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Photo-crosslinkable hydrogel-based 3D microfluidic culture device

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dc.contributor.authorLee, Youlee-
dc.contributor.authorLee, Jong Min-
dc.contributor.authorBae, Pan-Kee-
dc.contributor.authorChung, Il Yup-
dc.contributor.authorChung, Bong Hyun-
dc.contributor.authorChung, Bong Geun-
dc.date.accessioned2021-06-22T20:22:17Z-
dc.date.available2021-06-22T20:22:17Z-
dc.date.issued2015-04-
dc.identifier.issn0173-0835-
dc.identifier.issn1522-2683-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/18769-
dc.description.abstractWe developed the photo-crosslinkable hydrogel-based 3D microfluidic device to culture neural stem cells (NSCs) and tumors. The photo-crosslinkable gelatin methacrylate (GelMA) polymer was used as a physical barrier in the microfluidic device and collagen type I gel was employed to culture NSCs in a 3D manner. We demonstrated that the pore size was inversely proportional to concentrations of GelMA hydrogels, showing the pore sizes of 5 and 25 w/v% GelMA hydrogels were 34 and 4 m, respectively. It also revealed that the morphology of pores in 5 w/v% GelMA hydrogels was elliptical shape, whereas we observed circular-shaped pores in 25 w/v% GelMA hydrogels. To culture NSCs and tumors in the 3D microfluidic device, we investigated the molecular diffusion properties across GelMA hydrogels, indicating that 25 w/v% GelMA hydrogels inhibited the molecular diffusion for 6 days in the 3D microfluidic device. In contrast, the chemicals were diffused in 5 w/v% GelMA hydrogels. Finally, we cultured NSCs and tumors in the hydrogel-based 3D microfluidic device, showing that 53-75% NSCs differentiated into neurons, while tumors were cultured in the collagen gels. Therefore, this photo-crosslinkable hydrogel-based 3D microfluidic culture device could be a potentially powerful tool for regenerative tissue engineering applications.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherJohn Wiley & Sons Ltd.-
dc.titlePhoto-crosslinkable hydrogel-based 3D microfluidic culture device-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1002/elps.201400465-
dc.identifier.scopusid2-s2.0-84927702482-
dc.identifier.wosid000353052800004-
dc.identifier.bibliographicCitationElectrophoresis, v.36, no.7-8, pp 994 - 1001-
dc.citation.titleElectrophoresis-
dc.citation.volume36-
dc.citation.number7-8-
dc.citation.startPage994-
dc.citation.endPage1001-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.subject.keywordPlusNEURAL STEM-CELLS-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusPLATFORM-
dc.subject.keywordPlusCOCULTURE-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusMODEL-
dc.subject.keywordAuthorHydrogel-
dc.subject.keywordAuthorMicrofluidic device-
dc.subject.keywordAuthorStem cell-
dc.identifier.urlhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/elps.201400465-
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