Determination of cilnidipine, a new calcium antagonist, in human plasma using high performance liquid chromatography with tandem mass spectrometric detection

Anal Chim Acta. 2007 Sep 26;600(1-2):142-6. doi: 10.1016/j.aca.2006.11.072. Epub 2006 Dec 6.

Abstract

A rapid, sensitive and reliable high performance liquid chromatographic method coupled with tandem mass spectrometry (HPLC-MS/MS) has been developed and validated for the determination of cilnidipine, a relatively new calcium antagonist, in human plasma. The reversed-phase chromatographic system was interfaced with a TurboIonSpray (TIS) source. Nimodipine was employed as the internal standard (IS). Sample extracts following protein precipitation were injected into the HPLC-MS/MS system. The analyte and IS were eluted isocratically on a C18 column, with a mobile phase consisting of CH(3)OH and NH(4)Ac (96:4, v/v). The ions were detected by a triple quadrupole mass spectrometric detector in the negative mode. Quantification was performed using multiple reaction monitoring (MRM) of the transitions m/z 491.2-->122.1 and m/z 417.1-->122.1 for cilnidipine and for the IS, respectively. The analysis time for each run was 3.0 min. The calibration curve fitted well over the concentration range of 0.1-10 ngmL(-1), with the regression equation Y=(0.103+/-0.002)X+(0.014+/-0.003) (n=5), r=0.9994. The intra-day and inter-day R.S.D.% were less than 12.51% at all concentration levels within the calibration range. The recoveries were between 92.71% and 97.64%. The long-term stability and freeze-thaw stability were satisfying at each level. The present method provides a modern, rapid and robust tool for pharmacokinetic studies of cilnidipine.

MeSH terms

  • Adult
  • Calcium / antagonists & inhibitors*
  • Calcium / metabolism
  • Calcium Channel Blockers / blood*
  • Calcium Channel Blockers / pharmacokinetics
  • Chromatography, High Pressure Liquid / methods*
  • Dihydropyridines / blood*
  • Dihydropyridines / pharmacokinetics
  • Humans
  • Male
  • Tandem Mass Spectrometry / methods*
  • Temperature

Substances

  • Calcium Channel Blockers
  • Dihydropyridines
  • cilnidipine
  • Calcium