Please use this identifier to cite or link to this item:
http://hdl.handle.net/10603/429813
Title: | Paper microfluidic tools to improve the sensitivity and dynamic range of point of care immunoassays |
Researcher: | Sathishkumar, N |
Guide(s): | Toley, Bhushan J |
Keywords: | Engineering Engineering and Technology Engineering Chemical |
University: | Indian Institute of Science Bangalore |
Completed Date: | 2021 |
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,... |
Pagination: | xviii, 160 |
URI: | http://hdl.handle.net/10603/429813 |
Appears in Departments: | Chemical Engineering |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
01_title.pdf | Attached File | 25.34 kB | Adobe PDF | View/Open |
02_prelim pages.pdf | 271.54 kB | Adobe PDF | View/Open | |
03_table of contents.pdf | 187.54 kB | Adobe PDF | View/Open | |
04_abstract.pdf | 83.28 kB | Adobe PDF | View/Open | |
05_chapter 1.pdf | 87.26 kB | Adobe PDF | View/Open | |
06_chapter 2.pdf | 823.3 kB | Adobe PDF | View/Open | |
07_chapter 3.pdf | 1.41 MB | Adobe PDF | View/Open | |
08_chapter 4.pdf | 835.14 kB | Adobe PDF | View/Open | |
09_chapter 5.pdf | 1.19 MB | Adobe PDF | View/Open | |
10_chapter 6.pdf | 1.17 MB | Adobe PDF | View/Open | |
11_annexure.pdf | 3.64 MB | Adobe PDF | View/Open | |
80_recommendation.pdf | 122.8 kB | Adobe PDF | View/Open |
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