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将碳酸酐酶固定在改性聚醚砜膜上用于人工肺。

Immobilization of carbonic anhydrase on modified PES membranes for artificial lungs.

机构信息

Sichuan University, College Biomedical Engineering, Chengdu 610065, Sichuan, P. R. China.

College of Polymer Science and Engineering, State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu, 610065, P. R. China.

出版信息

J Mater Chem B. 2024 Feb 28;12(9):2364-2372. doi: 10.1039/d3tb02553e.

DOI:10.1039/d3tb02553e
PMID:38345129
Abstract

The introduction of carbonic anhydrase (CA) onto an extracorporeal membrane oxygenation (ECMO) membrane can improve the permeability of carbon dioxide (CO). However, existing CA-grafting methods have limitations, and the hemocompatibility of current substrate membranes of commercial ECMO is not satisfactory. In this study, a 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC)/-hydroxy succinimide (NHS) activation method is adopted to graft CA with CO-catalyzed conversion activity onto a polyethersulfone (PES) membrane, which is prepared by a phase inversion technique after crosslinking polymerization of 1-vinyl-2-pyrrolidone (VP) and acrylic acid (AA) in PES solution. The characterization results reveal that CA has been grafted onto the modified PES membrane successfully and exhibits catalytic activity. The kinetic parameters of esterase activity verify that the grafted amount of active CA increases with an increase in the concentration of the CA incubation solution. The CA-grafted membrane (CA-M) can accelerate the conversion of bicarbonate to CO in water and blood, which demonstrates the special catalytic activity towards bicarbonate of CA. Finally, blood compatibility tests prove that the CA-M does not lead to hemolysis, shows suppressed protein adsorption and increased coagulation time, and is suitable for application in ECMO. This work demonstrates a green and efficient method for preparing bioactive materials and has practical guiding significance for subsequent pulmonary membrane research and ECMO applications.

摘要

将碳酸酐酶 (CA) 引入体外膜肺氧合 (ECMO) 膜可以提高二氧化碳 (CO) 的通透性。然而,现有的 CA 接枝方法存在局限性,并且商业 ECMO 的现有基底膜的血液相容性并不令人满意。在这项研究中,采用 1-(3-二甲基氨基丙基)-3-乙基碳化二亚胺盐酸盐 (EDC)/-羟基琥珀酰亚胺 (NHS) 激活方法,将具有 CO 催化转化活性的 CA 接枝到聚醚砜 (PES) 膜上,该膜通过在 PES 溶液中交联聚合 1-乙烯基-2-吡咯烷酮 (VP) 和丙烯酸 (AA) 后通过相转化技术制备。表征结果表明,CA 已成功接枝到改性 PES 膜上并表现出催化活性。酯酶活性的动力学参数验证了接枝的活性 CA 数量随 CA 孵育溶液浓度的增加而增加。接枝 CA 的膜 (CA-M) 可以加速水中和血液中碳酸氢盐向 CO 的转化,这证明了 CA 对碳酸氢盐的特殊催化活性。最后,血液相容性测试证明 CA-M 不会导致溶血,显示出抑制蛋白质吸附和延长凝血时间的作用,适用于 ECMO 的应用。这项工作展示了一种绿色高效的制备生物活性材料的方法,对后续的肺膜研究和 ECMO 应用具有实际的指导意义。

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