@article {Vitale155937, author = {Flavia Vitale and Daniel G. Vercosa and Alexander V. Rodriguez and Sushma Sri Pamulapati and Frederik Seibt and Eric Lewis and J. Stephen Yan and Krishna Badhiwala and Mohammed Adnan and Gianni Royer-Carfagni and Michael Beierlein and Caleb Kemere and Matteo Pasquali and Jacob T. Robinson}, title = {Fluidic microactuation of flexible electrodes for neural recording}, elocation-id = {155937}, year = {2017}, doi = {10.1101/155937}, publisher = {Cold Spring Harbor Laboratory}, abstract = {Ultra-flexible microelectrodes that can bend and flex with the natural movement of the brain reduce the inflammatory response and improve the stability of long-term neural recordings.1-5 However, current methods to implant these highly flexible electrodes rely on temporary stiffening agents that increase the electrode size6-10 thus aggravating neural damage during implantation, which leads to cell loss and glial activation that persists even after the stiffening agents are removed or dissolve.11-13 A method to deliver thin, ultra-flexible electrodes deep into neural tissue without increasing the stiffness or size of the electrodes will enable minimally invasive electrical recordings from within the brain. Here we show that specially designed microfluidic devices can apply a tension force to ultra-flexible electrodes that prevents buckling without increasing the thickness or stiffness of the electrode during implantation. Additionally, these {\textquotedblleft}fluidic microdrives{\textquotedblright} allow us to precisely actuate the electrode position with micron-scale accuracy. To demonstrate the efficacy of our fluidic microdrives, we used them to actuate highly flexible carbon nanotube fiber (CNTf) microelectrodes11,14 for electrophysiology. We used this approach in three proof-of-concept experiments. First, we recorded compound action potentials in a soft model organism, the small cnidarian Hydra. Second, we targeted electrodes precisely to the thalamic reticular nucleus in brain slices and recorded spontaneous and optogenetically-evoked extracellular action potentials. Finally, we inserted electrodes more than 4 mm deep into the brain of rats and detected spontaneous individual unit activity in both cortical and subcortical regions. Compared to syringe injection, fluidic microdrives do not penetrate the brain and prevent changes in intracranial pressure by diverting fluid away from the injection site during insertion and actuation. Overall, the fluidic microdrive technology provides a robust new method to implant and actuate ultra-flexible neural electrodes.}, URL = {https://www.biorxiv.org/content/early/2017/06/26/155937}, eprint = {https://www.biorxiv.org/content/early/2017/06/26/155937.full.pdf}, journal = {bioRxiv} }