2011
DOI: 10.1007/s00604-011-0742-9
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Label-free electrochemical DNA biosensor based on a glassy carbon electrode modified with gold nanoparticles, polythionine, and graphene

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Cited by 46 publications
(22 citation statements)
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“…G/Au NR/PT modified GCE provided an excellent platform for further immobilization. CP was immobilized on G/Au NR/PT GCE both through strong Au-S bond Zhang and Huang, 2012), and the electrostatic interaction with the positively charge Au NRs (Lu et al, 2013). The presence of MCH aimed to block the nonspecific binding sites.…”
Section: Design Of Electrochemical Biosensormentioning
confidence: 99%
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“…G/Au NR/PT modified GCE provided an excellent platform for further immobilization. CP was immobilized on G/Au NR/PT GCE both through strong Au-S bond Zhang and Huang, 2012), and the electrostatic interaction with the positively charge Au NRs (Lu et al, 2013). The presence of MCH aimed to block the nonspecific binding sites.…”
Section: Design Of Electrochemical Biosensormentioning
confidence: 99%
“…Thionine was then electropolymerized on the G/Au NR GCE followed the reported method (Zhang and Huang, 2012). The deposition experiment was carried out from an acetate buffer solution (0.1 mol/L, pH ¼6.0) containing 0.5 mmol/L thionine using cyclic voltammetry (CV).…”
Section: Electrode Pretreatmentmentioning
confidence: 99%
“…This is in accordance with the literature [40], revealing that the TB attached on GO surface retained the redox properties. Absorption of Au NPs increased the conductivity of the TB-GO film, resulting in the increase of the redox peak current as the Au NPs acted as a conducting wire or an electron communication relay, which increased the electron transfer efficiency (curve c) [27,41]. When probe DNA was immobilized on the surface of the electrode, the redox peak current of TB decreased.…”
Section: Electrochemical Characterization Of the Different Modified Ementioning
confidence: 97%
“…When probe DNA was immobilized on the surface of the electrode, the redox peak current of TB decreased. After hybridization with target DNA, the peak current of the modified electrode further decreased, indicating that dsDNA formed an electron-transfer and mass-transfer blocking layer, which greatly inhibited the reaction on the electrode surface [27,42]. The CVs of the DNA biosensor in 0.1 M PBS (pH 7.0) at different scan rates were also studied.…”
Section: Electrochemical Characterization Of the Different Modified Ementioning
confidence: 99%
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