Optimized determination method for trans-10-hydroxy-2-decenoic acid content in royal jelly by high-performance liquid chromatography with an internal standard

J AOAC Int. 2007 Jan-Feb;90(1):244-9.

Abstract

An optimized reversed-phase high-performance liquid chromatography method was developed to detect the trans-10-hydroxy-2-decenoic acid (10-HDA) content in royal jelly cream and lyophilized powder. The sample was extracted using absolute ethanol. Chromatographic separation of 10-HDA and methyl 4-hydroxybenzoate as the internal standard was performed on a Nova-pak C18 column. The average recoveries were 95.0-99.2% (n = 5) with relative standard deviation (RSD) values of 1.3-2.1% for royal jelly cream and 98.0-100.0% (n = 5) with RSD values of 1.6-3.0% for lyophilized powder, respectively. The limits of detection and quantitation were 0.5 and 1.5 mg/kg, respectively, for both royal jelly cream and lyophilized powder. The method was validated for the determination of practical royal jelly products. The concentration of 10-HDA ranged from 1.26 to 2.21% for pure royal jelly cream samples and 3.01 to 6.19% for royal jelly lyophilized powder samples. For 30 royal jelly products, the 10-HDA content varied from not detectable to 0.98%.

MeSH terms

  • Animals
  • Bees
  • Chromatography, High Pressure Liquid / methods
  • Fatty Acids / chemistry*
  • Fatty Acids, Monounsaturated / analysis*
  • Freeze Drying
  • Indicators and Reagents
  • Kinetics
  • Royal Jelly

Substances

  • Fatty Acids
  • Fatty Acids, Monounsaturated
  • Indicators and Reagents
  • Royal Jelly
  • 10-hydroxy-2-decenoic acid