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在紧凑型临床前 PET/MR 扫描仪中对超极化 C 探针进行多频带回波平面波谱成像。

Multi-band echo-planar spectroscopic imaging of hyperpolarized C probes in a compact preclinical PET/MR scanner.

机构信息

Mallinckrodt Institute of Radiology, Washington University, St. Louis, Missouri, USA.

MR Solutions, Guildford, United Kingdom.

出版信息

Magn Reson Med. 2022 May;87(5):2120-2129. doi: 10.1002/mrm.29145. Epub 2021 Dec 31.

Abstract

PURPOSE

Hyperpolarized (HP) C MRI has enabled real-time imaging of specific enzyme-catalyzed metabolic reactions, but advanced pulse sequences are necessary to capture the dynamic, localized metabolic information. Herein we describe the design, implementation, and testing of a rapid and efficient HP C pulse sequence strategy on a cryogen-free simultaneous positron emission tomography/MR molecular imaging platform with compact footprint.

METHODS

We developed an echo planar spectroscopic imaging pulse sequence incorporating multi-band spectral-spatial radiofrequency (SSRF) pulses for spatially coregistered excitation of C metabolites with differential individual flip angles. Excitation profiles were measured in phantoms, and the SSRF-echo planar spectroscopic imaging sequence was tested in rats in vivo and compared to conventional echo planar spectroscopic imaging. The new sequence was applied for 2D dynamic metabolic imaging of HP [1- C]pyruvate and its molecular analog [1- C] -ketobutyrate at a spatial resolution of 5 mm × 5 mm × 20 mm and temporal resolution of 4 s. We also obtained simultaneous F-fluorodeoxyglucose positron emission tomography data for comparison with HP [1- C]pyruvate data acquired during the same scan session.

RESULTS

Measured SSRF excitation profiles corresponded well to Bloch simulations. Multi-band SSRF excitation facilitated efficient sampling of the multi-spectral kinetics of [1- C]pyruvate and [1- C] - . Whereas high pyruvate to lactate conversion was observed in liver, corresponding reduction of -ketobutyrate to [1- C] -hydroxybutyrate ( HB) was largely restricted to the kidneys and heart, consistent with the known expression pattern of lactate dehydrogenase B.

CONCLUSION

Advanced C SSRF imaging approaches are feasible on our compact positron emission tomography/MR platform, maximizing the potential of HP C technology and facilitating direct comparison with positron emission tomography.

摘要

目的

超极化(HP) C MRI 能够实时成像特定酶催化的代谢反应,但需要先进的脉冲序列来捕获动态的、局部的代谢信息。本文描述了在具有紧凑占地面积的无液氦的正电子发射断层扫描/磁共振(PET/MR)分子成像平台上,对快速高效的 HP C 脉冲序列策略的设计、实现和测试。

方法

我们开发了一种回波平面波谱成像脉冲序列,该序列结合了多带谱空间射频(SSRF)脉冲,用于对 C 代谢物进行空间配准激发,并具有不同的个体翻转角。在体模中测量了激发轮廓,并在体内对大鼠进行了 SSRF-回波平面波谱成像序列测试,并与传统的回波平面波谱成像进行了比较。该新序列用于 HP [1- C]丙酮酸及其分子类似物[1- C] -酮丁酸盐的 2D 动态代谢成像,空间分辨率为 5mm×5mm×20mm,时间分辨率为 4s。我们还同时获得了 F-氟脱氧葡萄糖正电子发射断层扫描数据,以便与同一扫描过程中采集的 HP [1- C]丙酮酸数据进行比较。

结果

测量的 SSRF 激发轮廓与 Bloch 模拟吻合较好。多带 SSRF 激发促进了[1- C]丙酮酸和[1- C] - 的多谱动力学的有效采样。在肝脏中观察到高丙酮酸向乳酸的转化,而相应的[1- C] -酮丁酸向[1- C] -羟基丁酸( HB)的还原主要局限于肾脏和心脏,这与乳酸脱氢酶 B 的已知表达模式一致。

结论

在我们的紧凑型 PET/MR 平台上,先进的 C SSRF 成像方法是可行的,最大限度地发挥了 HP C 技术的潜力,并促进了与正电子发射断层扫描的直接比较。

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