首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Application of statistical experimental design to the optimisation of microextraction by packed sorbent for the analysis of nonsteroidal anti-inflammatory drugs in human urine by ultra-high pressure liquid chromatography
【24h】

Application of statistical experimental design to the optimisation of microextraction by packed sorbent for the analysis of nonsteroidal anti-inflammatory drugs in human urine by ultra-high pressure liquid chromatography

机译:统计实验设计在填充吸附剂微萃取优化超高压液相色谱法分析人尿中非甾体类抗炎药中的应用

获取原文
获取原文并翻译 | 示例
           

摘要

A new approach based on microextraction by packed sorbent (MEPS) and a reversed-phase ultra-high pressure liquid chromatography (UHPLC) method was developed and validated for the determination and quantification of nonsteroidal anti-inflammatory drugs (NSAIDs) (acetylsalicylic acid, ketoprofen, diclofenac, naproxen and ibuprofen) in human urine. The important factors that could influence the extraction were previously screened using the Plackett-Burman design approach. The optimal MEPS extraction conditions were obtained using C18 phase as a sorbent, small sample volume (20μL) and a short time period (approximately 5min) for the entire sample preparation step. The analytes were separated on a core-shell column (Poroshell 120 EC-C18; 100mm×3.0mm; 2.7μm) using a binary mobile phase composed of aqueous 0.1% trifluoroacetic acid and acetonitrile in the gradient elution mode (4.5min of analysis time). The analytical method was fully validated based on linearity, limits of detection (LOD), limits of quantification (LOQ), inter- and intra-day precision and accuracy, and extraction yield. Under optimised conditions, excellent linearity (R~2>0.9991), limits of detection (1.07-16.2ngmL~(-1)) and precision (0.503-9.15% RSD) were observed for the target drugs. The average absolute recoveries of the analysed compounds extracted from the urine samples were 89.4-107%. The proposed method was also applied to the analysis of NSAIDs in human urine. The new approach offers an attractive alternative for the analysis of selected drugs from urine samples, providing several advantages including fewer sample preparation steps, faster sample throughput and ease of performance compared to traditional methodologies.
机译:开发了一种基于填充吸附剂(MEPS)微萃取和反相超高压液相色谱(UHPLC)方法的新方法,并已用于非甾体抗炎药(NSAIDs)(乙酰水杨酸,酮洛芬)的测定和定量验证,尿液中的双氯芬酸,萘普生和布洛芬)。先前使用Plackett-Burman设计方法筛选了可能影响提取的重要因素。在整个样品制备步骤中,使用C18相作为吸附剂,小样品量(20μL)和短时间段(约5分钟)可获得最佳的MEPS萃取条件。使用由0.1%三氟乙酸水溶液和乙腈组成的二元流动相,在梯度洗脱模式下(分析时间4.5分钟)在核-壳柱(Poroshell 120 EC-C18; 100mm×3.0mm;2.7μm)上分离分析物)。该分析方法已根据线性,检测限(LOD),定量限(LOQ),日间和日间精度和准确度以及提取得率进行了充分验证。在优化条件下,观察到目标药物具有良好的线性(R〜2> 0.9991),检出限(1.07-16.2ngmL〜(-1))和精密度(0.503-9.15%RSD)。从尿液样品中提取的分析化合物的平均绝对回收率为89.4-107%。所提出的方法还用于分析人类尿液中的NSAID。新方法为从尿液样本中选择的药物进行分析提供了一种有吸引力的替代方法,与传统方法相比,具有许多优点,包括更少的样品制备步骤,更快的样品通量和易于操作。

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