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在数秒内实现 [1-¹³C]丙酮酸的有序-统一 C 核极化,以及水和 SABRE 增强的相互作用。

Order-Unity C Nuclear Polarization of [1- C]Pyruvate in Seconds and the Interplay of Water and SABRE Enhancement.

机构信息

Integrative Biosciences, Department of Chemistry Karmanos Cancer Institute, Wayne State University, 5101 Cass Ave, Detroit, MI, 48202, USA.

Department of Chemistry, North Carolina State University, Raleigh, North Carolina, 27695-8204, USA.

出版信息

Chemphyschem. 2022 Jan 19;23(2):e202100839. doi: 10.1002/cphc.202100839. Epub 2021 Dec 9.

Abstract

Signal Amplification By Reversible Exchange in SHield Enabled Alignment Transfer (SABRE-SHEATH) is investigated to achieve rapid hyperpolarization of C spins of [1- C]pyruvate, using parahydrogen as the source of nuclear spin order. Pyruvate exchange with an iridium polarization transfer complex can be modulated via a sensitive interplay between temperature and co-ligation of DMSO and H O. Order-unity C (>50 %) polarization of catalyst-bound [1- C]pyruvate is achieved in less than 30 s by restricting the chemical exchange of [1- C]pyruvate at lower temperatures. On the catalyst bound pyruvate, 39 % polarization is measured using a 1.4 T NMR spectrometer, and extrapolated to >50 % at the end of build-up in situ. The highest measured polarization of a 30-mM pyruvate sample, including free and bound pyruvate is 13 % when using 20 mM DMSO and 0.5 M water in CD OD. Efficient C polarization is also enabled by favorable relaxation dynamics in sub-microtesla magnetic fields, as indicated by fast polarization buildup rates compared to the T spin-relaxation rates (e. g., ∼0.2 s versus ∼0.1 s , respectively, for a 6 mM catalyst-[1- C]pyruvate sample). Finally, the catalyst-bound hyperpolarized [1- C]pyruvate can be released rapidly by cycling the temperature and/or by optimizing the amount of water, paving the way to future biomedical applications of hyperpolarized [1- C]pyruvate produced via comparatively fast and simple SABRE-SHEATH-based approaches.

摘要

在屏蔽交换增强对齐转移(SABRE-SHEATH)的作用下,通过将 parahydrogen 作为核自旋序的来源,研究了信号放大,以实现 [1-13C]丙酮酸的 C 自旋的快速极化。通过温度和 DMSO 与 H2O 的共配位之间的敏感相互作用,可以调节丙酮酸与铱极化转移配合物的交换。通过在较低温度下限制 [1-13C]丙酮酸的化学交换,在不到 30s 的时间内实现了催化剂结合的 [1-13C]丙酮酸的 C 大于 50%的有序性(order-unity)极化。在催化剂结合的丙酮酸上,使用 1.4T NMR 光谱仪测量到 39%的极化率,并在原位积累结束时外推到 >50%。在包括游离和结合的丙酮酸的 30mM 丙酮酸样品中,当使用 20mM DMSO 和 0.5M CD3OD 时,测量到的最高极化率为 13%。在亚微特斯拉磁场中,有利的弛豫动力学也能实现有效的 C 极化,这表现为与 T 自旋弛豫率相比,极化快速积累速率更快(例如,对于 6mM 催化剂-[1-13C]丙酮酸样品,分别为 0.2s 与 0.1s)。最后,通过循环温度和/或优化水的量,可以快速释放催化剂结合的高极化 [1-13C]丙酮酸,为未来基于 SABRE-SHEATH 的相对快速和简单方法生产的高极化 [1-13C]丙酮酸的生物医学应用铺平了道路。

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