首页> 外文期刊>Journal of Chromatography, Biomedical Applications >Simultaneous determination of citalopram, fluoxetine, paroxetine and their metabolites in plasma by temperature-programmed packed capillary liquid chromatography with on-column focusing of large injection volumes
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Simultaneous determination of citalopram, fluoxetine, paroxetine and their metabolites in plasma by temperature-programmed packed capillary liquid chromatography with on-column focusing of large injection volumes

机译:程序升温填充毛细管液相色谱-大体积进样聚焦同时测定血浆中西酞普兰,氟西汀,帕罗西汀及其代谢物

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摘要

A miniaturized temperature-programmed packed capillary liquid chromatographic method with on-column large volume injection and UV detection for the simultaneous determination of the three selective serotonin reuptake inhibitors citalopram, fluoxetine, paroxetine and their metabolites in plasma is presented. An established reversed-phase C_8 solid-phase extraction method was employed, and the separation was carried out on a 3.5-μm Kromasil C_(18) 0.32 * 300 mm column with temperature-programming from 35 (e min) to 100 ℃ (10 min) at 1.3 ℃/min. The mobile phase consisted of acetonitrile-45 mM ammonium formate (pH 4.00) (25:75, v/v). The non-eluting sample focusing solvent composition acetonitrile-45 mM ammonium formate (pH 4.00) (3:97, v/v). allowed injection of 10 μl or more of the plasma extracts. The method was validated for the concentration range 0.05-5.0 μM, and the calibration curves were linear with coefficients of correlation >0.993. The limits of quantification for the antidepressants and their metabolites ranged from 0.05 to 0.26 μM. The within and between assay precision of relative peak height were in the range 2-22 and 2-15% relative standard deviation, respectively. The within and between assay recoveries were in the 61-99 and 54-92% range for the antidepressants, respectively, and between 52-102 and 51-102% for the metabolites.
机译:提出了一种柱上大体积进样和紫外检测的小型温度程序化填充毛细管液相色谱方法,用于同时测定血浆中三种选择性5-羟色胺再摄取抑制剂西酞普兰,氟西汀,帕罗西汀及其代谢物。使用已建立的反相C_8固相萃取方法,并在3.5μmKromasil C_(18)0.32 * 300 mm色谱柱上进行分离,并将程序升温设定为35(e min)至100℃(10分钟)在1.3℃/分钟。流动相由乙腈-45 mM甲酸铵(pH 4.00)(25:75,v / v)组成。非洗脱样品聚焦溶剂组合物乙腈-45 mM甲酸铵(pH 4.00)(3:97,v / v)。允许注射10μl或更多的血浆提取物。该方法的浓度范围为0.05-5.0μM,并且校正曲线为线性,相关系数> 0.993。抗抑郁药及其代谢产物的定量限为0.05至0.26μM。相对峰高的测定精度之间和之间的相对标准偏差分别为2-22和2-15%。对于抗抑郁药,试验内和试验间的回收率分别在61-99%和54-92%范围内,对于代谢物,在52-102%和51-102%之间。

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