...
首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Dispersive solid-phase microextraction method for sample extraction in the analysis of four tetracyclines in water and milk samples by high-performance liquid chromatography with diode-array detection
【24h】

Dispersive solid-phase microextraction method for sample extraction in the analysis of four tetracyclines in water and milk samples by high-performance liquid chromatography with diode-array detection

机译:分散固相微萃取方法通过高效液相色谱-二极管阵列检测法分析水和牛奶样品中的四个四环素,用于样品萃取

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

A dispersive solid-phase microextraction (dispersive-SPME) method for the determination of tetracycline, oxytetracycline,chlortetracycline and doxycycline is proposed. Different silica-based and polymeric sorbents were evaluated for their capacity to simultaneously preconcentrate tetracyclines (TCs) in the dispersive format from aqueous or organic solutions. Silica-based sorbents especially functionalized with primary amine, secondary amine, or carbonyl groups have showed higher capacity than polymeric sorbents under organic environment. In the proposed dispersive solid-phase microextraction method, after extraction with acetonitrile and salt-promoted partitioning, TCs were adsorbed to a small amount of dispersive silica-based primary and secondary amine sorbents, desorbed with a small volume of desorption solution, and determined by high-performance liquid chromatography with diode-array detection. Under the optimal conditions, recoveries were determined for surface water and milk samples spiked at 10 ng/mL and 50-150 ng/g, respectively, and quantification was achieved by matrix-matched calibration. The calibration curves of four TCs in both samples showed linearity with a correlation coefficient value above 0.997. Average recoveries ranged from 97.1 to 104.1% and the precision was from 2.0 to 5.6%. Limits of detection ranged from 0.7 to 3.5 ng/mL and from 7.9 to 35.3 ng/g for four TCs Surface in Surface water and milk samples, respectively.
机译:提出了一种测定四环素,土霉素,金霉素和强力霉素的分散固相微萃取法。评估了不同的二氧化硅基和聚合物吸附剂同时从水溶液或有机溶液中预浓缩分散形式的四环素(TC)的能力。在有机环境下,特别是被伯胺,仲胺或羰基官能化的二氧化硅基吸附剂比聚合物吸附剂具有更高的容量。在拟议的分散固相微萃取方法中,用乙腈萃取和盐促进的分配后,TCs吸附到少量的分散二氧化硅基伯胺和仲胺吸附剂上,并用少量解吸溶液解吸,并通过带有二极管阵列检测的高效液相色谱仪。在最佳条件下,分别测定加标浓度分别为10 ng / mL和50-150 ng / g的地表水和牛奶样品的回收率,并通过基质匹配校准实现定量。两个样品中四个TC的校准曲线均呈线性,相关系数值高于0.997。平均回收率在97.1%至104.1%之间,精度在2.0%至5.6%之间。地表水和牛奶样品中四个TCs的检出限分别为0.7至3.5 ng / mL和7.9至35.3 ng / g。

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