绿色金纳米颗粒的合成利用山楂果实提取物,表征,抗利什曼原虫,抗菌,抗氧化,和光催化活性

Mohammad Ali Ebrahimzadeh, Seyedeh Roya Alizadeh, Zahra Hashemi
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引用次数: 0

摘要

在这项研究中,金纳米颗粒的合成是由Sambucus ebulus (S. ebulus)果实提取物作为还原,封盖和稳定剂。在四氯酸氢(III)三水合物存在下,在65°C的温度下,以400转/分的转速搅拌,利用S. ebulus果提取物完成了金纳米颗粒(Au纳米颗粒)的生物合成。采用扫描电镜(FE-SEM)、能量色散x射线能谱(EDS)、傅里叶变换红外(FT-IR)、x射线衍射分析(XRD)和紫外可见光谱等分析方法对合成的SE-AuNPs进行了表征。565 nm处的强吸收峰证实了金纳米颗粒的形成。电镜结果显示,AuNPs多为球形,平均尺寸为116.2 nm。用XRD谱图证实了所制备纳米颗粒的立方晶结构,平均晶粒尺寸为28.471 nm。FT-IR分析证实了植物提取物中存在用于纳米颗粒合成的官能团。SE-AuNPs对革兰氏阳性菌和革兰氏阴性菌均表现出良好的抗菌活性,并表现出较强的抗利什曼原虫活性。SE-AuNPs具有良好的抗氧化活性,其IC50值为21.976µg/mL。制备的AuNPs在硼氢化钠和可见光条件下降解甲基橙(MO)。
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Green synthesis of gold nanoparticles using Sambucus ebulus fruit extract, characterization, and antileishmanial, antibacterial, antioxidant, and photocatalytic activities
In this study, gold nanoparticles were synthesized using the fruit extract of Sambucus ebulus (S. ebulus) as a reducing, capping, and stabilizing agent. Biogenic synthesis of gold nanoparticles (Au nanoparticles) was accomplished using S. ebulus fruit extract in the presence of hydrogen tetrachloroaurate(III) trihydrate at a temperature of 65 °C and the solution stirred at 400 rpm. The characterization of the synthesized nanoparticles (SE-AuNPs) was performed using different analytical methods, such as scanning electron microscopy (FE-SEM), energy dispersion X-ray spectroscopy (EDS), Fourier transform infrared (FT-IR), X-ray diffraction analysis (XRD), and UV-vis spectroscopy. A strong absorption peak at 565 nm confirmed the formation of the gold nanoparticle. On the basis of the electron microscopy results, AuNPs were mostly spherical with an average size of 116.2 nm. The cubic crystalline structure of the prepared nanoparticles was confirmed using the XRD pattern and the average crystallite size was obtained at 28.471 nm. FT-IR analysis confirmed the presence of functional groups in the plant extract for the synthesis of nanoparticles. SE-AuNPs showed good antibacterial activity against Gram-positive and Gram-negative bacteria tested and exhibited potent antileishmanial activity. Furthermore, SE-AuNPs showed excellent antioxidant activity that inhibited DPPH radicals with an IC50 value of 21.976 µg/mL. The prepared AuNPs acted to degrade methyl orange (MO), which was performed in sodium borohydride and visible light.
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