This work presents a simple, low cost method for creating microelectrodes for electrochemical paper-based analytical devices (ePADs). The microelectrodes were constructed by backfilling small holes made in polyester sheets using a CO2 laser etching system. To make electrical connections, the working electrodes were combined with silver screen-printed paper in a sandwich type two-electrode configuration. The devices were characterized using linear sweep voltammetry and the results are in good agreement with theoretical predictions for electrode size and shape. As a proof-of-concept, cysteine was measured using cobalt phthalocyanine as a redox mediator. The rate constant (kobs) for the chemical reaction between cysteine and the redox mediator was obtained by chronoamperometry and found to be on the order of 105 s−1 M−1. Using a microelectrode array, it was possible to reach a limit of detection of 4.8 μM for cysteine. The results show that carbon paste microelectrodes can be easily integrated with paper-based analytical devices.

Here we report a new microfluidic paper-based analytical device (mPAD) for quantifying metals in water. Metals represent an important class of water contaminants that come from a variety of sources including mining, transportation, manufacturing, waste management, and energy production. Current technologies for quantifying aquatic metals in water are expensive, relatively slow, tedious, provide inadequate performance, and are difficult to use in a field setting. As a result, a need exists for simple, portable, power-free measurement tools that enable rapid in-field quantification of aquatic metals. The reported metal test cards, referred to as the On-Target Water Chemistry test cards, represent a major improvement over previously reported linear distance-based detection systems comprised of paper. With the On-Target approach, the sample flows outwards radially and reacts with colorimetric complexing agents, significantly reducing assay time. The diameter of the resulting color formation is directly proportional to analyte concentration. The On-Target cards were used for detecting copper, iron, and zinc with detection limits as low as 0.1 ppm in ∼3 min and single ppb in combination with a membrane pre-concentration system.

A high-density amperometric electrode array containing 8192 individually addressable platinum working electrodes with an integrated potentiostat fabricated using Complementary Metal Oxide Semiconductor (CMOS) processes is reported. The array was designed to enable electrochemical imaging of chemical gradients with high spatiotemporal resolution. Electrodes are arranged over a 2 mm × 2 mm surface area into 64 subarrays consisting of 128 individual Pt working electrodes as well as Pt pseudo-reference and auxiliary electrodes. Amperometric measurements of norepinephrine in tissue culture media were used to demonstrate the ability of the array to measure concentration gradients in complex media. Poly(dimethylsiloxane) microfluidics were incorporated to control the chemical concentrations in time and space, and the electrochemical response at each electrode was monitored to generate electrochemical heat maps, demonstrating the array's imaging capabilities. A temporal resolution of 10 ms can be achieved by simultaneously monitoring a single subarray of 128 electrodes. The entire 2 mm × 2 mm area can be electrochemically imaged in 64 seconds by cycling through all subarrays at a rate of 1 Hz per subarray. Monitoring diffusional transport of norepinephrine is used to demonstrate the spatiotemporal resolution capabilities of the system.