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首页> 外文期刊>RSC Advances >Preparation and characterization of surface molecularly imprinted films coated on multiwall carbon nanotubes for recognition and separation of lysozyme with high binding capacity and selectivity
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Preparation and characterization of surface molecularly imprinted films coated on multiwall carbon nanotubes for recognition and separation of lysozyme with high binding capacity and selectivity

机译:涂在多壁碳纳米管上的表面分子印迹膜的制备和表征,用于识别和分离具有高结合能力和选择性的溶菌酶

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摘要

In this work, a series of facile and efficient molecularly imprinted polymers (MIPs) for the selective recognition and separation of lysozyme were synthesized by combining self-polymerization and nanosized matrix. The imprinted materials containing recognition sites for the lysozyme were formed via using both carboxyl-functionalized multi-walled carbon nanotubes (MWCNTs-COOH) as a support and dopamine (DA) with excellent biocompatibility as a functional monomer. The obtained polymers were characterized and evaluated by using field-emission scanning electron microscopy (FESEM), field-emission transmission electron microscopy (FETEM), nitrogen physisorption experiments, Fourier transform infrared (FT-IR) spectroscopy and thermogravimetric analysis (TGA). The optimum reaction conditions and adsorption performance of the resultant nanomaterials were also investigated. MIPs synthesized by this method exhibited excellent imprinting factor (4.1) and high binding capacity (418 mg g?1) for lysozyme. After six adsorption–desorption cycles, the adsorption capacity of the MIPs was only reduced by 7.4%. In addition, the prepared MIPs were used to separate and condense lysozyme from chicken egg white successfully, which showed potential values in industrial protein purification, basic biomedical research and clinical diagnostics.
机译:在这项工作中,通过结合自聚合和纳米级基质,合成了一系列用于选择性识别和分离溶菌酶的简便有效的分子印迹聚合物(MIP)。使用羧基官能化的多壁碳纳米管(MWCNTs-COOH)作为载体和具有出色生物相容性的多巴胺(DA)作为功能单体,通过 形成了含有溶菌酶识别位点的印迹材料。使用场发射扫描电子显微镜(FESEM),场发射透射电子显微镜(FETEM),氮物理吸附实验,傅立叶变换红外光谱(FT-IR)和热重分析(TGA)对所得聚合物进行表征和评估。还研究了所得纳米材料的最佳反应条件和吸附性能。用这种方法合成的MIP对溶菌酶表现出优异的印迹因子(4.1)和高结合能力(418 mg g ?1 )。经过六个吸附-解吸循环,MIP的吸附容量仅降低了7.4%。此外,制备的MIPs成功地从鸡蛋白中分离和浓缩了溶菌酶,在工业蛋白质纯化,基础生物医学研究和临床诊断中显示出潜在价值。

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