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Development and evaluation of a highly sensitive immunochromatographic strip test using gold nanoparticle for direct detection of Vibrio cholerae O139 in seafood samples

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dc.contributor.author Pengsuk C.
dc.contributor.author Chaivisuthangkura P.
dc.contributor.author Longyant S.
dc.contributor.author Sithigorngul P.
dc.date.accessioned 2021-04-05T03:33:08Z
dc.date.available 2021-04-05T03:33:08Z
dc.date.issued 2013
dc.identifier.issn 9565663
dc.identifier.other 2-s2.0-84871652158
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/14084
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-84871652158&doi=10.1016%2fj.bios.2012.10.011&partnerID=40&md5=4c435bc652aba84940593efb28574331
dc.description.abstract A strip test for the detection of Vibrio cholerae O139 was developed using two monoclonal antibodies (MAbs), namely VC-273 and VC-812, which specifically bind to the lipopolysaccharide and capsular polysaccharide of V. cholerae O139. The MAb VC-273 gold nanoparticle conjugate was sprayed onto a glass fiber pad that was placed adjacent to a sample chamber. MAb VC-812 and the goat anti-mouse immunoglobulin G (GAM) antibody were sprayed onto a nitrocellulose membrane in strips at positions designated as T and C, respectively. The test strips were assessed for their ability to directly detect V. cholerae O139 using samples dispersed in application buffer, and a 100μL aliquot of sample was applied to the sample chamber. The results were observable within 20min after application of the sample. In samples containing V. cholerae O139, the antigen was bound to the colloidal gold-conjugated MAb to form an antibody-antigen complex. This complex was captured by the MAbs at the T test line, resulting in the appearance of a reddish-purple band at the T position. The sensitivity of the test was determined to be 104cfumL-1. Direct detection of V. cholerae O139 in various fresh seafood samples could be accomplished with similar sensitivities. The detection limit was substantially improved to 1cfumL-1 of the original bacterial content after pre-incubation of the sample in alkaline peptone water for 12h. The V. cholerae strip test provides several advantages over other methods, including the speed and simplicity of use because there is no requirement for sophisticated equipment. © 2012 Elsevier B.V.
dc.subject Gold Nanoparticles
dc.subject Immunochromatography
dc.subject Monoclonal antibodies (mAb)
dc.subject Strip test
dc.subject Vibrio cholerae
dc.subject Antigens
dc.subject Glass fibers
dc.subject Metal nanoparticles
dc.subject Monoclonal antibodies
dc.subject Nitrocellulose
dc.subject Gold
dc.subject glass fiber
dc.subject gold nanoparticle
dc.subject immunoglobulin G antibody
dc.subject lipopolysaccharide
dc.subject monoclonal antibody
dc.subject polysaccharide
dc.subject pyroxylin
dc.subject water
dc.subject antibody production
dc.subject antigen antibody complex
dc.subject antigen binding
dc.subject article
dc.subject bacterium detection
dc.subject colony forming unit
dc.subject conjugation
dc.subject controlled study
dc.subject food analysis
dc.subject immunoaffinity chromatography
dc.subject limit of detection
dc.subject nonhuman
dc.subject process development
dc.subject process optimization
dc.subject sea food
dc.subject sensitivity analysis
dc.subject test strip
dc.subject thermostability
dc.subject Vibrio cholerae
dc.subject Animals
dc.subject Antibodies, Monoclonal
dc.subject Food Analysis
dc.subject Gold
dc.subject Humans
dc.subject Metal Nanoparticles
dc.subject Mice
dc.subject Seafood
dc.subject Sensitivity and Specificity
dc.subject Vibrio cholerae O139
dc.subject Bacteria
dc.subject Cellulose Nitrate
dc.subject Chromatography
dc.subject Glass Fibers
dc.subject Gold Compounds
dc.subject Bacteria (microorganisms)
dc.subject Capra hircus
dc.subject Vibrio cholerae
dc.title Development and evaluation of a highly sensitive immunochromatographic strip test using gold nanoparticle for direct detection of Vibrio cholerae O139 in seafood samples
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Biosensors and Bioelectronics. Vol 42, No.1 (2013), p.229-235
dc.identifier.doi 10.1016/j.bios.2012.10.011


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