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A colorimetric lateral flow immunoassay based on oriented antibody immobilization for sensitive detection of SARS-CoV-2.
Lee, Ae Sol; Kim, Su Min; Kim, Kyeong Rok; Park, Chulmin; Lee, Dong-Gun; Heo, Hye Ryoung; Cha, Hyung Joon; Kim, Chang Sup.
  • Lee AS; Graduate School of Biochemistry, Yeungnam University, Gyeongsan 38541, Republic of Korea.
  • Kim SM; Graduate School of Biochemistry, Yeungnam University, Gyeongsan 38541, Republic of Korea.
  • Kim KR; Graduate School of Biochemistry, Yeungnam University, Gyeongsan 38541, Republic of Korea.
  • Park C; Vaccine Bio Research Institute, College of Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Republic of Korea.
  • Lee DG; Vaccine Bio Research Institute, College of Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Republic of Korea.
  • Heo HR; Division of Infectious Diseases, Department of Internal Medicine, College of Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Republic of Korea.
  • Cha HJ; Senotherapy-based Metabolic Disease Control Research Center, Yeungnam University, Gyeongsan 38541, Republic of Korea.
  • Kim CS; Department of Chemical Engineering, Pohang University of Science and Technology, Pohang 37673, Republic of Korea.
Sens Actuators B Chem ; 379: 133245, 2023 Mar 15.
Article in English | MEDLINE | ID: covidwho-2165857
ABSTRACT
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes coronavirus disease 2019 (COVID-19). The high human-to-human transmission and rapid evolution of SARS-CoV-2 have resulted in a worldwide pandemic. To contain SARS-CoV-2, it is essential to efficiently control the transmission of the virus through the early diagnosis of infected individuals, including asymptomatic people. Therefore, a rapid and accurate assay is vital for the early diagnosis of SARS-CoV-2 in suspected individuals. In this study, we developed a colorimetric lateral flow immunoassay (LFIA) in which a CBP31-BC linker was used to immobilize antibodies on a cellulose membrane in an oriented manner. The developed LFIA enabled sensitive detection of cultured SARS-CoV-2 in 15 min with a detection limit of 5 × 104 copies/mL. The clinical performance of the LFIA for detecting SARS-CoV-2 was evaluated using 19 clinical samples validated by reverse transcription-polymerase chain reaction (RT-PCR). The LFIA detected all the positive and negative samples accurately, corresponding to 100% accuracy. Importantly, patient samples with low viral loads were accurately identified. Thus, the proposed method can provide a useful platform for rapid and accurate point-of-care testing of SARS-CoV-2 in infected individuals to efficiently control the COVID-19 pandemic.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Experimental Studies / Prognostic study Language: English Journal: Sens Actuators B Chem Year: 2023 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Experimental Studies / Prognostic study Language: English Journal: Sens Actuators B Chem Year: 2023 Document Type: Article