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Green synthesis, in vivo and in vitro pharmacological studies of Tamarindus indica based gold nanoparticles

机译:绿色合成,体内和体外药理学研究籼稻籼稻纳米粒子

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摘要

The current investigation aims to synthesize gold nanoparticles (AuNPs) from aqueous extract of Tamarindus indica and to evaluate the in vitro anti-bacterial and in vivo sedative and anelgescic activities of crude extract as well as synthesized AuNPs. Several methods have been reported to synthesize AuNPs; however, most of them were not ecofriendly. In the present study, the green synthesis of AuNPs has been carried out. Using the green synthesis method, AuNPs of T. indica were synthesized at room temperature (25 degrees C) by mixing 5 mL of HAuCl4 (1 mM) with 1 mL of T. indica seed extract solution. This extract solution was prepared by taking 5 gm dry seeds in 100 mL of double deionized water with continuous stirring for up to 24 h at 80 degrees C. The stability of AuNPs was confirmed with the help of relevant experimental techniques including ultraviolet-visible (UV/Vis) showing maximum absorbance at 535-540 nm, Fourier transform infrared showing a broad signal at 3464 cm(-1) which can be attributed to either amide or hydroxyl functionalities and atomic force microscopy analysis showed that the biomaterial surrounding AuNPs was agglomerated which proves the formation of discrete nanostructutres. These AuNPs have been evaluated for their antibacterial potential. The results revealed good antibacterial activity of the samples against. Klebsiella pneumonia, Bacillus subtilis and Staphylococcus epidermidis with 10-12 mm zone of inhibition range. The AuNPs were also found stable at high temperature, over a range of pH and in 1 mM salt solution. Moreover, the crude extract and respective AuNPs also exhibited interesting sedative and analgesic activities. Hence, we focused on phytochemicals-mediated synthesis of AuNPs considered as greatest attention in the treatment of anti-bacterial, analgesic, and sedative.
机译:目前的调查旨在将金纳米颗粒(AUNP)从Tamarindus indica的水性提取物合成,并评估体外抗细菌和体内镇静剂和粗提取物的额外的活性和合成的AUNPS。据报道了几种方法综合了AUNPS;然而,大多数都没有生态友好。在本研究中,已经进行了AUNP的绿色合成。使用绿色合成方法,通过将5ml HauCl4(1mM)与1ml T.ginga种子提取溶液混合,在室温(25℃)下合成T.T.pmina的AuNP。通过在80摄氏度的连续搅拌下在100ml双去离子水中服用5克的双去离子水中的5克干燥的种子来制备该提取物溶液。在包括紫外线可见的相关实验技术的帮助下,确认AUNP的稳定性(UV / VIS)显示在535-540nm处的最大吸光度,傅里叶变换红外线显示在3464cm(-1)的宽信号,其可归因于酰胺或羟基官能团和原子力显微镜分析显示,围绕剖腹症的生物材料是群体的凝聚证明了离散纳米结构的形成。这些AUNP已经评估了它们的抗菌潜力。结果揭示了样品的良好抗菌活性。 Klebsiella肺炎,枯草芽孢杆菌和葡萄球菌的抑制范围10-12毫米区域。在高温下,剖腹产均在高温下稳定,在一定的pH和1mM盐溶液中。此外,粗提物和各自的AUNP也表现出有趣的镇静剂和镇痛活性。因此,我们专注于植物化学症介导的抗菌,镇痛和镇静剂中被认为是最大的人类的合成。

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