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从批量吸附试验预测蛋白质动态结合能力。

Predicting protein dynamic binding capacity from batch adsorption tests.

机构信息

Department of Chemical Engineering, University of Virginia, Charlottesville, VA 22904, USA.

出版信息

Biotechnol J. 2012 Oct;7(10):1216-20. doi: 10.1002/biot.201200136. Epub 2012 Jun 14.

Abstract

The dynamic binding capacity (DBC) and its dependence on residence time influence the design and productivity of adsorption columns used in protein capture applications. This paper offers a very simple approach to predict the DBC of an adsorption column based on a measurement of the equilibrium binding capacity (EBC) and of the time needed to achieve one-half of the EBC in a batch adsorption test. The approach is based on a mass transfer kinetics model that assumes pore diffusion with a rectangular isotherm; however, the same approach is also shown to work for other systems where solute transport inside the particle occurs through other transport mechanisms.

摘要

动态结合容量 (DBC) 及其对停留时间的依赖性会影响用于蛋白质捕获应用的吸附柱的设计和生产效率。本文提供了一种非常简单的方法,可以根据批量吸附试验中测量的平衡结合容量 (EBC) 和达到 EBC 一半所需的时间来预测吸附柱的 DBC。该方法基于一个传质动力学模型,假设孔扩散具有矩形等温线;然而,同样的方法也适用于其他体系,其中颗粒内的溶质传输通过其他传输机制发生。

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