Drevet Mulard Eva, Gilard Véronique, Balayssac Stéphane, Rautureau Gilles J P
Institute of Chemistry and Biochemistry (ICBMS), UMR 5246, CNRS, University Lyon, F-69622 Villeurbanne, France.
France INSERM Research Unit 1033 LYOS, Lyon 1 University, F-69372 Lyon, France.
Molecules. 2025 Apr 19;30(8):1838. doi: 10.3390/molecules30081838.
Nuclear magnetic resonance (NMR) spectroscopy is a powerful analytical approach that enables both the structural determination and precise quantification of small molecules, such as metabolites. However, achieving precise quantification with NMR involves more than simply comparing integrals derived from NMR peaks to a concentration reference; quantitative NMR (qNMR) is a distinct and specialized application within the field. To obtain absolute quantitative results, spectra must be acquired under strict experimental conditions. Unfortunately, these acquisition parameters can be challenging to implement experimentally and often require trade-offs that compromise high throughput or practicality. In such situations, alternative strategies based on relative quantification and advanced software tools offer valuable solutions. This review aims to provide non-specialists with the key concepts and methodologies required for accurate NMR-based quantification in biomedical research, focusing on practical guidelines and experimental considerations. Unlike prior reviews, it prioritizes accessibility and practical implementation for researchers outside the field, emphasizing key experimental workflows and applications in biological and clinical studies. It clarifies the distinctions between absolute and relative concentration determinations and emphasizes the critical importance of sample preparation, pulse sequence selection, and rigorous control of experimental parameters. Recent technological advancements, such as high-field spectrometers and cryoprobes, have significantly enhanced the sensitivity and accuracy of NMR, enabling the reliable detection of low-concentration metabolites. Quantitative NMR thus offers critical potential in elucidating metabolic processes, supporting drug development, and aiding disease diagnosis.
核磁共振(NMR)光谱法是一种强大的分析方法,能够对小分子(如代谢物)进行结构测定和精确量化。然而,利用NMR实现精确量化不仅仅是简单地将NMR峰的积分与浓度参考值进行比较;定量核磁共振(qNMR)是该领域中一种独特的专门应用。为了获得绝对定量结果,必须在严格的实验条件下采集光谱。不幸的是,这些采集参数在实验中实施起来可能具有挑战性,并且常常需要进行权衡,这会影响高通量或实用性。在这种情况下,基于相对量化的替代策略和先进的软件工具提供了有价值的解决方案。本综述旨在为非专业人士提供生物医学研究中基于NMR的准确量化所需的关键概念和方法,重点关注实用指南和实验考虑因素。与以往的综述不同,它优先考虑该领域以外研究人员的可及性和实际应用,强调关键实验工作流程以及在生物学和临床研究中的应用。它阐明了绝对浓度测定和相对浓度测定之间的区别,并强调了样品制备、脉冲序列选择以及严格控制实验参数的至关重要性。最近的技术进步,如高场光谱仪和低温探头,显著提高了NMR的灵敏度和准确性,能够可靠地检测低浓度代谢物。因此,定量核磁共振在阐明代谢过程、支持药物开发和辅助疾病诊断方面具有关键潜力。