Farrant R D, Cupid B C, Nicholson J K, Lindon J C
Physical Sciences Research Unit, Glaxo Wellcome Medicines Research Centre, Stevenage, Herts, UK.
J Pharm Biomed Anal. 1997 Sep;16(1):1-5. doi: 10.1016/s0731-7085(96)01958-9.
The use of 2H NMR spectroscopy as a detector for HPLC has been investigated using the continuous flow method in which rat urine containing metabolites of N-dimethylformamide-d7 was employed as a test case. Three xenobiotic-related species, including DMF-d7 itself, were detected. It is shown that for small molecules which give relatively sharp 2H NMR resonances, 2H HPLC-NMR spectroscopy is a feasible technique. For larger molecules, the resulting broad lines are likely to preclude the determination of detailed structural information. However, extension of the approach is possible by the use of selectively 2H-labelled xenobiotics to determine HPLC retention times of metabolites with continuous-flow 2H NMR spectroscopy detection, followed by stop-flow 1H HPLC-NMR spectroscopy for structural characterisation.
已使用连续流动法研究了将2H核磁共振光谱用作高效液相色谱检测器的情况,其中以含有N-二甲基甲酰胺-d7代谢物的大鼠尿液作为测试实例。检测到三种与外源性物质相关的物质,包括DMF-d7本身。结果表明,对于给出相对尖锐的2H核磁共振共振峰的小分子,2H高效液相色谱-核磁共振光谱是一种可行的技术。对于较大的分子,由此产生的宽谱线可能会妨碍详细结构信息的测定。然而,通过使用选择性2H标记的外源性物质,采用连续流动2H核磁共振光谱检测来确定代谢物的高效液相色谱保留时间,随后采用停流1H高效液相色谱-核磁共振光谱进行结构表征,该方法是可以扩展的。