Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/14121
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dc.contributor.authorKeçili, Seren-
dc.contributor.authorKaymaz, Sumeyra Vural-
dc.contributor.authorÖzoğul, Beyzanur-
dc.contributor.authorTekin, H. Cumhur-
dc.contributor.authorElitaş, Meltem-
dc.date.accessioned2024-01-06T07:21:25Z-
dc.date.available2024-01-06T07:21:25Z-
dc.date.issued2023-
dc.identifier.issn0003-2654-
dc.identifier.issn1364-5528-
dc.identifier.urihttps://doi.org/10.1039/d3an01304a-
dc.identifier.urihttps://hdl.handle.net/11147/14121-
dc.description.abstractIntravenous fluids are being widely used in patients of all ages for preventing or treating dehydration in the intensive care units, surgeries in the operation rooms, or administering chemotherapeutic drugs at hospitals. Dextrose, Ringer, and NaCl solutions are widely received as intravenous fluids by hospitalized patients. Despite their widespread administration for over 100 years, studies on their influences on different cell types have been very limited. Increasing evidence suggests that treatment outcomes might be altered by the choice of the administered intravenous fluids. In this study, we investigated the influences of intravenous fluids on human endothelial (HUVEC) and monocyte (U937) cell lines using the magnetic levitation technique. Our magnetic levitation platform provides label-free manipulation of single cells without altering their phenotypic or genetic properties. It allows for monitoring and quantifying behavior of single cells by measuring their levitation heights, deformation indices, and areas. Our results indicate that HUVEC and U937 cell lines respond differently to different intravenous fluids. Dextrose solution decreased the viability of both cell lines while increasing the heterogeneity of areas, deformation, and levitation heights of HUVEC cells. We strongly believe that improved outcomes can be achieved when the influences of intravenous fluids on different cell types are revealed using robust, label-free, and efficient methods. Label-free analysis of cells exposed to intravenous fluids can be achieved through magnetic levitation technology coupled with cell-morphology characterization.en_US
dc.description.sponsorshipH. C. T. and M. E. are co-corresponding authors. H. C. T. acknowledges the financial support from The Scientific and Technological Research Council of Turkey (grant number 22AG032), the Outstanding Young Scientists Award funding (TUBA GEBIP 2020) from the [22AG032]; Scientific and Technological Research Council of Turkey [TUBA GEBIP 2020]; Outstanding Young Scientists Award; Turkish Academy of Science; 2022 Young Scientist Award (BAGEP) funding from Science Academy (Bilim Akademisi); Turkish Council of Higher Educationen_US
dc.description.sponsorshipH. C. T. and M. E. are co-corresponding authors. H. C. T. acknowledges the financial support from The Scientific and Technological Research Council of Turkey (grant number 22AG032), the Outstanding Young Scientists Award funding (TUBA GEBIP 2020) from the Turkish Academy of Science and the 2022 Young Scientist Award (BAGEP) funding from Science Academy (Bilim Akademisi). S. K. would like to thank the support of the Turkish Council of Higher Education for the 100/2000 CoHE doctoral scholarship. The authors would like to dedicate this article to the loving memories of those lost in the 2023 Kahramanmaras Earthquake.en_US
dc.language.isoenen_US
dc.publisherROYAL SOC CHEMISTRYen_US
dc.relation.ispartofAnalysten_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleInvestigating influences of intravenous fluids on HUVEC and U937 monocyte cell lines using the magnetic levitation methoden_US
dc.typeArticleen_US
dc.institutionauthor-
dc.departmentİzmir Institute of Technologyen_US
dc.identifier.volume148en_US
dc.identifier.issue22en_US
dc.identifier.startpage5588en_US
dc.identifier.endpage5596en_US
dc.identifier.wosWOS:001090298200001en_US
dc.identifier.scopus2-s2.0-85175264306en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1039/d3an01304a-
dc.identifier.pmid37872817en_US
dc.authorscopusid57216562865-
dc.authorscopusid57222252740-
dc.authorscopusid57960535800-
dc.authorscopusid25029174000-
dc.authorscopusid24080104200-
item.grantfulltextnone-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.dept03.01. Department of Bioengineering-
Appears in Collections: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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