Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Investigating the Therapeutic Effect of Folic Acid Conjugated Zno Nanoparticles on Human Triple Negative Breast Cancer Cell Line; [Istrazivanje Terapeutskog Efekta Nanocestica Zno Konjugovanih Sa Folnom Kiselinom Na Trostruko Negativnu Celijsku Liniju Raka Dojke Kod Ljudi] Publisher



Sabzandam S1 ; Zahmatkeshan M2, 3 ; Adel M4 ; Mehrdadian M5 ; Saliminia F3 ; Esmaeili F6
Authors
Show Affiliations
Authors Affiliations
  1. 1. Islamic Azad University, Department of Medical Nanotechnology, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Tehran, Iran
  2. 2. Iran University of Medical Sciences, Cellular and Molecular Research Center, Tehran, Iran
  3. 3. Iran University of Medical Sciences, Department of Medical Nanotechnology, Faculty of Advanced Technologies in Medicine, Tehran, Iran
  4. 4. Tabriz University of Medical Sciences, Department of Medical Nanotechnology, Tehran, Iran
  5. 5. Iran University of Medical Sciences, School of Medicine-International Campus, Tehran, Iran
  6. 6. Tehran University of Medical Sciences, Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran, Iran

Source: Materials Protection Published:2023


Abstract

Triple-negative breast cancer (TNBC) accounts for 15-20% of all invasive breast cancers and has a poor prognosis. ZnO NPs are promising anti-cancer agents. Moreover, folate alpha receptor (FRα) is a potential biomarker and therapeutic target because it is significantly expressed in TNBC. Therefore, ZnO and folic acid-conjugated ZnO (F-ZnO) NPs were synthesized by the sol-gel method. NPs were characterized by DLS, zeta potential, TEM, FTIR, and ICP-MS. FA-ZnO NPs had a mean diameter of 20 ± 2 nm and a surface charge of -15 mV, while ZnO NPs had a mean diameter of 40 ± 5 nm and a surface charge of -5 mV. The MTT assay and trypan blue test, respectively, were used to determine the cytotoxicity and viability percentage of ZnO and F-ZnO NPs at different concentrations of 2, 4, 8, 16, 32, 64 and 128 μg/mL for 12, 24, 48 and 72 hours (h) on the human TNBC cell line MDA-MB-231. The results indicated that both ZnO and F-ZnO NPs significantly reduced the viability of the cancer cells in a dose-dependent and time-dependent manner (p<0.05). The IC50 values for FA-ZnO NPs were approximately 3, 3.74, 4.38 and 5.5 times higher than those for ZnO NPs at 12- 24- 48- and 72-hour time points, respectively. The results suggest that F-ZnO NPs have the potential to be a good option for TNBC treatment and warrant further investigations. © 2023 Authors.