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Integrated targeted and non-targeted analysis of water sample extracts with micro-scale UHPLC–MS

机译:使用微型UHPLC-MS对水样提取物进行有针对性的综合分析

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摘要

class="kwd-title">Method name: Universal UHPLC–MS analysis enhanced by non-target screening class="kwd-title">Keywords: UHPLC–MS, Non-target, Pharmaceutical residues, Pesticides, Extraction, Cleanup, Retention time index, Database research class="head no_bottom_margin" id="idm139868908704032title">AbstractA sensitive method is introduced to detect selected pharmaceutical residues and polar pesticides with UHPLC–MS in water samples of different origin. Active or passive water sampling was combined with a laboratory solid-phase extraction cleanup and stable isotope dilution analysis. Recovery experiments demonstrated that the internal standard correction performed well for the compensation of matrix effects. Besides, the original targeted analysis approach was expanded by non-target analysis of the samples with only one more consecutive injection run needed. The key benefits of this multi-residue analysis are: class="first-line-outdent">
  • • Targeted analysis and quantification combined with non-target analysis on a micro-scale UHPLC–MS system usually employed for qualitative analysis only.
  • • The internal standards for targeted analysis were used in non-target runs to calculate the partition coefficient log P of unknown substances employing the retention time index (RTI).
  • • The filtering of database hits for two criteria (exact mass and partition coefficient) significantly reduced the list of suspects and at the same time rendered it possible to perform non-target analysis with lower mass accuracy (no lock-spray) in the range of 20–500 ppm.
  • 机译:<!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> <!-fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> class =“ kwd-title”>方法名称:通过非目标筛选增强了通用UHPLC-MS分析 class =“ kwd-title” >关键字: UHPLC–MS,非目标化合物,药物残留,农药,提取,净化,保留时间指数,数据库研究 class =“ head no_bottom_margin” id =“ idm139868908704032title”>摘要 A引入了灵敏的方法,通过UHPLC-MS检测不同来源的水样中的选定药物残留和极性农药。主动或被动水采样与实验室固相萃取净化和稳定的同位素稀释分析相结合。回收率实验表明,内标校正在补偿基质效应方面表现良好。此外,最初的目标分析方法通过对样品的非目标分析进行了扩展,只需要再进行一次连续进样即可。这种多残留分析的主要优点是: class =“ first-line-outdent”> <!-list-behavior =简单的前缀-word = mark-type = none最大标签大小= 9- >
  • •在通常仅用于定性分析的微型UHPLC-MS系统上,目标分析和定量与非目标分析相结合。
  • •针对目标分析的内部标准用于非目标运行中,利用保留时间指数(RTI)计算未知物质的分配系数logP。
  • •数据库筛选的结果两个标准(精确质量数和分配系数)显着减少了可疑物的数量,同时使得可以在20-500 ppm范围内以较低的质量准确度(无锁定喷雾)进行非目标分析。
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