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Ultra‐Sharp Nanowire Arrays Natively Permeate, Record, and Stimulate Intracellular Activity in Neuronal and Cardiac Networks
Author(s) -
Liu Ren,
Lee Jihwan,
Tchoe Youngbin,
Pre Deborah,
Bourhis Andrew M.,
D'AntonioChronowska Agnieszka,
Robin Gaelle,
Lee Sang Heon,
Ro Yun Goo,
Vatsyayan Ritwik,
Tonsfeldt Karen J.,
Hossain Lorraine A.,
Phipps M. Lisa,
Yoo Jinkyoung,
Nogan John,
Martinez Jennifer S.,
Frazer Kelly A.,
Bang Anne G.,
Dayeh Shadi A.
Publication year - 2022
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202108378
Subject(s) - intracellular , materials science , electrophysiology , nanowire , nanotechnology , scalability , biophysics , neuroscience , computer science , biology , microbiology and biotechnology , database
Intracellular access with high spatiotemporal resolution can enhance the understanding of how neurons or cardiomyocytes regulate and orchestrate network activity and how this activity can be affected with pharmacology or other interventional modalities. Nanoscale devices often employ electroporation to transiently permeate the cell membrane and record intracellular potentials, which tend to decrease rapidly with time. Here, one reports innovative scalable, vertical, ultrasharp nanowire arrays that are individually addressable to enable long‐term, native recordings of intracellular potentials. One reports electrophysiological recordings that are indicative of intracellular access from 3D tissue‐like networks of neurons and cardiomyocytes across recording days and that do not decrease to extracellular amplitudes for the duration of the recording of several minutes. The findings are validated with cross‐sectional microscopy, pharmacology, and electrical interventions. The experiments and simulations demonstrate that the individual electrical addressability of nanowires is necessary for high‐fidelity intracellular electrophysiological recordings. This study advances the understanding of and control over high‐quality multichannel intracellular recordings and paves the way toward predictive, high‐throughput, and low‐cost electrophysiological drug screening platforms.

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