首页> 外文期刊>Journal of separation science. >Simultaneous determination of caffeine, paracetamol, and ibuprofen in pharmaceutical formulations by high-performance liquid chromatography with UV detection and by capillary electrophoresis with conductivity detection
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Simultaneous determination of caffeine, paracetamol, and ibuprofen in pharmaceutical formulations by high-performance liquid chromatography with UV detection and by capillary electrophoresis with conductivity detection

机译:通过高效液相色谱-紫外检测和毛细管电泳-电导检测同时测定药物制剂中的咖啡因,扑热息痛和布洛芬

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摘要

Paracetamol, caffeine and ibuprofen are found in over-the-counter pharmaceutical formulations. In this work, we propose two new methods for simultaneous determination of paracetamol, caffeine and ibuprofen in pharmaceutical formulations. One method is based on high-performance liquid chromatography with diode-array detection and the other on capillary electrophoresis with capacitively coupled contactless conductivity detection. The separation by high-performance liquid chromatography with diode-array detection was achieved on a C-18 column (250x4.6 mm(2), 5 m) with a gradient mobile phase comprising 20-100% acetonitrile in 40 mmol L-1 phosphate buffer pH 7.0. The separation by capillary electrophoresis with capacitively coupled contactless conductivity detection was achieved on a fused-silica capillary (40 cm length, 50 m i.d.) using 10 mmol L-1 3,4-dimethoxycinnamate and 10 mmol L-1 -alanine with pH adjustment to 10.4 with lithium hydroxide as background electrolyte. The determination of all three pharmaceuticals was carried out in 9.6 min by liquid chromatography and in 2.2 min by capillary electrophoresis. Detection limits for caffeine, paracetamol and ibuprofen were 4.4, 0.7, and 3.4 mol L-1 by liquid chromatography and 39, 32, and 49 mol L-1 by capillary electrophoresis, respectively. Recovery values for spiked samples were between 92-107% for both proposed methods.
机译:在非处方药物制剂中发现了扑热息痛,咖啡因和布洛芬。在这项工作中,我们提出了两种同时测定药物制剂中扑热息痛,咖啡因和布洛芬的新方法。一种方法是基于具有二极管阵列检测功能的高效液相色谱法,另一种方法是基于具有电容耦合非接触电导率检测功能的毛细管电泳。在C-18色谱柱(250x4.6 mm(2),5 m)上采用包含20-100%乙腈和40 mmol L-1的梯度流动相,通过带有二极管阵列检测的高效液相色谱分离磷酸盐缓冲液pH 7.0。使用10 mmol L-1 3,4-二甲氧基肉桂酸酯和10 mmol L-1-丙氨酸在pH值调节下,在熔融石英毛细管(40 cm长,50 m id)上通过毛细管电泳与电容耦合非接触电导率检测进行分离氢氧化锂作为背景电解质,可达到10.4。通过液相色谱法在9.6分钟内通过毛细管电泳在2.2分钟内对所有三种药物进行测定。咖啡因,对乙酰氨基酚和布洛芬的检出限通过液相色谱法分别为4.4、0.7和3.4 mol L-1,通过毛细管电泳分别为39、32和49 mol L-1。对于这两种建议的方法,加标样品的回收率在92%至107%之间。

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