...
首页> 外文期刊>Analytica chimica acta >A multiresidue method for the simultaneous determination of ten macrolide antibiotics in human urine based on gradient elution liquid chromatography coupled to coulometric detection (HPLC-ECD)
【24h】

A multiresidue method for the simultaneous determination of ten macrolide antibiotics in human urine based on gradient elution liquid chromatography coupled to coulometric detection (HPLC-ECD)

机译:梯度洗脱液相色谱-库仑检测(HPLC-ECD)同时测定人尿中十种大环内酯类抗生素的多残留方法

获取原文
获取原文并翻译 | 示例

摘要

A new generation of coulometric detector coupled to a high performance liquid chromatograph (HPLC) was used in this work with the aim of developing a multiresidue method allowing for the first time the separation,in a single run,of ten commercially available macrolide antibiotics,erythromycin (ERY),dirithromycin (DIR),tylosin (TYL),tilmicosin (TILM),spiramycin (SPI),josamycin (JOS),kitasamycin (KIT),rosamicin (ROS),roxithromycin (ROX) and oleandomycin (OLE).The procedure was therefore fully optimised for the separation of standard mixtures of the ten macrolides using a gradient elution on a C8 reversed phase HPLC column,and very reasonable resolution was achieved among the thirteen signals,arising from these ten.In the following step,the quantification of all the macrolides was achieved in standard mixtures,using ROX as an internal standard (I.S.),with detection limits,on column,below 2.5 ng for each.The method was then applied to the determination of macrolides in human urine,after a simple and fast sample preparation procedure involving liquid-liquid extraction.Calibration curves were carried out using the method of matrix-matching.The detection limits for each drug,in the human urine,were below 3 ng injected (equivalent to an initial concentration in the urine below 0.06 mg l~(-1)).Overall recoveries of the entire method were estimated for each drug in human urine fortified at different levels of concentration within the linear range and averaged values were between 49.9 and 81.2% for low concentration levels and between 53.2 and 92.0% for high concentration levels for all macrolides.
机译:这项工作中使用了新一代的库仑检测器和高效液相色谱仪(HPLC),目的是开发一种多残留方法,首次允许一次分离十种市售大环内酯类抗生素红霉素。 (ERY),去甲霉素(DIR),泰乐菌素(TYL),替米考星(TILM),螺旋霉素(SPI),乔沙霉素(JOS),kitasamycin(KIT),玫瑰霉素(ROS),罗霉素(ROX)和oleandomycin(OLE)。因此,使用C8反相HPLC色谱柱上的梯度洗脱方法对十种大环内酯类化合物的标准混合物进行了完全优化,从这十种中分离出的十三种信号之间实现了非常合理的分离度。所有的大环内酯类化合物均以标准混合物的形式完成,使用ROX作为内标(IS),色谱柱的检出限为每个2.5 ng以下。该方法用于人体尿液中大环内酯类化合物的测定。简单,快速的样品制备过程,涉及液-液萃取。使用基质匹配法绘制校正曲线。人尿中每种药物的检出限均低于3 ng(相当于初始浓度)。尿液低于0.06 mg l〜(-1))。估计在线性范围内不同浓度水平下强化的人尿中每种药物的整体回收率,低浓度水平和平均值在49.9%至81.2%之间。所有大环内酯类药物的高浓度水平在53.2%和92.0%之间。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号