New HPLC-MS method for the simultaneous quantification of the antileukemia drugs imatinib, dasatinib, and nilotinib in human plasma

被引:88
|
作者
De Francia, Silvia [1 ]
D'Avolio, Antonio [2 ]
De Martino, Francesca [1 ]
Pirro, Elisa [1 ]
Baietto, Lorena [2 ]
Siccardi, Marco [2 ]
Simiele, Marco [2 ]
Racca, Silvia [1 ]
Saglio, Giuseppe [1 ]
Di Carlo, Francesco [1 ,2 ]
Di Perri, Giovanni
机构
[1] Univ Turin, Dept Biol & Clin Sci, S Luigi Gonzaga Hosp, I-10043 Orbassano, TO, Italy
[2] Univ Turin, Dept Infect Dis, Amedeo di Savoia Hosp, I-10149 Turin, Italy
关键词
Imatinib; Dasatinib; Nilotinib; HPLC-MS; Quantification; CHRONIC MYELOID-LEUKEMIA; KINASE INHIBITOR; METABOLITE CGP-74588; ST1571 GLEEVEC(TM); LIQUID; PHARMACOKINETICS; RESISTANCE; BMS-354825; MUTATIONS; CANCER;
D O I
10.1016/j.jchromb.2009.04.028
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new method using high performance liquid chromatography coupled with electrospray mass spectrometry is described for the quantification Of plasma concentration of tyrosine kinase inhibitors imatinib, dasatinib and nilotinib. A simple protein precipitation extraction procedure was applied on 250 mu l of plasma aliquots. Chromatographic separation of drugs and Internal Standard (quinoxaline) was achieved with a gradient (acetonitrile and water + formic acid 0.05%) on a C18 reverse phase analytical column with 20 min of analytical run. at flow rate of 1 ml/min. Mean intra-clay and inter-clay precision for all compounds were 4.3 and 11.4%; mean accuracy was 1.5%; extraction recovery ranged within 95 and 114%. Calibration curves ranged from 10,000 to 62.5 ng/ml. The limit of quantification was set at 78.1 ng/ml for imatinib and at 62.5 ng/ml for dasatinib and nilotinib. This novel developed methodology allows a specific, sensitive and reliable simultaneous determination of the three tyrosine kinase inhibitors imatinib, dasatinib and nilotinib in a single chromatographic run, useful for drugs estimation in plasma of patients affected by chronic myeloid leukemia. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1721 / 1726
页数:6
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