Université de Lyon, Institut des Sciences Analytiques, UMR 5280, CNRS, Université Lyon 1, ENS Lyon, 5 rue de la Doua, 69100, Villeurbanne, France; Oril Industrie, 13 rue Auguste Desgenetais, 76210, Bolbec, France.
Oril Industrie, 13 rue Auguste Desgenetais, 76210, Bolbec, France.
J Pharm Biomed Anal. 2018 Sep 10;159:237-244. doi: 10.1016/j.jpba.2018.06.058. Epub 2018 Jun 30.
On-line selective comprehensive two-dimensional chromatography combining Reversed Phase Liquid Chromatography and Supercritical Fluid Chromatography (sRPLCxSFC) was investigated for the analysis of chiral pharmaceutical compounds. Preliminary studies were carried out with the aim of overcoming instrumental constraints which are related to such 2D-coupling. The impact of both injection solvent and injection volume on the chiral SFC second separation was assessed with a view to limiting injection effects due to mobile phase compatibility issues between both dimensions. The resulting on-line sRPLCxSFC system was applied to the achiral x chiral analysis of a pharmaceutical sample. Using an Acquity BEH C18 column in the first dimension and a Chiralpak IC column in the second one, both chemical (achiral) and enantiomeric (chiral) purities could be evaluated in less than 50 min within a single run. Under such conditions, a detection limit of about 0.5% for R-enantiomer could be obtained with UV detection. The results obtained in sRPLCxSFC were compared to those obtained in conventional chiral 1D-SFC. Baseline resolution was obtained in both cases and the linearity in the detector response was on the same order of magnitude (R² > 0.99). Finally, despite current instrumental limitations (no commercially available system for sLCxSFC, large dwell volume and large extra-column volume in SFC), the on-line coupling of RPLC and SFC appears to be attractive and promising for rapid achiral/chiral analysis of complex pharmaceutical samples.
在线选择综合二维色谱结合反相液相色谱和超临界流体色谱(sRPLCxSFC)用于分析手性药物化合物。初步研究旨在克服与二维耦合相关的仪器限制。评估了进样溶剂和进样体积对手性 SFC 第二分离的影响,以期限制由于两个维度之间的流动相兼容性问题引起的进样效应。所得在线 sRPLCxSFC 系统应用于药物样品的非对映异构体 x 对映异构体分析。在第一维中使用 Acquity BEH C18 柱,在第二维中使用 Chiralpak IC 柱,在单次运行中可在不到 50 分钟的时间内评估化学(非对映异构体)和对映异构体(对映异构体)纯度。在这种条件下,使用紫外检测可获得约 0.5%R-对映异构体的检测限。sRPLCxSFC 中获得的结果与常规手性一维 SFC 中获得的结果进行了比较。在两种情况下均获得基线分离,并且检测器响应的线性度处于同一数量级(R²>0.99)。最后,尽管存在当前的仪器限制(没有商业上可用的 sLCxSFC 系统,SFC 中的停留体积大和柱外体积大),但 RPLC 和 SFC 的在线耦合似乎对手性药物复杂样品的快速非对映异构体/对映异构体分析具有吸引力和前景。