Determination of a new podophyllotoxin derivative, TOP-53, and its metabolite in rat plasma and urine by high-performance liquid chromatography with electrochemical detection

J Chromatogr B Biomed Sci Appl. 1997 Mar 7;690(1-2):283-8. doi: 10.1016/s0378-4347(96)00388-x.

Abstract

A high-performance liquid chromatographic method was developed for the determination of a new podophyllotoxin derivative, TOP-53 (I), and TOP-53 glucuronide (II) as its major metabolite in rat plasma and urine. For the analysis of I, the sample was chromatographed on a reversed-phase C18 column with electrochemical detection after consecutive two-step liquid-liquid extractions. Compound II was determined as I after enzymatic hydrolysis of II. This method was validated sufficiently with respect to specificity, accuracy, and precision. The limits of quantitation for both I and II were 2 ng/ml in plasma and 10 ng/ml in urine. The method is thus useful for the pharmacokinetic study of I.

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / blood*
  • Antineoplastic Agents, Phytogenic / pharmacokinetics
  • Antineoplastic Agents, Phytogenic / urine*
  • Chromatography, High Pressure Liquid
  • Drug Stability
  • Electrochemistry
  • Etoposide / analogs & derivatives*
  • Etoposide / blood
  • Etoposide / pharmacokinetics
  • Etoposide / urine
  • Glucuronates / blood
  • Glucuronates / urine
  • Rats
  • Sensitivity and Specificity

Substances

  • Antineoplastic Agents, Phytogenic
  • Glucuronates
  • TOP 53
  • TOP 53 glucuronide
  • Etoposide