A novel, rapid and sensitive UPLC-MS/MS method for the determination of macitentan in patients with pulmonary arterial hypertension


ALBAYRAK M., ATİLA A., Ucar E. Y., ARAZ Ö., KADIOĞLU Y.

BIOMEDICAL CHROMATOGRAPHY, cilt.33, sa.5, 2019 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 33 Sayı: 5
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1002/bmc.4502
  • Dergi Adı: BIOMEDICAL CHROMATOGRAPHY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Anahtar Kelimeler: macitentan, plasma, pulmonary arterial hypertension, UPLC-MS, MS, ENDOTHELIN-RECEPTOR ANTAGONIST, PHARMACOKINETICS, BOSENTAN
  • Atatürk Üniversitesi Adresli: Evet

Özet

Macitentan is an endothelin receptor antagonist commonly used in the treatment of pulmonary arterial hypertension (PAH). A novel, rapid, simple and sensitive UPLC-MS/MS method was developed and validated for pharmacokinetic study and the determination of macitentan in PAH patients. Macitentan and bosentan, which are used as internal standards, were detected using atmospheric pressure chemical ionization in positive ion and multiple reaction monitoring mode by monitoring the mass transitions m/z 589.1203.3 and 552.6311.5, respectively. Chromatographic separation was performed on a reverse-phase C18 column (5m, 4.6 x 150mm) with an isocratic mobile phase, which consisted of water containing 0.2% acetic acid-acetonitrile (90:10, v/v) at a flow rate of 1mL/min. Retention times were 1.97 and 1.72min for macitentan and IS, respectively. The calibration curve with high correlation coefficient (0.9996) was linear in the range 1-500ng/mL. The lower limit of quantitation and average recovery values were determined as 1ng/mL and 89.8%, respectively. This method is the first UPLC-MS/MS method developed and validated for the determination of macitentan from human plasma. The developed analytical method was fully validated for linearity, selectivity, specificity, accuracy, precision, sensitivity, stability, matrix effect and recovery according to US Food and Drug Administration guidelines. The developed method was applied successfully for pharmacokinetic study and the determination of macitentan in PAH patients.