Application of an LC-MS/MS method to the pharmacokinetics of TM-2, a potential antitumour agent, in rats

被引:6
作者
Men, Lei [1 ]
Zhao, Yunli [1 ]
Lin, Hongli [1 ]
Yang, Mingjing [1 ]
Liu, Hui [1 ]
Shao, Yanjie [1 ]
Fan, Ronghua [1 ]
Tang, Xing [1 ]
Yu, Zhiguo [1 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Peoples R China
关键词
a novel taxane derivative; pharmacokinetics; LC-MS; MS; antitumour; TISSUE DISTRIBUTION; IN-VITRO; METABOLISM; DOCETAXEL; PACLITAXEL; TAXANES; PLASMA;
D O I
10.1002/dta.1711
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
TM-2 is a novel semi-synthetic taxane derivative, selected for preclinical development based on its greater anticancer activity and lower toxicity compared with docetaxel. In this study, a rapid and sensitive analytical method based on ultra performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) has been developed for the determination of TM-2 in rat plasma. The biological samples were extracted with methyl tert-butyl ether and separated on a C-18 column (50mmx2.1mm, 1.7 mu m) using a mobile phase consisting of acetonitrile and 2mM ammonium acetate. The standard curves were linear over the range 5-1000ng/mL in rat plasma. The precision (relative standard deviation, RSD, %) were within 14.5%, and the accuracy (relative error, RE, %) ranged from -1.56 to 2.36%. Recovery and matrix effect were satisfactory in rat plasma. The validated method was successfully applied to pharmacokinetic studies after intravenous administration of TM-2 to rats. The pharmacokinetics of TM-2 in rats were characterized by a large volume of distribution and a long half-life of elimination after single dose (4, 8, and 16mg/kg), and a good correlation was observed between AUC and dose. The preclinical data will be useful for the design of subsequent trials of TM-2. Copyright (c) 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:544 / 549
页数:6
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