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首页> 外文期刊>Biomaterials >Au nanoparticles decorated C-60 nanoparticle-based label-free electrochemiluminesence aptasensor via a novel 'on-off-on' switch system
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Au nanoparticles decorated C-60 nanoparticle-based label-free electrochemiluminesence aptasensor via a novel 'on-off-on' switch system

机译:金纳米粒子通过新颖的“开-关-开”开关系统修饰了基于C-60纳米粒子的无标记电化学发光适体传感器

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摘要

Herein, a label-free electrochemiluminescence (ECL) aptasensor for highly sensitive determination of kanamycin was developed based on a novel "on-off-on" switch system. The first "switch on" state with remarkably high ECL intensity was obtained by the tri-layer composite films modified glassy carbon electrode towards the S2O82--O-2 system. To be specific, the first layer was the Au nanoparticles decorated C-60 nanoparticles (abbreviation as Au@nano-C-60) as inner-layer which was prepared by the in situ generating of Au nanoparticles onto the surface of bovine serum albumin decorated nano-C-60 nanoparticles. Then poly-L-histidine was first selected as a novel coreactant of S2O82--O-2 system and it was adsorbed on the Au@nano-C-60 modified electrode as inter-layer. Finally, a self-assembling layer of colloidal Au nanoparticles (AuNPs) was the outer-layer. The three layers were interaction by the Au-N covalent bond which could achieve a desirable initial amplified ECL signal. Successively, the capture probes (CPs) of the aptamer for the target of kanamycin was anchored on the resultant tri-layer composite films modified electrode. Later, the "switch off" state was made by the quenching effect of hemin/G-quadruplex DNAzymes towards S2O82--O-2 system according to the DNA hybridization reaction of an assistant probes (APs, guanine-rich nucleic acid) with CPs which could generate a large amount of hemin/G-quadruplex DNAzymes in the presence of hemin with a simple and label-free process. As expected, the second "switch on" state was the ECL signal recovery when the target of kanamycin was present, it is attributed to that the formation of the aptamer-kanamycin complex makes the quencher of hemin/G-quadruplex DNAzymes release from the sensing interface. With the association of "on-off-on" switch system, a linear response about 9 orders of magnitude for kanamycin detection was obtained from 0.15 nM to 170 mm as well as a detection limit down to 45 pM. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在此,基于新颖的“开-关-开”开关系统,开发了用于高灵敏度测定卡那霉素的无标记电化学发光(ECL)适体传感器。三层复合膜修饰的玻碳电极朝向S2O82--O-2系统获得了具有极高ECL强度的第一个“接通”状态。具体而言,第一层是Au纳米颗粒修饰的C-60纳米颗粒(缩写为Au @ nano-C-60)作为内层,它是通过在牛血清白蛋白修饰的表面上原位生成Au纳米颗粒而制备的纳米C-60纳米颗粒。然后首先选择聚L-组氨酸作为S2O82-O-2体系的新型共反应剂,并将其吸附在Au @ nano-C-60修饰电极上作为中间层。最后,胶体金纳米颗粒(AuNPs)的自组装层是外层。这三层通过Au-N共价键相互作用,可以实现理想的初始放大ECL信号。随后,将卡那霉素靶标的适体的捕获探针(CP)锚定在所得的三层复合膜修饰电极上。后来,根据辅助探针(AP,富含鸟嘌呤的核酸)与CP的DNA杂交反应,通过血红素/ G-四链体DNA酶对S2O82-O-2系统的猝灭作用来实现“关闭”状态在存在血红素的情况下,它可以通过简单且无标记的过程生成大量的血红素/ G-四链体DNA酶。不出所料,当存在卡那霉素的靶标时,第二个“开启”状态是ECL信号恢复,这归因于适体-卡那霉素复合物的形成使血红素/ G-四链体DNA酶的猝灭剂从传感中释放出来。接口。结合“ on-off-on”开关系统,卡那霉素的线性响应从0.15 nM到170 mm可达9个数量级,检出限低至45 pM。 (C)2015 Elsevier Ltd.保留所有权利。

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