New Signal Amplification Strategy Using Semicarbazide as Co-reaction Accelerator for Highly Sensitive Electrochemiluminescent Aptasensor Construction.

New Signal Amplification Strategy Using Semicarbazide as Co-reaction Accelerator for Highly Sensitive Electrochemiluminescent Aptasensor Construction.
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使用氨基脲作为共反应加速剂的新信号放大策略,用于构建高灵敏度电化学发光适体传感器。

DOI:
10.1021/acs.analchem.5b02848
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发表时间:
2015-10
影响因子:
7.4
通讯作者:
Chai Yaqin
Chai Yaqin
中科院分区:
化学1区
文献类型:
--
作者:
Ma Mengnan;Zhuo Ying;Yuan Ruo;Chai Yaqin

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一种高灵敏度的电致发光。(ECL)使用氨基脲构建适体传感器。(Sem)作为共反应加速剂,以促进CdTe量子点(CdTe QD)的ECL反应速率和过硫酸盐(S2O8.2-)的共反应物,以增强信号放大。共反应促进剂是一种物质,当它被引入到含有发光体和共反应物的ECL体系中时,它可以与共反应物而不是发光体相互作用,以促进发光体和共反应物的ECL反应速率,从而使ECL信号与仅存在发光体和共反应物的体系相比被显著放大。本工作首先通过Au−N键将Sem和Au纳米粒子(AuNPs)交替组装到空心Au纳米笼(AuNCs)表面,制备了(AuNPs-Sem)n-AuNCs多层纳米材料,用于固定凝血酶(TBA 2)的氨基端检测适体。值得注意的是,具有两个-NH 2末端基团的Sem不仅可以用作组装AuNP和AuNC的交联剂,还可以用作共反应加速剂,以提高CdTe QD和S2O8.2-的ECL反应速率,用于信号放大。在凝血酶(TB)存在的情况下,TBA 2信号探针可以被捕获在基于CdTe QD的传感界面上,以在S2O8.2−溶液中实现显著增强的ECL信号。因此,TBA 2信号探针中的Sem可以加速S2O8.2-的还原,产生更多的SO 4氧化介质。- ,这进一步促进了CdTe量子点的激发态的产生以发光。该传感器对TB浓度在1 × 10−7 ~ 1 nM范围内的定量检测具有很高的灵敏度,检测限为0.03 fM,表明该共反应加速器可以提供一种简单、高效、低成本的信号放大方法,并具有很大的应用潜力.
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.
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