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Development of an IoT-integrated multiplexed digital PCR system for quantitative detection o infectious diseases

Authors
Choi, Ji WookSeo, Won HoLee, Young SuhKim, So YoungKim, Bong SukLee, Kyoung G.Lee, Seok JaeChung, Bong Geun
Issue Date
Oct-2022
Publisher
Royal Society of Chemistry
Citation
Lab on a Chip, v.22, no.20, pp 3933 - 3941
Pages
9
Journal Title
Lab on a Chip
Volume
22
Number
20
Start Page
3933
End Page
3941
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/21687
DOI
10.1039/d2lc00726f
ISSN
1473-0197
1473-0189
Abstract
For rapid detection of the COVID-19 infection, the digital polymerase chain reaction (dPCR) with higher sensitivity and specificity has been presented as a promising method of point-of-care testing (POCT). Unlike the conventional real-time PCR (qPCR), the dPCR system allows absolute quantification of the target DNA without a calibration curve. Although a number of dPCR systems have previously been reported, most of these previous assays lack multiplexing capabilities. As different variants of COVID-19 have rapidly emerged, there is an urgent need for highly specific multiplexed detection systems. Additionally, the advances in the Internet of Things (IoT) technology have enabled the onsite detection of infectious diseases. Here, we present an IoT-integrated multiplexed dPCR (IM-dPCR) system involving sample compartmentalization, DNA amplification, fluorescence imaging, and quantitative analysis. This IM-dPCR system comprises three modules: a plasmonic heating-based thermal cycler, a multi-color fluorescence imaging set-up, and a firmware control module. Combined with a custom-developed smartphone application built on an IoT platform, the IM-dPCR system enabled automatic processing, data collection, and cloud storage. Using a self-priming microfluidic chip, 9 RNA groups (e.g., H1N1, H3N2, IFZ B, DENV2, DENV3, DENV4, OC43, 229E, and NL63) associated with three infectious diseases (e.g., influenza, dengue, and human coronaviruses) were analyzed with higher linearity (>98%) and sensitivity (1 copy per mu L). The IM-dPCR system exhibited comparable analytical accuracy to commercial qPCR platforms. Therefore, this IM-dPCR system plays a crucial role in the onsite detection of infectious diseases.
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