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在(超)高效液相色谱中使用电位检测和吸附/解吸结合动力学建模。

Use of potentiometric detection in (ultra) high performance liquid chromatography and modelling with adsorption/desorption binding kinetics.

机构信息

University of Antwerp, Department of Chemistry, Groenenborgerlaan 171, B-2020 Antwerp, Belgium.

出版信息

Anal Chim Acta. 2013 May 13;777:25-31. doi: 10.1016/j.aca.2013.03.031. Epub 2013 Mar 21.

Abstract

Observation of a potentiometric sensor's response behaviour after injection in flow injection analysis at different concentrations allowed studying "on" and "off" kinetics of the analyte's adsorption/diffusion behaviour. The alkaloid metergoline was mostly used as an example. k(on) and k(off) rate constant values were measured, and the association constant K(ass), and ΔG values of the analyte-surface interaction were calculated with an adsorption-based model which proved to be fully applicable. k(on) increased by decreasing the sensor dimensions, while koff was unaffected by miniaturization. Increasing acetonitrile concentrations in the running buffer increased k(off), while k(on) was unaffected. The experimentally determined ΔG values of the analyte-surface interaction showed a linear relation to the response of the sensor, in mV. This knowledge was applied to optimize the potentiometric detection of plant alkaloids in (U)HPLC. Sub-micromolar detection limits were obtained with the potentiometric detector/(U)HPLC combination. This is the first time that the response rates and the response itself can be modelled accurately for coated wire potentiometric sensors, and it is the first application of a potentiometric detector in UPLC.

摘要

在不同浓度下,通过在流动注射分析中对传感器进行注入观察其响应行为,可以研究分析物吸附/扩散行为的“开”和“关”动力学。以麦角新碱为例进行了研究。测量了 k(on)和 k(off)速率常数值,并使用基于吸附的模型计算了分析物-表面相互作用的缔合常数 K(ass)和 ΔG 值,该模型被证明完全适用。通过减小传感器的尺寸,k(on)增加,而 koff 不受微型化的影响。在运行缓冲液中增加乙腈浓度会增加 k(off),而 k(on)不受影响。通过实验确定的分析物-表面相互作用的 ΔG 值与传感器的 mV 响应呈线性关系。该知识已应用于优化(U)HPLC 中植物生物碱的电化学检测。通过电化学检测器/(U)HPLC 组合获得了亚微摩尔的检测限。这是首次可以准确地对涂覆线电化学传感器的响应速率和响应本身进行建模,也是首次在 UPLC 中应用电化学检测器。

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