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dc.contributor.authorJames-Pemberton, P
dc.contributor.authorLapinska, U
dc.contributor.authorHelliwell, M
dc.contributor.authorOlkhov, RV
dc.contributor.authorHedaux, OJ
dc.contributor.authorHyde, CJ
dc.contributor.authorShaw, AM
dc.date.accessioned2020-02-20T14:24:28Z
dc.date.issued2020-02-18
dc.description.abstractA multiplexed biophotonic assay platform has been developed using the localised particle plasmon in gold nanoparticles assembled in an array and functionalised for two assays: total IgG and C-reactive protein (CRP). A protein A/G (PAG) assay, calibrated with a NIST reference material, shows a maximum surface coverage of max = 7.13 ± 0.19 mRIU, equivalent to 1.5 ng mm-2 of F(ab)-presenting antibody. The CRP capture antibody has an equivalent surface binding density of max = 2.95 ± 0.41 mRIU indicating a 41% capture antibody availability. Free PAG binding to the functionalised anti-CRP surface shows that only 47 ± 3 % of CRP capture antibodies are correctly presenting Fab regions for antigen capture. The accuracy and precision of the CRP sensor assay was assessed with 54 blood samples containing spiked CRP in the range 2 – 160 mg/L. The mean accuracy was 0.42 mg/L with Confidence Interval (CI) at 95% from -14.7 to 13.8 mg/L and the precision had a Coefficient of Variation (CV) of 10.6% with 95% CI 0.9% - 20.2%. These biophotonic platform performance metrics indicate a CRP assay with 2 - 160 mg/L dynamic range, performed in 8 minutes from 5 L of whole blood without sample preparation.en_GB
dc.description.sponsorshipAttomarker Ltd.en_GB
dc.identifier.citationPublished online 18 February 2020en_GB
dc.identifier.doi10.1039/C9AN02516B
dc.identifier.urihttp://hdl.handle.net/10871/40951
dc.language.isoenen_GB
dc.publisherRoyal Society of Chemistryen_GB
dc.rights.embargoreasonUnder embargo until 18 February 2021 in compliance with publisher policyen_GB
dc.titleAccuracy and Precision Analysis for a Biophotonic Assay of C-Reactive Proteinen_GB
dc.typeArticleen_GB
dc.date.available2020-02-20T14:24:28Z
dc.identifier.issn0003-2654
dc.descriptionThis is the author accepted manuscript. The final version is available from the Royal Society of Chemistry via the DOI in this recorden_GB
dc.identifier.journalAnalysten_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
dcterms.dateAccepted2020-02-17
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2020-02-18
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2020-02-20T13:34:52Z
refterms.versionFCDAM
refterms.panelAen_GB


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