Determination of ifosfamide, 2- and 3-dechloroethyifosfamide using gas chromatography with nitrogen-phosphorus or mass spectrometry detection

Ther Drug Monit. 2000 Oct;22(5):613-20. doi: 10.1097/00007691-200010000-00018.

Abstract

A comparison was made between methods for determining ifosfamide (IF), 2- (2DCE) and 3-dechloroethylifosfamide (3DCE) using gas chromatography with nitrogen-phosphorus detection (GC-NPD) versus positive ion electron-impact ion-trap mass spectrometry (GC-MS2). Sample pretreatment involved liquid-liquid extraction with ethyl acetate after adding trofosfamide as internal standard and alkalinization. The GC-NPD was linear, specific, and sensitive for all analytes in the range of 0.0500-100 microg/mL with lower limits of quantification (LLQ) of 0.0500 microg/mL using a 50-microgL plasma sample. The GC-MS2 was linear, specific, and sensitive for IF, 2DCE, and 3DCE in the ranges of 0.250-100, 0.500-25.0, and 0.500-25.0 microg/mL, respectively, with LLQs of 0.250, 0.500, and 0.500 microg/mL. The ranges of accuracy, within-day precision, and between-day precision for analysis of all compounds with GC-NPD did not exceed 93.3% to 105.4%, 8.0% and 9.8%, respectively. The ranges of accuracy, within-day precision, and between-day precision for analysis of all compounds with GC-MS2 did not exceed 86.5% to 99.0%, 9.0% and 12.7%, respectively. In conclusion, GC-NPD proved to be superior to GC-MS2 in sensitivity, detection range, accuracy, and precisions. Therefore GC-NPD is the method of choice for fast un-derivatized determination of IF, 2DCE, and 3DCE in human plasma, and it can readily be used for clinical pharmacokinetic studies and routine monitoring of IF-treated patients in a hospital setting.

Publication types

  • Comparative Study
  • Evaluation Study

MeSH terms

  • Antineoplastic Agents, Alkylating / analysis*
  • Antineoplastic Agents, Alkylating / pharmacokinetics
  • Chromatography, Gas / standards
  • Cyclophosphamide / analogs & derivatives*
  • Cyclophosphamide / analysis*
  • Cyclophosphamide / pharmacokinetics
  • Drug Monitoring / standards*
  • Gas Chromatography-Mass Spectrometry / standards
  • Humans
  • Ifosfamide / analogs & derivatives*
  • Ifosfamide / analysis*
  • Ifosfamide / pharmacokinetics
  • Quality Control
  • Sensitivity and Specificity

Substances

  • Antineoplastic Agents, Alkylating
  • dechloroethylcyclophosphamide
  • Cyclophosphamide
  • dechloroethylifosfamide
  • Ifosfamide