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dc.identifier.urihttp://hdl.handle.net/11401/76283
dc.description.sponsorshipThis work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.en_US
dc.formatMonograph
dc.format.mediumElectronic Resourceen_US
dc.language.isoen_US
dc.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dc.typeDissertation
dcterms.abstractChoosing the right materials can be critical to biomedical device performance. Usually factors such as biocompatibility, function, and cost are considered. Here we focused on the interactions between proteins, cells, and the material surfaces used for their biomedical application. The influence of surface hydrophobicity and hydrophilicity on adsorbed fibrinogen conformation, orientation, fiber formation and platelet adhesion has been investigated to understand the interactions between blood components and the materials used in blood-contacting medical devices. The results indicate that fibrinogen adsorbed to either hydrophobic or hydrophilic polymer surfaces binds platelets, implying that both surfaces are potentially thrombogenic. We present a model for surface initiation of clots, which enabled the design of a quick screen for thrombogenesis and guides the innovation and design of new anti-thrombogenic materials. In addition, the interactions of polyisoprene (PI) and commercially Gutta-percha (nanoparticles filled PI) with dental pulp stem cells (DPSC) has been evaluated. The composition of three different kinds of Gutta-percha is consistent with their mechanical properties. The biocompatibility tests show that the Gutta-percha used in our study are non-cytotxic for human adult DPSCs, and could induce biomineralization by DPSCs without the addition of a chemical inducer. Then, the study of influence of PI substrates moduli on differentiation of DPSCs show that the “hard, G>2.3MPa†substrates can improve cell proliferation and induce biomineralization without chemical inducer. The results indicate that Gutta-percha, which is a filling material currently used in endodontic practice, can be potentially used in regeneration of the tooth, rather than obduration of the canal. PI as a polymer matrix can also be used in re-engineer scaffold for tooth regeneration therapy. Hence, the study of interface between protein/cells and substrates could help the choice of materials and the design of biomedical devices.
dcterms.available2017-09-20T16:49:55Z
dcterms.contributorGersappe, Dilipen_US
dcterms.contributorRafailovich, Miriam Hen_US
dcterms.contributorJones, Keithen_US
dcterms.contributorSimon, Marcia.en_US
dcterms.creatorZhang, Liudi
dcterms.dateAccepted2017-09-20T16:49:55Z
dcterms.dateSubmitted2017-09-20T16:49:55Z
dcterms.descriptionDepartment of Materials Science and Engineering.en_US
dcterms.extent108 pg.en_US
dcterms.formatApplication/PDFen_US
dcterms.formatMonograph
dcterms.identifierhttp://hdl.handle.net/11401/76283
dcterms.issued2015-05-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2017-09-20T16:49:55Z (GMT). No. of bitstreams: 1 Zhang_grad.sunysb_0771E_12588.pdf: 5912516 bytes, checksum: 4a7967d1bc0896b9b64d0f95997ab7b5 (MD5) Previous issue date: 2015en
dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectMaterials Science
dcterms.subjectdental pulp stem cell, fibrinogen, platelets, polymer substrate, thrombosis, tooth regeneration
dcterms.titleThe Role of Protein/Substrate Interface in the Functioning Biomedical Devices
dcterms.typeDissertation


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