Journal of Cluster Science

, Volume 29, Issue 6, pp 1107–1114 | Cite as

Functionalization of Ag Nanoparticles by Glutamic Acid and Conjugation of Ag@Glu by Thiosemicarbazide Enhances the Apoptosis of Human Breast Cancer MCF-7 Cells

  • Seyed Ataollah Sadat Shandiz
  • Ahmad Montazeri
  • Mansoreh Abdolhosseini
  • Somayeh Hadad Shahrestani
  • Mohammad Hedayati
  • Zeinab Moradi-Shoeili
  • Ali SalehzadehEmail author
Original Paper


In this study, we developed a novel thiosemicarbazide (TSC) conjugated with Ag nanoparticles functionalized by glutamic acid (Ag@Glu) for anticancer activities against human breast cancer MCF-7 cells. The Ag@Glu/TSC nanoparticles were characterized by UV–Vis diffuse reflectance spectroscopy, Fourier transform infrared (FTIR) spectroscopy, SEM, TEM, and XRD analyses. FTIR spectrum showed that the TSC was anchored on the Ag@Glu nanoparticles. The TEM and SEM images of the sample revealed that the Ag@Glu/TSC varied in morphology with a mean size of ~ 50 nm. In vitro cytotoxicity effect of Ag@Glu/TSC was performed using MTT assay toward human breast cancer MCF-7 cells. Moreover, Ag@Glu/TSC induced-apoptosis was evaluated using Hoechst 33258 staining, Caspase-3 activation assay, and annexin V/PI staining with flow cytometry analysis. The MTT assay result of Ag@Glu/TSC showed that the cell viability was in a dose-dependent manner (IC50 = 299.17 μg/mL). We found that Ag@Glu/TSC induce the apoptosis of MCF-7 cell through an increase in Caspase-3 and nuclear fragmentation. Furthermore, the percentage of early and late apoptotic cancer cells was increased as compared to untreated cells using annexin V/PI staining. Finally, we found that the novel Ag@Glu/TSC nanoparticles could inhibit the proliferation of MCF-7 cells by triggering apoptosis pathway, suggesting a new approach to treat breast cancer.


Caspase-3 Cytotoxicity Flow cytometry Nanoparticle 


Compliance with Ethical Standards

Conflict of interest

All of the authors have declared that no competing interests exist.


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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  • Seyed Ataollah Sadat Shandiz
    • 1
  • Ahmad Montazeri
    • 2
  • Mansoreh Abdolhosseini
    • 3
  • Somayeh Hadad Shahrestani
    • 3
  • Mohammad Hedayati
    • 4
  • Zeinab Moradi-Shoeili
    • 5
  • Ali Salehzadeh
    • 3
    Email author
  1. 1.Department of Biology, Central Tehran BranchIslamic Azad UniversityTehranIran
  2. 2.Young Researchers and Elite Club, Rasht BranchIslamic Azad UniversityRashtIran
  3. 3.Department of Biology, Rasht BranchIslamic Azad UniversityRashtIran
  4. 4.Department of Cell and Molecular BiologyUniversity of GuilanRashtIran
  5. 5.Department of Chemistry, Faculty of SciencesUniversity of GuilanRashtIran

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