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dc.contributor.advisorJongyoon Han.en_US
dc.contributor.authorWang, Ying-Chih, 1977-en_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Mechanical Engineering.en_US
dc.date.accessioned2008-02-27T22:12:52Z
dc.date.available2008-02-27T22:12:52Z
dc.date.copyright2007en_US
dc.date.issued2007en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/40358
dc.descriptionThesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2007.en_US
dc.descriptionIncludes bibliographical references (p. 135-141).en_US
dc.description.abstractSample preparation has long been the most important and costly process in bioanalyses. Conventional identification methods involve multiple purification steps combined with mass spectrometry or immunosensing. While well-developed and widely utilized, these methods require extensive human labor and exhibit limited resolving power for low abundance analytes. Due to the shear complexity and abundance variation of biosamples, rapid and ultra-sensitive diagnostic measurements of disease markers are still out of reach. To address this issue, we developed a novel nanofluidic concentrator, utilizing the unique concentration polarization effect of sub 50 nm nanofluidic filters. With the distinct ionic and molecular interaction at the nanoscale, nanofluidic systems can potentially outperform current sample preparation and molecular detection techniques. Aiming to investigate and expand the applications of these techniques, this thesis work involves the design and development of a highly efficient nanofluidic preconcentrator, which can achieve a million fold detectability enhancements without complex buffer arrangements. This thesis also includes an integrated preconcentration-immunosensing device.en_US
dc.description.abstract(cont.) By manipulating analyte concentrations, this integrated device not only increases the detection sensitivity, but also expands the dynamic range of given antibody-antigen couples. In addition, we also investigated the ion transfer at the micro-/nano-fluidic interface. Depending on the strength of the applied electric field across the nanochannel array, various phenomena such as concentration polarization, charge depletion, and nonlinear electrokinetic flows in the adjacent microfluidic channel can be observed and studied in situ by fluorescent microscopy. In summary, the nanofluidic concentrator we developed in this thesis facilitates sample preparation and detection of biomolecules from complex biological matrices and facilitates a further understanding of nanoscale molecular/fluid/ion transport phenomena by providing a well-controlled experimental platform.en_US
dc.description.statementofresponsibilityby Ying-Chih Wang.en_US
dc.format.extent141 p.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582
dc.subjectMechanical Engineering.en_US
dc.titleElectrokinetic trapping of biomolecules : novel nanofluidic devices for proteomic applicationsen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineering
dc.identifier.oclc187991167en_US


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