| Authors | فهیمه سادات واجدی,حسین دهقانی قربی,علی ضرابی |
| Journal | MAT SCI ENG C-MATER |
| Page number | 111627 |
| Volume number | 119 |
| IF | 8.457 |
| Paper Type | Full Paper |
| Published At | 2020-10-14 |
| Journal Grade | Scientific - research |
| Journal Type | Electronic |
| Journal Country | Iran, Islamic Republic Of |
| Journal Index | JCR |
Abstract
Breast cancer is one of the main reasons of women’s mortality. A novel ternary combination of ZnAl-layered
double hydroxides (LDH), cobalt ferrite (CoFe2O4) and N-graphene quantum dots (N-GQDs) proposes a pHsensitive
multifunctional nanocomposite that can improve therapeutic features of each compound; this is a
notable strategy to make biocompatible materials with unique properties for paclitaxel (PTX) delivery in breast
cancer cells. For proving the surface modification process of materials, electrochemical techniques including
cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were carried out. By coating PEG on the
surface of the N-GQDs/CoFe2O4/LDH, it developed a drug delivery system with low toxicity, an excellent
encapsulation efficiency 88.4%, drug loading capacity of ca. 31%, and slow and sustained release behavior (9%
after 72 h) under normal physiological conditions. Besides, a high drug release (~69%) at low-pH as a model of
the extracellular tumor environment indicated a pH-sensitive release behavior. Moreover, cell viability assay
proved the negligible cytotoxicity on normal cells (L929) and the improved growth inhibition effect of PTX/NGQDs/
CoFe2O4/LDH nanocarrier on MCF7 cancer cells. Blood compatibility test values with respect to red blood
cell aggregation (RBC), coagulation prothrombin time (PT), activated partial thromboplastin time (APTT), and
complement activation (C3 and C4 levels) remained within normal ranges without toxicity effect on RBCs and
complement factors. Overall, this novel designed PTX/N-GQDs/CoFe2O4/LDH nanocarrier with tremendously
biocompatible, slow-release and pH-dependent features could be considered as a theranostic candidate for
various anticancer drugs delivery and cancer therapy.