首页> 外文期刊>International journal of applied mechanics >PEGylated Thermo-Sensitive Bionic Magnetic Core-Shell Structure Molecularly Imprinted Polymers Based on Halloysite Nanotubes for Specific Adsorption and Separation of Bovine Serum Albumin
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PEGylated Thermo-Sensitive Bionic Magnetic Core-Shell Structure Molecularly Imprinted Polymers Based on Halloysite Nanotubes for Specific Adsorption and Separation of Bovine Serum Albumin

机译:基于Holloysite纳米管的聚乙二醇化热敏仿生磁芯 - 壳结构分子印迹聚合物,用于牛血清白蛋白的特异性吸附和分离

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摘要

Novel PEGylated thermo-sensitive bionic magnetic core-shell structure molecularly imprinted polymers (PMMIPs) for the specific adsorption and separation of bovine serum albumin (BSA) were obtained via a surface-imprinting technique. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), fourier transform infrared spectrometry (FT-IR), thermal gravimetric analysis (TGA), and specific surface area (BET), were adopted to demonstrate that novel PMMIPs were successfully synthesized. Subsequently, the prepared PMMIPs were used as the extractor for BSA and were combined with magnetic solid-phase extraction. The concentrations of BSA were detected by UV-vis spectrophotometry at 278 nm. The maximum adsorption capacity of the PMMIPs was 258 mg g(-1), which is much higher than that of non-imprinted polymer (PMNIPs). PMMIPs showed favorable selectivity for BSA against reference proteins, i.e., bovine hemoglobin, ovalbumin and lysozyme. PMMIPs were further used to recognize BSA in protein mixtures, milk, urine and sewage, these results revealed that approximately 96% of the ideal-state adsorption capacity of PMMIPs for BSA was achieved under complicated conditions. Regeneration and reusability studies demonstrated that adsorption capacity loss of the PMMIPs was not obvious after recycling for four times. Facile synthesis, excellent adsorption property and efficient selectivity for BSA trapping are features that highlight PMMIPs as an attractive candidate for biomacromolecular purification.
机译:通过表面积压印技术获得新型聚乙二醇化热敏仿生磁芯 - 壳结构的特异性吸附和分离牛血清白蛋白(BSA)。 X射线衍射(XRD),扫描电子显微镜(SEM),透射电子显微镜(TEM),振动样品磁体(VSM),傅里叶变换红外光谱(FT-IR),热重分析(TGA)和特定表面积(赌注)被采用证明新型PMMIP已成功综合。随后,使用制备的PMMIPS作为BSA的提取器,与磁性固相萃取组合。通过UV-Vis分光光度法在278nm处检测BSA的浓度。 PMMIP的最大吸附容量为258mg G(-1),远高于非印记聚合物(PMNIPS)。 PMMIPS对BSA对参考蛋白质,即牛血红蛋白,卵烧蛋白和溶菌酶进行了有利的选择性。 PMMIPS进一步用于识别蛋白质混合物,牛奶,尿液和污水中的BSA,这些结果表明,在复杂条件下,在BSA的PMMIPS的理想状态吸附能力约为96%。再生和可重用性研究表明,在回收4次后,PMMIPS的吸附能力损失并不明显。容易合成,优异的BSA诱捕性和有效的选择性是突出PMMIPS作为生物统治纯化有吸引力的候选的特征。

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