4.8 Article

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

Journal

BIOMATERIALS
Volume 52, Issue -, Pages 476-483

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2015.02.058

Keywords

Label-free; Electrochemiluminescence (ECL); On-off-on switch system; Au@nano-C-60; Hemin/G-quadruplex DNAzymes

Funding

  1. NNSF of China [51473136, 21275119, 21105081]
  2. Research Fund for the Doctoral Program of Higher Education (RFDP) [20110182120010]
  3. Specialized Research Fund for the Doctoral Program of Higher Education [20100182110015]
  4. Fundamental Research Funds for the Central Universities, China [XDJK2013A008, XDJK2013A027, XDJK2014A012]

Ask authors/readers for more resources

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.

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