Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/99718
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dc.contributorDepartment of Applied Physics-
dc.contributorDepartment of Biomedical Engineering-
dc.creatorLi, Len_US
dc.creatorSong, Men_US
dc.creatorLao, Xen_US
dc.creatorPang, SYen_US
dc.creatorLiu, Yen_US
dc.creatorWong, MCen_US
dc.creatorMa, Yen_US
dc.creatorYang, Men_US
dc.creatorHao, Jen_US
dc.date.accessioned2023-07-19T00:54:34Z-
dc.date.available2023-07-19T00:54:34Z-
dc.identifier.issn0264-1275en_US
dc.identifier.urihttp://hdl.handle.net/10397/99718-
dc.language.isoenen_US
dc.publisherElsevier Ltden_US
dc.rights© 2022 The Author(s). Published by Elsevier Ltd.en_US
dc.rightsThis is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Li, L., Song, M., Lao, X., Pang, S. -., Liu, Y., Wong, M. -., . . . Hao, J. (2022). Rapid and ultrasensitive detection of SARS-CoV-2 spike protein based on upconversion luminescence biosensor for COVID-19 point-of-care diagnostics. Materials and Design, 223, 111263 is available at https://doi.org/10.1016/j.matdes.2022.111263.en_US
dc.subjectUpconversion nanoparticlesen_US
dc.subjectAu nanorodsen_US
dc.subjectCOVID-19 point-of-care diagnosticsen_US
dc.subjectFRET effecten_US
dc.subjectSARS-CoV-2 spike proteinen_US
dc.titleRapid and ultrasensitive detection of SARS-CoV-2 spike protein based on upconversion luminescence biosensor for COVID-19 point-of-care diagnosticsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume223en_US
dc.identifier.doi10.1016/j.matdes.2022.111263en_US
dcterms.abstractHere, we firstly introduce a detection system consisting of upconversion nanoparticles (UCNPs) and Au nanorods (AuNRs) for an ultrasensitive, rapid, quantitative and on-site detection of SARS-CoV-2 spike (S) protein based on Förster resonance energy transfer (FRET) effect. Briefly, the UCNPs capture the S protein of lysed SARS-CoV-2 in the swabs and subsequently they are bound with the anti-S antibodies modified AuNRs, resulting in significant nonradiative transitions from UCNPs (donors) to AuNRs (acceptors) at 480 nm and 800 nm, respectively. Notably, the specific recognition and quantitation of S protein can be realized in minutes at 800 nm because of the low autofluorescence and high Yb-Tm energy transfer in upconversion process. Inspiringly, the limit of detection (LOD) of the S protein can reach down to 1.06 fg mL−1, while the recognition of nucleocapsid protein is also comparable with a commercial test kit in a shorter time (only 5 min). The established strategy is technically superior to those reported point-of-care biosensors in terms of detection time, cost, and sensitivity, which paves a new avenue for future on-site rapid viral screening and point-of-care diagnostics.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationMaterials and design, Nov. 2022, v. 223, 111263en_US
dcterms.isPartOfMaterials and designen_US
dcterms.issued2022-11-
dc.identifier.scopus2-s2.0-85140772431-
dc.identifier.eissn1873-4197en_US
dc.identifier.artn111263en_US
dc.description.validate202307 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextPolyU Internal Research Funden_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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