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Peer-reviewedCC BYMagnetic resonance imaging

Optimizing Saturation Time for Maximum CEST Contrast

  1. 1Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania 15203, USA

Abstract

Purpose To determine the optimal saturation time (T sat ) that maximizes the CEST contrast between a reference and a target signal, such as normal versus pathological tissues or pre- versus post-contrast conditions. Methods The optimal T sat (T sat, opt ) was determined from T 1 and a single measurement of the normalized saturated signal (S sat /S 0 ). We evaluated the analytically derived T sat, opt using simulation, phantom, and in vivo experiments. Results Theoretical analysis showed that the S sat /S 0 measured at T sat, opt is always higher than 0.37. When the repetition time (TR) is fixed or is very long (i.e., >5 T 1 ), the T sat, opt is independent of TR and can be derived from T 1 and S sat /S 0 measured at any T sat . When the steady state S sat /S 0 is 0.5 or 1/3, the T sat, opt equals to T 1 or T 1 /2, respectively. The analytically derived T sat, opt were validated by simulation, phantom and in vivo experiment results, and can be extended to include multiple CEST and non-CEST effects (excluding changes in T 1 ). The relative error of the T sat,opt is <10–15% for typical CEST contrasts of <5%. For very large contrast (e.g., >10% of S 0 ), more accurate estimation of T sat, opt can be obtained from the averaged S sat /S 0 of the reference and target signals. Conclusion T sat, opt can be determined from T 1 and a single measurement of the saturated signal. This approach simplifies optimization of T sat in CEST experiments, especially when using relatively high saturation powers or resonance frequencies close to water.

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BibTeX
@article{zhao2026optimizing,
  title = {{Optimizing Saturation Time for Maximum CEST Contrast}},
  author = {Yifan Zhao and Julius Juhyun Chung and Tao Jin},
  journal = {Magnetic resonance imaging},
  year = {2026},
  month = jul,
  doi = {10.1016/j.mri.2026.110747},
  url = {https://doi.org/10.1016/j.mri.2026.110747},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Optimizing Saturation Time for Maximum CEST Contrast
AU  - Yifan Zhao
AU  - Julius Juhyun Chung
AU  - Tao Jin
PY  - 2026
DA  - 2026/07/13
JO  - Magnetic resonance imaging
DO  - 10.1016/j.mri.2026.110747
UR  - https://doi.org/10.1016/j.mri.2026.110747
AB  - Purpose To determine the optimal saturation time (T sat ) that maximizes the CEST contrast between a reference and a target signal, such as normal versus pathological tissues or pre- versus post-contrast conditions. Methods The optimal T sat (T sat, opt ) was determined from T 1 and a single measurement of the normalized saturated signal (S sat /S 0 ). We evaluated the analytically derived T sat, opt using simulation, phantom, and in vivo experiments. Results Theoretical analysis showed that the S sat /S 0 measured at T sat, opt is always higher than 0.37. When the repetition time (TR) is fixed or is very long (i.e., >5 T 1 ), the T sat, opt is independent of TR and can be derived from T 1 and S sat /S 0 measured at any T sat . When the steady state S sat /S 0 is 0.5 or 1/3, the T sat, opt equals to T 1 or T 1 /2, respectively. The analytically derived T sat, opt were validated by simulation, phantom and in vivo experiment results, and can be extended to include multiple CEST and non-CEST effects (excluding changes in T 1 ). The relative error of the T sat,opt is <10–15% for typical CEST contrasts of <5%. For very large contrast (e.g., >10% of S 0 ), more accurate estimation of T sat, opt can be obtained from the averaged S sat /S 0 of the reference and target signals. Conclusion T sat, opt can be determined from T 1 and a single measurement of the saturated signal. This approach simplifies optimization of T sat in CEST experiments, especially when using relatively high saturation powers or resonance frequencies close to water.
SN  - 0730-725X
SN  - 1873-5894
ER  -