Assay of enzymic O-methylation of catechol oestrogens by high-performance liquid chromatography with coulometric detection

J Chromatogr. 1993 Aug 11;617(2):221-5. doi: 10.1016/0378-4347(93)80491-l.

Abstract

A simple and sensitive method for the determination of guaiaicol oestrogens enzymatically formed from 2- or 4-hydroxyoestradiol, by means of high-performance liquid chromatography with coulometric detection, has been developed. Catechol and guaiacol oestrogens were efficiently separated on a reversed-phase column, using 0.5% ammonium phosphate buffer (pH 3.0)-acetonitrile (59:41, v/v) as the mobile phase, and detected coulometrically in a screening-oxidation mode at +0.10 V and +0.35 V, respectively. The method was applied to the assay of in vitro enzymic O-methylation of catechol oestrogens. After 2- or 4-hydroxyoestradiol had been incubated with rat red blood cells in the presence of S-adenosylmethionine, the resulting guaiacols and unchanged substrate were percolated through an Extrelut-3 cartridge. The dried eluate was redissolved and directly injected. This simple procedure was as sensitive as the previously reported method using gas chromatography-mass spectrometry in a selected ion monitoring mode.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromatography, High Pressure Liquid / methods*
  • Electrochemistry
  • Erythrocytes / chemistry
  • Estrogens, Catechol / blood*
  • Male
  • Methylation
  • Rats
  • Rats, Inbred SHR
  • Sensitivity and Specificity

Substances

  • Estrogens, Catechol