An optimized fast-performance liquid chromatography method for analyzing lipoprotein profiles using microliter volumes of serum

Anal Biochem. 2008 May 15;376(2):268-74. doi: 10.1016/j.ab.2008.02.028. Epub 2008 Mar 4.

Abstract

Plasma or serum lipoprotein analysis is commonly carried out with a conventional size-exclusion fast-performance liquid chromatography method that requires large sample volumes (1-2 ml). To determine lipoprotein profiles of mice with this method, plasma or serum samples have to be pooled from a group of animals, which often requires sacrificing animals. Here we report an optimized anion-exchange chromatography method with simplified cholesterol collection and detection system. After 5-10 microl serum was injected for anion-exchange chromatography, a stepwise gradient was applied and fractions were collected on a 96-well plate. Cholesterol content in each well was measured using a fluorescence-based detection method. With this method, distinct lipoprotein peaks corresponding to high-density lipoprotein, low-density lipoprotein, and very-low-density lipoprotein, can be easily separated and identified with excellent resolution. The entire high-performance liquid chromatography run takes about 30min and the results are reproducible with a low variability. The small sample size allows analyzing the lipoprotein profile in a given mouse at a given time point with nonterminal bleeding. The method is simple to set up with commercially available parts and convenient to run.

MeSH terms

  • Animals
  • Blotting, Western
  • Chromatography, Gel
  • Chromatography, High Pressure Liquid / methods*
  • Humans
  • Lipoproteins / blood*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Rabbits
  • Rats
  • Reproducibility of Results

Substances

  • Lipoproteins