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Reliable permeability assay system in a microfluidic device mimicking cerebral vasculatures

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dc.contributor.authorYeon, Ju Hun-
dc.contributor.authorNa, Dokyun-
dc.contributor.authorChoi, Kyungsun-
dc.contributor.authorRyu, Seung-Wook-
dc.contributor.authorChoi, Chulhee-
dc.contributor.authorPark, Je-Kyun-
dc.date.available2020-11-20T02:40:26Z-
dc.date.issued2012-12-
dc.identifier.issn1387-2176-
dc.identifier.issn1572-8781-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/43515-
dc.description.abstractSince most of the bioavailable drugs are impermeable through the blood-brain barrier (BBB), development of a rapid and reliable permeability assay system has been a challenge in drug discovery targeting central nervous system (CNS). Here, we designed a microfluidic device to monitor the drug permeability into the CNS. Human umbilical vein endothelial cells (HUVECs) were shortly (2 similar to 3 h) incubated with astrocyte-conditioned medium after being trapped on microholes in the microfluidic device and tested for chip-based permeability measurement of drugs. The measured permeability values were highly correlated with those measured by conventional in vitro methods and the brain uptake index representing the quantity of transported substances across the in vivo BBB of rats. Using the microfluidic device, we could easily monitor the effect of hydrogen peroxide on the trans-endothelial permeability, which are consistent with the finding that the same treatment disrupted the formation of tight junctions between endothelial cells. Considering relatively short period of time needed for endothelial cell culture and ability to monitor the BBB physiology continuously, we propose that this novel system can be used as an invaluable first-line tool for CNS-related drug development.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherSPRINGER-
dc.titleReliable permeability assay system in a microfluidic device mimicking cerebral vasculatures-
dc.typeArticle-
dc.identifier.doi10.1007/s10544-012-9680-5-
dc.identifier.bibliographicCitationBIOMEDICAL MICRODEVICES, v.14, no.6, pp 1141 - 1148-
dc.description.isOpenAccessN-
dc.identifier.wosid000312124100020-
dc.identifier.scopusid2-s2.0-84877043911-
dc.citation.endPage1148-
dc.citation.number6-
dc.citation.startPage1141-
dc.citation.titleBIOMEDICAL MICRODEVICES-
dc.citation.volume14-
dc.type.docTypeArticle-
dc.publisher.location네델란드-
dc.subject.keywordAuthorBlood-brain barrier-
dc.subject.keywordAuthorMicrofluidics-
dc.subject.keywordAuthorCell trapping-
dc.subject.keywordAuthorPermeability assay-
dc.subject.keywordPlusBLOOD-BRAIN-BARRIER-
dc.subject.keywordPlusIN-VITRO MODEL-
dc.subject.keywordPlusDRUG PERMEABILITY-
dc.subject.keywordPlusP-GLYCOPROTEIN-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusVIVO-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusPREDICTION-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusTRANSPORT-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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