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A simple paper-based sensor with electrochemical detection was first developed for rapid, selective, and sensitive determination of acetylcholinesterase (AChE). The screen-printed graphene electrode was used as working electrode providing sensitivity for the sensor. The amperometric detection of AChE is based on the determination of thiocholine (TCh) produced from hydrolysis of acetylthiocholine chloride (ATCh) by AChE. To detect TCh, the ATCh immobilized sheet was stacked onto the detection sheet using double adhesive tape, then samples of AChE were dropped on the back side of an ATCh immobilized sheet with only 1min of incubation time. To avoid interference, glutathione (GSH), the potential of 0.5V vs. Ag/AgCl was applied onto a graphene electrode and the current, which depends on AChE concentration, was measured. Under optimized conditions, the limit of detection (LOD) from the experiment of AChE determination was 0.1U/mL with AChE concentration in range of 0.1-15U/mL. The data correlated well with the data obtained using spectrophotometric method. The developed sensor had been successfully applied to detect AChE in blood samples.

This work combines lab-on-paper methodology with nanoparticle science to develop a new tool for the simple and rapid determination of Hg(II). The resulting paper-based device enables measurement of Hg(II) from only 2 μL of sample solution. The color of the nanosilver in the test area immediately changes in the presence of Hg(II), and this change can be monitored by the naked eye. This method exhibits superior selectivity towards Hg(II) compared with the other metal ions tested. Furthermore, the results show a significant increase in the Hg(II) analytical signal when Cu(II) is added to the Ag Nanoplates at the test zone. With digital camera imaging and software processing, which are shown to further improve the quantitative capability of this technique, the linear detection range is 5–75 ppm Hg(II) with a limit of detection of 0.12 ppm. Using a pre-concentration scheme (based on repeated 2 μL applications of the test Hg(II) solution onto the same test zone) reduces the limit of detection to 2 ppb. The technique developed by this study provides a rapid, sensitive and selective detection method for aqueous Hg(II) samples and is especially suitable for remote field and environmental analysis.