Determination of chrysotoxine in rat plasma by liquid chromatography-tandem mass spectrometry and its application to a rat pharmacokinetic study

被引:10
|
作者
Fan, Jingjing [1 ]
Guan, Li [2 ]
Kou, Zeqi [2 ]
Feng, Feng [2 ]
Zhang, Yanbo [3 ]
Liu, Wenyuan [1 ]
机构
[1] China Pharmaceut Univ, Dept Pharmaceut Anal, Nanjing 210009, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, Dept Nat Med Chem, Nanjing 210009, Jiangsu, Peoples R China
[3] Univ Hong Kong, Li Ka Shing Fac Med, Sch Chinese Med, Pokfulam, Hong Kong, Peoples R China
关键词
Chrysotoxine; HPLC-MS/MS; Pharmacokinetics; Method validation; Bioavailability; DIODE-ARRAY DETECTION; DENDROBIUM; BIS(BIBENZYL)S; DERIVATIVES; BIBENZYL; PHENOLS;
D O I
10.1016/j.jchromb.2014.07.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Chrysotoxine (CTX), a naturally occurring bibenzyl compound isolated from Dendrobium species, has been reported to have neuroprotective effects. To evaluate its pharmacokinetics in rats, a rapid, sensitive and specific high performance liquid chromatography-tandem mass spectrometric (HPLC-MS/MS) method has been developed and validated for the quantification of CTX in rat plasma. Samples were pre-treated using a simple liquid-liquid extraction with ethyl acetate and the chromatographic separation was performed on a C-18 column with acetonitrile-water (90:10, v/v) as the mobile phase. CTX and the internal standard (wogonin) were detected using a tandem mass spectrometer in positive multiple reaction monitoring mode. Method validation revealed excellent linearity over the range 0.5-1000 ng/mL together with satisfactory intra- and inter-day precision, accuracy and recovery. Stability testing showed that CTX spiked into rat plasma was stable for 8 h at room temperature, for up to two weeks at -20 degrees C, and during three freeze-thaw cycles. Extracted samples were also observed to be stable over 24 h in an auto-sampler. The method was successfully used to investigate the pharmacokinetic profile of CTX after oral (100 mg/kg) and intravenous (25 mg/kg) administration in rats. CTX showed rapid excretion and low bioavailability in rats. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:57 / 62
页数:6
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