Organic electrochemical transistors (OECTs) are a burgeoning biosensing transducer platform due to their intrinsic amplification, high transconductance, and biocompatibility. To be successful in real world biosensing applications, however, stable performance should be demonstrated to avoid false analyte readings that could lead to dangerous misdiagnosis. This work demonstrates the stability of carefully prepared OECTs using commercially available PEDOT:PSS as the channel layer. These devices exhibit more than 99% retention of the baseline current over 50 transfer curve cycles and, importantly, after several changes in electrolyte solution. Furthermore, impressive stability is demonstrated during continuous measurements of the drain current. These results show that PEDOT:PSS OECTs are ready for biosensing applications requiring accurate continuous monitoring.

By simultaneously transducing and amplifying, transistors offer advantages over simpler, electrode-based transducers in electrochemical biosensors. However, transistor-based biosensors typically use static (i.e., DC) operation modes that are poorly suited for sensor architectures relying on the modulation of charge transfer kinetics to signal analyte binding. Thus motivated, here, we translate the AC “pulsed potential” approach typically used with electrochemical aptamer-based (EAB) sensors to an organic electrochemical transistor (OECT). Specifically, by applying a linearly sweeping square-wave potential to an aptamer-functionalized gate electrode, we produce current modulation across the transistor channel two orders of magnitude larger than seen for the equivalent, electrode-based biosensor. Unlike traditional EAB sensors, our aptamer-based OECT (AB-OECT) sensors critically maintain output current even with miniaturization. The pulsed transistor operation demonstrated here could be applied generally to sensors relying on kinetics-based signaling, expanding opportunities for noninvasive and high spatial resolution biosensing.

State-of-the-art tissue analogues used in high-fidelity, hands-on medical simulation modules can deliver lifelike appearance and feel but lack the capability to provide quantified, real-time assessment of practitioner performance. The monolithic fabrication of hybrid printed/textile piezoresistive strain sensors in a realistic Y/V plasty suture training pad is demonstrated. A class of 3D-printable organogels comprised of inexpensive and nonhazardous feedstocks is used as the sensing medium, and conductive composite threads are used as the electrodes. These organogels are comprised of a glycol-based deep-eutectic solvent (DES) serving as the ionic conductor and 3-trimethoxysilylmethacrylate-capped fumed silica particles serving as the gelating agent. Rheology measurements reveal the influence of fumed silica particle capping group on the mixture rheology. Freestanding strain sensors demonstrate a maximum strain amplitude of 300%, negligible signal drift, a monotonic sensor response, a low degree of hysteresis, and excellent cyclic stability. The increased contact resistance of the conductive thread electrodes used in place of wire electrodes do not make a significant impact on sensor performance. This work showcases the potential of these organogels utilized in sensorized tissue analogues and freestanding strain sensors for widespread applications in medical simulation and education.