Au nanoparticles decorated C60 nanoparticle-based label-free electrochemiluminesence aptasensor via a novel "on-off-on" switch system

被引:64
作者
Zhao, Min [1 ]
Zhuo, Ying [1 ]
Chai, Ya-Qin [1 ]
Yuan, Ruo [1 ]
机构
[1] Southwest Univ, Key Lab Luminescent & Real Time Analyt Chem, Minist Educ, Coll Chem & Chem Engn, Chongqing 400715, Peoples R China
关键词
Label-free; Electrochemiluminescence (ECL); On-off-on" switch system; Au@nano-C-60; Hemin/G-quadruplex DNAzymes; AQUEOUS-SOLUTION; ELECTROGENERATED CHEMILUMINESCENCE; SENSITIVE DETECTION; ENERGY-TRANSFER; QUANTUM DOTS; KANAMYCIN; APTAMER; DNA; AMPLIFICATION; BIOSENSOR;
D O I
10.1016/j.biomaterials.2015.02.058
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
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.
引用
收藏
页码:476 / 483
页数:8
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