Magnetic Particle Imaging (MPI)

Principal Investigator: Lawrence Wald
Title: “
Magnetic Particle Imaging (MPI) for Functional Brain Imaging in Humans”
BRAIN Category: 
Next Generation Human Imaging (RFA MH-14-217)

The Wald team plans to use an iron-oxide contrast agent to track blood volume, which will permit dramatically more sensitive imaging of human brain activity than existing methods.

NIH Webpages

Schematic set up and operating principle of the Magnetic Particle Imaging technology. Phillips MPI.

Schematic set up and operating principle of the Magnetic Particle Imaging technology. Phillips MPI.

Project Description

In this planning grant we propose several engineering developments to advance Magnetic Particle Imaging (MPI) to replace MRI as the next-generation functional brain imaging tool for human neuroscience. We assemble a group of technology experts to solve a myriad of identified and unidentified barriers, we employ simulation and bench-top experiments to characterize and test solutions for these technical obstacles and validate solutions by bench testing specific sub-sections of the imager. Finally we simulate the overall performance of the planned device and assess its benefit for human functional brain imaging. MPI is a young but extremely promising technology that uses the nonlinear magnetic response of iron- oxide nanoparticles to localize their presence in the body. MPI directly detects the nanoparticle’s magnetization rather than using secondary effects on the Magnetic Resonance relaxation times. Thus, while MPI and MRI share many technologies, the MPI method does not use the MR phenomena in any way. Our plan is to detect the activation-induced and resting-state changes in the iron-oxide concentration in the cerebral capillary network by monitoring the local iron oxide concentration (and thus local Cerebral Blood Volume, CBV). This CBV-contrast source is well-proven in animal and human fMRI studies which detect CBV changes by MRI using the same iron-oxide agents. But, by developing MPI as the detection modality, we show that there is a potential 120-fold increase in the contrast-to-noise ratio (CNR) of neuronal activation. This astronomical detection benefit dwarfs any potential benefit envisioned by improving MRI technology. For example, given that the BOLD CNR scales with the square of the magnet strength, this increase in CNR would be equivalent to a 30 Tesla MRI scanner, which is clearly infeasible. We envision the sensitivity boon will have an instantaneous and revolutionary impact on neuroscience. It will eliminate the need to perform group averaging to see an activation or networks, bringing analysis to the individual level needed to impact clinical medicine. By improving the basic detection methodology by 100 fold, we hope to revolutionize non-invasive functional imaging methods applicable to the human brain in health and disease.

Public Health Relevance Statement

In this planning grant, we will provide a roadmap that will allow us to develop Magnetic Particle Imaging (MPI) as a method for imaging the function of the human brain in health and disease. By producing a method that allows us to “see” the brain in operation with a clarity of up to 100-fold higher than existing MRI based methods, we hope to significantly impact our understanding of disease mechanisms.

NIH Spending Category

Bioengineering; Brain Disorders; Diagnostic Radiology; Neurosciences

Project Terms

Address; Animals; Architecture; base; Biomedical Engineering; Blood; Blood capillaries; Blood Volume; Brain; Brain imaging; capillary; Cerebrum; Clinical Medicine; Clinical Sciences; Data; design; Detection; detector; Development; Devices; Disease; electric field; Electronics; Engineering; Feedback; Foundations; Frequencies (time pattern); Functional Imaging; Functional Magnetic Resonance Imaging; Grant; Head; Health; hemodynamics; Human; Image; Imaging Device; imaging modality; improved; in vivo; Individual; Iron; iron oxide; magnetic field; Magnetic Resonance; Magnetic Resonance Imaging; Magnetism; Measures; Methodology; Methods; Modality; Modeling; Monitor; nanoparticle; Neurons; Neurosciences; next generation; Noise; Nuclear; operation; Optics; particle; Pathway interactions; Performance; Peripheral Nerve Stimulation; Phase; Positron-Emission Tomography; programs; public health relevance; Publishing; quantum; Regulation; Relaxation; research study; Resolution; response; Rest; Rodent; Rotation; Sampling; Shoulder; Simulate; simulation; Solutions; Source; Speed (motion); stem; Structure; Study Section; System; Technology; Testing; Time; Water

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