evaluated in human keratinocytes HaCaT cells (healthy cells) and tumor prostate PC-3 cells to determine toxicity and antitumor activity, respectively. The plant extract showed non or slight cytotoxic effects in both HaCaT and PC-3 cells at the tested concentrations. On the other hand, CuNPs synthesized with C. rosei extract showed an IC50 =120 ± 1.13 µg/mL in HaCaT cells, but in tumor PC-3 cells the IC50 = 491 ± 1.06 µg/mL. It is showed that C. rosei capping is insufficient to tune the oxidative stress in healthy cells exposed to CuNPs at higher concentrations, and, that higher concentrations of CuNPs are required to reduce the cell viability in <70 % in tumor PC-3 cells. Thus, a further study with different biogenic synthesized CuNPs particle size could determine different effects on the same models. It is also relevant to carry out in vitro analysis with other cancer cells and biomarkers.
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