SERS-ELISA using silica-encapsulated Au core-satellite nanotags for sensitive detection of SARS-CoV-2

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dc.contributor.authorQ Yu-
dc.contributor.authorH D Trinh-
dc.contributor.authorY Lee-
dc.contributor.authorTaejoon Kang-
dc.contributor.authorL Chen-
dc.contributor.authorS Yoon-
dc.contributor.authorJ Choo-
dc.date.accessioned2023-02-24T16:32:52Z-
dc.date.available2023-02-24T16:32:52Z-
dc.date.issued2023-
dc.identifier.issn0925-4005-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/31107-
dc.description.abstractThe sensitive detection of viruses is key to preventing the spread of infectious diseases. In this study, we develop a silica-encapsulated Au core-satellite (CS@SiO2) nanotag, which produces a strong and reproducible surface-enhanced Raman scattering (SERS) signal. The combination of SERS from the CS@SiO2 nanotags with enzyme-linked immunosorbent assay (ELISA) achieves a highly sensitive detection of SARS-CoV-2. The CS@SiO2 nanotag is constructed by assembling 32 nm Au nanoparticles (AuNPs) on a 75 nm AuNP. Then the core-satellite particles are encapsulated with SiO2 for facile surface modification and stability. The SERS-ELISA technique using the CS@SiO2 nanotags provides a great sensitivity, yielding a detection limit of 8.81 PFU mL-1, which is 10 times better than conventional ELISA and 100 times better than lateral flow assay strip method. SERS-ELISA is applied to 30 SARS-CoV-2 clinical samples and achieved 100% and 55% sensitivities for 15 and 9 positive samples with cycle thresholds < 30 and > 30, respectively. This new CS@SiO2-SERS-ELISA method is an innovative technique that can significantly reduce the false-negative diagnostic rate for SARS-CoV-2 and thereby contribute to overcoming the current pandemic crisis.-
dc.publisherElsevier-
dc.titleSERS-ELISA using silica-encapsulated Au core-satellite nanotags for sensitive detection of SARS-CoV-2-
dc.title.alternativeSERS-ELISA using silica-encapsulated Au core-satellite nanotags for sensitive detection of SARS-CoV-2-
dc.typeArticle-
dc.citation.titleSensors and Actuators B-Chemical-
dc.citation.number0-
dc.citation.endPage133521-
dc.citation.startPage133521-
dc.citation.volume382-
dc.contributor.affiliatedAuthorTaejoon Kang-
dc.contributor.alternativeNameYu-
dc.contributor.alternativeNameTrinh-
dc.contributor.alternativeName이연지-
dc.contributor.alternativeName강태준-
dc.contributor.alternativeNameChen-
dc.contributor.alternativeName윤상운-
dc.contributor.alternativeName주재범-
dc.identifier.bibliographicCitationSensors and Actuators B-Chemical, vol. 382, pp. 133521-133521-
dc.identifier.doi10.1016/j.snb.2023.133521-
dc.subject.keywordSurface-enhanced Raman scattering (SERS)-
dc.subject.keywordSERS-ELISA-
dc.subject.keywordSARS-CoV-2-
dc.subject.keywordInfectious disease-
dc.subject.keywordDiagnostics-
dc.subject.localSurface-enhanced Raman scattering-
dc.subject.localsurface-enhanced Raman scattering-
dc.subject.localsurface-enhanced raman scattering-
dc.subject.localSurface-enhanced Raman Scattering-
dc.subject.localSurface-enhanced Raman scattering (SERS)-
dc.subject.localSERS-ELISA-
dc.subject.localSARS-CoV-2-
dc.subject.localSARS-Cov-2-
dc.subject.localinfectious disease-
dc.subject.localInfectious diseases-
dc.subject.localinfectious diseaese-
dc.subject.localinfectious diseases-
dc.subject.localInfectious disease-
dc.subject.localInfectious Disease-
dc.subject.localdiagnostics-
dc.subject.localDiagnostic-
dc.subject.localDiagnostics-
dc.subject.localdiagnostic-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Bionanotechnology Research Center > 1. Journal Articles
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