Direct Write Assembly of Graphene/Poly(ε-Caprolactone) Composite Scaffolds and Evaluation of Their Biological Performance Using Mouse Bone Marrow Mesenchymal Stem Cells
dc.contributor.author | Deliormanli, AM | |
dc.date.accessioned | 2024-07-18T11:40:17Z | |
dc.date.available | 2024-07-18T11:40:17Z | |
dc.description.abstract | Scaffold and mesenchymal stem cell-based cartilage tissue engineering offers a favorable way for the repair and regeneration of injured cartilage. In this study, poly (epsilon-caprolactone) PCL scaffolds with grid-like structure having periodic lattice was manufactured by robocasting method in the presence of graphene nanoplatelets for cartilage tissue engineering applications. For this purpose, a PCL solution (20wt%) containing pristine graphene nanopowders in the form of platelets was prepared as printing ink and it was dispensed through a nozzle at room temperature to an ethanol bath at 4 degrees C. The construction of porous scaffolds was made by a layer-by-layer assembly. Results revealed that graphene additions were not detrimental to deposition process and the structure of the resultant scaffolds. In vitro cell tests indicated that the prepared grid-like graphene/PCL composite scaffolds have good cytocompatibility and non-toxicity for mouse bone marrow mesenchymal stem cells. The stem cells attached and proliferated well on the scaffolds and they also demonstrated a chondrogenic differentiation in the absence of transforming growth factors. | |
dc.identifier.issn | 0273-2289 | |
dc.identifier.other | 1559-0291 | |
dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/2289 | |
dc.language.iso | English | |
dc.publisher | SPRINGER | |
dc.subject | IN-VITRO CHONDROGENESIS | |
dc.subject | GRAPHENE OXIDE | |
dc.subject | DIFFERENTIATION | |
dc.subject | DEGRADATION | |
dc.subject | PCL | |
dc.subject | MEMBRANE | |
dc.subject | CYTOTOXICITY | |
dc.subject | COPOLYMERS | |
dc.title | Direct Write Assembly of Graphene/Poly(ε-Caprolactone) Composite Scaffolds and Evaluation of Their Biological Performance Using Mouse Bone Marrow Mesenchymal Stem Cells | |
dc.type | Article |