Department of Drug Chemistry and Technology , "Sapienza" University of Rome , P. le Aldo Moro 5 , 00185 Roma , Italy.
School of Pharmaceutical Sciences , University of Geneva , Rue Michel Servet, 1 , 1211 Geneva , 4, Switzerland.
Anal Chem. 2018 Sep 18;90(18):10828-10836. doi: 10.1021/acs.analchem.8b01907. Epub 2018 Sep 5.
This proof-of-concept work investigates the ultimate kinetic limits reachable in chiral supercritical fluid chromatography (SFC) with modern columns and advanced technological solutions. A commercial equipment (Waters Acquity UPC) has been in-house modified to minimize its overall extra-column variance through a series of technical adjustments including low-volume connecting tubings, reduced-volume flow cell, an in-house made external column oven, external low-dispersion injection system, and electronic temperature controller. Compared to the original (as-shipped) configuration, the extra-column variance on the low-dispersion equipment was reduced by more than 97%, from about 85 to slightly more than 2 μL (measured at 2.0 mL/min). This was mainly achieved thanks to the occurrence of fully developed turbulent regime with a proper selection of capillary i.d. at significantly smaller flow rates (1.5-4 mL/min; CO/methanol 80/20, v/v; 35 °C; back pressure regulator (BPR), 105 bar) than in entry-1 configuration. Ultrahigh efficiency columns of different geometries in-house packed with latest generation sub-2 μm UHPC-FPP-Whelk-O1 Chiral Stationary Phase (CSP) have been employed under sub- and supercritical fluid conditions. By carefully modulating the length and the internal diameter of connecting tubings in the function of column geometry, state of the art efficiencies (estimated in roughly 300 000 theoretical plates/m with reduced HETP of roughly 1.85) have been obtained on 4.6 mm i.d. chiral columns. Remarkably, for 3.0 mm × 100 mm (i.d. × length) columns, the efficiency gain on the fully modified SFC system (compared to an instrumental configuration where only the standard injector was replaced by the low-dispersion one) was greater than 90% for compounds with a retention factor of 1 and as large as 25% for retention factors of 2.5.
这项概念验证工作研究了现代色谱柱和先进技术解决方案在手性超临界流体色谱(SFC)中所能达到的最终动力学极限。一台商业设备(Waters Acquity UPC)经过内部改装,通过一系列技术调整,包括小体积连接管、小体积流通池、自制外部柱箱、内部低分散进样系统和电子温度控制器,最大限度地减少其整体柱外方差。与原始(发货)配置相比,低分散设备的柱外方差降低了 97%以上,从大约 85 微升至略高于 2 微升(在 2.0 毫升/分钟下测量)。这主要是由于在较小的流速(1.5-4 毫升/分钟;CO/甲醇 80/20,体积比;35°C;背压调节器(BPR),105 巴)下,通过适当选择毛细管内径,实现了完全发展的湍流状态,而在入口 1 配置下的流速要大得多。不同几何形状的超高效柱在亚临界和超临界流体条件下采用最新一代亚 2 微米 UHPC-FPP-Whelk-O1 手性固定相(CSP)进行内部装填。通过仔细调节连接管的长度和内径与柱几何形状的关系,在 4.6 毫米内径手性柱上获得了接近 300000 理论板/米的超高效率(通过大约 1.85 的 HETP 估算)。值得注意的是,对于 3.0 毫米×100 毫米(内径×长度)的柱子,与仅将标准进样器更换为低分散进样器的仪器配置相比,在完全改装的 SFC 系统上的效率增益对于保留因子为 1 的化合物大于 90%,对于保留因子为 2.5 的化合物则高达 25%。