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HERO ID
8175713
Reference Type
Journal Article
Title
é«ææ¶²ç¸è²è°±æ³åæ¶æµå®ä¼é©¬æ¿å°¼å主è¦ä»£è°¢ç©å»ç²åºä¼é©¬æ¿å°¼çè¡è¯æµåº¦
Author(s)
Luo, XX; Huang, L; Li, TF; Xue, XC; Wang, YH; Chen, Y; Yang, CQ; Feng, WY
Year
2018
Publisher
Chinese Journal of New Drugs Co. Ltd.
Volume
27
Issue
10
Page Numbers
1159-1164
Language
Chinese
Abstract
Objective: To establish a method for determining the concentrations of imatinib and its metabolites N-desmethyl imatinib in plasma by HPLC. Methods:Blood samples were pretreated by 1 molâ¢L-1 NaOH using ethyl acetate n-hexane (75:25) with dasatinib as an internal standard, then concentrated in vacuum, and the reconstituted solution was detected by HPLC. The analytical column was ZORBAX SB-C18 (250 mmÃ4.6 mm, 5 μm), mobile phase was acetonitrile-potassium dihydrogen phosphate buffer (0.025 molâ¢L-1 KH2PO3, pH value was adjusted to about 3.0 by H2PO3) (27:73, V/V) at a flow rate of 1.0 mLâ¢min-1. The detection wavelength was set at 267 nm, the temperature was kept at 35 â, and the injection volume was 20 μL. Results: The calibration curves had good linearity in the rang of 0.10~5.00 μgâ¢mL-1 for imatinib and 0.010~0.05 μgâ¢mL-1 for N-desmethyl imatinib (r=0.998 and 0.997, respectively). The limits of quantification of imatinib and N-desmethyl imatinib were 0.1 μgâ¢mL-1 and 0.01 μgâ¢mL-1, respectively. The extraction recoveries of low, medium and high concentration control samples were 86.02%, 87.31%, 88.21% for imatinib and 81.64%, 84.78%, 88.74% for N-desmethyl imatinib, respectively. The intra-day and inter-day RSD values were less than 15%. Conclusion: The method is simple, rapid and sensitive for drug monitoring and pharmacokinetic study on imatinib and N-desmethyl imatinib. © 2018, Chinese Journal of New Drugs Co. Ltd. All right reserved.
Keywords
HPLC; Imatinib; N-desmethyl imatinib; Therapeutic durg monitoring
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