首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Development and validation of UPLC-MS/MS method for simultaneous determination of gestodene and ethinyl estradiol in rat plasma.
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Development and validation of UPLC-MS/MS method for simultaneous determination of gestodene and ethinyl estradiol in rat plasma.

机译:UPLC-MS / MS法同时测定大鼠等离子体中粘滞与乙炔雌二醇的UPLC-MS / MS方法的开发与验证。

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摘要

A selective and sensitive ultra-performance liquid chromatography method with tandem mass spectrometric detection for simultaneous determination of gestodene (GES) and ethinyl estradiol (EE) in rat plasma was developed and validated. GES, EE and the internal standard, norgestrel, were extracted with ethyl acetate, derivatized (EE only) with dansyl chloride and then back-extracted into diethyl ether-hexane (2:1, v/v). The separation was performed on an ACQUITY UPLC BEH C(18) column with gradient elution using mobile phase consisting of acetonitrile and water (both containing 0.1% formic acid). The detection was carried out by means of electrospray ionization (ESI) mass spectrometry in positive ion mode with multiple-reaction monitoring. Calibration curves of GES and EE were linear (r(2) >or= 0.99) over the concentration ranges 1.59-159 and 0.196-78.4 ng/mL, respectively. The intra- and inter-day precisions were not more than 6.9 and 12.9% for GES and 10.6 and 9.0% for EE, and the accuracies were -2.5-8.0% for GES, and -7.2-0.19% for EE, respectively. The method herein described was superior to previous methods and was applicable to the pharmacokinetic study of GES and EE in rats.
机译:开发并验证了具有串联质谱检测的选择性和敏感的超高性能液相色谱法,用于同时测定大鼠等离子体中的粘滞(GES)和乙炔雌二醇(EE)。用乙酸乙酯,衍生化(EE仅)用癸酰氯萃取Ges,EE和内标Norgestrel,然后用氯化乙烷衍生化(EE),然后反萃取到乙醚 - 己烷(2:1,v / v)中。使用由乙腈和水(含有0.1%甲酸的水)组成的流动相,在渐变洗脱中进行分离,具有梯度洗脱(含有0.1%甲酸)。通过电喷雾电离(ESI)质谱法在具有多反应监测的正离子模式下进行检测。 GES和EE的校准曲线分别在浓度为1.59-159和0.196-78.4ng / ml上线性(R(2)>或= 0.99)。对于GES的GES和日间诊断的内部和日间诊断不大于6.9%,EE的10.6%和9.0%,对于GES的准确度分别为-2.5-8.0%,EE分别为-7.2-0.19%。本文所述的方法优于先前的方法,可应用于大鼠GES和EE的药代动力学研究。

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