鉴定单克隆抗体和蛋白质疫苗抗原生物物理特性的差示扫描量热法

M. Kirkitadze, Jian Hu, Mei Tang, B. Carpick
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引用次数: 4

摘要

背景:分析方法确认包括对验证特征子集的简化评估,目的是证明分析方法是科学合理的,适合其预期用途。与验证相反,分析方法的确认是在没有预定义的可接受标准的情况下进行的。确认可以作为方法验证的先决条件,或者当产品知识分析尚未建立为关键产品质量属性的测试时。本研究的重点是鉴别用于检测蛋白质疫苗抗原和单克隆抗体产物的热稳定性和三级结构的差示扫描量热法。通过对可重复性和中间精密度特性的评价,评价了分析参数的精密度。结论:该方法符合要求的性能指标,适用于不同类型的药材。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Qualification of a differential scanning calorimetry method for biophysical characterization of monoclonal antibodies and protein vaccine antigens
Background: Analytical method qualification consists of a simplified evaluation of a subset of validation characteristics with a goal to demonstrate that an analytical method is scientifically sound and suitable for its intended use. In contrast to validation, analytical method qualification is performed without predefined acceptability criteria. Qualification may be performed as a prerequisite to method validation, or when an assay for product knowledge has not yet been established as a test for a critical product quality attribute. Methodology The focus of this study was the qualification of a differential scanning calorimetry method that is used to examine thermal stability and tertiary structure of protein vaccine antigens and monoclonal antibody products. The analytical parameter evaluated was precision, through assessment of the characteristics of repeatability and intermediate precision. Conclusion: The results demonstrated that the assay met the desired performance characteristics, and is suitable...
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