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      Superparamagnetic iron oxide nanoparticles for their application in the human body: Influence of the surface

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          Abstract

          Iron oxide nanoparticles (IONs) are of great interest in nanomedicine for imaging, drug delivery, or for hyperthermia treatment. Although many research groups have focused on the synthesis and application of IONs in nanomedicine, little is known about the influence of the surface properties on the particles' behavior in the human body. This study analyzes the impact of surface coatings (dextran, polyvinyl alcohol, polylactide-co-glycolide) on the nanoparticles’ cytocompatibility, agglomeration, degradation, and the resulting oxidative stress induced by the particle degradation. All particles, including bare IONs (BIONs), are highly cytocompatible (>70%) and show no significant toxicity towards smooth muscle cells. Small-angle X-ray scattering profiles visualize the aggregation behavior of nanoparticles and yield primary particle sizes of around 20 nm for the investigated nanoparticles. A combined experimental setup of dynamic light scattering and phenanthroline assay was used to analyze the long-term agglomeration and degradation profile of IONs in simulated body fluids, allowing fast screening of multiple candidates. All particles degraded in simulated endosomal and lysosomal fluid, confirming the pH-dependent dissolution. The degradation rate decreased with the shrinking size of particles leading to a plateau. The fastest Fe 2+ release could be measured for the polyvinyl-coated IONs. The analytical setup is ideal for a quick preclinical study of IONs, giving often neglected yet crucial information about the behavior and toxicity of nanoparticles in the human body. Moreover, this study allows for the development and evaluation of novel ferroptosis-inducing agents.

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          Highlights

          • Effects of various coatings on the behavior of iron oxide nanoparticles.

          • Agglomeration and saturation magnetization influence their magnetophoretic behavior.

          • Fast experimental setup for screening the nanoparticles for usage in nanomedicine.

          • Usage of simulated body fluids.

          • Agglomeration and degradation directly affect each other.

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          Most cited references89

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          The role of iron and reactive oxygen species in cell death.

          The transition metal iron is essential for life, yet potentially toxic iron-catalyzed reactive oxygen species (ROS) are unavoidable in an oxygen-rich environment. Iron and ROS are increasingly recognized as important initiators and mediators of cell death in a variety of organisms and pathological situations. Here, we review recent discoveries regarding the mechanism by which iron and ROS participate in cell death. We describe the different roles of iron in triggering cell death, targets of iron-dependent ROS that mediate cell death and a new form of iron-dependent cell death termed ferroptosis. Recent advances in understanding the role of iron and ROS in cell death offer unexpected surprises and suggest new therapeutic avenues to treat cancer, organ damage and degenerative disease.
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            Magnetic iron oxide nanoparticles: synthesis, stabilization, vectorization, physicochemical characterizations, and biological applications.

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              PLGA-based nanoparticles: an overview of biomedical applications.

              Poly(lactic-co-glycolic acid) (PLGA) is one of the most successfully developed biodegradable polymers. Among the different polymers developed to formulate polymeric nanoparticles, PLGA has attracted considerable attention due to its attractive properties: (i) biodegradability and biocompatibility, (ii) FDA and European Medicine Agency approval in drug delivery systems for parenteral administration, (iii) well described formulations and methods of production adapted to various types of drugs e.g. hydrophilic or hydrophobic small molecules or macromolecules, (iv) protection of drug from degradation, (v) possibility of sustained release, (vi) possibility to modify surface properties to provide stealthness and/or better interaction with biological materials and (vii) possibility to target nanoparticles to specific organs or cells. This review presents why PLGA has been chosen to design nanoparticles as drug delivery systems in various biomedical applications such as vaccination, cancer, inflammation and other diseases. This review focuses on the understanding of specific characteristics exploited by PLGA-based nanoparticles to target a specific organ or tissue or specific cells. Copyright © 2012 Elsevier B.V. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Heliyon
                Heliyon
                Heliyon
                Elsevier
                2405-8440
                25 May 2023
                June 2023
                25 May 2023
                : 9
                : 6
                : e16487
                Affiliations
                [a ]Chair of Bioseparation Engineering, TUM School of Engineering and Design, Technical University of Munich, Germany
                [b ]Chair of Medical Materials and Implants, TUM School of Engineering and Design, Munich Institute of Biomedical Engineering, Technical University of Munich, Germany
                [c ]Division of Medicinal Chemistry, Otto Loewi Research Center, Medical University of Graz, Austria
                [d ]Division of Medical Physics and Biophysics, Gottfried Schatz Research Center, Medical University of Graz, Austria
                [e ]Institute of Inorganic Chemistry, Graz University of Technology, Stremayrgasse 9/IV, Graz, 8010, Austria
                [f ]BioTechMed-Graz, Austria
                Author notes
                []Corresponding author. Division of Medicinal Chemistry, Otto Loewi Research Center, Medical University of Graz, Austria. sebastian.schwaminger@ 123456medunigraz.at
                Article
                S2405-8440(23)03694-0 e16487
                10.1016/j.heliyon.2023.e16487
                10238907
                2abac6d9-fed9-4f49-9f22-bf8893a18124
                © 2023 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 15 March 2023
                : 16 May 2023
                : 18 May 2023
                Categories
                Research Article

                iron oxide nanoparticles,nanomedicine,simulated body fluids,cytocompatibility,agglomeration,magnetic separation

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