Microfluidic Device Design Informed by Red Blood Cell Morphology for Global Blood Diagnostics and Banking

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dc.contributor.advisorShevkoplyas, Sergey S.
dc.contributor.committeeMemberMajd, Sheereen
dc.contributor.committeeMemberAbidian, Mohammad Reza
dc.contributor.committeeMemberGifford, Howard C.
dc.contributor.committeeMemberWu, Tianfu
dc.contributor.committeeMemberSheehan, Vivien A.
dc.creatorTorabian, Kian
dc.creator.orcid0000-0002-5877-7416
dc.date.accessioned2020-06-04T03:40:04Z
dc.date.createdMay 2020
dc.date.issued2020-05
dc.date.submittedMay 2020
dc.date.updated2020-06-04T03:40:04Z
dc.description.abstractJust as blood diagnostic tests are ubiquitous in the clinic, blood component transfusions are among the most commonly performed medical procedures at the bedside. The many devices designed to process blood often rely on microscale flow of the complex non-Newtonian fluid. With approximately 40% of human blood comprised of red blood cells, flow dynamics are largely influenced by these relatively dense particles. Their delicate biconcave shape is essential to their deformability, aggregability, and overall viability, allowing them to bend, shear, expand, and stack as they navigate the microvasculature to deliver oxygen to surrounding tissues. As a result, shape and its many surrogates not only serve as biomarkers for their quality, but also can be exploited to improve diagnostic and blood banking devices. In this work we study red blood cells with altered morphology in various forms of sickle cell disease and in animal models with uniquely adapted vascular systems, and use our findings to develop three devices with applications in blood banking and diagnostics: a simple gravity-based device to replace industrial centrifuges that wash stored red blood cells prior to transfusion, a multi-layered microfluidic platform to separate whole blood into its component blood transfusion products, and a paper-based diagnostic device for the altered hemoglobin molecule responsible for sickle cell disease. We explore the limitations and challenges associated with current technologies used to study red blood cell deformability and aggregation, ranging from micropipettes to ektacytometers and aggregometers, with respect to balancing diagnostic robustness, methodological throughput, and access and affordability. Additionally, we take advantage of inexpensive and biomimetic microfluidic platforms to inform a design process for global health applications, considering the potential scope of these devices to improve access to some of the most widely used biomedical tools.
dc.description.departmentBiomedical Engineering, Department of
dc.format.digitalOriginborn digital
dc.format.mimetypeapplication/pdf
dc.identifier.citationPortions of this document appear in: Torabian, Kian, Dalia Lezzar, Nathaniel Z. Piety, Alex George, and Sergey S. Shevkoplyas. "Substituting sodium hydrosulfite with sodium metabisulfite Improves long-term stability of a distributable paper-based test kit for point-of-care screening for sickle cell anemia." Biosensors 7, no. 3 (2017): 39.
dc.identifier.urihttps://hdl.handle.net/10657/6721
dc.language.isoeng
dc.rightsThe author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. UH Libraries has secured permission to reproduce any and all previously published materials contained in the work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s).
dc.subjectsickle cell disease, ektacytometer, microfluidic, blood, red blood cell, erythrocyte, hemorheology, blood transfusion, blood banking, low-cost diagnostics, point-of-care diagnostics, global health, micropipette
dc.titleMicrofluidic Device Design Informed by Red Blood Cell Morphology for Global Blood Diagnostics and Banking
dc.type.dcmiText
dc.type.genreThesis
local.embargo.lift2022-05-01
local.embargo.terms2022-05-01
thesis.degree.collegeCullen College of Engineering
thesis.degree.departmentBiomedical Engineering, Department of
thesis.degree.disciplineBiomedical Engineering
thesis.degree.grantorUniversity of Houston
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy

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