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dc.contributor.advisorPaula T. Hammond and Michael F. Rubner.en_US
dc.contributor.authorBerg, Michael C., Ph. D. Massachusetts Institute of Technologyen_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Chemical Engineering.en_US
dc.date.accessioned2006-07-31T15:15:57Z
dc.date.available2006-07-31T15:15:57Z
dc.date.copyright2005en_US
dc.date.issued2005en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/33599
dc.descriptionThesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 2005.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstractThis thesis research focused on biological applications of ultra-thin weak polyelectrolyte multilayers with specific emphasis on cell patterning, drug delivery, and antibacterial coatings. All of these very different applications were studied using three different polymers - polyacrylic acid (PAA), poly(allylamine hydrochloride) (PAH), polyacrylamide (PAAm). The first part of this thesis focuses on patterning polyelectrolyte multilayers found to resist mammalian cell adhesion, with ligands that promote specific interactions for adhesion. It was found that by patterning PAH on polyelectrolyte multilayers, the patterned functional group density and thickness could be tuned through ink pH adjustment. By changing the surface density of amine groups in the PAH patterns, the ligand density could also be altered using specific chemistry to attach peptides containing the tri-peptide sequence, RGD, which is known to promote cell adhesion in a number of cell types. The RGD density in the patterned regions determined the number of cells attached and the amount of cytoskeletal protein organization. The second part is an evaluation of porous polyelectrolyte multilayers as a delivery system for controlled release of small molecule drugs. The loading and releasing properties of porous PAH/PAA multilayers were investigated using the two drugs, ketoprofen and cytochalasin D. It was determined that the amount of drug released was proportional to the number of porous layers. Nanoporous films showed zero-order release, whereas microporous films displayed Fickian diffusion. The efficacy of the released drugs was checked by monitoring the effect of released cytochalasin D on fibroblasts' division.en_US
dc.description.abstract(cont.) In the final part of this thesis, the antibacterial properties of both silver-loaded polyelectrolyte multilayers and superhydrophobic multilayers are examined. It was found that silver loaded multilayers killed bacteria to an extent greater than 99.99% for both airborne and waterborne models. Superhydrophobic films showed excellent anti-fouling properties for proteins, mammalian cells, and bacteria.en_US
dc.description.statementofresponsibilityby Michael C. Berg.en_US
dc.format.extent156 leavesen_US
dc.format.extent9505766 bytes
dc.format.extent9497559 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypeapplication/pdf
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.subjectChemical Engineering.en_US
dc.titleBiological applications of weal polyelectrolyte multilayersen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineering
dc.identifier.oclc64035839en_US


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