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用于生物分离的温度响应色谱法综述

Temperature-responsive chromatography for bioseparations: A review.

作者信息

Nagase Kenichi, Kanazawa Hideko

机构信息

Faculty of Pharmacy, Keio University, 1-5-30 Shibakoen, Minato, Tokyo, 105-8512, Japan.

Faculty of Pharmacy, Keio University, 1-5-30 Shibakoen, Minato, Tokyo, 105-8512, Japan.

出版信息

Anal Chim Acta. 2020 Nov 22;1138:191-212. doi: 10.1016/j.aca.2020.07.075. Epub 2020 Aug 12.

Abstract

In recent decades, in addition to existing small-molecule drug therapies, biomedical technology has also rapidly progressed, leading to the development of various therapies based on biopharmaceuticals and therapeutic cells. However, these materials require effective separation methods for their analysis and production. A representative separation method, which has been extensively studied, is the temperature-responsive chromatography system using poly(N-isopropylacrylamide) and its copolymers. Over the last 20 years, various temperature-responsive chromatographic techniques have been developed for the separation of different types of analytes by changing the copolymer composition, the polymer graft configuration, and the base materials of the stationary phase. The developed methods have been successfully applied for the separation of small-molecule drugs, peptides, and proteins, without affecting their biological activity, simply by changing the column temperature. Furthermore, temperature-modulated cell separation columns have been investigated for the separation of cells without changing their properties. Therefore, the developed methods can serve as effective tools for the current and future bioseparation of various biological compounds, biopharmaceutical proteins, and therapeutic cells that are currently used in therapies.

摘要

近几十年来,除了现有的小分子药物疗法外,生物医学技术也迅速发展,催生出了各种基于生物制药和治疗性细胞的疗法。然而,这些材料在分析和生产过程中需要有效的分离方法。一种经过广泛研究的代表性分离方法是使用聚(N-异丙基丙烯酰胺)及其共聚物的温度响应色谱系统。在过去20年中,通过改变共聚物组成、聚合物接枝构型和固定相的基础材料,已开发出各种温度响应色谱技术,用于分离不同类型的分析物。所开发的方法已成功应用于小分子药物、肽和蛋白质的分离,只需改变柱温,而不会影响它们的生物活性。此外,还研究了温度调制细胞分离柱用于细胞分离且不改变其特性的情况。因此,所开发的方法可作为当前和未来对各种生物化合物、生物制药蛋白质以及目前用于治疗的治疗性细胞进行生物分离的有效工具。

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