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Biomimetic Synthesis of Au-Nps using Cassia fistula Flower Extract and Studies of their Protein Interaction

机译:决明子花提取物对Au-NPS的仿生合成及其蛋白质相互作用研究

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Gold nanoparticles (Au-Nps) were synthesized by mediating Cassia fistula flower extract (CFFE) as reducing agent in absence and presence of sodium dodecyl sulphate (SDS) for the first time. Surface Plasmon Resonance (SPR) peak at around 550 nm was used for preliminary inference in the development of nanoparticles (Nps). With the increase in SDS the lambda(SPR) rises from 548 to 585 nm but the intensity of absorption decreased from pre to post cmc SDS. The Fourier transform infra-red (FTIR) was performed in absence and presence of SDS in order to ascertain the biomimetic reduction by CFFE and explain the bio-reduction of (Au3+) ions from the HAuCl4. For the preliminary size and dispersity of Au-Nps dynamic light scattering (DLS) was performed to observe the shape and crystallite size of Au-Nps,transmission electron microscopy (TEM) was performed which revealed multiple shapes and dispersity in the different conditions under which the synthesis was carried out. The synthesis was kinetically scanned by UV-visible spectroscopy that led to the assumption of pseudo first order kinetics with respect to HAuCl4 and CFFE reagents. The NPs were characterized with X-ray diffraction (XRD) for crystallinity and crystallite size. The protein interaction studies of Au-Nps with rabbit serum albumin (RSA) in absence and presence of SDS were accomplished by using UV-visible spectroscopy, DLS and fluorescence spectroscopy etc, that confirmed the denaturing and aggregation of the RSA protein in presence of SDS.
机译:首次在十二烷基硫酸钠(SDS)存在的情况下,介导决明子花提取物(CFFE)作为还原剂合成了金纳米颗粒(Au-Nps)。在550 nm左右的表面等离子体共振(SPR)峰用于纳米颗粒(Nps)发育的初步推断。随着[SDS]的增加,λ(SPR)从548 nm上升到585 nm,但吸收强度从cmc[SDS]前后降低。傅里叶变换红外 (FTIR) 在不存在和存在 SDS 的情况下进行,以确定 CFFE 的仿生还原并解释 HAuCl4 中 (Au3+) 离子的生物还原。对Au-Nps的初步尺寸和分散性进行动态光散射(DLS)观察Au-Nps的形状和微晶尺寸,并进行透射电子显微镜(TEM)分析,揭示了在不同条件下的多种形状和分散性。通过紫外-可见光谱对合成进行动力学扫描,从而假设 HAuCl4 和 CFFE 试剂的伪一级动力学。采用X射线衍射(XRD)对NPs的结晶度和晶粒尺寸进行了表征。利用紫外-可见光谱、DLS和荧光光谱等手段,研究了在SDS存在下Au-NPS与兔血清白蛋白(RSA)的相互作用,证实了RSA蛋白在SDS存在下的变性和聚集性。

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