Photo-crosslinkable hydrogel-based 3D microfluidic culture device

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dc.contributor.authorY Lee-
dc.contributor.authorJ M Lee-
dc.contributor.authorPan Kee Bae-
dc.contributor.authorI Y Chung-
dc.contributor.authorBong Hyun Chung-
dc.contributor.authorB G Chung-
dc.date.accessioned2017-04-19T10:03:45Z-
dc.date.available2017-04-19T10:03:45Z-
dc.date.issued2015-
dc.identifier.issn0173-0835-
dc.identifier.uri10.1002/elps.201400465ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/12588-
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 μm, 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.publisherWiley-
dc.titlePhoto-crosslinkable hydrogel-based 3D microfluidic culture device-
dc.title.alternativePhoto-crosslinkable hydrogel-based 3D microfluidic culture device-
dc.typeArticle-
dc.citation.titleElectrophoresis-
dc.citation.number7-
dc.citation.endPage1001-
dc.citation.startPage994-
dc.citation.volume36-
dc.contributor.affiliatedAuthorPan Kee Bae-
dc.contributor.affiliatedAuthorBong Hyun Chung-
dc.contributor.alternativeName이유리-
dc.contributor.alternativeName이종민-
dc.contributor.alternativeName배판기-
dc.contributor.alternativeName정일엽-
dc.contributor.alternativeName정봉현-
dc.contributor.alternativeName정봉근-
dc.identifier.bibliographicCitationElectrophoresis, vol. 36, no. 7, pp. 994-1001-
dc.identifier.doi10.1002/elps.201400465-
dc.subject.keywordHydrogel-
dc.subject.keywordMicrofluidic device-
dc.subject.keywordStem cell-
dc.subject.localHydrogels-
dc.subject.localhydrogel-
dc.subject.localhydrogels-
dc.subject.localHydrogel-
dc.subject.localmicrofluidic device-
dc.subject.localMicrofluidic devices-
dc.subject.localMicrofluidic device-
dc.subject.localstem cells-
dc.subject.localstem cell-
dc.subject.localStem cell-
dc.subject.localStem cells-
dc.subject.localStem Cell-
dc.description.journalClassY-
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