首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >A miniature condensed-phase membrane introduction mass spectrometry (CP-MIMS) probe for direct and on-line measurements of pharmaceuticals and contaminants in small, complex samples
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A miniature condensed-phase membrane introduction mass spectrometry (CP-MIMS) probe for direct and on-line measurements of pharmaceuticals and contaminants in small, complex samples

机译:微型冷凝相膜引入质谱(CP-MIMS)探针,用于对复杂小样本中的药物和污染物进行直接和在线测量

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摘要

RATIONALE High-throughput, automated analytical measurements are desirable in many analytical scenarios, as are rapid sample pre-screening techniques to identify 'positive' samples for subsequent measurements using more time-consuming conventional methodologies (e.g., liquid chromatography/mass spectrometry (LC/MS)). A miniature condensed-phase membrane introduction mass spectrometry (CP-MIMS) probe for the direct and continuous, on-line measurement of pharmaceuticals and environmental contaminants in small, complex samples is presented. METHODS A miniature polydimethylsiloxane hollow fibre membrane (PDMS-HFM) probe is coupled with an electrospray ionization (ESI) triple quadrupole mass spectrometer. Analytes are transported from the probe to the ESI source by a methanol acceptor phase. The probe can be autosampler mounted and directly inserted in small samples (≥400 μL) allowing continuous and simultaneous pptr-ppb level detection of target analytes (chlorophenols, triclosan, gemfibrozil, nonylphenol) in complex samples (artificial urine, beer, natural water, waste water, plant tissue). RESULTS The probe has been characterized and optimized for acceptor phase flow rate, sample mixing and probe washing. Signal response times, detection limits and calibration data are given for selected ion monitoring (SIM) and tandem mass spectrometry (MS/MS) measurements of target analytes at trace levels. Comparisons with flow cell type CP-MIMS systems are given. Analyte depletion effects are evaluated for small samples (≥400 μL). On-line measurements in small volumes of complex samples, temporally resolved reaction monitoring and in situ/in vivo demonstrations are presented. CONCLUSIONS The miniature CP-MIMS probe developed was successfully used for the direct, on-line detection of target analytes in small volumes (40 mL to 400 μL) of complex samples at pptr to low ppb levels. The probe can be readily automated as well as deployed for in situ/in vivo monitoring, including reaction monitoring, small sample measurements and direct insertion in living plant tissue.
机译:RATIONALE在许多分析场景中都需要高通量的自动化分析测量,以及快速的样品预筛​​选技术,以使用更耗时的常规方法(例如液相色谱/质谱法(LC /多发性硬化症))。提出了一种用于小型,复杂样品中药物和环境污染物的直接和连续在线测量的微型冷凝相膜引入质谱(CP-MIMS)探针。方法微型聚二甲基硅氧烷中空纤维膜(PDMS-HFM)探针与电喷雾电离(ESI)三重四极杆质谱仪耦合。通过甲醇受体相将分析物从探针传输到ESI源。探头可以安装在自动进样器上,并直接插入小样品(≥400μL)中,从而可以连续和同时检测pptr-ppb水平的复杂样品(人造尿液,啤酒,天然水,废水,植物组织)。结果该探针已针对受体相流速,样品混合和探针清洗进行了表征和优化。提供了信号响应时间,检测限和校准数据,用于痕量目标分析物的选定离子监测(SIM)和串联质谱(MS / MS)测量。给出了与流通池类型CP-MIMS系统的比较。对小样本(≥400μL)的分析物耗竭效果进行了评估。提出了少量复杂样品的在线测量,时间分辨反应监测以及原位/体内演示。结论开发的微型CP-MIMS探针已成功用于pptr至低ppb水平的小体积(40 mL至400μL)复杂样品中目标分析物的直接在线检测。该探针可以很容易地实现自动化,也可以部署在原位/体内监测中,包括反应监测,少量样品测量以及直接插入有生命的植物组织。

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