Citation: XIONG Shan, LI Jinglai, ZHU Xiuqing, WANG Xiaoying, LÜ Guiyuan, ZHANG Zhenqing. Determination of morroniside concentration in beagle plasma and its pharmacokinetics by high performance liquid chromatography-tandem mass spectrometry[J]. Chinese Journal of Chromatography, ;2014, 32(3): 290-293. doi: 10.3724/SP.J.1123.2013.11027 shu

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

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1. Zhejiang Chinese Medical University, Hangzhou 310053, China;

Corresponding author: LÜ Guiyuan, ZHANG Zhenqing,
Received Date: 14 November 2013
Available Online: 1 January 2014
Fund Project: 科技部“重大新药创制”科技重大专项(2012ZX09301003-001-007). (2012ZX09301003-001-007)

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×2.1 mm, 5 μm) 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. Pharmacokinetic parameters were fitted by software DAS 2.0. The methodological study showed a good linear relationship of 2-5000 μg/L (r=0.9966) with a sensitivity of 2 μg/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 pharmacokinetic study of morroniside in the beagle plasma samples. The area under the plasma concentration-time curves (AUC_(0-∞)) of morroniside after single ig administration doses of 5, 15 and 45 mg/kg were (1631.20±238.50), (3984.05±750.38) and (10397.64±3156.34) μg/L·h. The relationship between dose and AUC showed a good linearity. The pharmacokinetic property of morroniside was proposed to be linear pharmacokinetics.
- liquid chromatography-tandem mass spectrometry (LC-MS/MS),
- morroniside,
- plasma,
- beagle,
- pharmacokinetics
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