Effect of Short-Chain Organic Acids, Cations and Anions on the Retention of Citicoline Under Hydrophilic Interaction Liquid Chromatography Conditions

IF 1.3 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Sofiane Derbouz, Moulay-Hassane Guermouche, Saliha Guermouche, Ouassila Ferroukhi
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引用次数: 0

Abstract

The optimization of mobile phase composition in HPLC is crucial for achieving excellent chromatographic performance. Mobile phase additives are very often added to control retention, resolution, peak shape and efficiency. According to the Hofmeister series, additives are classified into chaotropic and kosmotropic agents. When ionizable compounds are analysed by hydrophilic interaction liquid chromatography (HILIC), additives can control the electrostatic interactions and affect the chromatographic parameters. In this study, citicoline, a neurotransmitter, was analysed under HILIC conditions using various additives. Due to the solubility limit in high organic content, the composition of the mobile phase was fixed at a 2/1 (V/V) acetonitrile/water ratio, and the salt concentration set to 25 mM. A total of 21 additives were tested, including short-chain organic acids (formic, acetic, propionic, trifluoroacetic and trichloroacetic acid), cations (lithium, sodium, potassium and ammonium) and anions (acetate, bromide, chloride, dihydrogen citrate, dihydrogen phosphate, nitrate, perchlorate and tetrafluoroborate). With additive-free mobile phases, weak retention of citicoline was observed, which can be explained by the small thickness of the water layer on the surface of the silica stationary phase and electrostatic repulsion between deprotonated silanols and negatively charged citicoline. However, the use of additives improves retention. Short-chain organic acids increased retention, but produce poor peak shape. Cations affected retention in the following order: \({{\varvec{L}}{\varvec{i}}}^{+}<{{\varvec{N}}{\varvec{H}}}_{4}^{+}<{{\varvec{N}}{\varvec{a}}}^{+}<{{\varvec{K}}}^{+}\), corresponding to the reversed Hofmeister series. The anions trend was: \({{\varvec{C}}{\varvec{H}}}_{3}{\varvec{C}}{{\varvec{O}}{\varvec{O}}}^{-}<{{\varvec{H}}}_{2}{{\varvec{P}}{\varvec{O}}}_{4}^{-}<{{\varvec{B}}{\varvec{r}}}^{-}<{{\varvec{C}}{\varvec{l}}}^{-}<{{\varvec{H}}}_{2}{{\varvec{C}}{\varvec{i}}{\varvec{t}}{\varvec{r}}{\varvec{a}}{\varvec{t}}{\varvec{e}}}^{-}<{{\varvec{N}}{\varvec{O}}}_{3}^{-}<{{\varvec{C}}{\varvec{l}}{\varvec{O}}}_{4}^{-}<{{\varvec{B}}{\varvec{F}}}_{4}^{-}\), which corresponds to the direct Hofmeister series, except for acetate and dihydrogen phosphate.

Abstract Image

亲水条件下短链有机酸、阳离子和阴离子对胞胆碱保留的影响
高效液相色谱中流动相组成的优化是实现高效液相色谱的关键。经常添加流动相添加剂来控制保留、分辨率、峰形和效率。根据霍夫迈斯特级数,添加剂可分为向混沌剂和向宇宙剂。在亲水相互作用液相色谱(HILIC)分析可电离化合物时,添加剂可以控制静电相互作用并影响色谱参数。在本研究中,胞胆碱,一种神经递质,分析了在HILIC条件下使用各种添加剂。由于高有机含量的溶解度限制,流动相的组成固定为2/1 (V/V)乙腈/水比,盐浓度设定为25 mM。共测试了21种添加剂,包括短链有机酸(甲酸、乙酸、丙酸、三氟乙酸和三氯乙酸)、阳离子(锂、钠、钾和铵)和阴离子(乙酸、溴化物、氯化物、柠檬酸二氢、磷酸二氢、硝酸盐、高氯酸盐和四氟硼酸盐)。在无添加剂的流动相中,胞二磷胆碱的保留较弱,这可以解释为二氧化硅固定相表面的水层厚度较小以及去质子化硅烷醇与带负电荷的胞二磷胆碱之间的静电斥力。然而,添加剂的使用提高了保留率。短链有机酸增加了保留率,但产生峰形差。阳离子影响保留率的顺序如下:\({{\varvec{L}}{\varvec{i}}}^{+}<{{\varvec{N}}{\varvec{H}}}_{4}^{+}<{{\varvec{N}}{\varvec{a}}}^{+}<{{\varvec{K}}}^{+}\),对应于颠倒的霍夫迈斯特级数。除乙酸和磷酸二氢外,阴离子趋势为:\({{\varvec{C}}{\varvec{H}}}_{3}{\varvec{C}}{{\varvec{O}}{\varvec{O}}}^{-}<{{\varvec{H}}}_{2}{{\varvec{P}}{\varvec{O}}}_{4}^{-}<{{\varvec{B}}{\varvec{r}}}^{-}<{{\varvec{C}}{\varvec{l}}}^{-}<{{\varvec{H}}}_{2}{{\varvec{C}}{\varvec{i}}{\varvec{t}}{\varvec{r}}{\varvec{a}}{\varvec{t}}{\varvec{e}}}^{-}<{{\varvec{N}}{\varvec{O}}}_{3}^{-}<{{\varvec{C}}{\varvec{l}}{\varvec{O}}}_{4}^{-}<{{\varvec{B}}{\varvec{F}}}_{4}^{-}\),与直接Hofmeister系列相对应。
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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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