A HPLC-fluorescence method for the quantification of abiraterone in plasma from patients with metastatic castration-resistant prostate cancer

被引:18
|
作者
Belleville, Tiphaine [1 ]
Noe, Gaelle [1 ]
Huillard, Olivier [2 ]
Thomas-Schoemann, Audrey [1 ,3 ]
Vidal, Michel [1 ,3 ]
Goldwasser, Francois [2 ,4 ]
Alexandre, Jerome [2 ,4 ]
Blanchet, Benoit [1 ]
机构
[1] Hop Cochin, AP HP, F-75674 Paris, France
[2] Hop Cochin, AP HP, Serv Cancerol Med, F-75674 Paris, France
[3] Univ Paris 05, PRES Sorbonne Paris Cite, CNRS UMR8638, Fac Pharm, Paris, France
[4] Univ Paris 05, Sorbonne Paris Cite, Inst Cochin,CNRS UMR8104, CARPEM,INSERM U 1016, Paris, France
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2015年 / 989卷
关键词
Abiraterone; HPLC; Fluorescence detection; Prostate cancer; Therapeutic drug monitoring; PHASE-I; OPEN-LABEL; ACETATE; MEN; RAT;
D O I
10.1016/j.jchromb.2015.03.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Abiraterone acetate is an oral prodrug of abiraterone, a selective inhibitor of CYP17, used for patients with metastatic castration-resistant prostate cancer (mCRPC). To date, a single liquid chromatographic-tandem mass spectroscopy method has been reported to assay abiraterone concentration in plasma from mCRPC patients. The aim of this study was to develop a simple and sensitive high performance liquid chromatographic (HPLC) method with fluorescence detection for quantification of abiraterone in plasma from mCRPC patients. After protein precipitation with acetonitrile and a liquid-liquid extraction with diethyl ether, abiraterone, and hydroxy-itraconazole (internal standard) were separated on a C8 Xterre (R) MS column using a mobile phase of acetonitrile and glycine buffer 88.4mM (pH 9.0) (60:40, v/v). Samples were eluted isocratically at a flow rate of 0.9 ml/min throughout an 11-min run. Fluorescence wavelengths' excitation and emission were 255 and 373 nm, respectively. The calibration was linear in the range 1.75-50 ng/ml. Inter- and intraday imprecision were less than 3.5 and 7%, respectively. This method is simple, sensitive, and selective. This analytical method was successfully applied to determine the steady-state plasma exposure to abiraterone in mCRPC patients. This method can be used in routine clinical practice to monitor plasma abiraterone concentrations in mCRPC patients. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:86 / 90
页数:5
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