Title of article :
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
Author/Authors :
Pursche، نويسنده , , S. and Ottmann، نويسنده , , O.G and Ehninger، نويسنده , , G. K. Schleyer ، نويسنده , , E.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
9
From page :
208
To page :
216
Abstract :
An isocratic and sensitive HPLC assay was developed allowing the determination of the new anticancer drug nilotinib (AMN107) in human plasma, urine, culture medium and cell samples. After protein precipitation with perchloric acid, AMN107 underwent an online enrichment using a Zirchrom-PBD precolumn, was separated on a Macherey-Nagel C18-HD column and finally quantified by UV-detection at 258 nm. The total run time is 25 min. The assay demonstrates linearity within a concentration range of 0.005–5.0 μg/ml in plasma (r2 = 0.9998) and 0.1–10.0 μg/ml in urine (r2 = 0.9913). The intra-day precision expressed as coefficients of variation ranged depending on the spiked concentration between 1.27–9.23% in plasma and 1.77–3.29% in urine, respectively. The coefficients of variation of inter-day precision was lower than 10%. Limit of detection was 0.002 μg/ml in plasma and 0.01 μg/ml in urine. The described method is stable, simple, economic and is routinely used for in vivo and in vitro pharmacokinetic studies of AMN107.
Keywords :
Nilotinib , Tyrosine kinase , chronic myelogenous leukaemia , BCR-ABL mutant , AMN107 , Intracellular concentration , Imatinb , HPLC
Journal title :
Journal of Chromatography B
Serial Year :
2007
Journal title :
Journal of Chromatography B
Record number :
1464479
Link To Document :
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