High-sensitivity lateral flow immunoassay with a fluorescent lanthanide nanoparticle label

dc.contributor.authorTeppo Salminen
dc.contributor.authorEtvi Juntunen
dc.contributor.authorSheikh M. Talha
dc.contributor.authorKim Pettersson
dc.contributor.organizationfi=biotekniikka|en=Biotechnology|
dc.contributor.organization-code1.2.246.10.2458963.20.98373201676
dc.contributor.organization-code2606202
dc.contributor.organization-code2610102
dc.converis.publication-id37233625
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/37233625
dc.date.accessioned2022-10-28T12:29:28Z
dc.date.available2022-10-28T12:29:28Z
dc.description.abstract<p>Lateral flow (LF) immunoassays are commonly used for point-of-care testing and typically incorporate visually read reporters, such as gold particles. To improve sensitivity and develop quantitative LF immunoassays, visual reporters can be replaced by fluorescent reporters detected by an instrument. In this study, we used fluorescent europium(III) chelate doped nanoparticle (Eu-np) reporters to develop a quantitative high-sensitivity LF immunoassay for free prostate specific antigen (fPSA). Furthermore, we tested different simplified formats of the assay and the effect of different modifiable parameters on the detection limit of the assay: dynamic range, assay duration and number of assay steps. The molar detection limits of the different assay formats were compared with published detection limits of LF immunoassays with different reporters. The cutoff was calculated from 11 female serum samples. The detection limit of the sensitivity optimized fPSA assay with fPSA spiked into pooled female serum was 0.01 ng/ml, which is approximately 100-fold lower than the most sensitive gold particle LF assays and 10-fold lower than other Eu-np and carbon nanoparticle based LF immunoassays. Thus, Eu-np reporters can be used to develop highly sensitive and quantitative LF immunoassays.<br /></p>
dc.format.pagerange39
dc.format.pagerange44
dc.identifier.eissn1872-7905
dc.identifier.jour-issn0022-1759
dc.identifier.olddbid176783
dc.identifier.oldhandle10024/159877
dc.identifier.urihttps://www.utupub.fi/handle/11111/32361
dc.identifier.urnURN:NBN:fi-fe2021042720494
dc.language.isoen
dc.okm.affiliatedauthorSalminen, Teppo
dc.okm.affiliatedauthorJuntunen, Etvi
dc.okm.affiliatedauthorTalha, Sheikh
dc.okm.affiliatedauthorPettersson, Kim
dc.okm.discipline318 Medical biotechnologyen_GB
dc.okm.discipline318 Lääketieteen bioteknologiafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier B.V.
dc.publisher.countryNetherlandsen_GB
dc.publisher.countryAlankomaatfi_FI
dc.publisher.country-codeNL
dc.relation.doi10.1016/j.jim.2018.12.001
dc.relation.ispartofjournalJournal of Immunological Methods
dc.relation.volume465
dc.source.identifierhttps://www.utupub.fi/handle/10024/159877
dc.titleHigh-sensitivity lateral flow immunoassay with a fluorescent lanthanide nanoparticle label
dc.year.issued2019

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