2011
DOI: 10.1039/c0lc00582g
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Nanocavity electrode array for recording from electrogenic cells

Abstract: We present a new nanocavity device for highly localized on-chip recordings of action potentials from individual cells in a network. Microelectrode recordings have become the method of choice for recording extracellular action potentials from high density cultures or slices. Nevertheless, interfacing individual cells of a network with high resolution still remains challenging due to an insufficient coupling of the signal to small electrodes, exhibiting diameters below 10 mm. We show that this problem can be ove… Show more

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Cited by 44 publications
(57 citation statements)
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“…We explain the excellent sealing of the electrode by the small opening which can be covered completely by the cell. Electron microscopy studies of the cell-chip interface reveal that the cell membrane seals the opening very well [24]. It did not escape out attention that we have not found any signals which stand out with their potassium contributions although we find examples for strong calcium and strong sodium currents.…”
Section: A Propagation Of Action Potentialsmentioning
confidence: 63%
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“…We explain the excellent sealing of the electrode by the small opening which can be covered completely by the cell. Electron microscopy studies of the cell-chip interface reveal that the cell membrane seals the opening very well [24]. It did not escape out attention that we have not found any signals which stand out with their potassium contributions although we find examples for strong calcium and strong sodium currents.…”
Section: A Propagation Of Action Potentialsmentioning
confidence: 63%
“…HL-1 cells generate action potentials spontaneously, pervading the entire cell population [32]. We have cultured cells and seeded them onto chips as previously described [24]. Briefly, the cells were kept in a T25 flask with a supplemented Claycomb medium (supplemented with 10% FBS, 100 μgml −1 penicillin-streptomycin, 0.1 mM norepinephrine, and 2 mM L-glutamine) in an incubator at 37 • C. After coalescing of the the cells to a confluent layer they were passaged using standard procedures.…”
Section: Experimental Methodsmentioning
confidence: 99%
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“…Wolfrum et al overcame this dilemma by creating micropores that interface the cells to larger electrodes. 10,11 A third approach involves decreasing the membrane impedance at the cell-electrode junction. In practice, this involves transiently rapturing the cell membrane by applying a zap voltage to a nanostructured electrode, thus allowing the electrodes to enter the cell and perform pseudo-intracellular recording until the raptured membrane reorganizes.…”
mentioning
confidence: 99%