Determination of midazolam and 1-hydroxymidazolam from plasma by gas chromatography coupled to methane negative chemical ionization mass spectrometry after sublingual administration of midazolam

J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Jun 1;879(19):1668-76. doi: 10.1016/j.jchromb.2011.04.009. Epub 2011 Apr 14.

Abstract

A sensitive and selective gas chromatographic mass spectrometric method for the determination of midazolam and its biologically active metabolite, 1-hydroxymidazolam, in rabbit plasma has been developed and validated. Sample preparation includes mixed-mode solid-phase extraction and derivatization with silylating reagents. Midazolam-d4 was used as an internal standard for the determination of parent drug and its active metabolite. The instrumentation consisted of a capillary column gas chromatography and a single quadrupole mass spectrometer with a negative chemical ionization. The method was found to be valid in terms of selectivity, linearity, precision, accuracy, and recovery over the concentration range of 2-200 ng/ml and 1-100 ng/ml for midazolam and 1-hydroxymidazolam, respectively. For both analytes, the lower limit of quantification was 2 ng/ml. Midazolam was stable in stock solutions stored three months at -20°C and in human plasma stored for three months at -80°C. In addition, no degradation of midazolam was found after three freeze-thaw cycles, in short-term stability at room temperature for 24h, or in post-preparative stability in the autosampler. The validity of the method was further tested by performing a pharmacokinetic study of sublingual administration of midazolam in rabbits. The method will be used in studies related to a formulation development of novel midazolam formulations for use in paediatric anaesthesia.

MeSH terms

  • Administration, Sublingual
  • Animals
  • Area Under Curve
  • Drug Stability
  • Gas Chromatography-Mass Spectrometry / methods*
  • Humans
  • Least-Squares Analysis
  • Male
  • Methane / chemistry
  • Midazolam / administration & dosage
  • Midazolam / analogs & derivatives*
  • Midazolam / blood*
  • Midazolam / chemistry
  • Midazolam / pharmacokinetics
  • Rabbits
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Solid Phase Extraction

Substances

  • 1-hydroxymethylmidazolam
  • Methane
  • Midazolam