聚合物基氨基酸固定相的制备及其在混合模式色谱中的应用

IF 1.2 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS Chromatographia Pub Date : 2024-02-06 DOI:10.1007/s10337-024-04311-5
Hanlin Zeng, Jingdong Peng, Huanjun Peng, Xiang Wang, Zilong Zhang, Hanqi Yang, Jiayu Yu, Jiajia Wu
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引用次数: 0

摘要

聚合物微球因其优异的性能而备受关注。本研究制备了一种聚合物基质的两性离子氨基酸固定相。以甲基丙烯酸聚缩水甘油酯二乙烯基苯(PGMA-DVB)微球为基质,通过环氧基团在 PGMA-DVB 微球基质表面的开环反应,成功地对 L-苯丙氨酸进行了改性。通过扫描电子显微镜、傅立叶变换红外光谱和元素分析对固定相进行了表征。苯丙氨酸修饰的固定相被用于 RPLC/HILIC 混合模式色谱,分别分离烷基苯、多环芳烃、酚类、核苷和核酸等探针。通过分离联苯异构体,证明了该固定相具有良好的空间选择性。所制备的固定相在碱性条件下(pH = 10)具有良好的稳定性,在有机溶剂流动相中的溶胀性较低。同时,该固定相在分离不同维生素(Rs > 5.3)以及分离和检测河水中的多环芳烃方面也表现出良好的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Preparation of Polymer-Based Amino Acid Stationary Phase and Its Application for Mixed-Mode Chromatography

Polymer microspheres have received attention because of their excellent properties. In this work, a polymer matrix zwitterionic amino acid stationary phase was prepared. Polyglycidyl methacrylate divinylbenzene (PGMA-DVB) microspheres was used as the matrix and successful modification with L-phenylalanine by ring-opening reaction of epoxy groups on the surface of PGMA-DVB microsphere matrix. The stationary phase was characterized by scanning electron microscopy, Fourier-transform infrared spectra, and elemental analysis. The phenylalanine-modified stationary phase was used in RPLC/HILIC mixed-mode chromatography for the separation of alkylbenzenes, polycyclic aromatic hydrocarbons, phenols, nucleosides and nucleic acids and etc. as probes, respectively. The good spatial selectivity of the stationary phase was demonstrated by the separation of biphenyl isomers. The prepared stationary phase showed good stability in alkaline condition (pH = 10) and low swelling in organic solvent mobile phase. Meanwhile, the stationary phase also showed good performance in the separation of different vitamins (Rs > 5.3), and the separation and detection of PAHs in river water.

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来源期刊
Chromatographia
Chromatographia 化学-分析化学
CiteScore
3.40
自引率
5.90%
发文量
103
审稿时长
2.2 months
期刊介绍: Separation sciences, in all their various forms such as chromatography, field-flow fractionation, and electrophoresis, provide some of the most powerful techniques in analytical chemistry and are applied within a number of important application areas, including archaeology, biotechnology, clinical, environmental, food, medical, petroleum, pharmaceutical, polymer and biopolymer research. Beyond serving analytical purposes, separation techniques are also used for preparative and process-scale applications. The scope and power of separation sciences is significantly extended by combination with spectroscopic detection methods (e.g., laser-based approaches, nuclear-magnetic resonance, Raman, chemiluminescence) and particularly, mass spectrometry, to create hyphenated techniques. In addition to exciting new developments in chromatography, such as ultra high-pressure systems, multidimensional separations, and high-temperature approaches, there have also been great advances in hybrid methods combining chromatography and electro-based separations, especially on the micro- and nanoscale. Integrated biological procedures (e.g., enzymatic, immunological, receptor-based assays) can also be part of the overall analytical process.
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