DC Field | Value | Language |
---|---|---|
dc.contributor.author | Oh, Seung Jun | ko |
dc.contributor.author | Park, Byung Hyun | ko |
dc.contributor.author | Jung, Jae Hwan | ko |
dc.contributor.author | Choi, Goro | ko |
dc.contributor.author | Lee, DohChang | ko |
dc.contributor.author | Kim, Do Hyun | ko |
dc.contributor.author | Seo, Tae Seok | ko |
dc.date.accessioned | 2016-04-14T02:50:02Z | - |
dc.date.available | 2016-04-14T02:50:02Z | - |
dc.date.created | 2015-11-09 | - |
dc.date.created | 2015-11-09 | - |
dc.date.created | 2015-11-09 | - |
dc.date.issued | 2016-01 | - |
dc.identifier.citation | BIOSENSORS & BIOELECTRONICS, v.75, pp.293 - 300 | - |
dc.identifier.issn | 0956-5663 | - |
dc.identifier.uri | http://hdl.handle.net/10203/203662 | - |
dc.description.abstract | We present a centrifugal microfluidic device which enables multiplex foodborne pathogen identification by loop-mediated isothermal amplification (LAMP) and colorimetric detection using Eriochrome Black T (EBT). Five identical structures were designed in the centrifugal microfluidic system to perform the genetic analysis of 25 pathogen samples in a high-throughput manner. The sequential loading and all-quoting of the LAMP cocktail, the primer mixtures, and the DNA sample solutions were accomplished by the optimized zigzag-shaped microchannels and RPM control. We targeted three kinds of pathogenic bacteria (Escherichia coli O157:H7, Salmonella typhimurlum and Vibrio parahaemolyticus) and detected the amplicons of the LAMP reaction by the EBT-mediated colorimetric method. For the limit-of-detection (LOD) test, we carried out the LAMP reaction on a chip with serially diluted DNA templates of E. coli O157:H7, and could observe the color change with 380 copies. The used primer sets in the LAMP reaction were specific only to the genomic DNA of E. coli O157:H7, enabling the on-chip selective, sensitive, and highthroughput pathogen identification with the naked eyes. The entire process was completed in 60 min. Since the proposed microsystem does not require any bulky and expensive instrumentation for endpoint detection, our microdevice would be adequate for point-of-care (POC) testing with high simplicity and high speed, providing an advanced genetic analysis microsystem for foodborne pathogen detection. | - |
dc.language | English | - |
dc.publisher | ELSEVIER ADVANCED TECHNOLOGY | - |
dc.title | Centrifugal loop-mediated isothermal amplification microdevice for rapid, multiplex and colorimetric foodborne pathogen detection | - |
dc.type | Article | - |
dc.identifier.wosid | 000362862000038 | - |
dc.identifier.scopusid | 2-s2.0-84941309557 | - |
dc.type.rims | ART | - |
dc.citation.volume | 75 | - |
dc.citation.beginningpage | 293 | - |
dc.citation.endingpage | 300 | - |
dc.citation.publicationname | BIOSENSORS & BIOELECTRONICS | - |
dc.identifier.doi | 10.1016/j.bios.2015.08.052 | - |
dc.contributor.localauthor | Lee, DohChang | - |
dc.contributor.localauthor | Kim, Do Hyun | - |
dc.contributor.localauthor | Seo, Tae Seok | - |
dc.contributor.nonIdAuthor | Choi, Goro | - |
dc.description.isOpenAccess | N | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordAuthor | Centrifugal microdevice | - |
dc.subject.keywordAuthor | Foodborne pathogen | - |
dc.subject.keywordAuthor | Loop-mediated isothermal amplification | - |
dc.subject.keywordAuthor | Colorimetric detection | - |
dc.subject.keywordAuthor | Multiplex detection | - |
dc.subject.keywordPlus | INFLUENZA-A VIRUS | - |
dc.subject.keywordPlus | IMMUNOCHROMATOGRAPHIC STRIP | - |
dc.subject.keywordPlus | BACTERIA | - |
dc.subject.keywordPlus | ASSAY | - |
dc.subject.keywordPlus | MICROSYSTEM | - |
dc.subject.keywordPlus | PLATFORMS | - |
dc.subject.keywordPlus | SYSTEM | - |
dc.subject.keywordPlus | DEVICE | - |
dc.subject.keywordPlus | CHIP | - |
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