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Analysis of cancer metabolism by imaging hyperpolarized nuclei: prospects for translation to clinical research.通过成像技术分析癌症代谢:向临床研究转化的前景。
Neoplasia. 2011 Feb;13(2):81-97. doi: 10.1593/neo.101102.
2
In situ detection of PHIP at 48 mT: demonstration using a centrally controlled polarizer.在 48 mT 下原位检测 PHIP:使用中央控制偏振器进行演示。
J Am Chem Soc. 2011 Jan 12;133(1):97-101. doi: 10.1021/ja108529m. Epub 2010 Dec 9.
3
Analysis of hyperpolarized dynamic 13C lactate imaging in a transgenic mouse model of prostate cancer.前列腺癌转基因小鼠模型中 13C 乳酸动态极化成像分析。
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4
Reversible interactions with para-hydrogen enhance NMR sensitivity by polarization transfer.与仲氢的可逆相互作用通过极化转移提高核磁共振灵敏度。
Science. 2009 Mar 27;323(5922):1708-11. doi: 10.1126/science.1168877.
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Producing and quantifying enriched para-H2.
Rev Sci Instrum. 2009 Jan;80(1):016108. doi: 10.1063/1.3072881.
6
PASADENA hyperpolarization of succinic acid for MRI and NMR spectroscopy.用于磁共振成像(MRI)和核磁共振波谱(NMR)的琥珀酸的帕萨迪纳超极化
J Am Chem Soc. 2008 Apr 2;130(13):4212-3. doi: 10.1021/ja7101218. Epub 2008 Mar 12.
7
Detecting tumor response to treatment using hyperpolarized 13C magnetic resonance imaging and spectroscopy.使用超极化13C磁共振成像和波谱检测肿瘤对治疗的反应。
Nat Med. 2007 Nov;13(11):1382-7. doi: 10.1038/nm1650. Epub 2007 Oct 28.
8
Towards hyperpolarized (13)C-succinate imaging of brain cancer.迈向脑癌的超极化(13)C-琥珀酸盐成像
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9
Ultra-fast three dimensional imaging of hyperpolarized 13C in vivo.体内超极化13C的超快三维成像。
MAGMA. 2005 Nov;18(5):245-56. doi: 10.1007/s10334-005-0007-x. Epub 2005 Nov 23.
10
Increase in signal-to-noise ratio of > 10,000 times in liquid-state NMR.在液态核磁共振中,信噪比提高超过10000倍。
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脉冲式注入仲氢发生器及丰度定量技术。

A pulsed injection parahydrogen generator and techniques for quantifying enrichment.

机构信息

Vanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, TN 37232-2310, United States.

出版信息

J Magn Reson. 2012 Jan;214(1):258-62. doi: 10.1016/j.jmr.2011.11.015. Epub 2011 Dec 2.

DOI:10.1016/j.jmr.2011.11.015
PMID:22188975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3268554/
Abstract

A device is presented for efficiently enriching parahydrogen by pulsed injection of ambient hydrogen gas. Hydrogen input to the generator is pulsed at high pressure to a catalyst chamber making thermal contact with the cold head of a closed-cycle cryocooler maintained between 15 and 20K. The system enables fast production (0.9 standard liters per minute) and allows for a wide range of production targets. Production rates can be systematically adjusted by varying the actuation sequence of high-pressure solenoid valves, which are controlled via an open source microcontroller to sample all combinations between fast and thorough enrichment by varying duration of hydrogen contact in the catalyst chamber. The entire enrichment cycle from optimization to quantification and storage kinetics are also described. Conversion of the para spin-isomer to orthohydrogen in borosilicate tubes was measured at 8 min intervals over a period of 64 h with a 12 T NMR spectrometer. These relaxation curves were then used to extract initial enrichment by exploiting the known equilibrium (relaxed) distribution of spin isomers with linear least squares fitting to a single exponential decay curve with an estimated error less than or equal to 1%. This procedure is time-consuming, but requires only one sample pressurized to atmosphere. Given that tedious matching to external references are unnecessary with this procedure, we find it to be useful for periodic inspection of generator performance. The equipment and procedures offer a variation in generator design that eliminate the need to meter flow while enabling access to increased rates of production. These tools for enriching and quantifying parahydrogen have been in steady use for 3 years and should be helpful as a template or as reference material for building and operating a parahydrogen production facility.

摘要

介绍了一种通过脉冲注入环境氢气来高效富集仲氢的装置。发生器输入的氢气在高压下脉冲进入与闭路循环致冷机的冷头保持在 15 到 20K 之间的热接触的催化剂室。该系统能够实现快速生产(0.9 标准升/分钟),并允许生产目标的广泛变化。通过改变高压电磁阀的致动顺序,可以系统地调整生产速率,该电磁阀通过开源微控制器进行控制,以通过改变催化剂室内的氢气接触时间来采样快速和彻底富集之间的所有组合。还描述了从优化到定量和存储动力学的整个富集周期。在 12T NMR 光谱仪上每隔 8 分钟测量一段时间为 64 小时的硼硅酸盐管中仲氢自旋异构体向正氢的转化。然后,利用已知的自旋异构体平衡(弛豫)分布,通过线性最小二乘拟合到单个指数衰减曲线,提取初始富集,该曲线具有估计误差小于或等于 1%。该过程很耗时,但仅需将一个样品加压至大气即可。由于此过程不需要与外部参考进行繁琐的匹配,因此我们发现它对于定期检查发生器性能很有用。该设备和程序提供了一种发生器设计的变化,消除了对流量计量的需求,同时能够提高生产速率。这些用于富集和定量仲氢的工具已经稳定使用了 3 年,应该有助于作为构建和运行仲氢生产设施的模板或参考材料。