Flow-Suppressed Hyperpolarized 13C Chemical Shift Imaging Using Velocity-Optimized Bipolar Gradient in Mouse Liver Tumors at 9.4 T
Flow-Suppressed Hyperpolarized 13C Chemical Shift Imaging Using Velocity-Optimized Bipolar Gradient in Mouse Liver Tumors at 9.4 T
复制标题
DOI:
10.1002/mrm.26578
复制
发表时间:
2017-11-01
影响因子:
3.3
通讯作者:
Kim, Dong-Hyun
中科院分区:
文献类型:
--
作者:
Lee, Hansol;Lee, Joonsung;Kim, Dong-Hyun
Purpose: To optimize and investigate the influence of bipolar gradients for flow suppression in metabolic quantification of hyperpolarized C-13 chemical shift imaging (CSI) of mouse liver at 9.4 T.Methods: The trade-off between the amount of flow suppression using bipolar gradients and T-2* effect from static spins was simulated. A free induction decay CSI sequence with alternations between the flow-suppressed and non-flowsuppressed acquisitions for each repetition time was developed and was applied to liver tumor-bearing mice via injection of hyperpolarized [1-C-13] pyruvate.Results: The in vivo results from flow suppression using the velocity-optimized bipolar gradient were comparable with the simulation results. The vascular signal was adequately suppressed and signal loss in stationary tissue was minimized. Application of the velocity-optimized bipolar gradient to tumorbearing mice showed reduction in the vessel-derived pyruvate signal contamination, and the average lactate/pyruvate ratio increased by 0.095 (P < 0.05) in the tumor region after flow suppression.Conclusion: Optimization of the bipolar gradient is essential because of the short C-13 T-2* and high signal in venous flow in the mouse liver. The proposed velocity-optimized bipolar gradient can suppress the vascular signal, minimizing T-2*-related signal loss in stationary tissues at 9.4 T. (C) 2016 International Society for Magnetic Resonance in Medicine.