Optimization of Microfluidic, Point of Care, Flow-Through, Bead-Based Microarrays: Towards Affordable Healthcare

dc.contributor.advisorMcDevitt, John T.en_US
dc.contributor.committeeMemberRichards-Kortum, Rebecca Raeen_US
dc.contributor.committeeMemberBiswal, Sibani Lisaen_US
dc.creatorChou, Jieen_US
dc.date.accessioned2014-09-30T20:11:33Zen_US
dc.date.available2014-09-30T20:11:33Zen_US
dc.date.created2012-12en_US
dc.date.issued2012-10-12en_US
dc.date.submittedDecember 2012en_US
dc.date.updated2014-09-30T20:11:33Zen_US
dc.description.abstractRecently, there has been much interest on the development of affordable, portable diagnostic devices for the detection of a wide range of analytes. Advancements in microfluidics and miniaturization bring promise for their use at the point of care over traditional, and for the most part laboratory-confined approaches. The integration of porous beads with microfluidics has demonstrated potential as highly sensitive sensing elements with the capability to detect multiple biological and chemical agents simultaneously. When used in a flow through microarray platform known as the Programmable Bio-Nano-Chip (p-BNC), these beads have demonstrated opportunities for detection of low volumes of sample under short analysis times. However, limitations in traditional microfluidic materials such as silicon and inefficient fractional capture of analytes by porous beads hinder the translation of the p-BNC into broad global and clinical adoption where tests are single use with short analysis times to detect low concentrations of sample. This dissertation aims to optimize the p-BNC through engineering design choices to enhance the performance and reduce the costs associated with the p-BNC. The development of a computational tool to model the porous bead-based system is described herein and used to lead in the design optimization of the system. This tool provides insights into the transport and capture of analytes within the bead array with capture performance as a function of flow rate, porosity, capture distances, molecular affinities, and binding densities. To transition away from a single use and expensive silicon-based microarray, a thermoplastics-based microarray, fabricated through the hot embossing of polyethylene from replicated molds from silicon, is developed and described. Further, to transition towards point of care conditions where sample volume is low and analysis times are short, the geometry of the bead microwell design is optimized to improve the fractional capture efficiency of analytes by the beads in flow through microcontainers. Finally, to improve the imprecision performance in bead-to-bead signal variation within the microarray, exploration of a split design and use of smaller beads reveal a decrease in imprecision.en_US
dc.format.mimetypeapplication/pdfen_US
dc.identifier.citationChou, Jie. "Optimization of Microfluidic, Point of Care, Flow-Through, Bead-Based Microarrays: Towards Affordable Healthcare." (2012) Diss., Rice University. <a href="https://hdl.handle.net/1911/77326">https://hdl.handle.net/1911/77326</a>.en_US
dc.identifier.urihttps://hdl.handle.net/1911/77326en_US
dc.language.isoengen_US
dc.rightsCopyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.en_US
dc.subjectMicrofluidicsen_US
dc.subjectPoint-of-careen_US
dc.subjectModelingen_US
dc.subjectGeometryen_US
dc.subjectOptimizationen_US
dc.subjectBeadsen_US
dc.titleOptimization of Microfluidic, Point of Care, Flow-Through, Bead-Based Microarrays: Towards Affordable Healthcareen_US
dc.typeThesisen_US
dc.type.materialTexten_US
thesis.degree.departmentBioengineeringen_US
thesis.degree.disciplineEngineeringen_US
thesis.degree.grantorRice Universityen_US
thesis.degree.levelDoctoralen_US
thesis.degree.nameDoctor of Philosophyen_US
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