基于比色法测定食品样品中l -半胱氨酸的简单且具有成本效益的聚合物修饰金纳米颗粒

Beeta Rani Khalkho, A. Saha, Bhuneshwari Sahu, M. Deb
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摘要

摘要本研究的目的是设计一种比色法测定l -半胱氨酸的方法。我们采用PVA覆盖的金纳米颗粒(GNPs)作为探针。采用紫外可见吸收光谱、透射电子显微镜(TEM)、傅里叶变换红外光谱(FTIR)、动态光散射(DLS)和Zeta电位分析仪对合成的GNPs进行了进一步的表征。结果表明,l -半胱氨酸的存在导致GNPs表面等离子体共振带在524 nm处猝灭。同时在670 nm处出现了新的吸光度。胶体GNPs的颜色由酒红色变为蓝色。GNPs的颜色变化是由于l -半胱氨酸的存在诱导了它们的聚集。基于这些观察结果,利用合成的GNPs开发了一种用于食品样品中l -半胱氨酸检测的新型比色传感器。值得注意的是,其他生物分子如丙氨酸、脯氨酸、苯丙氨酸、色氨酸、缬氨酸、精氨酸、谷氨酸、赖氨酸和组氨酸没有引起GNPs溶液颜色的任何变化。该比色探针对l -半胱氨酸具有良好的选择性和高灵敏度,检出限为2.0 μg mL-1。
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Simple and Cost Effective Polymer Modified Gold Nanoparticles Based on Colorimetric Determination of L-Cysteine in Food Samples
Abstract. The purpose of the present research was to design a method for the colorimetric determination of L-cysteine. We have employed PVA capped gold nanoparticles (GNPs) as a probe. The as-synthesized GNPs were further characterized by UV-vis absorption spectroscopy, transmission electron microscope (TEM), Fourier transform infrared spectroscopy (FTIR), dynamic light scattering (DLS) and Zeta potential analyser. The results show that the presence of L-cysteine caused the quenching of the surface plasmon resonance band of the GNPs at 524 nm. It was accompanied by the appearance of a new absorbance of a new absorbance band at 670 nm. The color of the colloidal GNPs changed from wine red to blue. The change in color of the GNPs was due to their aggregation induced by the presence of L-cysteine. Based on these observations, the as-synthesized GNPs were utilized to develop a novel colorimetric sensor for L-cysteine detection in food samples. Significantly, other biomolecules such as alanine, proline, phenylalanine, tryptophane, valine, arginine, glutamic acid, lysine and histidine did not cause any change in the color of the GNPs solutions. This colorimetric probe showed excellent selectivity and high sensitivity for L-cysteine with a detection limit of 2.0 μg mL-1.
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