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基于化学计量学设计和分析的非水亲水性相互作用和超临界流体色谱中咪唑啉和哌嗪类化合物的保留机制。

Retention mechanisms of imidazoline and piperazine-related compounds in non-aqueous hydrophilic interaction and supercritical fluid chromatography based on chemometric design and analysis.

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, Belgrade 11000, Serbia.

Chair and Department of Medical Chemistry, Faculty of Pharmacy, Medical University of Lublin, Jaczwsjiego 4, Lublin 20-090, Poland.

出版信息

J Chromatogr A. 2022 Aug 16;1678:463340. doi: 10.1016/j.chroma.2022.463340. Epub 2022 Jul 13.

Abstract

The experimental design methodology based on central composite design of experiments was applied to compare the retention mechanisms in supercritical fluid chromatography (SFC) and non-aqueous hydrophilic interaction liquid chromatography (NA-HILIC). The selected set consists of 26 compounds that belong to imidazoline and serotonin receptor ligands. The different chemometric tools (multiple linear regression, principal component analysis, parallel factor analysis) were used to examine the retention, as well as to identify the most significant retention mechanisms. The retention mechanism was investigated on two different stationary phases (diol, and mixed-mode diol). In NA-HILIC, the mobile phase contains acetonitrile as a main component, and methanolic solution of ammonium formate (+ 0.1% of formic acid) as a modifier. The same mobile phase modifier was used in SFC, with a difference in the main component of the mobile phase which was CO. The retention behaviour differs significantly between HILIC and SFC conditions. The retention pattern in HILIC mode was more partition-like, while in SFC the solute-sorbent interactions allowed retention. The retention mechanism between mixed-mode diol and the diol phases varies depending on the applied chromatographic mode, e.g., in HILIC the type of stationary phase significantly affects the elution order, while in SFC this was not the case. The HILIC retention behaviour was influenced by the number of tertiary amines-aliphatic, and N atom-centred fragments in tested compounds. On the other hand, the number of pyrrole and pyridine rings in the structure of the compound showed correlation with their SFC retention, simultaneously increasing the molecular weight and rapid elution of larger compounds. It was found that temperature surprisingly plays a major role in SFC mode. The increase in temperature reduces the relative contribution of enthalpy factors to total retention, so the separation in SFC was more entropy-controlled. For further pharmaceutical research and optimization, the SFC would be considered more beneficial compared to HILIC since it gives good selectivity in separation of chosen impurities.

摘要

基于中心复合实验设计的实验设计方法被应用于比较超临界流体色谱(SFC)和非水亲水性相互作用液相色谱(NA-HILIC)中的保留机制。所选的化合物集包括 26 种属于咪唑啉和血清素受体配体的化合物。使用不同的化学计量学工具(多元线性回归、主成分分析、平行因子分析)来检查保留情况,并确定最重要的保留机制。在两种不同的固定相(二醇和混合模式二醇)上研究了保留机制。在 NA-HILIC 中,流动相主要包含乙腈,甲醇溶液中的甲酸铵(+0.1%的甲酸)作为改性剂。在 SFC 中使用相同的流动相改性剂,只是流动相的主要成分不同,为 CO。HILIC 和 SFC 条件下的保留行为有很大的不同。在 HILIC 模式下,保留模式更像是分配,而在 SFC 中,溶质-固定相的相互作用允许保留。混合模式二醇和二醇相之间的保留机制因所应用的色谱模式而异,例如,在 HILIC 中,固定相的类型对洗脱顺序有显著影响,而在 SFC 中则不是。HILIC 的保留行为受到测试化合物中叔胺-脂肪族和 N 原子中心片段的数量的影响。另一方面,化合物结构中的吡咯环和吡啶环的数量与它们在 SFC 中的保留呈相关性,同时增加了分子量,使较大的化合物快速洗脱。研究发现,温度在 SFC 模式中出人意料地起着重要作用。温度的升高降低了焓因素对总保留的相对贡献,因此 SFC 中的分离更多是熵控制的。对于进一步的药物研究和优化,与 HILIC 相比,SFC 会被认为更有利,因为它在分离所选杂质方面具有良好的选择性。

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