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
[11]   Discovery of N-(2-chloro-6-methylphenyl)-2-(6-(4-(2-hydroxyethyl)-piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays [J].
Lombardo, LJ ;
Lee, FY ;
Chen, P ;
Norris, D ;
Barrish, JC ;
Behnia, K ;
Castaneda, S ;
Cornelius, LAM ;
Das, J ;
Doweyko, AM ;
Fairchild, C ;
Hunt, JT ;
Inigo, I ;
Johnston, K ;
Kamath, A ;
Kan, D ;
Klei, H ;
Marathe, P ;
Pang, SH ;
Peterson, R ;
Pitt, S ;
Schieven, GL ;
Schmidt, RJ ;
Tokarski, J ;
Wen, ML ;
Wityak, J ;
Borzilleri, RM .
JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (27) :6658-6661
[12]   Determination of imatinib mesylate and its main metabolite (CGP74588) in human plasma and murine specimens by ion-pairing reversed-phase high-performance liquid chromatography [J].
Oostendorp, Roos L. ;
Beijnen, Jos H. ;
Schellens, Jan H. M. ;
van Tellingen, Olaf .
BIOMEDICAL CHROMATOGRAPHY, 2007, 21 (07) :747-754
[13]   Pharmacokinetics and pharmacodynamics of imatinib in a phase I trial with chronic myeloid leukemia patients [J].
Peng, B ;
Hayes, M ;
Resta, D ;
Racine-Poon, A ;
Druker, BJ ;
Talpaz, M ;
Sawyers, CL ;
Rosamilia, M ;
Ford, J ;
Lloyd, P ;
Capdeville, R .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (05) :935-942
[14]   Trough imatinib plasma levels are associated with both cytogenetic and molecular responses to standard-dose imatinib in chronic myeloid leukemia [J].
Picard, Stephane ;
Titier, Karine ;
Etienne, Gabriel ;
Teilhet, Ernmanuelle ;
Ducint, Dominique ;
Bernard, Marie-Agnes ;
Lassalle, Regis ;
Marit, Gerald ;
Reiffers, Josy ;
Begaud, Bernard ;
Moore, Nicholas ;
Molimard, Mathieu ;
Mahon, Francois-Xavier .
BLOOD, 2007, 109 (08) :3496-3499
[15]   High-performance liquid chromatography method with ultraviolet detection for the quantification of the BCR-ABL inhibitor nilotinib (AMN107) in plasma, urine, culture medium and cell preparations [J].
Pursche, S. ;
Ottmann, O. G. ;
Ehninger, G. ;
Schleyer, E. .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2007, 852 (1-2) :208-216
[16]   Chronic myeloid leukemia [J].
Sawyers, CL .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (17) :1330-1340
[17]   Sequential ABL kinase inhibitor therapy selects for compound drug-resistant BCR-ABL mutations with altered oncogenic potency [J].
Shah, Neil P. ;
Skaggs, Brian J. ;
Branford, Susan ;
Hughes, Timothy P. ;
Nicoll, John M. ;
Paquette, Ronald L. ;
Sawyers, Charles L. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (09) :2562-2569
[18]   Mechanisms of resistance to STI571 in Philadelphia chromosome-associated leukemias [J].
Shah, NP ;
Sawyers, CL .
ONCOGENE, 2003, 22 (47) :7389-7395
[19]   Matrix effects: The Achilles heel of quantitative high-performance liquid chromatography-electrospray-tandem mass spectrometry [J].
Taylor, PJ .
CLINICAL BIOCHEMISTRY, 2005, 38 (04) :328-334
[20]   Quantification of imatinib in human plasma by high-performance liquid chromatography-tandem mass spectrometry [J].
Titier, Karine ;
Picard, Stephane ;
Ducint, Dominique ;
Teilhet, Emmanuelle ;
Moore, Nicholas ;
Berthaud, Patrice ;
Mahon, Francois-Xavier ;
Molimard, Mathieu .
THERAPEUTIC DRUG MONITORING, 2005, 27 (05) :634-640