Abstract
Metabolites in a urine extract are signal-enhanced by SABRE† hyperpolarization and detected using a benchtop NMR spectrometer. Quantification by standard addition is demonstrated for endogenic urinary nicotinamide (vitamin B3). Even higher sensitivity is achieved in an automated setup for multi-scan SABRE experiments. This hyperpolarization scheme is able to expedite biomarker detection and quantification, while maintaining low infrastructural requirements.
Supplementary materials
Title
ESI
Description
Experimental details on sample preparation, signal acquisition and data processing. Additional experiments for reproducibility, comparison of extract and lyophilized urine and concentration extimation of nicotinamide using nh-PHIP.
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Experimental data
Description
Unedited data for spectra shown in the main text and ESI in their native format (Magritek SpinSolve and Bruker).
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