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DOI: 10.18413/2313-8955-2015-1-3-104-111

DEVELOPMENT AND VALIDATION OF METHODS OF QUANTITATIVE DETERMINATION OF IMATINIB IN THE BLOOD PLASMA BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY WITH MASS SPECTROMETRIC DETECTION

The authors have developed a method of quantitative determination of an antitumor agent − a protein kinase inhibitor in the blood plasma by high performance liquid chromatography with tandem mass spectrometric detection. The analytical method range was from 0.03 to 3.83 g / ml in plasma. The method was used for the bioequivalence study of the reconstituted medicine containing imatinib as an active pharmaceutical ingredient compared with the reference.

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