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Investigating the Feasibility of In Vivo Perfusion Imaging Methods for Spinal Cord Using Hyperpolarized [C]t-Butanol and [C,N]Urea.利用超极化[C]叔丁醇和[C,N]尿素研究脊髓体内灌注成像方法的可行性。
Mol Imaging Biol. 2022 Jun;24(3):371-376. doi: 10.1007/s11307-021-01682-1. Epub 2021 Nov 15.
2
Assessing Prostate Cancer Aggressiveness with Hyperpolarized Dual-Agent 3D Dynamic Imaging of Metabolism and Perfusion.利用代谢与灌注的超极化双剂3D动态成像评估前列腺癌侵袭性
Cancer Res. 2017 Jun 15;77(12):3207-3216. doi: 10.1158/0008-5472.CAN-16-2083. Epub 2017 Apr 20.
3
Development of high resolution 3D hyperpolarized carbon-13 MR molecular imaging techniques.高分辨率三维超极化碳-13磁共振分子成像技术的发展
Magn Reson Imaging. 2017 May;38:152-162. doi: 10.1016/j.mri.2017.01.003. Epub 2017 Jan 7.
4
Spectrally selective three-dimensional dynamic balanced steady-state free precession for hyperpolarized C-13 metabolic imaging with spectrally selective radiofrequency pulses.采用谱选择性射频脉冲的超极化 13C 代谢成像的光谱选择性三维动态平衡稳态自由进动。
Magn Reson Med. 2017 Sep;78(3):963-975. doi: 10.1002/mrm.26480. Epub 2016 Oct 21.
5
Hyperpolarized C, N -Urea MRI for assessment of the urea gradient in the porcine kidney.超极化碳-13、氮-15尿素磁共振成像用于评估猪肾中的尿素梯度
Magn Reson Med. 2016 Dec;76(6):1895-1899. doi: 10.1002/mrm.26483. Epub 2016 Sep 26.
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Imaging Renal Urea Handling in Rats at Millimeter Resolution using Hyperpolarized Magnetic Resonance Relaxometry.使用超极化磁共振弛豫测量法以毫米分辨率对大鼠肾脏尿素处理进行成像
Tomography. 2016 Jun;2(2):125-135. doi: 10.18383/j.tom.2016.00127.
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Renal ischemia and reperfusion assessment with three-dimensional hyperpolarized C, N2-urea.利用三维超极化碳-13、氮-15尿素进行肾缺血再灌注评估。
Magn Reson Med. 2016 Nov;76(5):1524-1530. doi: 10.1002/mrm.26377. Epub 2016 Aug 22.
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Diabetes induced renal urea transport alterations assessed with 3D hyperpolarized C, N-Urea.使用3D超极化碳-13、氮-15尿素评估糖尿病引起的肾脏尿素转运改变。
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A general chemical shift decomposition method for hyperpolarized (13) C metabolite magnetic resonance imaging.一种用于超极化(13)C代谢物磁共振成像的通用化学位移分解方法。
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利用丙氨酸和水合丙酮酸的光谱抑制实现高时空分辨率的超极化 [1- C]丙酮酸和 [1- C]乳酸的 bSSFP 成像。

High spatiotemporal resolution bSSFP imaging of hyperpolarized [1- C]pyruvate and [1- C]lactate with spectral suppression of alanine and pyruvate-hydrate.

机构信息

Department of Radiology and Biomedical Imaging, University of California, San Francisco, California.

UC Berkeley-UCSF Graduate Program in Bioengineering, University of California, San Francisco and University of California, Berkeley, California.

出版信息

Magn Reson Med. 2018 Sep;80(3):1048-1060. doi: 10.1002/mrm.27104. Epub 2018 Feb 16.

DOI:10.1002/mrm.27104
PMID:29451329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5980670/
Abstract

PURPOSE

The bSSFP acquisition enables high spatiotemporal resolution for hyperpolarized C MRI at 3T, but is limited by spectral contamination from adjacent resonances. The purpose of this study was to develop a framework for in vivo dynamic high resolution imaging of hyperpolarized [1-C]pyruvate and [1-C]lactate generated in vivo at 3T by simplifying the spectrum through the use of selective suppression pulses.

METHODS

Spectral suppression pulses were incorporated into the bSSFP sequence for suppression of [1-C]alanine and [1-C]pyruvate-hydrate signals, leaving only the pyruvate and lactate resonances. Subsequently, the bSSFP pulse width, time-bandwidth, and repetition time were optimized for imaging these dual resonances.

RESULTS

The spectral suppression reduced both the alanine and pyruvate-hydrate signals by 85.5 ± 4.9% and had no significant effect on quantitation of pyruvate to lactate conversion (liver: = 0.400, kidney: = 0.499). High resolution (2 × 2 mm and 3 × 3 mm) sub-second 2D coronal projections and 3D 2.5 mm isotropic images were obtained in rats and tumor-bearing mice with 1.8-5 s temporal resolution, allowing for calculation of lactate-to-pyruvate ratios and .

CONCLUSION

The developed framework presented here shows the capability for dynamic high resolution volumetric hyperpolarized bSSFP imaging of pyruvate-to-lactate conversion on a clinical 3T MR scanner.

摘要

目的

bSSFP 采集在 3T 下实现了超高极化 C MRI 的高时空分辨率,但受到来自相邻共振的光谱干扰的限制。本研究的目的是开发一种框架,通过使用选择性抑制脉冲简化光谱,在 3T 下对体内产生的高极化 [1-C]丙酮酸和 [1-C]乳酸进行体内动态高分辨率成像。

方法

将光谱抑制脉冲纳入 bSSFP 序列中,以抑制 [1-C]丙氨酸和 [1-C]丙酮酸水合信号,仅留下丙酮酸和乳酸共振。随后,优化了 bSSFP 脉冲宽度、时带宽和重复时间,以对这两个共振进行成像。

结果

光谱抑制将丙氨酸和丙酮酸水合信号分别降低了 85.5±4.9%,对丙酮酸转化为乳酸的定量没有显著影响(肝: = 0.400,肾: = 0.499)。在大鼠和荷瘤小鼠中获得了高分辨率(2×2mm 和 3×3mm)亚秒二维冠状投影和 3D 2.5mm 各向同性图像,具有 1.8-5s 的时间分辨率,可计算乳酸与丙酮酸的比值和 。

结论

这里提出的开发框架展示了在临床 3T MR 扫描仪上进行动态高分辨率容积极化 bSSFP 成像以检测丙酮酸向乳酸转化的能力。