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dc.contributor.authorTaing, Meng-Houiten_US
dc.contributor.authorSweatman, Denisen_US
dc.contributor.editorDan V. Nicolauen_US
dc.date.accessioned2017-05-03T12:08:59Z
dc.date.available2017-05-03T12:08:59Z
dc.date.issued2006en_US
dc.date.modified2010-08-17T05:03:51Z
dc.identifier.doi10.1117/12.638652en_AU
dc.identifier.urihttp://hdl.handle.net/10072/13413
dc.description.abstractThis paper focuses on the design of an EIS (electrolyte on insulator on Silicon) structure as a detection method for pathogenic DNA. Current rapid detection methods rely on fluorescent labeling to determine binding affinity. Fluorescent quenching is seen by a change in activity as opposed to non-quenched states. Sensitive optical equipment is required to detect and distinguish these colour changes because they cannot be seen by the naked eye. The disadvantages of this is (1) a portable, independent device cannot be made since samples have to be brought back to the benchtop and (2) the obvious cost of acquiring and maintaining these optical detection systems. A low cost, portable electrical detection method has been investigated. The EIS structure (Electrolyte on Insulator on Silicon) provides a novel, label-free and simple to fabricate way to make a small field effect DNA detection sensor. The sensor responds to fluctuating capacitances caused by a depletion layer thickness change at the surface of the silicon substrate as a result of DNA adsorption onto the dielectric oxide/APTES (Aminopropylthioxysilane) surface. As DNA molecules diffuse to the sensor surface, they are bound to their complimentary capture probes. The negative charge exhibited by the DNA forces negative charge carriers in the silicon substrate to move away from the surface. This causes a depletion layer in n-type substrate to thicken and for a p-type to thin and can be observed as a change in capacitance. A low ionic solution strength will ensure that counter-ions do not affect the sensor measurements. The EIS sensor is designed to be later integrated into a complete lab on chip solution. A full lab on chip can incorporate the sensor to perform DNA quantity based measurements. Nucleic acids can be amplified by the on chip PCR system and then fed into the sensor to work out the DNA concentration. The sensor surface contains capture probes that will bind to the pathogen. They are held onto the sensor surface by the positively charged layer. The sensor will have onboard electronics to process the signals and determine the result of the measurements. The sensitivity of the sensor is on par with similar capacitance sensing technologies and is expected to be improved with later enhancements.en_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherSPIEen_US
dc.publisher.placeBellingham, WA USAen_US
dc.relation.ispartofstudentpublicationYen_AU
dc.relation.ispartofconferencenameBioMEMS and Nanotechnology IIen_US
dc.relation.ispartofconferencetitleProceedings of SPIE: Progress in Biomedical Optics and Imaging - Volume 6036, 2006en_US
dc.relation.ispartofdatefrom2005-12-11en_US
dc.relation.ispartofdateto2005-12-14en_US
dc.relation.ispartoflocationBrisbane, Queensland, Australiaen_US
dc.rights.retentionYen_AU
dc.subject.fieldofresearchcode299903en_US
dc.titleMicrofabricated EIS biosensor for detection of DNAen_US
dc.typeConference outputen_US
dc.type.descriptionE2 - Conference Publications (Non HERDC Eligible)en_US
dc.type.codeE - Conference Publicationsen_US
gro.facultyGriffith Sciences, Griffith School of Engineeringen_US
gro.date.issued2006
gro.hasfulltextNo Full Text
gro.griffith.authorTaing, Meng-Houit
gro.griffith.authorSweatman, Denis R.


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    Contains papers delivered by Griffith authors at national and international conferences.

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