Paper microfluidic tools to improve the sensitivity and dynamic range of point of care immunoassays

dc.contributor.guideToley, Bhushan J
dc.creator.researcherSathishkumar, N
dc.date.accessioned2022-12-22T05:19:26Z
dc.date.available2022-12-22T05:19:26Z
dc.date.awarded2022
dc.date.completed2021
dc.description.abstractOver the past decade, developing affordable home-based tests to diagnose infectious diseases has become a pressing need. The lateral flow immunoassay (LFIA) is the most successfully commercialized point-of-care immunoassay. However, it suffers from poor sensitivity compared to conventional laboratory techniques such as enzyme-linked immunosorbent assay (ELISA). Consequently, traditional LFIAs fail to deliver on the promise of bedside diagnostic testing for many applications. Paper-based microfluidic devices provide an alternative platform for performing molecular diagnosis at a low cost and have become popular for their simplicity. My research aimed to develop a portable paper-based signal-enhanced immunoassay device that satisfies WHO s ASSURED (affordable, sensitive, specific, user-friendly, rapid and robust, equipment-free and deliverable to end-users) criteria. Using the malarial antigen, PfHRP2, as a model analyte, we developed a gold nanoparticle-based LFIA to determine a baseline limit of detection (LOD). To improve upon the baseline LOD, we ported the ELISA assay into a paper microfluidic device using HRP and poly-HRP enzymes. In addition, we also explored the gold-based enhancement of the signal generated in gold nanoparticle-based LFIAs. Finally, we compared all the colorimetric signal enhancement techniques. While we observed a 4-fold improvement in LOD using the gold enhancement technique, the HRP and the poly-HRP based enhancement did not improve the LOD as expected. This was contrary to the popular belief that enzyme-based signal amplification would produce an improved LOD compared to gold nanoparticle-based LFIAs (despite the fact that a direct comparison was never performed). Using time-lapse imaging, we elucidated that the poor sensitivity in the paper-based ELISA platform is because of the kinetic limitations of the enzymatic amplification system. Finally, we built a 3D printed device housing Arduino-controlled electromagnets to automate the multiple steps of signal-enhanced immunoassays,...
dc.format.accompanyingmaterialNone
dc.format.dimensions30
dc.format.extentxviii, 160
dc.identifier.urihttp://hdl.handle.net/10603/429813
dc.languageEnglish
dc.publisher.institutionChemical Engineering
dc.publisher.placeBangalore
dc.publisher.universityIndian Institute of Science Bangalore
dc.rightsuniversity
dc.source.universityUniversity
dc.subject.keywordEngineering
dc.subject.keywordEngineering and Technology
dc.subject.keywordEngineering Chemical
dc.titlePaper microfluidic tools to improve the sensitivity and dynamic range of point of care immunoassays
dc.title.alternativePaper microfluidic tools to improve the sensitivity and dynamic range of point-of-care immunoassays
dc.type.degreePh.D.

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