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猪源胰酶中伪狂犬病病毒、脑心肌炎病毒、牛病毒性腹泻病毒和猪细小病毒的病毒灭活评估

Evaluation of viral inactivation of pseudorabies virus, encephalomyocarditis virus, bovine viral diarrhea virus and porcine parvovirus in pancreatin of porcine origin.

作者信息

Caruso C, Gobbi E, Biosa T, Andra' M, Cavallazzi U, Masoero L

机构信息

Department of Virology, Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta, Turin, Italy.

Department of Virology, Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta, Turin, Italy.

出版信息

J Virol Methods. 2014 Nov;208:79-84. doi: 10.1016/j.jviromet.2014.07.032. Epub 2014 Aug 7.

Abstract

Pancreatin is a substance containing enzymes, principally amylase, lipase, and protease. It is obtained from bovine or porcine pancreas and used in the treatment of pancreatic endocrine insufficiency in humans. Regulations and safety concerns mandate viral clearance (virus removal or inactivation) in biopharmaceuticals such as pancreatin. A virus validation study was performed to evaluate virus clearance achieved in the final step of drying under vacuum by testing a panel of four animal viruses: Pseudorabies virus (PRV), Encephalomyocarditis virus (EMCV), Bovine viral diarrhea virus (BVDV), and Porcine parvovirus (PPV). Because of the product's virucidal effect and high cytotoxicity, the starting material was diluted to a ratio of 0.67 g of dried pancreatin resuspended in 13.5 mL of cell culture medium followed by a 50-fold dilution in cell culture medium before spiking. After heating at 60±1°C for 5 h, the samples were diluted about 5-fold in cell culture medium and titered by the plaque assay method. The virus reduction factor ranged from 5.59 (for PPV) to 7.07 (for EMCV) and no viral plaque was observed, indicating that the process step was effective in the reduction and removal of virus contamination. Though no virus contamination events in pancreatin have been reported to date, evaluation of the production process for its ability to inactivate and/or remove virus contamination, particularly from zoonotic viral agents such as hepatitis E virus and Norovirus considered emerging pathogens, is necessary to ensure the viral safety of animal-derived biopharmaceuticals.

摘要

胰酶是一种含有多种酶的物质,主要包括淀粉酶、脂肪酶和蛋白酶。它是从牛或猪的胰腺中提取的,用于治疗人类胰腺内分泌功能不全。法规和安全问题要求对胰酶等生物制药进行病毒清除(病毒去除或灭活)。进行了一项病毒验证研究,通过检测一组四种动物病毒:伪狂犬病病毒(PRV)、脑心肌炎病毒(EMCV)、牛病毒性腹泻病毒(BVDV)和猪细小病毒(PPV),来评估在真空干燥的最后一步中实现的病毒清除效果。由于该产品具有杀病毒作用和高细胞毒性,起始物料被稀释至0.67 g干燥胰酶重悬于13.5 mL细胞培养基中的比例,然后在接种前在细胞培养基中进行50倍稀释。在60±1°C加热5小时后,样品在细胞培养基中稀释约5倍,并通过噬斑测定法进行滴定。病毒减少因子范围从5.59(针对PPV)到7.07(针对EMCV),且未观察到病毒噬斑,表明该工艺步骤在减少和去除病毒污染方面是有效的。尽管迄今为止尚未报道胰酶中有病毒污染事件,但评估生产工艺灭活和/或去除病毒污染的能力,特别是来自诸如戊型肝炎病毒和诺如病毒等人畜共患病毒病原体(被视为新兴病原体)的污染能力,对于确保动物源生物制药的病毒安全性是必要的。

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