Hubei Key Laboratory of Pollutant Analysis and Reuse Technology, Department of Chemistry, Hubei Normal University, Huangshi 435002, PR China.
Biosens Bioelectron. 2013 Sep 15;47:178-83. doi: 10.1016/j.bios.2013.03.029. Epub 2013 Mar 22.
A novel gold nanoprobe was prepared for the signal tracing of ultrasensitive nonenzymatic electrochemical immunoassay at a carbon nanotubes (CNTs)-based disposable immunosensor. The gold nanoprobe was prepared via in situ deposition of gold nanoparticles (Au NPs) on the polydopamine functionalized silica nanosphere followed by the labeling of signal antibodies. The immunosensor was prepared through the covalent immobilization of capturing antibodies on the CNTs modified screen-printed carbon electrode. After a sandwich-type immunoreaction on the immunosensor surface, the gold nanoprobes were captured onto the electrode surface to form immunocomplex. The multiple Au NPs on the attached nanoprobe composites were then measured by electrochemical stripping analysis to obtain signal response. This method provided a simple and controllable way to prepare a novel gold nanoprobe which greatly amplified the signal response of every single immuno-recognition event. The modification of electrode surface with CNTs also facilitated the stripping current enhancement of Au NPs resulting in the ultrahigh sensitivity of this immunoassay method. Using human IgG as a model analyte, the proposed method showed a wide linear range over three orders of magnitude with the detection limit down to 6.9pg/mL. Besides, this method showed excellent analytical performance with low cost, good portability, and acceptable reproducibility, stability and accuracy, thus providing great potentials for clinical applications.
一种新型金纳米探针被制备用于基于碳纳米管(CNT)的一次性免疫传感器上的超灵敏非酶电化学免疫分析中的信号追踪。该金纳米探针通过在聚多巴胺功能化的硅纳米球上原位沉积金纳米颗粒(Au NPs),然后标记信号抗体来制备。免疫传感器通过捕获抗体在 CNT 修饰的丝网印刷碳电极上的共价固定化来制备。在免疫传感器表面进行三明治型免疫反应后,金纳米探针被捕获到电极表面形成免疫复合物。然后通过电化学剥离分析测量附着在纳米探针复合材料上的多个 Au NPs 以获得信号响应。该方法提供了一种简单可控的方法来制备新型金纳米探针,极大地放大了每个免疫识别事件的信号响应。通过 CNT 修饰电极表面也促进了 Au NPs 的剥离电流增强,从而使这种免疫分析方法具有超高的灵敏度。用人 IgG 作为模型分析物,该方法在三个数量级范围内显示出宽的线性范围,检测限低至 6.9pg/mL。此外,该方法具有成本低、便携性好、重现性、稳定性和准确性可接受等优点,因此在临床应用中具有很大的潜力。