Quantitative determination of paclitaxel and its metabolites, 6α-hydroxypaclitaxel and p-3′-hydroxypaclitaxel, in human plasma using column-switching liquid chromatography/tandem mass spectrometry

被引:13
作者
Yamaguchi, Hiroaki [1 ]
Fujikawa, Asuka [1 ]
Ito, Hajime [1 ]
Tanaka, Nobuaki [1 ]
Furugen, Ayako [1 ]
Miyamori, Kazuaki [1 ]
Takahashi, Natsuko [2 ]
Ogura, Jiro [1 ]
Kobayashi, Masaki [1 ]
Yamada, Takehiro [3 ]
Mano, Nariyasu [4 ]
Iseki, Ken [1 ,3 ]
机构
[1] Hokkaido Univ, Fac Pharmaceut Sci, Sapporo, Hokkaido 0600812, Japan
[2] Hokkaido Univ, Grad Sch Med, Sapporo, Hokkaido 0608638, Japan
[3] Hokkaido Univ Hosp, Dept Pharm, Sapporo, Hokkaido 0608648, Japan
[4] Tohoku Univ Hosp, Dept Pharmaceut Sci, Sendai, Miyagi 9808574, Japan
关键词
paclitaxel; metabolite; human plasma; column-switching; QUANTIFICATION; ASSAY;
D O I
10.1002/bmc.2826
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A column-switching liquid chromatography/electrospray ionization tandem mass spectrometry to determine paclitaxel and its metabolites, 6-hydroxypaclitaxel and p-3-hydroxypaclitaxel, in human plasma was developed. The analytical system had a Shim-Pack MAYI-ODS (10x4.6mm i.d.) trapping column with deproteinization ability that concentrates analytes and removes water-soluble components. This method covered a linearity range of 55000ng/mL of concentrations in plasma for paclitaxel, a range of 0.87870ng/mL for 6-hydroxypaclitaxel and a range of 0.87435ng/mL for p-3-hydroxypaclitaxel. The intra-day precision and inter-day precision of analysis were less than 11.1%, and the accuracy was within +/- 14.4% at concentrations of 5, 50, 500 and 5000ng/mL for paclitaxel, 0.87, 8.7, 87 and 870ng/mL for 6-hydroxypaclitaxel, and 0.87, 8.7, 87 and 435ng/mL for p-3-hydroxypaclitaxel. The total run time was 30min. Our method was successfully applied to clinical pharmacokinetic investigation. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:539 / 544
页数:6
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