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dc.contributor.authorCiftci, Gonul Yenilmez
dc.contributor.authorSenkuytu, Elif
dc.contributor.authorIncir, Saadet Elif
dc.contributor.authorYuksel, Fatma
dc.contributor.authorOlcer, Zehra
dc.contributor.authorYildirim, Tuba
dc.contributor.authorKilic, Adem
dc.contributor.authorUludag, Yildiz
dc.date.accessioned2019-09-01T13:05:11Z
dc.date.available2019-09-01T13:05:11Z
dc.date.issued2016
dc.identifier.issn0956-5663
dc.identifier.issn1873-4235
dc.identifier.urihttps://dx.doi.org/10.1016/j.bios.2016.01.061
dc.identifier.urihttps://hdl.handle.net/20.500.12450/1199
dc.descriptionWOS: 000372558500047en_US
dc.descriptionPubMed ID: 26852202en_US
dc.description.abstractCancer, as one of the leading causes of death in the world, is caused by malignant cell division and growth that depends on rapid DNA replication. To develop anti-cancer drugs this feature of cancer could be exploited by utilizing DNA-damaging molecules. To achieve this, the paraben substituted cyclotetraphosphazene compounds have been synthesized for the first time and their effect on DNA (genotoxicity) has been investigated. The conventional genotoxicity testing methods are laborious, take time and are expensive. Biosensor based assays provide an alternative to investigate this drug/compound DNA interactions. Here for the first time, a new, easy and rapid screening method has been used to investigate the DNA damage, which is based on an automated biosensor device that relies on the real-time electrochemical profiling (REP (TM)) technology. Using both the biosensor based screening method and the in vitro biological assay, the compounds 9 and 11 (propyl and benzyl substituted cyclotetraphosphazene compounds, respectively), have resulted in higher DNA damage than the others with 65% and 80% activity reduction, respectively. (C) 2016 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipGebze Technical University (GTU) [BAP-2013-A-013]; BILGEM-TUBITAIC (The Scientific and Technological Research Council of Turkey) [S569000]en_US
dc.description.sponsorshipThe authors thank to Gebze Technical University (GTU) for the provided financial support (Grant no: BAP-2013-A-013). The project is also supported by BILGEM-TUBITAIC (The Scientific and Technological Research Council of Turkey) grant no: S569000. We gratefully acknowledge Bioelectronic Devices and Systems Group from BILGEM-TUBITAK for their contribution to the fabrication of the biochip and the sensing platform.en_US
dc.language.isoengen_US
dc.publisherELSEVIER ADVANCED TECHNOLOGYen_US
dc.relation.isversionof10.1016/j.bios.2016.01.061en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBiosensoren_US
dc.subjectElectrochemicalen_US
dc.subjectAmperometryen_US
dc.subjectCyclotetraphosphazenesen_US
dc.subjectParabensen_US
dc.subjectDNA interactionen_US
dc.subjectGenotoxicityen_US
dc.titleFirst paraben substituted cyclotetraphosphazene compounds and DNA interaction analysis with a new automated biosensoren_US
dc.typearticleen_US
dc.relation.journalBIOSENSORS & BIOELECTRONICSen_US
dc.authoridSenkuytu, Elif -- 0000-0002-3579-8062en_US
dc.identifier.volume80en_US
dc.identifier.startpage331en_US
dc.identifier.endpage338en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.department-temp[Ciftci, Gonul Yenilmez -- Senkuytu, Elif -- Incir, Saadet Elif -- Yuksel, Fatma -- Olcer, Zehra -- Kilic, Adem] Gebze Tech Univ, Dept Chem, TR-41400 Gebze, Kocaeli, Turkey -- [Uludag, Yildiz] Sci & Technol Res Council Turkey TUBITAK, UEKAE BILGEM, Bioelect Devices & Syst Grp, TR-41470 Gebze, Kocaeli, Turkey -- [Yildirim, Tuba] Amasya Univ, Fac Art & Sci, Dept Biol, TR-05100 Amasya, Turkeyen_US


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