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Updated: Jun 7, 2025

Spin Saturation Transfer Difference NMR SSTD NMR: A New Tool to Obtain Kinetic Parameters of Chemical Exchange Processes
Published on: November 12, 2016
Nonlinear parameter estimation with physics-constrained spectral-spatial priors for highly accelerated chemical
Chinh Dinh Nguyen1, HyungGoo R Kim1,2, Roh Eul Yoo3
1Department of Intelligent Precision Healthcare Convergence, Sungkyunkwan University, Suwon, Republic of Korea.
Abstract:
Objective.To develop a nonlinear, model-based parameter estimation method directly from incomplete measurements ink - wspace for robust spectral analysis in highly accelerated chemical exchange saturation transfer (CEST) magnetic resonance imaging (MRI).Approach. A CEST-specific, separable nonlinear model, which describes spectral decomposition using multi-pool Lorentzian functions (conventional magnetization transfer (MT), direct saturation of water signals (DS), amide, amine, and nuclear Overhauser effect) derived from the steady-state Bloch McConnel equation, is incorporated into a measurement model in CEST MRI. Furthermore, signal drop in saturation transfer experiments is formulated by an additional, separable nonlinear spectral prior indicating that the symmetric z-spectra synthesized using conventional MT and DS always remain higher or equal to the whole z-spectra with all pools. Given the above considerations, linear and nonlinear parameters in the proposed method are estimated in an alternating fashion directly from highly incomplete measurements ink - wspace by solving a constrained optimization problem with the physics-constrained spectral priors while imposing additional sparsity priors on spatial parameter maps.Main results.Compared with conventional methods, the proposed method yields clearer delineation of tumor-specific CEST maps without apparent artifact and noise.Significance.We successfully demonstrated the feasibility of the proposed method for CEST MRI with highly incomplete measurements thus enabling high-resolution whole brain CEST MRI in clinically reasonable imaging time.
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