» Articles » PMID: 37151731

Self-enhancement Lateral Flow Immunoassay for COVID-19 Diagnosis

Abstract

Equipment-free colorimetric-based lateral flow immunoassay (LFIA) is the most convenient and popular tool for various applications, including diagnostic tools requiring high sensitivity for the detection of pathogens. Thus, improvements and developments of LFIA are constantly being reported. Herein, we enriched the sensitivity of LFIA using the gold enhancement principle, emphasizing needlessly complicated apparatus, only one step for the strip test operation, and typical time incubation (15 min) process. Self-enhanced LFIA was then executed for subsequent flows by overlapping the additionally enhanced pad composed of gold ions and reducing agent on the conjugate pad and the sample pad. Self-enhanced LFIA was performed to detect SARS-CoV-2 antigens in saliva. The obtained result depicted that the achieved sensitivity was up to tenfold compared with that of conventional LFIA by visual measurements. The detection limits of self-enhanced LFIA detecting nucleocapsid protein antigens in the saliva sample was 0.50 and 0.10 ng/mL employed by naked eye detection and calibration curve-based calculation, respectively. When the proposed device was applied to 207 human saliva samples, the diagnostic performance presented a 96.10 % sensitivity and 99.23 % specificity. This self-enhanced LFIA could be implemented in large-scale production and demonstrates higher sensitivity with effortless use, which meets the requirements for point-of-care testing and on-field mass screening.

Citing Articles

Development of Detection Antibody Targeting the Linear Epitope in SARS-CoV-2 Nucleocapsid Protein with Ultra-High Sensitivity.

Wu F, Jiang Y, Yang H, Ma L Int J Mol Sci. 2024; 25(8).

PMID: 38674021 PMC: 11050370. DOI: 10.3390/ijms25084436.


Overlaid Lateral Flow Immunoassay for the Simultaneous Detection of Two Variant-Specific SARS-CoV-2 Neutralizing Antibodies.

Deenin W, Khongchareonporn N, Ruxrungtham K, Ketloy C, Hirankarn N, Wangkanont K Anal Chem. 2024; 96(14):5407-5415.

PMID: 38478766 PMC: 11270523. DOI: 10.1021/acs.analchem.3c05144.


Post-Assay Chemical Enhancement for Highly Sensitive Lateral Flow Immunoassays: A Critical Review.

Panferov V, Zherdev A, Dzantiev B Biosensors (Basel). 2023; 13(9).

PMID: 37754100 PMC: 10526817. DOI: 10.3390/bios13090866.

References
1.
Mistry D, Wang J, Moeser M, Starkey T, Lee L . A systematic review of the sensitivity and specificity of lateral flow devices in the detection of SARS-CoV-2. BMC Infect Dis. 2021; 21(1):828. PMC: 8371300. DOI: 10.1186/s12879-021-06528-3. View

2.
Igloi Z, Velzing J, Huisman R, GeurtsvanKessel C, Comvalius A, IJpelaar J . Clinical evaluation of the SD Biosensor SARS-CoV-2 saliva antigen rapid test with symptomatic and asymptomatic, non-hospitalized patients. PLoS One. 2021; 16(12):e0260894. PMC: 8694432. DOI: 10.1371/journal.pone.0260894. View

3.
Panraksa Y, Amin A, Graham B, Henry C, Chatterjee D . Immobilization of Proteinase K for urine pretreatment to improve diagnostic accuracy of active tuberculosis. PLoS One. 2021; 16(9):e0257615. PMC: 8454978. DOI: 10.1371/journal.pone.0257615. View

4.
Panferov V, Safenkova I, Zherdev A, Dzantiev B . Post-assay growth of gold nanoparticles as a tool for highly sensitive lateral flow immunoassay. Application to the detection of potato virus X. Mikrochim Acta. 2018; 185(11):506. DOI: 10.1007/s00604-018-3052-7. View

5.
Uwamino Y, Nagata M, Aoki W, Nakagawa T, Inose R, Yokota H . Accuracy of rapid antigen detection test for nasopharyngeal swab specimens and saliva samples in comparison with RT-PCR and viral culture for SARS-CoV-2 detection. J Infect Chemother. 2021; 27(7):1058-1062. PMC: 8052479. DOI: 10.1016/j.jiac.2021.04.010. View