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预平衡毛细管区带电泳或前沿分析:亲和毛细管电泳中平台峰条件的优势。

Pre-equilibrium capillary zone electrophoresis or frontal analysis: advantages of plateau peak conditions in affinity capillary electrophoresis.

作者信息

Østergaard Jesper, Hansen Steen H, Jensen Henrik, Thomsen Anne E

机构信息

Department of Analytical Chemistry, The Danish University of Pharmaceutical Sciences, Copenhagen, Denmark.

出版信息

Electrophoresis. 2005 Nov;26(21):4050-4. doi: 10.1002/elps.200500287.

Abstract

The feasibility of using the affinity CE methodologies pre-equilibrium CZE and CE frontal analysis was tested on interaction systems exhibiting rapid on-and-off kinetics. Experimentally, the methodologies differ only with respect to the volume of sample introduced into the capillary. Pre-equilibrium CZE has been considered amendable to interactions with slow on-and-off kinetics only; however, it has recently been applied in studies of interactions with fast on-and-off kinetics. The effect of varying the sample volume introduced hydrodynamically into the capillary on the apparent degree of complexation was studied. For two different binding systems, the fraction of free analyte was found to be overestimated using pre-equilibrium CZE as compared to volumes providing plateau peak conditions as used with frontal analysis. Results indicate that frontal analysis conditions lead to more robust binding assays and thus more reliable data. The validity of data obtained by pre-equilibrium CZE may be low, thus the use of an experimental setup providing plateau peaks is highly recommended. It is suggested that the effect of altering the sample volume on the degree of binding should be investigated as part of method development and validation.

摘要

在表现出快速结合和解离动力学的相互作用体系上,测试了使用亲和毛细管电泳方法(预平衡毛细管区带电泳和毛细管电泳前沿分析法)的可行性。实验上,这些方法仅在引入毛细管的样品体积方面有所不同。预平衡毛细管区带电泳一直被认为仅适用于具有缓慢结合和解离动力学的相互作用;然而,它最近已被应用于具有快速结合和解离动力学的相互作用研究中。研究了通过流体动力学方式引入毛细管的样品体积变化对表观络合程度的影响。对于两种不同的结合体系,发现与采用前沿分析法时提供平台峰条件的体积相比,使用预平衡毛细管区带电泳会高估游离分析物的比例。结果表明,前沿分析条件可导致更稳健的结合测定,从而获得更可靠的数据。通过预平衡毛细管区带电泳获得的数据有效性可能较低,因此强烈建议使用提供平台峰的实验装置。建议在方法开发和验证过程中,研究改变样品体积对结合程度的影响。

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