Abstract
Purpose: To develop a pulsed CEST magnetization-transfer method for rapidly acquiring relayed nuclear Overhauser enhancement (rNOE)–weighted images with magnetic transfer contrast (MTC) suppression at clinical field strength (3 T).
Methods: Using a pulsed CEST magnetization-transfer method with low saturation powers (B1) and long mixing time (tmix) to suppress contributions due to strong MTC from solid-like macromolecules, a low B1 also minimized direct water saturation. These MTC contributions were further reduced by subtracting the Z-spectral signals at two or three offsets by assuming that the residual MTC is a linear function between −3.5 ppm and −12.5 ppm.
Results: Phantom studies of a lactic acid (Lac) solution mixed with cross-linked bovine serum albumin show that strong MTC interference has a significant impact on the optimum B1 for detecting rNOEs, due to lactate binding. The MTC could be effectively suppressed using a pulse train with a B1 of 0.8 μT, a pulse duration (tp) of 40 ms, a tmix of 60 ms, and a pulse number (N) of 30, while rNOE signal was well maintained. As a proof of concept, we applied the method in mouse brain with injected hydrogel and a cell-hydrogel phantom. Results showed that rNOE-weighted images could provide good contrast between brain/cell and hydrogel.
Conclusion: The developed pulsed CEST magnetization-transfer method can achieve MTC suppression while preserving most of the rNOE signal at 3 T, which indicates the potential for translation of this technique to clinical applications related to mobile proteins/lipids change.
Methods: Using a pulsed CEST magnetization-transfer method with low saturation powers (B1) and long mixing time (tmix) to suppress contributions due to strong MTC from solid-like macromolecules, a low B1 also minimized direct water saturation. These MTC contributions were further reduced by subtracting the Z-spectral signals at two or three offsets by assuming that the residual MTC is a linear function between −3.5 ppm and −12.5 ppm.
Results: Phantom studies of a lactic acid (Lac) solution mixed with cross-linked bovine serum albumin show that strong MTC interference has a significant impact on the optimum B1 for detecting rNOEs, due to lactate binding. The MTC could be effectively suppressed using a pulse train with a B1 of 0.8 μT, a pulse duration (tp) of 40 ms, a tmix of 60 ms, and a pulse number (N) of 30, while rNOE signal was well maintained. As a proof of concept, we applied the method in mouse brain with injected hydrogel and a cell-hydrogel phantom. Results showed that rNOE-weighted images could provide good contrast between brain/cell and hydrogel.
Conclusion: The developed pulsed CEST magnetization-transfer method can achieve MTC suppression while preserving most of the rNOE signal at 3 T, which indicates the potential for translation of this technique to clinical applications related to mobile proteins/lipids change.
| Original language | English |
|---|---|
| Pages (from-to) | 254-267 |
| Journal | Magnetic Resonance in Medicine |
| Volume | 85 |
| Issue number | 1 |
| Online published | 1 Aug 2020 |
| DOIs | |
| Publication status | Published - Jan 2021 |
Research Keywords
- chemical exchange saturation transfer
- continuous wave-CEST/MT
- magnetization transfer contrast
- pulsed-CEST/MT
- relayed nuclear Overhauser enhancement
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Dive into the research topics of 'Relayed nuclear Overhauser enhancement imaging with magnetization transfer contrast suppression at 3 T'. Together they form a unique fingerprint.Projects
- 2 Finished
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GRF: Development of Theranostic Hydrogels for MRI-guided Brain Tumor Treatment
CHAN, W. Y. K. (Principal Investigator / Project Coordinator) & LEUNG, G. K. K. (Co-Investigator)
1/01/19 → 20/09/23
Project: Research
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TDG(CityU): Tracking molecules in the brain using magnetic resonance imaging (MRI)
CHAN, W. Y. K. (Principal Investigator / Project Coordinator)
1/09/18 → 28/07/21
Project: Research
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