Microfluidic cell disruption system employing a magnetically actuated diaphragm

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dc.contributor.authorHuh, Yun Sukko
dc.contributor.authorChoi, Jong Hyunko
dc.contributor.authorHuh, Kyoung Ae Kimko
dc.contributor.authorPark, Tae Jungko
dc.contributor.authorHong, Yeon Kiko
dc.contributor.authorKim, DoHyunko
dc.contributor.authorHong, Won-Hiko
dc.contributor.authorLee, SangYupko
dc.date.accessioned2010-11-19T06:20:37Z-
dc.date.available2010-11-19T06:20:37Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2007-12-
dc.identifier.citationELECTROPHORESIS, v.28, no.24, pp.4748 - 4757-
dc.identifier.issn0173-0835-
dc.identifier.urihttp://hdl.handle.net/10203/20156-
dc.description.abstractA microfluidic cell lysis chip equipped with a micromixer and SPE unit was developed and used for quantitative analysis of intracellular proteins. This miniaturized sample preparation system can be employed for any purpose where cell disruption is needed to obtain intracellular constituents for the subsequent analysis. This system comprises a magnetically actuated micromixer to disrupt cells, a hydrophobic valve to manipulate the cell lysate, and a packed porous polymerized monolith chamber for SPE and filtering debris from the cell lysate. Using recombinant Escherichia coli expressing intracellular enhanced green fluorescent protein (EGFP) and lipase as model bacteria, we optimized the cell disruption condition with respect to the lysis buffer composition, mixing time, and the frequency of the diaphragm in the micromixer, which was magnetically actuated by an external magnetic stirrer in the micromixer chamber. The lysed sample prepared under the optimal condition was purified by the packed SPE in the microfluidic chip. At a frequency of 1.96 Hz, the final cell lysis efficiency and relative fluorescence intensity of EGFP after the cell disruption process were greater than 90 and 94%, respectively. Thus, this microfluidic cell disruption chip can be used for the efficient lysis of cells for further analysis of intracellular contents in many applications.-
dc.description.sponsorshipThis work was supported by the Basic Research Program of the Korea Science & Engineering Foundation (grant no. R01- 2004-000-10681-0; Hong, W. H., Huh, Y. S. and Hong, Y. H.) and in part by MIC & IITA through IT Leading R&D Support Project (Lee, S. Y., Choi, J. H. and Park. T. J.).We thank Peter L. Bergquist, Macquarie University, New South Wales, Australia, for kindly providing the plasmid lipA-pET26b.en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleMicrofluidic cell disruption system employing a magnetically actuated diaphragm-
dc.typeArticle-
dc.identifier.wosid000252465600027-
dc.identifier.scopusid2-s2.0-37549067696-
dc.type.rimsART-
dc.citation.volume28-
dc.citation.issue24-
dc.citation.beginningpage4748-
dc.citation.endingpage4757-
dc.citation.publicationnameELECTROPHORESIS-
dc.identifier.doi10.1002/elps.200700366-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorKim, DoHyun-
dc.contributor.localauthorHong, Won-Hi-
dc.contributor.localauthorLee, SangYup-
dc.contributor.nonIdAuthorHuh, Yun Suk-
dc.contributor.nonIdAuthorChoi, Jong Hyun-
dc.contributor.nonIdAuthorHuh, Kyoung Ae Kim-
dc.contributor.nonIdAuthorPark, Tae Jung-
dc.contributor.nonIdAuthorHong, Yeon Ki-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorcell disruption-
dc.subject.keywordAuthorgreen fluorescent protein-
dc.subject.keywordAuthormagnetically actuated diaphragm micromixer-
dc.subject.keywordAuthormicrofluidic device-
dc.subject.keywordAuthorsolid-phase extraction-
dc.subject.keywordPlusDNA ANALYSIS-
dc.subject.keywordPlusCAPILLARY ELECTROPHORESIS-
dc.subject.keywordPlusSAMPLE PREPARATION-
dc.subject.keywordPlusLYSIS-
dc.subject.keywordPlusDEVICE-
dc.subject.keywordPlusSEPARATION-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusCHIP-
dc.subject.keywordPlusEXTRACTION-
dc.subject.keywordPlusSPORES-
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