Purpose
EPRI has surfaced as a promising non-invasive imaging modality that is capable of imaging tissue oxygenation. Due to extremely short spin-spin relaxation time, EPRI benefits from single point imaging and inherently suffers from limited spatial and temporal resolution, preventing localization of small hypoxic tissues and differentiation of hypoxia dynamics, making accelerated imaging a crucial issue.
Method
In this study, methods for accelerated single point imaging were developed by combining a bilateral k-space extrapolation technique with model-based reconstruction that benefits from dense sampling in the parameter domain (measurement of the T2* decay of an FID). In bilateral k-space extrapolation, more k-space samples are obtained in a sparsely sampled region by bilaterally extrapolating data from temporally neighboring k-spaces. To improve the accuracy of T2* estimation, a principal component analysis (PCA)-based method was implemented.
Result
In a computer simulation and a phantom experiment, the proposed methods showed its capability for reliable T2* estimation with high acceleration (8-fold, 15-fold, and 30-fold accelerations for 61×61×61, 95×95×95, and 127×127×127 matrix, respectively).
Conclusion
By applying bilateral k-space extrapolation and model-based reconstruction, improved scan times with higher spatial resolution can be achieved in the current SP-EPRI modality.