Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/50470
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKosker, Fatma Betül-
dc.contributor.authorAydın, Ömer-
dc.contributor.authorIcoz, Kutay-
dc.date.accessioned2023-04-08T10:01:02Z-
dc.date.available2023-04-08T10:01:02Z-
dc.date.issued2022-
dc.identifier.issn2079-6374-
dc.identifier.urihttps://doi.org/10.3390/bios12111013-
dc.identifier.urihttps://hdl.handle.net/11499/50470-
dc.description.abstractSimple staining of cells is a widely used method in basic medical diagnostics, education, and research laboratories. The stains are low-cost, but the extensive consumption results in excessive toxic waste generation. Thus, to decrease the amount of toxic waste resulting from the cell staining procedure is a need. In this study, we developed a magnetically driven and compartmentalized passive microfluidic chip to perform simple staining of human eukaryotic cells, K562 cells, and lymphocyte cells derived from patients. We demonstrated simple staining on cells with trypan blue, methylene blue, crystal violet, and safranin for high, medium, and low cell densities. The stained cells were imaged using a bright field optical microscope and a cell phone to count cells on the focal plane. The staining improved the color signal of the cell by 25-135-pixel intensity changes for the microscopic images. The validity of the protocol was determined using Jurkat and MDA-MB-231 cell lines as negative controls. In order to demonstrate the practicality of the system, lymphocyte cells derived from human blood samples were stained with trypan blue. The color intensity changes in the first and last compartments were analyzed to evaluate the performance of the chip. The developed method is ultra-low cost, significantly reduces the waste generated, and can be integrated with mobile imaging devices in terms of portability. By combining microfabrication technology with cell staining, this study reported a novel contribution to the field of microfluidic bioŞensors. In the future, we expect to demonstrate the detection of pathogens using this method.en_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.relation.ispartofBioŞensors-Baselen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectcell stainingen_US
dc.subjectpassive microfluidicsen_US
dc.subjectimmunomagnetic beadsen_US
dc.subjectcolour signalen_US
dc.subjecthuman eukaryotic cellsen_US
dc.subjectMicrofluidic Chipen_US
dc.subjectCultureen_US
dc.titleSimple Staining of Cells on a Chipen_US
dc.typeArticleen_US
dc.identifier.volume12en_US
dc.identifier.issue11en_US
dc.departmentPamukkale Universityen_US
dc.authoridAydın, Omer/0000-0002-9028-8786-
dc.authoridIcoz, Kutay/0000-0002-0947-6166-
dc.identifier.doi10.3390/bios12111013-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorwosidAydın, Omer/E-9342-2012-
dc.authorwosidIcoz, Kutay/J-2063-2015-
dc.identifier.pmid36421132en_US
dc.identifier.scopus2-s2.0-85147362776en_US
dc.identifier.wosWOS:000894897000001en_US
dc.institutionauthor-
dc.identifier.scopusqualityQ1-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept20.03. Biomedical Engineering-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Teknoloji Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Files in This Item:
File SizeFormat 
biosensors-12-01013-v2.pdf3.77 MBAdobe PDFView/Open
Show simple item record



CORE Recommender

SCOPUSTM   
Citations

2
checked on Jun 29, 2024

Page view(s)

30
checked on May 27, 2024

Download(s)

116
checked on May 27, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.