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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >On-line on-chip post-column derivatisation reactions for pre-ionisation of analytes and cluster analysis in gradient mu-liquid chromatography/electrospray mass spectrometry
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On-line on-chip post-column derivatisation reactions for pre-ionisation of analytes and cluster analysis in gradient mu-liquid chromatography/electrospray mass spectrometry

机译:在线芯片上柱后衍生化反应,用于分析物的预电离和梯度mu-液相色谱/电喷雾质谱中的聚类分析

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A system is presented that demonstrates the principle of on-line and on-chip post-column derivatisation reactions in micro-high-performance liquid chromatography (mu-HPLC) hyphenated to electrospray time-of-flight mass spectrometry (ESI-TOFMS). In this mu-HPLC-chip-MS set-up, the analytes are separated using gradient mu-HPLC and subsequently derivatised on-chip and detected. One of the major limitations of MS detection is its dependency on the degree of ionisation, which is widely variable and compound-specific. Optimising and controlling the degree of ionisation in a simple manner would allow MS detection to be truly generic. One way of achieving this is by pre-ionisation of analytes using simple derivatisation procedures that are both rapid and quantitative. Performing this in situ on the system described here overcomes issues of sample handling and efficiency losses when time-consuming "bench chemistry" is necessary prior to analysis. The power of the system is demonstrated by the separation of primary and secondary amines, which are subsequently derivatised with a positively charged phosphonium complex and detected in an enhanced manner. Typically, molecular cations (M+) are detected showing that the ionisation process is dominated by the phosphonium species, leading to more constant ionisation for a variety of compounds. In addition, stable isotopically labelled (C-12/C-13)-phosphonium reagent is used for the reactions, allowing for inherent signaloise (S/N) improvement and automated data processing using cluster analysis. A similar reaction scheme is used for the derivatisation of ketones and aldehydes, also demonstrating dramatic increases in sensitivity, especially with increasing temperature. Minimal loss in chromatographic fidelity in terms of retention times is observed by the introduction of the micromixer chip into the system. Optimal flow rates in mu-HPLC and ESI-MS are compatible with flow rates for the chip as well as a multitude of in-line optical detectors including UV and fluorescence. In addition, the micromixer chip can be positioned pre-column if preferred. The system is robust, easily fully automated and applicable to a wide variety of reactions. The system has a major advantage in its simple robust connection to the "normal scale" outside world. Copyright (C) 2002 John Wiley Sons, Ltd. [References: 14]
机译:提出了一个系统,该系统演示了用电喷雾飞行时间质谱(ESI-TOFMS)联用的微型高效液相色谱(mu-HPLC)中的在线和芯片上柱后衍生化反应的原理。在这种mu-HPLC-chip-MS设置中,使用梯度mu-HPLC分离分析物,然后在芯片上衍生化并检测。 MS检测的主要限制之一是其对电离度的依赖性,该电离度的变化范围广且具有化合物特异性。以简单的方式优化和控制电离度将使MS检测成为真正的通用检测。实现此目的的一种方法是使用快速且定量的简单衍生化程序对分析物进行预电离。当在分析之前需要耗时的“台式化学”时,在此处描述的系统上原位执行此操作可以克服样品处理和效率损失的问题。伯胺和仲胺的分离证明了该系统的功能,然后将其与带正电荷的phospho络合物衍生化并以增强的方式进行检测。通常,检测到分子阳离子(M +),表明电离过程受the类物质支配,从而导致各种化合物的电离更加恒定。此外,稳定的同位素标记的(C-12 / C-13)reagent试剂可用于反应,从而可以改善固有的信噪比(S / N)并使用聚类分析进行自动数据处理。类似的反应方案用于酮和醛的衍生化,也显示出灵敏度的显着提高,尤其是随着温度的升高。通过将微混合器芯片引入系统,可以观察到色谱保真度在保留时间方面的损失最小。 mu-HPLC和ESI-MS中的最佳流速与芯片的流速以及包括紫外线和荧光在内的多种在线光学检测器兼容。另外,如果优选的话,微混合器芯片可以定位在柱前。该系统功能强大,易于完全自动化,并适用于多种反应。该系统的主要优势在于与外部“正常规模”的简单牢固连接。版权所有(C)2002 John Wiley Sons,Ltd. [引用:14]

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