4.6 Article

Graphene Oxide Nanoparticles Modified Paper Electrode as a Biosensing Platform for Detection of the htrA Gene of O. tsutsugamushi

Journal

SENSORS
Volume 21, Issue 13, Pages -

Publisher

MDPI
DOI: 10.3390/s21134366

Keywords

scrub typhus; screen printed paper electrode; DNA sensor; electrochemical; htrA gene

Funding

  1. Department of Science and Technology (DST), Govt. of India [SP/YO/079/2017]
  2. Ministry of Education and Science of the Russian Federation on the program of Increase of Competitiveness of NITU MISIS among the leading world scientific and educational centers [K3-2016-019]

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The study developed an amperometric DNA sensor using graphene oxide nanoparticles modified paper electrodes, which showed excellent sensitivity and limit of detection for O. tsutsugamushi genomic DNA detection.
The unique structural and electrochemical properties of graphene oxide (GO) make it an ideal material for the fabrication of biosensing devices. Therefore, in the present study, graphene oxide nanoparticles modified paper electrodes were used as a low-cost matrix for the development of an amperometric DNA sensor. The graphene oxide was synthesized using the modified hummers method and drop cast on a screen-printed paper electrode (SPPE) to enhance its electrochemical properties. Further, the GO/SPPE electrode was modified with a 5 ' NH2 labeled ssDNA probe specific to the htrA gene of Orientia tsutsugamushi using carbodiimide cross-linking chemistry. The synthesized GO was characterized using UV-Vis, FTIR, and XRD. The layer-by-layer modification of the paper electrode was monitored via FE-SEM, cyclic voltammetry, and electrochemical impedance spectroscopy (EIS). The sensor response after hybridization with single-stranded genomic DNA (ssGDNA) of O. tsutsugamushi was recorded using differential pulse voltammetry (DPV). Methylene blue (1 mM in PBS buffer, pH 7.2) was used as a hybridization indicator and [Fe(CN)(6)](-3/-4) (2.5 mM in PBS buffer, pH 7.2) as a redox probe during electrochemical measurements. The developed DNA sensor shows excellent sensitivity (1228.4 mu A/cm(2)/ng) and LOD (20 pg/mu L) for detection of O. tsutsugamushi GDNA using differential pulse voltammetry (DPV).

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