Abstract

AbstractOne of the most prevalent cancers affecting women globally is breast cancer. Consequently, the development of cost‐effective and low‐risk treatment options remains a critical pursuit. This study describes the synthesis via water‐in‐oil‐in‐water (W/O/W) of a pH‐responsive nanocarrier for curcumin delivery, a promising anticancer drug. The nanocarrier comprises carboxymethyl starch (CMS), polyethylene glycol (PEG), and gamma alumina (γ‐Al2O3) nanoparticles. The molecular interactions between the nanocomposite components, its crystalline structure, surface morphology, size distribution, and surface charge were assessed via Fourier‐transformed infrared (FTIR) spectroscopy, field emission‐scanning electron microscopy (FE‐SEM), x‐ray diffraction (XRD), dynamic light scattering (DLS) and zeta potential, respectively. The nanocarrier showed a size ranging from 150 to 280 nm, zeta potential of +35.4 mV, drug loading of 47% and an encapsulation efficiency of 87%, which are among the maximum values reported to date for curcumin nanocarriers. A gradual drug release was observed, with 51% and 90% released after 72 h at pH 7.4 and 5.4, respectively, which corroborates the pH‐sensitivity of the nanocarrier. The cytotoxic effects of the curcumin‐loaded nanocomposite on MCF‐7 breast cancer cells and normal cells were investigated using methylthiazolyldiphenyl‐tetrazolium bromide (MTT) assay and flow cytometry. The results demonstrated that loading curcumin onto the hydrogel significantly enhances its penetration into MCF‐7 cells. Overall, this novel nanocomposite offers a promising approach for curcumin delivery in breast cancer treatment.

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