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采用实验方法学(DOE)的田口设计优化非去污剂处理对包膜病毒的灭活。

Optimization of non-detergent treatment for enveloped virus inactivation using the Taguchi design of experimental methodology (DOE).

机构信息

a Department of Recombinant Hepatitis B Vaccine, Production and Research Complex , Pasteur Institute of Iran , Tehran , Iran.

b Viral Vaccines Research Center , Pasteur Institute of Iran , Tehran , Iran.

出版信息

Prep Biochem Biotechnol. 2019;49(7):686-694. doi: 10.1080/10826068.2019.1599398. Epub 2019 Apr 29.

DOI:10.1080/10826068.2019.1599398
PMID:31035907
Abstract

In mammalian cell culture technology, viral contamination is one of the main challenges; and, so far, various strategies have been taken to remove or inactivate viruses in the cell-line production process. The suitability and feasibility of each method are determined by different factors including effectiveness in target virus inactivation, maintaining recombinant protein stability, easiness-in terms of the process condition, cost-effectiveness, and eco-friendliness. In this research, Taguchi design-of-experiments (DOE) methodology was used to optimize a non-detergent viral inactivation method via considering four factors of temperature, time, pH, and alcohol concentration in an unbiased (orthogonal) fashion with low influence of nuisance factors. Herpes Simplex Virus-1 (HSV1) and Vero cell-line were used as models for enveloped viruses and cell-line, respectively. Examining the cytopathic effects (CPE) in different dilutions showed that pH (4), alcohol (15%), time (120 min), and temperature (25 °C) were the optimal points for viral inactivation. Evaluating the significance of each parameter in the HSV-1 inactivation using Taguchi and ANOVA analyses, the contributions of pH, alcohol, temperature and time were 56.5%, 19.2%, 12%, and 12%, respectively. Examining the impact of the optimal viral treatment condition on the stability of model recombinant protein-recombinant human erythropoietin, no destabilization was detected.

摘要

在哺乳动物细胞培养技术中,病毒污染是主要挑战之一;到目前为止,已经采取了各种策略来去除或灭活细胞系生产过程中的病毒。每种方法的适用性和可行性取决于不同的因素,包括目标病毒灭活的有效性、保持重组蛋白稳定性、过程条件的难易程度、成本效益和生态友好性。在这项研究中,田口实验设计 (DOE) 方法被用于通过以无偏(正交)的方式考虑温度、时间、pH 和酒精浓度这四个因素来优化非去污剂病毒灭活方法,以最小化干扰因素的影响。单纯疱疹病毒 1 (HSV1) 和 Vero 细胞系分别被用作包膜病毒和细胞系的模型。通过不同稀释度检查细胞病变效应 (CPE),表明 pH 值(4)、酒精(15%)、时间(120 分钟)和温度(25°C)是病毒灭活的最佳点。使用田口和 ANOVA 分析评估每个参数对 HSV-1 灭活的重要性,pH、酒精、温度和时间的贡献分别为 56.5%、19.2%、12%和 12%。检查最佳病毒处理条件对模型重组蛋白-重组人促红细胞生成素稳定性的影响,未检测到蛋白不稳定。

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