CRP detection from serum for chip-based point-of-care testing system

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dc.contributor.authorKim, Chang-Hoonko
dc.contributor.authorAhn, Jae-Hyukko
dc.contributor.authorKim, Jee-Yeonko
dc.contributor.authorChoi, Ji-Minko
dc.contributor.authorLim, Kyung-Choonko
dc.contributor.authorPark, Tae-Jungko
dc.contributor.authorHeo, Nam-Suko
dc.contributor.authorLee, Hee-Guko
dc.contributor.authorKim, Jong-Wanko
dc.contributor.authorChoi, Yang-Kyuko
dc.date.accessioned2013-08-08T05:43:34Z-
dc.date.available2013-08-08T05:43:34Z-
dc.date.created2013-03-08-
dc.date.created2013-03-08-
dc.date.issued2013-03-
dc.identifier.citationBIOSENSORS & BIOELECTRONICS, v.41, pp.322 - 327-
dc.identifier.issn0956-5663-
dc.identifier.urihttp://hdl.handle.net/10203/174531-
dc.description.abstractMost of point-of-care testing (POCT) to improve facilitates in diagnosis, treatment, and monitoring of patients. POCT technique has still remained a quantitatively and accurately detective effect. In this article, we demonstrated that real human C-reactive protein (CRP) in serum was detected for a chip-based point-of-care testing application based on a nanogap-embedded field effect transistor (FET), and the results were compared with those obtained via the enzyme-linked immunosorbent assay (ELISA) method. The limit of detection (LOD), determined from the standard curve, was 0.1 ng/ml, which is comparable to that of commercialized ELISAs. We evaluated that an improved detection range (0.1 ng/ml to 100 ng/ml) was achieved by comparing with commercialized ELISA. Control experiments to determine selectivity and to discern false-positive/false-negative rates were also performed. This report is the first description of the detection of CRP in human serum using a silicon-based biosensor. (C) 2012 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER ADVANCED TECHNOLOGY-
dc.subjectC-REACTIVE PROTEIN-
dc.subjectSURFACE-PLASMON RESONANCE-
dc.subjectFIELD-EFFECT TRANSISTOR-
dc.subjectBIOSENSORS-
dc.subjectELISA-
dc.titleCRP detection from serum for chip-based point-of-care testing system-
dc.typeArticle-
dc.identifier.wosid000314191300046-
dc.identifier.scopusid2-s2.0-84870820491-
dc.type.rimsART-
dc.citation.volume41-
dc.citation.beginningpage322-
dc.citation.endingpage327-
dc.citation.publicationnameBIOSENSORS & BIOELECTRONICS-
dc.identifier.doi10.1016/j.bios.2012.08.047-
dc.contributor.localauthorChoi, Yang-Kyu-
dc.contributor.nonIdAuthorKim, Jee-Yeon-
dc.contributor.nonIdAuthorChoi, Ji-Min-
dc.contributor.nonIdAuthorLim, Kyung-Choon-
dc.contributor.nonIdAuthorPark, Tae-Jung-
dc.contributor.nonIdAuthorHeo, Nam-Su-
dc.contributor.nonIdAuthorLee, Hee-Gu-
dc.contributor.nonIdAuthorKim, Jong-Wan-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorC-reactive protein-
dc.subject.keywordAuthorCRP-
dc.subject.keywordAuthorNanogap-embedded FET-
dc.subject.keywordAuthorFET-based biosensor-
dc.subject.keywordAuthorPoint-of-care testing (POCT)-
dc.subject.keywordPlusC-REACTIVE PROTEIN-
dc.subject.keywordPlusSURFACE-PLASMON RESONANCE-
dc.subject.keywordPlusFIELD-EFFECT TRANSISTOR-
dc.subject.keywordPlusBIOSENSORS-
dc.subject.keywordPlusELISA-
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