首页> 外文期刊>Journal of Chromatography, Biomedical Applications >High-performance liquid chromatographic determination of cefepime inhuman plasma and in urine anddialysis flid using a column-switching technique
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High-performance liquid chromatographic determination of cefepime inhuman plasma and in urine anddialysis flid using a column-switching technique

机译:色谱柱切换技术高效液相色谱法测定人血浆中头孢吡肟和尿液及透析液中的含量

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A high-performance liquid chromatographic method with UV absorbance was developed for the analysis of cefepime inhuman plasma and urine, and in dialysis fluid. Detection was performed at 280 nm. The assay procedure for cefepime inplasma involves the addition of an internal standard (cefpirome) followed by treatment of the samples with trichioraceticacid,acetonitrile and dichioromethane. To quantify cefepime in diluted urine (1:20) and in the dialysis fluid, samples spikedwith the internal standard (cefpirome) were analysed using a column-switching technique. The HPLC column, Nucleosil C_(18),was equilibrated with an eluent mixture composed of acetonitrile—anirnonium acetate (pH 4). Linear detector responses were observed for the calibration curve standards in the range 0.5 to 100 #mu#g/ml, which spans what is currently thought to be the clinically relevant range for cefepime concentrations in body fluids. The limit of quantification was 0.5 #mu#g /mlin the three matrices. Extraction recoveries proved to be more than 84%. Precision, expressed as %RSD, was in the range 1.5 to 9%.Accuracy ranged from 93 to 105%. This method was used to follow the time course of the concentration of cefepinie in plasma,urine and dialysate outlet samples after a 10-mm infusion period of 2 g of this drug in patients with acute renal failure undergoing hemodiafiltration.
机译:开发了一种具有紫外吸收的高效液相色谱方法,用于分析人血浆和尿液中以及透析液中的头孢吡肟。在280nm处进行检测。头孢吡肟血浆的测定方法包括添加内标(头孢哌啶),然后用三氯乙酸,乙腈和二氯甲烷处理样品。为了定量稀释尿液(1:20)和透析液中的头孢吡肟,使用柱切换技术分析了掺有内标(头孢哌啶)的样品。 HPLC色谱柱Nucleosil C_(18)用由乙腈-乙酸铵(pH 4)组成的洗脱液混合物平衡。校准曲线标准品的线性检测器响应在0.5至100#mu#g / ml的范围内,该范围跨越了目前认为体液中头孢吡肟浓度的临床相关范围。三种基质的定量限为0.5#mu#g / ml。提取回收率证明超过84%。以%RSD表示的精度在1.5至9%的范围内,精度在93至105%的范围内。该方法用于追踪急性肾功能衰竭血液透析滤过患者10毫米输注2克这种药物后血浆,尿液和透析液出口样品中头孢哌尼浓度的时程。

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