Department of Engineering and Chemical Sciences, Karlstad University, Karlstad SE-651 88, Sweden.
Anal Chem. 2021 Apr 27;93(16):6385-6393. doi: 10.1021/acs.analchem.0c05142. Epub 2021 Apr 12.
A strategy to match any retention shifts due to increased or decreased pressure drop during supercritical fluid chromatography (SFC) method transfer is presented. The strategy relies on adjusting the co-solvent molarity without the need to adjust the back-pressure regulator. Exact matching can be obtained with minimal changes in separation selectivity. To accomplish this, we introduce the isomolar plot approach, which shows the variation in molar co-solvent concentration depending on the mass fraction of co-solvent, pressure, and temperature, here exemplified by CO-methanol. This plot allowed us to unify the effects of the co-solvent mass fraction and density on retention in SFC. The approach, which was verified on 12 known empirical retention models for each enantiomer of six basic pharmaceuticals, allowed us to numerically calculate the apparent retention factor for any column pressure drop. The strategy can be implemented either using a mechanistic approach if retention models are known or empirically by iteratively adjusting the co-solvent mass fraction. As a rule of thumb for the empirical approach, we found that the relative mass fraction adjustment needed is proportional to the relative change in the retention factor caused by a change in the pressure drop. Different proportionality constants were required to match retention in the case of increasing or decreasing pressure drops.
提出了一种策略,以匹配由于超临界流体色谱 (SFC) 方法转移过程中压降增加或减少而导致的任何保留移动。该策略依赖于调整共溶剂的摩尔浓度,而无需调整背压调节阀。通过最小的分离选择性变化可以实现精确匹配。为了实现这一点,我们引入了等摩尔图方法,该方法显示了摩尔共溶剂浓度随共溶剂质量分数、压力和温度的变化,这里以 CO-甲醇为例。该图允许我们统一 SFC 中共溶剂质量分数和密度对保留的影响。该方法在六种基本药物的每个对映体的 12 个已知经验保留模型上进行了验证,允许我们数值计算任何柱压降的表观保留因子。该策略可以通过使用已知保留模型的机械方法或通过迭代调整共溶剂质量分数的经验方法来实现。对于经验方法,我们发现相对质量分数调整的需要与由压降变化引起的保留因子的相对变化成正比。对于增加或减少压降的情况,需要不同的比例常数来匹配保留。