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

机译:猪源性胰酶对伪狂犬病病毒,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

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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 degrees 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. (C) 2014 Elsevier B.V. All rights reserved.
机译:胰酶是一种含有酶的物质,主要是淀粉酶,脂肪酶和蛋白酶。它是从牛或猪的胰腺中获得的,用于治疗人的胰腺内分泌功能不全。法规和安全问题要求在生物药物(如胰酶)中清除病毒(清除病毒或使其失活)。通过测试一组四种动物病毒:伪狂犬病病毒(PRV),脑心肌炎病毒(EMCV),牛病毒性腹泻病毒(BVDV)和猪病毒,进行了病毒验证研究,以评估在真空干燥的最后步骤中获得的病毒清除率细小病毒(PPV)。由于该产品具有杀病毒作用和高细胞毒性,因此将原料稀释至重悬于13.5 mL细胞培养基中的0.67 g干燥胰酶的比例,然后在加标之前在细胞培养基中稀释50倍。在60 +/- 1摄氏度下加热5小时后,将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。病毒减少因子的范围从5.59(对于PPV)到7.07(对于EMCV),没有观察到病毒斑块,表明该工艺步骤可有效减少和去除病毒污染。尽管迄今尚无胰酶中病毒污染事件的报道,但为了确保其灭活和/或清除病毒污染能力的能力,特别是从人畜共患的病毒性药物(例如戊型肝炎病毒和诺如病毒)中进行评估,对于生产过程的评估是必要的。动物来源生物药品的病毒安全性。 (C)2014 Elsevier B.V.保留所有权利。

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