Development and validation of a liquid chromatography/tandem mass spectrometry assay for the quantification of methyl protodioscin in rat plasma: application to a pharmacokinetic study

被引:11
作者
Cao, Xiuzhen [3 ]
Yao, Zhihong [1 ]
Chen, Haifeng [2 ]
Dai, Yi
Sun, Pinghua
Yei, Wencai
Yao, Xinsheng [3 ]
机构
[1] Jinan Univ, Pharmaceut Coll, Guangzhou 510632, Peoples R China
[2] Tsinghua Univ, Res Inst, Key Lab Res & Dev Tradit Chinese Med & Nat Produc, Shenzhen 518057, Peoples R China
[3] Shenyang Pharmaceut Univ, Dept Nat Prod Chem, Shenyang 110016, Peoples R China
关键词
methyl protodioscin; rat plasma; HPLC-MS/MS; pharmacokinetics;
D O I
10.1002/bmc.948
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
A high performance liquid chromatography/tandem mass spectrometry assay was first developed and validated for the quantification of methyl protodioscin (MPD), a natural furostanol saponin with distinct antitumor activity, in rat plasma with 17 alpha-ethinylestradiol as internal standard (IS). Methanol-mediated protein precipitation was employed for plasma sample pretreatment. The separation was achieved on a C-18 column (150 x 4.6 mm, id., 5 mu m) by isocratic elution with methanol-water (72:28, v/v) as mobile phase at a flow rate of 1.0 mL/min. Ion acquisition was performed in selective reaction monitoring positive mode by monitoring the transition of m/z 1085.7 -> 1053.7 for MPD, and in selective ion monitoring negative mode by monitoring the deprotonated ion m/z 295.5 for IS. The assay was linear over the concentration range of 2.024-270.0 mu g/mL with 2.024 mu g/mL as the lower limit of quantification. It was specific, accurate, precise and reproducible with intra- and inter-run RSD <8.3% and RE between -11.5 and 12.8%. The assay was successfully applied to a preclinical pharmacokinetic study after an intravenous dose of 40 mg/kg MPD to rats. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:408 / 413
页数:6
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