REVIEW ARTICLE ON MAGNETIC PARTICLE IMAGING (MPI)
1Himal Rai, 1Avinash Chaubey, 1Prashant Kumar Jha*, 1Debasis Roy, 1Rupam Gayen, 2Satish Kumar Jha, 1Supriyo Roy
1Brainware University Kolkata, India.
2Bhaikaka University, Karamsad, Gujarat
Corresponding Author: Prashant Kumar Jha
DOI: https://doi.org/10.62502/ijmi/3njqg492
ABSTRACT
Due to concerns regarding the complications associated with gadolinium-based contrast agents (GBCAs) in MRI scans, the field of radiology is shifting towards safer options such as superparamagnetic iron oxide nanoparticles (SPIONs) and Magnetic Particle Imaging (MPI). MPI, an innovative tomographic technology, employs SPION tracers to achieve real-time, high-definition imaging without the use of ionizing radiation, thereby ensuring safety by operating at excitation frequencies below 25 kHz. The chemical and physical characteristics of MPI highlight its safety compared to other imaging modalities, utilizing the nonlinear magnetization curve of SPIONs for radiation-free imaging. Tracers like Resovist and Feraheme influence spatial resolution and signal intensity in MPI. Applications of MPI encompass effective cell tracking, promising advancements in vascular imaging, and potential uses in oncology and functional imaging. The assessment concludes that MPI is a low-risk approach, particularly benefiting patients with chronic kidney disease and those susceptible to iodinated contrast, with future directions focusing on refining techniques, creating more advanced nanoparticles, and broadening applications across various medical domains.
Keywords: Magnetic Particle Imaging, Contrast Media, SPION
Article Received: Feb-16, 2024 | Accepted: Feb-28, 2024 | Published: March-20, 2024
Introduction
The realm of radiology is evolving swiftly, particularly with the use of gadolinium-based contrast agents (GBCAs) in magnetic resonance imaging (MRI) due to their safety profile. However, recent findings have highlighted potential complications of these agents, particularly for patients with nephrogenic systemic fibrosis (NSF), especially those with stage 4 or 5 renal disease (known as chronic kidney disease or CKD, with a glomerular filtration rate below 30 ml/min per 1.73 m2). Avoiding the risk posed by GBCAs is crucial, especially for vulnerable patients. As an alternative, superparamagnetic iron oxide nanoparticles (SPIONs) have emerged, with Magnetic Particle Imaging (MPI) being a notable advancement in this domain. MPI is a novel tomographic technology that utilizes a tracer called a superparamagnetic iron oxide nanoparticle (SPION), consisting of a surface coating (typically polyethylene glycol, carboxy dextran, or dextran) surrounding a core of magnetite (Fe3O4) or maghemite (Fe2O3). This technique enables real-time, high-resolution, and highly sensitive imaging without ionizing radiation, making it safer for specific applications compared to other imaging methods. By adjusting the magnetic properties of an iron oxide nanoparticle with a magnetic field gradient, which is generated by the nonlinear magnetic properties of the nanoparticle, MPI can achieve exceptional image clarity. This unique approach allows MPI excitation frequencies to remain below 25 kHz, independent of wavelength, while achieving a resolution that is more than six orders of magnitude finer than the wavelength, typically in millimeters [1,2,3].
Spatial coding in MPI is achieved through external magnetic gradient fields, while signal production involves periodically changing external magnetic fields. By employing sophisticated tracers and optimized scanner configurations, MPI can achieve a spatial resolution of approximately 1 mm. The essence of MPI lies in leveraging small magnetic particle technology, which is not only widely employed for its non-destructive nature but also for its ease and speed of deployment. Its radiation-free characteristic makes it patient-friendly, utilizing the nonlinear magnetization curve of superparamagnetic nanoparticles, particularly SPIO.
The breakdown of these particles in the liver post-imaging is standard since they are already part of clinical MRI practices. Signal creation involves the use of periodically changing external magnetic fields, while spatial coding utilizes external magnetic gradient fields. Advanced tracers and optimal scanner setups contribute to achieving the desired spatial resolution of around 1 mm. Furthermore, the MPI scanner maximizes the unique properties of SPIOs by applying specific magnetic fields through a multi-layered coil topology, adapting its response accordingly. The primary signal for 3D visualization is the tracer response, which is amplified through receiving coils.
The core essence of magnetic particle imaging (MPI) hinges on the utilization of SPION (superparamagnetic iron oxide nanoparticle) tracers, which are vital components that enable the technique. These tracers consist of iron oxide nanoparticles exhibiting spontaneous magnetization under the influence of an applied magnetic field, facilitating the identification of bodily fluids like blood. Unlike the human body, which lacks a magnetic interface for magnetic field imaging, even a minor magnetic field can induce a directional shift. Notably, the properties of SPIONs significantly impact the resolution and signal intensity achievable with MPI.
Current MPI tracers in use, such as Resovist and Feraheme, are not developed solely based on MPI physics but rather employ imaging principles. For instance, the T2 relaxation time is shortened in MRI by incorporating Nano magnetic material, which introduces magnetic micro- gradients to external magnetic fields, causing a loss of phase coherence in resonance protons and resulting in signal voids in the MR image.
MPI finds diverse applications, notably in cell tracking. Feraheme, following its FDA approval, has demonstrated efficacy due to its small size and easy absorption by body cells, making it suitable for cell tracking. Notably, there are no known side effects even for individuals with kidney issues receiving iodinated sensitive contrast.
Innovative approaches have been explored to tailor tracers compliant with MPI physics theory. Modifications in particle size and shape have yielded tracers with significant saturation magnetization, excellent resolution, and sensitivity in MPI, surpassing commercially available options like VivoTrax. These bespoke tracers have proven effective in real-time and extended monitoring of stem cells in vivo. Additionally, MPI holds promise in vascular imaging, surpassing the standard CT perfusion method, which carries ionizing radiation risks. MPI's capabilities have been demonstrated in measuring cerebral blood flow in live mice and imaging stroke-related perfusion changes in rodents.
Moreover, MPI's potential extends to cancer imaging by leveraging the enhanced permeability and retention (EPR) effect, allowing for tumor detection even in early stages. Functional imaging applications of MPI include assessing organ function and monitoring therapies through dynamic SPION distribution imaging, demonstrating high sensitivity and reduced scan duration. In conclusion, MPI stands as a low-risk diagnostic imaging method, benefiting patients with chronic kidney disease and those at risk with iodinated contrast. Its non-invasive, radiation-free nature coupled with high resolution and sensitivity is revolutionizing diagnostic imaging, with ongoing advancements focusing on refining tracer properties and expanding applications across diverse medical fields. Future trends in MPI entail optimizing imaging techniques, developing advanced MNPs, and integrating with other imaging modalities for comprehensive diagnostic approaches. Efforts to address safety concerns and standardize protocols are expected to drive wider adoption of MPI in research and clinical settings, pavingthe way for breakthroughs in medical imaging and diagnostics.
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