Institute of Pharmaceutical Sciences, Pharmaceutical (Bio-)Analysis, University of Tübingen, Auf der Morgenstelle 8, 72076 Tübingen, Germany.
Institute of Pharmaceutical Sciences, Pharmaceutical (Bio-)Analysis, University of Tübingen, Auf der Morgenstelle 8, 72076 Tübingen, Germany; Chair of Environmental Chemistry and Bioanalytics, Faculty of Chemistry, Nicolaus Copernicus University in Torun, 7 Gagarin Str., PL-87-100 Toruń, Poland.
J Chromatogr A. 2023 Jul 19;1701:464069. doi: 10.1016/j.chroma.2023.464069. Epub 2023 May 14.
With the increasing numbers of nucleic acid-based pharmaceuticals like antisense oligonucleotides (ASO), small interfering ribonucleic acid (siRNA) entering the market, research facilities, pharmaceutical industries and also regulatory authorities have been looking for efficient analytical methods for these synthetic oligonucleotides (ON). Besides of conventional one-dimensional (1D) reversed-phase liquid chromatography with or without ion-pairing (IP-RP-LC, RP-LC), hydrophilic liquid chromatography (HILIC) and mixed-mode chromatography (MMC), two-dimensional (2D) approaches combining two orthogonal chromatographic techniques also become more relevant due to the high structural complexity of oligonucleotides. Recently, we tested a polybutylene terephthalate(PBT)-based stationary phase under ion-pairing free RP mode for the liquid chromatography electrospray ionization mass spectrometry (LC-ESI-MS) analysis of siRNA (Patisiran). In this study, retention profile and chromatographic orthogonality, respectively, were compared to other LC-modes like HILIC, IP-RPLC, another ion-pair free cholesterol-bonded RPLC and MMC considering their normalized retention times. Finally, because of higher orthogonality, the ion-pairing free PBT-bonded RPLC as first dimension (D) was hyphenated with HILIC in the second dimension (D) in a selective comprehensive 2D-LC setup leading to an enhanced resolution for peak purity evaluation of the main ON entities.
随着越来越多的基于核酸的药物,如反义寡核苷酸 (ASO)、小干扰核糖核酸 (siRNA) 进入市场,研究机构、制药行业和监管机构一直在寻找这些合成寡核苷酸 (ON) 的有效分析方法。除了常规的一维(1D)反相液相色谱法(带或不带离子对)(IP-RP-LC、RP-LC)、亲水液相色谱法(HILIC)和混合模式色谱法(MMC)外,由于寡核苷酸的结构高度复杂,二维(2D)方法结合两种正交色谱技术也变得更加相关。最近,我们在无离子对反相模式下测试了一种基于聚对苯二甲酸丁二醇酯 (PBT) 的固定相,用于液相色谱-电喷雾电离质谱 (LC-ESI-MS) 分析 siRNA(Patisiran)。在这项研究中,分别根据归一化保留时间,与其他 LC 模式(如 HILIC、IP-RPLC、另一种无离子对的胆固醇键合反相 HPLC 和 MMC)比较保留特征和色谱正交性。最后,由于更高的正交性,无离子对的 PBT 键合反相 HPLC 作为第一维(D)与第二维(D)的 HILIC 串联,在选择性综合 2D-LC 装置中实现了主要 ON 实体的峰纯度评估的增强分辨率。