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LC-MS/MS quantification of next-generation biotherapeutics: A case study for an IgE binding Nanobody in cynomolgus monkey plasma

机译:LC-MS / MS定量分析下一代生物疗法:食蟹猴血浆中结合IgE的纳米抗体的案例研究

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Background: Nanobodies? are therapeutic proteins derived from the smallest functional fragments of heavy chain-only antibodies. The development and validation of an LC-MS/MS-based method for the quantification of an IgE binding Nanobody in cynomolgus monkey plasma is presented. Results: Nanobody quantification was performed making use of a proteotypic tryptic peptide chromatographically enriched prior to LC-MS/MS analysis. The validated LLOQ at 36 ng/ml was measured with an intra- and inter-assay precision and accuracy 20%. The required sensitivity could be obtained based on the selectivity of 2D LC combined with MS/MS. No analyte specific tools for affinity purification were used. Plasma samples originating from a PK/PD study were analyzed and compared with the results obtained with a traditional ligand-binding assay. Excellent correlations between the two techniques were obtained, and similar PK parameters were estimated. Conclusion: A 2D LC-MS/MS method was successfully developed and validated for the quantification of a next generation biotherapeutic.
机译:背景:纳米抗体?是源自仅重链抗体的最小功能片段的治疗性蛋白质。提出了开发和验证基于LC-MS / MS的食蟹猴血浆中IgE结合纳米抗体定量方法。结果:在LC-MS / MS分析之前,使用色谱富集的蛋白型胰蛋白酶肽对纳米​​抗体进行定量。以批内和批间精密度和准确度<20%的方式测量经验证的36 ng / ml LLOQ。可以基于2D LC与MS / MS的选择性来获得所需的灵敏度。没有使用用于亲和纯化的分析物专用工具。分析了来自PK / PD研究的血浆样品,并将其与传统配体结合测定所获得的结果进行了比较。获得了两种技术之间的极好的相关性,并估计了相似的PK参数。结论:成功开发了二维LC-MS / MS方法,并验证了该方法可用于下一代生物治疗药物的定量。

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