1986
DOI: 10.1109/tbme.1986.325894
|View full text |Cite
|
Sign up to set email alerts
|

Thin-Film Multiple Electrode Probes: Possibilities and Limitations

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
27
0

Year Published

1999
1999
2016
2016

Publication Types

Select...
5
5

Relationship

0
10

Authors

Journals

citations
Cited by 93 publications
(27 citation statements)
references
References 20 publications
0
27
0
Order By: Relevance
“…In the case where the same electrical signal is simultaneously recorded on 36 of the 37 microelectrodes of the array, the crosstalk signal on the 37th microelectrode could be as high as at 100 Hz. At first sight, this perturbation level may seem unacceptable [32], however, for the particular application of measuring streaming potentials of cartilage, much of the frequency content of the signal is below 30 Hz. In this frequency range, the crosstalk induced by one electrode is lower than 0.1% [ Fig.…”
Section: Discussionmentioning
confidence: 99%
“…In the case where the same electrical signal is simultaneously recorded on 36 of the 37 microelectrodes of the array, the crosstalk signal on the 37th microelectrode could be as high as at 100 Hz. At first sight, this perturbation level may seem unacceptable [32], however, for the particular application of measuring streaming potentials of cartilage, much of the frequency content of the signal is below 30 Hz. In this frequency range, the crosstalk induced by one electrode is lower than 0.1% [ Fig.…”
Section: Discussionmentioning
confidence: 99%
“…Over the past several decades, studies of electroactive cells have been carried out by using a variety of recording techniques, including glass micropipette intracellular and patch-clamp electrodes (1,3), voltage-sensitive dyes (4,5), multielectrode arrays (MEAs) (6)(7)(8), and planar FETs (9)(10)(11). The latter 2 recording techniques use welldeveloped microfabrication methods to allow for direct multiplexed detection on a scale not possible with micropipette technology, although the MEAs and FETs exhibit limited signalto-noise ratios (S/N) and detection areas that make cellular and subcellular recording difficult (12,13).…”
mentioning
confidence: 99%
“…Specifically, in previous studies the device or electrode density defined by fabrication process, could be used to describe the true signal spatial resolution -that is the distance at which distinct signals can be resolved by adjacent detectors. Moreover, scaling down the size of individual metal electrodes to achieve more localized detection is difficult due to corresponding increases in their impedance (7,8) that intrinsically limits the resolution of such passive recordings. Voltage-and calcium-sensitive optical dyes can provide excellent temporal and spatial resolution over wide fields (9, 10) but typically not simultaneously.…”
mentioning
confidence: 99%