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dc.contributor.authorRoberts, Jonathan M.
dc.contributor.authorBradshaw, David J.
dc.contributor.authorLynch, Richard J. M.
dc.contributor.authorHigham, Susan M.
dc.contributor.authorValappil, Sabeel P.
dc.date.accessioned2023-02-02T10:18:45Z
dc.date.available2023-02-02T10:18:45Z
dc.date.issued2021-10-30
dc.identifierhttps://chesterrep.openrepository.com/bitstream/handle/10034/627498/Roberts%20et%20al%20PDPT%20accepted%20version.pdf?sequence=3
dc.identifier.citationRoberts, J. M., Bradshaw, D. J., Lynch, R. J. M., Higham. S. M., & Valappil, S. P. (2021). Quantifying the demineralisation of enamel using a hyperspectral camera measuring fluorescence loss. Photodiagnosis and Photodynamic Therapy, 36, 102603. https://doi.org/10.1016/j.pdpdt.2021.102603en_US
dc.identifier.issn1572-1000
dc.identifier.doi10.1016/j.pdpdt.2021.102603
dc.identifier.urihttp://hdl.handle.net/10034/627498
dc.description.abstractBackground The gold standard for quantifying mineral loss of enamel is transverse microradiography (TMR) and is complimented by the non-destructive quantitative light induced fluorescence (QLF) which measures changes in autofluorescence. Fluorescence loss has been shown to correlate with mineral loss. Building upon the established method, the use of hyperspectral fluorescence imaging (HI) allows the capture of a broader range of wavelengths to quantify fluorescence changes more accurately. Methods Bovine Enamel was demineralised within the dual constant depth film fermenter over 14 days and analysed using TMR, QLF and HI. The mineral change values were compared using Pearson's Correlation Coefficient. Results The analysis showed a statistically significant correlation that was equal between TMR and HI (r = 0.844) and TMR and QLF (r = 0.844), but weaker between QLF and HI (r = 0.811). Conclusions The correlations indicate that HI is a promising valid non-destructive method for quantifying mineral loss from bovine enamel that is as accurate as QLF and complements TMR.en_US
dc.publisherElsevieren_US
dc.relation.urlhttps://doi.org/10.1016/j.pdpdt.2021.102603en_US
dc.relation.urlhttps://www.sciencedirect.com/science/article/pii/S157210002100421Xen_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.subjectMicrobiologyen_US
dc.subjectBiofilmen_US
dc.subjectFluorescence imagingen_US
dc.titleQuantifying the Demineralisation of Enamel Using a Hyperspectral Camera Measuring Fluorescence Lossen_US
dc.typeArticleen_US
dc.identifier.eissn1873-1597en_US
dc.contributor.departmentUniversity of Liverpool; GlaxoSmithKline Consumer Healthcare; University of Chesteren_US
dc.identifier.journalPhotodiagnosis and Photodynamic Therapyen_US
or.grant.openaccessYesen_US
rioxxterms.funderEngineering and Physical Sciences Research Council (EPSRC), GlaxoSmithKline plc (GSK)en_US
rioxxterms.identifier.projectEngineering and Physical Sciences Research Council (EPSRC)- GlaxoSmithKline plc (GSK) Industrial CASE Studentship (#15220088)en_US
rioxxterms.versionAMen_US
rioxxterms.versionofrecord10.1016/j.pdpdt.2021.102603en_US
rioxxterms.licenseref.startdate2022-10-30
dcterms.dateAccepted2021-10-22
rioxxterms.publicationdate2021-10-30
dc.date.deposited2023-02-02en_US


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