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首页> 外文期刊>Luminescence: The journal of biological and chemical luminescence >Determination of the pseudoephedrine content in pharmaceutical formulations and in biological fluids using a microbore HPLC system interfaced to a microfluidic chemiluminescence detectorl
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Determination of the pseudoephedrine content in pharmaceutical formulations and in biological fluids using a microbore HPLC system interfaced to a microfluidic chemiluminescence detectorl

机译:使用与微流化学发光检测器连接的微孔HPLC系统测定药物制剂和生物液体中伪麻黄碱的含量

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A novel automated precolumn derivatization followed by separation using liquid chromatography for the determination of pseudoephedrine (PSE) by a microfluidic chemiluminescence detector has been developed. An on-line derivatization procedure was utilized by converting PSE into a highly light emitting species in a Ru(bipy)(3)(2+)-peroxydisulphate chemiluminescence (CL) system by derivatizing it with a 1.0 M formaldehyde solution. The derivatized analyte was directly injected into a microbore high-performance liquid chromatography (HPLC) system coupled to an on-chip chemiluminescence detector. The newly developed highly selective, sensitive and fast HPLC-CL method was validated and successfully applied for the analysis of PSE in pharmaceutical formulations and a human urine sample. The selectivity of the method is not only due to the HPLC separation but is also due to the highly selective detection principle of the Ru(bipy)(3)(2+)-peroxydisulphate CL system used. There was no interference observed from the common preservatives and excipients used in pharmaceutical preparations, which did not show any significant CL signal. The retention time of PSE was less than 3 min, and the detection limits and quantification limits were found to be 5.7 and 26.0 mu g L-1, respectively. Copyright (C) 2015 John Wiley & Sons, Ltd.
机译:开发了一种新型的自动柱前衍生化方法,然后使用液相色谱法进行分离,以通过微流化学发光检测器测定伪麻黄碱(PSE)。使用在线衍生化程序,方法是通过用1.0 M甲醛溶液将PSE转化为Ru(bipy)(3)(2 +)-过二硫酸盐化学发光(CL)系统中的PSE使其成为高发光物质。将衍生的分析物直接注入与芯片上化学发光检测器耦合的微孔高效液相色谱(HPLC)系统中。新开发的高选择性,灵敏和快速的HPLC-CL方法得到验证,并成功用于药物制剂和人尿液样品中PSE的分析。该方法的选择性不仅归因于HPLC分离,还归因于所用Ru(bipy)(3)(2 +)-过氧二硫酸盐CL系统的高选择性检测原理。没有观察到来自药物制剂中常用的防腐剂和赋形剂的干扰,它们没有显示任何明显的CL信号。 PSE的保留时间少于3分钟,检测限和定量限分别为5.7和26.0μg L-1。版权所有(C)2015 John Wiley&Sons,Ltd.

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