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开发一种通用的高通量寡核苷酸 LC-MS 方法以加速药物发现。

Development of a Versatile High-through-put Oligonucleotide LC-MS Method to Accelerate Drug Discovery.

机构信息

Pharmacokinetics, Dynamics, Metabolism, and Bioanalytics, Merck & Co., Inc., Boston, Massachusetts, 02115, USA.

Biology-Discovery, Merck & Co., Inc., West Point, Pennsylvania, 19446, USA.

出版信息

AAPS PharmSciTech. 2024 Oct 10;25(7):239. doi: 10.1208/s12249-024-02934-3.

Abstract

Liquid chromatography-mass spectrometry (LC-MS) is an effective tool for high-throughput quantification of oligonucleotides that is crucial for understanding their biological roles and developing diagnostic tests. This paper presents a high-throughput LC-MS/MS method that may be versatilely applied for a wide range of oligonucleotides, making it a valuable tool for rapid screening and discovery. The method is demonstrated using an in-house synthesized MALAT-1 Antisense oligonucleotide (ASO) as a test case. Biological samples were purified using a reversed liquid-liquid extraction process automated by a liquid handling workstation and analyzed with ion-pairing LC-MS/MS. The assay was evaluated for sensitivity (LLOQ = 2 nM), specificity, precision, accuracy, recovery, matrix effect, and stability in rat cerebrospinal fluid (CSF) and plasma. Besides some existing considerations such as column selection, ion-pairing reagent, and sample purification, our work focused on the following four subtopics: 1) selecting the appropriate Multiple Reaction Monitoring (MRM) transition to maximize sensitivity for trace-level ASO in biological samples; 2) utilizing a generic risk-free internal standard (tenofovir) to avoid crosstalk interference from the oligo internal standard commonly utilized in the LC-MS assay; 3) automating the sample preparation process to increase precision and throughput; and 4) comparing liquid-liquid extraction (LLE) and solid-phase extraction (SPE) as sample purification methods in oligo method development. The study quantified the concentration of MALAT-1 ASO in rat CSF and plasma after intrathecal injection and used the difference between the two matrices to evaluate the injection technique. The results provide a solid foundation for further internal oligonucleotide discovery and development.

摘要

液相色谱-质谱联用(LC-MS)是一种高通量定量寡核苷酸的有效工具,对于理解其生物学作用和开发诊断测试至关重要。本文提出了一种高通量 LC-MS/MS 方法,可广泛应用于多种寡核苷酸,是快速筛选和发现的有价值的工具。该方法使用内部合成的 MALAT-1 反义寡核苷酸(ASO)作为测试案例进行了演示。生物样品通过由液体处理工作站自动化的反相液-液萃取过程进行纯化,并采用离子对 LC-MS/MS 进行分析。该测定法的灵敏度(LLOQ=2 nM)、特异性、精密度、准确度、回收率、基质效应和稳定性在大鼠脑脊液(CSF)和血浆中进行了评估。除了柱选择、离子对试剂和样品纯化等一些现有考虑因素外,我们的工作还集中在以下四个子主题上:1)选择适当的多重反应监测(MRM)转换,以最大限度地提高痕量生物样品中 ASO 的灵敏度;2)利用通用无风险内标(替诺福韦)避免通常在 LC-MS 测定中使用的寡体内标引起的串扰干扰;3)自动化样品制备过程以提高精密度和通量;4)比较液-液萃取(LLE)和固相萃取(SPE)作为寡核苷酸方法开发中的样品纯化方法。该研究定量测定了鞘内注射后 MALAT-1 ASO 在大鼠 CSF 和血浆中的浓度,并使用两种基质之间的差异来评估注射技术。研究结果为进一步的内部寡核苷酸发现和开发提供了坚实的基础。

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