Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/111633
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dc.contributorDepartment of Applied Physicsen_US
dc.creatorWei, Yen_US
dc.creatorSong, Men_US
dc.creatorLi, Len_US
dc.creatorMa, Yen_US
dc.creatorLao, Xen_US
dc.creatorLiu, Yen_US
dc.creatorLi, Gen_US
dc.creatorHao, Jen_US
dc.date.accessioned2025-03-04T06:43:33Z-
dc.date.available2025-03-04T06:43:33Z-
dc.identifier.issn2095-8226en_US
dc.identifier.urihttp://hdl.handle.net/10397/111633-
dc.language.isoenen_US
dc.publisherScience in China Pressen_US
dc.rights© The Author(s) 2024.en_US
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made.en_US
dc.rightsThe images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.en_US
dc.rightsTo view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.en_US
dc.rightsThe following publication Wei, Y., Song, M., Li, L. et al. Enhanced long-lasting luminescence nanorods for ultrasensitive detection of SARS-CoV-2 N protein. Sci. China Mater. 68, 253–260 (2025) is available at https://10.1007/s40843-024-3148-9.en_US
dc.subjectBiosensoren_US
dc.subjectHigh sensitivityen_US
dc.subjectNucleocapsid proteinen_US
dc.subjectPersistent luminescenceen_US
dc.subjectZn2GeO4:Mn, Cren_US
dc.titleEnhanced long-lasting luminescence nanorods for ultrasensitive detection of SARS-CoV-2 N proteinen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage253en_US
dc.identifier.epage260en_US
dc.identifier.volume68en_US
dc.identifier.issue2en_US
dc.identifier.doi10.1007/s40843-024-3148-9en_US
dcterms.abstractPersistent luminescence nanomaterials can remain luminescence when the light source is turned off, which exhibits promise in biosensor and bioimaging fields since they have the ability to completely eradicate tissue autofluorescence. Although significant progress has been made in the persistent luminescence biosensing, there is still a dearth of long-afterglow detection platform with low limit of detection (LOD) and high sensitivity. Herein, Zn2GeO4:Mn, Cr persistently luminescent nanorods (PLNRs) with superior persistent luminescence and long afterglow time were developed. The addition of Cr3+ manifestly improves persistent luminescence intensity and afterglow duration through creating a deep defect trap. Then the biosensors were constructed by combining the Zn2GeO4:Mn,Cr PLNRs-antibody and Fe3O4 magnetic nanoparticles (MNPs)-antibody for nucleocapsid protein detection based on electrostatic attraction. The LOD value for nucleocapsid protein realizes as low as 39.82 ag/mL, which is much lower than the previously reported persistent luminescent-based biosensors. Accordingly, the low detection sensitivity is attributed to fluorescence resonance energy transfer. In addition, high specificity is also achieved. Therefore, the as-prepared Zn2GeO4:Mn,Cr persistently luminescent materials can act as the promising candidate in biosensors applications. This strategy provides effective guidance for the development of biosensing platforms with high sensitivity and specificity. (Figure presented.)en_US
dcterms.accessRightsopen accessen_US
dcterms.alternative用于SARS-CoV-2 N蛋白超灵敏检测的增强型长余辉 发光纳米棒en_US
dcterms.bibliographicCitationScience China materials, Jan. 2025, v. 68, no. 2, p. 253-260en_US
dcterms.isPartOfScience China materialsen_US
dcterms.issued2025-01-
dc.identifier.scopus2-s2.0-85209076907-
dc.identifier.eissn2199-4501en_US
dc.description.validate202503 bchyen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_TA-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextPolyU Grantsen_US
dc.description.pubStatusPublisheden_US
dc.description.TASpringer Nature (2024)en_US
dc.description.oaCategoryTAen_US
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