• 文献标题:   A novel nanocomposite matrix based on graphene oxide and ferrocene-branched organically modified sol-gel/chitosan for biosensor application
  • 文献类型:   Article
  • 作  者:   PENG HP, HUANG ZJ, ZHENG YJ, CHEN W, LIU AL, LIN XH
  • 作者关键词:   graphene oxide, chitosan, ferrocenebranched organically modified solgel, glucose oxidase, biosensor
  • 出版物名称:   JOURNAL OF SOLID STATE ELECTROCHEMISTRY
  • ISSN:   1432-8488 EI 1433-0768
  • 通讯作者地址:   Fujian Med Univ
  • 被引频次:   17
  • DOI:   10.1007/s10008-014-2415-1
  • 出版年:   2014

▎ 摘  要

A novel platform for the fabrication of a glucose biosensor was successfully constructed by entrapping glucose oxidase (GOD) in a ferrocene (Fc)-branched organically modified silica material (ormosil)/chitosan (CS)/graphene oxide (GO) nanocomposite. The morphology, structure, and electrochemistry of the nanocomposite were characterized by transmission electron microscopy, X-ray powder diffraction, UV-vis spectroscopy, Fourier transform infrared spectroscopy, and electrochemical techniques. Results demonstrated that the proposed electrochemical platform not only provided an excellent microenvironment to maintain the bioactivity of the immobilized enzyme, but also effectively prevented the leakage of both the enzyme and mediator from the matrix and retained the electrochemical activity of Fc. Furthermore, dispersing GO within the Fc-branched ormosil/CS matrix could significantly improve the stability of GO and make it exhibit a positive charge, which was more favorable for the further immobilization of biomolecules, such as GOD, with higher loading. Moreover, it could also improve the conductivity of the matrix film and facilitate the electron shuttle between the mediator and electrode. Under optimal conditions, the designed biosensor to glucose exhibited a wide and useful linear range of 0.02 to 5.39 mM with a low detection limit of 6.5 mu M. The value of K (M) (app) was 4.21 mM, indicating that the biosensor possesses higher biological affinity to glucose. The present approach could be used efficiently for the linkage of other redox mediators and immobilize other biomolecules in the process of fabricating novel biosensors.