Simultaneous determination of gemcitabine and gemcitabine-squalene by liquid chromatography- Tandem mass spectrometry in human plasma

被引:28
作者
Khoury, Hania
Deroussent, Alain
Reddy, L. Harivardhan
Couvreur, Patrick
Vassal, Gilles
Paci, Angelo [1 ]
机构
[1] Inst Gustave Roussy, UPRES EA 3535 Pharmacol & New Canc Treatment, IFR554, F-94800 Villejuif, France
[2] Univ Paris 11, F-94800 Villejuif, France
[3] Univ Paris 11, CNRS, Fac Pharm IFR 141, UMR 8612, F-92296 Chatenay Malabry, France
[4] Inst Gustave Roussy, IFR54, F-94800 Villejuif, France
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2007年 / 858卷 / 1-2期
关键词
gemcitabine; gemcitabine-squalene; mass spectrometry; cancer; Nucleosides analogues;
D O I
10.1016/j.jchromb.2007.08.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Gemcitabine-squalene is a new prodrug that self-organizes in water forming nanoassemblies. It exhibits better anti-cancer properties in vitro and in vivo than gemcitabine. A liquid chromatography/tandem mass spectrometry assay of gemcitabine-squalene and gemcitabine was developed in human plasma in order to quantitate gemcitabine and its squalene conjugate. After protein precipitation with acetonitrile/methanol (90/10, v/v), the compounds were analyzed by reversed-phase high performance liquid chromatography and detected by tandem mass spectrometry using multiple reaction monitoring. The method was linear over the concentration range of 10-10,000 ng/ml of human plasma for both compounds with an accuracy lower than 10.4% and a precision below 14.8%. The method showed a lower limit of quantitation of 10 ng/ml of human plasma for dFdC and dFdC-SQ. A preliminary in vivo study in mice was shown as application of the method as no significant difference between human and mice plasma for the analysis of dFdC and dFdC-SQ was demonstrated. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:71 / 78
页数:8
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