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Lawsone assisted preparation of carbon nanofibers for the selective detection of miRNA molecules

dc.contributor.authorSahtani, Karima
dc.contributor.authorAykut, Yakup
dc.contributor.authorTanık, Nilay A
dc.contributor.buuauthorSahtani, Karima
dc.contributor.buuauthorAYKUT, YAKUP
dc.contributor.buuauthorTanık, Nilay A
dc.contributor.departmentFen Bilimleri Enstitüsü
dc.contributor.departmentTekstil Mühendisliği Bölümü
dc.contributor.departmentMühendislik Fakültesi
dc.contributor.departmentTekstil Mühendisliği Bölümü
dc.contributor.scopusid57299680900
dc.contributor.scopusid55320835000
dc.contributor.scopusid57195994912
dc.date.accessioned2025-05-13T06:47:03Z
dc.date.issued2022-01-01
dc.description.abstractBACKGROUND: microRNA (miRNA) molecules are considered as biomarkers and have promising future for early-stage cancer diagnosis. Lawsone (Law) enriched carbon nanofibers (CNFs) were prepared via electrospinning process for the selective miRNA detection. Anti-miRNA molecules were attached on the CNFs immobilized screen printed electrodes (SPE) and used for the detection of miRNA molecules by observing guanine oxidation signal via differential pulse voltammetry (DPV) method. Three different miRNA molecules including the target (miRNA), single-base mismatched (SM.miRNA) and non-complementary (NC.miRNA) were hybridized with the previously attached anti-miRNA molecules (with guanine [PolyT(G)] and without guanine [PolyT(I)]) on the CNFs immobilized SPE surfaces. RESULTS: Guanine oxidation signal decreased after the hybridization of miRNA with anti-miRNA molecules on CNF immobilized SPE surfaces. Guanine oxidation signal was not detected on the PolyT(I) attached samples, but the existence of guanine oxidation signal was clear detected after the addition of miRNA molecules on the previously attached PolyT(I). Because no hybridization of anti-miRNA molecules with the non-complementary miRNA (NC.miRNA) molecules occurred, the guanine oxidation signal was not significantly decreased after the interaction of NC.miRNA with the attached PolyT(G). Since there was no hybridization between the NC.miRNA molecules with the attached PolyT(I) on the SPEs, weak guanine peaks were detected at PolyT(I)-NC.miRNA samples as a result of the existence of residual NC.miRNA molecules on SPE after washing. CONCLUSIONS: The measurement results confirm the enhanced selectivity of the miRNA molecules by using CNFs with SPEs and the developed biosensory system could be used to detect the specific RNA molecules. © 2021 Society of Chemical Industry (SCI).
dc.identifier.doi10.1002/jctb.6937
dc.identifier.endpage269
dc.identifier.issn0268-2575
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85117353089
dc.identifier.startpage254
dc.identifier.urihttps://hdl.handle.net/11452/51812
dc.identifier.volume97
dc.indexed.scopusScopus
dc.language.isoen
dc.publisherJohn Wiley and Sons Ltd
dc.relation.journalJournal of Chemical Technology and Biotechnology
dc.relation.tubitak118M231
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectMiRNA
dc.subjectGuanine oxidation
dc.subjectElectrospinning
dc.subjectCarbon nanofiber
dc.subjectBiosensors
dc.subject.scopusElectrochemical Biosensors for DNA Damage Assessment
dc.titleLawsone assisted preparation of carbon nanofibers for the selective detection of miRNA molecules
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentFen Bilimleri Enstitüsü/Tekstil Mühendisliği Bölümü
local.contributor.departmentMühendislik FakültesiTekstil Mühendisliği Bölümü
local.indexed.atScopus
relation.isAuthorOfPublication9b6d7d6e-e8d2-4636-86ab-37eae699c9d3
relation.isAuthorOfPublication.latestForDiscovery9b6d7d6e-e8d2-4636-86ab-37eae699c9d3

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