Determination of morroniside concentration in beagle plasma and its pharmacokinetics by high performance liquid chromatography-tandem mass spectrometry

A sensitive, simple and specific high performance liquid chromatography-electrospray ionization tandem mass spectrometry (LC-MS/MS) method was developed for the determination of morroniside in the plasma of beagles administered via intragastric (ig) doses of morroniside. The method employed paeoniflorin as the internal standard and extracted by simple protein precipitation. The separation was achieved using an Inertsil ODS-SP column (50 mm x 2. 1 mm, 5 mu m) with mobile phases of 1 mmol/L sodium formate aqueous solution and acetonitrile (gradient elution) at a flow rate of 0.4 mL/min. The detection was accomplished by a mass spectrometer using multiple reaction monitoring (MRM) in positive mode. Pharmacoldnetic parameters were fitted by software DAS 2. 0. The methodological study showed a good linear relationship of 2-5 000 mu g/L (r= 0.996 6) with a sensitivity of 2 mu g/L as the limit of quantification. The precision, accuracy, mean recoveries and the matrix effects were satisfied with the requirements of biological sample measurement. The method described above was successfully applied to the pharmacoldnetic study of morroniside in the beagle plasma samples. The area under the plasma concentration-time curves (AUC((0-infinity))) of morroniside after single ig administration doses of 5, 15 and 45 mg/kg were (1 631. 20 +/- 238. 50), (3 984. 05 +/- 750. 38) and (10 397. 64 +/- 3 156. 34) mu g/L . h. The relationship between dose and AUC showed a good linearity. The pharmacokinetic property of morroniside was proposed to be linear pharmacokinetics.