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Original scientific paper

https://doi.org/10.5562/cca3997

Facile Design of Superparamagnetic Core-Shell EDC-Ascorbate-Fe3O4 Nanocomposites for Targeted Delivery of Doxorubicin to Triple Negative Breast Tumor by Fenton Reaction

S. H. Mirjalili ; Department of Chemistry, Yazd Branch, Islamic Azad University, Yazd, Iran
Mohammad Reza Nateghi ; Department of Chemistry, Yazd Branch, Islamic Azad University, Yazd, Iran *
F. Kalantari-Fotooh ; Department of Chemistry, Yazd Branch, Islamic Azad University, Yazd, Iran

* Corresponding author.


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Abstract

Triple negative breast cancer (TNBC) phenotype accounts for its significant resistance to chemotherapy and other therapeutic procedures. So, the establishment of better and effective therapeutic procedures has become a challenge during recent years. Doxorubicin is a potent chemotherapeutic candidate but its prominent side effects can be subsided via its combination with nanocarriers. So, the present study was aimed to design ascorbic acid modified biopolymeric EDC/NHS-modified magnetic nanoparticles (MNP@MNP@AA-EDC/NHS-DOX for doxorubicin drug delivery to the triple negative breast cancers cell lines of MDA-MB-231, MDA-MB-468 and HCC1937. Monodisperse Fe3O4 MNPs were prepared by chemical co-precipitation method. According to the SEM and DLS results, MNP@AA-EDC/NHS-DOX, MNPs@AA, MNP@AA-MNP@AA-EDC/NHS and MNP@AA-EDC/NHS-DOX had average particle diameter of 53, 79 and 95 nm, respectively. While, XRD analysis showed that the MNP material had the strongest Fe crystal peak, while surface modified MNP@AA-EDC/NHS-DOX did not alter the characteristic properties of MNPs. VSM magnetization analysis revealed that MNP@AA-EDC/NHS-DOX exhibited sufficient paramagnetic potential in the presence of external magnetic field. The TG analysis showed that thermal decomposition capacity of present nanocomposites was: MNPs > MNP@AA-EDC/NHS > AA-MNPs > MNP@AA-EDC/NHS-DOX. AA-modified MNPs did not completely lose their thermal stability as compared to other modifications. Alamar blue analysis revealed that the bare MNPs did have non-significant cytotoxicity in MDA-MB-231, MDA-MB-468 and HCC1937 cell lines (p > 0.001). While, MNP@AA-EDC/NHS-DOX at 0.1, 1.0 and 10 μg/mL DOX concentrations showed significantly lowered cell survival percentages as compared to the free DOX regimens after 24 and 72h. While, HCC1937 cell line had the most accumulation of free (1.42 > 0.93 > 0.9 pg DOX/cell) and conjugated DOX (2.64 > 2.2 > 1.91 pg DOX/cell) after 6 h of incubation period as compared to MDA-MB-468 and MDA-MB-231, respectively (* p < 0.05). Present results provide a new insight into the design of paramagnetic targeted drug delivery nanocomposite system to overcome the obstacles and side effects of conventional chemotherapeutic agents.

Keywords

triple negative breast cancer; ascorbic acid modified MNPs; ferromagnetism; doxorubicin; Fenton reaction

Hrčak ID:

313325

URI

https://hrcak.srce.hr/313325

Publication date:

10.12.2023.

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