Development and validation of an HPLC-DAD analysis for pharmacopoeial qualification of industrial Capsicum extracts

J Chromatogr Sci. 2015 Jan;53(1):16-23. doi: 10.1093/chromsci/bmu004. Epub 2014 Feb 20.

Abstract

A reverse-phase high-performance liquid chromatography method was developed to quantify capsaicin (trans-8-methyl-N-vanillyl-6-nonenamid), dihydrocapsaicin (8-methyl-N-vanillylnonanamide) and the main capsaicinoid contents of Capsicum extracts. The chromatographic separation was carried out on a C8 column using isocratic mobile phase consisting of 40% (v/v) acetonitrile and 60% (v/v) orthophosphoric acid solution with flow rate of 1.5 mL/min. The concentration of the eluting compounds was monitored by a diode-array detector at wavelength of 281 nm. The method was evaluated for number of validation characteristics (selectivity, accuracy (confidence intervals <1%), repeatability and intermediate precision (RSD% < 2.5%), limit of detection (LOD), limit of quantification (LOQ) and calibration range). The LOD was 0.25 µg/mL and the LOQ was 0.5 µg/mL. Using methanolic solutions of United States Pharmacopoeia (USP) Capsaicin and Dihydrocapsaicin Reference Standards, the method was linear over the concentration range 0.0005-0.5000 mg/mL for both capsaicinoids. The method was applied to qualify capsaicinoid content of two industrial capsicum extracts according to the USP 29.

Publication types

  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • Capsaicin / analogs & derivatives
  • Capsaicin / analysis
  • Capsicum / chemistry*
  • Chromatography, High Pressure Liquid / methods*
  • Chromatography, High Pressure Liquid / standards
  • Limit of Detection
  • Plant Extracts / analysis*
  • Reference Standards

Substances

  • Plant Extracts
  • Capsaicin
  • dihydrocapsaicin