Advanced characterization of magnetization dynamics in iron oxide magnetic nanoparticle tracers.

Characterization of the magnetization dynamics of single-domain magnetic nanoparticles (MNPs) is important for magnetic particle imaging (MPI), magnetic resonance imaging (MRI), and emerging medical diagnostic/therapeutic technologies. Depending on particle size and temperature, nanoparticle magnetization relaxation time constants span from nanoseconds to seconds. In solution, relaxation occurs via coupled Brownian and Néel relaxation mechanisms. Even though their coexistence complicates analysis, the presence of two timescales presents opportunities for more direct control of magnetization behavior if the two processes can be understood, isolated, and tuned. Using high frequency coils and sample temperature tunability, we demonstrate unambiguous determination of the specific relaxation processes for iron oxide nanoparticles using both time and frequency domain techniques. Furthermore, we study the evolution of the fast dynamics at ≈ 10 nanosecond timescales, for magnetic field amplitudes relevant to MPI.

The effects of intraparticle structure and interparticle interactions on the magnetic hysteresis loop of magnetic nanoparticles.

Technologically relevant magnetic nanoparticles for biomedicine are rarely noninteracting single-domain nanoparticles; instead, they are often interacting, with complex physical and magnetic structures. In this paper, we present both experimental and simulated magnetic hysteresis loops of a system of magnetic nanoparticles with significant interparticle interactions and a well-defined intraparticle structure which are used for magnetic nanoparticle hyperthermia cancer treatment. Experimental measurements were made at 11 K on suspensions of magnetic nanoparticles dispersed in H2O which have been frozen in a range of applied magnetic fields to tune the interparticle interactions. Micromagnetic simulations of hysteresis loops investigated the roles of particle orientation with respect to the field and of particle chaining in the shape of the hysteresis loops. In addition, we present an analysis of the magnetic anisotropy arising from the combination of magnetocrystalline and shape anisotropy, given the well-defined internal structure of the nanoparticles. We find that the shape of the experimental hysteresis loops can be explained by the internal magnetic structure, modified by the effects of interparticle interactions from chaining.

Bio-Nano-Magnetic Materials for Localized Mechanochemical Stimulation of Cell Growth and Death.

Magnetic nanoparticles are promising new tools for therapeutic applications, such as magnetic nanoparticle hyperthermia therapy and targeted drug delivery. Recent in vitro studies have demonstrated that a force application with magnetic tweezers can also affect cell fate, suggesting a therapeutic potential for magnetically modulated mechanical stimulation. The magnetic properties of nanoparticles that induce physical responses and the subtle responses that result from mechanically induced membrane damage and/or intracellular signaling are evaluated. Magnetic particles with various physical, geometric, and magnetic properties and specific functionalization can now be used to apply mechanical force to specific regions of cells, which permit the modulation of cellular behavior through the use of spatially and time controlled magnetic fields. On one hand, mechanochemical stimulation has been used to direct the outgrowth on neuronal growth cones, indicating a therapeutic potential for neural repair. On the other hand, it has been used to kill cancer cells that preferentially express specific receptors. Advances made in the synthesis and characterization of magnetic nanomaterials and a better understanding of cellular mechanotransduction mechanisms may support the translation of mechanochemical stimulation into the clinic as an emerging therapeutic approach.

Physics of heat generation using magnetic nanoparticles for hyperthermia.

Magnetic nanoparticle hyperthermia and thermal ablation have been actively studied experimentally and theoretically. In this review, we provide a summary of the literature describing the properties of nanometer-scale magnetic materials suspended in biocompatible fluids and their interactions with external magnetic fields. Summarised are the properties and mechanisms understood to be responsible for magnetic heating, and the models developed to understand the behaviour of single-domain magnets exposed to alternating magnetic fields. Linear response theory and its assumptions have provided a useful beginning point; however, its limitations are apparent when nanoparticle heating is measured over a wide range of magnetic fields. Well-developed models (e.g. for magnetisation reversal mechanisms and pseudo-single domain formation) available from other fields of research are explored. Some of the methods described include effects of moment relaxation, anisotropy, nanoparticle and moment rotation mechanisms, interactions and collective behaviour, which have been experimentally identified to be important. Here, we will discuss the implicit assumptions underlying these analytical models and their relevance to experiments. Numerical simulations will be discussed as an alternative to these simple analytical models, including their applicability to experimental data. Finally, guidelines for the design of optimal magnetic nanoparticles will be presented.

Exploring the magnetic behavior of nickel-coordinated pyrogallol[4]arene nanocapsules.

The magnetic behavior of nickel-seamed C-propylpyrogallol[4]arene dimeric and hexameric nanocapsular assemblies has been investigated in the solid state using a SQUID magnetometer. These dimeric and hexameric capsular entities show magnetic differentiation both in terms of moment per nanocapsule and potential antiferromagnetic interactions within individual nanocapsules. The weak antiferromagnetic behavior observed at low temperatures indicates dipolar interactions between neighboring nickel atoms; however, this effect is higher in the hexameric nickel-seamed assembly. The differences in magnetic behavior of dimer versus hexamer can be attributed to different coordination environments and metal arrangements in the two nanocapsular assemblies.