Li Ze-Yun, Li Qing, Lü Jiang, Ling Jun-Hong, Yu Xi-Hua, Chen Xiao-Hui, Bi Kai-Shun
School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
J Pharm Anal. 2011 Feb;1(1):8-12. doi: 10.1016/S2095-1779(11)70002-8. Epub 2012 Jan 30.
A simple, rapid and sensitive liquid chromatography-mass spectrometry (LC-MS) method was developed for the determination of salidroside in rat plasma and study of its pharmacokinetics after oral administration of suspension of and Fructus into Wistar rats. Plasma sample of 200 μL was extracted with acetic ether-isopropanol (2:1) and the extraction was performed on a Kromasil C column (150 mm × 4. 6 mm, 5 μm) with the mobile phase of methanol-water (41:59, v/v) within a run time of 6.0 min. The analyte was monitored with positive electrospray ionization (ESI) by selected ion monitoring (SIM) mode. The target ions were m/z 323.05 for salidroside and m/z 411.05 for internal Standard (IS) geniposide. A good linear relationship was obtained over the range of 5.0-500.0 ng/mL and the lower limit of quantification was 5.0 ng/mL. The validated method was successfully applied to the pharmacokinetic study of salidroside in rat plasma after oral administration of suspension of and Fructus .