2020
DOI: 10.1016/j.bios.2020.112524
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Portable and multiplexed lateral flow immunoassay reader based on SERS for highly sensitive point-of-care testing

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Cited by 93 publications
(57 citation statements)
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“…45 Each SERS nanotag was mixed with its corresponding target for 5 minutes to enable the selective capture of the analytes forming immuno-complexes. 30 Each biomarker's LF strips were then dipped into the assigned immuno-complex solutions in the 96 well-plate for 10 minutes to allow the solutions to migrate upward by capillary force. This led to formation and accumulation of sandwich complexes on the test lines due to the presence of pre-immobilised capture antibodies.…”
Section: Quantitative Sers Detection Of Slpa and Toxbmentioning
confidence: 99%
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“…45 Each SERS nanotag was mixed with its corresponding target for 5 minutes to enable the selective capture of the analytes forming immuno-complexes. 30 Each biomarker's LF strips were then dipped into the assigned immuno-complex solutions in the 96 well-plate for 10 minutes to allow the solutions to migrate upward by capillary force. This led to formation and accumulation of sandwich complexes on the test lines due to the presence of pre-immobilised capture antibodies.…”
Section: Quantitative Sers Detection Of Slpa and Toxbmentioning
confidence: 99%
“…The control lines remained colored for all concentrations, indicating that the LF strips were working correctly. 30 The LF strips were then washed out with 0.01 M Tris buffer (pH 8.4) for 5 minutes to remove the excess immuno-complex solutions from the strips surface to avoid the Raman background signal that can interfere with the test lines scan. This enabled highly sensitive quantitative detection for both biomarkers test lines using a handheld Raman spectrometer to acquire their SERS signals in 0.5 s. Each test line was scanned in orbital raster scanning (ORS) mode to acquire the average SERS signal from test line zones and to reduce the SERS signal variability between repeated scans.…”
Section: Quantitative Sers Detection Of Slpa and Toxbmentioning
confidence: 99%
See 2 more Smart Citations
“…Development of coloration readers suitable for standard LFT is a way of how to improve the assay. e reader devices are especially desired in pointof-care testing [66]. e improved LFT assays are quantitative or at least semiquantitative with acceptable accuracy of concentration range determination.…”
Section: Instrumentation Of Lft For Point-of-care Diagnosismentioning
confidence: 99%