4.8 Article

Practical and regenerable electrochemical aptasensor based on nanoporous gold and thymine-Hg2+-thymine base pairs for Hg2+ detection

期刊

BIOSENSORS & BIOELECTRONICS
卷 90, 期 -, 页码 542-548

出版社

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2016.10.018

关键词

Hg2+; Nanoporous gold; Electrochemistry; Thymine-Hg2+-thymine; Amplification

资金

  1. National Natural Science Foundation of China [51521006, 51378190, 51278176, 51408206, 51579098, 51579096]
  2. National Program for Support of Top-Notch Young Professionals of China
  3. Program for New Century Excellent Talents in University [NCET-13-0186]
  4. Scientific Research Fund of Hunan Provincial Education Department [521293050]
  5. Program for Changjiang Scholars and Innovative Research Team in University [IRT-13R17]
  6. Fundamental Research Funds for the Central Universities
  7. Hunan Provincial Innovation Foundation for Postgraduate [CX20158091]
  8. Shanghai Tongji Gao Tingyao Environmental Science and Technology Development Foundation
  9. International S & T Cooperation Program of China [2015DFG92750]

向作者/读者索取更多资源

A simple, practical and reusable electrochemical aptasensor, based on thymine-Hg2+-thymine (T-Hg2+-T) coordination chemistry and nanoporous gold (NPG) for signal amplification, was designed for sensitive and selective detection of mercury ions (Hg2+). The thiol modified T-rich hairpin capture probe was self-assembled onto the surface of the NPG modified electrode for hybridizing with ferrocene-labeled T-rich probe in the presence of Hg2+ via T-Hg2+-T coordination chemistry. As a result, the hairpin capture probe was opened, and the ferrocene tags were close to the NPG modified electrode. Taking advantage of the amplification effect of NPG electrode for increasing the reaction sites of thiol modified capture probe, the proposed electrochemical aptasensor could detect Hg2+ quantitatively in the range of 0.01-5000 nM, with a detection limit as low as 0.0036 nM which is much lower than the maximum contamination level for He in drinking water defined by the U.S. Environmental Protection Agency. Moreover, the proposed electrochemical aptasensor can be regenerated by adding cysteine and Hg2+. The aptasensor was also used to detect Hg2+ from real water samples, and the results showed excellent agreement with the values determined by atomic fluorescence spectrometer. This aptasensor showed a promising potential for on-site detecting Hg2+ in drinking water.

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