Publication:
Impact of reaction variables and PEI/L-cysteine ratio on the optical properties and cytocompatibility of cationic Ag2S quantum dots as NIR bio-imaging probes

dc.contributor.departmentDepartment of Chemistry
dc.contributor.departmentGraduate School of Sciences and Engineering
dc.contributor.kuauthorAcar, Havva Funda Yağcı
dc.contributor.kuauthorDuman, Fatma Demir
dc.contributor.kuauthorDurmuşoğlu, Emek Göksu
dc.contributor.kuauthorKhodadust, Rouhollah
dc.contributor.kuauthorYağcı, Mustafa Barış
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.contributor.schoolcollegeinstituteGRADUATE SCHOOL OF SCIENCES AND ENGINEERING
dc.date.accessioned2024-11-09T12:32:02Z
dc.date.issued2016
dc.description.abstractNear-infrared emitting semiconductor quantum dots (NIRQDs) are popular fluorescent probes due to better penetration depth and elimination of tissue autofluorescence. Here, we demonstrate one pot aqueous synthesis of cytocompatible, strongly luminescent, cationic Ag2S NIRQDs utilizing a mixed coating composed of branched polyethyleneimine (PEI)-25 kDa and L-cysteine (Cys) as in vitro luminescent tags and in vivo optical imaging agents. Ultrasmall sizes, a clear first excitonic peak in the absorption spectra, relatively narrow emission peaks with maxima between 730 and 775 nm and a Stokes shift less than 100 nm were obtained. Lifetime measurements indicate excitonic and defect-related emissions. Interestingly, not the emission maxima but the intensity was influenced by the Cys amount more dramatically. PEI/Cys 60/40 mol ratio provided the highest quantum yield reported until now for Ag2S NIRQD (157%) emitting at such a short wavelength. Low molecular weight PEI failed to produce luminescent QDs. Cytotoxicity evaluation of the most strongly luminescing NIRQDs, revealed the PEI/Cys (mol mol(-1)) 50/50 composition as the non-toxic composition below 2.4 mu g Ag per mL concentration. Others had low-toxicity. In vitro microscopy experiments showed endosomal distribution of NIRQDs in Hela cells and strong NIR signal. In vivo imaging study demonstrated that Ag2S NIRQDs could effectively be used as strong optical imaging agents.
dc.description.fulltextYES
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.issue81
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuTÜBİTAK
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TÜBİTAK)
dc.description.versionPublisher version
dc.description.volume6
dc.identifier.doi10.1039/c6ra13804g
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR00850
dc.identifier.issn2046-2069
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85030155995
dc.identifier.urihttps://doi.org/10.1039/c6ra13804g
dc.identifier.wos382482200058
dc.keywordsIn-Vivo
dc.keywordsAqueous Synthesis
dc.keywordsHighly Luminescent
dc.keywordsDrug-Delivery
dc.keywordsNanocrystals
dc.keywordsNanoparticles
dc.keywordsEmission
dc.keywordsWindow
dc.keywordsTemperature
dc.keywordsStability
dc.language.isoeng
dc.publisherRoyal Society of Chemistry (RSC)
dc.relation.grantno113Z164
dc.relation.ispartofRSC Advances
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/855
dc.subjectChemistry, Multidisciplinary
dc.titleImpact of reaction variables and PEI/L-cysteine ratio on the optical properties and cytocompatibility of cationic Ag2S quantum dots as NIR bio-imaging probes
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorDuman, Fatma Demir
local.contributor.kuauthorKhodadust, Rouhollah
local.contributor.kuauthorDurmuşoğlu, Emek Göksu
local.contributor.kuauthorYağcı, Mustafa Barış
local.contributor.kuauthorAcar, Havva Funda Yağcı
local.publication.orgunit1College of Sciences
local.publication.orgunit1GRADUATE SCHOOL OF SCIENCES AND ENGINEERING
local.publication.orgunit2Department of Chemistry
local.publication.orgunit2Graduate School of Sciences and Engineering
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relation.isOrgUnitOfPublication3fc31c89-e803-4eb1-af6b-6258bc42c3d8
relation.isOrgUnitOfPublication.latestForDiscovery035d8150-86c9-4107-af16-a6f0a4d538eb
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