• Türkçe
    • English
  • English 
    • Türkçe
    • English
  • Login
View Item 
  •   DSpace Home
  • Araştırma Çıktıları | TR-Dizin | WoS | Scopus | PubMed
  • Scopus İndeksli Yayınlar Koleksiyonu
  • View Item
  •   DSpace Home
  • Araştırma Çıktıları | TR-Dizin | WoS | Scopus | PubMed
  • Scopus İndeksli Yayınlar Koleksiyonu
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

Investigation of the Effect of Silver Nanoparticles Obtained from Primula Vulgaris Extracts by Applying the Green Synthesis Method on MCF-7 Cells

xmlui.dri2xhtml.METS-1.0.item-rights

info:eu-repo/semantics/closedAccess

Date

2024

Author

Ciftci, Harun
Er Caliskan, Cigdem
Yazici, Burcu
Tekcan, Akin
Ozturk, Kubra

Metadata

Show full item record

Abstract

In recent years, the use of nanoparticles has gained significant attention in cancer research due to their unique properties and potential as targeted drug delivery systems. This study focuses on the synthesis and characterization of Primula vulgaris stabilized silver nanoparticles (PVAgNPs) and the evaluation of in vitro cytotoxicity against MCF-7 cells. In this study, PVAgNPs were synthesized separately from the flower (PVAgNPsF), leaf (PVAgNPsL), and root (PVAgNPsR) extracts of Primula vulgaris (PV). The PVAgNPs were characterized by various analytical techniques, including UV-Visible absorption spectroscopy, Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction, Dynamic Light Scattering (DLS), zeta potential, and scanning electron microscopy (SEM). The maximum absorption wavelengths are obtained at 437 nm for the PVAgNPsR samples and at 440 nm for the PVAgNPsF and PVAgNPsL samples. Based on the XRD spectra, PVAgNPs were found to have a cubic crystal structure. On average, the zeta potential values of PVAgNPs ranged from-14 to-28 mV, indicating that they were quite stable. SEM analysis showed that the synthesized PVAgNPs were predominantly spherical in shape and ranged in size from 40 to 89 nm. The iCELLigence Real-Time Cell Analysis (RTCA) system was used to evaluate the efficacy of the synthesized PVAgNPs against MCF-7 cell lines. After 24 h of incubation, the inhibitory concentrations (IC50) of PVAgNPsL PVAgNPsR, and PVAgNPsF Were determined to be 30.37, 36.74, and 57.64 µg/mL, respectively, indicating that PVAgNPs have an in vitro cytotoxic effect on MCF-7 cells. In conclusion, PVAgNPs were successfully synthesized using a green synthesis approach. In addition, a thorough characterization of these nanoparticles was carried out, confirming their structural properties, and demonstrating their efficacy against MCF-7 cell lines. These results highlight the potential of PVAgNPs as promising candidates for the development of novel anticancer drugs. However, further studies are required to evaluate their feasibility and efficacy for future therapeutic applications. © 2024, Iranian Institute of Research and Development in Chemical Industries. All rights reserved.

Volume

43

Issue

7

URI

https://hdl.handle.net/20.500.12450/4326

Collections

  • Scopus İndeksli Yayınlar Koleksiyonu [1574]



DSpace software copyright © 2002-2015  DuraSpace
Contact Us | Send Feedback
Theme by 
@mire NV
 

 




| Instruction | Guide | Contact |

DSpace@Amasya

by OpenAIRE
Advanced Search

sherpa/romeo

Browse

All of DSpaceCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsTypeDepartmentPublisherCategoryLanguageAccess TypeThis CollectionBy Issue DateAuthorsTitlesSubjectsTypeDepartmentPublisherCategoryLanguageAccess Type

My Account

LoginRegister

DSpace software copyright © 2002-2015  DuraSpace
Contact Us | Send Feedback
Theme by 
@mire NV
 

 


|| Instruction || Guide || Library || Amasya University || OAI-PMH ||

Amasya Üniversitesi Kütüphane ve Dokümantasyon Daire Başkanlığı, Amasya, Turkey
If you find any errors in content, please contact: openaccess@amasya.edu.tr

Creative Commons License
DSpace@Amasya by Amasya University Institutional Repository is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 Unported License..

DSpace@Amasya: