Determination of toosendanin in rat plasma by ultra-performance liquid chromatography-electrospray ionization-mass spectrometry and its application in a pharmacokinetic study

被引:12
|
作者
Wang, Xintang [1 ,2 ,3 ]
Wang, Changhong [2 ,3 ,4 ]
Wang, Zhengtao [1 ,2 ,3 ,4 ]
机构
[1] China Pharmaceut Univ, Dept Pharmacognosy, Nanjing 210038, Jiangsu, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Inst Chinese Mat Med, MOE Key Lab Standardizat Chinese Med, Shanghai 201210, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Inst Chinese Mat Med, SATCM Key Lab New Resources & Qual Evaluat Chines, Shanghai 201210, Peoples R China
[4] Shanghai R&D Ctr Standardizat Chinese Med, Shanghai 201210, Peoples R China
关键词
toosendanin; pharmacokinetics; UPLC-ESI; MS; rat plasma;
D O I
10.1002/bmc.2779
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Toosendanin (TSN) is a major triterpenoid existing in Melia toosendan, which has been used as a digestive tract parasiticide and insecticide but with serious hepatotoxicity. An ultra-performance liquid chromatographyelectrospray ionizationmass spectrometry method was developed for determination of TSN in rat plasma. Plasma samples were separated on Acquity UPLCTM BEH C18 column with acetonitrile and water as flow phase by gradient elution and determined by quadrupole mass spectrometer in negative selective ion monitoring mode. Usolic acid was used as internal standard. The calibration curves were linear over 0.023.0?mu g/mL for TSN with a lower limit of quantification (LLOQ) of 20?ng/mL in rat plasma. The extraction recoveries of TSN were within 74.380.7% with an accuracy of 94.5108.9%. The intra- and inter-day precision values of the assay at three quality control levels were 8.813.8% and <13.9% at LLOQ level, respectively. The method was successfully applied to a pharmacokinetic study of TSN in rats after a single intravenous and oral administration of 2 and 60?mg/kg. The shorter Tmax, higher Vd and Cl of TSN after oral administration indicated that TSN could be absorbed, distributed and eliminated quickly in rats in vivo. The absolute bioavailability of TSN after oral administration was 9.9%. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:222 / 227
页数:6
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