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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Felodipine quantification in human plasma by high-performance liquid chromatography coupled to tandem mass spectrometry
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Felodipine quantification in human plasma by high-performance liquid chromatography coupled to tandem mass spectrometry

机译:高效液相色谱-串联质谱法测定人血浆中非洛地平的含量

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摘要

A rapid, sensitive, robust and specific method was developed for the determination and quantitation of felodipine, in human blood plasma by liquid chromatography coupled with tandem mass spectrometry using nimodipine as internal standard. Felodipine was extracted from 0.5 mL human plasma by use of a liquid/liquid procedure using diethyl ether/hexane (80/20, v/v) as eluent. The method included a chromatographic run of 5 min using a C-18 analytical column (100 mm x 4.6 mm i.d.) and the calibration curve was linear over the range from 0.02 to 10 ng mL(-1) (r(2) > 0.994). The between-run precision, determined as relative standard deviation of replicate quality controls, was 5.7% (0.06 ng mL(-1)), 7.1% (0.6 ng mL(-1)) and 6.8% (7.5 ng mL(-1)). The between-run accuracy was +/- 0.0, 2.1 and 3.1% for the above-mentioned concentrations, respectively. (C) 2004 Elsevier B.V. All rights reserved.
机译:建立了一种快速,灵敏,鲁棒且特异的方法,通过液相色谱-串联质谱法(以尼莫地平为内标)测定和测定人血浆中的非洛地平。通过使用二乙醚/己烷(80/20,v / v)作为洗脱剂的液/液方法从0.5mL人血浆中提取非洛地平。该方法包括使用C-18分析柱(100 mm x 4.6 mm内径)进行5分钟的色谱分析,校正曲线在0.02至10 ng mL(-1)范围内呈线性(r(2)> 0.994 )。两次运行之间的精密度被确定为重复质量控制的相对标准偏差,分别为5.7%(0.06 ng mL(-1)),7.1%(0.6 ng mL(-1))和6.8%(7.5 ng mL(-1) ))。对于上述浓度,批间准确度分别为+/- 0.0、2.1和3.1%。 (C)2004 Elsevier B.V.保留所有权利。

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