Whole blood microsampling for the quantitation of estetrol without derivatization by liquid chromatography-tandem mass spectrometry

被引:31
作者
Nys, Gwenael [1 ]
Gallez, Anne [2 ]
Kok, Miranda G. M. [1 ]
Cobraiville, Gael [1 ]
Servais, Anne-Catherine [1 ]
Piel, Geraldine [3 ]
Pequeux, Christel [2 ]
Fillet, Marianne [1 ]
机构
[1] Univ Liege, Lab Anal Med, Ctr Interdisciplinary Res Med, Quartier Hop, Ave Hippocrate 15, B-4000 Liege, Belgium
[2] Univ Liege, Lab Tumor & Dev Biol, GIGA Canc, Quartier Hop, CHU B23,Ave Hippocrate 15, B-4000 Liege, Belgium
[3] Univ Liege, Lab Pharmaceut Technol & Biopharm, CIRM, Quartier Hop, Ave Hippocrate 15, B-4000 Liege, Belgium
关键词
Estetrol; UHPLC-MS/MS; Volumetric absorptive microsampling; Ammonium fluoride; Pharmacokinetic study; DRIED BLOOD; CLINICAL-APPLICATIONS; ION SUPPRESSION; HUMAN SERUM; LC-MS/MS; ESTROGENS; BIOANALYSIS; METABOLISM; ESTRADIOL; QUANTIFICATION;
D O I
10.1016/j.jpba.2017.02.060
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Quantitative bioanalysis and especially pharmacokinetic studies are challenging since only low volumes of biological material are available and low concentrations (ng/ml) are often expected. In this context, volumetric absorptive microsampling (VAMS) devices were developed to accurately collect 10 or 20 mu l of whole blood from tested subjects. In this study, we present the development and validation of ultra-high performance liquid chromatography coupled to tandem mass spectrometry method after VAMS sampling for the quantitation of estetrol (E4), a potentially new medicine for hormone replacement, contraception and osteoporosis therapies. Interestingly, a very simple sample preparation procedure was developed without any derivatization step. Even if lack of sensitivity is a common consideration when using negative ionization mode, we demonstrated in this work that an excellent sensitivity could be reached by carefully optimizing the nature and concentration of the mobile phase additive. After the optimization of every experimental parameter, the stability, selectivity, trueness, precision and accuracy of the final method were successfully demonstrated. In addition, the excellent performances of the method were confirmed by two independent proof-of-concept pharmacokinetic studies of E4 after VAMS collection in a murine model. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:258 / 265
页数:8
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