Department of Chemical engineering, North University of China, Taiyuan, Shanxi 030051, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Aug 1;878(23):2077-86. doi: 10.1016/j.jchromb.2010.06.007. Epub 2010 Jun 11.
By adopting the novel surface molecular imprinting technique put forward by us not long ago, a creatinine molecule-imprinted material with high performance was prepared. The functional macromolecule polymethacrylic acid (PMAA) was first grafted on the surfaces of micron-sized silica gel particles in the manner of "grafting from" using 3-methacryloxypropyltrimethoxysilane (MPS) as intermedia, resulting in the grafted particles PMAA/SiO(2). Subsequently, the molecular imprinting was carried out towards the grafted macromolecule PMAA using creatinine as template and with ethylene glycol diglycidyl ether (EGGE) as crosslinker by right of the intermolecular hydrogen bonding and electrostatic interaction between the grafted PMAA and creatinine molecules. Finally, the creatinine-imprinted material MIP-PMAA/SiO(2) was obtained. The binding character of MIP-PMAA/SiO(2) for creatinine was investigated in depth with both batch and column methods and using N-hydroxysuccinimide and creatine as two contrast substances, whose chemical structures are similar to creatinine to a certain degree. The experimental results show that the surface-imprinted material MIP-PMAA/SiO(2) has excellent binding affinity and high recognition selectivity for creatinine. Before imprinting, PMAA/SiO(2) particles nearly has not recognition selectivity for creatinine, and the selectivity coefficients of PMAA/SiO(2) for creatinine relative to N-hydroxysuccinimide and creatine are only 1.23 and 1.30, respectively. However, after imprinting, the selectivity coefficients of MIP-PMAA/SiO(2) for creatinine in respect to N-hydroxysuccinimide and creatine are remarkably enhanced to 11.64 and 12.87, respectively, displaying the excellent recognition selectivity and binding affinity towards creatinine molecules.
采用我们不久前提出的新颖表面分子印迹技术,制备了一种高性能的肌酐分子印迹材料。首先,通过 3-甲氧基丙基三甲氧基硅烷(MPS)作为中间体,以“从接枝”的方式将官能大分子甲基丙烯酸丙酯(PMAA)接枝到微米级硅胶颗粒表面,得到接枝颗粒 PMAA/SiO(2)。随后,以肌酐为模板,以乙二醇二缩水甘油醚(EGGE)为交联剂,利用接枝 PMAA 和肌酐分子之间的分子间氢键和静电相互作用,对接枝大分子 PMAA 进行分子印迹。最后,得到肌酐印迹材料 MIP-PMAA/SiO(2)。通过批量和柱方法,使用 N-羟基琥珀酰亚胺和肌酸作为两种对比物质,深入研究了 MIP-PMAA/SiO(2)对肌酐的结合特性,其化学结构在一定程度上与肌酐相似。实验结果表明,表面印迹材料 MIP-PMAA/SiO(2)对肌酐具有优异的结合亲和力和高识别选择性。印迹前,PMAA/SiO(2)颗粒对肌酐几乎没有识别选择性,PMAA/SiO(2)对肌酐相对于 N-羟基琥珀酰亚胺和肌酸的选择性系数仅分别为 1.23 和 1.30。然而,印迹后,MIP-PMAA/SiO(2)对 N-羟基琥珀酰亚胺和肌酸的选择性系数分别显著提高到 11.64 和 12.87,对肌酐分子表现出优异的识别选择性和结合亲和力。