A regenerating self-assembled gold nanoparticle-containing electrochemical impedance sensor

We report on the development of an electrochemical reductive desorption protocol for repeated regeneration of gold electrodes modified with multi-layers of self-assembled surfaces for use in electrochemical sensing. The gold electrodes were first modified with 1,6-hexanedithiol to which gold nanopar...

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Veröffentlicht in:Biosensors & bioelectronics 2014-06, Vol.56, p.328-333
Hauptverfasser: Mahmoud, Amr M., Tang, Thompson, Jed Harrison, D., Lee, William E., Jemere, Abebaw B.
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Sprache:eng
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Zusammenfassung:We report on the development of an electrochemical reductive desorption protocol for repeated regeneration of gold electrodes modified with multi-layers of self-assembled surfaces for use in electrochemical sensing. The gold electrodes were first modified with 1,6-hexanedithiol to which gold nanoparticles were attached in a subsequent modification step. Attachment of thiolated single-stranded nucleic acid oligomers to the gold nanoparticles completed the electrochemical sensor. The changes of electrode behavior after each assembly and desorption processes were investigated by cyclic voltammetry, electrochemical impedance spectroscopy and X-ray photoelectron spectroscopy techniques. The self-assembled sensor showed a wide dynamic range (0.1–100nM), a low detection limit (20pM) and high reproducibility (4.4% RSD) for complementary nucleic acid target molecules, along with reusability. On a single gold electrode, the complete sensor–target structure could be assembled and disassembled at least four times with 90% of its original signal intact. •We report a reductive desorption technique for removal of multi-layer self-assembled structures on gold electrode.•The desorption technique allowed us repeated analysis performed via multi-layer molecular self-assembly and electrochemical detection.•A single electrode could be assembled and disassembled many times with at least 90% of its initial response intact.•The demonstration made here has significant implications for integration of electrochemical sensors and for automated electrochemical analysis.
ISSN:0956-5663
1873-4235
DOI:10.1016/j.bios.2014.01.019