稳态变章动角法在快速测定长t1中的应用——一种可用于超极化MR分子探针设计的方法

Marc Jupin, A. Gamliel, Y. Hovav, J. Sosna, J. Gomori, R. Katz‐Brull
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引用次数: 1

摘要

在溶解动态核极化技术中,具有长t1的分子探针是首选。没有直接成键质子的小分子13C核或质子位置被氘核取代的sp3 13C核可以满足这一要求。这种新型分子探针的T1测定对于超偏振观测的成功至关重要。虽然反演恢复方法基本上仍然是T1测量的标准,但我们在这里表明,稳态可变章动角方法更快,可能更适合于确定热平衡中相对较长的T1。具体来说,本文确定了一种新的分子探针[均匀标记(UL)-13C6, UL- 2h8]2-脱氧-d-葡萄糖的T1,并与[UL-13C6, UL- 2h7]d-葡萄糖的T1进行了比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Application of the Steady-State Variable Nutation Angle Method for Faster Determinations of Long T1s—An Approach Useful for the Design of Hyperpolarized MR Molecular Probes
In the dissolution-dynamic nuclear polarization technique, molecular probes with long T1s are preferred. 13C nuclei of small molecules with no directly bonded protons or sp3 13C nuclei with proton positions substituted by deuterons may fulfill this requirement. The T1 determination of such new molecular probes is crucial for the success of the hyperpolarized observation. Although the inversion-recovery approach remained by and large the standard for T1 measurements, we show here that the steady-state variable nutation angle approach is faster and may be better suited for the determination of relatively long T1s in thermal equilibrium. Specifically, the T1 of a new molecular probe, [uniformly labeled (UL)-13C6, UL-2H8]2-deoxy-d-glucose, is determined here and compared to that of [UL-13C6, UL-2H7]d-glucose.
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