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Effects of Deuteration of 13C-Enriched Phospholactate on Efficiency of Parahydrogen-Induced Polarization by Magnetic Field Cycling

机译:富集13C的磷酸酯对磁场循环中对氢诱导极化效率的影响

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摘要

We report herein a large-scale (>10 g) synthesis of isotopically enriched 1-13C-phosphoenolpyruvate and 1-13C-phosphoenolpyruvate-d2 for application in hyperpolarized imaging technology. The 1-13C-phosphoenolpyruvate-d2 was synthesized with 57% overall yield (over two steps), and >98% H isotopic purity, representing an improvement over the previous report. The same outcome was achieved for 1-13C-phosphoenolpyruvate. These two unsaturated compounds with C=C bonds were employed for parahydrogen-induced polarization via pairwise parahydrogen addition in aqueous medium. We find that deuteration of 1-13C-phosphoenolpyruvate resulted in overall increase of 1H T1 of nascent hyperpolarized protons (4.30 ± 0.04 s versus 2.06 ± 0.01 s) and H polarization (~2.5% versus ~0.7%) of the resulting hyperpolarized 1-13C-phospholactate. The nuclear spin polarization of nascent parahydrogen-derived protons was transferred to 1-13C nucleus via magnetic field cycling procedure. The proton T1 increase in hyperpolarized deuterated 1-13C-phospholactate yielded approximately 30% better 13C polarization compared to non-deuterated hyperpolarized 1-13C-phospholactate. Analysis of T1 relaxation revealed that deuteration of 1-13C-phospholactate may have resulted in approximately 3-fold worse H→13C polarization transfer efficiency via magnetic field cycling. Since magnetic field cycling is a key polarization transfer step in the Side-Arm Hydrogenation approach, the presented findings may guide more rationale design of contrast agents using parahydrogen polarization of a broad range of 13C hyperpolarized contrast agents for molecular imaging employing 13C MRI. The hyperpolarized 1-13C-phospholactate-d2 is of biomedical imagingrelevance because it undergoes in vivo dephosphorylation and becomes 13C hyperpolarized lactate, which as we show canbe detected in the brain using 13C hyperpolarized MRI; an implication for future imaging of neurodegenerative diseasesand dementia.
机译:我们在此报告了同位素富集的1- 13 C-磷酸烯醇丙酮酸和1- 13 C-磷酸烯醇丙酮酸-d2的大规模(> 10 g)合成,用于超极化成像技术。合成了1- 13 C-磷酸烯醇式丙酮酸-d2,总产率为57%(分两步),且同位素纯度> 98%, H,与以前的方法相比有所改进报告。 1- 13 C-磷酸烯醇丙酮酸获得了相同的结果。通过在水性介质中成对的对氢加成,将这两个具有C = C键的不饱和化合物用于对氢诱导的极化。我们发现1- 13 C-磷酸烯醇丙酮酸的氘化导致新生超极化质子的 1 H T1总体增加(4.30±0.04 s对2.06±0.01 s),并且<产生的超极化1- 13 C-磷酸乳酸的sup> H极化(〜2.5%对〜0.7%)。通过磁场循环程序将新生的对氢衍生质子的核自旋极化转移至1- 13 C核。与未氘化的超极化1- 13 13 C-乳酸中的质子T1增加约好 13 C极化30% > C-磷酸乳酸。 T1弛豫的分析表明,通过磁场循环,1- 13 C-乳酸乳酸的氘化可能导致H→ 13 C极化传输效率降低约3倍。由于磁场循环是侧臂加氢方法中的关键极化转移步骤,因此,本文发现的结果可能会指导使用更宽范围的 13 C超极化造影剂的对氢极化进行造影剂的更合理设计。 13 C MRI进行分子成像1- 13 C-磷酸乳酸-d2的超极化是生物医学成像具有相关性,因为它在体内经历了去磷酸化作用并变成了 13 C超极化乳酸,正如我们所显示的,使用 13 C超极化MRI在大脑中进行检测;对神经退行性疾病的未来影像学意义和痴呆症。

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