Development and validation of an ultra-performance liquid chromatography-tandem mass spectrometry method for the quantification of the antimalarial drug pyronaridine in human whole blood

 Development and validation of an ultra-performance liquid chromatography-tandem mass spectrometry method for the quantification of the antimalarial drug pyronaridine in human whole blood

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Practical Solutions and Value

Practical Solutions

  • Developed a fast and accurate method to quantify pyronaridine in whole blood
  • Reduced sample volume required to 50 µL
  • Eliminated matrix effect and ion enhancement or suppression
  • Improved sensitivity and reduced carry-over in the chromatographic system

Value

  • Supported future PK studies of pyronaridine, especially in special populations like children and pregnant women
  • Enabled assessment of the terminal elimination half-life of pyronaridine up to 42 days post-treatment initiation
  • Enhanced sensitivity for accurate quantification of pyronaridine in whole blood
  • Demonstrated stability of pyronaridine for up to 315 days when stored at -70°C

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