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缓冲成分与中性配位体的络合:第一部分。对常见缓冲性质的影响。

Complexation of buffer constituents with neutral complexation agents: part I. Impact on common buffer properties.

机构信息

Charles University in Prague , Faculty of Science, Department of Physical and Macromolecular Chemistry, Prague, Czech Republic.

出版信息

Anal Chem. 2013 Sep 17;85(18):8518-25. doi: 10.1021/ac4013804. Epub 2013 Aug 29.

Abstract

The complexation of buffer constituents with the complexation agent present in the solution can very significantly influence the buffer properties, such as pH, ionic strength, or conductivity. These parameters are often crucial for selection of the separation conditions in capillary electrophoresis or high-pressure liquid chromatography (HPLC) and can significantly affect results of separation, particularly for capillary electrophoresis as shown in Part II of this paper series (Beneš, M.; Riesová, M.; Svobodová, J.; Tesařová, E.; Dubský, P.; Gaš, B. Anal. Chem. 2013, DOI: 10.1021/ac401381d). In this paper, the impact of complexation of buffer constituents with a neutral complexation agent is demonstrated theoretically as well as experimentally for the model buffer system composed of benzoic acid/LiOH or common buffers (e.g., CHES/LiOH, TAPS/LiOH, Tricine/LiOH, MOPS/LiOH, MES/LiOH, and acetic acid/LiOH). Cyclodextrins as common chiral selectors were used as model complexation agents. We were not only able to demonstrate substantial changes of pH but also to predict the general complexation characteristics of selected compounds. Because of the zwitterion character of the common buffer constituents, their charged forms complex stronger with cyclodextrins than the neutral ones do. This was fully proven by NMR measurements. Additionally complexation constants of both forms of selected compounds were determined by NMR and affinity capillary electrophoresis with a very good agreement of obtained values. These data were advantageously used for the theoretical descriptions of variations in pH, depending on the composition and concentration of the buffer. Theoretical predictions were shown to be a useful tool for deriving some general rules and laws for complexing systems.

摘要

缓冲成分与溶液中配合剂的络合作用会显著影响缓冲液的性质,如 pH 值、离子强度或电导率。这些参数通常是选择毛细管电泳或高压液相色谱 (HPLC) 分离条件的关键因素,并且会显著影响分离结果,对于毛细管电泳尤其如此,如本论文系列的第二部分所示(Beneš, M.; Riesová, M.; Svobodová, J.; Tesařová, E.; Dubský, P.; Gaš, B. Anal. Chem. 2013, DOI: 10.1021/ac401381d)。在本文中,我们从理论和实验两方面证实了缓冲成分与中性配合剂络合的影响,实验对象是由苯甲酸/LiOH 或常见缓冲液(如 CHES/LiOH、TAPS/LiOH、Tricine/LiOH、MOPS/LiOH、MES/LiOH 和乙酸/LiOH)组成的模型缓冲液系统。我们使用常见的手性选择剂环糊精作为模型配合剂。我们不仅能够证明 pH 值的显著变化,还能够预测所选化合物的一般络合特性。由于常见缓冲成分的两性离子特性,它们的带电形式与环糊精的络合作用比中性形式更强。这一点通过 NMR 测量得到了充分证明。此外,通过 NMR 和亲和毛细管电泳确定了所选化合物两种形式的络合常数,所得值非常吻合。这些数据有利于对 pH 值随缓冲液组成和浓度变化的理论描述。理论预测被证明是一种有用的工具,可用于推导络合体系的一些一般规则和定律。

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