A quantitative method for the determination of bosutinib in human plasma using high-performance liquid chromatography and ultraviolet detection.

Abstract:

BACKGROUND:We propose a simple, sensitive, and fast high-performance liquid chromatography ultraviolet detection (HPLC-UV) method for the quantitative determination of bosutinib in human plasma. METHODS:Plasma samples were processed using an Oasis hydrophilic-lipophilic balance extraction cartridge (1 mL, 30 mg). Bosutinib and the internal standard imatinib were separated using a mobile phase of 0.5% Na2 PO4 H2 O (pH 3.5)-acetonitrile-methanol (55:25:20, v/v/v) on a CAPCELL PAK C18 MG II reversed-phase column 250 nm×4.6 nm i.d., at a flow rate of 1.0 mL/min, with ultraviolet detection at 250 nm. RESULTS:The calibration curve exhibited linearity over the bosutinib concentration range of 25-1500 ng/mL at 250 nm, with coefficient of variation for intraday precision of 2.42%, 6.04%, and 1.11% for 100, 250, and 1500 ng/mL, respectively, of bosutinib. The lower limit of detection was 20 ng/mL. The extraction recovery rates for bosutinib ranged from 84.36% to 85.82%. The intra- and interday precision was below 8.7%, and the accuracy ranged from -5.95% to 5.85% over the linear range. No notable matrix effects or astaticism were observed. CONCLUSION:The proposed HPLC-UV method was successfully applied as an assay to detect bosutinib in human plasma.

journal_name

J Clin Lab Anal

authors

Sumimoto T,Nakahara R,Sato Y,Itoh H

doi

10.1002/jcla.22201

subject

Has Abstract

pub_date

2018-01-01 00:00:00

issue

1

eissn

0887-8013

issn

1098-2825

journal_volume

32

pub_type

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