TwinDemic detection: A non-enzymatic signal amplification system for on-site detection of multiple respiratory viruses
- Authors
- Lim, Jaewoo; Ahn, Jin Woo; Maeng, Inhee; Lee, Jina; Kim, Ryunhyung; Mun, Byenggeol; Kim, Sunjoo; Jang, Hyowon; Kang, Taejoon; Jung, Juyeon; Haam, Seungjoo; Kim, Eunjung; Oh, Seung Jae; Lim, Eun-Kyung
- Issue Date
- Feb-2025
- Publisher
- Elsevier BV
- Keywords
- Influenza A; Microfluidic chip; Non-enzymatic signal amplification; Point-of-care testing; severe acute respiratory syndrome coronavirus 2
- Citation
- Sensors and Actuators, B: Chemical, v.424
- Indexed
- SCIE
SCOPUS
- Journal Title
- Sensors and Actuators, B: Chemical
- Volume
- 424
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/74826
- DOI
- 10.1016/j.snb.2024.136933
- ISSN
- 0925-4005
1873-3077
- Abstract
- The simultaneous occurrence of multiple respiratory viruses, such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2 [CoV]) and influenza A virus (IAV), presents a challenge for accurate diagnosis and treatment. To address this, we developed the TwinDemic Detection (TDD) system—an integrated point-of-care diagnostic platform that can simultaneously detect CoV and IAV using a multi-respiratory virus identification approach. The TDD system contains a transparent poly(methyl methacrylate) microfluidic chip with a hydrogel-based gene detection sensor and a handheld fluorescence reader. This system uses a fuel-stimulated DNA probe to detect viral RNA and amplify the fluorescence signal without the need for enzymatic or thermal controls. The system's performance was tested using 45 human nasopharyngeal samples; results revealed positive and negative predictive values of 93.3 % and 96.7 % for CoV, and 100 % and 96.7 % for IAV, respectively. This system enables the accurate and simultaneous detection of multiple respiratory viruses for public health surveillance and shows potential for use as a point-of-care molecular test to monitor a wider range of viruses in the future. © 2024 The Authors
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