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Sensitive Chemiluminescence Immunoassay by Capillary Electrophoresis with Gold Nanoparticles

机译:纳米金毛细管电泳灵敏的化学发光免疫分析

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This technical note describes a new chemiluminescence immunoassay hyphenated to capillary electrophoresis (CE-based CL-IA) with gold nanoparticles (AuNPs) technique for biological molecules determination. AuNPs were used as a protein label reagent in the light of its excellent catalytic effect to the CL reaction of luminol and hydrogen peroxide. AuNPs conjugate with antibody (Ab) to form tagged antibody (Ab~(*)), and then Ab~(*) link to antigen (Ag) to produce an Ab~(*)-Ag complex by a noncompetitive immunoreaction. The mixture of the excess Ab~(*) and the Ab~(*)-Ag complex was baseline separated and detected within 5 min under the optimized conditions. This new protocol was evaluated with human immunoglobulin G (IgG) as the target molecule. The calibration curve of IgG was in the range of 0.008-5 (mu)g/mL with a correlation coefficient of 0.995. The detection limit (S/N velence 3) of IgG was 1.14 X 10~(-3) (mu)g/mL (7.1 pmol/L, 0.39 amol). The proposed AuNPs enhanced CE-based CL-IA method was successfully applied for the quantification of IgG in human sera from patients. It proves that the present method could be developed into a new and sensitive biochemical analysis technique.
机译:本技术说明介绍了一种新的化学发光免疫分析方法,该方法通过金纳米颗粒(AuNPs)技术与毛细管电泳(基于CE的CL-IA)联用。由于AuNPs对鲁米诺和过氧化氢的CL反应具有出色的催化作用,因此被用作蛋白质标记试剂。 AuNP与抗体(Ab)缀合形成标记的抗体(Ab _(*)),然后Ab _(*)与抗原(Ag)连接,通过非竞争性免疫反应产生Ab〜(*)-Ag复合物。基线分离过量的Ab〜(*)和Ab〜(*)-Ag复合物的混合物,并在优化条件下5分钟内检测到。以人免疫球蛋白G(IgG)为靶分子评估了该新方案。 IgG的校准曲线在0.008-5μg/ mL的范围内,相关系数为0.995。 IgG的检出限(S / N限3)为1.14 X 10〜(-3)μg/ mL(7.1 pmol / L,0.39 amol)。所提出的AuNPs增强的基于CE的CL-IA方法已成功用于定量患者人血清中的IgG。证明了本方法可以发展成为一种新的敏感的生化分析技术。

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