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dc.contributor.authorNaegle, Kristen Men_US
dc.contributor.otherMassachusetts Institute of Technology. Biological Engineering Division.en_US
dc.date.accessioned2007-07-18T13:16:45Z
dc.date.available2007-07-18T13:16:45Z
dc.date.copyright2006en_US
dc.date.issued2006en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/37962
dc.descriptionThesis (S.M.)--Massachusetts Institute of Technology, Biological Engineering Division, 2006.en_US
dc.descriptionIncludes bibliographical references (leaves 44-45).en_US
dc.description.abstractThere is a great need in the fields of biology, medicine, and pharmaceuticals to create high-throughput devices for the detection of specific cell states in a heterogeneous mixture of cells. The desire is to differentiate among diseased and healthy cells, cell age, and cell type with the minimum amount of sample pretreatment. This project addresses this need by developing microfluidic devices that exploit the adhesion differences between cell states and cell types to rapidly count cells of different types without the need for labels. There are two avenues in which to explore cell adhesion differences with these devices, the first is a net electrostatic change at the surface of the cell wall and the second is the presence of specific cell-membrane adhesion proteins. It is hypothesized that the forced interaction of the cell wall with the microfabricated microcapillary walls would result in a differential velocity based on cell type that could be detected simply using a microscope and video camera or an interferometer. The eventual integration of cell velocity detection would result in a portable all-inclusive lab-on-a-chip system that could be used in the field for detecting the presence of diseases, such as malaria and cancer as well as in a lab setting for drug discovery.en_US
dc.description.statementofresponsibilityby Kristen M. Naegle.en_US
dc.format.extent50 leavesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582
dc.subjectBiological Engineering Division.en_US
dc.titleTowards a microfluidic disease detection deviced based on cellular adhesion differencesen_US
dc.typeThesisen_US
dc.description.degreeS.M.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.identifier.oclc144608662en_US


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