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Bioactive Carbon Dots from Clove Residue: Synthesis, Characterization, and Osteogenic Properties

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dc.contributor.authorHong, Hye-Sun-
dc.contributor.authorPark, Hee-Jung-
dc.contributor.authorLee, Ji-Min-
dc.contributor.authorChen, Zu-Yu-
dc.contributor.authorKim, Tae-Woo-
dc.contributor.authorSeo, Yong-Seok-
dc.contributor.authorKang, Jun-Won-
dc.contributor.authorSeo, Young-Kwon-
dc.date.accessioned2025-03-12T07:00:19Z-
dc.date.available2025-03-12T07:00:19Z-
dc.date.issued2025-02-
dc.identifier.issn2227-9059-
dc.identifier.issn2227-9059-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/57982-
dc.description.abstractBackground/Objectives: Bone regeneration using nanomaterial-based approaches shows promise for treating critical bone defects. However, developing sustainable and cost-effective therapeutic materials remains challenging. This study investigates the osteogenic potential of clove-derived carbon dots (C-CDs) for bone regeneration applications. Methods: C-CDs were synthesized using a green hydrothermal method. The osteogenic potential was evaluated in human bone marrow-derived mesenchymal stem cells (hBM-MSCs) and validated using ectopic bone formation and calvarial defect models. Results: C-CDs demonstrated uniform morphology (similar to 10 nm) with efficient cellular uptake. In vitro studies showed successful osteogenic differentiation through the upregulation of RUNX2, ALP, COL1A1, and BMP-2 mediated by Wnt/beta-catenin/GSK3 beta and BMP signaling pathways. In vivo models have also demonstrated that C-CDs are effective in promoting bone regeneration. Conclusions: These findings establish C-CDs as promising candidates for bone regeneration therapy, offering a sustainable alternative to current treatments. While optimization is needed, their demonstrated osteogenic properties warrant further development for regenerative medicine applications.-
dc.format.extent22-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleBioactive Carbon Dots from Clove Residue: Synthesis, Characterization, and Osteogenic Properties-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/biomedicines13020527-
dc.identifier.scopusid2-s2.0-85218913942-
dc.identifier.wosid001431031500001-
dc.identifier.bibliographicCitationBiomedicines, v.13, no.2, pp 1 - 22-
dc.citation.titleBiomedicines-
dc.citation.volume13-
dc.citation.number2-
dc.citation.startPage1-
dc.citation.endPage22-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusMESENCHYMAL STEM-CELLS-
dc.subject.keywordPlusNANOPARTICLE SIZE-
dc.subject.keywordPlusQUANTUM DOTS-
dc.subject.keywordPlusBONE-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordAuthorcarbon dots-
dc.subject.keywordAuthorclove-
dc.subject.keywordAuthorgreen synthesis-
dc.subject.keywordAuthorbone regeneration-
dc.subject.keywordAuthorosteogenic differentiation-
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