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dc.contributor.authorZhang, Y-
dc.contributor.authorCai, X-
dc.contributor.authorChoi, SW-
dc.contributor.authorKim, C-
dc.contributor.authorWang, LHV-
dc.contributor.authorXia, YN-
dc.date.accessioned2016-03-31T08:29:03Z-
dc.date.available2016-03-31T08:29:03Z-
dc.date.created2013-07-31-
dc.date.issued2010-11-
dc.identifier.issn0142-9612-
dc.identifier.other2010-OAK-0000027899-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/15409-
dc.description.abstractVisualizing cells in three-dimensional (3D) scaffolds has been one of the major challenges in tissue engineering. Most current imaging modalities either suffer from poor penetration depth or require exogenous contrast agents. Here, we demonstrate photoacoustic microscopy (PAM) of the spatial distribution and temporal proliferation of cells inside three-dimensional porous scaffolds with thicknesses over 1 mm. Specifically, we evaluated the effects of seeding and culture methods on the spatial distribution of melanoma cells. Spatial distribution of the cells in the scaffold was well-resolved in PAM images. Moreover, the number of cells in the scaffold was quantitatively measured from the as-obtained volumetric information. The cell proliferation profile obtained from PAM correlated well with what was obtained using the traditional 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. (C) 2010 Elsevier Ltd. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherELSEVIER-
dc.relation.isPartOfBIOMATERIALS-
dc.subjectInverse opal scaffolds-
dc.subjectPhotoacoustic microscopy-
dc.subjectMelanoma-
dc.subjectTissue engineering-
dc.subjectBiomedical imaging-
dc.subjectIN-VIVO-
dc.subjectPOLYMER SCAFFOLDS-
dc.subject3D SCAFFOLDS-
dc.subjectTISSUE-
dc.subjectDIFFERENTIATION-
dc.subjectTOMOGRAPHY-
dc.subjectMIGRATION-
dc.subjectPERFUSION-
dc.subjectDESIGN-
dc.titleChronic label-free volumetric photoacoustic microscopy of melanoma cells in three-dimensional porous scaffolds-
dc.typeArticle-
dc.contributor.college전자전기공학과-
dc.identifier.doi10.1016/j.biomaterials.2010.07.089-
dc.author.googleZhang, Y-
dc.author.googleCai, X-
dc.author.googleChoi, SW-
dc.author.googleKim, C-
dc.author.googleWang, LHV-
dc.author.googleXia, YN-
dc.relation.volume31-
dc.relation.issue33-
dc.relation.startpage8651-
dc.relation.lastpage8658-
dc.contributor.id11117022-
dc.relation.journalBIOMATERIALS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOMATERIALS, v.31, no.33, pp.8651 - 8658-
dc.identifier.wosid000283912700016-
dc.date.tcdate2019-01-01-
dc.citation.endPage8658-
dc.citation.number33-
dc.citation.startPage8651-
dc.citation.titleBIOMATERIALS-
dc.citation.volume31-
dc.contributor.affiliatedAuthorKim, C-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc38-
dc.type.docTypeArticle-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlus3D SCAFFOLDS-
dc.subject.keywordPlusTISSUE-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusPERFUSION-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordAuthorInverse opal scaffolds-
dc.subject.keywordAuthorPhotoacoustic microscopy-
dc.subject.keywordAuthorMelanoma-
dc.subject.keywordAuthorTissue engineering-
dc.subject.keywordAuthorBiomedical imaging-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-

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