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Hyperthermic effects of dissipative structures of magnetic nanoparticles in large alternating magnetic fields

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TLDR
Numerically compared the magnetic loss in rotatable nanoparticles in aqueous media with that of non-rotatable nanoparticle anchored to localised structures to shed new light on the design of targeted magnetic hyperthermia treatments.
Abstract
Targeted hyperthermia treatment using magnetic nanoparticles is a promising cancer therapy. However, the mechanisms of heat dissipation in the large alternating magnetic field used during such treatment have not been clarified. In this study, we numerically compared the magnetic loss in rotatable nanoparticles in aqueous media with that of non-rotatable nanoparticles anchored to localised structures. In the former, the relaxation loss in superparamagnetic nanoparticles has a secondary maximum because of slow rotation of the magnetic easy axis of each nanoparticle in the large field in addition to the known primary maximum caused by rapid Neel relaxation. Irradiation of rotatable ferromagnetic nanoparticles with a high-frequency axial field generates structures oriented in a longitudinal or planar direction irrespective of the free energy. Consequently, these dissipative structures significantly affect the conditions for maximum hysteresis loss. These findings shed new light on the design of targeted magnetic hyperthermia treatments.

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Journal ArticleDOI

Fundamentals and advances in magnetic hyperthermia

TL;DR: A broad overview of magnetic hyperthermia addressing new perspectives and the progress on relevant features such as the ad hoc preparation of magnetic nanoparticles, physical modeling of magnetic heating, methods to determine the heat dissipation power of magnetic colloids including the development of experimental apparatus and the influence of biological matrices on the heating efficiency is presented in this article.
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Magnetic nanoparticle heating and heat transfer on a microscale: Basic principles, realities and physical limitations of hyperthermia for tumour therapy.

TL;DR: Practical aspects, limitations, and the state of the art for the application of magnetic heating in magnetic particle hyperthermia as thermal treatment of small tumours are illuminated.
Journal ArticleDOI

Magnetic Properties of Magnetic Nanoparticles for Efficient Hyperthermia.

TL;DR: This work discusses some of the physics principles for effective heating of MNPs focusing on the role of surface anisotropy, interface exchange an isotropy and dipolar interactions, and some physical and practical limitations of using MNPs in magnetic hyperthermia.
Journal ArticleDOI

Physics of heat generation using magnetic nanoparticles for hyperthermia

TL;DR: A summary of the literature describing the properties of nanometer-scale magnetic materials suspended in biocompatible fluids and their interactions with external magnetic fields and the implicit assumptions underlying these analytical models are provided.
References
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Journal Article

Thermal Fluctuations of a Single-Domain Particle

Brown
- 01 Jan 1963 - 
Journal ArticleDOI

Thermal Fluctuations of a Single-Domain Particle

TL;DR: In this article, the Langevin equation of the Fokker-planck partial differential equation is replaced by a random-field term, which can be avoided by using the fluctuation-dissipation theorem.
Journal ArticleDOI

Heating magnetic fluid with alternating magnetic field

TL;DR: In this paper, the authors developed analytical relationships and computations of power dissipation in magnetic fluid (ferrofluid) subjected to alternating magnetic field and showed that the dissipation results from the orientational relaxation of particles having thermal fluctuations in a viscous medium.
Journal ArticleDOI

Progress in applications of magnetic nanoparticles in biomedicine

TL;DR: A progress report on the biomedical applications of magnetic nanoparticles since 2003 is presented in this paper, with a focus on magnetic actuation for in vitro non-viral transfection and tissue engineering.
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Coadministration of a tumor-penetrating peptide enhances the efficacy of cancer drugs.

TL;DR: Mouse tumor models show that coinjection of the iRGD peptide increases the tumor penetration and antitumor activity of several cancer drugs, including the cytotoxic agent doxorubicin and the therapeutic antibody trastuzumab (Herceptin), without increasing their harmful effects on healthy tissue.
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