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      An ionic liquid supported CeO2 nanoshuttles–carbon nanotubes composite as a platform for impedance DNA hybridization sensing

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      Biosensors and Bioelectronics
      Elsevier BV

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          Abstract

          A novel nanocomposite membrane, comprising of nanosized shuttle-shaped cerium oxide (CeO(2)), single-walled carbon nanotubes (SWNTs) and hydrophobic room temperature ionic liquid (RTIL) 1-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF(6)), was developed on the glassy carbon electrode (GCE) for electrochemical sensing of the immobilization and hybridization of DNA. The properties of the CeO(2)-SWNTs-BMIMPF(6)/GCE, the characteristics of the immobilization and hybridization of DNA were studied by cyclic voltammetry and electrochemical impedance spectroscopy (EIS) using [Fe(CN)(6)](3-/4-) as the redox indicator. The synergistic effect of nano-CeO(2), SWNTs and RTIL could dramatically enhance the sensitivity of DNA hybridization recognition. The electron transfer resistance (R(et)) of the electrode surface increased after the immobilization of probe ssDNA on the CeO(2)-SWNTs-BMIMPF(6) membrane and rose further after the hybridization of the probe ssDNA with its complementary sequence. The remarkable difference between the R(et) value at the probe DNA-immobilized electrode and that at the hybridized electrode could be used for label-free EIS detection of the target DNA. The sequence-specific DNA of phosphoenolpyruvate carboxylase (PEPCase) gene from transgenically modified rape was detected by this DNA electrochemical biosensor. Under optimal conditions, the dynamic range for detecting the sequence-specific DNA of the PEPCase gene was from 1.0x10(-12) mol/L to 1.0x10(-7) mol/L, and the detection limit was 2.3x10(-13) mol/L, suggesting that the CeO(2)-SWNTs-BMIMPF(6) nanocomposite hold great promises for the applications in sensitive electrochemical biosensor.

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          Author and article information

          Journal
          Biosensors and Bioelectronics
          Biosensors and Bioelectronics
          Elsevier BV
          09565663
          April 2009
          April 2009
          : 24
          : 8
          : 2417-2422
          Article
          10.1016/j.bios.2008.12.024
          19167208
          5de96ce9-037d-4122-9d1a-02ad51fcde3e
          © 2009

          https://www.elsevier.com/tdm/userlicense/1.0/

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