Optimization of a high-performance liquid chromatography method to quantify bilirubin and separate it from its photoproducts: effect of column length, Ph, mobile phase composition, and flow rate

Appl Biochem Biotechnol. 2006 Dec;135(3):209-18. doi: 10.1385/abab:135:3:209.

Abstract

A rapid reversed-phase (RP) high-performance liquid chromatography method for the isolation of bilirubin from its photoproducts (e.g., biliverdin) is reported. The method is based on isocratic elution using methanol:water as the mobile phase. A 24 full-factorial experimental design approach was adopted. For the optimization, the best separation was obtained using a flow rate of 1.50 mL/min, a mobile phase of 99:1 methanol:water (v/v) at pH 3.60, and a 150 x 4.6 mm id RP (C18) column containing 5-microm particles. These conditions produced the fastest total retention time of 3.38 +/- 0.055 min, and other chromatographic parameters were acceptable. Under the optimum conditions, a linear calibration curve for bilirubin was obtained over the 1.0-40.0 microg/L concentration range studied. The limit of quantification was 0.79 g/L and the limit of detection was 0.24 microg/L. Bilirubin in solution was monitored by ultraviolet detection at 450 nm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bilirubin / isolation & purification*
  • Bilirubin / radiation effects
  • Chromatography, High Pressure Liquid / instrumentation*
  • Chromatography, High Pressure Liquid / methods*
  • Hydrogen-Ion Concentration
  • Light
  • Microfluidics / methods
  • Phase Transition
  • Photochemistry / methods
  • Reproducibility of Results
  • Sensitivity and Specificity

Substances

  • Bilirubin