Rapid and sensitive analysis of vincristine in human plasma using on-line extraction combined with liquid chromatography/tandem mass spectrometry

被引:34
作者
Corona, Giuseppe [1 ,2 ]
Casetta, Bruno [3 ]
Sandron, Sara [1 ,2 ]
Vaccher, Emanuela [4 ]
Toffoli, Giuseppe [1 ,2 ]
机构
[1] Natl Canc Inst, Div Expt & Clin Pharmacol, Aviano, PN, Italy
[2] Ctr Mol Biomed, Aviano, PN, Italy
[3] Appl Biosyst Inc, I-20052 Monza, MI, Italy
[4] Natl Canc Inst, Med Oncol Div A, Aviano, PN, Italy
关键词
D O I
10.1002/rcm.3390
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
A simple and rapid method has been developed and validated for the quantitation of vincristine in human plasma by liquid chromatography/tandem mass spectrometry (LC/MS/MS) with atmospheric pressure chemical ionization using on-line solid-phase extraction. The method uses vinblastine as internal standard and the sample preparation is limited just to a plasma protein precipitation step. Further sample clean-up is carried out on-line through a perfusion column preceding an analytical phenyl LC column, the latter directly connected to the mass spectrometer. Quantitation is performed in multiple reaction monitoring mode using the transitions of m/z 825.3 -> 765.3 and 811.3 -> 751.3 for vincristine and vinblastine respectively. The assay was linear (r(2) >= 0.99) in a concentration range from 0.1 to 500 ng/mL. Carry-over, measured on the experimental set-up, was less than 0.04%. Recovery for vincristine and the internal standard was within 90-95%. The intra-day and inter-day assay precision ranged from 1.2% to 6.8% RSD while mean percentage deviation from nominal value ranged from 0.01% to 6.1%. The proposed assay was found suitable for pharmacokinetics investigations and clinical therapeutic drug monitoring especially in pediatric cancer patients. Copyright (C) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:519 / 525
页数:7
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