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Detection of immunoglobulin G based on nanoparticle surface energy transfers from fluorescein isothiocyanate to gold nanoparticles

机译:基于从异硫氰酸荧光素到金纳米粒子的纳米粒子表面能转移,检测免疫球蛋白G

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In this paper, a simple and sensitive approach for human immunoglobulin G (hIgG) detection is described based on nanoparticle surface energy transfer (NSET) from fluorescein isothiocyanate (FITC) to gold nanoparticles (GNPs). The assay consisted of polyclonal goat anti-IgG antibody labeled luminescent FITC as the donor and GNPs as the acceptor. In the initial stage, with the energy transfer from FITC to GNPs, the FITC fluorescence was effectively quenched. Upon the introduction of IgG, effective competitive binding to the polyclonal goat anti-IgG antibody labeled FITC occurred, which significantly hindered the NSET, and thus recovered the fluorescence of FITC. The change in fluorescent intensity produced a novel strategy for the detection of hIgG. The recovered fluorescence of FITC was linearly proportional to the concentration of hIgG in the range of 4.0 ?— 10a?’9 to 2.2 ?— 10a?’7 g mLa?’1 with a detection limit of 8.3 ?— 10a?’10 g mLa?’1. This method was applied to the determination of hIgG in human serum samples via a standard addition method, and the recovery rate obtained was 98.7a€“105.0%.
机译:在本文中,基于从异硫氰酸荧光素(FITC)到金纳米颗粒(GNP)的纳米颗粒表面能转移(NSET),描述了一种简单而灵敏的人类免疫球蛋白G(hIgG)检测方法。该测定法包括标记为发光FITC的多克隆山羊抗IgG抗体作为供体,GNPs作为受体。在初始阶段,随着能量从FITC传递到GNP,FITC荧光被有效地猝灭。引入IgG后,与多克隆山羊抗IgG抗体标记的FITC发生了有效的竞争结合,这显着阻碍了NSET,从而恢复了FITC的荧光。荧光强度的变化产生了检测hIgG的新策略。 FITC的回收荧光与hIgG浓度成线性比例,在4.0?-10a?'9至2.2?-10a?'7 g mLa?'1范围内,检出限为8.3?-10a?'10 g mLa?'1。该方法通过标准加入法用于人血清中人IgG的测定,回收率为98.7a×105.0%。

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