Synthesis and properties of alginate-based nanoparticles incorporated with different inorganic nanoparticulate modifiers for enhanced encapsulation and controlled release of favipiravir

Alginate is a naturally occurring polysaccharide that consists of guluronic and man-nuronic acid residues. Although it has been widely exploited in drug delivery because of its favor-able properties (biocompatibility, ease of processing, and gelling capability under mild conditions), most alginate-based systems show poor sustained-release drug release because of the high erosion rate of alginate-based hydrogels. This study exploited the effect of three inorganic nanoparticulate modifiers (including montmorillonite clay material, silver nanoparticles, and iron-based magnetic nanoparticles) on the encapsulation and controlled release of favipiravir, which served as a model for poorly soluble drugs. Structures of the generated nanoparticles were characterized by using UV- visible spectroscopy, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), and thermogravimetric analysis (TGA) to examine interac-tions between the loaded drug and the components of the nanoparticles. The incorporation of var-ious nanoparticulate modifiers into alginate-based nanoparticles had little effect on the drug release mechanism, with all modified nanoparticles following a Super Case-II transport mechanism in which the drug release rate was governed by the relaxation of the polymeric chains. However, nanoparticles incorporated with different modifiers show variations in porosity and hydrophilicity. This caused ultimate changes in drug encapsulation efficiency and release sustainability.(c) 2023 The Author(s). Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

Automated summary

This study investigated the encapsulation and controlled release of favipiravir using three inorganic nanoparticulate modifiers. While the release mechanism of the drug was not significantly affected by the modifiers, the incorporation of different types of nanoparticles led to variations in porosity and hydrophilicity, which ultimately influenced the drug encapsulation efficiency and release sustainability.