Determination of midazolam and its hydroxy metabolites in human plasma and oral fluid by liquid chromatography/electrospray ionization ion trap tandem mass spectrometry

Midazolam (MDZ), a short‐acting benzodiazepine, is a widely accepted probe drug for CYP3A phenotyping. Published methods for its analysis have used either therapeutic doses of MDZ, or, if employing lower doses, were mostly unable to quantify the two hydroxy metabolites. In the present study, a sensi...

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Bibliographic Details
Published in:Rapid communications in mass spectrometry 2007-01, Vol.21 (9), p.1531-1540
Main Authors: Link, Bettina, Haschke, Manuel, Wenk, Markus, Krähenbühl, Stephan
Format: Article
Language:English
Subjects:
Chromatography, High Pressure Liquid - methods
Humans
Hypnotics and Sedatives - blood
Hypnotics and Sedatives - pharmacokinetics
Midazolam - analogs & derivatives
Midazolam - blood
Midazolam - pharmacokinetics
Reproducibility of Results
Saliva - chemistry
Spectrometry, Mass, Electrospray Ionization - methods
Tandem Mass Spectrometry - methods
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Summary:Midazolam (MDZ), a short‐acting benzodiazepine, is a widely accepted probe drug for CYP3A phenotyping. Published methods for its analysis have used either therapeutic doses of MDZ, or, if employing lower doses, were mostly unable to quantify the two hydroxy metabolites. In the present study, a sensitive and specific liquid chromatography/electrospray ionization tandem mass spectrometry method was developed and validated for the quantitative determination of MDZ and two of its metabolites (1′‐hydroxymidazolam (1′‐OHMDZ) and 4‐hydroxymidazolam (4‐OHMDZ)) in human plasma and oral fluid. After liquid‐liquid extraction with hexane/dichloromethane (73:27, v/v), the analytes were separated on a Luna C18(2) (100 × 2.1 mm) analytical column using gradient elution. Detection was achieved using tandem mass spectrometry on an ion trap mass spectrometer. Midazolam‐d6 was used as internal standard for quantification. The calibration curves were linear (R2 >0.998) between 0.05 and 20 ng/mL for MDZ and both metabolites in both matrices. Using 1 mL samples, the limit of detection was 0.025 ng/mL and the limit of quantification was 0.05 ng/mL for MDZ and the hydroxy metabolites in both matrices. Intra‐ and inter‐day accuracies, determined at three different concentrations, were between 92.1 and 102.3% and the corresponding coefficients of variation were
ISSN:0951-4198
1097-0231
DOI:10.1002/rcm.2987