Department of Chemical Engineering, North University of China, Taiyuan 030051, China.
Colloids Surf B Biointerfaces. 2010 Jun 1;77(2):206-13. doi: 10.1016/j.colsurfb.2010.01.025. Epub 2010 Feb 4.
The crosslinked copolymeric microspheres (HEMA/NVP) of N-vinylpyrrolidone (NVP) and 2-hydroxyethyl methacrylate (HEMA) were prepared using inverse suspension polymerization method. Subsequently, the reaction of methacryloyl chloride with the hydroxyl groups on the surfaces of HEMA/NVP microspheres was performed, leading to the introduction of polymerisable double bonds onto the surfaces of microspheres HEMA/NVP. Afterward, methacrylic acid was allowed to be graft-polymerized on microspheres HEMA/NVP in the manner of "grafting from", resulting in the grafted microspheres PMAA-HEMA/NVP. The grafted microspheres PMAA-HEMA/NVP were fully characterized with several means. The graft-polymerization of MAA on microspheres HEMA/NVP was studied in detail, and the optimal reaction conditions were determined. Thereafter, the adsorption property of the grafted microspheres PMAA-HEMA/NVP for lysozyme as a basic protein model was preliminarily examined to explore the feasibility of removing deleterious basic protein such as density lipoprotein from blood. The experimental results indicate that the PMAA grafting degree on microspheres HEMA/NVP is limited because an enwinding polymer layer as a kinetic barrier on the surfaces of HEMA/NVP microspheres will be formed during the graft-polymerization, and block the graft-polymerization. In order to enhance PMAA grafting degree, reaction temperature, monomer concentration and the used amount of initiator should be effectively controlled. The experimental results also reveal that the grafted microspheres PMAA-HEMA/NVP possess very strong adsorption ability for lysozyme by right of strong electrostatic interaction.
采用反相悬浮聚合法制备了 N-乙烯基吡咯烷酮(NVP)和 2-羟乙基甲基丙烯酸酯(HEMA)的交联共聚微球(HEMA/NVP)。然后,使丙烯酰氯与 HEMA/NVP 微球表面的羟基反应,在微球 HEMA/NVP 的表面上引入可聚合的双键。之后,通过“从接枝”的方式使甲基丙烯酸接枝聚合在 HEMA/NVP 微球上,得到接枝微球 PMAA-HEMA/NVP。用多种手段对接枝微球 PMAA-HEMA/NVP 进行了充分的表征。详细研究了 MAA 在 HEMA/NVP 微球上的接枝聚合反应,并确定了最佳反应条件。此后,初步考察了接枝微球 PMAA-HEMA/NVP 对溶菌酶作为基本蛋白模型的吸附性能,以探索从血液中去除有害的基本蛋白如脂蛋白的可行性。实验结果表明,由于在接枝聚合过程中在 HEMA/NVP 微球表面上形成了作为动力学障碍的包缠聚合物层,因此微球 HEMA/NVP 上的 PMAA 接枝程度是有限的。为了提高 PMAA 的接枝程度,应有效控制反应温度、单体浓度和引发剂用量。实验结果还表明,接枝微球 PMAA-HEMA/NVP 通过强静电相互作用对溶菌酶具有很强的吸附能力。