首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >On-line separation and quantification of virus antigens of different serotypes in multivalent vaccines by capillary zone electrophoresis: A case study for quality control of foot-and-mouth disease virus vaccines
【24h】

On-line separation and quantification of virus antigens of different serotypes in multivalent vaccines by capillary zone electrophoresis: A case study for quality control of foot-and-mouth disease virus vaccines

机译:用毛细管电泳在多价疫苗中不同血清型病毒抗原的在线分离和定量 - 一种口蹄疫病毒疫苗质量控制的案例研究

获取原文
获取原文并翻译 | 示例
           

摘要

Accurate quantification of effective antigens of different serotypes is crucial for quality control of multivalent vaccines but challenging. A simple and rapid capillary zone electrophoresis (CZE) method was developed for on-line separation and quantification of foot-and-mouth disease virus (FMDV) antigens in monovalent and bivalent FMDV vaccines. The FMDV peak identity in CZE was demonstrated by the study of FMDV dissociation combined with high performance size exclusion chromatography (HPSEC) analysis. After optimizing CZE conditions including UV detecting wavelength, injection volume, and separation voltage, both serotype A and O FMDV showed good reproducibility (RSD <5%) and linear responses (R-2 =0.999) between the peak area and FMDV content in the concentration range of 15-400 mu g/mL. The two serotypes of FMDV with similar size had different migration time in CZE according to their different zeta potential, which allows them to be separated and quantified, with accuracy of <10% relative error. CZE was then successfully applied for antigen quantification of commercial O monovalent and A/O bivalent FMDV vaccines. Compared with HPSEC, CZE was not only able to quantify each serotype of FMDV, but also free from interference of nucleic acids impurities. In summary, the CZE can be a simple, rapid, and reliable tool for quality control of monovalent and bivalent FMDV vaccines. The CZE method can also be further extended to the quality control of other multivalent virus and virus like particle vaccines. (C) 2020 Elsevier B.V. All rights reserved.
机译:不同血清型有效抗原的准确定量对于多价疫苗的质量控制至关重要,但具有挑战性。建立了一种简单快速的毛细管区带电泳(CZE)方法,用于在线分离和定量检测单价和二价口蹄疫疫苗中的口蹄疫病毒(FMDV)抗原。通过对口蹄疫病毒解离的研究,结合高效液相色谱(HPSEC)分析,证实了CZE中口蹄疫病毒峰的一致性。优化了CZE条件,包括紫外检测波长、进样量和分离电压,在15-400μg/mL的浓度范围内,A型和O型口蹄疫病毒的峰面积与口蹄疫病毒含量之间均表现出良好的重现性(RSD<5%)和线性响应(R-2=0.999)。根据zeta电位的不同,大小相似的两种血清型口蹄疫病毒在CZE中的迁移时间不同,这使得它们能够被分离和定量,准确度相对误差<10%。CZE随后成功地应用于商用O单价和A/O二价FMDV疫苗的抗原定量。与HPSEC相比,CZE不仅能够定量检测口蹄疫的各个血清型,而且不受核酸杂质的干扰。总之,CZE可以作为一种简单、快速、可靠的工具,用于单价和二价口蹄疫疫苗的质量控制。CZE方法还可以进一步扩展到其他多价病毒和病毒样颗粒疫苗的质量控制。(C) 2020爱思唯尔B.V.版权所有。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号