Publication:
An easy-to-fabricate microfluidic shallow trench induced three-dimensional cell culturing and imaging (STICI3D) platform

dc.contributor.coauthorCoşkun, Umut Can
dc.contributor.coauthorRehman, Ateeq Ur
dc.contributor.coauthorGülle, Merve
dc.contributor.coauthorErten, Ahmet
dc.contributor.departmentN/A
dc.contributor.departmentDepartment of Physics
dc.contributor.departmentDepartment of Electrical and Electronics Engineering
dc.contributor.departmentN/A
dc.contributor.kuauthorBaşer, Hatice Nur
dc.contributor.kuauthorBaysal, Kemal
dc.contributor.kuauthorKiraz, Alper
dc.contributor.kuauthorKul, Demet
dc.contributor.kuauthorKuş, Funda
dc.contributor.kuauthorMorova, Berna
dc.contributor.kuprofileFaculty Member
dc.contributor.kuprofileFaculty Member
dc.contributor.kuprofileResearcher
dc.contributor.otherDepartment of Physics
dc.contributor.otherDepartment of Electrical and Electronics Engineering
dc.contributor.researchcenterKoç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM)
dc.contributor.schoolcollegeinstituteGraduate School of Sciences and Engineering
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.contributor.yokidN/A
dc.contributor.yokid119184
dc.contributor.yokid22542
dc.contributor.yokidN/A
dc.contributor.yokidN/A
dc.contributor.yokidN/A
dc.date.accessioned2024-11-09T12:31:23Z
dc.date.issued2022
dc.description.abstractCompared to the established monolayer approach of two-dimensional cell cultures, three-dimensional (3D) cultures more closely resemble in vivo models; that is, the cells interact and form clusters mimicking their organization in native tissue. Therefore, the cellular microenvironment of these 3D cultures proves to be more clinically relevant. In this study, we present a novel easy-to-fabricate microfluidic shallow trench induced 3D cell culturing and imaging (STICI3D) platform, suitable for rapid fabrication as well as mass manufacturing. Our design consists of a shallow trench, within which various hydrogels can be formed in situ via capillary action, between and fully in contact with two side channels that allow cell seeding and media replenishment, as well as forming concentration gradients of various molecules. Compared to a micropillar-based burst valve design, which requires sophisticated microfabrication facilities, our capillary-based STICI3D can be fabricated using molds prepared with simple adhesive tapes and razors alone. The simple design supports the easy applicability of mass-production methods such as hot embossing and injection molding as well. To optimize the STICI3D design, we investigated the effect of individual design parameters such as corner radii, trench height, and surface wettability under various inlet pressures on the confinement of a hydrogel solution within the shallow trench using Computational Fluid Dynamics simulations supported with experimental validation. We identified ideal design values that improved the robustness of hydrogel confinement and reduced the effect of end-user dependent factors such as hydrogel solution loading pressure. Finally, we demonstrated cultures of human mesenchymal stem cells and human umbilical cord endothelial cells in the STICI3D to show that it supports 3D cell cultures and enables precise control of cellular microenvironment and real-time microscopic imaging. The easy-to-fabricate and highly adaptable nature of the STICI3D platform makes it suitable for researchers interested in fabricating custom polydimethylsiloxane devices as well as those who are in need of ready-to-use plastic platforms. As such, STICI3Ds can be used in imaging cell-cell interactions, angiogenesis, semiquantitative analysis of drug response in cells, and measurement of transport through cell sheet barriers.
dc.description.fulltextYES
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue10
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuTÜBİTAK
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TÜBİTAK)
dc.description.sponsorshipNational Center for High Performance Computing of Turkey
dc.description.versionPublisher version
dc.description.volume7
dc.formatpdf
dc.identifier.doi10.1021/acsomega.1c05118
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR03490
dc.identifier.issn2470-1343
dc.identifier.linkhttps://doi.org/10.1021/acsomega.1c05118
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85126748427
dc.identifier.urihttps://hdl.handle.net/20.500.14288/1937
dc.identifier.wos783601100008
dc.keywordsMesenchymal stromal cellsin-vitro
dc.keywordsScaffolds
dc.keywordsHydrogels
dc.keywordsSystems
dc.keywordsAssays
dc.keywordsModel
dc.languageEnglish
dc.publisherAmerican Chemical Society (ACS)
dc.relation.grantno119E138
dc.relation.grantno1006212019
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/10285
dc.sourceACS Omega
dc.subjectChemistry
dc.subjectMultidisciplinary
dc.titleAn easy-to-fabricate microfluidic shallow trench induced three-dimensional cell culturing and imaging (STICI3D) platform
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authoridN/A
local.contributor.authorid0000-0001-8969-590X
local.contributor.authorid0000-0001-7977-1286
local.contributor.authoridN/A
local.contributor.authoridN/A
local.contributor.authoridN/A
local.contributor.kuauthorBaşer, Hatice Nur
local.contributor.kuauthorBaysal, Kemal
local.contributor.kuauthorKiraz, Alper
local.contributor.kuauthorKul, Demet
local.contributor.kuauthorKuş, Funda
local.contributor.kuauthorMorova, Berna
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relation.isOrgUnitOfPublication21598063-a7c5-420d-91ba-0cc9b2db0ea0
relation.isOrgUnitOfPublication.latestForDiscovery21598063-a7c5-420d-91ba-0cc9b2db0ea0

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