{"id":{"repo_id":"mit","oai_identifier":"oai:dspace.mit.edu:1721.1/156298"},"canonical_url":"https://search.dev.ndltd.org/etd/mit/oai:dspace.mit.edu:1721.1/156298","repository":{"repo_id":"mit","name":"MIT","base_url":"https://dspace.mit.edu/oai/request"},"display":{"title":"Low-Cost Electronic Microfluidics for Multiplexed Point-of-Care Biomarker Detection","abstract":"As we have seen in recent years, point-of-care (PoC) systems are vital elements in healthcare, as they can aid in disease detection, monitoring, and treatment, and even inform public policy. However, while qualitative (yes/no) PoC sensors are abundant (i.e. pregnancy tests, rapid COVID19 tests), low-cost, automated, quantitative PoC platforms are limited. Yet, given the importance of quantitative biomarker detection for nuanced analysis of patient health for chronic and fast acting diseases, there remains a persistent need for PoC systems capable of cost-effective detection of low abundance markers in blood. This thesis explores methodology for development of an automated low-cost system for the measurement of protein biomarkers in blood. By prioritizing accessibility, affordability, and automation, I focus on addressing unmet needs in PoC platform development which often prevent translation of these systems to PoC settings. Focusing primarily on cytokine biomarkers, notably IL-6, this thesis proposes modular solutions designed for seamless integration into existing clinical workflows. Chapter 2 introduces a sample-to-answer PoC workflow, consolidating blood testing steps through at-site sample collection, on-chip blood-to-plasma separation, and a bead-based electrochemical assay. Leveraging microfluidics and electronics, this system offers a rapid 30-minute assay time. It was validated by measuring spiked IL-6 concentrations in human blood, with applications demonstrated in CAR-T patient monitoring and small molecule detection for drug regulation. Chapter 3 introduces Microfluidics via Inkjet-Printing and Xurography (MINX), the first rapid prototyping technique which combines tape-based microfluidics with multiplexed electrodes. MINX was employed to fabricate low-cost PoC biosensors for detecting cytokine biomarkers. In Chapter 4, this modular fabrication method was extended to create the first integrated PoC system featuring tape-based microfluidic valves for automated fluidic and electrical controls. This MINX PoC platform was validated through detection of IL-6 in human plasma. Finally, Chapter 5 outlines future directions, emphasizing real-time dynamic control to enhance assay tunability. These advancements in PoC platforms hold promise for improving protein biomarker detection accessibility and affordability.","abstract_html":"As we have seen in recent years, point-of-care (PoC) systems are vital elements in healthcare, as they can aid in disease detection, monitoring, and treatment, and even inform public policy. However, while qualitative (yes/no) PoC sensors are abundant (i.e. pregnancy tests, rapid COVID19 tests), low-cost, automated, quantitative PoC platforms are limited. Yet, given the importance of quantitative biomarker detection for nuanced analysis of patient health for chronic and fast acting diseases, there remains a persistent need for PoC systems capable of cost-effective detection of low abundance markers in blood. This thesis explores methodology for development of an automated low-cost system for the measurement of protein biomarkers in blood. By prioritizing accessibility, affordability, and automation, I focus on addressing unmet needs in PoC platform development which often prevent translation of these systems to PoC settings. Focusing primarily on cytokine biomarkers, notably IL-6, this thesis proposes modular solutions designed for seamless integration into existing clinical workflows. Chapter 2 introduces a sample-to-answer PoC workflow, consolidating blood testing steps through at-site sample collection, on-chip blood-to-plasma separation, and a bead-based electrochemical assay. Leveraging microfluidics and electronics, this system offers a rapid 30-minute assay time. It was validated by measuring spiked IL-6 concentrations in human blood, with applications demonstrated in CAR-T patient monitoring and small molecule detection for drug regulation. Chapter 3 introduces Microfluidics via Inkjet-Printing and Xurography (MINX), the first rapid prototyping technique which combines tape-based microfluidics with multiplexed electrodes. MINX was employed to fabricate low-cost PoC biosensors for detecting cytokine biomarkers. In Chapter 4, this modular fabrication method was extended to create the first integrated PoC system featuring tape-based microfluidic valves for automated fluidic and electrical controls. This MINX PoC platform was validated through detection of IL-6 in human plasma. Finally, Chapter 5 outlines future directions, emphasizing real-time dynamic control to enhance assay tunability. These advancements in PoC platforms hold promise for improving protein biomarker detection accessibility and affordability.","abstract_has_math":false,"creators":["Kikkeri, Kruthika"],"institution":"Massachusetts Institute of Technology","degree_name":"Doctoral","degree_level":null,"degree_discipline":null,"degree_department":"Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science","school":null,"contributors":[],"advisors":["Voldman, Joel"],"committee_chairs":[],"committee_members":[],"year":2024,"date_issued":"2024-05","date_published":"2024-05","updated_at":"2026-07-22T22:21:34Z","subjects":[],"languages":[],"rights":["In Copyright - Educational Use Permitted","Copyright retained by author(s)"],"rights_urls":["https://rightsstatements.org/page/InC-EDU/1.0/"],"identifier_entries":[]},"links":{"outbound_url":"https://hdl.handle.net/1721.1/156298","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Voldman, Joel"]},{"key":"dc:contributor.department","label":"Department","values":["Massachusetts Institute of Technology. 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However, while qualitative (yes/no) PoC sensors are abundant (i.e. pregnancy tests, rapid COVID19 tests), low-cost, automated, quantitative PoC platforms are limited. Yet, given the importance of quantitative biomarker detection for nuanced analysis of patient health for chronic and fast acting diseases, there remains a persistent need for PoC systems capable of cost-effective detection of low abundance markers in blood. This thesis explores methodology for development of an automated low-cost system for the measurement of protein biomarkers in blood. By prioritizing accessibility, affordability, and automation, I focus on addressing unmet needs in PoC platform development which often prevent translation of these systems to PoC settings. Focusing primarily on cytokine biomarkers, notably IL-6, this thesis proposes modular solutions designed for seamless integration into existing clinical workflows. Chapter 2 introduces a sample-to-answer PoC workflow, consolidating blood testing steps through at-site sample collection, on-chip blood-to-plasma separation, and a bead-based electrochemical assay. Leveraging microfluidics and electronics, this system offers a rapid 30-minute assay time. It was validated by measuring spiked IL-6 concentrations in human blood, with applications demonstrated in CAR-T patient monitoring and small molecule detection for drug regulation. Chapter 3 introduces Microfluidics via Inkjet-Printing and Xurography (MINX), the first rapid prototyping technique which combines tape-based microfluidics with multiplexed electrodes. MINX was employed to fabricate low-cost PoC biosensors for detecting cytokine biomarkers. In Chapter 4, this modular fabrication method was extended to create the first integrated PoC system featuring tape-based microfluidic valves for automated fluidic and electrical controls. This MINX PoC platform was validated through detection of IL-6 in human plasma. Finally, Chapter 5 outlines future directions, emphasizing real-time dynamic control to enhance assay tunability. These advancements in PoC platforms hold promise for improving protein biomarker detection accessibility and affordability."]},{"key":"dc:description.degree","label":"Dc Description Degree","values":["Ph.D."]},{"key":"dc:title","label":"Title","values":["Low-Cost Electronic Microfluidics for Multiplexed Point-of-Care Biomarker Detection"]}]}],"canonical_facts":{"dc:contributor.advisor":["Voldman, Joel"],"dc:contributor.department":["Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science"],"dc:creator":["Kikkeri, Kruthika"],"dc:date.accessioned":["2024-08-21T18:54:54Z"],"dc:date.available":["2024-08-21T18:54:54Z"],"dc:date.issued":["2024-05"],"dc:description.abstract":["As we have seen in recent years, point-of-care (PoC) systems are vital elements in healthcare, as they can aid in disease detection, monitoring, and treatment, and even inform public policy. However, while qualitative (yes/no) PoC sensors are abundant (i.e. pregnancy tests, rapid COVID19 tests), low-cost, automated, quantitative PoC platforms are limited. Yet, given the importance of quantitative biomarker detection for nuanced analysis of patient health for chronic and fast acting diseases, there remains a persistent need for PoC systems capable of cost-effective detection of low abundance markers in blood. This thesis explores methodology for development of an automated low-cost system for the measurement of protein biomarkers in blood. By prioritizing accessibility, affordability, and automation, I focus on addressing unmet needs in PoC platform development which often prevent translation of these systems to PoC settings. Focusing primarily on cytokine biomarkers, notably IL-6, this thesis proposes modular solutions designed for seamless integration into existing clinical workflows. Chapter 2 introduces a sample-to-answer PoC workflow, consolidating blood testing steps through at-site sample collection, on-chip blood-to-plasma separation, and a bead-based electrochemical assay. Leveraging microfluidics and electronics, this system offers a rapid 30-minute assay time. It was validated by measuring spiked IL-6 concentrations in human blood, with applications demonstrated in CAR-T patient monitoring and small molecule detection for drug regulation. Chapter 3 introduces Microfluidics via Inkjet-Printing and Xurography (MINX), the first rapid prototyping technique which combines tape-based microfluidics with multiplexed electrodes. MINX was employed to fabricate low-cost PoC biosensors for detecting cytokine biomarkers. In Chapter 4, this modular fabrication method was extended to create the first integrated PoC system featuring tape-based microfluidic valves for automated fluidic and electrical controls. This MINX PoC platform was validated through detection of IL-6 in human plasma. Finally, Chapter 5 outlines future directions, emphasizing real-time dynamic control to enhance assay tunability. These advancements in PoC platforms hold promise for improving protein biomarker detection accessibility and affordability."],"dc:description.degree":["Ph.D."],"dc:identifier.uri":["https://hdl.handle.net/1721.1/156298"],"dc:publisher":["Massachusetts Institute of Technology"],"dc:rights":["In Copyright - Educational Use Permitted","Copyright retained by author(s)"],"dc:rights.uri":["https://rightsstatements.org/page/InC-EDU/1.0/"],"dc:title":["Low-Cost Electronic Microfluidics for Multiplexed Point-of-Care Biomarker Detection"],"dc:type":["Thesis"],"thesis:degree_name":["Doctoral","Doctor of Philosophy"]},"updated_at":"2026-07-22T22:21:34Z"}