Elucidation of stress-induced degradation products of mangiferin: Method development and validation

Biomed Chromatogr. 2017 Aug;31(8). doi: 10.1002/bmc.3935. Epub 2017 Mar 13.

Abstract

The degradation behavior of mangiferin, under various ICH Q1A(R2) recommended stress conditions, was studied using an isocratic elution with mobile phase (pH 2.4), composed of acetonitrile and 1% orthophosphoric acid (12:88 v/v) at a flow rate of 1.0 mL/min, with λmax 262 nm. It was suitably adapted for LC-MS studies by replacing with 1% acetic acid (ACN-1% acetic acid; 18:82) and the pH was adjusted to 3.0. Extensive degradation was found to occur during alkaline medium stress studies at 2.31 min of retention time at λmax of 235 nm. The mass spectrum of mangiferin, 3 h after treatment with 0.1 M NaOH, clearly shows the rupture of the tricyclic ring, indicating that a fragment at m/z - 269 was formed. Furthermore, the results were supported by nuclear magnetic resonance as well. However, no degradation was observed in other stress conditions.

Keywords: LC-MS-MS; degaradation products; mass spectra; xanthone ring.

MeSH terms

  • Anti-Inflammatory Agents / chemistry*
  • Antioxidants / chemistry*
  • Chromatography, Liquid
  • Drug Stability
  • Hydrolysis
  • Magnetic Resonance Spectroscopy
  • Mangifera / chemistry
  • Plant Extracts / chemistry*
  • Tandem Mass Spectrometry
  • Xanthones / chemistry*

Substances

  • Anti-Inflammatory Agents
  • Antioxidants
  • Mangifera indica extract
  • Plant Extracts
  • Xanthones
  • mangiferin