Controlled curcumin delivery via carboxymethyl starch‐modified gamma alumina nanoparticles in a polyethylene glycol‐based hydrogel

Author:

Adeli Fatemeh1,Pourmadadi Mehrab2,Abdouss Majid1,Rahdar Abbas34,Fathi‐karkan Sonia56,Samandari Saeed Saber78,Díez‐Pascual Ana M.9ORCID

Affiliation:

1. Department of Chemistry Amirkabir University of Technology Tehran Iran

2. Protein Research Center Shahid Beheshti Uinversity Tehran Iran

3. Department of Physics, Faculty of Sciences University of Zabol Zabol Iran

4. Key Laboratory of Modeling and Simulation‐based Reliability and Optimization University of Zabol Zabol Iran

5. Natural Products and Medicinal Plants Research Center North Khorasan University of Medical Sciences Bojnurd Iran

6. Department of Advanced Sciences and Technologies in Medicine, School of Medicine North Khorasan University of Medical Sciences Bojnurd Iran

7. New Technologies Research Center Amirkabir University of Technology Tehran Iran

8. Composites Research Laboratory CRLab Amirkabir University of Technology Tehran Iran

9. Universidad de Alcalá Facultad de Ciencias, Departamento de Química Analítica, Química Física e Ingeniería Química Alcalá de Henares Madrid Spain

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.

Publisher

Wiley

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