Liquid chromatography/electrospray ionization mass spectrometry method for the determination of the active metabolite M-1 of suplatast tosilate in human plasma

Biomed Chromatogr. 2007 Dec;21(12):1297-302. doi: 10.1002/bmc.894.

Abstract

A liquid chromatography/electrospray ionization mass spectrometry (LC/ESIMS) method for the determination of 4-(3-ethoxy-2-hydroxypropoxy) acrylanilide (M-1), the active metabolite of suplatast tosilate, in human plasma was established. Plasma samples were extracted with diethyl ether, separated on a C(18) column with a mobile phase of acetonitrile-10 mm ammonium acetate solution containing 0.1% formic acid (28:72, v/v) and detected by ESIMS. The method was linear over the concentration range 0.15-60.0 ng/mL. The lowest limit of quantification was 0.15 ng/mL. The intra- and inter-run relative standard deviations obtained from three validation runs were all less than 8.6%, and the intra- and inter-run relative errors were all less than 3.1%. The method was successfully applied for the evaluation of pharmacokinetic profiles of M-1 in healthy volunteers.

MeSH terms

  • Acetates / chemistry
  • Acetonitriles / chemistry
  • Arylsulfonates / blood*
  • Arylsulfonates / pharmacokinetics
  • Chromatography, Liquid / methods*
  • Formates / chemistry
  • Histamine Antagonists / blood*
  • Histamine Antagonists / pharmacokinetics
  • Humans
  • Reference Values
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Solutions / chemistry
  • Spectrometry, Mass, Electrospray Ionization / methods*
  • Sulfonium Compounds / blood*
  • Sulfonium Compounds / pharmacokinetics
  • Time Factors

Substances

  • Acetates
  • Acetonitriles
  • Arylsulfonates
  • Formates
  • Histamine Antagonists
  • Solutions
  • Sulfonium Compounds
  • formic acid
  • suplatast tosilate
  • ammonium acetate
  • acetonitrile