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A SPR biosensor based on signal amplification using antibody-QD conjugates for quantitative determination of multiple tumor markers

机译:基于信号放大的SPR生物传感器使用抗体-QD偶联物定量测定多种肿瘤标志物

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摘要

The detection of tumor markers is very important in early cancer diagnosis; however, tumor markers are usually present at very low concentrations, especially in the early stages of tumor development. Surface plasmon resonance (SPR) is widely used to detect biomolecular interactions; it has inherent advantages of being high-throughput, real-time, and label-free technique. However, its sensitivity needs essential improvement for practical applications. In this study, we developed a signal amplification strategy using antibody-quantum dot (QD) conjugates for the sensitive and quantitative detection of α-fetoprotein (AFP), carcinoembryonic antigen (CEA) and cytokeratin fragment 21-1 (CYFRA 21-1) in clinical samples. The use of a dual signal amplification strategy using AuNP-antibody and antibody-QD conjugates increased the signal amplification by 50-folds. The constructed SPR biosensor showed a detection limit as low as 0.1 ng/mL for AFP, CEA, and CYFRA 21-1. Moreover, the results obtained using this SPR biosensor were consistent with those obtained using the electrochemiluminescence method. Thus, the constructed SPR biosensor provides a highly sensitive and specific approach for the detection of tumor markers. This SPR biosensor can be expected to be readily applied for the detection of other tumor markers and can offer a potentially powerful solution for tumor screening.
机译:肿瘤标志物的检测在早期癌症诊断中非常重要。然而,肿瘤标志物通常以非常低的浓度存在,尤其是在肿瘤发展的早期阶段。表面等离振子共振(SPR)被广泛用于检测生物分子之间的相互作用。它具有高通量,实时和无标签技术的固有优势。但是,其灵敏度需要针对实际应用进行必要的改进。在这项研究中,我们开发了使用抗体-量子点(QD)共轭物的信号放大策略,用于灵敏和定量检测α-甲胎蛋白(AFP),癌胚抗原(CEA)和细胞角蛋白片段21-1(CYFRA 21-1)在临床样品中。使用AuNP抗体和抗体QD偶联物的双重信号放大策略的使用使信号放大倍数增加了50倍。所构建的SPR生物传感器对AFP,CEA和CYFRA 21-1的检测极限低至0.1µng / mL。而且,使用该SPR生物传感器获得的结果与使用电化学发光方法获得的结果一致。因此,构建的SPR生物传感器为检测肿瘤标志物提供了高度灵敏和特异性的方法。可以预期该SPR生物传感器可以很容易地用于检测其他肿瘤标志物,并且可以为肿瘤筛查提供潜在的强大解决方案。

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