Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/12390
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dc.contributor.authorKara, Aylinen_US
dc.contributor.authorDistler, Thomasen_US
dc.contributor.authorPolley, Christianen_US
dc.contributor.authorSchneidereit, Dominiken_US
dc.contributor.authorSeitz, Hermannen_US
dc.contributor.authorFriedrich, Oliveren_US
dc.contributor.authorTıhmınlıoğlu, Fundaen_US
dc.contributor.authorBoccaccini, Aldo Ren_US
dc.date.accessioned2022-08-16T08:53:01Z-
dc.date.available2022-08-16T08:53:01Z-
dc.date.issued2022-06-
dc.identifier.urihttps://doi.org/10.1016/j.mtbio.2022.100309-
dc.identifier.urihttps://hdl.handle.net/11147/12390-
dc.description.abstractThree-dimensional (3D) printing technology enables the design of personalized scaffolds with tunable pore size and composition. Combining decellularization and 3D printing techniques provides the opportunity to fabricate scaffolds with high potential to mimic native tissue. The aim of this study is to produce novel decellularized bone extracellular matrix (dbECM)-reinforced composite-scaffold that can be used as a biomaterial for bone tissue engineering. Decellularized bone particles (dbPTs, ∼100 ​μm diameter) were obtained from rabbit femur and used as a reinforcement agent by mixing with gelatin (GEL) in different concentrations. 3D scaffolds were fabricated by using an extrusion-based bioprinter and crosslinking with microbial transglutaminase (mTG) enzyme, followed by freeze-drying to obtain porous structures. Fabricated 3D scaffolds were characterized morphologically, mechanically, and chemically. Furthermore, MC3T3-E1 mouse pre-osteoblast cells were seeded on the dbPTs reinforced GEL scaffolds (GEL/dbPTs) and cultured for 21 days to assess cytocompatibility and cell attachment. We demonstrate the 3D-printability of dbPTs-reinforced GEL hydrogels and the achievement of homogenous distribution of the dbPTs in the whole scaffold structure, as well as bioactivity and cytocompatibility of GEL/dbPTs scaffolds. It was shown that Young's modulus and degradation rate of scaffolds were enhanced with increasing dbPTs content. Multiphoton microscopy imaging displayed the interaction of cells with dbPTs, indicating attachment and proliferation of cells around the particles as well as into the GEL-particle hydrogels. Our results demonstrate that GEL/dbPTs hydrogel formulations have potential for bone tissue engineering.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofMaterials Today Bioen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBone tissue engineeringen_US
dc.subjectComposite scaffoldsen_US
dc.subjectDecellularized bone extracellular matrixen_US
dc.subjectThree-dimensional printingen_US
dc.subjectMicrobial transglutaminaseen_US
dc.title3D printed gelatin/decellularized bone composite scaffolds for bone tissue engineering: Fabrication, characterization and cytocompatibility studyen_US
dc.typeArticleen_US
dc.authorid0000-0001-8302-913Xen_US
dc.authorid0000-0002-3715-8253en_US
dc.institutionauthorKara, Aylinen_US
dc.institutionauthorTıhmınlıoğlu, Fundaen_US
dc.departmentİzmir Institute of Technology. Chemical Engineeringen_US
dc.departmentİzmir Institute of Technology. Bioengineeringen_US
dc.identifier.wosWOS:000813479900001en_US
dc.identifier.scopus2-s2.0-85132223046en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1016/j.mtbio.2022.100309-
dc.identifier.pmid35757025-
dc.contributor.affiliation01. Izmir Institute of Technologyen_US
dc.contributor.affiliationFriedrich-Alexander Universität Erlangen-Nürnbergen_US
dc.contributor.affiliationUniversität Rostocken_US
dc.contributor.affiliationFriedrich-Alexander Universität Erlangen-Nürnbergen_US
dc.contributor.affiliationUniversität Rostocken_US
dc.contributor.affiliationFriedrich-Alexander Universität Erlangen-Nürnbergen_US
dc.contributor.affiliation01. Izmir Institute of Technologyen_US
dc.contributor.affiliationFriedrich-Alexander Universität Erlangen-Nürnbergen_US
dc.relation.issn2590-0064en_US
dc.description.volume15en_US
dc.identifier.scopusqualityQ1-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.languageiso639-1en-
item.fulltextWith Fulltext-
crisitem.author.dept01.01. Units Affiliated to the Rectorate-
crisitem.author.dept03.02. Department of Chemical Engineering-
Appears in Collections:Bioengineering / Biyomühendislik
Chemical Engineering / Kimya Mühendisliği
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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