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Stable and reproducible nano-electrospray ionization of aqueous solutions and untreated biological samples using ion current limitation combined with polarity reversing

机译:使用离子电流限制与极性反转相结合的方法,对水溶液和未处理的生物样品进行稳定且可重现的纳米电喷雾电离

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Owing to its high chemical sensitivity and low sample consumption, nanoelectrospray ionization mass spectrometry (nESI-MS) is nowadays widely used in various fields such as chemistry, biology, medicine, pharmaceutical industry, clinical assessment and forensic science. The key analytical limitations of conventional nESI-MS analysis include low stability and poor tip-to-tip reproducibility of analyte signals due to the common clogging of glass capillary tips and the occurrence of electric discharge, especially for the analysis of aqueous solutions. In this study, the nESI current was greatly reduced and the corona discharge was efficiently quenched using a 10 GΩ resistor placed in series between a pulled glass capillary and a high voltage power supply. Additionally, polarity reversing was applied for the in situ salt removal and higher signal intensity than in conventional nESI. Furthermore, by closing the back side of the pulled glass capillary during the analysis the sample flow rate could be reduced down to ca. 1 nL min?1. This combined approach allows the analysis of various aqueous solutions and untreated biological samples without tip clogging and electric discharge both in positive and negative modes with enhanced chemical sensitivity, high signal durability (up to several hours per sample) and excellent tip-to-tip reproducibility (80–90%). We believe that the proposed approach may solve many current problems and significantly advance nESI mass spectrometry in the very near future.
机译:纳米电喷雾电离质谱法(nESI-MS)具有较高的化学敏感性和较低的样品消耗量,因此如今已广泛用于化学,生物学,医药,制药工业,临床评估和法医科学等各个领域。常规nESI-MS分析的关键分析限制包括稳定性低和分析物信号的点对点重现性差,这是由于玻璃毛细管针头的普遍堵塞和放电的发生,特别是对于水溶液的分析。在这项研究中,使用串联在拉制玻璃毛细管和高压电源之间的10GΩ电阻,nESI电流大大降低,电晕放电得以有效淬灭。此外,极性反转用于原位除盐,并且比常规nESI具有更高的信号强度。此外,通过在分析过程中关闭拉出的玻璃毛细管的背面,可以将样品流速降低到大约。最小1 nL 1。这种组合的方法可以分析各种水溶液和未经处理的生物样品,而不会出现正向和负向模式的尖端堵塞和放电现象,具有增强的化学敏感性,高信号耐久性(每个样品长达数小时)和出色的尖端到尖端重现性(80–90%)。我们认为,所提出的方法可能会解决许多当前的问题,并在不远的将来极大地促进nESI质谱的发展。

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