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头柱场放大进样的见解:第二部分。阳离子化合物通过短水柱进行电动进样后电泳系统行为的研究。

Insights into head-column field-amplified sample stacking: Part II. Study of the behavior of the electrophoretic system after electrokinetic injection of cationic compounds across a short water plug.

作者信息

Šesták Jozef, Thormann Wolfgang

机构信息

Clinical Pharmacology Laboratory, Institute for Infectious Diseases, University of Bern, Bern, Switzerland; Institute of Analytical Chemistry of the Czech Academy of Sciences, v. v. i., Brno, Czechia.

Clinical Pharmacology Laboratory, Institute for Infectious Diseases, University of Bern, Bern, Switzerland.

出版信息

J Chromatogr A. 2017 Aug 25;1512:124-132. doi: 10.1016/j.chroma.2017.06.073. Epub 2017 Jun 30.

Abstract

Part I on head-column field-amplified sample stacking comprised a detailed study of the electrokinetic injection of a weak base across a short water plug into a phosphate buffer at low pH. The water plug is converted into a low conductive acidic zone and cationic analytes become stacked at the interface between this and a newly formed phosphoric acid zone. The fundamentals of electrokinetic processes occurring thereafter were studied experimentally and with computer simulation and are presented as part II. The configuration analyzed represents a discontinuous buffer system. Computer simulation revealed that the phosphoric acid zone at the plug-buffer interface becomes converted into a migrating phosphate buffer plug which corresponds to the cationically migrating system zone of the phosphate buffer system. Its mobility is higher than that of the analytes such that they migrate behind the system zone in a phosphate buffer comparable to the applied background electrolyte. The temporal behaviour of the current and the conductivity across the water plug were monitored and found to reflect the changes in the low conductivity plug. Determination of the buffer flow in the capillary revealed increased pumping caused by the mismatch of electroosmosis within the low conductivity plug and the buffer. This effect becomes elevated with increasing water plug length. For plug lengths up to 1% of the total column length the flow quickly drops to the electroosmotic flow of the buffer and simulations with experimentally determined current and flow values predict negligible band dispersion and no loss of resolution for both low and large molecular mass components.

摘要

第一部分关于柱头场放大样品堆积,详细研究了弱酸在短水柱中电动进样至低pH值磷酸盐缓冲液的过程。水柱转变为低导电酸性区,阳离子分析物在该区与新形成的磷酸区之间的界面处堆积。之后通过实验和计算机模拟研究了后续发生的电动过程的基本原理,并在第二部分进行了阐述。所分析的配置代表了一种不连续缓冲系统。计算机模拟表明,柱头 - 缓冲液界面处的磷酸区转变为迁移的磷酸盐缓冲液柱,其对应于磷酸盐缓冲系统的阳离子迁移系统区。其迁移率高于分析物,使得它们在与施加的背景电解质相当的磷酸盐缓冲液中在系统区后面迁移。监测了水柱上电流和电导率的时间行为,发现其反映了低导电柱的变化。对毛细管中缓冲液流动的测定表明,由于低导电柱内电渗与缓冲液的不匹配导致泵送增加。随着水柱长度增加,这种效应增强。对于长度达到柱总长度1%的水柱,流动迅速降至缓冲液的电渗流,并且用实验确定的电流和流动值进行的模拟预测,对于低分子量和大分子质量组分,谱带展宽可忽略不计且分辨率无损失。

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