2011
DOI: 10.1007/s11432-011-4384-7
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Silicon-based microelectrode arrays for stimulation and signal recording of in vitro cultured neurons

Abstract: Microelectrode arrays (MEAs) for stimulation and signal recording of in vitro cultured neurons are presented. Each MEA is composed of 60 independent electrodes with 59 working ones and one reference one. These electrodes are divided into 30 pairs. Through each pair of electrodes, four independent states can be realized to define the accessing modes of neurons cultured on the surface of the electrodes. A total MEA covers an area of 10 mm×10 mm. MEAs are fabricated in a silicon-based semiconductor process. An im… Show more

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Cited by 4 publications
(3 citation statements)
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“…Conventionally, MEAs were fabricated from materials such as glass, 10-12 silicon, 13,14 and polymers. [15][16][17] Glass MEAs are of particular interest for their benecial characteristics such as biocompatibility, planarity and transparency.…”
Section: Introductionmentioning
confidence: 99%
“…Conventionally, MEAs were fabricated from materials such as glass, 10-12 silicon, 13,14 and polymers. [15][16][17] Glass MEAs are of particular interest for their benecial characteristics such as biocompatibility, planarity and transparency.…”
Section: Introductionmentioning
confidence: 99%
“…Microelectrode arrays, composed of 60 independent electrodes, for stimulation and signal recording of in vitro cultured neurons were coupled with impedance measurements [ 85 , 86 ]. The extracellular signal recording in the presence of acetylcholine and other stimulants has been carried out and the results indicate that microelectrodes array systems can be used for extracellular stimulation, recording, simultaneous stimulation and recording, and isolation of PC12 cells network cultured in vitro [ 85 , 87 ].…”
Section: Cellular Eventsmentioning
confidence: 99%
“…In 1972, Charles A. Thomas Jr. invented microelectrode array (MEA), which could be used to measure the electrical activities of neuronal networks cultured on its surface and implemented patch clamp's limitation that the electrophysiological characteristics of only one single neuron could be tested each time [1]. After half a century, scientists have developed multiple types of MEAs and established neuron culturing techniques on MEA to investigate neuronal networks' electrophysiological characteristics, such as spontaneous and triggered action potentials [2][3][4][5]. While limited by the traditional data analysis methods, most of the MEA experiments required long recording time and complicated statistical computation.…”
Section: Introductionmentioning
confidence: 99%