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Updated: Jul 20, 2026

Untargeted Metabolomics from Biological Sources Using Ultraperformance Liquid Chromatography-High Resolution Mass Spectrometry UPLC-HRMS
Published on: May 20, 2013
Aqueous LC-MS/MS quantification of α-/β-nicotinamide mononucleotide in dietary supplements using a pentabromophenyl
Chng Sze Hoei1, Nian-Hua Wu2, Chao-Ming Tsen3
1Department of Family Medicine, Tungs' Taichung MetroHarbor Hospital, Taichung, 435403, Taiwan.
Abstract:
In this study, we developed an LC-MS/MS method that enables baseline separation and quantification of α- and β-nicotinamide mononucleotide (NMN) isomers under fully aqueous reversed-phase conditions. At first, three commonly used reversed-phase columns (Polar C18, F5, and PBr) were evaluated, and only the PBr phase provided sufficient stereoselectivity through enhanced π-π stacking, dipole-dipole interactions, and halogen bonding. Using 0.1 % formic acid in water as the mobile phase, the two isomers were baseline resolved within 3 min. The method was validated for linearity, sensitivity, precision, accuracy, and matrix effects. When applied to eight commercial NMN supplements, the analysis revealed substantial variation in isomer composition, including undeclared or inaccurately labeled ingredients. Overall, this work presents the first LC-MS/MS approach capable of isomer-specific NMN analysis under fully aqueous reversed-phase conditions, offering a robust and environmentally compatible platform for product authentication, quality control, and potential applications in pharmacokinetics and metabolomics.

