Paper microfluidic tools to improve the sensitivity and dynamic range of point of care immunoassays
| dc.contributor.guide | Toley, Bhushan J | |
| dc.creator.researcher | Sathishkumar, N | |
| dc.date.accessioned | 2022-12-22T05:19:26Z | |
| dc.date.available | 2022-12-22T05:19:26Z | |
| dc.date.awarded | 2022 | |
| dc.date.completed | 2021 | |
| dc.description.abstract | Over 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.accompanyingmaterial | None | |
| dc.format.dimensions | 30 | |
| dc.format.extent | xviii, 160 | |
| dc.identifier.uri | http://hdl.handle.net/10603/429813 | |
| dc.language | English | |
| dc.publisher.institution | Chemical Engineering | |
| dc.publisher.place | Bangalore | |
| dc.publisher.university | Indian Institute of Science Bangalore | |
| dc.rights | university | |
| dc.source.university | University | |
| dc.subject.keyword | Engineering | |
| dc.subject.keyword | Engineering and Technology | |
| dc.subject.keyword | Engineering Chemical | |
| dc.title | Paper microfluidic tools to improve the sensitivity and dynamic range of point of care immunoassays | |
| dc.title.alternative | Paper microfluidic tools to improve the sensitivity and dynamic range of point-of-care immunoassays | |
| dc.type.degree | Ph.D. |
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