A Novel Enzyme-Free Biosensor Based on Porous Core-Shell Metal Organic Frame Nanocomposites Modified Electrode for Highly Sensitive Detection of Uric Acid and Dopamine
A novel enzyme-free biosensor based on porous metal organic frame nanocomposites, i.e., core-shell structured Au@NC@GC nanocomposites, has been constructed for simultaneous determination of uric acid (UA) and dopamine (DA). Au@ZIF-8@ZIF-67 was prepared through a seed-mediated growth method and carbo...
Saved in:
Published in | Journal of biomedical nanotechnology Vol. 15; no. 7; p. 1443 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
01.07.2019
|
Subjects | |
Online Access | Get more information |
Cover
Loading…
Summary: | A novel enzyme-free biosensor based on porous metal organic frame nanocomposites, i.e., core-shell structured Au@NC@GC nanocomposites, has been constructed for simultaneous determination of uric acid (UA) and dopamine (DA). Au@ZIF-8@ZIF-67 was prepared through a seed-mediated growth method and carbonized in nitrogen atmosphere to synthesize a nanoporous hybrid carbon materials (Au@NC@GC). Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) studies demonstrate that the as-prepared Au@NC@GC modified glassy carbon electrode (Au@NC@GC-GCE) possesses a high selectivity and sensitivity for simultaneous detections of UA and DA. It exhibited wide linear responses for UA and DA in the range from 10
M to 600
M and 10
M to 150
M, with the detection limits of 0.773 nM and 0.746 nM, respectively (S/N = 3). Moreover, this novel electrochemical biosensor could be further utilized in biological analysis (i.e., human serum), and the satisfactory recovery results of UA and DA could be readily obtained. These afore-mentioned results further manifest that the as-prepared biosensors are capable for quantitatively monitoring UA and DA in serum, verifying the possibility for its future promising applications in real biological or clinic samples analysis. |
---|---|
ISSN: | 1550-7033 |
DOI: | 10.1166/jbn.2019.2791 |