Advances in Magnetic Nanoparticles: Biocompatibility, Toxicity, and Biomedical Applications

A special issue of Magnetochemistry (ISSN 2312-7481). This special issue belongs to the section "Applications of Magnetism and Magnetic Materials".

Deadline for manuscript submissions: 28 February 2025 | Viewed by 909

Special Issue Editor

Special Issue Information

Dear Colleagues,

Magnetic nanoparticles (MNPs) have great potential in various areas such as medicine, cancer therapy and diagnostics, biosensing, and material science.

With the development of nanotechnology, the emergence of novel antitumor techniques that utilize magnetic nanoparticles (MNPs) such as magnetic hyperthermia and magnetomechanical stress have been the subject of much attention and study in recent years as anticancer tools. In magnetic hyperthermia, an external alternating magnetic field is used to heat the area of the cancer tissue due to the local heating of the magnetic nanoparticles, which are preferentially accumulated in cancer cells due to altered iron metabolism. This treatment leads to cellular effects such as decreased cell viability, cytoskeleton damage, the elevation of oxidative stress, cell cycle arrest, and cellular death by apoptosis. By taking advantage of differences in the thermal resistance of normal and tumor cells, magnetic hyperthermia can kill tumor cells selectively, thus lowering the side effects.

In this Special Issue, special attention will be paid to the utilization of strategies for the functionalization of MNPs in order to improve their biocompatibility and to direct their application by binding biofunctional molecules such as antibodies, ligands, or receptors; this will provide high selectivity and sensitivity for many biological applications.  

A relatively novel technique whose popularity has soared in recent years for the treatment of cancer is magnetomechanical stress. In this technique, the magnetic field exerts magnetic forces on the magnetic nanoparticles; in turn, this exerts mechanical forces on malignant and non-malignant cell membranes, causing damage and cell death primarily to cancerous tissues.

This Special Issue will focus on current approaches to the use of magnetic nanoparticles, magnetic hyperthermia, and magnetomechanical stress in the search for a multifunctional therapy in cancer, with an improved therapeutic index for treatment without the occurrence of non-additive side effects in normal tissue.

Prof. Dr. Rumiana Tzoneva
Guest Editor

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Keywords

  • magnetic nanoparticles
  • biocompatibility
  • magnetic hyperthermia
  • magnetomechanical stress
  • cancer cells
  • cell death
  • cytoskeleton damage
  • cell cycle arres
  • oxidative stress

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Published Papers (1 paper)

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Research

17 pages, 8054 KiB  
Article
Incorporation of Superparamagnetic Magnetic–Fluorescent Iron Oxide Nanoparticles Increases Proliferation of Human Mesenchymal Stem Cells
by Willian Pinheiro Becker, Juliana Barbosa Torreão Dáu, Wanderson de Souza, Rosalia Mendez-Otero, Rosana Bizon Vieira Carias and Jasmin
Magnetochemistry 2024, 10(10), 77; https://doi.org/10.3390/magnetochemistry10100077 - 12 Oct 2024
Viewed by 683
Abstract
Mesenchymal stem cells (MSCs) have significant therapeutic potential and their use requires in-depth studies to better understand their effects. Labeling cells with superparamagnetic iron oxide nanoparticles allows real-time monitoring of their location, migration, and fate post-transplantation. This study aimed to investigate the efficacy [...] Read more.
Mesenchymal stem cells (MSCs) have significant therapeutic potential and their use requires in-depth studies to better understand their effects. Labeling cells with superparamagnetic iron oxide nanoparticles allows real-time monitoring of their location, migration, and fate post-transplantation. This study aimed to investigate the efficacy and cytotoxicity of magnetic–fluorescent nanoparticles in human adipose tissue-derived mesenchymal stem cells (hADSCs). The efficacy of Molday ION rhodamine B (MIRB) labeling in hADSCs was evaluated and their biocompatibility was assessed using various techniques and differentiation assays. Prussian blue and fluorescence staining confirmed that 100% of the cells were labeled with MIRB and this labeling persisted for at least 3 days. Transmission electron microscopy revealed the internalization and clustering of the nanoparticles on the outer surface of the cell membrane. The viability assay showed increased cell viability 3 days after nanoparticle exposure. Cell counts were higher in the MIRB-treated group compared to the control group at 3 and 5 days and an increased cell proliferation rate was observed at 3 days post-exposure. Adipogenic, osteogenic, and chondrogenic differentiation was successfully achieved in all groups, with MIRB-treated cells showing an enhanced differentiation rate into adipocytes and osteocytes. MIRB was efficiently internalized by hADSCs but induced changes in cellular behavior due to the increased cell proliferation rate. Full article
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