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The enhanced diffusional mixing for latex immunoagglutination assay in a microfluidic device

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dc.contributor.authorHan, Jin-Hee-
dc.contributor.authorKim, Kye-Seong-
dc.contributor.authorYoon, Jeong-Yeol-
dc.date.accessioned2022-10-07T11:32:23Z-
dc.date.available2022-10-07T11:32:23Z-
dc.date.issued2007-02-
dc.identifier.issn0003-2670-
dc.identifier.issn1873-4324-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/172339-
dc.description.abstractLatex immunoagglutination assay in a microfluidic device is expected to be even easier than its large-sized, commercialized counterpart. However, such demonstration has had a limited success due to the difficulties in mixing in a microfluidic device, especially for the microparticles used in latex immunoagglutination assay. The primary goal of this work is to improve diffusional mixing towards the successful latex immunoagglutination in a microfluidic devices without any non-specific binding. To this end, SDS (sodium dodecyl sulfate, an ionic surfactant) or Tween 80 (polyethylene sorbitol ester, a non-ionic surfactant) was added to the antibody-conjugated polystyrene (PS) microparticle suspension. These surfactant-added particle suspensions were mixed with the target antigen solution at the Y-junction of a microfluidic device. The immunoagglutination and the diffusion behavior were visually identified with an inverted light microscope. Both surfactants showed some problems such as non-specific binding (with SDS) or very poor diffusion (with Tween 80). As an alternative approach, therefore, highly carboxylated PS microparticles, where the surface is saturated with carboxyl-terminated side chains, were evaluated without using any surfactants. These particles showed very low non-specific binding comparable to that with Tween 80 and good diffusional mixing equivalent to that with SIDS. (c) 2006 Elsevier B.V. All rights reserved.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleThe enhanced diffusional mixing for latex immunoagglutination assay in a microfluidic device-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.aca.2006.11.044-
dc.identifier.scopusid2-s2.0-33846548080-
dc.identifier.wosid000244386000003-
dc.identifier.bibliographicCitationAnalytica Chimica Acta, v.584, no.2, pp 252 - 259-
dc.citation.titleAnalytica Chimica Acta-
dc.citation.volume584-
dc.citation.number2-
dc.citation.startPage252-
dc.citation.endPage259-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.subject.keywordPlusPROTEIN ADSORPTION-
dc.subject.keywordPlusIMMUNOASSAYS-
dc.subject.keywordPlusFORCES-
dc.subject.keywordPlusFLOW-
dc.subject.keywordAuthorlatex immunoagglutination assay-
dc.subject.keywordAuthordiffusional mixing-
dc.subject.keywordAuthormicrofluidic device-
dc.subject.keywordAuthornon-specific binding-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0003267006022124?via%3Dihub-
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