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dc.contributor.authorTeng, W-
dc.contributor.authorBAN, CHANGILL-
dc.contributor.authorHahn, JH-
dc.date.accessioned2015-07-22T19:04:43Z-
dc.date.available2015-07-22T19:04:43Z-
dc.date.created2015-06-18-
dc.date.issued2015-03-
dc.identifier.issn1932-1058-
dc.identifier.other2015-OAK-0000033008en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/13208-
dc.description.abstractThis paper describes a new and facile approach for the formation of pore-spanning bilayer lipid membranes (BLMs) within a poly(dimethylsiloxane) (PDMS) microfluidic device. Commercially, readily available polycarbonate (PC) membranes are employed for the support of BLMs. PC sheets with 5 mu m, 2 mu m, and 0.4 mu m pore diameters, respectively, are thermally bonded into a multilayer-stack, reducing the pore density of 0.4 mu m-pore PC by a factor of 200. The BLMs on this support are considerably stable (a mean lifetime: 17 h). This multilayer-stack PC (MSPC) membrane is integrated into the PDMS chip by an epoxy bonding method developed to secure durable bonding under the use of organic solvents. The microchip has a special channel for guiding a micropipette in the proximity of the MSPC support. With this on-site injection technique, tens to hundreds of nanoliters of solutions can be directly dispensed to the support. Incorporating gramicidin ion channels into BLMs on the MSPC support has confirmed the formation of single BLMs, which is based on the observation from current signals of 20 pS conductance that is typical to single channel opening. Based on the bilayer capacitance (1.4 pF), about 15% of through pores across the MSPC membrane are estimated to be covered with BLMs. (C) 2015 AIP Publishing LLC.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherAMER INST PHYSICS-
dc.relation.isPartOfBIOMICROFLUIDICS-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleFormation of lipid bilayer membrane in a poly(dimethylsiloxane) microchip integrated with a stacked polycarbonate membrane support and an on-site nanoinjector-
dc.typeArticle-
dc.contributor.college화학과en_US
dc.identifier.doi10.1063/1.4919066-
dc.author.googleTeng, Wen_US
dc.author.googleBan, Cen_US
dc.author.googleHahn, JHen_US
dc.relation.volume9en_US
dc.relation.issue2en_US
dc.contributor.id10085220en_US
dc.relation.journalBIOMICROFLUIDICSen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIEen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOMICROFLUIDICS, v.9, no.2-
dc.identifier.wosid000353829200028-
dc.date.tcdate2018-03-23-
dc.citation.number2-
dc.citation.titleBIOMICROFLUIDICS-
dc.citation.volume9-
dc.contributor.affiliatedAuthorBAN, CHANGILL-
dc.contributor.affiliatedAuthorHahn, JH-
dc.identifier.scopusid2-s2.0-84928346232-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.scptc0*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle; Proceedings Paper-
dc.subject.keywordPlusMECHANICAL-PROPERTIES-
dc.subject.keywordPlusCHANNEL RECORDINGS-
dc.subject.keywordPlusPOROUS MEMBRANES-
dc.subject.keywordPlusRECONSTITUTION-
dc.subject.keywordPlusARRAY-
dc.subject.keywordPlusCONDUCTANCE-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusLIFETIME-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryPhysics, Fluids & Plasmas-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaPhysics-

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Dept of Chemistry
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