Université de Nantes, CNRS, CEISAM, UMR 6230, B.P. 92208, 2 rue de la Houssinière, F-44322 Nantes Cedex 03, France.
J Pharm Biomed Anal. 2011 Jan 5;54(1):252-7. doi: 10.1016/j.jpba.2010.07.046. Epub 2010 Aug 6.
Quantitative analysis of metabolic mixtures by (1)H 1D NMR offers a limited potential for precise quantification of biomarkers, due to strong overlap between the peaks. Two-dimensional spectroscopy is a powerful tool to unambiguously and simultaneously measure a larger number of metabolite contributions. However, it is still rarely used for quantification, first because quantitative analysis by 2D NMR requires a calibration procedure due to the multi-impulsional nature of 2D NMR experiments, and above all because of the prohibitive experiment duration that is necessary to obtain such a calibration curve. In this work, we develop and evaluate a 2D (1)H INADEQUATE protocol for a fast determination of metabolite concentrations in complex mixtures. The 2D pulse sequence is carefully optimized and evaluated in terms of precision and linearity. Quantitative (1)H INADEQUATE 2D spectra of metabolic mixtures are obtained in 7 min with a repeatability better than 2% for metabolite concentrations as small as 100 μM and an excellent linearity. The method described in this work allows a fast and precise quantification of metabolic mixtures, and it forms a promising tool for metabonomic studies.
基于 (1)H 1D NMR 的代谢混合物的定量分析由于峰之间的强重叠,因此仅提供了对生物标志物进行精确定量的有限潜力。二维光谱是一种强大的工具,可以明确且同时测量更多数量的代谢物贡献。然而,它仍然很少用于定量分析,首先是因为二维 NMR 实验的多脉冲性质需要校准程序,其次是因为获得这种校准曲线所需的实验时间过长。在这项工作中,我们开发并评估了一种用于快速测定复杂混合物中代谢物浓度的 2D(1)H INADEQUATE 方案。该二维脉冲序列在精度和线性度方面进行了仔细的优化和评估。通过该方法,在 7 分钟内可以获得代谢混合物的 2D INADEQUATE 图谱,对于低至 100 μM 的代谢物浓度,其重复性优于 2%,并且具有极好的线性度。本文所描述的方法可以快速准确地定量代谢混合物,是代谢组学研究的有前途的工具。