Freie Universität Berlin, Institute of Pharmacy, Königin-Luise-Str. 2+4, 14195 Berlin, Germany.
Freie Universität Berlin, Institute of Pharmacy, Königin-Luise-Str. 2+4, 14195 Berlin, Germany.
J Pharm Biomed Anal. 2019 Jan 5;162:47-59. doi: 10.1016/j.jpba.2018.08.061. Epub 2018 Sep 3.
This review covers literature investigating methods for enantioselective chromatography using supercritical fluids as mobile phase constituents (SFC) in the field of bioanalysis. It provides an overview on method development and screening approaches published in scientific literature 2014-2018. Chiral stationary phases are used to create a chiral environment that allows for discrimination of enantiomers. Especially polysaccharide-based stationary phases are used in methods of recent investigations. In comparison to HPLC chiral SFC separation provides more selective cavity effects of inclusion-type chiral separation phases. Modifier and additive choices as well as further operating conditions like backpressure, temperature and flow rate are summarized and critically discussed. Further on, observed sample pretreatment and possible detection techniques are presented. SFC hyphenated to mass detection was found of major relevance and is therefore further discussed. Coupling of SFC with different detectors allows for straightforward use in bioanalysis. Interfacing MS detectors is generally performed including a make-up pump. Thus, applied make-up conditions were also reviewed. While most of the chiral separations in HPLC are performed in normal phase mode, and thus, challenge MS hyphenation, SFC-MS hyphenation can be easily achieved. This allows for convenient application in chiral trace analyses, often required in bioanalysis. Even worse in enantioseparation than in achiral chromatography, method development in SFC suffers from a lack of knowledge in separation mechanisms and thus approaches are often quite unique and most often achieved by screening using a One-Factor-at-a-Time (OFAT) design. Broad screening experiments with methodical approaches still appear as method of choice for now.
本文综述了使用超临界流体作为手性色谱流动相组成部分(SFC)在生物分析领域进行对映选择性色谱的文献。综述涵盖了 2014 年至 2018 年期间在科学文献中发表的方法开发和筛选方法。手性固定相用于创建手性环境,以实现对映异构体的区分。特别是多糖基固定相在最近研究方法中得到了广泛应用。与 HPLC 相比,手性 SFC 分离提供了更具选择性的包含型手性分离相的空腔效应。对改性剂和添加剂的选择以及其他操作条件(如背压、温度和流速)进行了总结和批判性讨论。此外,还介绍了观察到的样品预处理和可能的检测技术。SFC 与质谱检测联用被认为具有重要意义,因此进行了进一步讨论。SFC 与不同检测器的联用允许直接用于生物分析。接口 MS 检测器通常包括一个制备泵。因此,还审查了应用的制备条件。虽然大多数 HPLC 中的手性分离是在正相模式下进行的,因此对 MS 联用具有挑战性,但 SFC-MS 联用可以很容易地实现。这使得在生物分析中经常需要的痕量手性分析中可以方便地应用。与手性分析相比,在非手性色谱中,SFC 中的方法开发受到分离机制知识不足的限制,因此方法通常非常独特,并且最常通过使用 One-Factor-at-a-Time (OFAT) 设计进行筛选来实现。广泛的筛选实验和系统的方法仍然是目前的首选方法。