新的信号放大策略:利用氨基脲作为共反应加速剂构建高灵敏度的电化学适体传感器。
New Signal Amplification Strategy Using Semicarbazide as Co-reaction Accelerator for Highly Sensitive Electrochemiluminescent Aptasensor Construction.
机构信息
Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University , Chongqing 400715, China.
出版信息
Anal Chem. 2015 Nov 17;87(22):11389-97. doi: 10.1021/acs.analchem.5b02848. Epub 2015 Oct 26.
A highly sensitive electrochemiluminescent (ECL) aptasensor was constructed using semicarbazide (Sem) as co-reaction accelerator to promote the ECL reaction rate of CdTe quantum dots (CdTe QDs) and the co-reactant of peroxydisulfate (S2O8(2-)) for boosting signal amplification. The co-reaction accelerator is a species that when it is introduced into the ECL system containing luminophore and co-reactant, it can interact with co-reactant rather than luminophore to promote the ECL reaction rate of luminophore and co-reactant; thus the ECL signal is significantly amplified in comparison with that in which only luminophore and co-reactant are present. In this work, the ECL signal probes were first fabricated by alternately assembling the Sem and Au nanoparticles (AuNPs) onto the surfaces of hollow Au nanocages (AuNCs) via Au-N bond to obtain the multilayered nanomaterials of (AuNPs-Sem)n-AuNCs for immobilizing amino-terminated detection aptamer of thrombin (TBA2). Notably, the Sem with two -NH2 terminal groups could not only serve as cross-linking reagent to assemble AuNPs and AuNCs but also act as co-reaction accelerator to enhance the ECL reaction rate of CdTe QDs and S2O8(2-) for signal amplification. With the sandwich-type format, TBA2 signal probes could be trapped on the CdTe QD-based sensing interface in the presence of thrombin (TB) to achieve a considerably enhanced ECL signal in S2O8(2-) solution. As a result, the Sem in the TBA2 signal probes could accelerate the reduction of S2O8(2-) to produce the more oxidant mediators of SO4(•-), which further boosted the production of excited states of CdTe QDs to emit light. With the employment of the novel co-reaction accelerator Sem, the proposed ECL biosensor exhibited ultrahigh sensitivity to quantify the concentration of TB from 1 × 10(-7) to 1 nM with a detection limit of 0.03 fM, which demonstrated that the co-reaction accelerator could provide a simple, efficient, and low-cost approach for signal amplification and hold great potential for other ECL biosensors construction.
一种高灵敏度的电化学发光(ECL)适体传感器是通过使用氨基半卡巴肼(Sem)作为共反应加速剂来构建的,以促进碲化镉量子点(CdTe QDs)的 ECL 反应速率和过二硫酸盐(S2O8(2-))作为共反应物,以增强信号放大。共反应加速剂是一种物质,当它被引入到包含发光体和共反应物的 ECL 系统中时,它可以与共反应物相互作用而不是与发光体相互作用,从而促进发光体和共反应物的 ECL 反应速率;因此,与仅存在发光体和共反应物的情况相比,ECL 信号得到了显著放大。在这项工作中,首先通过通过 Au-N 键将 Sem 和金纳米粒子(AuNPs)交替组装到中空金纳米笼(AuNCs)的表面上来制备 ECL 信号探针,以获得(AuNPs-Sem)n-AuNCs 的多层纳米材料,用于固定氨端检测凝血酶(TBA2)的适体。值得注意的是,具有两个 -NH2 末端基团的 Sem 不仅可以用作交联试剂来组装 AuNPs 和 AuNCs,还可以作为共反应加速剂来增强 CdTe QDs 和 S2O8(2-)的 ECL 反应速率,以实现信号放大。在存在凝血酶(TB)的情况下,TBA2 信号探针可以被捕获在基于 CdTe QD 的传感界面上,从而在 S2O8(2-)溶液中实现相当大的增强的 ECL 信号。结果,TBA2 信号探针中的 Sem 可以加速 S2O8(2-)的还原,产生更多的氧化剂介质 SO4(•-),这进一步促进了 CdTe QDs 激发态的产生以发光。通过使用新型共反应加速剂 Sem,所提出的 ECL 生物传感器对 TB 的浓度从 1×10(-7)到 1 nM 进行了超灵敏定量,检测限为 0.03 fM,这表明共反应加速剂可以为信号放大提供一种简单、高效、低成本的方法,并为其他 ECL 生物传感器的构建提供了巨大的潜力。