Clinical Validation of a Colorimetric Loop-Mediated Isothermal Amplification Using a Portable Device for the Rapid Detection of SARS-CoV-2

Quick and reliable mass testing of infected people is an effective tool for the contingency of SARS-CoV-2. During the COVID-19 pandemic, Point-of-Care (POC) tests using Loop-Mediated Isothermal Amplification (LAMP) arose as a useful diagnostic tool. LAMP tests are a robust and fast alternative to Po...

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Veröffentlicht in:Diagnostics (Basel) 2023-04, Vol.13 (7), p.1355
Hauptverfasser: Raddatz, Bruna W, Rabello, Felipe J, Benedetti, Rafael, Steil, Gisleine J, Imamura, Louise M, Kim, Edson Y S, Santiago, Erika B, Hartmann, Luís F, Predebon, João V, Delfino, Bruna M, Nogueira, Meri B, Dos Santos, Jucélia S, da Silva, Breno G, Nicollete, Diego R P, Almeida, Bernardo M M de, Rogal, Jr, Sergio R, Figueredo, Marcus V M
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Sprache:eng
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Zusammenfassung:Quick and reliable mass testing of infected people is an effective tool for the contingency of SARS-CoV-2. During the COVID-19 pandemic, Point-of-Care (POC) tests using Loop-Mediated Isothermal Amplification (LAMP) arose as a useful diagnostic tool. LAMP tests are a robust and fast alternative to Polymerase Chain Reaction (PCR), and their isothermal property allows easy incorporation into POC platforms. The main drawback of using colorimetric LAMP is the reported short-term stability of the pre-mixed reagents, as well as the relatively high rate of false-positive results. Also, low-magnitude amplification can produce a subtle color change, making it difficult to discern a positive reaction. This paper presents Hilab Molecular, a portable device that uses the Internet of Things and Artificial Intelligence to pre-analyze colorimetric data. In addition, we established manufacturing procedures to increase the stability of colorimetric RT-LAMP tests. We show that ready-to-use reactions can be stored for up to 120 days at -20 °C. Furthermore, we validated both the Hilab Molecular device and the Hilab RT-LAMP test for SARS-CoV-2 using 581 patient samples without any purification steps. We achieved a sensitivity of 92.93% and specificity of 99.42% (samples with CT ≤ 30) when compared to RT-qPCR.
ISSN:2075-4418
2075-4418
DOI:10.3390/diagnostics13071355