Simultaneous quantitation of nicotinamide riboside and nicotinamide in dietary supplements via HPTLC–UV with confirmation by online HPTLC–ESI–MS

Author:

Neamţu Andreea Silvia1,Biţă Andrei2,Scorei Ion Romulus3,Rău Gabriela4,Bejenaru Ludovic Everard2,Bejenaru Cornelia5,Rogoveanu Otilia-Constantina6,Oancea Carmen Nicoleta1,Radu Antonia5,Pisoschi Cătălina Gabriela7,Neamţu Johny8,Mogoşanu George Dan2

Affiliation:

1. 1 Doctoral School, University of Medicine and Pharmacy of Craiova, 2 Petru Rareş Street, 200349 Craiova, Dolj County, Romania

2. 2 Department of Pharmacognosy & Phytotherapy, Faculty of Pharmacy, University of Medicine and Pharmacy of Craiova, 2 Petru Rareş Street, 200349 Craiova, Dolj County, Romania

3. 3 BioBoron Research Institute, S.C. Natural Research S.R.L., 31B Dunării Street, 207465 Podari Commune, Dolj County, Romania

4. 4 Department of Organic Chemistry, Faculty of Pharmacy, University of Medicine and Pharmacy of Craiova, 2 Petru Rareş Street, 200349 Craiova, Dolj County, Romania

5. 5 Department of Pharmaceutical Botany, Faculty of Pharmacy, University of Medicine and Pharmacy of Craiova, 2 Petru Rareş Street, 200349 Craiova, Dolj County, Romania

6. 6 Department of Physical Medicine and Rehabilitation, Faculty of Medicine, University of Medicine and Pharmacy of Craiova, 2 Petru Rareş Street, 200349 Craiova, Dolj County, Romania

7. 7 Department of Biochemistry, Faculty of Pharmacy, University of Medicine and Pharmacy of Craiova2 Petru Rareş Street, 200349 Craiova, Dolj County, Romania

8. 8 Department of Physics, Faculty of Pharmacy, University of Medicine and Pharmacy of Craiova2 Petru Rareş Street, 200349 Craiova, Dolj County, Romania

Abstract

The identification and quantitation of nicotinamide riboside (NAR) and its main related compound (nicotinamide) were achieved using high-performance thin-layer chromatography (HPTLC)–ultraviolet (UV) densitometry with confirmation by online electrospray ionization (ESI)–mass spectrometry (MS). As the stationary phase, HPTLC Si 60 F254 glass plates were employed; the mobile phase was ethanol–1 M ammonium acetate–formic acid (7:1:0.1, v/v/v). No derivatization was applied, and UV densitometry was performed in the absorbance mode (270 nm). The method was validated by specificity, linearity, accuracy, precision, and robustness.

Publisher

Akademiai Kiado Zrt.

Subject

General Chemistry

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