Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13491
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dc.contributor.authorYodmongkol S.
dc.contributor.authorThaweboon S.
dc.contributor.authorThaweboon B.
dc.contributor.authorPuttharugsa C.
dc.contributor.authorSutapun B.
dc.contributor.authorAmarit R.
dc.contributor.authorSomboonkaew A.
dc.contributor.authorSrikhirin T.
dc.date.accessioned2021-04-05T03:24:16Z-
dc.date.available2021-04-05T03:24:16Z-
dc.date.issued2016
dc.identifier.issn214922
dc.identifier.other2-s2.0-84956625420
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13491-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84956625420&doi=10.7567%2fJJAP.55.02BE03&partnerID=40&md5=3470acc7a6bb84227318002263155fcc
dc.description.abstractIn this study, surface plasmon resonance imaging (SPR imaging) was developed for the detection of Candida albicans which is a causal agent of oral infection. The detection was based on the sandwich assay. The capture antibody was covalently immobilized on the mixed self assemble monolayers (SAMs). The ratio of mixed SAMs between 11-mercaptoundecanoic acid and 3-mercaptopropanol was varied to find the optimal ratio for use as a sensor surface. The results showed that the suitable surface for C. albicans detection was SAM of carboxylic (mixed SAMs 1 : 0), even though mixed SAMs 1 : 40 had a high detection signal in comparison to mixed SAMs 1 : 0, but the non-specific signal was higher. The detection limit was 107 cells/ml for direct detection, and was increased to 106 cells/ml with sandwich antibody. The use of polyclonal C. albicans antibody as capture and sandwich antibody showed good selectivity against the relevant oral bacteria including Escherichia coli, Streptococcus mutan, Staphylococcus aureus, β-streptococci, and Lactobacillus casei. SPR platform in this study could detect C. albicans from the mixed microbial suspension without requirement of skillful technician. This SPR imaging biosensor could be applied for Candida identification after cultivation. © 2016 The Japan Society of Applied Physics.
dc.subjectAntibodies
dc.subjectBacteria
dc.subjectBiosensors
dc.subjectCandida
dc.subjectChemical detection
dc.subjectEscherichia coli
dc.subjectPlasmons
dc.subjectSignal detection
dc.subjectYeast
dc.subject11-mercaptoundecanoic acid
dc.subjectDetection limits
dc.subjectDirect detection
dc.subjectLactobacillus casei
dc.subjectSelf-assemble monolayers
dc.subjectStaphylococcus aureus
dc.subjectSurface plasmon resonance biosensor
dc.subjectSurface plasmon resonance imaging
dc.subjectSurface plasmon resonance
dc.titleApplication of surface plasmon resonance biosensor for the detection of Candida albicans
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJapanese Journal of Applied Physics. Vol 55, No.2 (2016)
dc.identifier.doi10.7567/JJAP.55.02BE03
Appears in Collections:Scopus 1983-2021

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