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研究提高 PHIP-SAH 产生的 C13-丙酮酸中的超极化水平。

Studies to enhance the hyperpolarization level in PHIP-SAH-produced C13-pyruvate.

机构信息

Dept. Molecular Biotechnology and Health Sciences, Via Nizza 52, Torino, Italy.

Dept. Molecular Biotechnology and Health Sciences, Via Nizza 52, Torino, Italy.

出版信息

J Magn Reson. 2018 Apr;289:12-17. doi: 10.1016/j.jmr.2018.01.019. Epub 2018 Jan 31.

Abstract

The use of [1-C]pyruvate, hyperpolarized by dissolution-Dynamic Nuclear Polarization (d-DNP), in in vivo metabolic studies has developed quickly, thanks to the imaging probe's diagnostic relevance. Nevertheless, the cost of a d-DNP polarizer is quite high and the speed of hyperpolarization process is relatively slow, meaning that its use is limited to few research laboratories. ParaHydrogen Induced Polarization Side Arm Hydrogenation (PHIP-SAH) (Reineri et al., 2015) is a cost effective and easy-to-handle method that produces C-MR hyperpolarization in [1-C]pyruvate and other metabolites. This work aims to identify the main determinants of the hyperpolarization levels observed in C13-pyruvate using this method. By dissecting the various steps of the PHIP-SAH procedure, it has been possible to assess the role of several experimental parameters whose optimization must be pursued if this method is to be made suitable for future translational steps. The search for possible solutions has led to improvements in the polarization of sodium [1-C]pyruvate from 2% to 5%. Moreover, these results suggest that observed polarization levels could be increased considerably by an automatized procedure which would reduce the time required for the work-up passages that are currently carried out manually. The results reported herein mean that the attainment of polarization levels suitable for the metabolic imaging applications of these hyperpolarized substrates show significant promise.

摘要

由于成像探针具有诊断相关性,因此[1-C]丙酮酸经溶解动态核极化(d-DNP)超极化后在体内代谢研究中的应用迅速发展。然而,d-DNP 极化器的成本相当高,且超极化过程的速度相对较慢,这意味着其使用仅限于少数研究实验室。ParaHydrogen Induced Polarization Side Arm Hydrogenation (PHIP-SAH)(Reineri 等人,2015)是一种具有成本效益且易于操作的方法,可在[1-C]丙酮酸和其他代谢物中产生 C-MR 极化。本工作旨在确定使用该方法在 C13-丙酮酸中观察到的超极化水平的主要决定因素。通过剖析 PHIP-SAH 过程的各个步骤,可以评估几个实验参数的作用,如果要将该方法用于未来的转化步骤,则必须对其进行优化。为了寻找可能的解决方案,我们对钠[1-C]丙酮酸的极化进行了改进,使其从 2%提高到 5%。此外,这些结果表明,通过自动化程序可以大大提高观察到的极化水平,该程序可以减少目前手动进行的工作流程所需的时间。本文报道的结果表明,实现适合这些超极化底物代谢成像应用的极化水平具有很大的潜力。

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