Publication:
Evaluation of cytotoxic and genotoxic potential of avobenzone and octocrylene on human skin fibroblast cells

dc.contributor.authorVatan, Özgür
dc.contributor.authorSevinç, Duygu
dc.contributor.authorYılmaz Çelik, Dilek
dc.contributor.authorAurelie Allounan, A. Carine
dc.contributor.authorTeksoy, Özgün
dc.contributor.authorOral, Neylan
dc.contributor.authorHüriyet, Hüzeyfe
dc.contributor.authorÇavaş, Tolga
dc.contributor.authorÇinkılıç, Nilüfer
dc.contributor.buuauthorVATAN, ÖZGÜR
dc.contributor.buuauthorSevinç, Duygu
dc.contributor.buuauthorYılmaz Çelik, Dilek
dc.contributor.buuauthorAurelie Allounan, A. Carine
dc.contributor.buuauthorTeksoy, Özgün
dc.contributor.buuauthorOral, Neylan
dc.contributor.buuauthorHüriyet, Hüzeyfe
dc.contributor.buuauthorÇAVAŞ, TOLGA
dc.contributor.buuauthorÇİNKILIÇ, NİLÜFER
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentBiyoloji Bölümü
dc.contributor.orcid0000-0002-7687-3284
dc.contributor.orcid0000-0003-1620-1918
dc.contributor.researcheridAAH-5296-2021
dc.contributor.researcheridISV-0209-2023
dc.contributor.researcheridO-7508-2015
dc.contributor.researcheridJOX-7778-2023
dc.contributor.researcheridJOR-9588-2023
dc.contributor.researcheridJOL-2743-2023
dc.contributor.researcheridEDJ-3505-2022
dc.contributor.researcheridJOX-5573-2023
dc.contributor.researcheridCVI-9578-2022
dc.contributor.researcheridEQD-6980-2022
dc.date.accessioned2024-09-26T06:49:32Z
dc.date.available2024-09-26T06:49:32Z
dc.date.issued2023-12-31
dc.description.abstractWe investigated the cytotoxic and genotoxic effects of the organic UVA filter avobenzone (AVB), and the UVB filter octocrylene (OCT), found alone or in combination in different sunscreen formulations, on normal human skin fibroblast cells (CCD-1118Sk). To achieve this purpose, we used XTT viability assay, single cell gel electrophoresis (comet) assay and reactive oxygen species (ROS) assay. For cytotoxicity, CCD-1118Sk cells were exposed to various concentrations of AVB (32-800 mu M), and OCT (130-6500 mu M). The IC50 values were 100.2 and 1390.95 mu M for AVB and OCT, respectively. IC12.5, IC25 and IC50 concentrations were chosen for genotoxicity testing. The comet assay revealed DNA damage at the two highest concentrations of AVB and all OCT concentrations. The rate of DNA damage was significantly higher than in the control groups. Co-treatment with AVB and OCT increased the level of DNA damage and intracellular oxidative stress compared with AVB and OCT treatment alone. Finally, our study showed that the UVA filter AVB, with the UVB filter OCT, may induce cytotoxic and genotoxic effects on human skin fibroblast cells.Highlights Avobenzone and octocrylene are UV filters used in sunscreen products. Healthy human skin fibroblast cell line CCD-1118Sk was used for cytotoxic and genotoxic assays. Cotreatment with avobenzone and octocrylene caused more severe DNA damage than their treatment alone. Our findings will contribute to the limited number of cytotoxicity and genotoxicity studies and lead to more detailed studies on the use of these two chemicals.
dc.identifier.doi10.1080/26895293.2023.2270171
dc.identifier.issn2689-5293
dc.identifier.issue1
dc.identifier.urihttps://doi.org/10.1080/26895293.2023.2270171
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/26895293.2023.2270171
dc.identifier.urihttps://hdl.handle.net/11452/45277
dc.identifier.volume16
dc.identifier.wos001089869500001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherTaylor & Francis Ltd
dc.relation.bapKUAP(F)-2015/70
dc.relation.journalAll Life
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectIn-vitro
dc.subjectUv filters
dc.subjectDamage
dc.subjectPhotostability
dc.subjectProducts
dc.subjectAssay
dc.subjectDna
dc.subjectUv filters
dc.subjectAvobenzone
dc.subjectOctocrylene
dc.subjectCytotoxicity
dc.subjectGenotoxicity
dc.subjectScience & technology - other topics
dc.titleEvaluation of cytotoxic and genotoxic potential of avobenzone and octocrylene on human skin fibroblast cells
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentFen Edebiyat Fakültesi/Biyoloji Bölümü
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relation.isAuthorOfPublicatione2d73980-fde0-4719-a06f-304443cac871
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relation.isAuthorOfPublication.latestForDiscovery1de6fd1a-3db1-46bc-9a57-31cc24b984ad

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