Department of Chemistry and Polymer Science , Stellenbosch University , Private Bag X1 , Matieland 7602 , South Africa.
Institute of Viticulture and Oenology , DLR Rheinpfalz , Neustadt an der Weinstraße 67435 , Germany.
Anal Chem. 2018 Oct 2;90(19):11643-11650. doi: 10.1021/acs.analchem.8b03234. Epub 2018 Sep 20.
Comprehensive two-dimensional liquid chromatography (LC × LC) and ion mobility spectrometry-mass spectrometry (IMS-MS) are increasingly being used to address challenges associated with the analysis of highly complex samples. In this work, we evaluate the potential of the combination of these techniques in the form of a comprehensive three-dimensional LC × LC × IMS separation system. As application, hydrophilic interaction chromatography (HILIC) × reversed phase LC (RP-LC) × IMS-high-resolution MS (HR-MS) was used to analyze a range of phenolic compounds, including hydrolyzable and condensed tannins, flavonoids, and phenolic acids in several natural products. A protocol for the extraction and visualization of the four-dimensional data obtained using this approach was developed. We show that the combination of HILIC, RP-LC, and IMS offers excellent separation of complex phenolic samples in three dimensions. Benefits associated with the incorporation of IMS include improved MS sensitivity and mass-spectral data quality. IMS also provided separation of trimeric procyanidin isomeric species that could not be differentiated by HILIC × RP-LC or HR-MS. On the traveling wave IMS (TWIMS) system used here, both IMS separation performance and the extent of second dimension (D) undersampling depend on the upper mass scan limit, which might present a limitation for the analysis of larger molecular ions. The performance of the LC × LC × IMS system was characterized in terms of practical peak capacity and separation power, using established theory and taking undersampling and orthogonality into account. An average increase in separation performance by a factor of 13 was found for the samples analyzed here when IMS was incorporated into the HILIC × RP-LC-MS workflow.
二维液相色谱(LC×LC)和离子淌度谱-质谱联用(IMS-MS)技术越来越多地被用于解决高度复杂样品分析所面临的挑战。在这项工作中,我们评估了这两种技术相结合的潜力,即建立一个全面的三维 LC×LC×IMS 分离系统。作为应用实例,亲水作用色谱(HILIC)×反相液相色谱(RP-LC)×IMS-高分辨质谱(HR-MS)被用于分析一系列酚类化合物,包括几种天然产物中的可水解和缩合单宁、类黄酮和酚酸。本研究开发了一种提取和可视化该方法获得的四元数据的方案。结果表明,HILIC、RP-LC 和 IMS 的组合在三维空间内提供了对复杂酚类样品的优异分离。将 IMS 纳入其中的好处包括提高了 MS 灵敏度和质谱数据质量。IMS 还提供了无法通过 HILIC×RP-LC 或 HR-MS 区分的三聚原花青素异构体的分离。在本研究中使用的行波 IMS(TWIMS)系统中,IMS 分离性能和二维(D)欠采样的程度取决于上质量扫描极限,这可能对分析更大的分子离子存在限制。采用已建立的理论并考虑欠采样和正交性,从实际峰容量和分离能力的角度对 LC×LC×IMS 系统的性能进行了表征。当将 IMS 纳入 HILIC×RP-LC-MS 工作流程时,发现这里分析的样品的分离性能平均提高了 13 倍。