Superparamagnetic iron oxide nanoparticle (SPION) contrast agents for MRI generally consist of a biocompatible polymer coating or matrix with superparamagnetic (ferri- or ferromagnetic) iron oxide cores [1
]. Superparamagnetic particles are nanoscale particles in which quantum effects dominate over bulk effects. For iron oxides, this generally translates to diameters of less than 30 nm. They exhibit strong magnetization in the presence of an applied field; however, upon removal of the field, they retain no permanent magnetization, making them ideal for in vivo
applications where magnetic dipole-induced aggregation of particles within the vasculature would have the potential to cause embolization.
Inside the scanner, the SPIONs cause local perturbations of the magnetic field around the particles, resulting in detectable variations of the relaxation times of nearby proton spins after a probing RF pulse has been applied. Specifically, these local distortions increase proton dephasing, providing contrast enhancement in T2
-weighted (spin-spin or transverse) MR images. In fact, the resulting T2
-weighted images show signal intensity decreases, known as negative contrast, in regions where the SPIONs have aggregated [4
Although many of these particles eventually end up naturally in the liver, the leaky vasculature present in solid tumors also promotes extravasation and accumulation—an effect known as “enhanced permeability and retention (EPR)—thereby providing contrast highlighting of the tumor against the surrounding tissue. The contrast effects are amplified when reactive cells associated with tumors also take up the particles (e.g., [5
]). Implanted or injected cells that have been doped with SPIONs also can be tracked via T2
-weighted MR imaging for applications in regenerative medicine and cell targeting (For review see [7
Though FDA-cleared, the main commercially available agents, such as Feridex/Comidex, have been withdrawn from the market [8
]. Recently, a new SPION-based MRI contrast agent, Feraheme (also known as Ferumoxytol—AMAG Pharmaceuticals), has received a significant amount of attention due to its FDA-cleared status for use in humans, and there is keen interest to understand its magnetic properties. Feraheme is a SPION coated with a low molecular weight semi-synthetic carbohydrate. It is particularly indicated for the treatment of iron deficiency anemia in adult patients with chronic kidney disease [9
]. Feraheme has a hydrodynamic diameter of ca
. 30 nm and, most importantly for other potential biomedical applications, the carboxylated polymer coating allows for the bio-functionalization of the particle’s surface [10
To date, the molecular weight and iron release profile of feraheme have been investigated [11
], as have some of the basic magnetic properties [10
], and these studies have focused on bio-functionalization and MRI contrast. A thorough evaluation of the magnetic properties of Feraheme and consideration of its potential use in other biomedical applications, such as magnetic fluid hyperthermia (MFH), cell tracking/loading optimization, nanomagnetic cellular actuation, and nanomagnetic drug and gene delivery, have not yet been reported (For reviews of these applications see [1
Magnetic fluid hyperthermia is a technique that utilizes the coupling of radiofrequency magnetic fields with magnetic nanoparticles to preferentially heat the particles compared to surrounding diamagnetic tissue. As the body is primarily diamagnetic, magnetic fields pass through relatively unimpeded, allowing the applied RF magnetic field to penetrate deep into tissue and deposit significant amounts of energy, primarily but not exclusively in the form of heat, to targets where MNPs have accumulated either via extravasation through leaky tumor vasculature or via biomolecular targeting of cell surface receptors. Herein, we present morphological and magnetic characterization data for Feraheme as well as the results of a preliminary evaluation of the suitability of this SPION for MFH applications.
3. Experimental Section
3.1. Feraheme Samples
Vials of Feraheme (17 mL) were purchased commercially and consisted of 510 mg of elemental iron per vial (30 mg/mL of iron and 122 mg/mL of particles). Several different lot numbers were used and showed no significant differences in measurements. They were stored at the recommended temperature of 20 °C before use, and were used before the expiration date on the vial. Samples for SQUID magnetometry analysis were freeze-dried. The label states that the material containing the iron oxide particles is “polyglucose sorbitol carboxymethylether”, but no analysis of the organic part was attempted.
3.2. High Resolution Transmission Electron Microscopy (HRTEM)
Microscopy was performed on a JEOL 2010F HRTEM at 200 kV. Copper TEM grids were prepared by diluting Feraheme 50 times in double-distilled, deionized water. This solution was then pipetted onto TEM grids, which were placed over filter paper to absorb any excess fluid. The Formvar TEM grids were then covered and allowed to dry overnight. Particle size analysis was conducted by measuring the diameter of 232 particles using NIH ImageJ. Energy dispersive X-ray spectroscopy (EDX) analysis (Oxford Instruments EDS X-ray Microanalysis System coupled to the HRTEM microscope) and selected area electron diffraction were performed on one sample of Feraheme prepared as described above.
3.3. Superconducting Quantum Interference Device (SQUID) Magnetometry
Analysis of the magnetic properties of Feraheme was conducted using data acquired with a Quantum Design MPMS XL superconducting quantum interference device (SQUID) magnetometer. A sample of Feraheme was freeze-dried and 11.35 mg (dry weight) was packed into gel caps for insertion into the instrument. The background signal from the gel-caps is known to be significantly less than the signal arising from the sample, so the background was not subtracted. Magnetic hysteresis loops (magnetization [M] vs. applied magnetic field [H]) were measured at 5 K and 300 K in fields up to ±7 T. The temperature dependence of magnetization was measured after cooling from 300 K to 5 K in a 10 mT field and subsequently measured while warming in a 10 mT field. Zero-field-cooled magnetization was measured upon warming from 5 K in static field of about 1 mT after cooling from 300 K to 5 K in zero field.
3.4. Magnetic Fluid Hyperthermia (MFH)
The suitability of Feraheme for magnetic fluid hyperthermia (MFH) applications was evaluated using an Ambrell AC coil system running at 340 kHz and 37.5 kA/m. Stock Feraheme suspensions were diluted in distilled water to concentrations of 2, 10, 15 and 30 mg/mL (particles) and 1 mL of the new suspensions was then sealed in a sealed PVC vial. The temperature of the suspension was monitored and recorded automatically at 10 s. intervals with an Optical probe (Neoptix Reflex with NEOLink Software) inserted into the suspension. Water without Feraheme particles was evaluated at the same intervals as a control. The starting temperature for both the suspension and the water control was 12 °C. These measurements were repeated four times for each concentration and for the water control.
Magnetic micro- and nanoparticles are being increasingly employed in biomedical research and, in some cases, clinical diagnostic applications. FDA clearance of Feraheme opens up the possibility of using these particles for biomedical applications other than MRI contrast enhancement. The aim of this study was to better understand the morphological and magnetic properties of these particles in order to begin to evaluate the potential for using Feraheme in clinical applications such as magnetic fluid hyperthermia, in vivo cell targeting and actuation, magnetically targeted drug delivery and in vivo cell tracking.
The superparamagnetic nature of the magnetic cores described here as well as the biocompatible nature of the polymer matrix makes Feraheme ideal for in vivo applications where aggregation of blocked magnetic particles has the potential to cause embolism. The size of the particles allows them to escape the body’s Reticuloendothelial surveillance system (RES), while the relatively high magnetic moment (>25 Am2/kg) for a polymer/iron oxide composite, provides an indication that they could be used for intracellular loading in cell targeting applications.
Initial evaluation of the heating ability of Feraheme also indicates that the particles have the potential to be used in magnetic fluid hyperthermia applications. The significant and rapid heating above ambient temperature shown here in the higher concentrations indicate that these particles have the potential to induce cell apoptosis and necrosis if delivered to solid tumors at appropriate concentrations. However, it should be noted that these experiments, like many evaluations of magnetic nanoparticles for hyperthermia applications, were done in water without flow. In the body, blood flow through the tissue provides an effective mechanism for heat transport, likely limiting the clinical effectiveness somewhat or requiring higher MNP concentrations. Another caveat to this analysis is that the starting temperature for these experiments was below body temperature (12 °C). Starting at body temperature would likely result in a slower temperature rise and may not result in the full temperature increase observed over duration of this experiment.
The data provided in this study provide a sound foundation for further evaluation of the potential of Feraheme in biomedical and clinical applications beyond their current use in as MRI contrast agents. The field of Mesoscale Magnetic Biomaterials—magnetic biomaterials that range is size from nanometers to microns—is growing rapidly, with applications spanning from those already in use in the clinic and pathology laboratories, such as MRI contrast and cell separation, to more advanced and futuristic applications in cancer treatment, tissue engineering and regenerative medicine. For all of these in vivo applications, the development and use of biocompatible magnetic nanoparticles will be a pre-requisite. In addition, re-purposing formulations that are already in use may provide a shorter route to the clinic for many of these applications. The work presented here represents an initial step in investigating this idea by rigorously characterizing Feraheme and conducting a preliminary investigation for one of these potential future applications—magnetic fluid hyperthermia.