Stability studies on trans-rosmarinic acid and GC-MS analysis of its degradation product

J Pharm Biomed Anal. 2011 Jul 15;55(5):1010-6. doi: 10.1016/j.jpba.2011.04.003. Epub 2011 Apr 8.

Abstract

The stability of trans-rosmarinic acid (trans-RA, an important phenolic compound with anti-oxidant, anti-inflammatory, anti-bacterial, and anti-viral properties) exposed to different stress conditions (daylight, higher temperatures, different solvents, and humidity) was investigated. Gas chromatography-mass spectrometry (GC-MS) was used to analyse the degraded samples, and structural identification of degradation products was assigned based upon MS fragmentation pattern. The GC-MS method was validated in terms of linearity, precision as repeatability, accuracy, limit of detection (LOD), limit of quantitation (LOQ) and recovery. The stability experiments were performed on pure trans-RA and on trans-RA present in commercially available rosemary extract. The cis-isomer of RA was the only degradation product. The results showed that trans-RA was readily isomerized into its cis-form within a few hours when dissolved in ethanol, methanol or tetrahydrofuran, and exposed to darkness or daylight at different temperatures. Isomerization took place to a greater extent in protic than in aprotic solvents. Trans-RA in the solid state was found to be stable for up to three months under all tested conditions. The described GC-MS method was also applied to the determination of trans-RA in eight different species of Lamiaceae family.

MeSH terms

  • Calibration
  • Chemistry Techniques, Analytical / methods
  • Chemistry, Pharmaceutical / methods
  • Cinnamates / analysis*
  • Depsides / analysis*
  • Ethanol / chemistry
  • Furans / chemistry
  • Gas Chromatography-Mass Spectrometry / methods*
  • Isomerism
  • Limit of Detection
  • Methanol / chemistry
  • Models, Chemical
  • Reproducibility of Results
  • Rosmarinic Acid
  • Solvents / chemistry
  • Temperature

Substances

  • Cinnamates
  • Depsides
  • Furans
  • Solvents
  • Ethanol
  • tetrahydrofuran
  • Methanol