Shaping Magnetic Hyperthermia Properties through Nanoparticle Surface‐Ligand Design: Implications for Cellular Responses

Magnetic iron oxide nanoparticles have attracted increasing attention for their potential use in biomedicine over the last few decades. Their inherent characteristics have enabled novel therapeutic approaches such as magnetic hyperthermia. To maximize the therapeutic efficacy, several research efforts have been focused on the optimization of these nanoparticles in terms of their size, morphology, and crystal structure etc. However, no consensus has been reached regarding the optimal surface design. To gain deeper insight into this complex phenomenon, the influence of a variety of surface ligands on the magnetic, hyperthermic, and colloidal behaviors of the magnetic iron oxide nanoparticles, along with their influence on cellular viability, is investigated. The results revealed that the molecular structure of the ligands, including both the anchoring group and molecular chain, plays a critical role in determining the above-mentioned properties and performance. This work lays the groundwork for surface engineering of magnetic nanoparticles, emphasizing the need to consider the magneto-hyperthermic performance, colloidal stabilities, and the cellular interactions as interconnected factors that critically influence their clinical applicability.

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Publication Details

Journal
Small
Published
2025-10-25
DOI
https://doi.org/10.1002/smll.202507665
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
Field-Weighted Citation Impact
0.00

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article

Shaping Magnetic Hyperthermia Properties through Nanoparticle Surface‐Ligand Design: Implications for Cellular Responses

Bradley J. Nelson, Salvador Pané, Lukas Hertle, Xiangzhong Chen et al.
Small
Nanoparticle-Based Drug Delivery
article

Shaping Magnetic Hyperthermia Properties through Nanoparticle Surface‐Ligand Design: Implications for Cellular Responses

Bradley J. Nelson, Salvador Pané, Lukas Hertle, Xiangzhong Chen, Josep Puigmartí‐Luis, Eneko Garaio, Alberto López‐Ortega, Marta Estrader, Valentin Gantenbein, Hao Ye, Joaquim Llacer‐Wintle, Iain C. Paul, Alba Martínez‐Jiménez de Allo, Sarina Nigg
article en

Abstract

Magnetic iron oxide nanoparticles have attracted increasing attention for their potential use in biomedicine over the last few decades. Their inherent characteristics have enabled novel therapeutic approaches such as magnetic hyperthermia. To maximize the therapeutic efficacy, several research efforts have been focused on the optimization of these nanoparticles in terms of their size, morphology, and crystal structure etc. However, no consensus has been reached regarding the optimal surface design. To gain deeper insight into this complex phenomenon, the influence of a variety of surface ligands on the magnetic, hyperthermic, and colloidal behaviors of the magnetic iron oxide nanoparticles, along with their influence on cellular viability, is investigated. The results revealed that the molecular structure of the ligands, including both the anchoring group and molecular chain, plays a critical role in determining the above-mentioned properties and performance. This work lays the groundwork for surface engineering of magnetic nanoparticles, emphasizing the need to consider the magneto-hyperthermic performance, colloidal stabilities, and the cellular interactions as interconnected factors that critically influence their clinical applicability.

SmallVol. 21(50)
Institució Catalana de Recerca i Estudis Avançats (ES), Universidad Pública de Navarra (UPNA) (ES), Institute of Inorganic Chemistry of the Slovak Academy of Sciences (SK), Robotics Research (United States) (US), Guangdong Institute of Intelligent Manufacturing (CN), Yiwu Science and Technology Research Institute (CN), Institut de Nanociència i Nanotecnologia de la Universitat de Barcelona, Universitat de Barcelona (ES)
National Science Foundation, European Commission, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, National Natural Science Foundation of China, Generalitat de Catalunya, Eidgenössische Technische Hochschule Zürich, Agencia Estatal de Investigación, European Social Fund
Openalex Percentile: Top 80%
Nanoparticle-Based Drug Delivery
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