4.7 Article

Preparation of pH-sensitive chitosan/polyvinylpyrrolidone/alpha-Fe2O3 nanocomposite for drug delivery application: Emphasis on ameliorating restrictions

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DOI: 10.1016/j.ijbiomac.2021.01.067

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Chitosan; Polyvinylpyrrolidone; Iron oxide; pH-sensitive nanocarrier; Drug delivery

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In this study, nanocomposites of hematite/chitosan/polyvinylpyrrolidone were synthesized as a drug carrier for doxorubicin, exhibiting pH-sensitive and controlled release properties. The chemical and physical interactions within the nanocomposites were confirmed through analyses, and they demonstrated good cytotoxicity and anticancer effects in cell experiments.
Chitosan (CS)/polyvinylpyrrolidone (PVP)/hematite (alpha-Fe2O3) nanocomposites loaded with Doxorubicin (drug model) were synthesized via an oil-in-water emulsification method to develop a biocompatible and pH-sensitive drug nanocarrier for the first time. A hydrogel, including CS, PVP, and alpha-Fe2O3, was fabricated successfully with glutaraldehyde (GA) as the cross-linker. Incorporating alpha-Fe2O3 into CS/PVP hydrogel improved the pH-sensitivity and developed beneficial hydrogel. FTIR and XRD analysis illustrated physical interactions between polymer-polymer, polymer-drug, and crystalline behavior of prepared nanocomposite. These analyses also confirmed chemical bonding in nanocomposite's structure. The FE-SEM analysis showed successful impregnation of a-Fe2O3 into CS/PVP matrix and spherical structure. To clarify the size distribution and surface charge of the drug-loaded nanocomposite (CS/PVP/alpha-Fe2O3/Dox), DLS and zeta analyses were conducted. They showed the mean size of nanocomposites at about 247 nm. Drug-loaded CS/PVP/alpha-Fe2O3 nanocomposite and CS/PVP/Dox were studied for their release behavior and kinetics. Furthermore, the effect of alpha-Fe2O3 on release from CS/PVP/alpha-Fe2O3/Dox nanocomposite was investigated. That showed an increase in encapsulation of Doxorubicin and beneficial release behavior such as slow-release and retention effect. The release from this drug-loaded nanocomposite revealed excellent pH-sensitive and controlled release of the drug. Besides, the in vitro cytotoxicity and cell apoptosis were studied to recognize biological properties. These analyses revealed that drug-loaded nanocomposite caused high inhibition to MCF-7 cells in presence of alpha-Fe2O3 and proved the hematite's anticancer effect. By and large, this study confirmed CS/PVP/alpha-Fe2O3 nanocomposites as a potential candidate for the controlled pH-sensitive release of the drug. (C) 2021 Published by Elsevier B.V.

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