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首页> 外文期刊>Vaccine >Size-exclusion HPLC provides a simple, rapid, and versatile alternative method for quality control of vaccines by characterizing the assembly of antigens
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Size-exclusion HPLC provides a simple, rapid, and versatile alternative method for quality control of vaccines by characterizing the assembly of antigens

机译:体积排阻HPLC通过表征抗原装配为疫苗质量控制提供了一种简单,快速,通用的替代方法

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摘要

The assembly of antigen structure is often crucial to the potency of vaccines. Currently adopted methods like animal testing and ultracentrifugation take long time and are difficult to automate for multiple samples. Here we develop a size-exclusion high-performance liquid chromatography (SE-HPLC) method to characterize the assembly of antigen structure during both manufacturing process and storage. Three important vaccine antigens including inactivated foot and mouth disease virus (FMDV), which is a virus vaccine; and two virus-like particles (VLPs) vaccines involving hepatitis B core antigen (HBcAg)VLPs, and hepatitis B surface antigen (HBsAg) VLPs, were successfully analyzed using commercially available TSK gel columns with pore size above 45 nm. Combined with other analytical methods including SDS-PAGE, dynamic light scattering, wavelength scan, and multi-angle laser light scattering, the SE-HPLC method was proven to be a simple, rapid, and reliable tool for antigen particles assembly analysis. Specifically, for FMDV whole virus particle, SE-HPLC was used to analyze 146S content in vaccine preparations and the thermal dissociation of the 146S. For HBcAg-VLPs that are expressed in recombinant Escherichia coli, its expression level during cell culture process was quantitatively monitored by SE-HPLC. The SE-HPLC also showed applicability for quality check of HBsAg vaccine preparations by monitoring the product consistency of different lot number and the product stability during storage. Results shown in this work clearly demonstrated that SE-HPLC method has potential as a versatile alternative technology for control of the final product by both manufacturers and the regulatory agencies. (C) 2015 Elsevier Ltd. All rights reserved.
机译:抗原结构的组装通常对疫苗的效力至关重要。目前采用的方法(例如动物测试和超速离心)需要很长时间,并且很难自动化处理多个样品。在这里,我们开发了一种排阻高效液相色谱(SE-HPLC)方法,以表征制造过程和存储过程中抗原结构的组装。三种重要的疫苗抗原包括灭活的口蹄疫病毒(FMDV),它是一种病毒疫苗;使用孔径大于45 nm的市售TSK凝胶柱成功地分析了两种涉及乙型肝炎核心抗原(HBcAg)VLP和乙型肝炎表面抗原(HBsAg)VLP的病毒样颗粒(VLP)疫苗。结合SDS-PAGE,动态光散射,波长扫描和多角度激光散射等其他分析方法,SE-HPLC方法被证明是一种简单,快速且可靠的抗原颗粒组装分析工具。具体而言,对于FMDV全病毒颗粒,使用SE-HPLC分析疫苗制剂中146S的含量和146S的热解离。对于在重组大肠杆菌中表达的HBcAg-VLP,通过SE-HPLC定量监测其在细胞培养过程中的表达水平。 SE-HPLC还通过监测不同批号的产品一致性和储存过程中的产品稳定性,还显示出适用于HBsAg疫苗制剂质量检查的适用性。这项工作中显示的结果清楚地表明,SE-HPLC方法具有作为制造商和监管机构控制最终产品的通用替代技术的潜力。 (C)2015 Elsevier Ltd.保留所有权利。

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