Determination of residual solvents in bulk pharmaceuticals by thermal desorption/gas chromatography/mass spectrometry

Chem Pharm Bull (Tokyo). 2000 Dec;48(12):1894-7. doi: 10.1248/cpb.48.1894.

Abstract

Thermal desorption (TD) techniques followed by capillary GC/MS were applied for the analysis of residual solvents in bulk pharmaceuticals. Solvents desorbed from samples by heating were cryofocused at the head of a capillary column prior to GC/MS analysis. This method requires a very small amount of sample and no sample pretreatment. Desorption temperature was set at the point about 20 degrees C higher than the melting point of each sample individually. The relative standard deviations of this method tested by performing six consecutive analyses of 8 different samples were 1.1 to 3.1%, and analytical results of residual solvents were in agreement with those obtained by direct injection of N,N-dimethylformamide solution of the samples into the GC. This novel TD/GC/MS method was demonstrated to be very useful for the identification and quantification of residual solvents in bulk pharmaceuticals.

MeSH terms

  • Chemistry, Pharmaceutical / methods
  • Drug Contamination
  • Gas Chromatography-Mass Spectrometry*
  • Pharmaceutical Preparations / analysis*
  • Quality Control
  • Reference Standards
  • Solvents / analysis*
  • Temperature

Substances

  • Pharmaceutical Preparations
  • Solvents