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Cited 9 time in webofscience Cited 9 time in scopus
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dc.contributor.authorPark, J-
dc.contributor.authorToner, M-
dc.contributor.authorYarmush, ML-
dc.contributor.authorTilles, AW-
dc.date.accessioned2016-04-01T08:32:02Z-
dc.date.available2016-04-01T08:32:02Z-
dc.date.created2009-09-03-
dc.date.issued2006-11-
dc.identifier.issn1613-4982-
dc.identifier.other2006-OAK-0000018617-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/28189-
dc.description.abstractAn extracorporeal bioartificial liver (BAL) device containing viable hepatocytes has the potential to provide temporary hepatic support to liver failure patients, serving as a bridge to transplantation while awaiting a suitable donor. In some patients, providing temporary hepatic support may be sufficient to allow adequate regeneration of the host liver, thereby eliminating the need for a liver transplant. Although the BAL device is a promising technology for the treatment of liver failure, there are several technical challenges that must be overcome in order to develop systems with sufficient processing capacity and of manageable size. In this study, the authors describe the critical issues involved in developing a BAL device. They also discuss their experiences in hepatocyte culture optimization within the context of a microchannel flat-plate BAL device.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherSPRINGER HEIDELBERG-
dc.relation.isPartOfMICROFLUIDICS AND NANOFLUIDICS-
dc.subjectoxygen-
dc.subjecthepatocyte-
dc.subjectmicrogrooves-
dc.subjectbioreactor-
dc.subjectshear stress-
dc.subjectOXYGEN-UPTAKE RATES-
dc.subjectI CLINICAL-TRIAL-
dc.subjectPHASE-I-
dc.subjectCULTURED-HEPATOCYTES-
dc.subjectHEPATIC-FAILURE-
dc.subjectEXPERIENCE-
dc.subjectPERFUSION-
dc.subjectSYSTEM-
dc.subjectCELLS-
dc.subjectMULTICENTER-
dc.titleMicrochannel bioreactors for bioartificial liver support-
dc.typeArticle-
dc.contributor.college기계공학과-
dc.identifier.doi10.1007/S10404-006-0095-6-
dc.author.googlePark, J-
dc.author.googleToner, M-
dc.author.googleYarmush, ML-
dc.author.googleTilles, AW-
dc.relation.volume2-
dc.relation.issue6-
dc.relation.startpage525-
dc.relation.lastpage535-
dc.contributor.id10093923-
dc.relation.journalMICROFLUIDICS AND NANOFLUIDICS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCIE-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationMICROFLUIDICS AND NANOFLUIDICS, v.2, no.6, pp.525 - 535-
dc.identifier.wosid000242225600007-
dc.date.tcdate2019-02-01-
dc.citation.endPage535-
dc.citation.number6-
dc.citation.startPage525-
dc.citation.titleMICROFLUIDICS AND NANOFLUIDICS-
dc.citation.volume2-
dc.contributor.affiliatedAuthorPark, J-
dc.identifier.scopusid2-s2.0-33750340227-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc7-
dc.description.scptc6*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusOXYGEN-UPTAKE RATES-
dc.subject.keywordPlusPHASE-I-
dc.subject.keywordPlusCULTURED-HEPATOCYTES-
dc.subject.keywordPlusCLINICAL-EXPERIENCE-
dc.subject.keywordPlusCONTROLLED-TRIAL-
dc.subject.keywordPlusFAILURE-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusPERFUSION-
dc.subject.keywordPlusDIALYSIS-
dc.subject.keywordPlusASSIST-
dc.subject.keywordAuthoroxygen-
dc.subject.keywordAuthorhepatocyte-
dc.subject.keywordAuthormicrogrooves-
dc.subject.keywordAuthorbioreactor-
dc.subject.keywordAuthorshear stress-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryInstruments & Instrumentation-
dc.relation.journalWebOfScienceCategoryPhysics, Fluids & Plasmas-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaInstruments & Instrumentation-
dc.relation.journalResearchAreaPhysics-

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