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利用经优化的静电和疏水相互作用的温敏阴离子聚合物刷修饰珠实现抗体药物分离。

Antibody drug separation using thermoresponsive anionic polymer brush modified beads with optimised electrostatic and hydrophobic interactions.

机构信息

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

Department of Materials Engineering, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo, 113-8656, Japan.

出版信息

Sci Rep. 2020 Jul 27;10(1):11896. doi: 10.1038/s41598-020-68707-7.

DOI:10.1038/s41598-020-68707-7
PMID:32719404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7385495/
Abstract

Antibody drugs play an important role in biopharmaceuticals, because of the specificity for target biomolecules and reduction of side effects. Thus, separation and analysis techniques for these antibody drugs have increased in importance. In the present study, we develop functional chromatography matrices for antibody drug separation and analysis. Three types of polymers, poly(N-isopropylacrylamide (NIPAAm)-co-2-acrylamido-2-methylpropanesulfonic acid (AMPS)-co-N-phenyl acrylamide (PhAAm)), P(NIPAAm-co-AMPS-co-n-butyl methacrylate (BMA)), and P(NIPAAm-co-AMPS-co-tert-butylacrylamide (tBAAm)), were modified on silica beads through atom transfer radical polymerisation. Rituximab elution profiles were observed using the prepared beads-packed column. Rituximab adsorption at high temperature and elution at low temperature from the column were observed, as a result of the temperature-modulated electrostatic and hydrophobic interactions. Using the column, rituximab purification from contaminants was performed simply by changing the temperature. Additionally, three types of antibody drugs were separated using the column through temperature-modulated hydrophobic and electrostatic interactions. These results demonstrate that the temperature-responsive column can be applied for the separation and analysis of biopharmaceuticals through a simple control of the column temperature.

摘要

抗体药物在生物制药中发挥着重要作用,因为它们对靶生物分子具有特异性,并减少了副作用。因此,这些抗体药物的分离和分析技术变得越来越重要。在本研究中,我们开发了用于抗体药物分离和分析的功能型色谱基质。通过原子转移自由基聚合,在硅胶珠上修饰了三种聚合物:聚(N-异丙基丙烯酰胺(NIPAAm)-共-2-丙烯酰胺基-2-甲基丙磺酸(AMPS)-共-N-苯基丙烯酰胺(PhAAm))、P(NIPAAm-co-AMPS-co-正丁基甲基丙烯酸酯(BMA))和 P(NIPAAm-co-AMPS-co-叔丁基丙烯酰胺(tBAAm))。使用制备的珠粒填充柱观察到利妥昔单抗的洗脱曲线。观察到利妥昔单抗在高温下的吸附和在低温下从柱上的洗脱,这是由于温度调制的静电和疏水相互作用。通过改变温度,使用该柱可简单地从杂质中纯化利妥昔单抗。此外,通过温度调制的疏水和静电相互作用,使用该柱分离了三种类型的抗体药物。这些结果表明,通过简单地控制柱温,该温度响应柱可用于生物制药的分离和分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/2e38f709442f/41598_2020_68707_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/a7c0f3a63a08/41598_2020_68707_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/8297c71aef22/41598_2020_68707_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/dc1ca37375f7/41598_2020_68707_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/662ab0c4f656/41598_2020_68707_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/35ea877a56b7/41598_2020_68707_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/cbb96cbb2dcf/41598_2020_68707_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/2e38f709442f/41598_2020_68707_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/a7c0f3a63a08/41598_2020_68707_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/8297c71aef22/41598_2020_68707_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/dc1ca37375f7/41598_2020_68707_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/662ab0c4f656/41598_2020_68707_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/35ea877a56b7/41598_2020_68707_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/cbb96cbb2dcf/41598_2020_68707_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde5/7385495/2e38f709442f/41598_2020_68707_Fig7_HTML.jpg

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