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Non-invasive in vivo monitoring of transplanted stem cells in 3D-bioprinted constructs using near-infrared fluorescent imaging

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dc.contributor.authorKim, Soon Hee-
dc.contributor.authorKwon, Jin Seon-
dc.contributor.authorCho, Jae Gu-
dc.contributor.authorPark, Kate G.-
dc.contributor.authorLim, Tae Hyeon-
dc.contributor.authorKim, Moon Suk-
dc.contributor.authorChoi, Hak Soo-
dc.contributor.authorPark, Chan Hum-
dc.contributor.authorLee, Sang Jin-
dc.date.accessioned2021-11-20T17:40:54Z-
dc.date.available2021-11-20T17:40:54Z-
dc.date.created2021-08-30-
dc.date.issued2021-05-
dc.identifier.issn2380-6761-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/128141-
dc.description.abstractCell-based tissue engineering strategies have been widely established. However, the contributions of the transplanted cells within the tissue-engineered scaffolds to the process of tissue regeneration remain poorly understood. Near-infrared (NIR) fluorescence imaging systems have great potential to non-invasively monitor the transplanted cell-based tissue constructs. In this study, labeling mesenchymal stem cells (MSCs) using a lipophilic pentamethine indocyanine (CTNF127, emission at 700 nm) as a NIR fluorophore was optimized, and the CTNF127-labeled MSCs (NIR-MSCs) were printed embedding in gelatin methacryloyl bioink. The NIR-MSCs-loaded bioink showed excellent printability. In addition, NIR-MSCs in the 3D constructs showed high cell viability and signal stability for an extended period in vitro. Finally, we were able to non-invasively monitor the NIR-MSCs in constructs after implantation in a rat calvarial bone defect model, and the transplanted cells contributed to tissue formation without specific staining. This NIR-based imaging system for non-invasive cell monitoring in vivo could play an active role in validating the cell fate in cell-based tissue engineering applications.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-
dc.titleNon-invasive in vivo monitoring of transplanted stem cells in 3D-bioprinted constructs using near-infrared fluorescent imaging-
dc.typeArticle-
dc.contributor.affiliatedAuthorCho, Jae Gu-
dc.identifier.doi10.1002/btm2.10216-
dc.identifier.scopusid2-s2.0-85103170837-
dc.identifier.wosid000632929800001-
dc.identifier.bibliographicCitationBIOENGINEERING & TRANSLATIONAL MEDICINE, v.6, no.2-
dc.relation.isPartOfBIOENGINEERING & TRANSLATIONAL MEDICINE-
dc.citation.titleBIOENGINEERING & TRANSLATIONAL MEDICINE-
dc.citation.volume6-
dc.citation.number2-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusAMNIOTIC-FLUID-
dc.subject.keywordPlusBONE-FORMATION-
dc.subject.keywordPlusDEFECTS-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusREGENERATION-
dc.subject.keywordPlusSCAFFOLD-
dc.subject.keywordPlusSTROMAL CELLS-
dc.subject.keywordPlusTHICKNESS-
dc.subject.keywordPlusTISSUE-
dc.subject.keywordAuthorinfrared fluorescence-
dc.subject.keywordAuthorinvasive monitoring-
dc.subject.keywordAuthornear&amp-
dc.subject.keywordAuthor#8208-
dc.subject.keywordAuthornon&amp-
dc.subject.keywordAuthor#8208-
dc.subject.keywordAuthorscaffold monitoring-
dc.subject.keywordAuthorstem cell tracking-
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