Ultrafast molecular diagnosis-based solid-phase photonic PCR for respiratory pathogen variant discrimination

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dc.contributor.authorS E Seo-
dc.contributor.authorK H Kim-
dc.contributor.authorH Oh-
dc.contributor.authorJinyeong Kim-
dc.contributor.authorS Kim-
dc.contributor.authorY K Kim-
dc.contributor.authorJung Joo Hong-
dc.contributor.authorKyong-Cheol Ko-
dc.contributor.authorH Cho-
dc.contributor.authorD Y Lee-
dc.contributor.authorH I Kim-
dc.contributor.authorK G Lee-
dc.contributor.authorO S Kwon-
dc.date.accessioned2024-09-27T16:33:32Z-
dc.date.available2024-09-27T16:33:32Z-
dc.date.issued2024-
dc.identifier.issn1616-301X-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/36014-
dc.description.abstractThe need for an accurate and rapid diagnosis platform for highly contagious viruses, such as pandemic viruses, has rapidly increased. Conventional diagnostic methods in the initial stage of quarantine for the prevention of epidemic spread have encountered limitations such as a long operation time, occupation of a large space, and high cost per single operation. Here, a highly sensitive and selective portable diagnostic platform based on solid-phase photonic polymerase chain reaction (SP-PCR) is reported. The thermal cycle is operated by the photothermal energy converted from the photon energy of a light-emitting diode (LED) through a gold layer to phonons. The formation of an amplicon, which is immobilized through N-heterocyclic carbene, is confirmed through fluorescence on the surface of the miniaturized SP-PCR chip. The practical applicability of the newly developed diagnosis platform for the recognition of the presence of a SARS-CoV-2-specific genome sequence is demonstrated utilizing 100 clinical samples, including 72 COVID-19-positive clinical samples and 28 negative samples.-
dc.publisherWiley-
dc.titleUltrafast molecular diagnosis-based solid-phase photonic PCR for respiratory pathogen variant discrimination-
dc.title.alternativeUltrafast molecular diagnosis-based solid-phase photonic PCR for respiratory pathogen variant discrimination-
dc.typeArticle-
dc.citation.titleAdvanced Functional Materials-
dc.citation.number38-
dc.citation.endPage2402972-
dc.citation.startPage2402972-
dc.citation.volume34-
dc.contributor.affiliatedAuthorJinyeong Kim-
dc.contributor.affiliatedAuthorJung Joo Hong-
dc.contributor.affiliatedAuthorKyong-Cheol Ko-
dc.contributor.alternativeName서성은-
dc.contributor.alternativeName김경호-
dc.contributor.alternativeName오한슬-
dc.contributor.alternativeName김진영-
dc.contributor.alternativeName김수민-
dc.contributor.alternativeName김유경-
dc.contributor.alternativeName홍정주-
dc.contributor.alternativeName고경철-
dc.contributor.alternativeName조해인-
dc.contributor.alternativeName이도연-
dc.contributor.alternativeName김형일-
dc.contributor.alternativeName이경G-
dc.contributor.alternativeName권오석-
dc.identifier.bibliographicCitationAdvanced Functional Materials, vol. 34, no. 38, pp. 2402972-2402972-
dc.identifier.doi10.1002/adfm.202402972-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Korea Preclinical Evaluation Center > 1. Journal Articles
Ochang Branch Institute > Division of National Bio-Infrastructure > National Primate Research Center > 1. Journal Articles
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