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用于表征磷酰二胺吗啉代寡聚物的二维液相色谱/质谱工作流程的开发。

Development of a two-dimensional liquid chromatography/mass spectrometry workflow for characterization of phosphorodiamidate morpholino oligomers.

作者信息

Wei Tao, Wang Mingming, Cai Bao Zhong

机构信息

Process Development, Sarepta Therapeutics, Inc., Cambridge, MA 02142, USA.

Process Development, Sarepta Therapeutics, Inc., Cambridge, MA 02142, USA.

出版信息

J Chromatogr A. 2025 Aug 30;1757:466129. doi: 10.1016/j.chroma.2025.466129. Epub 2025 Jun 6.

Abstract

A sensitive two-dimensional liquid chromatography/mass spectrometry (2D-LC/MS) workflow was developed for characterization of phosphorodiamidate morpholino oligomers (PMOs) for the first time. This workflow employed strong cation exchange chromatography (SCX) as the first dimension (D), and hydrophilic interaction chromatography (HILIC) as the second dimension (D), with ammonium formate as MS-compatible salt in both dimensions. Peaks of interest were collected using multiple heart cutting (MHC) and transferred to D HILIC for online desalting and orthogonal separation prior to high resolution MS (HR-MS) analysis for impurity identification. Active solvent modulation (ASM) was utilized to address the elution strength incompatibility between D SCX and D HILIC, allowing for improved peak shape leading to enhanced resolution, and increased peak capacity by the 2D-LC approach. This workflow was initially demonstrated by analyzing a 30-mer PMO spiked with n-1 deletion impurity markers and was subsequently applied to effectively elucidate the impurity profiles of three PMO drug substances (ranging from 22-mer to 30-mer), affording identification of impurities at low levels. The impurity profiles suggested common impurity classes were formed in the PMOs, despite varying lengths or sequences, and were structurally related to their parent PMOs. This 2D-LC/MS workflow improves PMO impurity characterization by increasing peak capacity, providing high MS sensitivity, and enabling streamlined impurity analysis with short data turnaround time.

摘要

首次开发了一种灵敏的二维液相色谱/质谱联用(2D-LC/MS)工作流程,用于对磷酰二胺吗啉代寡聚物(PMO)进行表征。该工作流程采用强阳离子交换色谱(SCX)作为第一维(D1),亲水相互作用色谱(HILIC)作为第二维(D2),在两个维度中均使用甲酸铵作为与质谱兼容的盐。使用多次中心切割(MHC)收集感兴趣的峰,并将其转移至D2 HILIC进行在线脱盐和正交分离,然后进行高分辨率质谱(HR-MS)分析以鉴定杂质。利用活性溶剂调制(ASM)解决D1 SCX和D2 HILIC之间的洗脱强度不兼容性问题,从而改善峰形,提高分辨率,并通过二维液相色谱方法增加峰容量。该工作流程最初通过分析添加了n-1缺失杂质标记物的30聚体PMO进行了验证,随后应用于有效阐明三种PMO原料药(22聚体至30聚体)的杂质谱,能够鉴定低水平的杂质。杂质谱表明,尽管PMO的长度或序列不同,但在其中形成了常见的杂质类别,并且这些杂质在结构上与其母体PMO相关。这种二维液相色谱/质谱联用工作流程通过增加峰容量、提供高质谱灵敏度以及实现具有短数据周转时间的简化杂质分析,改进了PMO杂质表征。

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