Efficient Parahydrogen-Induced 13C Hyperpolarization on a Microfluidic Device

被引:2
|
作者
Barker, Sylwia J. [1 ,2 ]
Dagys, Laurynas [1 ,3 ]
Levitt, Malcolm H. [1 ]
Utz, Marcel [1 ,2 ]
机构
[1] Univ Southampton, Sch Chem, Southampton SO17 1BJ, England
[2] Karlsruhe Inst Technol, Inst Microstruct Technol, D-76131 Karlsruhe, Germany
[3] Vilnius Univ, Inst Chem Phys, LT-01513 Vilnius, Lithuania
基金
欧洲研究理事会; 英国工程与自然科学研究理事会;
关键词
ON-A-CHIP; NUCLEAR-MAGNETIC-RESONANCE; NMR; SINGLET; KINETICS; TOOL;
D O I
10.1021/jacs.4c03271
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We show the direct production and detection of C-13-hyperpolarized fumarate by parahydrogen-induced polarization (PHIP) in a microfluidic lab-on-a-chip (LoC) device and achieve 8.5% C-13 polarization. This is the first demonstration of C-13-hyperpolarization of a metabolite by PHIP in a microfluidic device. LoC technology allows the culture of mammalian cells in a highly controlled environment, providing an important tool for the life sciences. In-situ preparation of hyperpolarized metabolites greatly enhances the ability to quantify metabolic processes in such systems by microfluidic NMR. PHIP of H-1 nuclei has been successfully implemented in microfluidic systems, with mass sensitivities in the range of pmol/s. However, metabolic NMR requires high-yield production of hyperpolarized metabolites with longer spin life times than is possible with H-1. This can be achieved by transfer of the polarization onto C-13 nuclei, which exhibit much longer T-1 relaxation times. We report an improved microfluidic PHIP device, optimized using a finite element model, that enables the direct and efficient production of C-13-hyperpolarized fumarate.
引用
收藏
页码:18379 / 18386
页数:8
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