Chitosan/Alginate Nanogels Containing Multicore Magnetic Nanoparticles for Delivery of Doxorubicin

• Main Authors: Sérgio R. S. Veloso (Author), Eva S. Marta (Author), Pedro V. Rodrigues (Author), Cacilda Moura (Author), Carlos O. Amorim (Author), Vítor S. Amaral (Author), Miguel A. Correa-Duarte (Author), Elisabete M. S. Castanheira (Author)
• Format: Book
• Published: MDPI AG, 2023-08-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Summary

In this study, multicore-like iron oxide (Fe₃O₄) and manganese ferrite (MnFe₂O₄) nanoparticles were synthesized and combined with nanogels based on chitosan and alginate to obtain a multimodal drug delivery system. The nanoparticles exhibited crystalline structures and displayed sizes of 20 ± 3 nm (Fe₃O₄) and 11 ± 2 nm (MnFe₂O₄). The Fe₃O₄ nanoparticles showed a higher saturation magnetization and heating efficiency compared with the MnFe₂O₄ nanoparticles. Functionalization with citrate and bovine serum albumin was found to improve the stability and modified surface properties. The nanoparticles were encapsulated in nanogels, and provided high drug encapsulation efficiencies (~70%) using doxorubicin as a model drug. The nanogels exhibited sustained drug release, with enhanced release under near-infrared (NIR) laser irradiation and acidic pH. The nanogels containing BSA-functionalized nanoparticles displayed improved sustained drug release at physiological pH, and the release kinetics followed a diffusion-controlled mechanism. These results demonstrate the potential of synthesized nanoparticles and nanogels for controlled drug delivery, offering opportunities for targeted and on-demand release in biomedical applications.

Item Description

10.3390/pharmaceutics15092194
1999-4923