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氙气超极化化学交换饱和转移磁共振成像剂的绝对宿主浓度及交换动力学映射

Mapping of Absolute Host Concentration and Exchange Kinetics of Xenon Hyper-CEST MRI Agents.

作者信息

Kunth Martin, Witte Christopher, Schröder Leif

机构信息

Molecular Imaging, Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Campus Berlin-Buch, Robert-Roessle-Str. 10, 13125 Berlin, Germany.

Translational Molecular Imaging, Deutsches Krebsforschungszentrum, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.

出版信息

Pharmaceuticals (Basel). 2021 Jan 21;14(2):79. doi: 10.3390/ph14020079.

Abstract

Xenon magnetic resonance imaging (MRI) provides excellent sensitivity through the combination of spin hyperpolarization and chemical exchange saturation transfer (CEST). To this end, molecular hosts such as cryptophane-A or cucurbit[]urils provide unique opportunities to design switchable MRI reporters. The concentration determination of such xenon binding sites in samples of unknown dilution remains, however, challenging. Contrary to H CEST agents, an internal reference of a certain host (in this case, cryptophane-A) at micromolar concentration is already sufficient to resolve the entire exchange kinetics information, including an unknown host concentration and the xenon spin exchange rate. Fast echo planar imaging (EPI)-based Hyper-CEST MRI in combination with Bloch-McConnell analysis thus allows quantitative insights to compare the performance of different emerging ultra-sensitive MRI reporters.

摘要

通过自旋超极化与化学交换饱和转移(CEST)相结合,氙磁共振成像(MRI)具有出色的灵敏度。为此,诸如穴番-A或葫芦脲等分子主体为设计可切换的MRI报告分子提供了独特的机会。然而,在未知稀释度的样品中确定此类氙结合位点的浓度仍然具有挑战性。与氢CEST试剂不同,微摩尔浓度的特定主体(在这种情况下为穴番-A)的内部参考已经足以解析整个交换动力学信息,包括未知的主体浓度和氙自旋交换率。因此,基于快速回波平面成像(EPI)的超CEST MRI与布洛赫-麦康奈尔分析相结合,能够进行定量分析,以比较不同新型超灵敏MRI报告分子的性能。

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