Abstract
Purpose
Phosphomono- and diesters (PME and PDE) are important metabolites that are potential biomarkers for a number of cancers. We designed a new NMR pulse sequence, i.e., 1H–31P soft-heteronuclear single quantum correlation (HSQC), specifically for noninvasively detecting PME and PDE in biological samples.
Procedure
The nonselective 1H refocusing π pulses in the conventional heteronuclear single quantum correlation pulse sequence are replaced by selective π pulses. When the selective pulses are offset on the CH2O resonances, the homonuclear couplings between the NCH2 and CH2O protons are effectively removed, and the spectrum of PME and PDE is significantly enhanced.
Results
The sensitivity of this pulse sequence has been demonstrated with milk and mouse brain samples. A soft-HSQC spectrum, where only PME and PDE signals appear, can be recorded from these biological samples in minutes with remarkably high signal-to-noise ratio.
Conclusion
This pulse sequence provides a new and quick method for in vivo studies of phosphorus metabolite in the human brain and other tissues for medical purposes.
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Acknowledgments
The authors thank the National Natural Science Foundation of China (nos. 21120102038, 21173257, 20921004, and 21005085) and the National Major Basic Research Program of China (no. 2009CB918603) for their financial support.
Conflict of Interest
The authors have no conflicts of interest.
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Mao, Xa., Jiang, B., Jiang, L. et al. 1H–31P Soft-HSQC Pulse Sequence Specifically for Detecting Phosphomono- and Diesters in Biological Samples. Mol Imaging Biol 15, 245–249 (2013). https://doi.org/10.1007/s11307-012-0607-6
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DOI: https://doi.org/10.1007/s11307-012-0607-6