首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Determination of azelnidipine in human plasma by liquid chromatography-electrospray ionization-mass spectrometry.
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Determination of azelnidipine in human plasma by liquid chromatography-electrospray ionization-mass spectrometry.

机译:液相色谱-电喷雾电离质谱法测定人血浆中的氮卓尼平。

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摘要

A liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS) method for the determination of azelnidipine in human plasma was established. Nicardipine was used as the internal standard (IS). After adjustment to a basic pH with sodium hydroxide solution (0.1 M), plasma samples were extracted with cyclohexane-diethyl ether (1:1, v/v) and separated on a C(18) column with a mobile phase of 20 mM ammonium acetate solution-methanol-formic acid (25:75:0.5, v/v). The electrospray ionization was employed in a single quadrupole mass spectrometer for the determination. The method was linear over the concentration range of 0.05-40 ng/ml. The lower limit of quantification (LLOQ) was 0.05 ng/ml. The intra- and inter-run standard deviations were less than 9.5% and 11.0%, respectively. The method was successfully applied to study the pharmacokinetics of azelnidipine in healthy Chinese volunteers.
机译:建立了液相色谱-电喷雾电离质谱法(LC-ESI-MS)测定人血浆中的氮卓尼平的方法。尼卡地平用作内标(IS)。用氢氧化钠溶液(0.1 M)调节至碱性pH后,用环己烷-二乙醚(1:1,v / v)提取血浆样品,并在C(18)色谱柱上分离,流动相为20 mM铵乙酸盐溶液-甲醇-甲酸(25:75:0.5,v / v)。电喷雾电离在单四极杆质谱仪中进行测定。该方法在0.05-40 ng / ml的浓度范围内是线性的。定量下限(LLOQ)为0.05 ng / ml。批内和批间标准偏差分别小于9.5%和11.0%。该方法已成功地用于研究阿兹尼地平在健康中国志愿者中的药代动力学。

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