Lovejoy Lauren Kline, Foley Joe P
R&D Medicine Development and Supply, Analytical Development, GSK, Collegeville, PA 19426, USA; Drexel University, Department of Chemistry, 32 South 32nd St., Disque Hall 305, Philadelphia, PA 19104, USA.
Drexel University, Department of Chemistry, 32 South 32nd St., Disque Hall 305, Philadelphia, PA 19104, USA.
J Chromatogr A. 2024 Aug 30;1731:465178. doi: 10.1016/j.chroma.2024.465178. Epub 2024 Jul 20.
This paper discusses the development of an analytical method by an alternative separation approach, sequential elution liquid chromatography (SE-LC), to separate permanently charged ions (anions), weak acids, and neutral compounds using anion exchange and reversed-phase columns in tandem. SE-LC separates classes of compounds by group by employing two or more elution modes. Advantages to using SE-LC over conventional HPLC are a greater peak capacity and a reduced separation disorder. Importantly, the same HPLC as used for a conventional HPLC separation may be used to afford a successful SE-LC separation. Mobile phase selection and gradient optimization are integral for a successful SE-LC class separation of permanent anions, weak acids, and neutral compounds and will be discussed in detail in this paper. The most successful (best resolution and repeatability) SE-LC separation was achieved by applying isocratic elution at low pH to elute the weak acids, followed by an acetonitrile gradient to elute the neutral compounds, and last a sodium methanesulfonate gradient to elute the anionic compounds using a superficially porous C18 column coupled with a strong anion exchange (SAX) column. Repeatability (RSD) in the retention times and peak areas of the analytes was less than 0.25 % and 1.5 %, respectively.
本文讨论了一种分析方法的开发,该方法采用一种替代分离方法——顺序洗脱液相色谱法(SE-LC),通过串联使用阴离子交换柱和反相柱来分离永久带电离子(阴离子)、弱酸和中性化合物。SE-LC通过采用两种或更多种洗脱模式按组分离化合物类别。与传统高效液相色谱法(HPLC)相比,使用SE-LC的优势在于更大的峰容量和减少的分离紊乱。重要的是,用于传统HPLC分离的同一台HPLC可用于成功进行SE-LC分离。流动相的选择和梯度优化对于成功实现永久阴离子、弱酸和中性化合物的SE-LC类别分离至关重要,本文将对此进行详细讨论。最成功(分辨率和重复性最佳)的SE-LC分离是通过在低pH下采用等度洗脱来洗脱弱酸,然后采用乙腈梯度洗脱中性化合物,最后采用甲磺酸钠梯度洗脱阴离子化合物实现的,使用的是表面多孔C18柱与强阴离子交换(SAX)柱联用。分析物保留时间和峰面积的重复性(相对标准偏差,RSD)分别小于0.25%和1.5%。