Stefańska Marta, Müntener Thomas, Hiller Sebastian
Biozentrum, University of Basel, Basel, Switzerland.
Commun Chem. 2025 Aug 1;8(1):223. doi: 10.1038/s42004-025-01626-8.
Towards target diagnostics of low-concentrated molecules in biofluids, NMR spectroscopy faces limitations due to low sensitivity, signal overlap, and high equipment costs. Hyperpolarization methods such as photo-chemically induced dynamic nuclear polarization (photo-CIDNP) can mitigate some of these challenges. In this study, we explore the potential of steady-state photo-CIDNP to quantify target molecules in urine samples. Matrix interference poses a significant challenge to quantitative measurements, and we thus establish two counteracting methods: spiking and biofluid dilution. Experiments conducted in both high (14.1 T) and low (1.9 T) magnetic fields demonstrate the effectiveness of photo-CIDNP-based quantification at micromolar levels for the analytes sumatriptan and paracetamol. We report limits of quantification (LOQs) in complex matrices down to 3.5 μM and average errors of less than 26% with the spiking method and less than 11% using biofluid dilution. This proof-of-concept study highlights the potential of NMR supported by photo-CIDNP as a target diagnostic tool for rapid drug quantification and clinical monitoring applications, especially with low-cost benchtop NMR devices.
对于生物流体中低浓度分子的靶向诊断,核磁共振波谱法由于灵敏度低、信号重叠和设备成本高而面临局限性。光化学诱导动态核极化(photo-CIDNP)等超极化方法可以缓解其中一些挑战。在本研究中,我们探索了稳态photo-CIDNP在定量尿液样本中靶分子方面的潜力。基质干扰对定量测量构成重大挑战,因此我们建立了两种抵消方法:加标法和生物流体稀释法。在高(14.1 T)和低(1.9 T)磁场中进行的实验证明了基于photo-CIDNP的定量方法在微摩尔水平上对分析物舒马曲坦和对乙酰氨基酚的有效性。我们报告了在复杂基质中使用加标法时低至3.5 μM的定量限(LOQ)以及平均误差小于26%,使用生物流体稀释法时平均误差小于11%。这项概念验证研究突出了由photo-CIDNP支持的核磁共振作为快速药物定量和临床监测应用的靶向诊断工具的潜力,特别是对于低成本的台式核磁共振设备。