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Development of a membrane solid-phase extraction method based on polyethyleneimine modified MWNTs for on-line extraction and preconcentration of acidic proteins in serum samples

机译:基于聚乙烯亚胺修饰的多壁碳纳米管的膜固相萃取方法的在线提取和血清样品中酸性蛋白的预浓缩

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A membrane solid-phase extraction method based on polyethyleneimine modified multi-walled carbon nanotubes (MWNTs) for the on-line separation and concentration of acidic proteins in serum sample, followed by UV-Vis spectrophotometric determination, is developed. In this study, the polyethyleneimine was noncovalently adsorbed on the outer surface of the MWNTs and then the polyethyleneimine modified MWNTs (PEIa€“MWNTs) were filtered through a membrane to form an adsorbent layer. The alkalescent PEI coating provided high-density homogeneous functional groups on MWNTs' sidewall and led to homogeneous dispersion of MWNTs in aqueous solutions. The PEIa€“MWNTs membrane was applied to on-line separation of proteins in serum and exhibited excellent extraction and concentration ability for acidic proteins. Factors, which affected the efficiency of proteins extraction and their subsequent spectrophotometric determination, were studied and optimized. Under optimized conditions, the retention and recovery efficiencies of 100% and 92% for 25 ??g mLa?’1 of BSA solution were achieved, along with a RSD value of 1.9% at a flow rate of 30 ??L sa?’1. The limit of method detection was 1.0 ??g mLa?’1 with an enrichment factor of 12. The maximum adsorption capacity for BSA was 112 mg ga?’1 MWNTs. The method was applied to isolating acidic proteins from bovine serum sample and obtained satisfactory results.
机译:建立了一种基于聚乙烯亚胺修饰的多壁碳纳米管(MWNTs)的膜固相萃取方法,用于血清样品中酸性蛋白的在线分离和浓缩,然后进行紫外可见分光光度法测定。在这项研究中,聚乙烯亚胺非共价吸附在MWNTs的外表面上,然后将聚乙烯亚胺改性的MWNTs(PEIa“ MWNTs)通过膜过滤,形成吸附剂层。碱性PEI涂层在MWNT的侧壁上提供了高密度的均质官能团,并导致MWNT在水溶液中的均匀分散。 PEIa?MWNTs膜用于在线分离血清中的蛋白质,对酸性蛋白质具有优异的提取和浓缩能力。研究和优化了影响蛋白质提取效率及其后续分光光度法测定的因素。在最佳条件下,对于25 ?? g mLa?'1的BSA溶液,保留和回收效率分别为100%和92%,在30 ?? L sa?'的流速下的RSD值为1.9%。 1。方法检测的极限为1.0 ?? g mLa?1,富集系数为12。BSA的最大吸附容量为112 mg ga?'1 MWNTs。该方法用于牛血清样品中酸性蛋白的分离,获得了满意的结果。

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