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Colored imaging of magnetic nanoparticles (MNP) is a promising noninvasive method for medical applications such as therapy and diagnosis. This study investigates the capability of the magnetoelectric sensor and projected gradient descent (PGD) algorithm for colored particle detection. In the first step, the required circumstances for image reconstruction are studied via a simulation approach for different signal-to-noise ratios (SNR). The spatial accuracy of the reconstructed image is evaluated based on the correlation coefficient (CC) factor. The inverse problem is solved using the PGD method, which is adapted according to a nonnegativity constraint in the complex domain. The MNP characterizations are assessed through a magnetic particle spectrometer (MPS) for different types. In the experimental investigation, the real and imaginary parts of the MNP's response are used to detect the spatial distribution and particle type, respectively. The experimental results indicate that the average phase difference for CT100 and ARA100 particles is 14 degrees, which is consistent with the MPS results and could satisfy the system requirements for colored imaging. The experimental evaluation showed that the magnetoelectric sensor and the proposed approach could be potential candidates for color bio-imaging applications. [ABSTRACT FROM AUTHOR]

Imaging of magnetic nanoparticles (MNPs) is of great interest in the medical sciences. By using resonant magnetoelectric sensors, higher harmonic excitations of MNPs can be measured and mapped in space. The proper reconstruction of particle distribution via solving the inverse problem is paramount for any imaging technique. For this, the forward model needs to be modeled accurately. However, depending on the state of the magnetoelectric sensors, the projection axis for the magnetic field may vary and may not be known accurately beforehand. As a result, the projection axis used in the model may be inaccurate, which can result in inaccurate reconstructions and artifact formation. Here, we show an approach for mapping MNPs that includes sources of uncertainty to both select the correct particle distribution and the correct model simultaneously. [ABSTRACT FROM AUTHOR]