Automated direct high-performance liquid chromatographic assay for estetrol, estriol, cortisone and cortisol in serum and amniotic fluid

J Chromatogr. 1991 Jul 17;568(1):35-44. doi: 10.1016/0378-4347(91)80338-d.

Abstract

An automated direct assay for the simultaneous determination of unconjugated estetrol, estriol, cortisone and cortisol in serum and amniotic fluid, using high-performance liquid chromatography with electrochemical detection and ultraviolet detection, has been developed. The analysis time is ca. 1 h. This system offers good reproducibility with low coefficients of variation (estetrol, 2.3%; estriol, 2.3%; cortisone, 2.6%; cortisol, 1.9%). Detection limits are low enough for routine determinations (estetrol and estriol, 150 pg; cortisone and cortisol, 5 ng). Comparison of the values measured by the present method and by radioimmunoassay revealed significant correlations for estetrol (r = 0.787, p less than 0.01), estriol (r = 0.957, p less than 0.01), cortisone (r = 0.956, p less than 0.01) and cortisol (r = 0.865, p less than 0.01). This system proved to be valuable in monitoring feto-placental function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amniotic Fluid / chemistry*
  • Chromatography, High Pressure Liquid / methods*
  • Cortisone / analysis*
  • Cortisone / blood*
  • Estetrol / analysis*
  • Estetrol / blood*
  • Estriol / analysis*
  • Estriol / blood*
  • Female
  • Humans
  • Hydrocortisone / analysis
  • Hydrocortisone / blood*
  • Pregnancy

Substances

  • Estetrol
  • Estriol
  • Cortisone
  • Hydrocortisone