Martinelli, EleonoraAkouissi, OutmanLiebi, LucaFurfaro, IvanMaulà, DesiréeSavoia, NathanRemy, AntoineNikles, LaetitiaRoux, AdrienStoppini, LucLacour, Stéphanie P.2025-01-252025-01-252025-01-242024-10-1810.1126/sciadv.adp80542-s2.0-85206693130https://infoscience.epfl.ch/handle/20.500.14299/24390739413178Traditional microelectrode arrays (MEAs) are limited to measuring electrophysiological activity in two dimen- Attribution creative commons sions, failing to capture the complexity of three-dimensional (3D) tissues such as neural organoids and spheroids. noncommercial Here, we introduce a flower-shaped MEA (e-Flower) that can envelop submillimeter brain spheroids following ac- license 4.0 (cc BY-nc). tuation by the sole addition of the cell culture medium. Inspired by soft microgrippers, its actuation mechanism leverages the swelling properties of a polyacrylic acid hydrogel grafted to a polyimide substrate hosting the electrical interconnects. Compatible with standard electrophysiology recording systems, the e-Flower does not require additional equipment or solvents and is ready to use with preformed 3D tissues. We designed an e-Flower achieving a curvature as low as 300 micrometers within minutes, a value tunable by the choice of reswelling media and hydrogel cross-linker concentration. Furthermore, we demonstrate the ability of the e-Flower to detect spontaneous neural activity across the spheroid surface, demonstrating its potential for comprehensive neural signal recording.enfalsetext::journal::journal article::research article