Nanoflake-like SnS2 matrix for glucose biosensing based on direct electrochemistry of glucose oxidase

A novel biosensor is developed based on immobilization of proteins on nanoflake-like SnS₂ modified glass carbon electrode (GCE). With glucose oxidase (GOD) as a model, direct electrochemistry of the GOD/nanoflake-like SnS₂ is studied. The prepared SnS₂ has large surface area and can offer favorable...

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Veröffentlicht in:Biosensors & bioelectronics 2011-07, Vol.26 (11), p.4337-4341
Hauptverfasser: Yang, Zhanjun, Ren, Yanyan, Zhang, Yongcai, Li, Juan, Li, Hongbo, Hu, Xiaochun Huang Xiaoya, Xu, Qin
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Sprache:eng
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Zusammenfassung:A novel biosensor is developed based on immobilization of proteins on nanoflake-like SnS₂ modified glass carbon electrode (GCE). With glucose oxidase (GOD) as a model, direct electrochemistry of the GOD/nanoflake-like SnS₂ is studied. The prepared SnS₂ has large surface area and can offer favorable microenvironment for facilitating the electron transfer between protein and electrode surface. The properties of GOD/SnS₂ are characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), UV-vis spectroscopy, Fourier transform infrared spectroscopy (FTIR) and cyclic voltammetry (CV), respectively. The immobilized enzyme on nanoflake-like SnS₂ retains its native structure and bioactivity and exhibits a surface-controlled, reversible two-proton and two-electron transfer reaction with the apparent electron transfer rate constant (k(s)) of 3.68 s⁻¹. The proposed biosensor shows fast amperometric response (8s) to glucose with a wide linear range from 2.5 × 10⁻⁵ M to 1.1 × 10⁻³ M, a low detection limit of 1.0 × 10⁻⁵ M at signal-to-noise of 3 and good sensitivity (7.6 ± 0.5 mA M⁻¹ cm⁻²). The resulting biosensor has acceptable operational stability, good reproducibility and excellent selectivity and can be successfully applied in the reagentless glucose sensing at -0.45 V. It should be worthwhile noting that it opens a new avenue for fabricating excellent electrochemical biosensor.
ISSN:0956-5663
1873-4235
DOI:10.1016/j.bios.2011.04.031