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dc.contributor.advisorMichael F. Rubner and Robert E. Cohen.en_US
dc.contributor.authorSwiston, Albert Josephen_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Materials Science and Engineering.en_US
dc.date.accessioned2010-10-08T20:38:02Z
dc.date.available2010-10-08T20:38:02Z
dc.date.copyright2010en_US
dc.date.issued2010en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/59006
dc.descriptionThesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2010.en_US
dc.descriptionThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.en_US
dc.descriptionCataloged from student submitted PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstractPolymer multilayers may be built through the sequential ("layer-by-layer") adsorption of species (polymers, nanoparticles) with specific interactions (electrostatic, hydrogen-bonding). Multilayered heterostructures - films comprised of multiple lamellar regions or strata, each of which consisting of several bilayers of electrostatically complexed or hydrogen-bonded materials - may be assembled and patterned into precise geometries. These heterostructures maintain the functions and capabilities of each lamellar region, and thus complex, stimuli-responsive films with multiple functionalities may be fabricated and patterned with high fidelity. This thesis describes a method to fabricate such heterostructured devices for single-cell functionalization. These devices may be attached to the surface of living immune system cells, conferring new functions without impairing native cellular behaviors. The first part of this thesis focuses on the techniques to create a heterostructured backpack. Photolithographic methods were developed to geometrically pattern multilayer films into a desired size and shape. A host of polymer multilayer systems labile at physiologically relevant pH's were built and tested as a way to release the backpack from its fabrication substrate. Therapeutically and diagnostically interesting materials, such as magnetic nanoparticles, biodegradable polymers, and quantum dots were built into the backpack's payload region. Finally, a film that non-cytotoxically adheres the backpack to the cell surface was developed and optimized as the celladhesive region. How backpack attachment affect native cell behavior is of utmost importance. Backpack attachment was found to be non-cytotoxic to B lymphocytes, and T cells were still able to migrate on ICAM-coated surfaces. Backpacks could be made with specific chemistries that could activate desirable cell behavior, such as activating dendritic cells, which demonstrates that backpacks need not be passive objects but rather actively engage with the attached cell to create hybrid bio-synthetic devices. The last part of this thesis describes how backpacks can be used as functional phagocytosis-resistant particles that may be used to increase in vivo circulation time or functionalize phagocytic cells. This presents exciting opportunities for immunoengineering applications, such as using immune cells to invade solid tumors and deliver cytotoxic payloads.en_US
dc.description.statementofresponsibilityby Albert Joseph Swiston Jr.en_US
dc.format.extent195 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/1721.1/7582en_US
dc.subjectMaterials Science and Engineering.en_US
dc.titleFunctional "backpacks" for cellular engineeringen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineering
dc.identifier.oclc666492547en_US


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