Magnetic particle imaging (MPI) has been shown to provide remarkable contrast for imaging applications such as angiography, stem cell tracking, and cancer imaging. Recently, there is growing interest in the functional imaging capabilities of MPI, where 'color MPI' techniques have explored separating different nanoparticles, which could potentially be used to distinguish nanoparticles in different states or environments. Viscosity mapping is a promising functional imaging application for MPI, as increased viscosity levels in vivo have been associated with numerous diseases such as hypertension, atherosclerosis, and cancer. In this work, we propose a viscosity mapping technique for MPI through the estimation of the relaxation time constant of the nanoparticles. Importantly, the proposed time constant estimation scheme does not require any prior information regarding the nanoparticles. We validate this method with extensive experiments in an in-house magnetic particle spectroscopy (MPS) setup at four different frequencies (between 250 Hz and 10.8 kHz) and at three different field strengths (between 5 mT and 15 mT) for viscosities ranging between 0.89 mPa · s-15.33 mPa · s. Our results demonstrate the viscosity mapping ability of MPI in the biologically relevant viscosity range.

Magnetic particle imaging (MPI) is a novel imaging modality with important potential applications, such as angiography, stem cell tracking, and cancer imaging. Recently, there have been efforts to increase the functionality of MPI via multi-color imaging methods that can distinguish the responses of different nanoparticles, or nanoparticles in different environmental conditions. The proposed techniques typically rely on extensive calibrations that capture the differences in the harmonic responses of the nanoparticles. In this paper, we propose a method to directly estimate the relaxation time constant of the nanoparticles from the MPI signal, which is then used to generate a multi-color relaxation map. The technique is based on the underlying mirror symmetry of the adiabatic MPI signal when the same region is scanned back and forth. We validate the proposed method via simulations, and via experiments on our in-house magnetic particle spectrometer setup at 10.8 kHz and our in-house MPI scanner at 9.7 kHz. Our results show that nanoparticles can be successfully distinguished with the proposed technique, without any calibration or prior knowledge about the nanoparticles.

Magnetic particle imaging (MPI) uses superparamagnetic iron oxide (SPIO) nanoparticles as biomedical imaging tracers. The potential applications of MPI have recently been broadened by the introduction of "color" MPI techniques that can distinguish different nanoparticles and/or environments, e.g., by exploiting the relaxation behavior of SPIOs. One of the important applications of color MPI techniques is viscosity mapping. In this work, we show relaxation-based color MPI experiments that can distinguish the biologically relevant viscosity range of up to 5 mPa s. To find the optimal drive field parameters for viscosity, we compare color MPI results at three different frequencies. We show that frequencies around 10 kHz are well-suited for viscosity mapping using the multicore cluster Nanomag-MIP nanoparticles, providing a one-to-one mapping between the estimated relaxation time constant and viscosity.

Magnetic Particle Imaging (MPI) is an emerging medical imaging modality that images the spatial distribution of superparamagnetic iron oxide (SPIO) nanoparticles using their nonlinear response to applied magnetic fields. In standard x-space approach to MPI, the image is reconstructed by gridding the speed-compensated nanoparticle signal to the instantaneous position of the field free point (FFP). However, due to safety limits on the drive field, the field-of-view (FOV) needs to be covered by multiple relatively small partial field-of-views (pFOVs). The image of the entire FOV is then pieced together from individually processed pFOVs. These processing steps can be sensitive to non-ideal signal conditions such as harmonic interference, noise, and relaxation effects. In this work, we propose a robust x-space reconstruction technique, Partial FOV Center Imaging (PCI), with substantially simplified pFOV processing. PCI first forms a raw image of the entire FOV by mapping MPI signal directly to pFOV center locations. The corresponding MPI image is then obtained by deconvolving this raw image by a compact kernel, whose fully-known shape solely depends on the pFOV size. We analyze the performance of the proposed reconstruction via extensive simulations, as well as imaging experiments on our in-house FFP MPI scanner. The results show that PCI offers a trade-off between noise robustness and interference robustness,