Rapid UHPLC method for simultaneous determination of vancomycin, terbinafine, spironolactone, furosemide and their metabolites: application to human plasma and urine

Anal Sci. 2010;26(7):755-9. doi: 10.2116/analsci.26.755.

Abstract

The ultra high performance liquid chromatography (UHPLC)-UV method for the simultaneous determination of furosemide, saluamine (furosemide metabolite), spironolactone, carnenone (spironolactone active metabolite), terbinafine, N-desmethylcarboxy terbinafine (terbinafine metabolite) and vancomycin in human plasma and urine is proposed. Good separation of the analytes was achieved with the gradient RP-UHPLC-UV with the mobile phase composed as acetonitrile and 0.1% formic acid. The determined substances were eluted from a Hypersil GOLD C(18)e (50 mm x 2.1 mm, 1.7 microm particles) column in 3.3 min. Good linear relationships were observed for all of the analytes (R(2) higher than 0.994). The limit of detection (LOD) values varied from 0.01 to 0.07 microg ml(-1), with vancomycin as an exception (0.11 microg ml(-1)). After protein precipitation and solid-phase extraction, samples of plasma and urine were analyzed. Thanks to the short analysis time and small quantities of urine or plasma needed, this method can be applied to routine clinical analysis.

MeSH terms

  • Blood Chemical Analysis / methods*
  • Calibration
  • Chromatography, High Pressure Liquid / methods*
  • Furosemide / blood
  • Furosemide / metabolism
  • Furosemide / urine
  • Humans
  • Naphthalenes / blood
  • Naphthalenes / metabolism
  • Naphthalenes / urine
  • Reproducibility of Results
  • Spironolactone / blood
  • Spironolactone / metabolism
  • Spironolactone / urine
  • Terbinafine
  • Time Factors
  • Urinalysis / methods*
  • Vancomycin / blood
  • Vancomycin / metabolism
  • Vancomycin / urine

Substances

  • Naphthalenes
  • Spironolactone
  • Vancomycin
  • Furosemide
  • Terbinafine