Publications by authors named "Cindi L Dennis"

Article Synopsis
  • High-crystal-quality nanoferrites with short ligands, like oleic acid, have been found to improve sensitivity and spatial resolution in magnetic particle imaging (MPI) due to their ability to form uniaxial assemblies.
  • A one-pot thermal decomposition method was developed to create magnetic nano-objects (MNOs) that show strong magnetic interactions and reproducibility, with sizes ranging from 12 to 27 nm, affecting their response and chain formation capabilities.
  • The study revealed that these ferrite MNOs significantly enhance signal and spatial resolution compared to existing MPI tracers, with results indicating the importance of optimizing the frequency and field amplitude for effective imaging and thermal performance.
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Temperature is a fundamental physical quantity important to the physical and biological sciences. Measurement of temperature within an optically inaccessible three-dimensional (3D) volume at microscale resolution is currently limited. Thermal magnetic particle imaging (T-MPI), a temperature variant of magnetic particle imaging (MPI), hopes to solve this deficiency.

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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.

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The magnetic properties of nickel-seamed C-pyrogallol[4]arene (PgC Ni) hexamers and dimers are studied for the first time in solution. The combination of small-angle neutron scattering and superconducting quantum interference device magnetometer measurements of the solution species reveal their paramagnetic and weakly antiferromagnetic behaviour. Surprisingly, the magnetic results indicated the presence of an unprecedented 13 Å-radius species, larger than both the dimeric and hexameric nanocapsules with both octahedral and square-planar metal centers.

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We report here on the reproducibility of measurements on a second-order gradiometer superconducting quantum interference device magnetometer of two different yttrium iron garnet spheres, both having a diameter of 1 mm: 1) the National Institute of Standards and Technology magnetic moment standard reference material (SRM) and 2) a commercial sample. It has been suggested that rotating the sample rod around its axis can move the sample center toward the center of the second-order gradiometer coil. The observed value of the magnetic moment will be theoretically a minimum when the radial offset is 0, and this value will increase in a "quadratic" manner with the radial offset.

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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 HO which have been frozen in a range of applied magnetic fields to tune the interparticle interactions.

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Magnetic iron oxide nanoparticles (MIONs) have established a niche as a nanomedicine platform for diagnosis and therapy, but they present a challenging surface for ligand functionalization which limits their applications. On the other hand, coating MIONs with another material such as gold to enhance these attachments introduces other complications. Incomplete coating may expose portions of the iron oxide core, or the coating process may alter their magnetic properties.

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The presence of a large applied magnetic field removes the degeneracy of the vacuum energy states for spin-up and spin-down neutrons. For polarized neutron reflectometry, this must be included in the reference potential energy of the Schrödinger equation that is used to calculate the expected scattering from a magnetic layered structure. For samples with magnetization that is purely parallel or antiparallel to the applied field which defines the quantization axis, there is no mixing of the spin states (no spin-flip scattering) and so this additional potential is constant throughout the scattering region.

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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.

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Three chloride-bridged lanthanide compounds, [Ln4Cl6(CH3OH)12(OH)2]·4Cl·2CH3OH [Ln = Gd (), Dy () and Er ()], have been unexpectedly isolated by the reactions of LnCl3·6H2O and N,N'-bis(salicylidene)-1,2-(phenylene-diamine) (H2L). X-ray crystallographic analysis reveals a triclinic cell with a unique defect-dicubane {Ln4} core and the structure across this series is nominally isomorphic. Measurements of direct current magnetic susceptibility and isothermal magnetization give insight into the relevant cluster Hamiltonians for , , and , and alternating current susceptibility shows slow relaxation in , but not in or down to 2 K and up to 1 kHz.

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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.

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The differences in magnetic properties of metal-based nanometric assemblies are due to distinct contributions from host-guest interactions, structural integrity, and magnetic interactions. To disentangle these contributions, it is necessary to control the self-assembly process that forms these entities. Herein we study the effect of host-to-guest ratios to identify remarkably different structural-magnetic contributions of C-methylpyrogallol[4]arene⊂ferrocene/(PgC1)2⊂Fc dimers vs (PgC1)3⊂Fc nanotubes.

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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.

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Solid-state proton nuclear magnetic resonance (NMR) measurements are performed successfully on polymer blend thin films through the use of synthetic mica as a substrate. When used as a substrate, synthetic fluorophlogopite mica with its proton-free, diamagnetic character, allows for adequate measurement sensitivity while minimally perturbing the proton thin-film spectra, especially relative to more commonly available natural micas. Specifically, we use multiple-pulse techniques in the presence of magic-angle spinning to measure the degree of mixing in two different polymer blend thin films, polystyrene/poly(xylylene ether) and poly(1-methyladamantyl methacrylate) (PMAdMA)/triphenylsulfonium perfluorobutanesulfonate (TPS-PFBS), spin-coated onto mica substrates.

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Iridescent Schiller layers were prepared by centrifugation of beta-FeOOH sols with an initial particle concentration of 10(14) particles/mL, reducing the Schiller layer formation time from over 2 months to 3 weeks. The formation and structure of the Schiller layers were investigated using optical and transmission electron microscopy. Microscopy studies revealed the self-assembly to proceed by the formation of two-dimensional particle arrays followed by the stacking of these arrays to form the final iridescent state.

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The magnetic properties of 10 nm diameter surfactant-coated cobalt (Co) nanoparticles in 1,2-dichlorobenzene (DCB) are investigated by a series of sequential magnetic moment (m) vs temperature (T) measurements. A rapid rise in magnetic moment around 250 K during warming and an abrupt drop at 234 K during cooling are observed when a nonsaturating external magnetic field is applied. Differential scanning calorimetry (DSC) measurements demonstrate that the rapid rise and abrupt drop in magnetization are associated with the melting and freezing of the solvent.

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