| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1212208 | Journal of Chromatography B | 2015 | 4 Pages |
•A method for the analysis of ruscogenin was developed.•The method produced a linear range of 2–1000 ng/mL ruscogenin in rat plasma.•The method was successful at detecting ruscogenin from treated rats.
A sensitive and rapid ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method was developed to determine ruscogenin in rat plasma using midazolam as the internal standard (IS). Sample preparation was accomplished through a liquid–liquid extraction procedure with ethyl acetate to 0.2 mL plasma sample. The analyte and IS were separated on an Acquity UPLC BEH C18 column (2.1 mm × 50 mm, 1.7 μm) with the mobile phase of acetonitrile and 1% formic acid in water with gradient elution at a flow rate of 0.40 mL/min. Ruscogenin and IS were eluted at 1.74 and 1.11 min, respectively. The detection was performed on a triple quadrupole tandem mass spectrometer equipped with positive-ion electrospray ionization (ESI) by multiple reactions monitoring (MRM) of the transitions at m/z 431.2 → 287.0 for ruscogenin and m/z 326.2 → 291.1 for IS. The linearity of this method was found to be within the concentration range of 2–1000 ng/mL with a lower limit of quantification of 2 ng/mL. Only 2.0 min was needed for an analytical run. The matrix effect was 92.4–107.3% for ruscogenin. The intra- and inter-day precision (RSD%) were less than 11.2% and accuracy (RE%) was within ±9.8%. The recovery ranged from 75.4% to 86.3%. Ruscogenin was sufficiently stable under all relevant analytical conditions. The method was also successfully applied to the pharmacokinetic study of ruscogenin in rats.
