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预测大型生物分子高效液相色谱分离中的带宽。I. 尺寸排阻研究以及溶质斯托克斯直径与颗粒孔径的作用。

Predicting bandwidth in the high-performance liquid chromatographic separation of large biomolecules. I. Size-exclusion studies and the role of solute stokes diameter versus particle pore diameter.

作者信息

Ghrist B F, Stadalius M A, Snyder L R

出版信息

J Chromatogr. 1987 Jan 30;387:1-19. doi: 10.1016/s0021-9673(01)94510-8.

DOI:10.1016/s0021-9673(01)94510-8
PMID:3558619
Abstract

Column plate numbers, N, were measured for 12 different proteins as a function of mobile phase flow-rate in two gel filtration systems (either denaturing or non-denaturing conditions). These data were used to extend a previous model that predicts bandwidths in reversed-phase and ion-exchange chromatography. Restriction of diffusion of large molecules within column packing pores is now defined more precisely, with a single relationship describing this effect for both reversed-phase and size-exclusion chromatography (SEC) (and presumably other high-performance liquid chromatography systems). Separations by gel filtration (SEC) are now included in our general model. A total of 17 flow-rate studies were carried out, involving different proteins, columns and/or mobile phase conditions (denaturing or non-denaturing). Comparisons of plate numbers predicted by the model with experimental values were satisfactory in 15 out of 17 cases. The remaining two cases appear to represent "non-well-behaved" systems, where experimental bandwidths were higher than predicted values by more than 20%. Initial attempts at understanding the origin of these non-ideal effects are described.

摘要

在两种凝胶过滤系统(变性或非变性条件)中,测定了12种不同蛋白质的柱板数N与流动相流速的函数关系。这些数据用于扩展先前预测反相和离子交换色谱带宽的模型。现在更精确地定义了大分子在柱填料孔隙内的扩散限制,用一个单一关系描述反相色谱和尺寸排阻色谱(SEC)(可能还有其他高效液相色谱系统)中的这种效应。凝胶过滤(SEC)分离现在包含在我们的通用模型中。总共进行了17项流速研究,涉及不同的蛋白质、色谱柱和/或流动相条件(变性或非变性)。在17个案例中,有15个案例模型预测的柱板数与实验值的比较令人满意。其余两个案例似乎代表“行为不佳”的系统,其中实验带宽比预测值高出20%以上。描述了初步尝试理解这些非理想效应的起源。

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