Pregled bibliografske jedinice broj: 1131641
Current status of the lateral flow immunoassay for the detection of SARS-CoV-2 in nasopharyngeal swabs
Current status of the lateral flow immunoassay for the detection of SARS-CoV-2 in nasopharyngeal swabs // Biochemia medica, 31 (2021), 2; 230-239 doi:10.11613/BM.2021.020601 (međunarodna recenzija, pregledni rad, znanstveni)
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Naslov
Current status of the lateral flow immunoassay for
the detection of SARS-CoV-2 in nasopharyngeal swabs
Autori
Somborac Bačura, Anita ; Dorotić, Marija ; Grošić, Leonarda ; Džimbeg, Monika ; Dodig, Slavica
Izvornik
Biochemia medica (1330-0962) 31
(2021), 2;
230-239
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, pregledni rad, znanstveni
Ključne riječi
COVID-19 ; immunoassay ; nasopharynx ; SARS-CoV-2 antigen testing
Sažetak
Early detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and diagnosis of coronavirus disease 2019 (COVID- 19) are priorities during the pandemic. Symptomatic and suspected asymptomatic individuals should be tested for COVID-19 to confirm infection and to be excluded from social interactions. As molecular testing capacity is overloaded during the pandemic, rapid antigen tests, such as lateral flow immunoassays (LFIAs), can be a useful tool as they allow greater test availability and obtain results in a very short time. This short review aims to present the analytical properties of LFIAs in the detection of SARS-CoV-2 in nasopharyngeal swabs. Lateral flow immunoassay is a method that combines thin-layer chromatography and indirect immunochemical sandwich method and allows the detection of a specific SARS-CoV-2 antigen in nasopharyngeal swabs. Swab specimens should be adequately collected and tested as soon as possible. Users should pay attention to quality control and possible interferences. Antigen tests for SARS- CoV-2 show high sensitivity and specificity in cases with high viral loads, and should be used up to five days after the onset of the first symptoms of COVID-19. False positive results may be obtained when screening large populations with a low prevalence of COVID-19 infection, while false negative results may happen due to improper specimen collection or insufficient amount of antigen in the specimen. So as to achieve reliable results, a diagnostic accuracy study of a specific rapid antigen test should be performed.
Izvorni jezik
Engleski
Znanstvena područja
Javno zdravstvo i zdravstvena zaštita, Farmacija, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
POVEZANOST RADA
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE