1. Academic Validation
  2. Simultaneous determination of aurantio-obtusin, chrysoobtusin, obtusin and 1-desmethylobtusin in rat plasma by UHPLC-MS/MS

Simultaneous determination of aurantio-obtusin, chrysoobtusin, obtusin and 1-desmethylobtusin in rat plasma by UHPLC-MS/MS

  • Biomed Chromatogr. 2014 Mar;28(3):369-74. doi: 10.1002/bmc.3030.
Wei-dong Zhang 1 Peng-yuan Wang Ying Wang Qing Wang Yi Gu Jun Cao Shao-qing Wang Xiao-juan Wang
Affiliations

Affiliation

  • 1 Department of Pharmacy, School of Stomatology, Fourth Military Medical University, 145 West Changle Road, Xi'an, 710032, People's Republic of China.
Abstract

A sensitive and reliable ultra-high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry (UHPLC-MS/MS) method was developed and validated for the simultaneous determination of four active components of Semen Cassiae extract (aurantio-obtusin, chrysoobtusin, obtusin and 1-desmethylobtusin) in rat plasma after oral administration. Chromatographic separation was achieved on an Agilent Poroshell 120 C18 column with gradient elution using a mobile phase that consisted of acetonitrile-ammonium acetate in water (30 mm) at a flow rate of 0.4 mL/min. Detection was performed by a triple-quadrupole tandem mass spectrometer in multiple reaction monitoring mode. The calibration curve was linear over a range of 3.24-1296 ng/mL for aurantio-obtusin, 0.77-618 ng/mL for chrysoobtusin, 34.55-1818 ng/mL for obtusin and 1.86-1485 ng/mL for 1-desmethylobtusin. Inter- and intra-day assay variation was <15%. All analytes were shown to be stable during all sample storage and analysis procedures.

Keywords

1-desmethylobtusin; UHPLC-MS/MS; aurantio-obtusin; chrysoobtusin; obtusin; semen cassiae.

Figures
Products