Poly(dimethyl siloxane)-based protein chip for simultaneous detection of multiple samples: Use of glycidyl methacrylate photopolymer for site-specific protein immobilization

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dc.contributor.authorPark, Kyoung-Hwanko
dc.contributor.authorPark, Hyun-Gyuko
dc.contributor.authorKim, Joon-Hoko
dc.contributor.authorSeong, Ki-Hunko
dc.date.accessioned2010-11-15T06:34:40Z-
dc.date.available2010-11-15T06:34:40Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2006-12-
dc.identifier.citationBIOSENSORS & BIOELECTRONICS, v.22, no.5, pp.613 - 620-
dc.identifier.issn0956-5663-
dc.identifier.urihttp://hdl.handle.net/10203/19919-
dc.description.abstractThis paper describes fabrication of a poly(dimethyl siloxane) (PDMS)-based chip to analyze multiple protein interactions utilizing glycidyl methacrylate (GMA) photopolymer for a site-specific immobilization of capture proteins in a closed system. First, using one direction channels of a PDMS mold having cross-channels, GMA micropads were prepared by photopolymerizing GMA solution by 365 nm light irradiation at predetermined positions. After the first mold was replaced with a second mold having higher height or directly without mold changing, capture proteins were allowed to be covalently immobilized onto the surface of the epoxide-activated GMA pads. Following immobilization, poly(ethylene glycol) diacrylate (PEG-DA) precursor was photopolymerized at specific regions to generate plugs for prevention of mixing between different sample injection channels, diminishing the need of a mold changing for sample injections. Final chip was assembled by connecting separated sample injection channels using a connector mold. The viability of this strategy was successfully demonstrated by simultaneous detection of two different antigen-antibody interactions. (c) 2006 Elsevier B.V. All rights reserved.-
dc.description.sponsorshipThis research was supported by Samsung Advanced Institute of Technology (SAIT), Center for Ultramicrochemical Process Systems sponsored by KOSEF and Brain Korea 21 (BK 21) project.en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherELSEVIER ADVANCED TECHNOLOGY-
dc.subjectMICROFLUIDIC SYSTEMS-
dc.subjectFABRICATION-
dc.subjectDEVICES-
dc.subjectDNA-
dc.subjectEXPRESSION-
dc.subjectHYDROGELS-
dc.subjectPOLYMER-
dc.subjectMICROSTRUCTURES-
dc.subjectHYBRIDIZATION-
dc.subjectMICROARRAY-
dc.titlePoly(dimethyl siloxane)-based protein chip for simultaneous detection of multiple samples: Use of glycidyl methacrylate photopolymer for site-specific protein immobilization-
dc.typeArticle-
dc.identifier.wosid000242230800006-
dc.identifier.scopusid2-s2.0-33750969698-
dc.type.rimsART-
dc.citation.volume22-
dc.citation.issue5-
dc.citation.beginningpage613-
dc.citation.endingpage620-
dc.citation.publicationnameBIOSENSORS & BIOELECTRONICS-
dc.identifier.doi10.1016/j.bios.2006.01.029-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorPark, Hyun-Gyu-
dc.contributor.nonIdAuthorKim, Joon-Ho-
dc.contributor.nonIdAuthorSeong, Ki-Hun-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorglycidyl methacrylate-
dc.subject.keywordAuthorpoly(dimethyl siloxane) (PDMS)-
dc.subject.keywordAuthormicrofluidics-
dc.subject.keywordAuthorpoly(ethylene glycol) diacrylate-
dc.subject.keywordAuthorbiomolecular immobilization-
dc.subject.keywordPlusMICROFLUIDIC SYSTEMS-
dc.subject.keywordPlusFABRICATION-
dc.subject.keywordPlusDEVICES-
dc.subject.keywordPlusDNA-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusHYDROGELS-
dc.subject.keywordPlusPOLYMER-
dc.subject.keywordPlusMICROSTRUCTURES-
dc.subject.keywordPlusHYBRIDIZATION-
dc.subject.keywordPlusMICROARRAY-
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