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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Salmonella typhi determination using voltammetric amplification of nanoparticles: A highly sensitive strategy for metalloimmunoassay based on a copper-enhanced gold label
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Salmonella typhi determination using voltammetric amplification of nanoparticles: A highly sensitive strategy for metalloimmunoassay based on a copper-enhanced gold label

机译:纳米颗粒伏安法扩增伤寒沙门氏菌:基于铜标记的金标记的金属免疫测定的高灵敏度策略

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A highly sensitive electrochemical amplification immunoassay for Salmonella typhi (S. typhi) determination has been developed for the first time by using a copper-enhanced gold nanoparticle label coupled with anodic stripping voltammetry. Monoclonal antibodies for S. typhi were first immobilized oil polystyrene microwells and then Captured by S. typhi bacteria. After an immunoreaction occurred, a polyclonal, antibody-colloidal gold Conjugate was added to bind to the S. typhi bacteria. Next, a copper-enhancer Solution containing ascorbic acid and copper (II) Sulfate was added into the polystyrene microwells. The ascorbic acid was employed to reduce the copper(II) ions to copper(0), which Was Subsequently deposited onto the gold nanoparticle tags. After the copper was dissolved in nitric acid, the released copper ions were detected by anodic stripping voltammetry. The amount of deposited copper was related to the amount of gold nanoparticle tag present, which was controlled by the amount S. typhi attached to the polyclonal antibody-colloidal gold conjugate. Therefore, the anodic stripping peak Current was linearly dependent on the S. typhi concentration over concentration range of 1.30 x 10(2) cfu/mL to 2.6 x 10(3) cfu/mL in a logarithmic plot, with a detection limit as low as 98.9 cfu/mL. The influences of the relevant experimental variables, such as the concentration of copper and the reaction time of S. typhi with antibody, were investigated. We also Successfully applied this method to determine the presence of S. typhi in human serum. Our results are a step towards developing more sensitive and reliable nanoparticle immunoassays. (C) 2008 Elsevier B.V. All rights reserved.
机译:通过使用铜增强的金纳米颗粒标记结合阳极溶出伏安法,首次开发了用于伤寒沙门氏菌(S. typhi)测定的高灵敏度电化学扩增免疫测定法。伤寒沙门氏菌的单克隆抗体首先固定在油性聚苯乙烯微孔中,然后被伤寒沙门氏菌捕获。发生免疫反应后,添加多克隆抗体胶体金结合物以结合伤寒沙门氏菌。接着,将包含抗坏血酸和硫酸铜(II)的铜增强剂溶液添加到聚苯乙烯微孔中。使用抗坏血酸将铜(II)离子还原为铜(0),然后将其沉积到金纳米粒子标签上。铜溶解在硝酸中后,通过阳极溶出伏安法检测释放的铜离子。铜的沉积量与存在的金纳米颗粒标签的量有关,金纳米颗粒标签的量由附着于多克隆抗体-胶体金结合物上的伤寒沙门氏菌的量控制。因此,在对数图中,阳极溶出峰电流在1.30 x 10(2)cfu / mL到2.6 x 10(3)cfu / mL的浓度范围内与伤寒沙门氏菌浓度呈线性关系,检出限低为98.9 cfu / mL。研究了相关实验变量对铜浓度和伤寒沙门氏菌与抗体反应时间的影响。我们还成功地应用了这种方法来确定人血清中是否存在伤寒链球菌。我们的结果是朝着开发更灵敏和可靠的纳米粒子免疫测定迈出的一步。 (C)2008 Elsevier B.V.保留所有权利。

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