Ultra-Sensitive Detection of Mercury by Using Field-Effect Transistor Biosensors Based on Single-Walled Carbon Nanotubes.

In recent years, the amount of mercury discharged by human activities has continued to increase. Most of the mercury in surface water settles into the sediment, where it can be directly or indirectly transformed into mercury ion (Hg2+) compounds (such as dimethylmercury) under the action of microorganisms. Hg2+ display high toxicity and bioaccumulation in food, such as fish and rice, and thus the contamination of mercury ion is a serious concern for human health. Practical Hg2+ detection methods are usually limited by the sensitivity and selectivity of the used methods, such as colorimetric determination and fluorescence biosensor based on the solution phase. Therefore, it is urgent to develop Hg2+ detection methods in the practical environment with high sensitivity and selectivity. DNA is low-cost, relatively stable, and has been used for different fields. In this study, DNA for Hg2+detection was absorbed on the surface of single-walled carbon nanotubes (SWNTs) by using 1,5-diaminonaphthalene (DAN) based on field-effect transistor (FET) biosensors. The interaction between DNA and Hg2+ can be directly converted into electrical signals based on the SWNTs biosensors. The experimental results showed that the limit of detection (LOD) of Hg2+ without the phase-locked amplifier was about 42.6 pM. The function of the phase-locked amplifier is to achieve fast detection of the biosensor with strong anti-noise ability. Intriguingly, the sensitivity of the biosensor combined with a phase-locked amplifier to detect Hg2+ was further improved to be 5.14 pM compared with some current methods of biosensors. Furthermore, this biosensor has an excellent selectivity and practical detection in tap water, which demonstrates its high performance and low cost in practical application in Hg2+ detection. These results show this method for Hg2+ detection using SWNTs biosensors with a phase-locked amplifier is promising.