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High-throughput and trace analysis of diazepam in plasma using DART-MS/MS and its pharmacokinetic application. | LitMetric

High-throughput and trace analysis of diazepam in plasma using DART-MS/MS and its pharmacokinetic application.

Anal Biochem

Research Center for Drug Metabolism, School of Life Sciences, Jilin University, Changchun, 130012, PR China; Beijing Institute of Drug Metabolism, Beijing, 102209, PR China. Electronic address:

Published: December 2021

AI Article Synopsis

  • A new high-throughput method using DART-MS/MS has been developed to quantitatively analyze diazepam in rat plasma with just 25 μL of sample and a quick 15-second acquisition time.
  • The method demonstrated strong linearity for diazepam detection between 10-2000 ng/mL, with low variability and high accuracy in results.
  • Successful application of this method in pharmacokinetic studies highlights its potential for sensitive and accurate bioanalysis of diazepam and possibly other drugs.

Article Abstract

A high-throughput quantitative analytical method based on Direct Analysis in Real Time tandem mass spectrometry (DART-MS/MS) has been developed and validated for the determination of diazepam in rat plasma, whereby analyzing of each sample needs merely 25 μL plasma, simple solid phase extraction sample preparation and 15 s acquisition time. The multiple reaction monitoring (MRM) transitions at m/z 285.2 → 193.1 and 316.0 → 270.0 were selected for the monitoring of diazepam and its internal standard clonazepam respectively. A good linearity within the range of 10-2000 ng/mL, an intra- and inter-day precisions within <7.78% as to an accuracy ranging from 1.04% to 7.92% have been achieved. The method has been successfully applied to the pharmacokinetic study of diazepam in rats' plasma after a single intragastric administration at a dose of 10 mg/kg. The results indicate that this method fulfills the requirements of the bioanalysis in sensitivity and accuracy. It shows considerable promise for application of DART-MS to the quantitative investigation of other drugs.

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Source
http://dx.doi.org/10.1016/j.ab.2021.114435DOI Listing

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