首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Preparation of magnetic molecularly imprinted polymers based on a deep eutectic solvent as the functional monomer for specific recognition of lysozyme
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Preparation of magnetic molecularly imprinted polymers based on a deep eutectic solvent as the functional monomer for specific recognition of lysozyme

机译:基于深度共晶溶剂的磁性分子印迹聚合物作为溶菌酶特异性识别的功能单体的制备

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摘要

A magnetized molecularly imprinted polymer (MIP) was prepared via a surface-imprinting technique. An allyl-based deep eutectic solvent was chosen as the functional monomer to obtain the polymer for specific recognition of lysozyme. It was deposited on silica-coated magnetite nanoparticles. The structure of the polymer was confirmed by X-ray diffraction, Fourier transform infrared spectrometry, transmission electron microscopy, thermogravimetric analysis and vibrating sample magnetometry. The maximum binding capacity of the imprinted polymer is found to be 108 mg center dot g(-1), which is higher than that of non-imprinted polymer. Compared to reference proteins such as cytochrome C, bovine hemoglobin and bovine serum albumin, the MIP shows favorable selectivity for lysozyme. Besides, the imprinted polymer can be further used to specifically recognize lysozyme from the protein mixture and chicken egg white. Reusability studies demonstrate that the polymer can be recycled four times without significant loss of adsorption capacity. The LOD of the method is 12.8 mu g center dot mL(-1). The relative standard deviations (for n = 3) are 1.38% for precision and 2.76% for repeatability. Its facile synthesis, high adsorption performance and excellent selectivity to capture lysozyme make this polymer an attractive candidate to be applied in biomacromolecular purification.
机译:通过表面积压印技术制备磁化分子印迹聚合物(MIP)。选择基于烯丙基的深共晶溶剂作为功能性单体,得到聚合物,用于特异性识别溶菌酶。它沉积在二氧化硅涂覆的磁铁矿纳米粒子上。通过X射线衍射,傅里叶变换红外光谱,透射电子显微镜,热重分析和振动样品磁力证实了聚合物的结构。发现印迹聚合物的最大结合能力为108mg中心点G(-1),其高于非印记聚合物的中心点G(-1)。与参考蛋白如细胞色素C,牛血红蛋白和牛血清白蛋白相比,MIP显示出溶菌酶的有利选择性。此外,印迹聚合物可以进一步用于特异性地识别来自蛋白质混合物和鸡蛋白的溶菌酶。可重用性研究表明,聚合物可以再循环四次,而不会显着损失吸附能力。该方法的床位是12.8μg中心点M1(-1)。相对标准偏差(对于n = 3)为精度为1.38%,可重复性为2.76%。其容易合成,高吸附性能和优异的捕获溶菌酶的选择性使得该聚合物是待应用于生物重致纯化的有吸引力的候选者。

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