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Nowadays, we are assisting in the exceptional growth in research relating to the development of wearable devices for sweat analysis. Sweat is a biofluid that contains useful health information and allows a non-invasive, continuous and comfortable collection. For this reason, it is an excellent biofluid for the detection of different analytes. In this work, electrochemical sensors based on polyaniline thin films deposited on the flexible substrate polyethylene terephthalate coated with indium tin oxide were studied. Polyaniline thin films were abstained by the potentiostatic deposition technique, applying a potential of +2 V vs. SCE for 90 s. To improve the sensor performance, the electronic substrate was modified with reduced graphene oxide, obtained at a constant potential of −0.8 V vs. SCE for 200 s, and then polyaniline thin films were electrodeposited on top of the as-deposited substrate. All samples were characterized by XRD, SEM, EDS, static contact angle and FT-IR/ATR analysis to correlate the physical-chemical features with the performance of the sensors. The obtained electrodes were tested as pH sensors in the range from 2 to 8, showing good behavior, with a sensitivity of 62.3 mV/pH, very close to a Nernstian response, and a reproducibility of 3.8%. Interference tests, in the presence of competing ions, aimed to verify the selectivity, were also performed. Finally, a real sweat sample was collected, and the sweat pH was quantified with both the proposed sensor and a commercial pH meter, showing an excellent concordance.

Silver ions, the most toxic form of silver, can be present in drinking water due to their release from silver nanoparticles which are widely used in consumer products. Due to their adverse health effects, a quick portable approach for detection in drinking water is needed. Herein we report on the development of an electrochemical sensor for silver ions detection in tap water using linear sweep voltammetry with in situ pH control; enabled by closely space interdigitated electrode arrays. The in situ pH control approach, allows the pH of a test solution to be tailored to pH 3 thereby eliminating the current need for acid addition. A calibration curve between 0.2 -10 µM was established for silver detection in sodium acetate when 1.25 V and 1.65 V was applied at the protonator electrode during deposition and stripping, respectively, as a proof of concept study. For the final application in tap water, 1.65 V was applied at the protonator electrode during deposition and stripping. The chlorine ions, present in tap water as a consequence of the disinfection process, facilitated the silver detection and no additional electrolyte had to be added. Combination of complexation of silver ions with chlorine coupled with in situ pH control resulted in linear calibration range between 0.25 and 2 µM in tap water without the need of acidification.