4.7 Article

Synthesis of core-shell structured Au@Bi2S3 nanorod and its application as DNA immobilization matrix for electrochemical biosensor construction

Journal

CHINESE CHEMICAL LETTERS
Volume 31, Issue 1, Pages 181-184

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2019.04.056

Keywords

DNA biosensor; Au@Bi2S3 nanorods; Electrochemical impedance spectroscopy; Core-shell structure; Bi3+-N bond; Probe immobilization

Funding

  1. National Natural Science Foundation of China [21802064, 21275127]
  2. Natural Science Foundation of Fujian Province, China [2018J01435, 2017J01419]
  3. Foundation of Key Laboratory of Sensor Analysis of Tumor Marker, Ministry of Education, Qingdao University of Science and Technology

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The core-shell structured Au@Bi2S3 nanorods have been prepared through direct in-situ growth of Bi2S3 at the surface of pre-synthesized gold nanorods. The product was characterized by X-ray diffraction, transmission electron microscopy and energy-dispersive X-ray spectroscopy. Then the obtained Au@Bi2S3 nanorods were coated onto glassy carbon electrode to act as a scaffold for fabrication of electrochemical DNA biosensor on the basis of the coordination of -NH2 modified on 5'-end of probe DNA and Au@Bi2S3. Electrochemical characterization assays demonstrate that the Au@Bi2S3 nanorods behave as an excellent electronic transport channel to promote the electron transfer kinetics and increase the effective surface area by their nanosize effect. The hybridization experiments reveal that the Au@Bi2S3 matrix-based DNA biosensor is capable of recognizing complementary DNA over a wide concentration ranging from 10 fmol/L. to 1 nmol/L. The limit of detection was estimated to be 2 fmol/L (S/N = 3). The biosensor also presents remarkable selectivity to distinguish fully complementary sequences from base-mismatched and non-complementary ones, showing great promising in practical application. (C) 2019 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.

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