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

被引:89
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
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2009年 / 877卷 / 18-19期
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
相关论文
共 22 条
[1]   Evolving concepts in the management of chronic myeloid leukemia: recommendations from an expert panel on behalf of the European LeukemiaNet [J].
Baccarani, Michele ;
Saglio, Giuseppe ;
Goldman, John ;
Hochhaus, Andreas ;
Simonsson, Bengt ;
Appelbaum, Frederick ;
Apperley, Jane ;
Cervantes, Francisco ;
Cortes, Jorge ;
Deininger, Michael ;
Gratwohl, Alois ;
Guilhot, Frangois ;
Horowitz, Mary ;
Hughes, Timothy ;
Kantarjian, Hagop ;
Larson, Richard ;
Niederwieser, Dielger ;
Silver, Richard ;
Hehlmann, Rudiger .
BLOOD, 2006, 108 (06) :1809-1820
[2]   High-throughput quantification of the anti-leukemia drug ST1571 (Gleevec™) and its main metabolite (CGP 74588) in human plasma using liquid chromatography-tandem mass spectrometry [J].
Bakhtiar, R ;
Lohne, J ;
Ramos, L ;
Khemani, L ;
Hayes, M ;
Tse, F .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2002, 768 (02) :325-340
[3]   Quantification of the anti-leukemia drug ST1571 (Gleevec™) and its metabolite (CGP 74588) in monkey plasma using a semi-automated solid phase extraction procedure and liquid chromatography-tandem mass spectrometry [J].
Bakhtiar, R ;
Khemani, L ;
Hayes, M ;
Bedman, T ;
Tse, F .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2002, 28 (06) :1183-1194
[4]   Dynamics of BCR-ABL kinase domain mutations in chronic myeloid leukemia after sequential treatment with multiple tyrosine kinase inhibitors [J].
Cortes, Jorge ;
Jabbour, Elias ;
Kantarjian, Hagop ;
Yin, C. Cameron ;
Shan, Jianqin ;
O'Brien, Susan ;
Garcia-Manero, Guillermo ;
Giles, Francis ;
Breeden, Megan ;
Reeves, Nubia ;
Wierda, William G. ;
Jones, Dan .
BLOOD, 2007, 110 (12) :4005-4011
[5]   Imatinib as a paradigm of targeted therapies [J].
Druker, BJ .
ADVANCES IN CANCER RESEARCH, VOL 91, 2004, 91 :1-+
[6]   Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. [J].
Druker, BJ ;
Talpaz, M ;
Resta, DJ ;
Peng, B ;
Buchdunger, E ;
Ford, JM ;
Lydon, NB ;
Kantarjian, H ;
Capdeville, R ;
Ohno-Jones, S ;
Sawyers, CL .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (14) :1031-1037
[7]   Src in cancer: deregulation and consequences for cell behaviour [J].
Frame, MC .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2002, 1602 (02) :114-130
[8]   Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification [J].
Gorre, ME ;
Mohammed, M ;
Ellwood, K ;
Hsu, N ;
Paquette, R ;
Rao, PN ;
Sawyers, CL .
SCIENCE, 2001, 293 (5531) :876-880
[9]   Preclinical pharmacokinetics and in vitro metabolism of dasatinib (BMS-354825): a potent oral multi-targeted kinase inhibitor against SRC and BCR-ABL [J].
Kamath, Amrita V. ;
Wang, Jian ;
Lee, Francis Y. ;
Marathe, Punit H. .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2008, 61 (03) :365-376
[10]   Nilotinib in imatinib-resistant CML and Philadelphia chromosome-positive ALL [J].
Kantarjian, Hagop ;
Giles, Francis ;
Wunderle, Lydia ;
Bhalla, Kapil ;
O'Brien, Susan ;
Wassmann, Barbara ;
Tanaka, Chiaki ;
Manley, Paul ;
Rae, Patricia ;
Mietlowski, William ;
Bochinski, Kathy ;
Hochhaus, Andreas ;
Griffin, James D. ;
Hoelzer, Dieter ;
Albitar, Maher ;
Dugan, Margaret ;
Cortes, Jorge ;
Alland, Leila ;
Ottmann, Oliver G. .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (24) :2542-2551