Show simple item record

dc.contributor.advisorXuanhe Zhao.en_US
dc.contributor.authorParada Hernandez, Germán Alberto.en_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Chemical Engineering.en_US
dc.date.accessioned2020-02-10T21:39:03Z
dc.date.available2020-02-10T21:39:03Z
dc.date.issued2019en_US
dc.identifier.urihttps://hdl.handle.net/1721.1/123727
dc.descriptionThesis: Ph. D., Massachusetts Institute of Technology, Department of Chemical Engineering, 2019en_US
dc.descriptionCataloged from PDF version of thesis. "June 2019." Vita.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstractHydrogels are crosslinked polymer networks with high water contents that can be designed to have similar properties as native tissue. Due to the tunability and unique properties of this class of materials, they are considered ideal biomaterials and have been explored for a variety of tissue engineering and biomedical applications. The widespread adoption of these materials outside research lab settings, however, has been hampered by multiple technical and non-technical limitations. We have addressed two of the technical limitations identified: Poor mechanical robustness and integration with non-hydrogel surfaces, and the lack of quantitative predictions of the hydrogel properties (based on the hydrogel's composition and structure). In this thesis we introduce a set of tough materials based on an interpenetrating network hydrogel architecture, and several strategies used to robustly adhere these materials to inorganic and elastomeric substrates.en_US
dc.description.abstractThese strategies are used to introduce thin hydrogel layers on flat surfaces and selected medical devices. Subsequently, we characterize the mechanical, biocompatibility, antifouling, functional and blood compatibility properties of various coated surfaces, as compared to those of pristine surfaces, for medical device applications. Addressing the second limitation, we have developed an Ideal Reversible Polymer Network (IRPN) system that shows a single relaxation timescale due to the minimization of defects present on its structure. This system, which features 4-arm end-functionalized macromers with reversible crosslinks, enables predictions of its viscoelastic properties under shear deformation using Maxwell-based frameworks. The predictions are validated using a PEG hydrogel featuring boronic acid-diol reversible bonding and the data matches well the model predictions up to a critical strain boundary (which is estimated using scaling arguments).en_US
dc.description.abstractWe hope this work enables the design and formulation of hydrogel-based materials and devices that can be employed to reduce clinical complications and healthcare-related challenges.en_US
dc.description.statementofresponsibilityby Germán Alberto Parada Hernandez.en_US
dc.format.extent143 pagesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectChemical Engineering.en_US
dc.titleIdeal reversible polymer networks : theory and applicationsen_US
dc.typeThesisen_US
dc.description.degreePh. D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.identifier.oclc1138415547en_US
dc.description.collectionPh.D. Massachusetts Institute of Technology, Department of Chemical Engineeringen_US
dspace.imported2020-02-10T21:39:03Zen_US
mit.thesis.degreeDoctoralen_US
mit.thesis.departmentChemEngen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record