首页> 外文期刊>Journal of separation science. >Trace analysis of rimantadine in human urine after dispersive liquid liquid microextraction followed by liquid chromatography-post column derivatization
【24h】

Trace analysis of rimantadine in human urine after dispersive liquid liquid microextraction followed by liquid chromatography-post column derivatization

机译:分散液液体微萃取后液相色谱柱衍生术后人类尿液中的痕量分析 - 液相色谱柱衍生化

获取原文
获取原文并翻译 | 示例
           

摘要

The first dispersive liquid liquid microextraction scheme followed by liquid chromatography-post column derivatization for the determination of the antiviral drug rimantadine in urine samples is demonstrated. The effect of the type and volume of organic extraction solvent, type and volume of disperser solvent, sample pH, ionic strength, extraction time, and centrifugation speed on the extraction efficiency were studied. Rimantadine and the internal standard (amantadine) were chromatographed using a reversed phase monolithic stationary phase with a mixture of equal volumes of methanol and phosphate buffer (pH = 3) as mobile phase. On-line postcolumn derivatization of the analyte was performed using a "two-stream" manifold with o-phthalaldehyde and N-acetyl-cysteine at alkaline medium. Under the optimized extraction conditions, the enrichment factor of rimantadine was 58. The linear range was 5-100 mu g/L with correlation coefficient r of 0.9984 while the limit of detection achieved was 0.5 mu g/L. The within-day and between-day precision for the tested concentration levels were less than 14.3% and the mean recoveries obtained from the spiked samples were ranged between 87.5 and 113.9%. The main advantages of the proposed method are the simplicity of operation, rapidity, low cost, and low limit of detection of the analyte.
机译:证明了第一分散液液体微萃取方案,然后进行液相色谱柱衍生化,用于测定尿液样品中的抗病毒药物rimantadine。研究了有机萃取溶剂的类型和体积,分散剂溶剂的类型和体积,样品pH,离子强度,提取时间和对提取效率的离心速度。使用反相单片固定相色谱分离,用相等体积的甲醇和磷酸盐缓冲液(pH = 3)作为流动相,通过反相单片固定相进行色谱分离。使用碱性介质的“双流”歧管和N-乙酰基半胱氨酸的“两料流”歧管进行分析物的在线后衍生化。在优化的提取条件下,Rimantadine的富集因子为58.线性范围为5-100μg,相关系数R为0.9984,而获得的检测限为0.5μg/ L。测试浓度水平的日期和白天的精度小于14.3%,并且从尖刺样品获得的平均回收率在87.5和113.9%之间。所提出的方法的主要优点是简单的操作,快速,低成本和分析物检测的低限制。

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