Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/429813
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dc.date.accessioned2022-12-22T05:19:26Z-
dc.date.available2022-12-22T05:19:26Z-
dc.identifier.urihttp://hdl.handle.net/10603/429813-
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.extentxviii, 160-
dc.languageEnglish-
dc.rightsuniversity-
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.creator.researcherSathishkumar, N-
dc.subject.keywordEngineering-
dc.subject.keywordEngineering and Technology-
dc.subject.keywordEngineering Chemical-
dc.contributor.guideToley, Bhushan J-
dc.publisher.placeBangalore-
dc.publisher.universityIndian Institute of Science Bangalore-
dc.publisher.institutionChemical Engineering-
dc.date.completed2021-
dc.date.awarded2022-
dc.format.dimensions30-
dc.format.accompanyingmaterialNone-
dc.source.universityUniversity-
dc.type.degreePh.D.-
Appears in Departments:Chemical Engineering

Files in This Item:
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01_title.pdfAttached File25.34 kBAdobe PDFView/Open
02_prelim pages.pdf271.54 kBAdobe PDFView/Open
03_table of contents.pdf187.54 kBAdobe PDFView/Open
04_abstract.pdf83.28 kBAdobe PDFView/Open
05_chapter 1.pdf87.26 kBAdobe PDFView/Open
06_chapter 2.pdf823.3 kBAdobe PDFView/Open
07_chapter 3.pdf1.41 MBAdobe PDFView/Open
08_chapter 4.pdf835.14 kBAdobe PDFView/Open
09_chapter 5.pdf1.19 MBAdobe PDFView/Open
10_chapter 6.pdf1.17 MBAdobe PDFView/Open
11_annexure.pdf3.64 MBAdobe PDFView/Open
80_recommendation.pdf122.8 kBAdobe PDFView/Open


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