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dc.contributor.authorPancrazio, Josephen_US
dc.contributor.authorBey, Paul Jr.en_US
dc.contributor.authorLoloee, Arashen_US
dc.contributor.authorManne, SubbaRaoen_US
dc.contributor.authorChao, Hui-Chuanen_US
dc.contributor.authorHoward, Lornen_US
dc.contributor.authorGosney, W. Miltonen_US
dc.contributor.authorBorkholder, Daviden_US
dc.contributor.authorKovacs, Gregoryen_US
dc.contributor.authorManos, Patriciaen_US
dc.contributor.authorCuttino, Daviden_US
dc.contributor.authorStenger, Daviden_US
dc.date.accessioned2008-02-01T18:12:37Zen_US
dc.date.available2008-02-01T18:12:37Zen_US
dc.date.issued1998-10en_US
dc.identifier.citationBiosensors & Bioelectronics 13 (1998) 971-979en_US
dc.identifier.urihttp://hdl.handle.net/1850/5555en_US
dc.descriptionRIT community members may access full-text via RIT Libraries licensed databases: http://library.rit.edu/databases/en_US
dc.description.abstractAn extracellular recording system incorporating an electrode array and an amplifier/stimulator CMOS chip is described and characterized. Important features of this custom VLSI chip include 16 instrumentation amplifiers with a gain of 50 and the incorporation of a cross-point array allowing designation of an extracellular microelectrode as either a stimulator or sensor. The planar array consisted of 32 microelectrodes, 14,um in diameter, and four larger reference electrodes. Microelectrodes, interconnecting traces, and bond pads were patterned with a 500-run layer of gold. The interconnecting traces were passivated with a I-,um thick layer of silicon nitride to provide chemical and electrical insulation and microelectrode impedance was lowered utilizing electrode position of platinum black. The amplifier exhibited a nearly flat frequency response with high pass and low pass corner frequencies of 0.7 Hz and 50 kHz, respectively. The input referred noise over the 50 kHz bandwidth was 12-16 ,uVRMS' well below the magnitude of previously reported extracellular potentials. Crosstalk between neighboring channels resulted in an output signal below the amplifier noise level, even for relatively large extracellular potentials. Using this system, extracellular recordings were demonstrated yielding typical peak-to-peak biopotentials of magnitude 0.9-2.1 mV and 100-400,uV for chick cardiac myocytes and rat spinal cord neurons, respectively. The key components of this extracellular recording system can be manufactured using industry standard thin film photolithographic techniques. © 1998 Elsevier Science S.A. All rights reserved.en_US
dc.description.sponsorshipThe work at Southern Methodist University was supported in part by the late W. W. Caruth through the Communities Foundation of Texas, the National Science Foundation under Grant Nos. D1R-9109777 and D1R9317891, the University of North Texas, and the Texas Advanced Technology Program under Grant No. 003613-016. EffOlts at the Naval Research Laboratory and Science Application International Corporation were supported by the OSD Counterproliferation Support Program through DARPA and the Naval Research Laboratory contract N000 14-95-C-2128. The opinions and assertions contained herein are the private ones of the authors and are not to be construed as official or reflecting the view of the Department of the Navy.en_US
dc.language.isoen_USen_US
dc.publisherElsevier www.elsevier.com/locate/biosen_US
dc.subjectAmplifieren_US
dc.subjectCardiac myocytesen_US
dc.subjectCMOSen_US
dc.subjectExtracellular recordingen_US
dc.subjectSpinal cord neuronsen_US
dc.titleDescription and demonstration of a CMOS amplifier-based-system with measurement and stimulation capability for bioelectrical signal transductionen_US
dc.typeArticleen_US
dc.identifier.urlhttp://dx.doi.org/10.1016/S0956-5663(98)00006-2


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