The Effects of Polymer Coating of Gold Nanoparticles on Oxidative Stress and DNA Damage

ArticleAçık Erişim

Özet

Gold nanoparticles (AuNPs) have been widely used in many biological and biomedical applications. In this regard, their surface modification is of paramount importance in order to increase their cellular uptake, delivery capability, and optimize their distribution inside the body. The aim of this study was to examine the effects of AuNPs on cytotoxicity, oxidant/antioxidant parameters, and DNA damage in HepG2 cells and investigate the potential toxic effects of different surface modifications such as polyethylene glycol (PEG) and polyethyleneimine (PEI; molecular weights of 2,000 (low molecular weight [LMW]) and 25,000 (high molecular weight [HMW]). The study groups were determined as AuNPs, PEG-coated AuNPs (AuNPs/PEG), low-molecular weight polyethyleneimine-coated gold nanoparticles (AuNPs/PEI LMW), and high-molecular weight polyethyleneimine-coated gold nanoparticles (AuNPs/PEI HMW). After incubating HepG2 cells with different concentrations of nanoparticles for 24 hours, half maximal inhibitory concentrations (the concentration that kills 50% of the cells) were determined as 166.77, 257.73, and 198.44 µg/mL for AuNPs, AuNPs/PEG, and AuNPs/PEI LMW groups, respectively. Later, inhibitory concentration 30 (IC30, the concentration that kills 30% of the cells) doses were calculated, and further experiments were performed on cells that were exposed to IC30 doses. Although intracellular reactive oxygen species levels significantly increased in all nanoparticles, AuNPs as well as AuNPs/PEG did not cause any changes in oxidant/antioxidant parameters. However, AuNPs/PEI HMW particularly induced oxidative stress as evidence of alterations in lipid peroxidation and protein oxidation. These results suggest that at IC30 doses, AuNPs do not affect oxidative stress and DNA damage significantly. Polyethylene glycol coating does not have an impact on toxicity, however PEI coating (particularly HMW) can induce oxidative stress. © The Author(s) 2020.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/13964Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1177/1091581820927646Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorSen, Gamze Tilbe
dc.contributor.authorOzkemahli, Gizem
dc.contributor.authorShahbazi, Reza
dc.contributor.authorErkekoglu, Pınar
dc.contributor.authorUlubayram, Kezban
dc.contributor.authorKocer-Gumusel, Belma
dc.date.accessioned2026-10-18T20:28:45.687536416Z
dc.date.available2026-10-18T20:28:45.687536416Z
dc.date.issued2020
dc.description.abstractGold nanoparticles (AuNPs) have been widely used in many biological and biomedical applications. In this regard, their surface modification is of paramount importance in order to increase their cellular uptake, delivery capability, and optimize their distribution inside the body. The aim of this study was to examine the effects of AuNPs on cytotoxicity, oxidant/antioxidant parameters, and DNA damage in HepG2 cells and investigate the potential toxic effects of different surface modifications such as polyethylene glycol (PEG) and polyethyleneimine (PEI; molecular weights of 2,000 (low molecular weight [LMW]) and 25,000 (high molecular weight [HMW]). The study groups were determined as AuNPs, PEG-coated AuNPs (AuNPs/PEG), low-molecular weight polyethyleneimine-coated gold nanoparticles (AuNPs/PEI LMW), and high-molecular weight polyethyleneimine-coated gold nanoparticles (AuNPs/PEI HMW). After incubating HepG2 cells with different concentrations of nanoparticles for 24 hours, half maximal inhibitory concentrations (the concentration that kills 50% of the cells) were determined as 166.77, 257.73, and 198.44 µg/mL for AuNPs, AuNPs/PEG, and AuNPs/PEI LMW groups, respectively. Later, inhibitory concentration 30 (IC30, the concentration that kills 30% of the cells) doses were calculated, and further experiments were performed on cells that were exposed to IC30 doses. Although intracellular reactive oxygen species levels significantly increased in all nanoparticles, AuNPs as well as AuNPs/PEG did not cause any changes in oxidant/antioxidant parameters. However, AuNPs/PEI HMW particularly induced oxidative stress as evidence of alterations in lipid peroxidation and protein oxidation. These results suggest that at IC30 doses, AuNPs do not affect oxidative stress and DNA damage significantly. Polyethylene glycol coating does not have an impact on toxicity, however PEI coating (particularly HMW) can induce oxidative stress. © The Author(s) 2020.
dc.identifier.doi10.1177/1091581820927646
dc.identifier.eissn1092-874X
dc.identifier.endpage340
dc.identifier.issn1091-5818
dc.identifier.issue4
dc.identifier.pmid32483993
dc.identifier.scopus2-s2.0-85085880887
dc.identifier.startpage328
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13964
dc.identifier.volume39
dc.identifier.wosWOS:000537487000001
dc.language.isoen
dc.publisherSAGE Publications Inc.
dc.relation.ispartofInternational Journal of Toxicology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectDNA damage
dc.subjectgold nanoparticles
dc.subjectoxidative stress
dc.subjectpolyethylene glycol
dc.subjectpolyethyleneimine
dc.subjectreactive oxygen species
dc.subjectsurface modification
dc.subjectCatalase
dc.subjectCell Survival
dc.subjectGlutathione
dc.subjectGlutathione Peroxidase
dc.subjectGold
dc.subjectHep G2 Cells
dc.subjectHumans
dc.subjectMetal Nanoparticles
dc.subjectPolyethylene Glycols
dc.subjectSuperoxide Dismutase
dc.subjectantioxidant
dc.subjectDNA
dc.subjectgold nanoparticle
dc.subjectmacrogol
dc.subjectmalonaldehyde
dc.subjectreactive oxygen metabolite
dc.subjectmetal nanoparticle
dc.subjectArticle
dc.subjectcoating (procedure)
dc.subjectcontrolled study
dc.subjectcytotoxicity
dc.subjectdispersity
dc.subjectenzyme activity
dc.titleThe Effects of Polymer Coating of Gold Nanoparticles on Oxidative Stress and DNA Damage
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus31
rdl.citation.wos28
rdl.departmentFaculty of Pharmacy, Department of Toxicology, Erzincan Binali Yildirim University, Erzincan, Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)