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Electrochemical biosensor array characterization

dc.contributor.authorJibson, Matthew William, author
dc.contributor.authorChen, Thomas Wei, advisor
dc.contributor.authorTobet, Stuart A., committee member
dc.contributor.authorHenry, Charles S., committee member
dc.contributor.authorMaciejewski, Anthony A., committee member
dc.date.accessioned2007-01-03T04:41:11Z
dc.date.available2007-01-03T04:41:11Z
dc.date.issued2009
dc.descriptionDepartment Head: Anthony A. Maciejewski.
dc.description.abstractNeurotransmitters play an important role in central nervous systems. Nitric oxide, a neurotransmitter, is important in this development. Of interest is detecting molecular gradients that are essential in the development of tissue and organ systems. Molecular gradients are difficult to detect because of the relative large size of the cells compared to the electrochemical sensors used in sensing systems. Furthermore, in order to detect a gradient, an sensor array must be used in order to collect real-time spatial data. Due to this requirement of a sensor array, it is difficult to construct a device with discrete parts, since it would be quite large. Thus, an integrated sensor must be constructed. Integration allows components to be small enough to have many sensors in the area of a cell, and is thus able to sense a chemical image, or gradient. Previous work has resulted in the production of a chip with an array of 21 sensor sites of individual and specific design with the purpose of testing hypotheses relating the shape, size, distance and configuration to the output signal strength. The electrodes are on the micron scale, and are capable of performing electrochemistry on living cells. The sensor sites were characterized using differential pulse voltammetry to find their relative performance. Based on these results, further tests were performed to test hypotheses regarding the shape, size, distance and configuration of the electrodes. The lower detection limit is found on two of the best sensors. A proof-of-concept test is done with a living mouse-ovary slice, which showed results similar to those in the literature. Results show that the important design characteristics are working-electrode size (larger is better), and the ratio of the areas of the working to auxiliary electrode (smaller ratio is better). The other design characteristics (distance, shape, configuration) played, in general, did not have much impact on the output. Conclusions about the design of future chips is made based on these findings.
dc.format.mediummasters theses
dc.identifier2009_summer_Jibson_ECEN.pdf
dc.identifierETDF2009100001ECEN
dc.identifier.urihttp://hdl.handle.net/10217/26587
dc.languageEnglish
dc.language.isoeng
dc.publisherColorado State University. Libraries
dc.relationCatalog record number (MMS ID): 991012184649703361
dc.relationR857.B54.J537 2009
dc.relation.ispartof2000-2019
dc.rightsCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.
dc.titleElectrochemical biosensor array characterization
dc.typeText
dcterms.rights.dplaThis Item is protected by copyright and/or related rights (https://rightsstatements.org/vocab/InC/1.0/). You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
thesis.degree.disciplineElectrical and Computer Engineering
thesis.degree.grantorColorado State University
thesis.degree.levelMasters
thesis.degree.nameMaster of Science (M.S.)

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