重组牛生长激素中工艺特异性大肠杆菌宿主细胞污染物蛋白的免疫配位定量分析。

M L Whitmire, L C Eaton
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引用次数: 11

摘要

我们开发了一种阈值系统免疫oligand测定法,用于定量somavuabove(正常序列重组牛生长激素)中残留的、工艺特异性的大肠杆菌宿主细胞污染物蛋白(HCP)。该分析的动态范围为2至160 ng/mL,定量限为2 ng/mL。上述实验室标准中指定的somavav6次重复的日分析精密度(CV)为3.0%。本标准多次测定运行(共69个实验室标准重复)的累积分析精密度为8.4%。保守的警戒限度为100 ng/mL,以确保在化学计量抗体过量的条件下每个测定样品的分析精度。虽然该试验是设计用于谱释放规格试验,但它也被用于验证通过专有的somavubove纯化工艺去除HCP。这种用法符合与“表征良好”的重组生物制药蛋白相关的监管指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An immunoligand assay for quantitation of process specific Escherichia coli host cell contaminant proteins in a recombinant bovine somatotropin.

We have developed a Threshold System immunoligand assay for the quantitation of residual, process-specific, Escherichia coli host cell contaminant proteins (HCP) in somavubove (a normal sequence recombinant bovine somatotropin). The assay has a dynamic range of 2 to 160 ng/mL, with a limit of quantitation of 2 ng/mL. Daily analytical precision (CV) for six replicates of the designated somavubove laboratory standard is 3.0%. Cumulative analytical precision for multiple assay runs of this standard (a total of 69 laboratory standard replicates) is 8.4%. A conservative alert limit of 100 ng/mL has been assigned in order to assure analytical precision for each assay sample under conditions of stoichiometric antibody excess. Although the assay was designed for use as a profile-release specification assay, it has also been used to validate removal of HCP by the proprietary somavubove purification process. This use is consistent with regulatory guidelines related to "well characterized" recombinant biopharmaceutical proteins.

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