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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 catecholamines by flow-injection analysis and high-performance liquid chromatography with chemiluminescence detection.
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Determination of catecholamines by flow-injection analysis and high-performance liquid chromatography with chemiluminescence detection.

机译:流动注射分析和高效液相色谱-化学发光检测法测定儿茶酚胺。

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摘要

A chemiluminescence (CL) detection of catecholamines [norepinephrine (NE), epinephrine (E), dopamine (DA) and L-dopa (LD)] is described for the flow-injection (FI) and high-performance liquid chromatographic (HPLC) determination of these compounds. The detection method is based on the inhibition effect of catecholamines (CAs) on the CL reaction of luminol with iodine in the alkaline medium. The proposed FI method allows the determination of CAs in pharmaceutical preparations for the purpose of drug quality control. The calibration curves show good linearity in the concentration range of: 1.1-20.0 microg l(-1) (NE), 0.5-5.0 microg l(-1) (E), 0.6-9.0 microg l(-1) (DA) and 0.6-10.0 microg l(-1) (LD). The limits of detection (defined as a signal-to-noise ratio of 3) are: 0.34 microg l(-1) (NE), 0.15 microg l(-1) (E) and 0.18 microg l(-1) (DA, LD). The HPLC procedure was successfully applied for the determination of catecholamines (NE, E, DA) in human urine after solid-phase extraction (SPE). In a simple run time CAs can be determined in 20 min. The chromatographic linear ranges are: 5.0-72.0 microg l(-1) (NE), 5.0-48.0 microg l(-1) (E) and 5.0-96.0 microg l(-1) (DA). The limits of detection for three urinary CAs are: 0.71 microg l(-1) (NE), 0.26 microg l(-1) (E) and 0.73 microg l(-1) (DA).
机译:化学发光(CL)检测儿茶酚胺[去甲肾上腺素(NE),肾上腺素(E),多巴胺(DA)和左旋多巴(LD)]用于流动注射(FI)和高效液相色谱(HPLC)这些化合物的测定。该检测方法基于儿茶酚胺(CAs)对鲁米诺与碘在碱性介质中的CL反应的抑制作用。所提出的FI方法可以确定药物制剂中的CA,以达到药物质量控制的目的。校准曲线在以下浓度范围内显示良好的线性:1.1-20.0 microg l(-1)(NE),0.5-5.0 microg l(-1)(E),0.6-9.0 microg l(-1)(DA)和0.6-10.0 microg l(-1)(LD)。检测极限(定义为3的信噪比)为:0.34 microg l(-1)(NE),0.15 microg l(-1)(E)和0.18 microg l(-1)(DA ,LD)。固相萃取(SPE)后,HPLC方法成功地用于测定人尿中的儿茶酚胺(NE,E,DA)。在简单的运行时间内,可以在20分钟内确定CA。色谱线性范围为:5.0-72.0 microg l(-1)(NE),5.0-48.0 microg l(-1)(E)和5.0-96.0 microg l(-1)(DA)。三个尿液CA的检出限为:0.71微克l(-1)(NE),0.26微克l(-1)(E)和0.73微克l(-1)(DA)。

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