DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ko, S | ko |
dc.contributor.author | Kim, B | ko |
dc.contributor.author | Jo, SS | ko |
dc.contributor.author | Oh, SY | ko |
dc.contributor.author | Park, Je-Kyun | ko |
dc.date.accessioned | 2013-03-07T18:02:53Z | - |
dc.date.available | 2013-03-07T18:02:53Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 2007-08 | - |
dc.identifier.citation | BIOSENSORS & BIOELECTRONICS, v.23, pp.51 - 59 | - |
dc.identifier.issn | 0956-5663 | - |
dc.identifier.uri | http://hdl.handle.net/10203/90856 | - |
dc.description.abstract | A sensitive and rapid electrochemical microchip fabricated by assembling a surface-functionalized poly(dimethylsiloxane) (PDMS) microchannel with an interdigitated array (IDA) gold electrode was developed for the detection of human cardiac troponin I (cTnI) in the early diagnosis of acute myocardial infarction. Anti-cTnI was immobilized onto the internal surface of the PDMS channel on which protein G layer had been generated by silanization. To reduce electrode fouling, a PDMS channel was assembled with an IDA chip after surface treatment. The detection experiments were performed with successive injection of cTnI, alkaline phosphatase (AP)-labeled anti-cTnI, and p-aminophenylphosphate. Then, cyclic voltammograms were obtained by the oxidation peak current proportionally to the concentration of enzymatic product, p-aminophenol. The optimal packing density of anti-cTnI on the surface of the PDMS channel was determined at the anti-cTnI concentration of 30 mu g/n-d for the highest electrochemical signal. These demonstrate that the proper orientation and best packing density of antibody as well as no electrode fouling contributed to the low detection limit (148 pg/ml) of cTnI within 8 min. (C) 2007 Elsevier B.V. All rights reserved. | - |
dc.language | English | - |
dc.publisher | ELSEVIER ADVANCED TECHNOLOGY | - |
dc.subject | ACUTE MYOCARDIAL-INFARCTION | - |
dc.subject | SUBARACHNOID HEMORRHAGE | - |
dc.subject | ENZYME-IMMUNOASSAY | - |
dc.subject | IMMUNOSENSOR | - |
dc.subject | MARKERS | - |
dc.subject | MONOLAYERS | - |
dc.subject | ELECTRODE | - |
dc.subject | SYSTEMS | - |
dc.subject | INJURY | - |
dc.subject | SERUM | - |
dc.title | Electrochemical detection of cardiac troponin I using a microchip with the surface-functionalized poly(dimethylsiloxane) channel | - |
dc.type | Article | - |
dc.identifier.wosid | 000250325400006 | - |
dc.identifier.scopusid | 2-s2.0-34548488733 | - |
dc.type.rims | ART | - |
dc.citation.volume | 23 | - |
dc.citation.beginningpage | 51 | - |
dc.citation.endingpage | 59 | - |
dc.citation.publicationname | BIOSENSORS & BIOELECTRONICS | - |
dc.identifier.doi | 10.1016/j.bios.2007.03.013 | - |
dc.contributor.localauthor | Park, Je-Kyun | - |
dc.contributor.nonIdAuthor | Ko, S | - |
dc.contributor.nonIdAuthor | Kim, B | - |
dc.contributor.nonIdAuthor | Jo, SS | - |
dc.contributor.nonIdAuthor | Oh, SY | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordAuthor | electrochemical microchip | - |
dc.subject.keywordAuthor | human cardiac troponin I | - |
dc.subject.keywordAuthor | surface-functionalized PDMS channel | - |
dc.subject.keywordAuthor | alkaline phosphatase | - |
dc.subject.keywordPlus | ACUTE MYOCARDIAL-INFARCTION | - |
dc.subject.keywordPlus | SUBARACHNOID HEMORRHAGE | - |
dc.subject.keywordPlus | ENZYME-IMMUNOASSAY | - |
dc.subject.keywordPlus | IMMUNOSENSOR | - |
dc.subject.keywordPlus | MARKERS | - |
dc.subject.keywordPlus | MONOLAYERS | - |
dc.subject.keywordPlus | ELECTRODE | - |
dc.subject.keywordPlus | SYSTEMS | - |
dc.subject.keywordPlus | INJURY | - |
dc.subject.keywordPlus | SERUM | - |
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