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完整 mAb LC-MS 用于临床前研究的药物浓度测定:生物分析方法性能和体内样本。

Intact mAb LC-MS for drug concentration from pre-clinical studies: bioanalytical method performance and in-life samples.

机构信息

Bioanalysis, Immunogenicity & Biomarkers, GSK, 1250 S. Collegeville Rd., Collegeville, PA 19426, USA.

Scientific Operations, Waters Corporation, 34 Maple St, Milford, MA 01757, USA.

出版信息

Bioanalysis. 2020 Oct;12(19):1389-1403. doi: 10.4155/bio-2020-0168. Epub 2020 Sep 25.

DOI:10.4155/bio-2020-0168
PMID:32975433
Abstract

Antibody biotherapeutic measurement from pharmacokinetic studies has not been traditionally based on intact molecular mass as is the case for small molecules. However, recent advancements in protein capture and mass spectrometer technology have enabled intact mass detection and quantitation for dosed biotherapeutics. A bioanalytical method validation is part of the regulatory requirement for sample analysis to determine drug concentration from in-life study samples. Here, an intact protein LC-MS assay is subjected to mock bioanalytical method validation, and unknown samples are compared between intact protein LC-MS and established bioanalytical assay formats: Ligand-binding assay and peptide LC-MS/MS. Results are presented from the intact and traditional bioanalytical method evaluations, where the in-life sample concentrations were comparable across method types with associated data analyses presented. Furthermore, for intact protein LC-MS, modification monitoring and evaluation of data processing parameters is demonstrated.

摘要

抗体生物治疗药物的药代动力学研究中的测量方法并不像小分子药物那样基于完整的分子质量。然而,最近蛋白质捕获和质谱仪技术的进步使得对给药的生物治疗药物的完整质量检测和定量成为可能。生物分析方法验证是样品分析的监管要求的一部分,目的是从体内研究样品中确定药物浓度。在这里,对完整蛋白 LC-MS 分析方法进行了模拟生物分析方法验证,并将完整蛋白 LC-MS 与已建立的生物分析测定方法格式:配体结合测定法和肽 LC-MS/MS 进行了未知样品的比较。提供了完整蛋白和传统生物分析方法评估的结果,其中方法类型之间的体内样本浓度具有可比性,并给出了相关数据分析。此外,对于完整蛋白 LC-MS,还展示了修饰监测和数据处理参数的评估。

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