| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 183973 | Electrochimica Acta | 2015 | 8 Pages |
•A facile and reusable electrochemical method for selectively detection Hg2+ based on T-Hg2+-T duplex using undecorated graphene directly as the sensing platform was constructed.•Graphene was directly immobilized on the glass carbon electrode, which was used as the ferrocene-tagged probe DNA carrier and amplified the electrochemical signal.•Target-induced surface hybridization can cause the form of ds-DNA and the decrease of redox current signal because of the remarkable difference in the affinity of graphene with ds-DNA and short ss-DNA fragments.•This approach for Hg2+ detection is high sensitivity, adequate selectivity, and excellent reusability.•This strategy allowed the minimal reagents and working steps making it possible for Hg2+ detection in real environmental samples.
A simple, signal-off and reusable electrochemical biosensor was developed for sensitive and selective detection of mercury(II) based on thymine–mercury(II)–thymine (T–Hg2+–T) complex and the remarkable difference in the affinity of graphene with double strand DNA (ds-DNA) and single strand DNA (ss-DNA). Our system was composed of ferrocene-tagged probe DNA and graphene. Due to the noncovalent assembly, the ferrocene-tagged probe ss-DNA was immobilized on the surface of graphene nanosheets directly and employed to amplify the electrochemical signal. In the presence of Hg2+, the ferrocene-labeled T-rich DNA probe hybridized with target probe to form ds-DNA via the Hg2+-mediated coordination of T-Hg2+-T base pairs. As a result, the duplex DNA complex kept away from the graphene surface due to the weak affinity of graphene and ds-DNA, and the redox current decreased substantially. Meanwhile, the graphene decorated GCE surface was released for the reusability. Under the optimal conditions, the proposed sensor showed a linear concentration range from 25 pM to 10 μM with a detection limit of 5 pM for Hg2+ detection. The strategy afforded exquisite selectivity for Hg2+ against other metal ions in real environmental samples.
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