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Scaffold-Free Three-Dimensional Cell Culturing Using Magnetic Levitation

dc.contributor.author Türker, Esra
dc.contributor.author Demirçak, Nida
dc.contributor.author Arslan Yıldız, Ahu
dc.contributor.other 03.01. Department of Bioengineering
dc.contributor.other 01.01. Units Affiliated to the Rectorate
dc.contributor.other 01. Izmir Institute of Technology
dc.contributor.other 03. Faculty of Engineering
dc.coverage.doi 10.1039/c8bm00122g
dc.date.accessioned 2020-01-21T08:11:24Z
dc.date.available 2020-01-21T08:11:24Z
dc.date.issued 2018-07
dc.description.abstract Three-dimensional (3D) cell culture has emerged as a pioneering methodology and is increasingly utilized for tissue engineering, 3D bioprinting, cancer model studies and drug development studies. The 3D cell culture methodology provides artificial and functional cellular constructs serving as a modular playground prior to animal model studies, which saves substantial efforts, time and experimental costs. The major drawback of current 3D cell culture methods is their dependency on biocompatible scaffolds, which often require tedious syntheses and fabrication steps. Herein, we report an easy-to-use methodology for the formation of scaffold-free 3D cell culture and cellular assembly via magnetic levitation in the presence of paramagnetic agents. To paramagnetize the cell culture environment, three different Gadolinium(iii) chelates were utilized, which led to levitation and assembly of cells at a certain levitation height. The assembly and close interaction of cells at the levitation height where the magnetic force was equilibrated with gravitational force triggered the formation of complex 3D cellular structures. It was shown that Gd(iii) chelates provided an optimal levitation that induced intercellular interactions in scaffold-free format without compromising cell viability. NIH 3T3 mouse fibroblasts and HCC827 non-small-cell lung cancer cells were evaluated via the magnetic levitation system, and the formation of 3D cell culture models was validated for both cell lines. Hereby, the developed magnetic levitation system holds promises for complex cellular assemblies and 3D cell culture studies. en_US
dc.description.sponsorship IYTE BAP; 2016IYTE70 en_US
dc.identifier.citation Türker, E., Demirçak, N., and Arslan Yıldız, A. (2018). Scaffold-free three-dimensional cell culturing using magnetic levitation. Biomaterials Science, 6(7), 1745-1753. doi:10.1039/c8bm00122g en_US
dc.identifier.doi 10.1039/c8bm00122g en_US
dc.identifier.issn 2047-4830
dc.identifier.issn 2047-4830
dc.identifier.issn 2047-4849
dc.identifier.scopus 2-s2.0-85049070854
dc.identifier.uri https://doi.org/10.1039/C8BM00122G
dc.identifier.uri https://hdl.handle.net/11147/7606
dc.language.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.relation.ispartof Biomaterials Science en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Cell culture en_US
dc.subject Magnetic levitation en_US
dc.subject 3D cellular structure en_US
dc.subject Biocompatible scaffolds en_US
dc.subject Gadolinium compounds en_US
dc.title Scaffold-Free Three-Dimensional Cell Culturing Using Magnetic Levitation en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id 0000-0003-0348-0575
gdc.author.institutional Türker, Esra
gdc.author.institutional Türker, Esra
gdc.author.institutional Arslan Yıldız, Ahu
gdc.author.institutional Arslan Yıldız, Ahu
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.description.department İzmir Institute of Technology. Bioengineering en_US
gdc.description.endpage 1753 en_US
gdc.description.issue 7 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 1745 en_US
gdc.description.volume 6 en_US
gdc.description.wosquality Q2
gdc.identifier.openalex W2800428612
gdc.identifier.pmid 29700506
gdc.identifier.wos WOS:000447710700007
gdc.openalex.fwci 4.482
gdc.openalex.normalizedpercentile 1.0
gdc.openalex.toppercent TOP 1%
gdc.opencitations.count 72
gdc.scopus.citedcount 73
gdc.wos.citedcount 74
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