Department of Analytical Chemistry, Faculty of Chemistry, Universidad Complutense de Madrid, 28040, Madrid, Spain.
Department of Analytical Chemistry, Faculty of Chemistry, Universidad Complutense de Madrid, 28040, Madrid, Spain.
Talanta. 2020 May 1;211:120761. doi: 10.1016/j.talanta.2020.120761. Epub 2020 Jan 17.
A simple, fast and sensitive amperometric immunosensing method for the determination of the clinically relevant cytokine interferon gamma (IFN-γ) in saliva complying the requirements demanded for this kind of sample is reported. The target analyte was sandwiched between a specific capture antibody covalently immobilized on a screen-printed electrode functionalized by the diazonium salt grafting of p-aminobenzoic acid, and a biotinylated detector antibody labeled with a streptavidin-horseradish peroxidase conjugate. The amperometric responses measured at - 0.20 V vs Ag pseudo-reference electrode upon addition of hydrogen peroxide in the presence of hydroquinone as the redox mediator allowed a calibration plot with a linear range between 2.5 and 2000 pg mL and a low limit of detection (1.6 pg mL) to be obtained. In addition, a good selectivity against other non-target proteins was achieved. The developed method was validated by analyzing a WHO 1st International Standard for IFN-γ. In addition, the immunosensor was used for the determination of the endogenous IFN-γ in saliva with results in excellent agreement with those obtained by a commercial ELISA kit.
本文报道了一种简单、快速、灵敏的安培免疫传感方法,用于测定唾液中与临床相关的细胞因子干扰素 γ(IFN-γ),该方法符合对这种样品的要求。目标分析物被夹在通过对氨基苯甲酸的重氮盐接枝功能化的、共价固定在丝网印刷电极上的特异性捕获抗体,和生物素化的检测抗体之间,该检测抗体标记有链霉亲和素-辣根过氧化物酶偶联物。在存在氢醌作为氧化还原介体的情况下,加入过氧化氢后,在 - 0.20 V 对银伪参比电极测量的安培响应允许获得线性范围在 2.5 和 2000 pg mL 之间且检测限低至 1.6 pg mL 的校准曲线。此外,还实现了对其他非目标蛋白的良好选择性。通过分析世界卫生组织的 IFN-γ 第 1 国际标准对所开发的方法进行了验证。此外,该免疫传感器还用于测定唾液中的内源性 IFN-γ,其结果与商业 ELISA 试剂盒的结果非常吻合。