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Development of BioPoly® materials for use in prosthetic heart valve replacements

dc.contributor.authorDean, Harold, author
dc.contributor.authorJames, Sue, advisor
dc.contributor.authorDasi, Prasad, committee member
dc.contributor.authorOrton, Chris, committee member
dc.date.accessioned2007-01-03T08:03:02Z
dc.date.available2007-01-03T08:03:02Z
dc.date.issued2012
dc.description.abstractSince their conception in the 1950s, prosthetic heart valves (HV) have suffered clinical complications. Mechanical HVs, made from synthetic materials and with unnatural hemodynamics, are prone to thrombus formation without anti-coagulation therapy. Bioprosthetic HVs, made from fixed natural tissues, do not generally elicit thrombogenicity, but require long-term antiplatelet therapy and have a shorter lifespan due to calcification and tearing. Polymeric and fabric leaflet HVs potentially have the durability of a mechanical HV with the natural hemodynamics of a bioprosthetic valve; however, previous polymeric leaflet HVs did have problems with thrombus formation and calcification and very little research has been done on fabric leaflet HVs. This research aimed to explore the possibility to improve the hemocompatibility and long term in vivo performance of polymeric and fabric HV leaflets by improving polymer surface chemistry. The overall goal of the current project was to develop BioPoly materials for cardiovascular applications. The percent crystallinity, mechanical properties (i.e. tensile and bending), surface contact angle and hemocompatibility with whole blood of hyaluronan (HA) treated linear low density polyethylene (LLDPE) film and polyethylene terephtalate (PET) fabric were compared to untreated LLDPE film and PET fabric. Both processes were successful in incorporating HA into the base polymer structures. The swelling method used with the LLDPE allowed for HA concentrations ranging from 0.5% to 1.5%. The open weave of the PET fabric resulted in more controllable HA integration with a range from 0.25% to 3.5% HA. The process used to integrate HA maintained original tensile and bending properties and reduced surface water contact angle compared to LLDPE controls (86.7±2.3° to 39.0±1.1°). Increasing HA content did not further reduce contact angle when the additional surface dip was utilized. Whole blood clotting was significantly less on the HA-treated materials than the control LLDPE and PET, with clotting becoming negligible at the higher HA concentrations, as confirmed by free hemoglobin and scanning electron microscopy (SEM). The reduction of contact angle in the HA-treated LLDPE indicates the hydrophilic nature of the composite which resulted in better anti-thrombogenic properties.
dc.format.mediumborn digital
dc.format.mediummasters theses
dc.identifierDean_colostate_0053N_11011.pdf
dc.identifierETDF2012500027MCEN
dc.identifier.urihttp://hdl.handle.net/10217/65321
dc.languageEnglish
dc.language.isoeng
dc.publisherColorado State University. Libraries
dc.relation.ispartof2000-2019
dc.rightsCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.
dc.subjectheart valve
dc.subjectthrombus
dc.subjectpolyethylene
dc.subjecthemocompatible
dc.titleDevelopment of BioPoly® materials for use in prosthetic heart valve replacements
dc.typeText
dcterms.rights.dplaThis Item is protected by copyright and/or related rights (https://rightsstatements.org/vocab/InC/1.0/). You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
thesis.degree.disciplineMechanical Engineering
thesis.degree.grantorColorado State University
thesis.degree.levelMasters
thesis.degree.nameMaster of Science (M.S.)

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