Chemical characterization and neuroprotective properties of copper nanoparticles green-synthesized bynigella sativaL. seed aqueous extract against methadone-induced cell death in adrenal phaeochromocytoma (PC12) cell line

dc.contributor.authorYan, Wen
dc.contributor.authorLiu, Yutang
dc.contributor.authorMansooridara, Shirin
dc.contributor.authorKalantari, Atoosa Shahriyari
dc.contributor.authorSadeghian, Nastaran
dc.contributor.authorTaslimi, Parham
dc.contributor.authorZangeneh, Akram
dc.contributor.authorTaslimi, Parham
dc.contributor.authorSadeghian, Nastaran
dc.date.accessioned2025-10-18T10:02:08Z
dc.date.created2020
dc.date.issued2020
dc.departmentFakülteler, Fen Fakültesi, Biyoteknoloji Bölümü
dc.description.abstractRecently, scientists have used the metallic nanoparticles especially copper nanoparticles for formulating many new neuroprotective supplements in the field of neurology. Also, we know the role ofNigella sativaL. in increasing the physiological activities of the central nervous system in traditional medicine. In the present study, we decided to prepare and formulate a new neuroprotective supplement (copper nanoparticles in aqueous medium usingN. sativaseed aqueous extract) in thein vitrocondition. The organometallic chemistry tests such as Fourier Transformed Infrared Spectroscopy (FT-IR), UV-Visible Spectroscopy (UV-Vis), Field Emission Scanning Electron Microscopy (FE-SEM), and Transmission Electron Microscopy (TEM) were used for characterizing of copper nanoparticles. In the FT-IR test, the presence of many antioxidant compounds with related bonds caused excellent condition for reducing copper in the copper nanoparticles. In UV-Vis, the clear peak in the wavelength of 569 nm showed the copper nanoparticles formation. Also, in the TEM and FE-SEM images, the copper nanoparticles had the size of 19.5 nm. In the biological part of the current study, methadone significantly (p <= 0.01) decreased cell viability, mitochondrial membrane potential, and increased inflammatory cytokines concentrations, caspase-3 activity, and DNA fragmentation. CuNPs-treated cell cutlers significantly (p <= 0.01) increased cell viability and mitochondrial membrane potential, and decreased inflammatory cytokines concentrations, caspase-3 activity, and DNA fragmentation in the high concentration of methadone-treated adrenal phaeochromocytoma (PC12) cells. For investigating the antioxidant properties of copper nanoparticles, the 2,2-diphenyl-1-picrylhydrazyl (DPPH) test was used in the presence of butylated hydroxytoluene as the positive control. The copper nanoparticles inhibited half of the DPPH molecules in the concentration of 171 mu g/mL. In this study, we concluded that copper nanoparticles biosynthesized byN. sativaL. seed suppressed methadone-induced cell death in PC12 cells.
dc.identifier.doi10.1080/17458080.2020.1778167
dc.identifier.endpage296
dc.identifier.issn1745-8080
dc.identifier.issn1745-8099
dc.identifier.issue1
dc.identifier.orcidZangeneh, Akram/0000-0001-8129-8432
dc.identifier.orcidTaslimi, Parham/0000-0002-3171-0633
dc.identifier.scopus2-s2.0-85087496043
dc.identifier.scopusqualityQ2
dc.identifier.startpage280
dc.identifier.urihttps://doi.org/10.1080/17458080.2020.1778167
dc.identifier.urihttps://hdl.handle.net/11772/20417
dc.identifier.volume15
dc.identifier.wosWOS:000545194000001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherTaylor & Francis Ltd
dc.relation.ispartofJournal of Experimental Nanoscience
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzWoS_20251016
dc.subjectChemical Characterization
dc.subjectCopper Nanoparticles
dc.subjectNeuroprotective Supplement
dc.subjectMethadone
dc.subjectPc12
dc.titleChemical characterization and neuroprotective properties of copper nanoparticles green-synthesized bynigella sativaL. seed aqueous extract against methadone-induced cell death in adrenal phaeochromocytoma (PC12) cell line
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationdadfa319-65b8-4543-92b4-bea49e0139e9
relation.isAuthorOfPublication7f83844e-1b57-4c97-b59d-6bd6facb1def
relation.isAuthorOfPublication.latestForDiscoverydadfa319-65b8-4543-92b4-bea49e0139e9

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