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聚乙烯亚胺功能化碳点及其前体共固定在硅胶上用于亲水作用色谱。

Polyethyleneimine-functionalized carbon dots and their precursor co-immobilized on silica for hydrophilic interaction chromatography.

机构信息

CAS Key Laboratory of Chemistry of Northwestern Plant Resources and Key Laboratory for Natural Medicine of Gansu Province, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, 730000, China; University of Chinese Academy of Sciences, Chinese Academy of Sciences, Beijing, 100039, China.

CAS Key Laboratory of Chemistry of Northwestern Plant Resources and Key Laboratory for Natural Medicine of Gansu Province, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, 730000, China.

出版信息

J Chromatogr A. 2019 Jul 19;1597:142-148. doi: 10.1016/j.chroma.2019.03.026. Epub 2019 Mar 18.

Abstract

A new strategy based on synergistic effect of the carbon dots and their precursor was proposed to enhance the selectivity of hydrophilic interaction liquid chromatography (HILIC). In this work, polyethyleneimine (PEI) and PEI-functionalized carbon dots (PEICDs) mix-grafted silica packing material was prepared to act as a novel HILIC stationary phase. Both inner and outer surface of the porous silica are decorated with the mixture of PEI and carbon dots. This stationary phase, namely Sil-PEI/CDs, demonstrate enhanced retention ability and selectivity toward polar analytes, with which 11 nucleosides and nucleobases and 9 ginsenosides can be nicely separated. The Sil-PEI/CDs (RSD 0.12% - 0.54%) exhibited even better stability than the traditional PEI modified stationary phase (RSD 0.39% - 0.87%) within 40 h of continuously elution. And excellent column efficiency was observed from Sil-PEI/CDs (∼65,000 plates/m for cytidine). The strategy of mixed stabilization revealed a new method to prepare good performanced carbon dots based chromatographic column.

摘要

提出了一种基于碳点及其前体协同效应的新策略,以增强亲水性相互作用液相色谱(HILIC)的选择性。在这项工作中,制备了聚乙烯亚胺(PEI)和 PEI 功能化碳点(PEICDs)混合接枝硅胶填充材料,用作新型 HILIC 固定相。多孔硅胶的内表面和外表面都用 PEI 和碳点的混合物进行了修饰。这种固定相,即 Sil-PEI/CDs,表现出对极性分析物更强的保留能力和选择性,可将 11 种核苷和碱基以及 9 种人参皂苷很好地分离。Sil-PEI/CDs(RSD 0.12% - 0.54%)在连续洗脱 40 小时内表现出比传统的 PEI 改性固定相(RSD 0.39% - 0.87%)更好的稳定性。从 Sil-PEI/CDs (约 65,000 板/m 用于胞嘧啶)观察到出色的柱效。混合稳定策略为制备性能良好的基于碳点的色谱柱提供了一种新方法。

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