Introduction
Organs-on-chip (OoCs) are dynamic tissue culture devices which mimic microphysiological environments to recapitulate in vivo-like organ functions in vitro and thus enhance the efficiency of drug development and disease modelling [1]. Among the key features distinguishing OoCs from established tissue culture technologies, automated monitoring of biological cues, such as charged species, is essential to reduce user intervention and improve system's ease of use and reliability [2]. In this respect, dynamic electric sensing can meet user needs without recurring to terminal optical labeling and microscopy techniques, which deteriorate cells' wellbeing.