Elahi Nahid Jalalian, Salehmoghadam Masoud, Taherzadeh Danial, Hashemzadeh Alireza, Darroudi Majid
NanoBioEletrochemistry Research Center, Bam University of Medical Sciences, Bam, Iran.
Department of Biology, Payem-e-Noor University of Mashhad, Mashhad, Iran.
Recent Pat Biotechnol. 2019;13(3):228-238. doi: 10.2174/1872208313666190118123141.
The green synthesizing procedure of Silver nanoparticles (AgNPs) has been performed through the usage of a natural polysaccharide; Arabic gum (AG) as a stabilizing/ capping agent. For characterization of AgNPs, TEM, particle size analyzer and UV-Vis were used.
The aim of our project was to identify biosynthesized AgNPs for sensing ammonia and to explore its toxicity on Neuro-2A cells. We also reviewed the patents for biosynthesized AgNO3 and ammonia sensing. The optimal conditions for the synthesis of AgNPs in AG consist of utilizing (0.1g) AG in dH2O (70 ml), 10 ml of 1 mM silver solution and 0.1 mM (AA) at 70°C stirring for 30 minutes. The AgNPs cytotoxicity was evaluated on Neuro-2A cells; consequently, ammonia was sensed with the lowest possible concentration of 10-6.
Particle size analyzer displayed the mean diameter of about 70 nm for the sphericalshaped Ag-NPs. UV-Vis revealed that the prepared AgNPs were ammonia sensitive in solution as the concentration of ammonia was increased. The cytotoxicity of AgNPs indicated lower Cell viability at higher concentrations of the AG-capped AgNPs.
By synthesis of AgNPs in GA by using AA, we successfully prepared a sensor to diagnose ammonia in a cell and sensing its level at concentrations of 10-6 M. In this study, no therapeutic application has been shown, but this method could be utilized industrially for therapeutic purposes in the future.
银纳米颗粒(AgNPs)的绿色合成过程是通过使用天然多糖阿拉伯胶(AG)作为稳定剂/封端剂来进行的。使用透射电子显微镜(TEM)、粒度分析仪和紫外可见光谱仪对AgNPs进行表征。
我们项目的目的是鉴定用于检测氨的生物合成AgNPs,并探索其对神经母细胞瘤细胞(Neuro-2A)的毒性。我们还查阅了生物合成硝酸银和氨传感的专利。在AG中合成AgNPs的最佳条件包括在70毫升去离子水中使用0.1克AG、10毫升1毫摩尔的银溶液和0.1毫摩尔的抗坏血酸(AA),在70°C搅拌30分钟。评估了AgNPs对Neuro-2A细胞的细胞毒性;因此,以低至10⁻⁶的浓度检测氨。
粒度分析仪显示球形Ag-NPs的平均直径约为70纳米。紫外可见光谱表明,随着氨浓度的增加,制备的AgNPs在溶液中对氨敏感。AgNPs的细胞毒性表明,在较高浓度的AG封端的AgNPs下细胞活力较低。
通过使用AA在GA中合成AgNPs,我们成功制备了一种传感器,用于诊断细胞中的氨并检测其在10⁻⁶ M浓度下的水平。在本研究中,未显示出治疗应用,但该方法未来可在工业上用于治疗目的。