Determination of thymidine phosphorylase activity by a non-radiochemical assay using reversed-phase high-performance liquid chromatography

J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Jun 25;820(2):271-275. doi: 10.1016/j.jchromb.2005.04.009.

Abstract

Thymidine phosphorylase (TP) catalyses the conversion of thymidine into thymine. A non-radiochemical assay procedure for TP was developed in which thymine was detected at 265 nm after separation with reversed-phase HPLC. A complete separation of thymidine and thymine was achieved in 6 min and the minimum amount of thymine that could be detected was 0.8 pmol. The assay was linear with reaction times, up to at least 4 h, and protein concentrations up to at least 65 microg/ml. Population analysis showed no differences in TP activity between man and women or with increasing age.

Publication types

  • Validation Study

MeSH terms

  • Chromatography, High Pressure Liquid / methods*
  • Humans
  • Kinetics
  • Leukocytes / enzymology*
  • Radiochemistry
  • Thymidine Phosphorylase / metabolism*

Substances

  • Thymidine Phosphorylase