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dc.contributor.authorDextras, Philip
dc.contributor.authorPayer, Kristofor Robert
dc.contributor.authorBurg, Thomas P.
dc.contributor.authorShen, Wenjiang
dc.contributor.authorWang, Ying-Chih
dc.contributor.authorHan, Jongyoon
dc.contributor.authorManalis, Scott R.
dc.date.accessioned2012-03-01T21:27:50Z
dc.date.available2012-03-01T21:27:50Z
dc.date.issued2011-02
dc.date.submitted2010-09
dc.identifier.issn1057-7157
dc.identifier.otherINSPEC Accession Number: 11804841
dc.identifier.urihttp://hdl.handle.net/1721.1/69557
dc.description.abstractWe report on a fabrication and packaging process for a microsystem consisting of a mass-based protein detector and a fully integrated preconcentrator. Preconcentration of protein is achieved by means of a nanofluidic concentrator (NC), which takes advantage of fast nonlinear electroosmotic flow near a nanochannel-microchannel junction to concentrate charged molecules inside a volume of fluid on the order of 1 pL. Detection of preconcentrated protein samples is accomplished by passing them through a suspended microchannel resonator (SMR), which is a hollow resonant cantilever serially connected to the NC on the same device. The transit of a preconcentrated sample produces a transient shift in the cantilever's resonance frequency that is proportional to the density of the sample and, hence, the concentration of protein contained in it. A device containing both NC and SMR structures was produced using a novel fabrication process which simultaneously satisfies the separate packaging requirements of the two structures. The initial testing of this prototype device has demonstrated that the integrated SMR can accurately measure the concentration of a bovine serum albumin solution, that was preconcentrated using the integrated NC. Future improvements in the fabrication process will allow site-specific surface modification of the device and compatibility with separation methods, which will create opportunities for its application to immunoassays and universal detection.en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (Contract R01CA119402)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH Cell Decision Process Center P50-GM68762)en_US
dc.language.isoen_US
dc.publisherInstitute of Electrical and Electronics Engineersen_US
dc.relation.isversionofhttp://dx.doi.org/10.1109/JMEMS.2010.2093563en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourceProf. Manalis via Howard Silveren_US
dc.titleFabrication and Characterization of an Integrated Microsystem for Protein Preconcentration and Sensingen_US
dc.typeArticleen_US
dc.identifier.citationDextras, Philip et al. “Fabrication and Characterization of an Integrated Microsystem for Protein Preconcentration and Sensing.” Journal of Microelectromechanical Systems 20.1 (2011): 221–230.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Microsystems Technology Laboratoriesen_US
dc.contributor.approverManalis, Scott R.
dc.contributor.mitauthorManalis, Scott R.
dc.contributor.mitauthorDextras, Philip
dc.contributor.mitauthorPayer, Kristofor Robert
dc.contributor.mitauthorBurg, Thomas P.
dc.contributor.mitauthorWang, Ying-Chih
dc.contributor.mitauthorHan, Jongyoon
dc.relation.journalJournal of Microelectromechanical Systemsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsDextras, Philip; Payer, Kristofor R.; Burg, Thomas P.; Shen, Wenjiang; Wang, Ying-Chih; Han, Jongyoon; Manalis, Scott R.en
dc.identifier.orcidhttps://orcid.org/0000-0001-5223-9433
dc.identifier.orcidhttps://orcid.org/0000-0001-7215-1439
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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